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Mark Daly

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Genes & Molecular Sequences

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Samira Bahl; Roberta L Beauchamp; Colby Chiang; Mark J Daly; James F Gusella; Benjamin M Neale; Michael E Talkowski; Vijaya Ramesh
Lack of association of rare functional variants in TSC1/TSC2 genes with autism spectrum disorder.
Jacqueline I Goldstein; George B Grant; Christina M Hultman; Jared Maguire; Steven A McCarroll; Jennifer L Moran; Jason Carey; Kimberly Chambert; Andrew Crenshaw; Mark J Daly; Menachem Fromer; Colm O'Dushlaine; Shaun Purcell; Pamela Sklar; Christine Stevens; Patrick F Sullivan; Benjamin M Neale
zCall: a rare variant caller for array-based genotyping: genetics and population analysis.
Kasper Lage; Blake C Ballif; Søren Brunak; Mark J Daly; Patricia K Donahoe; Joshua M Gorham; Steven C Greenway; Sonia M Mesquita; William T Pu; Amy E Roberts; Jill A Rosenfeld; Ayellet V Segrè; Christine E Seidman; Jonathan G Seidman; Lisa G Shaffer; Leslie B Smoot; Niels Tommerup; Hiroko Wakimoto; Alexandre C Pereira; Lars A Larsen
Genetic and environmental risk factors in congenital heart disease functionally converge in protein networks driving heart development.

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All Publications

2013: Samira Bahl; Roberta L Beauchamp; Colby Chiang; Mark J Daly; James F Gusella; Benjamin M Neale; Michael E Talkowski; Vijaya Ramesh
Lack of association of rare functional variants in TSC1/TSC2 genes with autism spectrum disorder.
Molecular autism 2013;4(1):5.
2012: Jacqueline I Goldstein; George B Grant; Christina M Hultman; Jared Maguire; Steven A McCarroll; Jennifer L Moran; Jason Carey; Kimberly Chambert; Andrew Crenshaw; Mark J Daly; Menachem Fromer; Colm O'Dushlaine; Shaun Purcell; Pamela Sklar; Christine Stevens; Patrick F Sullivan; Benjamin M Neale
zCall: a rare variant caller for array-based genotyping: genetics and population analysis.
Bioinformatics (Oxford, England) 2012;28(19):2543-5.
2012: Kasper Lage; Blake C Ballif; Søren Brunak; Mark J Daly; Patricia K Donahoe; Joshua M Gorham; Steven C Greenway; Sonia M Mesquita; William T Pu; Amy E Roberts; Jill A Rosenfeld; Ayellet V Segrè; Christine E Seidman; Jonathan G Seidman; Lisa G Shaffer; Leslie B Smoot; Niels Tommerup; Hiroko Wakimoto; Alexandre C Pereira; Lars A Larsen
Genetic and environmental risk factors in congenital heart disease functionally converge in protein networks driving heart development.
Proceedings of the National Academy of Sciences of the United States of America 2012;109(35):14035-40.
2012: John F Staropoli; Winnie Xin; Jose E Abdenur; Rosemary Barone; Scott H Coppel; Mark J Daly; Naser Elbalalesy; Amel Karaa; Andrew Kirby; Karen B Leydiker; Elaine T Lim; Marcy E MacDonald; Stephen G Romansky; Katherine B Sims; Susan L Cotman
A homozygous mutation in KCTD7 links neuronal ceroid lipofuscinosis to the ubiquitin-proteasome system.
American journal of human genetics 2012;91(1):202-8.
2012: Colby Chiang; Mark J Daly; Carl Ernst; Richard L M Faull; James F Gusella; Ira M Hall; Carrie Hanscom; Adrian Heilbut; Jessie C Jacobsen; Andrew Kirby; Charles Lee; Amelia M Lindgren; Marcy E MacDonald; C McLaughlan; Ryan E Mills; Cynthia C Morton; Toshiro K Ohsumi; Suzanne J Reid; Skye R Rudiger; Yiping Shen; Russell G Snell; C Simon Bawden; Ian Blumenthal; Mark L Borowsky; Michael E Talkowski
Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integration.
Nature genetics 2012;44(4):390-7, S1.
2012: Yi Yu; Mark J Daly; Robyn Reynolds; Bernard Rosner; Johanna M Seddon
Prospective assessment of genetic effects on progression to different stages of age-related macular degeneration using multistate Markov models.
Investigative ophthalmology & visual science 2012;53(3):1548-56.
2012: G A Walford; J G Wilson; B Neale; S F A Grant; J I Rotter; D S Siscovick; J B Meigs; C S Fox; Tamara Isakova; Mark J Daly; J S Pankow; D W Bowden; T Green; J C Florez
Common genetic variants differentially influence the transition from clinically defined states of fasting glucose metabolism.
Diabetologia 2012;55(2):331-9.
2012: Lillian M Zwemer; Andrew Chess; Mark J Daly; Andrew Kirby; Benjamin R Thompson; Alexander Zak; Alexander A Gimelbrant
Autosomal monoallelic expression in the mouse.
Genome biology 2012;13(2):R10.
2012: Nicholette D Palmer; Bong H Roh; Assiamira Ferrara; Goncalo R Abecasis; David Altshuler; Najaf Amin; Ping An; Kristin Ardlie; Yavuz Ariyurek; Yurii S Aulchenko; Beverley Balkau; Inês Barroso; Philip Barter; John P Beilby; Rafn Benediktsson; Amanda J Bennett; Yoav Ben-Shlomo; Richard N Bergman; Sven Bergmann; Roza Blagieva; Murielle Bochud; Bernhard O Boehm; Michael Boehnke; Eric Boerwinkle; Amélie Bonnefond; Lori L Bonnycastle; Dorret I Boomsma; Knut Borch-Johnsen; Ingrid B Borecki; Stefan R Bornstein; Kristina Bengtsson Boström; Yvonne Böttcher; Nabila Bouatia-Naji; Bert Bravenboer; Eric Brunner; Thomas A Buchanan; Suzannah Bumpstead; Suzannah J Bumpstead; Noël P Burtt; Harry Campbell; Antonio Cao; Stephane Cauchi; Christine Cavalcanti-Proença; Guillaume Charpentier; Yii-Der Ida Chen; Peter Chines; Peter S Chines; Robert Clarke; Lachlan J M Coin; Francis S Collins; Cyrus Cooper; Matthew N Cooper; Marilyn Cornelis; David J Couper; Gabe Crawford; Laura Crisponi; Mark J Daly; Ian N M Day; Eco J C de Geus; George V Dedoussis; Abbas Dehghan; Panos Deloukas; Jerome Delplanque; Christian Dina; Alex Doney; Alex S F Doney; Josée Dupuis; Shah Ebrahim; Josephine M Egan; Amanda Elliott; Amanda L Elliott; Katherine S Elliott; Paul Elliott; Michael R Erdos; Annette C Fedson; Teresa Ferreira; Luigi Ferrucci; Antje Fischer-Rosinsky; Jose C Florez; Nita G Forouhi; Caroline S Fox; Christopher S Franklin; Paul W Franks; Rune Frants; Maria Grazia Franzosi; Timothy M Frayling; Philippe Froguel; Pilar Galan; Martha Ganser; Christian Gieger; Nicole L Glazer; Anna L Gloyn; Anuj Goel; Mark O Goodarzi; Jürgen Graessler; Harald Grallert; Niels Grarup; Todd Green; Simon Griffin; Leif Groop; Christopher J Groves; Scott Grundy; Candace Guiducci; Rhian Gwilliam; Ulf Gyllensten; Samy Hadjadj; Göran Hallmans; Naomi Hammond; Anders Hamsten; Xijing Han; Torben Hansen; Anna-Liisa Hartikainen; Neelam Hassanali; Andrew T Hattersley; Caroline Hayward; Simon C Heath; Peter Henneman; Serge Hercberg; Christian Herder; Andrew A Hicks; Winston A Hide; David R Hillman; Aroon D Hingorani; Graham A Hitman; Albert Hofman; Oliver M Hofmann; Jouke Jan Hottenga; Frank B Hu; Jennie Hui; Joe Hung; David J Hunter; Cornelia Huth; Kristian Hveem; Thomas Illig; Erik Ingelsson; Bo Isomaa; Anne U Jackson; Marjo-Riitta Jarvelin; Paul R V Johnson; Toby Johnson; Torben Jørgensen; Antti Jula; Marika Kaakinen; Stavroula Kanoni; WEN KAO; W H Linda Kao; Jaakko Kaprio; Fredrik Karpe; Y Antero Kesaniemi; Mika Kivimaki; Norman Klopp; Beatrice Knight; Augustine Kong; Seppo Koskinen; Peter Kovacs; Peter Kraft; Meena Kumari; Johanna Kuusisto; Kirsten Ohm Kyvik; Markku Laakso; Taina Lajunen; Claudia Langenberg; G Mark Lathrop; Torsten Lauritzen; Debbie A Lawlor; Olivier Le Bacquer; Cécile Lecoeur; Man Li; Yun Li; Aloysius Lieverse; Lars Lind; Cecilia M Lindgren; Ruth J F Loos; Jian'an Luan; Valeriya Lyssenko; Reedik Mägi; Patrik K E Magnusson; Robert Mahley; Massimo Mangino; Alisa K Manning; Michael Marmot; Michel Marre; María Teresa Martínez-Larrad; Jarred B McAteer; Steven A McCarroll; Steve A McCarroll; Mark I McCarthy; Laura J McCulloch; Ruth McPherson; James B Meigs; Christa Meisinger; Thomas Meitinger; David Melzer; Pierre Meneton; David Meyre; Kristian Midthjell; Braxton D Mitchell; Karen L Mohlke; Vincent Mooser; Mario A Morken; Andrew D Morris; Andrew P Morris; Sutapa Mukherjee; Silvia Naitza; Narisu Narisu; David M Nathan; Pau Navarro; Matthew J Neville; Peter Nilsson; Jeffrey R O'Connell; Ben A Oostra; Marco Orrù; Katharine R Owen; Ruth Pakyz; Colin N A Palmer; Lyle J Palmer; James S Pankow; Giuseppe Paolisso; Cristian Pattaro; François Pattou; Felicity Payne; Daniel Pearson; John F Peden; Nancy L Pedersen; Oluf Pedersen; Leena Peltonen; Brenda W J H Penninx; Markus Perola; John R B Perry; Ann-Kristin Petersen; Andreas F H Pfeiffer; Irene Pichler; Carl Platou; Ozren Polasek; Danielle Posthuma; Simon C Potter; Anneli Pouta; Peter Paul Pramstaller; Peter P Pramstaller; Christine Proença; Inga Prokopenko; Michael A Province; Bruce M Psaty; Lu Qi; Joshua Randall; Wolfgang Rathmann; Soumya Raychaudhuri; N William Rayner; Nigel W Rayner; Kenneth Rice; Samuli Ripatti; Fernando Rivadeneira; Neil R Robertson; Rosa Maria Roccasecca; Ghislain Rocheleau; Michael Roden; Olov Rolandsson; Jerome I Rotter; Igor Rudan; Aimo Ruokonen; Denis Rybin; Veikko Salomaa; Michael J Sampson; Annelli Sandbaek; Manjinder Sandhu; Serena Sanna; Richa Saxena; Avan Aihie Sayer; Paul Scheet; David Schlessinger; Peter Schwarz; Laura J Scott; Angelo Scuteri; Udo Seedorf; Ayellet V Segrè; Manuel Serrano-Ríos; Praveen Sethupathy; Stephen J Sharp; Beverley Shields; Beverley M Shields; Peter Shrader; Alan R Shuldiner; Gunnar Sigurdsson; Eric Sijbrands; Eric J G Sijbrands; Kaisa Silander; Angela Silveira; Laila Simpson; Andrew Singleton; David S Siscovick; Rob Sladek; George Davey Smith; Nicholas L Smith; Kijoung Song; Nicole Soranzo; Ulla Sovio; Thomas Sparsø; Timothy D Spector; Joachim Spranger; Kari Stefansson; Lincoln D Stein; Valgerdur Steinthorsdottir; Klaus Strassburger; Heather M Stringham; Michael Stumvoll; Qi Sun; Amy Swift; Amy J Swift; Holly Syddall; Ann-Christine Syvänen; Toshiko Tanaka; Barbara Thorand; Gudmar Thorleifsson; Unnur Thorsteinsdottir; Jean Tichet; Nicholas J Timpson; Anke Tönjes; Tiinamaija Tuomi; Jaakko Tuomilehto; Manuela Uda; Andre Uitterlinden; André G Uitterlinden; Timo T Valle; Rob M van Dam; Ko Willems van Dijk; Cornelia M van Duijn; Timon W van Haeften; Thijs van Herpt; Mandy van Hoek; Jana V van Vliet-Ostaptchouk; Dhiraj Varma; Sophie Visvikis-Siest; Veronique Vitart; Nicole Vogelzangs; Benjamin F Voight; Peter Vollenweider; Gérard Waeber; Peter J Wagner; Mark Walker; Andrew Walley; Gudmundur Bragi Walters; Kim L Ward; Nicholas J Wareham; Richard M Watanabe; Dawn M Waterworth; Hugh Watkins; Michael N Weedon; Ryan P Welch; Eleanor Wheeler; H-Erich Wichmann; Cisca Wijmenga; Sarah H Wild; Gonneke Willemsen; Cristen J Willer; Gordon H Williams; James F Wilson; Jacqueline Witteman; Jaqueline C M Witteman; Alan F Wright; Guanming Wu; John W G Yarnell; Carina Zabena; Eleftheria Zeggini; Diana Zelenika; Björn Zethelius; Guangju Zhai; Jing Hua Zhao; M Carola Zillikens; Barry I Freedman; Charles N Rotimi; Jasmin Divers; Lingyi Lu; Megan E Rudock; Carl D Langefeld; Michele M Sale; Adebowale Adeyemo; Pamela J Hicks; Donald W Bowden; Julie T Ziegler; Maggie C Y Ng; Daniel Shriner; Matthew E Talbert; Maria R Wing; Meredith A Bostrom; Joshua P Lewis; S Sandy An; Jessica N Cooke; Caitrin W McDonough; Jessica M Hester; Robert Sladek
A genome-wide association search for type 2 diabetes genes in African Americans.
PloS one 2012;7(1):e29202.
2011: Soumya Raychaudhuri; Robyn Reynolds; Stephan Ripke; Albert K Tai; Perciliz L Tan; Soumya Vemuri; Yi Yu; Donald J Zack; Betsy Campochiaro; Peter A Campochiaro; Kimberly Chin; Mark J Daly; Sivakumar Gowrisankar; Oleg Iartchouk; Nicholas Katsanis; Kate Montgomery; Johanna M Seddon
A rare penetrant mutation in CFH confers high risk of age-related macular degeneration.
Nature genetics 2011;43(12):1232-6.
2011: Manuel A Rivas; Phil Schumm; Yashoda Sharma; Mark S Silverberg; Christine Stevens; Leif Törkvist; Ramnik J Xavier; Clarence K Zhang; David Altshuler; Mélissa Beaudoin; Gabrielle Boucher; Steven R Brant; Noel Burtt; Judy H Cho; Mauro D'Amato; Marla C Dubinsky; Richard H Duerr; David Ellinghaus; Tim Fennell; Andre Franke; Stacey Gabriel; Agnes Gardet; Philippe Goyette; Todd Green; Jonas Halfvarson; Talin Haritunians; Andrew Kirby; Joshua M Korn; Finny Kuruvilla; Caroline Lagacé; Anna Latiano; Guillaume Lettre; Ken Sin Lo; Dermot P B McGovern; Benjamin Neale; John D Rioux; Stephan Ripke; Mark J Daly
Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease.
Nature genetics 2011;43(11):1066-73.
2011: Johanna M Seddon; Yi Yu; Mark J Daly; Robyn Reynolds; Bernard Rosner
Risk models for progression to advanced age-related macular degeneration using demographic, environmental, genetic, and ocular factors.
Ophthalmology 2011;118(11):2203-11.
2011: Kate M Im; Louise Izatt; Anna Jakubowska; Esther M John; Christiana Kartsonaki; Karin Kast; Tomas Kirchhoff; Robert J Klein; Joshua Korn; Yael Laitman; Conxi Lazaro; Flavio Lejbkowicz; Jan Lubinski; Phuong L Mai; Lesley McGuffog; Hanne E J Meijers-Heijboer; Alfons Meindl; Marco Montagna; Jonathan Morrison; Patrick J Morrison; Steven Narod; Katherine L Nathanson; Susan L Neuhausen; Heli Nevanlinna; Kenneth Offit; Clare T Oliver; Olufunmilayo I Olopade; Ana Osorio; Hilmi Ozcelik; Joan Paterson; Bernard Peissel; Susan Peock; Pedro Perez-Segura; Paolo Peterlongo; Catherine Phelan; Marion Piedmonte; Radka Platte; Mary Porteous; Sabine Preisler-Adams; Timothy R Rebbeck; Gad Rennert; Mark T Rogers; Matti A Rookus; Wendy S Rubinstein; Rita K Schmutzler; V Shane Pankratz; Lucy E Side; Christian F Singer; Olga M Sinilnikova; Melissa C Southey; Dominique Stoppa-Lyonnet; Mary-Beth Terry; Amanda Ewart Toland; Nadine Tung; Christi J van Asperen; Cees E Van Roozendaal; Raymonda Varon-Mateeva; Laurence Venat-Bouvet; Joseph Vijai; Lisa Walker; Xianshu Wang; Barbara Wappenschmidt; Jeffrey N Weitzel; Kristiina Aittomäki; David M Altshuler; Irene L Andrulis; Antonis C Antoniou; Rosa B Barkardottir; Mary S Beattie; Javier Benitez; Ignacio Blanco; Paweł Blecharz; Bernardo Bonanni; Carole Brewer; Saundra S Buys; Trinidad Caldes; Maria Adelaide Caligo; Salina Chan; Georgia Chenevix-Trench; Clement Y Chow; Andrew G Clark; J Margriet Collée; Margaret Cook; Fergus J Couch; Andrew Thomas Crenshaw; Mary B Daly; Mark J Daly; Emma D'Andrea; Michael Dean; Helmut Deissler; Peter Devilee; Susan M Domchek; Mercedes Durán; Douglas F Easton; Ros Eeles; D Gareth Evans; Zachary Fredericksen; Eitan Friedman; Debra Frost; Judy Garber; Mia M Gaudet; Gord Glendon; Andrew K Godwin; Todd Green; Mark H Greene; Candace Guiducci; Ute Hamann; Thomas V O Hansen; Sue Healey; Shirley Hodgson; Frans B Hogervorst; Nicoline Hoogerbrugge; John L Hopper; Tomasz Huzarski; Bert Gold
Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers.
Human genetics 2011;130(5):685-99.
2011: Ida J Hatoum; Chris Cotsapas; Mark J Daly; Danielle M Greenawalt; Marc L Reitman; Lee M Kaplan
Heritability of the weight loss response to gastric bypass surgery.
The Journal of clinical endocrinology and metabolism 2011;96(10):E1630-3.
2011: Yi Yu; Donald J Zack; Haraldur Sigurdsson; R Theodore Smith; Lucia Sobrin; Eric H Souied; Kari Stefansson; Perciliz L Tan; Gudmar Thorleifsson; Unnur Thorsteinsdottir; André G Uitterlinden; Cornelia M van Duijn; Johannes R Vingerling; Rando Allikmets; Paul N Baird; Gaetano R Barile; timothy wayne behrens; Tushar R Bhangale; Milam A Brantley; Gabriëlle H S Buitendijk; Betsy Campochiaro; Peter A Campochiaro; Usha Chakravarthy; Kimberly A Chin; Mark J Daly; Evangelos Evangelou; Jesen Fagerness; Robert R Graham; Omar Gustafsson; Robyn H Guymer; Ruth Hogg; John Ioannidis; Nicholas Katsanis; Caroline C W Klaver; Aaron Y Lee; Phil H Lee; Nicolas Leveziel; Joanna E Merriam; Ward Ortmann; Soumya Raychaudhuri; Robyn Reynolds; Andrea J Richardson; Stephan Ripke; Luba D Robman; Johanna M Seddon
Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration.
Human molecular genetics 2011;20(18):3699-709.
2011: Sara Caroline Widaa; Anand Swaroop; E Shyong Tai; Wan Ting Tay; Herman A Taylor; Natalie Van Zuydam; Jie Jin Wang; James G Wilson; Tin Aung; Matthew Brooks; Monika Buraczynska; Ching J Chen; Mary Frances Cotch; Mark J Daly; Alex S F Doney; Todd Green; Per-Henrik Groop; Vilmundur Gudnason; Kustaa Hietala; Sudha K Iyengar; Richard A Jensen; Barbara E Klein; Ronald Klein; Graham P Leese; Yiyuan Liu; Paul Mitchell; Andrew D Morris; Colin N A Palmer; Alan Penman; Jerome I Rotter; Niina Sandholm; Seang-Mei Saw; Xueling Sim; David S Siscovick; Albert V Smith; Tien Y Wong
Candidate gene association study for diabetic retinopathy in persons with type 2 diabetes: the Candidate gene Association Resource (CARe).
Investigative ophthalmology & visual science 2011;52(10):7593-602.
2011: Aiden Corvin; mark daniel cossburn; Isabelle Cournu-Rebeix; Mathew B Cox; Wendy Cozen; Bruce A C Cree; Anne H Cross; Daniele Cusi; Sandra D'alfonso; Mark J Daly; Emma Davis; Paul I W de Bakker; Philip L De Jager; Marc Debouverie; Panos Deloukas; Marie Beatrice D'hooghe; Alexander Dilthey; Katherine Dixon; Rita Dobosi; Peter Donnelly; Serge Dronov; Bénédicte Dubois; Audrey Duncanson; Sarah Edkins; David Ellinghaus; Irina Elovaara; Federica Esposito; Bertrand Fontaine; Claire Fontenille; Simon Foote; Andre Franke; Colin Freeman; Daniela Galimberti; Angelo Ghezzi; Eleni Giannoulatou; Matthew Gillman; Joseph Glessner; Refujia Gomez; An Goris; Olivier Gout; Colin Graham; Struan F A Grant; Emma Gray; Franca Rosa Guerini; Rhian Gwilliam; David A Hafler; Jonathan L Haines; Hakon Hakonarson; Per Hall; Naomi Hammond; Anders Hamsten; Hanne F Harbo; Hans-Peter Hartung; Stephen L Hauser; Clive Hawkins; Stanley Hawkins; Rob N Heard; Simon Heath; Garrett Hellenthal; Bernhard Hemmer; Jan Hillert; Jeremy Hobart; Muna Hoshi; Sarah E Hunt; Carmen Infante-Duarte; Gillian Ingram; Wendy Ingram; Talat Islam; Adrian J Ivinson; Maja Jagodic; Janusz Jankowski; Alagurevathi Jayakumar; Michael Kabesch; Anu Kemppinen; Allan G Kermode; Trevor J Kilpatrick; Cecilia Kim; Norman Klopp; Ingrid Kockum; Keijo Koivisto; Cordelia Langford; Malin Larsson; Mark Lathrop; Jeannette S Lechner-Scott; Maurizio A Leone; Virpi Leppä; Stephen Leslie; Jennifer Liddle; Ulrika Liljedahl; Robin R Lincoln; Jenny Link; Jianjun Liu; Aslaug R Lorentzen; Sara Lupoli; Fabio Macciardi; Thomas Mack; Hugh S Markus; Mark Marriott; Roland Martin; Vittorio Martinelli; Deborah Mason; Christopher G Mathew; Owen T McCann; Jacob McCauley; Gil McVean; Frank Mentch; Inger-Lise Mero; Tania Mihalova; Xavier Montalban; John Mottershead; Loukas Moutsianas; Marcin P Mycko; Kjell-Morten Myhr; Paola Naldi; Jorge R Oksenberg; William Ollier; Tomas Olsson; Annette Bang Oturai; Alison Page; Colin N A Palmer; Aarno Palotie; Nikolaos A Patsopoulos; Jean Pelletier; Leena Peltonen; Marc L Perez; Margaret Pericak-Vance; Laura Piccio; Trevor Pickersgill; Fredrik Piehl; Matti Pirinen; Robert Plomin; Susan Pobywajlo; Simon C Potter; Hong L Quach; Patricia P Ramsay; Anna Rautanen; Rathi Ravindrarajah; Mauri Reunanen; Richard Reynolds; Michelle Ricketts; John D Rioux; Neil Robertson; Mariaemma Rodegher; Sabine Roesner; Justin P Rubio; Ina-Maria Rückert; Janna Saarela; Marco Salvetti; Erika Salvi; Adam Santaniello; Stephen Sawcer; Catherine A Schaefer; Stefan Schreiber; Christian Schulze; Rodney J Scott; Finn Sellebjerg; Krzysztof W Selmaj; David Sexton; Ling Shen; Brigid Simms-Acuna; Sheila Skidmore; Patrick M A Sleiman; Cathrine Smestad; Helle Bach Søndergaard; Per Soelberg Sørensen; Chris C A Spencer; Anne Spurkland; Jim Stankovich; Graeme J Stewart; Amy Strange; Richard C Strange; Zhan Su; Anna-Maija Sulonen; Emilie Sundqvist; Ann-Christine Syvänen; Francesca Taddeo; Bruce Taylor; Pentti Tienari; Ayman Tourbah; Richard C Trembath; Ewa Tronczynska; Niall Tubridy; Jane Vickery; Pablo Villoslada; Ananth C Viswanathan; Matthew J Waller; Kai Wang; James Wason; Paul Weston; Pamela Whittaker; H-Erich Wichmann; Sara Caroline Widaa; Ernest Willoughby; Juliane Winkelmann; Michael Wittig; Nicholas W Wood; Jacqueline Yaouanq; John Zajicek; Haitao Zhang; Frauke Zipp; Rebecca Zuvich; Filippo Martinelli Boneschi; Roby Abraham; Lars Alfredsson; Kristin Ardlie; Cristin Aubin; Amie Baker; Katharine Baker; Maria Ban; Gavin Band; Sergio E Baranzini; Lisa F Barcellos; Céline Bellenguez; Laura Bergamaschi; Roberto Bergamaschi; Allan Bernstein; Achim Berthele; Hannah Blackburn; Jenefer M Blackwell; Mike Boggild; Izaura Lima Bomfim; David R Booth; Jonathan P Bradfield; Elvira Bramon; David Brassat; Simon A Broadley; Matthew A Brown; Dorothea Buck; Suzannah J Bumpstead; Helmut Butzkueven; Ruggero Capra; William M Carroll; Juan P Casas; Paola Cavalla; Elisabeth G Celius; Sabine Cepok; Rosetta Chiavacci; Françoise Clerget-Darpoux; Katleen Clysters; Manuel Comabella; Giancarlo Comi; Alastair Compston
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Nature 2011;476(7359):214-9.
2011: Chris Cotsapas; Mark J Daly; Philip L De Jager; James T Elder; Robert R Graham; Peter Gregersen; David A Hafler; Lars Klareskog; Kasper Lage; Benjamin M Neale; Stephen S Rich; Elizabeth Rossin; Katherine A Siminovitch; John A Todd; David A van Heel; Benjamin F Voight; chris wallace; Cisca Wijmenga; Jane Worthington; Gonçalo R Abecasis; Jeffrey C Barrett; Timothy Behrens; Judy Cho
Pervasive sharing of genetic effects in autoimmune disease.
PLoS genetics 2011;7(8):e1002254.
2011: Jessica Shea; Brian Thomson; Vineeta Agarwala; David Altshuler; Eric Banks; Noël P Burtt; Mark J Daly; Mark Depristo; Stacey Gabriel; Leif Groop; Candace Guiducci; Sekar Kathiresan; Jared Maguire; Robert C Onofrio; Anthony A Philippakis
Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction.
Nature genetics 2011;43(8):801-5.
2011: M Isabel Lucena; Michael Miller; Mariam Molokhia; Jose Maria Navarro; Matthew R Nelson; Itsik Pe'er; Munir Pirmohamed; Manuel Romero-Gomez; Francisco Ruiz-Cabello; Yufeng Shen; Camilla Stephens; Bruno H C Stricker; Thomas J Urban; Paul B Watkins; Qun-Ying Yue; Guruprasad P Aithal; Raúl J Andrade; Emmanuelle Bondon-Guitton; Alfonso Carvajal; Anita Conforti; Ann K Daly; Mark J Daly; Christopher P Day; John F Dillon; Peter T Donaldson; Michel Eichelbaum; Aris Floratos; Robert J Fontana; David B Goldstein; Max Groome; Luisa Ibanez
Susceptibility to amoxicillin-clavulanate-induced liver injury is influenced by multiple HLA class I and II alleles.
Gastroenterology 2011;141(1):338-47.
2011: Mark A DePristo; Eric Banks; Ryan Poplin; Kiran V Garimella; Jared R Maguire; Christopher Hartl; Anthony A Philippakis; Guillermo del Angel; Manuel A Rivas; Matt Hanna; Aaron McKenna; Tim J Fennell; Andrew M Kernytsky; Andrey Y Sivachenko; Kristian Cibulskis; Stacey B Gabriel; David Altshuler; Mark J Daly
A framework for variation discovery and genotyping using next-generation DNA sequencing data.
Nature genetics 2011;43(5):491-8.
2011: Michael E Talkowski; Carl Ernst; Adrian Heilbut; Colby Chiang; Carrie Hanscom; Amelia Lindgren; Andrew Kirby; Shangtao Liu; Bhavana Muddukrishna; Toshiro K Ohsumi; Yiping Shen; Mark Borowsky; Mark J Daly; Cynthia C Morton; James Gusella
Next-generation sequencing strategies enable routine detection of balanced chromosome rearrangements for clinical diagnostics and genetic research.
American journal of human genetics 2011;88(4):469-81.
2011: Benjamin M Neale; Manuel A Rivas; Benjamin F Voight; David Altshuler; Bernie Devlin; Marju Orho-Melander; Sekar Kathiresan; Shaun M Purcell; Kathryn Roeder; Mark J Daly
Testing for an unusual distribution of rare variants.
PLoS genetics 2011;7(3):e1001322.
2011: Carl A Anderson; Gabrielle Boucher; Charlie W Lees; Andre Franke; Mauro D'Amato; Kent D Taylor; James C Lee; Philippe Goyette; Marcin Imielinski; Anna Latiano; Caroline Lagacé; Regan Scott; Leila Amininejad; Suzannah Bumpstead; Leonard Baidoo; Robert N Baldassano; Murray Barclay; Theodore M Bayless; Stephan Brand; Carsten Büning; Jean-Frédéric Colombel; Lee A Denson; Martine De Vos; Marla Dubinsky; Cathryn Edwards; David Ellinghaus; Rudolf S N Fehrmann; James A B Floyd; Timothy Florin; Denis Franchimont; Lude Franke; Michel Georges; Jürgen Glas; Nicole L Glazer; Stephen L Guthery; Talin Haritunians; Nicholas K Hayward; Jean-Pierre Hugot; Gilles Jobin; Debby Laukens; Ian Craig Lawrance; Marc Lémann; Arie Levine; Cecile Libioulle; Edouard Louis; Dermot P McGovern; Monica Milla; Grant W Montgomery; Katherine I Morley; Craig Mowat; Aylwin Ng; William Newman; Roel A Ophoff; Laura Papi; Orazio Palmieri; Laurent Peyrin-Biroulet; Julián Panés; Anne Phillips; Natalie J Prescott; Deborah D Proctor; Rebecca Roberts; Richard Russell; Paul Rutgeerts; Jeremy Sanderson; Miquel Sans; Philip Schumm; Frank Seibold; Yashoda Sharma; Lisa A Simms; Mark Seielstad; A Hillary Steinhart; Stephan R Targan; Leonard H van den Berg; Morten Vatn; Hein Verspaget; Thomas Walters; cisca wijmenga; David C Wilson; Harm-Jan Westra; Ramnik J Xavier; Zhen Z Zhao; Cyriel Y Ponsioen; Vibeke Andersen; Leif Torkvist; Maria Gazouli; Nicholas P Anagnou; Tom H Karlsen; Limas Kupcinskas; Jurgita Sventoraityte; John C Mansfield; Subra Kugathasan; Mark S Silverberg; Jonas Halfvarson; Jerome I Rotter; Christopher G Mathew; Anne M Griffiths; Richard Gearry; Tariq Ahmad; Steven R Brant; Mathias Chamaillard; Jack Satsangi; Judy H Cho; Stefan Schreiber; Mark J Daly; Jeffrey C Barrett; Miles Parkes; Vito Annese; Hakon Hakonarson; Graham Radford-Smith; Richard H Duerr; Séverine Vermeire; Rinse K Weersma; John D Rioux
Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.
Nature genetics 2011;43(3):246-52.
2011: Eimear E Kenny; Minseung Kim; Alexander Gusev; Jennifer K Lowe; Jacqueline Salit; J Gustav Smith; Sirisha Kovvali; Hyun Min Kang; Christopher Newton-Cheh; Mark J Daly; Markus Stoffel; David Altshuler; Jeffrey M Friedman; Eleazar Eskin; Jan L Breslow; Itsik Pe'er
Increased power of mixed models facilitates association mapping of 10 loci for metabolic traits in an isolated population.
Human molecular genetics 2011;20(4):827-39.
2011: Lucia Sobrin; Robyn Reynolds; Yi Yu; Jesen Fagerness; Nicolas Leveziel; Paul S Bernstein; Eric H Souied; Mark J Daly; Johanna M Seddon
ARMS2/HTRA1 locus can confer differential susceptibility to the advanced subtypes of age-related macular degeneration.
American journal of ophthalmology 2011;151(2):345-52.e3.
2011: Yi Yu; Mark J Daly; Jesen Fagerness; Robyn Reynolds; Bernard Rosner; Johanna M Seddon
Association of variants in the LIPC and ABCA1 genes with intermediate and large drusen and advanced age-related macular degeneration.
Investigative ophthalmology & visual science 2011;52(7):4663-70.
2011: Eleonora A M Festen; Philippe Goyette; Todd Green; Gabrielle Boucher; Claudine Beauchamp; Gosia Trynka; Patrick C Dubois; Caroline Lagacé; Pieter C F Stokkers; Daan W Hommes; Donatella Barisani; Orazio Palmieri; Vito Annese; David A van Heel; Rinse Weersma; Mark J Daly; Cisca Wijmenga; John D Rioux
A meta-analysis of genome-wide association scans identifies IL18RAP, PTPN2, TAGAP, and PUS10 as shared risk loci for Crohn's disease and celiac disease.
PLoS genetics 2011;7(1):e1001283.
2011: Elizabeth J Rossin; Kasper Lage; Soumya Raychaudhuri; Ramnik J Xavier; Diana Tatar; Yair Benita; Chris Cotsapas; Mark J Daly
Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biology.
PLoS genetics 2011;7(1):e1001273.
2010: Kiran Musunuru; James P Pirruccello; Ron Do; Gina M Peloso; Candace Guiducci; Carrie Sougnez; Kiran V Garimella; Sheila Fisher; Justin Abreu; Andrew J Barry; Tim Fennell; Eric Banks; Lauren Ambrogio; Kristian Cibulskis; Andrew Kernytsky; Elena Gonzalez; Nicholas Rudzicz; James C Engert; Mark A DePristo; Mark J Daly; Jonathan C Cohen; Helen H Hobbs; David Altshuler; Gustav Schonfeld; Stacey B Gabriel; Pin Yue; Sekar Kathiresan
Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemia.
The New England journal of medicine 2010;363(23):2220-7.
2010: Andre Franke; Dermot P B McGovern; Jeffrey C Barrett; Kai Wang; Graham L Radford-Smith; Tariq Ahmad; Charlie W Lees; Tobias Balschun; James Lee; Rebecca Roberts; Carl A Anderson; Joshua C Bis; Suzanne Bumpstead; David Ellinghaus; Eleonora M Festen; Michel Georges; Todd Green; Talin Haritunians; Luke Jostins; Anna Latiano; Christopher G Mathew; Grant W Montgomery; Natalie J Prescott; Soumya Raychaudhuri; Jerome I Rotter; Philip Schumm; Yashoda Sharma; Lisa A Simms; Kent D Taylor; David Whiteman; cisca wijmenga; Robert N Baldassano; Murray Barclay; Theodore M Bayless; Stephan Brand; Carsten Büning; Albert Cohen; Jean-Frederick Colombel; Mario Cottone; Laura Stronati; Ted Denson; Martine De Vos; Renata D'Inca; Marla Dubinsky; Cathryn Edwards; Tim Florin; Denis Franchimont; Richard Gearry; Jürgen Glas; Andre Van Gossum; Stephen L Guthery; Jonas Halfvarson; Hein W Verspaget; Jean-Pierre Hugot; Amir Karban; Debby Laukens; Ian Craig Lawrance; Marc Lemann; Arie Levine; Cecile Libioulle; Edouard Louis; Craig Mowat; William Newman; Julián Panés; Anne Phillips; Deborah D Proctor; Miguel Regueiro; Richard Russell; Paul Rutgeerts; Jeremy Sanderson; Miquel Sans; Frank Seibold; A Hillary Steinhart; Pieter C F Stokkers; Leif Torkvist; Gerd Kullak-Ublick; David Wilson; Thomas Walters; Stephan R Targan; Steven R Brant; John D Rioux; Mauro D'Amato; Rinse K Weersma; Subra Kugathasan; Anne M Griffiths; John C Mansfield; Severine Vermeire; Richard H Duerr; Mark S Silverberg; Jack Satsangi; Stefan Schreiber; Judy H Cho; Vito Annese; Hakon Hakonarson; Mark J Daly; Miles Parkes
Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.
Nature genetics 2010;42(12):1118-25.
2010: Themistocles L Assimes; Hilma Hólm; Sekar Kathiresan; Muredach P Reilly; Gudmar Thorleifsson; Benjamin F Voight; Jeanette Erdmann; Christina Willenborg; Dhananjay Vaidya; Changchun Xie; Chris C Patterson; Thomas M Morgan; Mary Susan Burnett; Mingyao Li; Mark A Hlatky; Joshua W Knowles; John R Thompson; Devin Absher; Carlos Iribarren; Alan Go; Stephen P Fortmann; Stephen Sidney; Neil Risch; Hua Tang; Richard Myers; Klaus Berger; Monika Stoll; Svati H Shah; Gudmundur Thorgeirsson; Karl Andersen; Aki S Havulinna; J Enrique Herrera; Nauder Faraday; Yoonhee Kim; Brian G Kral; Rasika A Mathias; Ingo Ruczinski; Bhoom Suktitipat; Alexander F Wilson; Lisa R Yanek; Lewis C Becker; Patrick Linsel-Nitschke; Wolfgang Lieb; Inke R König; Christian Hengstenberg; Marcus Fischer; Klaus Stark; Wibke Reinhard; Janina Winogradow; Martina Grassl; Anika Grosshennig; Michael Preuss; Stefan Schreiber; H-Erich Wichmann; Christa Meisinger; Jean Yee; Yechiel Friedlander; Ron Do; James B Meigs; Gordon Williams; David M Nathan; Calum A MacRae; Liming Qu; Robert L Wilensky; William H Matthai; Atif N Qasim; Hakon Hakonarson; Augusto D Pichard; Kenneth M Kent; Lowell Satler; Joseph M Lindsay; Ron Waksman; Christopher W Knouff; Dawn M Waterworth; Max C Walker; Vincent E Mooser; Jaume Marrugat; Gavin Lucas; Isaac Subirana; Joan Sala; Rafael Ramos; Nicola Martinelli; Oliviero Olivieri; Elisabetta Trabetti; Giovanni Malerba; Pier Franco Pignatti; Candace Guiducci; Daniel Mirel; Melissa Parkin; Joel N Hirschhorn; Rosanna Asselta; Stefano Duga; Kiran Musunuru; Mark J Daly; Shaun Purcell; Sandra Eifert; Peter S Braund; Benjamin J Wright; Anthony J Balmforth; Stephen G Ball; Willem H Ouwehand; Panos Deloukas; Michael Scholz; Francois Cambien; Andreas Huge; Thomas Scheffold; Veikko Salomaa; Domenico Girelli; Christopher B Granger; Leena Peltonen; Pascal P McKeown; David Altshuler; Olle Melander; Joseph M Devaney; Stephen E Epstein; Daniel J Rader; Roberto Elosua; James C Engert; Sonia S Anand; Alistair Hall; Andreas Ziegler; Christopher J O'Donnell; John A Spertus; David Siscovick; Stephen M Schwartz; Diane M Becker; Unnur Thorsteinsdottir; Kari Stefansson; Heribert Schunkert; Nilesh J Samani; Thomas Quertermous
Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies.
Journal of the American College of Cardiology 2010;56(19):1552-63.
2010: Agnès Gardet; Yair Benita; Chun Li; Bruce E Sands; Isabel Ballester; Christine Stevens; Joshua R Korzenik; John D Rioux; Mark J Daly; Ramnik J Xavier; Daniel K Podolsky
LRRK2 is involved in the IFN-gamma response and host response to pathogens.
Journal of immunology (Baltimore, Md. : 1950) 2010;185(9):5577-85.
2010: Mia M. Gaudet; Tomas Kirchhoff; Todd Green; Joseph Vijai; Joshua M Korn; Candace Guiducci; Ayellet V Segrè; Kate McGee; Lesley McGuffog; Christiana Kartsonaki; Jonathan Morrison; Sue Healey; Olga M Sinilnikova; Dominique Stoppa-Lyonnet; Sylvie Mazoyer; Marion Gauthier-Villars; Hagay Sobol; Michel Longy; Marc Frenay; Frans B L Hogervorst; Matti A Rookus; J Margriet Collée; Nicoline Hoogerbrugge; Kees E P van Roozendaal; Marion Piedmonte; Wendy Rubinstein; Stacy Nerenstone; Linda Van Le; Stephanie V Blank; Trinidad Caldés; Miguel de la Hoya; Heli Nevanlinna; Kristiina Aittomäki; Conxi Lazaro; Ignacio Blanco; Adalgeir Arason; Oskar T Johannsson; Rosa B Barkardottir; Peter Devilee; Olofunmilayo I Olopade; Susan L Neuhausen; Xianshu Wang; Zachary S Fredericksen; Paolo Peterlongo; Siranoush Manoukian; Monica Barile; Alessandra Viel; Paolo Radice; Catherine M Phelan; Steven Narod; Gad Rennert; Flavio Lejbkowicz; Anath Flugelman; Irene L Andrulis; Gord Glendon; Hilmi Ozcelik; Amanda E Toland; Marco Montagna; Emma D'Andrea; Eitan Friedman; Yael Laitman; Ake Borg; Mary Beattie; Susan J Ramus; Susan M Domchek; Katherine L Nathanson; Tim Rebbeck; Amanda B Spurdle; Xiaoqing Chen; Helene Holland; Esther M John; John L Hopper; Saundra S Buys; Mary B Daly; Melissa C Southey; Mary Beth Terry; Nadine Tung; Thomas V Overeem Hansen; Finn C Nielsen; Mark H Greene; Mark I Greene; Phuong L Mai; Ana Osorio; Mercedes Durán; Raquel Andres; Javier Benítez; Jeffrey N Weitzel; Judy Garber; Ute Hamann; Susan Peock; Margaret Cook; Clare Oliver; Debra Frost; Radka Platte; D Gareth Evans; Fiona Lalloo; Ros Eeles; Louise Izatt; Lisa Walker; Jacqueline Eason; Julian Barwell; Andrew K Godwin; Rita K Schmutzler; Barbara Wappenschmidt; Stefanie Engert; Norbert Arnold; Dorothea Gadzicki; Michael Dean; Bert Gold; Robert J. Klein; Fergus J Couch; Georgia Chenevix-Trench; Douglas F Easton; Mark J Daly; Antonis C Antoniou; David M Altshuler; Kenneth Offit
Common genetic variants and modification of penetrance of BRCA2-associated breast cancer.
PLoS genetics 2010;6(10):e1001183.
2010: Sarah E Calvo; Elena J Tucker; Alison G Compton; Denise M Kirby; Gabriel Crawford; Noel P Burtt; Manuel Rivas; Candace Guiducci; Damien L Bruno; Olga A Goldberger; Michelle C Redman; Esko Wiltshire; Callum J Wilson; David Altshuler; Stacey B Gabriel; Mark J Daly; David R Thorburn; Vamsi K Mootha
High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency.
Nature genetics 2010;42(10):851-8.
2010: Ida Surakka; Kati Kristiansson; Verneri Anttila; Michael Inouye; Chris Barnes; Loukas Moutsianas; Veikko Salomaa; Mark J Daly; Aarno Palotie; Leena Peltonen; Samuli Ripatti
Founder population-specific HapMap panel increases power in GWA studies through improved imputation accuracy and CNV tagging.
Genome research 2010;20(10):1344-51.
2010: David M Altshuler; Richard A Gibbs; Leena Peltonen; David M Altshuler; Richard A Gibbs; Leena Peltonen; Emmanouil Dermitzakis; Stephen F Schaffner; Fuli Yu; Leena Peltonen; Emmanouil Dermitzakis; Penelope E Bonnen; David M Altshuler; Richard A Gibbs; Paul I W de Bakker; Panos Deloukas; Stacey B Gabriel; Rhian Gwilliam; Sarah Hunt; Michael Inouye; Xiaoming Jia; Aarno Palotie; Melissa Parkin; Pamela Whittaker; Fuli Yu; Kyle Chang; Alicia Hawes; Lora R Lewis; Yanru Ren; David Wheeler; Richard A Gibbs; Donna Marie Muzny; Chris Barnes; Katayoon Darvishi; Matthew Hurles; Joshua M Korn; Kati Kristiansson; Charles Lee; Steven A McCarrol; James Nemesh; Emmanouil Dermitzakis; Alon Keinan; Stephen B Montgomery; Samuela Pollack; Alkes L Price; Nicole Soranzo; Penelope E Bonnen; Richard A Gibbs; Claudia Gonzaga-Jauregui; Alon Keinan; Alkes L Price; Fuli Yu; Verneri Anttila; Wendy Brodeur; Mark J Daly; Stephen Leslie; Gil McVean; Loukas Moutsianas; Huy Nguyen; Stephen F Schaffner; Qingrun Zhang; Mohammed J R Ghori; Ralph McGinnis; William McLaren; Samuela Pollack; Alkes L Price; Stephen F Schaffner; Fumihiko Takeuchi; Sharon R Grossman; Ilya Shlyakhter; Elizabeth B Hostetter; Pardis C Sabeti; Clement Adebamowo; Morris W Foster; Deborah R Gordon; Julio Licinio; Maria Cristina Manca; Patricia A Marshall; Ichiro Matsuda; Duncan Ngare; Vivian Ota Wang; Deepa Reddy; Charles N Rotimi; Charmaine D Royal; Richard R Sharp; Changqing Zeng; Lisa D Brooks; Jean E McEwen
Integrating common and rare genetic variation in diverse human populations.
Nature 2010;467(7311):52-8.
2010: Soumya Raychaudhuri; Joshua M Korn; Steven A McCarroll; David Altshuler; Pamela Sklar; Shaun Purcell; Mark J Daly
Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function.
PLoS genetics 2010;6(9):.
2010: Aaron McKenna; Matthew Hanna; Eric Banks; Andrey Sivachenko; Kristian Cibulskis; Andrew Kernytsky; Kiran Garimella; David Altshuler; Stacey Gabriel; Mark J Daly; Mark A DePristo
The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data.
Genome research 2010;20(9):1297-303.
2010: Ayellet V Segrè; Leif Groop; Vamsi K Mootha; Mark J Daly; David Altshuler
Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traits.
PLoS genetics 2010;6(8):.
2010: Soumya Raychaudhuri; Stephan Ripke; Mingyao Li; Benjamin M Neale; Jesen Fagerness; Robyn Reynolds; Lucia Sobrin; Anand Swaroop; Gonçalo Abecasis; Johanna M Seddon; Mark J Daly
Associations of CFHR1-CFHR3 deletion and a CFH SNP to age-related macular degeneration are not independent.
Nature genetics 2010;42(7):553-5; author reply 555-6.
2010: Benjamin F Voight; Laura J Scott; Valgerdur Steinthorsdottir; Andrew P Morris; Christian Dina; Ryan P Welch; Eleftheria Zeggini; Cornelia Huth; Yurii S Aulchenko; Gudmar Thorleifsson; Laura J McCulloch; Teresa Ferreira; Harald Grallert; Najaf Amin; Guanming Wu; Cristen J Willer; Soumya Raychaudhuri; Steve A McCarroll; Claudia Langenberg; Oliver M Hofmann; Josée Dupuis; Lu Qi; Ayellet V Segrè; Mandy van Hoek; Pau Navarro; Kristin Ardlie; Beverley Balkau; Rafn Benediktsson; Amanda J Bennett; Roza Blagieva; Eric Boerwinkle; Lori L Bonnycastle; Kristina Bengtsson Boström; Bert Bravenboer; Suzannah Bumpstead; Noisël P Burtt; Guillaume Charpentier; Peter S Chines; Marilyn Cornelis; David J Couper; Gabe Crawford; Alex S F Doney; Katherine S Elliott; Amanda Elliott; Michael R Erdos; Caroline S Fox; Christopher S Franklin; Martha Ganser; Christian Gieger; Niels Grarup; Todd Green; Simon Griffin; Christopher J Groves; Candace Guiducci; Samy Hadjadj; Neelam Hassanali; Christian Herder; Bo Isomaa; Anne U Jackson; Paul R V Johnson; Torben Jørgensen; WEN KAO; Norman Klopp; Augustine Kong; Peter Kraft; Johanna Kuusisto; torsten lauritzen; Man Li; Aloysius Lieverse; Cecilia M Lindgren; Valeriya Lyssenko; Michel Marre; Thomas Meitinger; Kristian Midthjell; Mario A Morken; Narisu Narisu; Peter Nilsson; Katharine R Owen; Felicity Payne; John R B Perry; Ann-Kristin Petersen; Carl Platou; Christine Proença; Inga Prokopenko; Wolfgang Rathmann; N William Rayner; Neil R Robertson; Ghislain Rocheleau; Michael Roden; Michael J Sampson; Richa Saxena; Beverley M Shields; Peter Shrader; Gunnar Sigurdsson; Thomas Sparsø; Klaus Strassburger; Heather M Stringham; Qi Sun; Amy J Swift; Barbara Thorand; Jean Tichet; Tiinamaija Tuomi; Rob M van Dam; Timon W van Haeften; Thijs van Herpt; Jana V van Vliet-Ostaptchouk; Gudmundur Bragi Walters; Michael N Weedon; cisca wijmenga; Jacqueline Witteman; Richard N Bergman; Stephane Cauchi; Francis S Collins; Anna L Gloyn; Ulf Gyllensten; Torben Hansen; Winston Hide; Graham A Hitman; Albert Hofman; David J Hunter; Kristian Hveem; Markku Laakso; Karen L Mohlke; Andrew D Morris; Colin N A Palmer; Peter P Pramstaller; Igor Rudan; Eric Sijbrands; Lincoln D Stein; Jaakko Tuomilehto; Andre Uitterlinden; Mark Walker; Nicholas J Wareham; Richard M Watanabe; Gonçalo R Abecasis; Bernhard O Boehm; Harry Campbell; Mark J Daly; Andrew T Hattersley; Frank B Hu; James B Meigs; James S Pankow; Oluf Pedersen; H-Erich Wichmann; Inês Barroso; Jose C Florez; Timothy M Frayling; Leif Groop; Rob Sladek; Unnur Thorsteinsdottir; James F Wilson; Thomas Illig; Philippe Froguel; Cornelia M van Duijn; Kari Stefansson; David Altshuler; Michael Boehnke; Mark I McCarthy
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.
Nature genetics 2010;42(7):579-89.
2010: Andrew Kirby; Hyun Min Kang; Claire M Wade; Chris Cotsapas; Emrah Kostem; Buhm Han; Nick Furlotte; Eun Yong Kang; Manuel Rivas; Molly A Bogue; Kelly A Frazer; Frank M Johnson; Erica J Beilharz; David R Cox; Eleazar Eskin; Mark J Daly
Fine mapping in 94 inbred mouse strains using a high-density haplotype resource.
Genetics 2010;185(3):1081-95.
2010: Paul I W de Bakker; Benjamin M Neale; Mark J Daly
Meta-analysis of genome-wide association studies.
Cold Spring Harbor protocols 2010;2010(6):pdb.top81.
2010: Benjamin M Neale; Jesen Fagerness; Robyn Reynolds; Lucia Sobrin; Margaret Parker; Soumya Raychaudhuri; Perciliz L Tan; Edwin C Oh; Joanna E Merriam; Eric Souied; Paul S Bernstein; Binxing Li; Jeanne M Frederick; Kang Zhang; Milam A Brantley; Aaron Y Lee; Donald J Zack; Betsy Campochiaro; Peter A Campochiaro; Stephan Ripke; R Theodore Smith; Gaetano R Barile; Nicholas Katsanis; Rando Allikmets; Mark J Daly; Johanna M Seddon
Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC).
Proceedings of the National Academy of Sciences of the United States of America 2010;107(16):7395-400.
2010: Dermot P B McGovern; Agnès Gardet; Leif Törkvist; Philippe Goyette; Jonah Essers; Kent D Taylor; Benjamin M Neale; Rick T H Ong; Caroline Lagacé; Chun Li; Todd Green; Christine R Stevens; Claudine Beauchamp; Phillip R Fleshner; Marie Carlson; Mauro D'Amato; Jonas Halfvarson; Martin L Hibberd; Mikael Lördal; Leonid Padyukov; Angelo Andriulli; Elisabetta Colombo; Anna Latiano; Orazio Palmieri; Edmond-Jean Bernard; Colette Deslandres; Daan W Hommes; Dirk J de Jong; Pieter C Stokkers; Rinse K Weersma; Yashoda Sharma; Mark S Silverberg; Judy H Cho; Jing Wu; Kathryn Roeder; Steven R Brant; L Phillip Schumm; Richard H Duerr; Marla C Dubinsky; Nicole L Glazer; Talin Haritunians; Andy Ippoliti; Gil Y Melmed; David S Siscovick; Eric A Vasiliauskas; Stephan R Targan; Vito Annese; cisca wijmenga; Sven Pettersson; Jerome I Rotter; Ramnik J Xavier; Mark J Daly; John D Rioux; Mark Seielstad
Genome-wide association identifies multiple ulcerative colitis susceptibility loci.
Nature genetics 2010;42(4):332-7.
2010: Lindsay C Burrage; Annie E Baskin-Hill; David S Sinasac; Jonathan Singer; Colleen Croniger; Andrew Kirby; E J Kulbokas; Mark J Daly; Eric S Lander; Karl W Broman; Joseph H Nadeau
Genetic resistance to diet-induced obesity in chromosome substitution strains of mice.
Mammalian genome : official journal of the International Mammalian Genome Society 2010;21(3-4):115-29.
2010: Lucia Sobrin; Julian B Maller; Benjamin M Neale; Robyn C Reynolds; Jesen A Fagerness; Mark J Daly; Johanna M Seddon
Genetic profile for five common variants associated with age-related macular degeneration in densely affected families: a novel analytic approach.
European journal of human genetics : EJHG 2010;18(4):496-501.
2010: Rameen Beroukhim; Craig H Mermel; Dale Porter; Guo Wei; Soumya Raychaudhuri; Jerry Donovan; Jordi Barretina; Jesse S Boehm; Jennifer Dobson; Mitsuyoshi Urashima; Kevin T Mc Henry; Reid M Pinchback; Azra H Ligon; Yoon-Jae Cho; Leila Haery; Heidi Greulich; Michael Reich; Wendy Winckler; Michael S Lawrence; Barbara A Weir; Kumiko E Tanaka; Derek Chiang; Adam J Bass; Alice Loo; Carter Hoffman; John Prensner; Ted Liefeld; Qing Gao; Derek Yecies; Sabina Signoretti; Elizabeth Maher; Frederic J Kaye; Hidefumi Sasaki; Joel E Tepper; Jonathan A Fletcher; Josep Tabernero; José Baselga; Ming-Sound Tsao; Francesca Demichelis; Mark A Rubin; Pasi A Janne; Mark J Daly; Carmelo Nucera; Ross Levine; Benjamin L Ebert; Stacey Gabriel; Anil K Rustgi; Cristina R Antonescu; Marc Ladanyi; Anthony Letai; Levi A Garraway; Massimo Loda; David G Beer; Lawrence True; Aikou Okamoto; Scott L Pomeroy; Samuel Singer; Todd R Golub; Eric S Lander; Gad Getz; William R Sellers; Matthew Meyerson
The landscape of somatic copy-number alteration across human cancers.
Nature 2010;463(7283):899-905.
2010: Eveliina Jakkula; Virpi Leppä; Anna-Maija Sulonen; Teppo Varilo; Suvi Kallio; Anu Kemppinen; Shaun Purcell; Keijo Koivisto; Pentti J Tienari; Marja-Liisa Sumelahti; Irina Elovaara; Tuula Pirttilä; Mauri Reunanen; Arpo Aromaa; Annette Bang Oturai; Helle Bach Søndergaard; Hanne F Harbo; Inger-Lise Mero; Stacey B Gabriel; Daniel B Mirel; Stephen L Hauser; Ludwig Kappos; Chris Polman; Philip L De Jager; David A Hafler; Mark J Daly; Aarno Palotie; Janna Saarela; Leena Peltonen
Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene.
American journal of human genetics 2010;86(2):285-91.
2009: Marcin Imielinski; Robert N Baldassano; Anne Griffiths; Richard K Russell; Vito Annese; Marla Dubinsky; Subra Kugathasan; Jonathan P Bradfield; Thomas D Walters; Patrick Sleiman; Cecilia E Kim; Aleixo Muise; Kai Wang; Joseph T Glessner; Shehzad Saeed; Haitao Zhang; Edward C Frackelton; Cuiping Hou; James H Flory; George Otieno; Rosetta M Chiavacci; Robert W Grundmeier; Massimo Castro; Anna Latiano; Bruno Dallapiccola; Joanne Stempak; Debra J Abrams; Kent Taylor; Dermot McGovern; Gary Silber; Iwona Wrobel; Antonio Quiros; Jeffrey C Barrett; Sarah Hansoul; Dan L Nicolae; Judy H Cho; Richard H Duerr; John D Rioux; Steven R Brant; Mark S Silverberg; Kent D Taylor; M Michael Barmuda; Alain Bitton; Themistocles Dassopoulos; Lisa Datta; Todd Green; Anne M Griffiths; Emily O Kistner; Michael T Murtha; Miguel D Regueiro; Jerome I Rotter; L Philip Schumm; A Hillary Steinhart; Stephen R Targan; Ramnik J Xavier; Cecile Libioulle; Cynthia Sandor; Mark Lathrop; Jacques Belaiche; Olivier Dewit; Ivo Gut; Simon Heath; Debby Laukens; Myriam Mni; Paul Rutgeerts; André Van Gossum; Diana Zelenika; Denis Franchimont; J P Hugot; Martine de Vos; Severine Vermeire; Edouard Louis; Lon R Cardon; Carl A Anderson; Hazel Drummond; Elaine Nimmo; Tariq Ahmad; Natalie J Prescott; Clive M Onnie; Sheila A Fisher; Jonathan Marchini; Jilur Ghori; Suzannah Bumpstead; Rhian Gwillam; Mark Tremelling; Panos Delukas; John Mansfield; Derek Jewell; Jack Satsangi; Christopher G Mathew; Miles Parkes; Michel Georges; Mark J Daly; Melvin B Heyman; George D Ferry; Barbara Kirschner; Jessica Lee; Jonah Essers; Richard Grand; Michael Stephens; Arie Levine; David Piccoli; John Van Limbergen; Salvatore Cucchiara; Dimitri S Monos; Stephen L Guthery; Lee Denson; David C Wilson; Straun F A Grant; Mark Daly; Mark S Silverberg; Jack Satsangi; Hakon Hakonarson
Common variants at five new loci associated with early-onset inflammatory bowel disease.
Nature genetics 2009;41(12):1335-40.
2009: Soumya Raychaudhuri; Brian P Thomson; Elaine F Remmers; Stephen Eyre; Anne Hinks; Candace Guiducci; Joseph J Catanese; Gang Xie; Eli A Stahl; Robert Chen; Lars Alfredsson; Christopher I Amos; Kristin G Ardlie; Anne Barton; John Bowes; Noel P Burtt; Monica Chang; Jonathan Coblyn; Karen H Costenbader; Lindsey A Criswell; J Bart A Crusius; Jing Cui; Phillip L De Jager; Bo Ding; Paul Emery; Edward Flynn; Pille Harrison; Lynne J Hocking; Tom W J Huizinga; Daniel L Kastner; Xiayi Ke; Fina A S Kurreeman; Annette T Lee; Xiangdong Liu; Yonghong Li; Paul Martin; Ann W Morgan; Leonid Padyukov; David M Reid; Mark Seielstad; Michael F Seldin; Nancy A Shadick; Sophia Steer; Paul P Tak; Wendy Thomson; Annette H M van der Helm-van Mil; Irene E van der Horst-Bruinsma; Michael E Weinblatt; Anthony G Wilson; Gert Jan Wolbink; Paul Wordsworth; David Altshuler; Elizabeth W Karlson; Rene E M Toes; Niek de Vries; Ann B Begovich; Katherine A Siminovitch; Jane Worthington; Lars Klareskog; Peter K Gregersen; Mark J Daly; Robert M Plenge
Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis risk.
Nature genetics 2009;41(12):1313-8.
2009: Ivana V Yang; Claire M Wade; Hyun Min Kang; Scott Alper; Holly Rutledge; Brad Lackford; Eleazar Eskin; Mark J Daly; David A Schwartz
Identification of novel genes that mediate innate immunity using inbred mice.
Genetics 2009;183(4):1535-44.
2009: John D Rioux; Philippe Goyette; Timothy J Vyse; Lennart Hammarström; Michelle M A Fernando; Todd Green; Philip L De Jager; Sylvain Foisy; Joanne Wang; Paul I W de Bakker; Stephen Leslie; Gilean McVean; Leonid Padyukov; Lars Alfredsson; Vito Annese; David A Hafler; Qiang Pan-Hammarstrom; Ritva Matell; Stephen J Sawcer; Alastair D Compston; Bruce A C Cree; Daniel B Mirel; Mark J Daly; timothy wayne behrens; Lars Klareskog; Peter K Gregersen; Jorge R Oksenberg; Stephen L Hauser
Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases.
Proceedings of the National Academy of Sciences of the United States of America 2009;106(44):18680-5.
2009: Lauren A Weiss; Dan E Arking; Mark J Daly; Aravinda Chakravarti
A genome-wide linkage and association scan reveals novel loci for autism.
Nature 2009;461(7265):802-8.
2009: Jonah B Essers; Jessica J Lee; Subra Kugathasan; Christine R Stevens; Richard J Grand; Mark J Daly
Established genetic risk factors do not distinguish early and later onset Crohn's disease.
Inflammatory bowel diseases 2009;15(10):1508-14.
2009: Chris Cotsapas; Elizabeth K Speliotes; Ida J Hatoum; Danielle M Greenawalt; Radu Dobrin; Pek Y Lum; Christine Suver; Eugene Chudin; Daniel Kemp; Marc Reitman; Benjamin F Voight; Benjamin M Neale; Eric E Schadt; Joel N Hirschhorn; Lee M Kaplan; Mark J Daly
Common body mass index-associated variants confer risk of extreme obesity.
Human molecular genetics 2009;18(18):3502-7.
2009: Eimear E Kenny; Alexander Gusev; Kaitlin Riegel; Dieter Lütjohann; Jennifer K Lowe; Jacqueline Salit; Julian B Maller; Markus Stoffel; Mark J Daly; David Altshuler; Jeffrey M Friedman; Jan L Breslow; Itsik Pe'er; Ephraim Sehayek
Systematic haplotype analysis resolves a complex plasma plant sterol locus on the Micronesian Island of Kosrae.
Proceedings of the National Academy of Sciences of the United States of America 2009;106(33):13886-91.
2009: Mark J Daly
Assessing significance in genetic association studies.
Cold Spring Harbor protocols 2009;2009(8):pdb.top58.
2009: Philip L De Jager; Xiaoming Jia; Joanne Wang; Paul I W de Bakker; Linda Ottoboni; Neelum T Aggarwal; Laura Piccio; Soumya Raychaudhuri; Dong Tran; Cristin Aubin; Rebeccah Briskin; Susan Romano; Sergio E Baranzini; Jacob McCauley; Margaret Pericak-Vance; Jonathan L Haines; Rachel A Gibson; Yvonne Naeglin; Bernard Uitdehaag; Paul Matthews; Ludwig Kappos; Chris Polman; Wendy L McArdle; David P Strachan; Denis Evans; Anne H Cross; Mark J Daly; Alastair Compston; Stephen J Sawcer; Howard L Weiner; Stephen L Hauser; David A Hafler; Jorge R Oksenberg
Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci.
Nature genetics 2009;41(7):776-82.
2009: Ann K Daly; Peter T Donaldson; Pallav Bhatnagar; Yufeng Shen; Itsik Pe'er; Aris Floratos; Mark J Daly; David B Goldstein; Sally John; Matthew R Nelson; Julia Graham; B Kevin Park; John F Dillon; William Bernal; Heather J Cordell; Munir Pirmohamed; Guruprasad P Aithal; Christopher P Day
HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin.
Nature genetics 2009;41(7):816-9.
2009: Soumya Raychaudhuri; Robert M Plenge; Elizabeth J Rossin; Aylwin C Y Ng; Shaun M Purcell; Pamela Sklar; Edward M Scolnick; Ramnik J Xavier; David Altshuler; Mark J Daly
Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions.
PLoS genetics 2009;5(6):e1000534.
2009: E A M Festen; Philippe Goyette; R Scott; V Annese; Alexandra Zhernakova; J Lian; C Lefèbvre; Steven R Brant; Judy H Cho; Mark S Silverberg; Kent D Taylor; Dirk J de Jong; Pieter C F Stokkers; D Mcgovern; O Palmieri; J-P Achkar; Ramnik Xavier; Mark J Daly; Richard H Duerr; Cisca Wijmenga; Rinse Weersma; John D Rioux
Genetic variants in the region harbouring IL2/IL21 associated with ulcerative colitis.
Gut 2009;58(6):799-804.
2009: Anu Kemppinen; Minna Suvela; Pentti J Tienari; Irina Elovaara; Keijo Koivisto; Tuula Pirttilä; Mauri Reunanen; Ilkka Rautakorpi; Jan Hillert; Frida Lundmark; Annette Oturai; Lars Ryder; Hanne F Harbo; Elisabeth G Celius; Aarno Palotie; Mark J Daly; Leena Peltonen; Janna Saarela
MYO9B polymorphisms in multiple sclerosis.
European journal of human genetics : EJHG 2009;17(6):840-3.
2009: J Gustav Smith; Jennifer K Lowe; Sirisha Kovvali; Julian B Maller; Jacqueline Salit; Mark J Daly; Markus Stoffel; David M Altshuler; Jeffrey M Friedman; Jan L Breslow; Christopher Newton-Cheh
Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae.
Heart rhythm : the official journal of the Heart Rhythm Society 2009;6(5):634-41.
2009: John Ioannidis; Gilles Thomas; Mark J Daly
Validating, augmenting and refining genome-wide association signals.
Nature reviews. Genetics 2009;10(5):318-29.
2009: Suvi P Kallio; Eveliina Jakkula; Shaun Purcell; Minna Suvela; Keijo Koivisto; Pentti J Tienari; Irina Elovaara; Tuula Pirttilä; Mauri Reunanen; Denis Bronnikov; Markku Viander; Seppo Meri; Jan Hillert; Frida Lundmark; Hanne F Harbo; Aslaug R Lorentzen; Philip L De Jager; Mark J Daly; David A Hafler; Aarno Palotie; Leena Peltonen; Janna Saarela
Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS.
Human molecular genetics 2009;18(9):1670-83.
2009: Johanna M Seddon; Robyn Reynolds; Julian Maller; Jesen A Fagerness; Mark J Daly; Bernard Rosner
Prediction model for prevalence and incidence of advanced age-related macular degeneration based on genetic, demographic, and environmental variables.
Investigative ophthalmology & visual science 2009;50(5):2044-53.
2009: Alan Huett; Aylwin Ng; Zhifang Cao; Petric Kuballa; Masaaki Komatsu; Mark J Daly; Daniel K Podolsky; Ramnik Xavier
A novel hybrid yeast-human network analysis reveals an essential role for FNBP1L in antibacterial autophagy.
Journal of immunology (Baltimore, Md. : 1950) 2009;182(8):4917-30.
2009: D T Miller; Y Shen; Lauren A Weiss; J Korn; I Anselm; C Bridgemohan; G F Cox; H Dickinson; J Gentile; D J Harris; V Hegde; R Hundley; O Khwaja; S Kothare; C Luedke; R Nasir; A Poduri; K Prasad; P Raffalli; A Reinhard; S E Smith; M M Sobeih; J S Soul; J Stoler; M Takeoka; W-H Tan; J Thakuria; R Wolff; R Yusupov; James Gusella; Mark J Daly; B-L Wu
Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders.
Journal of medical genetics 2009;46(4):242-8.
2009: Philip L De Jager; Clare Baecher-Allan; Lisa M Maier; Ariel T Arthur; Linda Ottoboni; Lisa Barcellos; Jacob McCauley; Stephen Sawcer; An Goris; Janna Saarela; Roman Yelensky; Alkes Price; Virpi Leppa; Nick Patterson; Paul I W de Bakker; Dong Tran; Cristin Aubin; Susan Pobywajlo; Elizabeth Rossin; Xinli Hu; Charles W Ashley; Edwin Choy; John D Rioux; Margaret Pericak-Vance; Adrian Ivinson; David R Booth; Graeme J Stewart; Aarno Palotie; Leena Peltonen; Bénédicte Dubois; Jonathan L Haines; Howard L Weiner; Alastair Compston; Stephen L Hauser; Mark J Daly; David Reich; Jorge R Oksenberg; David A Hafler
The role of the CD58 locus in multiple sclerosis.
Proceedings of the National Academy of Sciences of the United States of America 2009;106(13):5264-9.
2009: Sekar Kathiresan; Benjamin F Voight; Shaun Purcell; Kiran Musunuru; Diego Ardissino; Pier M Mannucci; Sonia Anand; James C Engert; Nilesh J Samani; Heribert Schunkert; Jeanette Erdmann; Muredach P Reilly; Daniel J Rader; Thomas Morgan; John A Spertus; Monika Stoll; Domenico Girelli; Pascal P McKeown; Chris C Patterson; David S Siscovick; Christopher J O'Donnell; Roberto Elosua; Leena Peltonen; Veikko Salomaa; Stephen M Schwartz; Olle Melander; David Altshuler; Diego Ardissino; Pier Angelica Merlini; Carlo Berzuini; Luisa Bernardinelli; Flora Peyvandi; Marco Tubaro; Patrizia Celli; Maurizio Ferrario; Raffaela Fetiveau; Nicola Marziliano; Giorgio Casari; Michele Galli; Flavio Ribichini; Marco Rossi; francesco bernardi; Pietro Zonzin; Alberto Piazza; Pier M Mannucci; Stephen M Schwartz; David S Siscovick; Jean Yee; Yechiel Friedlander; Roberto Elosua; Jaume Marrugat; Gavin Lucas; Isaac Subirana; Joan Sala; Rafael Ramos; Sekar Kathiresan; James B Meigs; Gordon Williams; David M Nathan; Calum A MacRae; Christopher J O'Donnell; Veikko Salomaa; Aki S Havulinna; Leena Peltonen; Olle Melander; Goran Berglund; Benjamin F Voight; Sekar Kathiresan; Joel N Hirschhorn; Rosanna Asselta; Stefano Duga; Marta Spreafico; Kiran Musunuru; Mark J Daly; Shaun Purcell; Benjamin F Voight; Shaun Purcell; James Nemesh; Joshua M Korn; Steven A McCarroll; Stephen M Schwartz; Jean Yee; Sekar Kathiresan; Gavin Lucas; Isaac Subirana; Roberto Elosua; Aarti Surti; Candace Guiducci; Lauren Gianniny; Daniel Mirel; Melissa Parkin; Noel Burtt; Stacey B Gabriel; Nilesh J Samani; John R Thompson; Peter S Braund; Benjamin J Wright; Anthony J Balmforth; Stephen G Ball; Heribert Schunkert; Jeanette Erdmann; Patrick Linsel-Nitschke; Wolfgang Lieb; Andreas Ziegler; Inke König; Christian Hengstenberg; Marcus Fischer; Klaus Stark; Anika Grosshennig; Michael Preuss; H-Erich Wichmann; Stefan Schreiber; Heribert Schunkert; Nilesh J Samani; Jeanette Erdmann; Willem Ouwehand; Christian Hengstenberg; Panos Deloukas; Michael Scholz; Francois Cambien; Muredach P Reilly; Mingyao Li; Zhen Chen; Robert Wilensky; William Matthai; Atif Qasim; Hakon H Hakonarson; Joe Devaney; Mary-Susan Burnett; Augusto D Pichard; Kenneth M Kent; Lowell Satler; Joseph M Lindsay; Ron Waksman; Christopher W Knouff; Dawn M Waterworth; Max C Walker; Vincent Mooser; Stephen E Epstein; Daniel J Rader; Thomas Scheffold; Klaus Berger; Monika Stoll; Andreas Huge; Domenico Girelli; Nicola Martinelli; Oliviero Olivieri; Roberto Corrocher; Thomas Morgan; John A Spertus; Pascal McKeown; Chris C Patterson; Heribert Schunkert; Erdmann Erdmann; Patrick Linsel-Nitschke; Wolfgang Lieb; Andreas Ziegler; Inke R König; Christian Hengstenberg; Marcus Fischer; Klaus Stark; Anika Grosshennig; Michael Preuss; H-Erich Wichmann; Stefan Schreiber; Hilma Hólm; Gudmar Thorleifsson; Unnur Thorsteinsdottir; Kari Stefansson; James C Engert; Ron Do; Changchun Xie; Sonia Anand; Sekar Kathiresan; Diego Ardissino; Pier M Mannucci; David Siscovick; Christopher J O'Donnell; Nilesh J Samani; Olle Melander; Roberto Elosua; Leena Peltonen; Veikko Salomaa; Stephen M Schwartz; Alistair Hall; David Altshuler
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
Nature genetics 2009;41(3):334-41.
2009: Jennifer K Lowe; Julian B Maller; Itsik Pe'er; Benjamin M Neale; Jacqueline Salit; Eimear E Kenny; Jessica L Shea; Ralph Burkhardt; J Gustav Smith; Weizhen Ji; Martha Noel; Jia Nee Foo; Maude L Blundell; Vita Skilling; Laura Garcia; Marcia L Sullivan; Heather E Lee; Anna Labek; Hope Ferdowsian; Steven B Auerbach; Richard P Lifton; Christopher Newton-Cheh; Jan L Breslow; Markus Stoffel; Mark J Daly; David Altshuler; Jeffrey M Friedman
Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae.
PLoS genetics 2009;5(2):e1000365.
2009: Mark S Silverberg; Judy H Cho; John D Rioux; Dermot P B McGovern; Jing Wu; Vito Annese; Jean-Paul Achkar; Philippe Goyette; Regan Scott; Wei Xu; M Michael Barmada; Lambertus Klei; Mark J Daly; Clara Abraham; Theodore M Bayless; Fabrizio Bossa; Anne M Griffiths; Andrew F Ippoliti; Raymond G Lahaie; Anna Latiano; Pierre Paré; Deborah D Proctor; Miguel D Regueiro; A Hillary Steinhart; Stephan R Targan; L Philip Schumm; Emily O Kistner; Annette T Lee; Peter K Gregersen; Jerome I Rotter; Steven R Brant; Kent D Taylor; Kathryn Roeder; Richard H Duerr
Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study.
Nature genetics 2009;41(2):216-20.
2009: Alexander Gusev; Jennifer K Lowe; Markus Stoffel; Mark J Daly; David Altshuler; Jan L Breslow; Jeffrey M Friedman; Itsik Pe'er
Whole population, genome-wide mapping of hidden relatedness.
Genome research 2009;19(2):318-26.
2009: Chiara Sabatti; Susan K Service; Anna-Liisa Hartikainen; Anneli Pouta; Samuli Ripatti; Jae Brodsky; Chris G Jones; Noah A Zaitlen; Teppo Varilo; Marika Kaakinen; Ulla Sovio; Aimo Ruokonen; Jaana Laitinen; Eveliina Jakkula; Lachlan Coin; Clive Hoggart; ANDREW COLLINS; Hannu Turunen; Stacey Gabriel; Paul Elliot; Mark I McCarthy; Mark J Daly; Marjo-Riitta Järvelin; Nelson B Freimer; Leena Peltonen
Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.
Nature genetics 2009;41(1):35-46.
2009: Alan Huett; Steven A McCarroll; Mark J Daly; Ramnik J Xavier
On the level: IRGM gene function is all about expression.
Autophagy 2009;5(1):96-9.
2009: J Sissons; Bo-Shiun Yan; Alexander V Pichugin; A Kirby; Mark J Daly; Igor Kramnik
Multigenic control of tuberculosis resistance: analysis of a QTL on mouse chromosome 7 and its synergism with sst1.
Genes and immunity 2009;10(1):37-46.
2009: Jesen A Fagerness; Julian B Maller; Benjamin M Neale; Robyn C Reynolds; Mark J Daly; Johanna M Seddon
Variation near complement factor I is associated with risk of advanced AMD.
European journal of human genetics : EJHG 2009;17(1):100-4.
2008: Haifeng Shao; Lindsay C Burrage; David S Sinasac; Annie E Hill; Sheila R Ernest; William O'Brien; Hayden-William Courtland; Karl Jepsen; Andrew Kirby; E J Kulbokas; Mark J Daly; Karl W Broman; Eric S Lander; Joseph H Nadeau
Genetic architecture of complex traits: large phenotypic effects and pervasive epistasis.
Proceedings of the National Academy of Sciences of the United States of America 2008;105(50):19910-4.
2008: Eveliina Jakkula; Karola Rehnström; Teppo Varilo; Olli P H Pietiläinen; Tiina Paunio; Nancy L Pedersen; Ulf deFaire; Marjo-Riitta Järvelin; Juha Saharinen; Nelson Freimer; Samuli Ripatti; Shaun Purcell; ANDREW COLLINS; Mark J Daly; Aarno Palotie; Leena Peltonen
The genome-wide patterns of variation expose significant substructure in a founder population.
American journal of human genetics 2008;83(6):787-94.
2008: David Altshuler; Mark J Daly; Eric S Lander
Genetic mapping in human disease.
Science (New York, N.Y.) 2008;322(5903):881-8.
2008: Edwin Choy; Roman Yelensky; Sasha Bonakdar; Robert M Plenge; Richa Saxena; Philip De Jager; Stanley Y Shaw; Cara S Wolfish; Jacqueline M Slavik; Chris Cotsapas; Manuel Rivas; Emmanouil T Dermitzakis; Ellen Cahir-McFarland; Elliott Kieff; David Hafler; Mark J Daly; David Altshuler
Genetic analysis of human traits in vitro: drug response and gene expression in lymphoblastoid cell lines.
PLoS genetics 2008;4(11):e1000287.
2008: Ralph Burkhardt; Eimear E Kenny; Jennifer K Lowe; Andrew Birkeland; Rebecca Josowitz; Martha Noel; Jacqueline Salit; Julian B Maller; Itsik Pe'er; Mark J Daly; David Altshuler; Markus Stoffel; Jeffrey M Friedman; Jan L Breslow
Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13.
Arteriosclerosis, thrombosis, and vascular biology 2008;28(11):2078-84.
2008: Dale R Nyholt; K Steven LaForge; Mikko Kallela; Kirsi Alakurtti; Verneri Anttila; Markus Färkkilä; Eija Hämaläinen; Jaakko Kaprio; Mari A Kaunisto; Andrew C Heath; Grant W Montgomery; Hartmut Göbel; Unda Todt; Michel D Ferrari; Lenore J Launer; Rune R Frants; Gisela M Terwindt; Boukje de Vries; W M Monique Verschuren; Jan Brand; Tobias Freilinger; Volker Pfaffenrath; Andreas Straube; Dennis G Ballinger; Yiping Zhan; Mark J Daly; David R Cox; Martin Dichgans; Arn van den Maagdenberg; Christian Kubisch; Nicholas G Martin; Maija Wessman; Leena Peltonen; Aarno Palotie
A high-density association screen of 155 ion transport genes for involvement with common migraine.
Human molecular genetics 2008;17(21):3318-31.
2008: Soumya Raychaudhuri; Elaine F Remmers; Annette T Lee; Rachel Hackett; Candace Guiducci; Noël P Burtt; Lauren Gianniny; Benjamin D Korman; Leonid Padyukov; Fina A S Kurreeman; Monica Chang; Joseph J Catanese; Bo Ding; Sandra Wong; Annette H M van der Helm-van Mil; Benjamin M Neale; Jonathan Coblyn; Jing Cui; Paul P Tak; Gert Jan Wolbink; J Bart A Crusius; Irene E van der Horst-Bruinsma; Lindsey A Criswell; Christopher I Amos; Michael F Seldin; Daniel Kastner; Kristin G Ardlie; Lars Alfredsson; Karen H Costenbader; David Altshuler; Tom W J Huizinga; Nancy A Shadick; Michael E Weinblatt; Niek de Vries; Jane Worthington; Mark Seielstad; Rene E M Toes; Elizabeth W Karlson; Ann B Begovich; Lars Klareskog; Peter K Gregersen; Mark J Daly; Robert M Plenge
Common variants at CD40 and other loci confer risk of rheumatoid arthritis.
Nature genetics 2008;40(10):1216-23.
2008: Joshua M Korn; Finny G Kuruvilla; Steven A McCarroll; Alec Wysoker; James Nemesh; Simon Cawley; Earl Hubbell; Jim Veitch; Patrick J Collins; Katayoon Darvishi; Charles Lee; Marcia M Nizzari; Stacey B Gabriel; Shaun Purcell; Mark J Daly; David Altshuler
Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs.
Nature genetics 2008;40(10):1253-60.
2008: Steven A McCarroll; Finny G Kuruvilla; Joshua M Korn; Simon Cawley; James Nemesh; Alec Wysoker; Michael H Shapero; Paul I W de Bakker; Julian B Maller; Andrew Kirby; Amanda Elliott; Melissa Parkin; Earl Hubbell; Teresa Webster; Rui Mei; James Veitch; Patrick J Collins; Robert Handsaker; Steve Lincoln; Marcia Nizzari; John Blume; Keith W Jones; Rich Rava; Mark J Daly; Stacey B Gabriel; David Altshuler
Integrated detection and population-genetic analysis of SNPs and copy number variation.
Nature genetics 2008;40(10):1166-74.
2008: C Labbé; Philippe Goyette; C Lefebvre; C Stevens; T Green; M K Tello-Ruiz; Z Cao; A L Landry; J Stempak; V Annese; A Latiano; Steven R Brant; Richard H Duerr; K D Taylor; Judy H Cho; A Hillary Steinhart; Mark J Daly; Mark S Silverberg; Ramnik Xavier; John D Rioux
MAST3: a novel IBD risk factor that modulates TLR4 signaling.
Genes and immunity 2008;9(7):602-12.
2008: Steven A McCarroll; Alan Huett; Petric Kuballa; Shannon D Chilewski; Aimee Landry; Philippe Goyette; Michael C Zody; Jennifer L Hall; Steven R Brant; Judy H Cho; Richard H Duerr; Mark S Silverberg; Kent D Taylor; John D Rioux; David Altshuler; Mark J Daly; Ramnik Xavier
Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease.
Nature genetics 2008;40(9):1107-12.
2008: Robert R Graham; Chris Cotsapas; Leela Davies; Rachel Hackett; Christopher J Lessard; Joanlise M Leon; Noël P Burtt; Candace Guiducci; Melissa Parkin; Casey Gates; Robert M Plenge; timothy wayne behrens; Joan E Wither; John D Rioux; Paul R Fortin; Deborah Cunninghame Graham; Andrew K Wong; Timothy J Vyse; Mark J Daly; David Altshuler; Kathy L Moser; Patrick M Gaffney
Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus.
Nature genetics 2008;40(9):1059-61.
2008: Manuel A R Ferreira; Michael C O'Donovan; Yan A Meng; Ian R Jones; Douglas M Ruderfer; Lisa Jones; Jinbo Fan; George Kirov; Roy H Perlis; Elaine K Green; Jordan W Smoller; Detelina Grozeva; Jennifer Stone; Ivan Nikolov; Kimberly Chambert; Marian L Hamshere; Vishwajit L Nimgaonkar; Valentina Moskvina; Michael E Thase; Sian Caesar; Gary S Sachs; Jennifer Franklin; Katherine Gordon-Smith; Kristin G Ardlie; Stacey B Gabriel; Christine Fraser; Brendan Blumenstiel; Matthew Defelice; Gerome Breen; Michael Gill; Derek W Morris; Amanda Elkin; Walter J Muir; McGhee Kevin; Richard Williamson; Donald J MacIntyre; Alan W MacLean; Clair David St; Michelle Robinson; Margaret Van Beck; Ana C P Pereira; Radhika Kandaswamy; Andrew McQuillin; David A Collier; Nicholas J Bass; Allan H Young; Jacob Lawrence; Ian Nicol Ferrier; Adebayo Anjorin; Anne Farmer; David Curtis; Edward M Scolnick; Peter McGuffin; Mark J Daly; Aiden P Corvin; Peter A Holmans; Douglas H Blackwood; Hugh M Gurling; Michael J Owen; Shaun M Purcell; Pamela Sklar; Nick Craddock
Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.
Nature genetics 2008;40(9):1056-8.
2008: Jeffrey C Barrett; Sarah Hansoul; Dan L Nicolae; Judy H Cho; Richard H Duerr; John D Rioux; Steven R Brant; Mark S Silverberg; Kent D Taylor; M Michael Barmada; Alain Bitton; Themistocles Dassopoulos; Lisa Datta; Todd Green; Anne M Griffiths; Emily O Kistner; Michael T Murtha; Miguel D Regueiro; Jerome I Rotter; L Philip Schumm; A Hillary Steinhart; Stephan R Targan; Ramnik J Xavier; Cecile Libioulle; Cynthia Sandor; Mark Lathrop; Jacques Belaiche; olivier dewit; Ivo Gut; Simon Heath; Debby Laukens; Myriam Mni; Paul Rutgeerts; André Van Gossum; Diana Zelenika; Denis Franchimont; Jean-Pierre Hugot; Martine de Vos; Severine Vermeire; Edouard Louis; Lon R Cardon; Carl A Anderson; Hazel Drummond; Elaine Nimmo; Tariq Ahmad; Natalie Prescott; Clive M Onnie; Sheila A Fisher; Jonathan Marchini; Jilur Ghori; Suzannah Bumpstead; Rhian Gwilliam; Mark Tremelling; Panos Deloukas; John Mansfield; Derek Jewell; Jack Satsangi; Christopher G Mathew; Miles Parkes; Michel Georges; Mark J Daly
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.
Nature genetics 2008;40(8):955-62.
2008: Verneri Anttila; Dale R Nyholt; Mikko Kallela; Ville Artto; Salli Vepsäläinen; Eveliina Jakkula; Annika Wennerström; Päivi Tikka-Kleemola; Mari A Kaunisto; Eija Hämäläinen; Elisabeth Widén; Joseph D Terwilliger; Kathleen Ries Merikangas; Grant W Montgomery; Nicholas G Martin; Mark J Daly; Jaakko Kaprio; Leena Peltonen; Markus Färkkilä; Maija Wessman; Aarno Palotie
Consistently replicating locus linked to migraine on 10q22-q23.
American journal of human genetics 2008;82(5):1051-63.
2008: Eleftheria Zeggini; Laura J Scott; Richa Saxena; Benjamin F Voight; Jonathan L Marchini; Tianle Hu; Paul I W de Bakker; Goncalo Abecasis; Peter Almgren; Gitte Andersen; Kristin Ardlie; Kristina Bengtsson Boström; Richard N Bergman; Lori L Bonnycastle; Knut Borch-Johnsen; Noël P Burtt; Hong Chen; Peter S Chines; Mark J Daly; Parimal Deodhar; Chia-Jen Ding; Alex S F Doney; William L Duren; Katherine S Elliott; Michael R Erdos; Timothy M Frayling; Rachel Freathy; Lauren Gianniny; Harald Grallert; Niels Grarup; Christopher J Groves; Candace Guiducci; Torben Hansen; Christian Herder; Graham A Hitman; Thomas Hughes; Bo Isomaa; Anne U Jackson; Torben Jørgensen; Augustine Kong; Kari Kubalanza; Finny G Kuruvilla; Johanna Kuusisto; Claudia Langenberg; Hana Lango; torsten lauritzen; Yun Li; Cecilia M Lindgren; Valeriya Lyssenko; Amanda F Marvelle; Christa Meisinger; Kristian Midthjell; Karen L Mohlke; Mario A Morken; Andrew D Morris; Narisu Narisu; Peter Nilsson; Katharine R Owen; Colin N A Palmer; Felicity Payne; John R B Perry; Elin Pettersen; Carl Platou; Inga Prokopenko; Lu Qi; Li Qin; Nigel W Rayner; Matthew Rees; Jeffrey J Roix; Anelli Sandbaek; Beverley Shields; Marketa Sjögren; Valgerdur Steinthorsdottir; Heather M Stringham; Amy J Swift; Gudmar Thorleifsson; Unnur Thorsteinsdottir; Nicholas J Timpson; Tiinamaija Tuomi; Jaakko Tuomilehto; Mark Walker; Richard Watanabe; Michael Weedon; Cristen J Willer; Thomas Illig; Kristian Hveem; Frank B Hu; Markku Laakso; kari stefansson; Oluf Pedersen; Nicholas J Wareham; Inês Barroso; Andrew T Hattersley; Francis S Collins; Leif Groop; Mark I McCarthy; Michael Boehnke; David Altshuler
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.
Nature genetics 2008;40(5):638-45.
2008: Itsik Pe'er; Roman Yelensky; David Altshuler; Mark J Daly
Estimation of the multiple testing burden for genomewide association studies of nearly all common variants.
Genetic epidemiology 2008;32(4):381-5.
2008: Catarina D Campbell; Andrew Kirby; James Nemesh; Mark J Daly; Joel N Hirschhorn
A survey of allelic imbalance in F1 mice.
Genome research 2008;18(4):555-63.
2008: P Goyette; C Lefebvre; A Ng; Steven R Brant; J H Cho; R H Duerr; M S Silverberg; K D Taylor; A Latiano; G Aumais; C Deslandres; G Jobin; V Annese; Mark J Daly; R J Xavier; J D Rioux
Gene-centric association mapping of chromosome 3p implicates MST1 in IBD pathogenesis.
Mucosal immunology 2008;1(2):131-8.
2008: Hyun Min Kang; Noah A Zaitlen; Claire M Wade; Andrew Kirby; David Heckerman; Mark J Daly; Eleazar Eskin
Efficient control of population structure in model organism association mapping.
Genetics 2008;178(3):1709-23.
2008: Lauren A Weiss; Yiping Shen; Joshua M Korn; Dan E Arking; David T Miller; Ragnheidur Fossdal; Evald Saemundsen; Hreinn Stefansson; Manuel A R Ferreira; Todd Green; Orah S Platt; Douglas M Ruderfer; Christopher Walsh; David Altshuler; Aravinda Chakravarti; Rudolph E Tanzi; Kari Stefansson; Susan L Santangelo; James Gusella; Pamela Sklar; Bai-Lin Wu; Mark J Daly
Association between microdeletion and microduplication at 16p11.2 and autism.
The New England journal of medicine 2008;358(7):667-75.
2008: Petric Kuballa; Alan Huett; John D Rioux; Mark J Daly; Ramnik Xavier
Impaired autophagy of an intracellular pathogen induced by a Crohn's disease associated ATG16L1 variant.
PloS one 2008;3(10):e3391.
2008: Hyung-Goo Kim; Shotaro Kishikawa; Anne W Higgins; Ihn Sik Seong; Diana J Donovan; Yiping Shen; Eric Lally; Lauren A Weiss; Juliane Najm; Kerstin Kutsche; Maria Descartes; Lynn Holt; Stephen Braddock; Robin Troxell; Lee Kaplan; Fred Volkmar; Ami Klin; Katherine Tsatsanis; David J Harris; Ilse Noens; David L Pauls; Mark J Daly; Marcy E MacDonald; Cynthia C Morton; Bradley J Quade; James Gusella
Disruption of neurexin 1 associated with autism spectrum disorder.
American journal of human genetics 2008;82(1):199-207.
2007: Robert M Plenge; Chris Cotsapas; Leela Davies; Alkes L Price; Paul I W de Bakker; Julian Maller; Itsik Pe'er; Noel P Burtt; Brendan Blumenstiel; Matt DeFelice; Melissa Parkin; Rachel Barry; Wendy Winslow; Claire Healy; Robert R Graham; Benjamin M Neale; Elena Izmailova; Ronenn Roubenoff; Alexander N Parker; Roberta Glass; Elizabeth W Karlson; Nancy Maher; David A Hafler; David M Lee; Michael F Seldin; Elaine F Remmers; Annette T Lee; Leonid Padyukov; Lars Alfredsson; Jonathan Coblyn; Michael E Weinblatt; Stacey B Gabriel; Shaun Purcell; Lars Klareskog; Peter K Gregersen; Nancy A Shadick; Mark J Daly; David Altshuler
Two independent alleles at 6q23 associated with risk of rheumatoid arthritis.
Nature genetics 2007;39(12):1477-82.
2007: Pardis C Sabeti; Patrick Varilly; Ben Fry; Jason Lohmueller; Elizabeth Hostetter; Chris Cotsapas; Xiaohui Xie; Elizabeth H Byrne; Steven A McCarroll; Rachelle Gaudet; Stephen F Schaffner; Eric S Lander; Kelly A Frazer; Dennis G Ballinger; David R Cox; David Hinds; Laura L Stuve; Richard A Gibbs; John W Belmont; Andrew Boudreau; Paul Hardenbol; Suzanne M Leal; Shiran Pasternak; David A Wheeler; Thomas D Willis; Fuli Yu; Huanming Yang; Changqing Zeng; Yang Gao; Haoran Hu; Weitao Hu; Chaohua Li; Wei Lin; Siqi Liu; Hao Pan; Xiaoli Tang; Jian Wang; Wei Wang; Jun Yu; Bo Zhang; Qingrun Zhang; Hongbin Zhao; Hui Zhao; Jun Zhou; Stacey B Gabriel; Rachel Barry; Brendan Blumenstiel; Amy Camargo; Matthew Defelice; Maura Faggart; Mary Goyette; Supriya Gupta; Jamie Moore; Huy Nguyen; Robert C Onofrio; Melissa Parkin; Jessica Roy; Erich Stahl; Ellen Winchester; Liuda Ziaugra; David Altshuler; Yan Shen; Zhijian Yao; Wei Huang; Xun Chu; Yungang He; Li Jin; Yangfan Liu; Yayun Shen; Weiwei Sun; Haifeng Wang; Yi Wang; Ying Wang; Xiaoyan Xiong; Liang Xu; Mary Waye; Stephen K W Tsui; Hong Xue; J Tze-Fei Wong; Luana M Galver; Jian-Bing Fan; Kevin Gunderson; Sarah S Murray; Arnold R Oliphant; Mark S Chee; Alexandre Montpetit; Fanny Chagnon; Vincent Ferretti; Martin Leboeuf; Jean-François Olivier; Michael S Phillips; Stéphanie Roumy; Clémentine Sallée; Andrei Verner; Thomas J Hudson; Pui-Yan Kwok; Dongmei Cai; Daniel C Koboldt; Raymond D Miller; Ludmila Pawlikowska; Patricia Taillon-Miller; Ming Xiao; Lap-Chee Tsui; William Mak; You Qiang Song; Paul K H Tam; Yusuke Nakamura; Takahisa Kawaguchi; Takuya Kitamoto; Takashi Morizono; Atsushi Nagashima; Yozo Ohnishi; Akihiro Sekine; Toshihiro Tanaka; Tatsuhiko Tsunoda; Panos Deloukas; Christine P Bird; Marcos Delgado; Emmanouil T Dermitzakis; Rhian Gwilliam; Sarah Hunt; Jonathan Morrison; Don Powell; Barbara E Stranger; Pamela Whittaker; David R Bentley; Mark J Daly; Paul I W de Bakker; Jeff Barrett; Yves R Chretien; Julian Maller; Steve McCarroll; Nick Patterson; Itsik Pe'er; Alkes Price; Shaun Purcell; Daniel J Richter; Pardis Sabeti; Richa Saxena; Stephen F Schaffner; Pak C Sham; Patrick Varilly; David Altshuler; Lincoln D Stein; Lalitha Krishnan; Albert Vernon Smith; Marcela K Tello-Ruiz; Gudmundur A Thorisson; Aravinda Chakravarti; Peter E Chen; David J Cutler; Carl S Kashuk; Shin Lin; Goncalo Abecasis; Weihua Guan; Yun Li; Heather M Munro; Zhaohui Steve Qin; Daryl J Thomas; Gilean McVean; Adam Auton; Leonardo Bottolo; Niall Cardin; Susana Eyheramendy; Colin Freeman; Jonathan Marchini; Simon Myers; Chris Spencer; Matthew Stephens; Peter Donnelly; Lon R Cardon; Geraldine Clarke; David M Evans; Andrew P Morris; Bruce S Weir; Tatsuhiko Tsunoda; Todd A Johnson; James C Mullikin; Stephen T Sherry; Michael Feolo; Andrew Skol; Houcan Zhang; Changqing Zeng; Hui Zhao; Ichiro Matsuda; Yoshimitsu Fukushima; Darryl R Macer; Eiko Suda; Charles N Rotimi; Clement Adebamowo; Ike Ajayi; Toyin Aniagwu; Patricia A Marshall; Chibuzor Nkwodimmah; Charmaine D M Royal; Mark F Leppert; Missy Dixon; Andy Peiffer; Renzong Qiu; Alastair Kent; Kazuto Kato; Norio Niikawa; ISAAC FOLORUNSO ADEWOLE; Bartha M Knoppers; Morris W Foster; Ellen Wright Clayton; Jessica Watkin; Richard A Gibbs; John W Belmont; Donna Muzny; Lynne Nazareth; Erica Sodergren; George Weinstock; David A Wheeler; Imtaz Yakub; Stacey B Gabriel; Robert C Onofrio; Daniel J Richter; Liuda Ziaugra; Bruce W Birren; Mark J Daly; David Altshuler; Richard K Wilson; Lucinda L Fulton; Jane Rogers; John Burton; Nigel P Carter; Christopher M Clee; Mark Griffiths; Matthew C Jones; Kirsten McLay; Robert W Plumb; Mark T Ross; Sarah K Sims; David L Willey; Zhu Chen; Hua Han; Le Kang; Martin Godbout; John C Wallenburg; Paul L'Archevêque; Guy Bellemare; Koji Saeki; Hongguang Wang; Daochang An; Hongbo Fu; Qing Li; Zhen Wang; Renwu Wang; Arthur L Holden; Lisa D Brooks; Jean E McEwen; Mark S Guyer; Vivian Ota Wang; Jane L Peterson; Michael Shi; Jack Spiegel; Lawrence M Sung; Lynn F Zacharia; Francis S Collins; Karen Kennedy; Ruth Jamieson; John Stewart
Genome-wide detection and characterization of positive selection in human populations.
Nature 2007;449(7164):913-8.
2007: Kelly A Frazer; Dennis G Ballinger; David R Cox; David Hinds; Laura L Stuve; Richard A Gibbs; John W Belmont; Andrew Boudreau; Paul Hardenbol; Suzanne M Leal; Shiran Pasternak; David A Wheeler; Thomas D Willis; Fuli Yu; Huanming Yang; Changqing Zeng; Yang Gao; Haoran Hu; Weitao Hu; Chaohua Li; Wei Lin; Siqi Liu; Hao Pan; Xiaoli Tang; Jian Wang; Wei Wang; Jun Yu; Bo Zhang; Qingrun Zhang; Hongbin Zhao; Hui Zhao; Jun Zhou; Stacey B Gabriel; Rachel Barry; Brendan Blumenstiel; Amy Camargo; Matthew Defelice; Maura Faggart; Mary Goyette; Supriya Gupta; Jamie Moore; Huy Nguyen; Robert C Onofrio; Melissa Parkin; Jessica Roy; Erich Stahl; Ellen Winchester; Liuda Ziaugra; David Altshuler; Yan Shen; Zhijian Yao; Wei Huang; Xun Chu; Yungang He; Li Jin; Yangfan Liu; Yayun Shen; Weiwei Sun; Haifeng Wang; Yi Wang; Ying Wang; Xiaoyan Xiong; Liang Xu; Mary Waye; Stephen K W Tsui; Hong Xue; J Tze-Fei Wong; Luana M Galver; Jian-Bing Fan; Kevin Gunderson; Sarah S Murray; Arnold R Oliphant; Mark S Chee; Alexandre Montpetit; Fanny Chagnon; Vincent Ferretti; Martin Leboeuf; Jean-François Olivier; Michael S Phillips; Stéphanie Roumy; Clémentine Sallée; Andrei Verner; Thomas J Hudson; Pui-Yan Kwok; Dongmei Cai; Daniel C Koboldt; Raymond D Miller; Ludmila Pawlikowska; Patricia Taillon-Miller; Ming Xiao; Lap-Chee Tsui; William Mak; You Qiang Song; Paul K H Tam; Yusuke Nakamura; Takahisa Kawaguchi; Takuya Kitamoto; Takashi Morizono; Atsushi Nagashima; Yozo Ohnishi; Akihiro Sekine; Toshihiro Tanaka; Tatsuhiko Tsunoda; Panos Deloukas; Christine P Bird; Marcos Delgado; Emmanouil T Dermitzakis; Rhian Gwilliam; Sarah Hunt; Jonathan Morrison; Don Powell; Barbara E Stranger; Pamela Whittaker; David R Bentley; Mark J Daly; Paul I W de Bakker; Jeff Barrett; Yves R Chretien; Julian Maller; Steve McCarroll; Nick Patterson; Itsik Pe'er; Alkes Price; Shaun Purcell; Daniel J Richter; Pardis Sabeti; Richa Saxena; Stephen F Schaffner; Pak C Sham; Patrick Varilly; David Altshuler; Lincoln D Stein; Lalitha Krishnan; Albert Vernon Smith; Marcela K Tello-Ruiz; Gudmundur A Thorisson; Aravinda Chakravarti; Peter E Chen; David J Cutler; Carl S Kashuk; Shin Lin; Goncalo Abecasis; Weihua Guan; Yun Li; Heather M Munro; Zhaohui Steve Qin; Daryl J Thomas; Gilean McVean; Adam Auton; Leonardo Bottolo; Niall Cardin; Susana Eyheramendy; Colin Freeman; Jonathan Marchini; Simon Myers; Chris Spencer; Matthew Stephens; Peter Donnelly; Lon R Cardon; Geraldine Clarke; David M Evans; Andrew P Morris; Bruce S Weir; Tatsuhiko Tsunoda; James C Mullikin; Stephen T Sherry; Michael Feolo; Andrew Skol; Houcan Zhang; Changqing Zeng; Hui Zhao; Ichiro Matsuda; Yoshimitsu Fukushima; Darryl R Macer; Eiko Suda; Charles N Rotimi; Clement Adebamowo; Ike Ajayi; Toyin Aniagwu; Patricia A Marshall; Chibuzor Nkwodimmah; Charmaine D M Royal; Mark F Leppert; Missy Dixon; Andy Peiffer; Renzong Qiu; Alastair Kent; Kazuto Kato; Norio Niikawa; ISAAC FOLORUNSO ADEWOLE; Bartha M Knoppers; Morris W Foster; Ellen Wright Clayton; Jessica Watkin; Richard A Gibbs; John W Belmont; Donna Muzny; Lynne Nazareth; Erica Sodergren; George M Weinstock; David A Wheeler; Imtaz Yakub; Stacey B Gabriel; Robert C Onofrio; Daniel J Richter; Liuda Ziaugra; Bruce W Birren; Mark J Daly; David Altshuler; Richard K Wilson; Lucinda L Fulton; Jane Rogers; John Burton; Nigel P Carter; Christopher M Clee; Mark Griffiths; Matthew C Jones; Kirsten McLay; Robert W Plumb; Mark T Ross; Sarah K Sims; David L Willey; Zhu Chen; Hua Han; Le Kang; Martin Godbout; John C Wallenburg; Paul L'Archevêque; Guy Bellemare; Koji Saeki; Hongguang Wang; Daochang An; Hongbo Fu; Qing Li; Zhen Wang; Renwu Wang; Arthur L Holden; Lisa D Brooks; Jean E McEwen; Mark S Guyer; Vivian Ota Wang; Jane L Peterson; Michael Shi; Jack Spiegel; Lawrence M Sung; Lynn F Zacharia; Francis S Collins; Karen Kennedy; Ruth Jamieson; John Stewart
A second generation human haplotype map of over 3.1 million SNPs.
Nature 2007;449(7164):851-61.
2007: Julian Maller; Jesen Fagerness; Robyn C Reynolds; Benjamin M Neale; Mark J Daly; Johanna M Seddon
Variation in complement factor 3 is associated with risk of age-related macular degeneration.
Nature genetics 2007;39(10):1200-1.
2007: Teri A Manolio; Laura Lyman Rodriguez; Lisa Brooks; Goncalo Abecasis; Dennis G Ballinger; Mark J Daly; Peter Donnelly; Stephen Faraone; Kelly A Frazer; Stacey Gabriel; Pablo Gejman; Alan Guttmacher; Emily L Harris; Thomas R Insel; John R Kelsoe; Eric Lander; Norma McCowin; Matthew D Mailman; Elizabeth G Nabel; James Ostell; Elizabeth Pugh; Stephen T Sherry; Patrick F Sullivan; John F Thompson; James Warram; David Wholley; Patrice M Milos; Francis S Collins
New models of collaboration in genome-wide association studies: the Genetic Association Information Network.
Nature genetics 2007;39(9):1045-51.
2007: Shaun Purcell; Benjamin Neale; Kathe Todd-Brown; Lori Thomas; Manuel A R Ferreira; David Bender; Julian Maller; Pamela Sklar; Paul I W de Bakker; Mark J Daly; Pak C Sham
PLINK: a tool set for whole-genome association and population-based linkage analyses.
American journal of human genetics 2007;81(3):559-75.
2007: Kelly A Frazer; Eleazar Eskin; Hyun Min Kang; Molly A Bogue; David Hinds; Erica J Beilharz; Robert V Gupta; Julie Montgomery; Matt M Morenzoni; Geoffrey B Nilsen; Charit L Pethiyagoda; Laura L Stuve; Frank M Johnson; Mark J Daly; Claire M Wade; David R Cox
A sequence-based variation map of 8.27 million SNPs in inbred mouse strains.
Nature 2007;448(7157):1050-3.
2007: David A Hafler; Alastair Compston; Stephen Sawcer; Eric S Lander; Mark J Daly; Philip De Jager; Paul I W de Bakker; Stacey B Gabriel; Daniel B Mirel; Adrian J Ivinson; Margaret Pericak-Vance; Simon G Gregory; John D Rioux; Jacob McCauley; Jonathan L Haines; Lisa F Barcellos; Bruce A C Cree; Jorge R Oksenberg; Stephen L Hauser
Risk alleles for multiple sclerosis identified by a genomewide study.
The New England journal of medicine 2007;357(9):851-62.
2007: Sophie Astrof; Andrew Kirby; Kerstin Lindblad-Toh; Mark J Daly; Richard O Hynes
Heart development in fibronectin-null mice is governed by a genetic modifier on chromosome four.
Mechanisms of development 2007;124(7-8):551-8.
2007: Philip De Jager; Denis Franchimont; Alicja Waliszewska; Alain Bitton; Albert Cohen; Diane Langelier; J Belaiche; Severine Vermeire; Lisa Farwell; An Goris; Cecile Libioulle; NIRAJ JANI; Themistocles Dassopoulos; Gillian P Bromfield; Bruno Dubois; J H Cho; Steven R Brant; Richard H Duerr; Haifeng Yang; J I Rotter; M S Silverberg; A Hillary Steinhart; Mark J Daly; Daniel K Podolsky; E Louis; David A Hafler; John D Rioux
The role of the Toll receptor pathway in susceptibility to inflammatory bowel diseases.
Genes and immunity 2007;8(5):387-97.
2007: Manuel A R Ferreira; Pak Sham; Mark J Daly; Shaun Purcell
Ascertainment through family history of disease often decreases the power of family-based association studies.
Behavior genetics 2007;37(4):631-6.
2007: STEPHEN CHANOCK; Teri Manolio; Michael Boehnke; Eric Boerwinkle; David J Hunter; Gilles Thomas; Joel N Hirschhorn; Goncalo Abecasis; David Altshuler; Joan E Bailey-Wilson; Lisa D Brooks; Lon R Cardon; Mark J Daly; Peter Donnelly; Joseph Fraumeni; Nelson B Freimer; Daniela S Gerhard; Chris Gunter; Alan E Guttmacher; Mark S Guyer; Emily L Harris; Josephine Hoh; Robert Hoover; C Augustine Kong; Kathleen Ries Merikangas; Cynthia C Morton; Lyle Palmer; Elizabeth G Phimister; John P Rice; Jerry Roberts; Charles Rotimi; Margaret A Tucker; Kyle J Vogan; Sholom Wacholder; Ellen M Wijsman; Deborah M Winn; Francis S Collins
Replicating genotype-phenotype associations.
Nature 2007;447(7145):655-60.
2007: Richa Saxena; Benjamin F Voight; Valeriya Lyssenko; Noël P Burtt; Paul I W de Bakker; Hong Chen; Jeffrey J Roix; Sekar Kathiresan; Joel N Hirschhorn; Mark J Daly; Thomas Hughes; Leif Groop; David Altshuler; Peter Almgren; Jose C Florez; Joanne Meyer; Kristin Ardlie; Kristina Bengtsson Boström; Bo Isomaa; Guillaume Lettre; Ulf Lindblad; Helen N Lyon; Olle Melander; Christopher Newton-Cheh; Peter Nilsson; Marju Orho-Melander; Lennart Råstam; Elizabeth K Speliotes; Marja-Riitta Taskinen; Tiinamaija Tuomi; Candace Guiducci; Anna Berglund; Joyce Carlson; Lauren Gianniny; Rachel Hackett; Liselotte Hall; Johan Holmkvist; Esa Laurila; Marketa Sjögren; Maria Sterner; Aarti Surti; Margareta Svensson; Malin Svensson; Ryan Tewhey; Brendan Blumenstiel; Melissa Parkin; Matthew Defelice; Rachel Barry; Wendy Brodeur; Jody Camarata; Nancy Chia; Mary Fava; John Gibbons; Bob Handsaker; Claire Healy; Kieu Nguyen; Casey Gates; Carrie Sougnez; Diane Gage; Marcia Nizzari; Stacey B Gabriel; Gung-Wei Chirn; Qicheng Ma; Hemang Parikh; Delwood Richardson; Darrell Ricke; Shaun Purcell
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.
Science (New York, N.Y.) 2007;316(5829):1331-6.
2007: Jose C Florez; M Sjögren; Christina M Agapakis; Noël P Burtt; Peter Almgren; Ulf Lindblad; G Berglund; Tiinamaija Tuomi; Daniel Gaudet; Mark J Daly; Kristin G Ardlie; J N Hirschhorn; David Altshuler; Leif Groop
Association testing of common variants in the insulin receptor substrate-1 gene (IRS1) with type 2 diabetes.
Diabetologia 2007;50(6):1209-17.
2007: John D Rioux; Ramnik Xavier; Kent D Taylor; Mark S Silverberg; Philippe Goyette; Alan Huett; Todd Green; Petric Kuballa; M. Michael Barmada; Lisa Datta; Yin Yao Shugart; Anne M Griffiths; Stephan R Targan; Andrew Ippoliti; Edmond-Jean Bernard; Ling Mei; Dan L Nicolae; Miguel Regueiro; L Philip Schumm; A Hillary Steinhart; Jerome I Rotter; Richard H Duerr; Judy H Cho; Mark J Daly; Steven R Brant
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.
Nature genetics 2007;39(5):596-604.
2007: Robert R Graham; Chieko Kyogoku; Snaevar Sigurdsson; Irina Vlasova - St. Louis; Leela R L Davies; Emily C Baechler; Robert M Plenge; Thearith Koeuth; Ward A Ortmann; Geoffrey Hom; Jason W Bauer; Clarence Gillett; Noël P Burtt; Deborah S Cunninghame-Graham; Robert C Onofrio; Michelle Petri; Iva Gunnarsson; Elisabet Svenungsson; Lars Rönnblom; Gunnel Nordmark; Peter K Gregersen; Kathy Moser; Patrick M Gaffney; Lindsey A Criswell; Timothy J Vyse; Ann-Christine Syvänen; Paul R Bohjanen; Mark J Daly; timothy wayne behrens; David Altshuler
Three functional variants of IFN regulatory factor 5 (IRF5) define risk and protective haplotypes for human lupus.
Proceedings of the National Academy of Sciences of the United States of America 2007;104(16):6758-63.
2007: Wendy Winckler; Michael Weedon; Robert R Graham; Steven A McCarroll; Shaun Purcell; Peter Almgren; Tiinamaija Tuomi; Daniel Gaudet; Kristina Bengtsson Boström; Mark Walker; Graham A Hitman; Andrew T Hattersley; Mark I McCarthy; Kristin G Ardlie; Joel N Hirschhorn; Mark J Daly; Timothy M Frayling; Leif Groop; David Altshuler
Evaluation of common variants in the six known maturity-onset diabetes of the young (MODY) genes for association with type 2 diabetes.
Diabetes 2007;56(3):685-93.
2007: Tai Wai Yeo; Philip De Jager; Simon G Gregory; Lisa F Barcellos; Amie Walton; An Goris; Chiara Fenoglio; Maria Ban; Craig J Taylor; Reyna S Goodman; Emily Walsh; Cara S Wolfish; Roger HORTON; James A Traherne; Stephan Beck; John Trowsdale; Stacy J Caillier; Adrian J Ivinson; Todd Green; Susan Pobywajlo; Eric S Lander; Margaret Pericak-Vance; Jonathan L Haines; Mark J Daly; Jorge R Oksenberg; Stephen L Hauser; Alastair Compston; David A Hafler; John D Rioux; Stephen Sawcer
A second major histocompatibility complex susceptibility locus for multiple sclerosis.
Annals of neurology 2007;61(3):228-36.
2007: Mark S Silverberg; Richard H Duerr; Steven R Brant; Gillian P Bromfield; Lisa Datta; NIRAJ JANI; Sunanda V Kane; Jerome I Rotter; L Philip Schumm; A Hillary Steinhart; Kent D Taylor; Huiying Yang; Judy H Cho; John D Rioux; Mark J Daly
Refined genomic localization and ethnic differences observed for the IBD5 association with Crohn's disease.
European journal of human genetics : EJHG 2007;15(3):328-35.
2007: Kitai Kim; Paul Lerou; Akiko Yabuuchi; Claudia Lengerke; Kitwa Ng; Jason West; Andrew Kirby; Mark J Daly; George Q Daley
Histocompatible embryonic stem cells by parthenogenesis.
Science (New York, N.Y.) 2007;315(5811):482-6.
2007: Shaun Purcell; Mark J Daly; Pak C Sham
WHAP: haplotype-based association analysis.
Bioinformatics (Oxford, England) 2007;23(2):255-6.
2007: Sonia Brescianini; Truc T Trinh; M Stoll; S Schreiber; John D Rioux; Mark J Daly
IBD5 is associated with an extensive complicated Crohn's disease feature: implications from genotype-phenotype analysis.
Gut 2007;56(1):149-50.
2007: Lauren A Weiss; Shaun Purcell; Skye Waggoner; Kate Lawrence; David Spektor; Mark J Daly; Pamela Sklar; David Skuse
Identification of EFHC2 as a quantitative trait locus for fear recognition in Turner syndrome.
Human molecular genetics 2007;16(1):107-13.
2006: Jose C Florez; Richa Saxena; Wendy Winckler; Noël P Burtt; Peter Almgren; Kristina Bengtsson Boström; Tiinamaija Tuomi; Daniel Gaudet; Kristin G Ardlie; Mark J Daly; David Altshuler; Joel N Hirschhorn; Leif Groop
The Krüppel-like factor 11 (KLF11) Q62R polymorphism is not associated with type 2 diabetes in 8,676 people.
Diabetes 2006;55(12):3620-4.
2006: Ad van Bodegraven; Christine R Curley; Karen A Hunt; Alienke J Monsuur; Ronald K Linskens; Clive M Onnie; J B A Crusius; Vito Annese; Anna Latiano; Mark S Silverberg; Alain Bitton; Sheila A Fisher; A Hillary Steinhart; Alastair Forbes; Jeremy Sanderson; Natalie Prescott; David P Strachan; Raymond J Playford; Christopher G Mathew; Cisca Wijmenga; Mark J Daly; John D Rioux; David A van Heel
Genetic variation in myosin IXB is associated with ulcerative colitis.
Gastroenterology 2006;131(6):1768-74.
2006: Richard H Duerr; Kent D Taylor; Steven R Brant; John D Rioux; Mark S Silverberg; Mark J Daly; A Hillary Steinhart; Clara Abraham; Miguel Regueiro; Anne Griffiths; Themistocles Dassopoulos; Alain Bitton; Huiying Yang; Stephan R Targan; Lisa Datta; Emily O Kistner; L Philip Schumm; Annette T Lee; Peter K Gregersen; M. Michael Barmada; Jerome I Rotter; Dan L Nicolae; Judy H Cho
A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.
Science (New York, N.Y.) 2006;314(5804):1461-3.
2006: Helen N Lyon; Jose C Florez; Todd Bersaglieri; Richa Saxena; Wendy Winckler; Peter Almgren; Ulf Lindblad; Tiinamaija Tuomi; Daniel Gaudet; Xiaofeng Zhu; Richard Cooper; Kristin G Ardlie; Mark J Daly; David Altshuler; Leif Groop; Joel N Hirschhorn
Common variants in the ENPP1 gene are not reproducibly associated with diabetes or obesity.
Diabetes 2006;55(11):3180-4.
2006: Paul I W de Bakker; Noël P Burtt; Robert R Graham; Candace Guiducci; Roman Yelensky; Jared A Drake; Todd Bersaglieri; Kathryn L Penney; Johannah Butler; Stanton Young; Robert C Onofrio; Helen N Lyon; Daniel O Stram; Christopher A Haiman; Matthew L Freedman; Xiaofeng Zhu; Richard Cooper; Leif Groop; Laurence N Kolonel; Brian Henderson; Mark J Daly; Joel N Hirschhorn; David Altshuler
Transferability of tag SNPs in genetic association studies in multiple populations.
Nature genetics 2006;38(11):1298-303.
2006: Mousumi Mutsuddi; Derek W Morris; Skye G Waggoner; Mark J Daly; Edward M Scolnick; Pamela Sklar
Analysis of high-resolution HapMap of DTNBP1 (Dysbindin) suggests no consistency between reported common variant associations and schizophrenia.
American journal of human genetics 2006;79(5):903-9.
2006: Steven Wiltshire; Paul I W de Bakker; Mark J Daly
The value of gene-based selection of tag SNPs in genome-wide association studies.
European journal of human genetics : EJHG 2006;14(11):1209-14.
2006: Richa Saxena; Lauren Gianniny; Noël P Burtt; Valeriya Lyssenko; Candace Giuducci; Marketa Sjögren; Jose C Florez; Peter Almgren; Bo Isomaa; Marju Orho-Melander; Ulf Lindblad; Mark J Daly; Tiinamaija Tuomi; Joel N Hirschhorn; Kristin G Ardlie; Leif C Groop; David Altshuler
Common single nucleotide polymorphisms in TCF7L2 are reproducibly associated with type 2 diabetes and reduce the insulin response to glucose in nondiabetic individuals.
Diabetes 2006;55(10):2890-5.
2006: Paul I W de Bakker; Gil McVean; Pardis C Sabeti; Marcos M Miretti; Todd Green; Jonathan Marchini; Xiayi Ke; Alienke J Monsuur; Pamela Whittaker; Marcos Delgado; Jonathan Morrison; Angela Richardson; Emily C Walsh; Xiaojiang Gao; Luana Galver; John Hart; David A Hafler; Margaret Pericak-Vance; John A Todd; Mark J Daly; John Trowsdale; Cisca Wijmenga; Timothy J Vyse; Stephan Beck; Sarah Shaw Murray; Mary Carrington; Simon Gregory; Panos Deloukas; John D Rioux
A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC.
Nature genetics 2006;38(10):1166-72.
2006: Julian Maller; Sarah George; Shaun Purcell; Jesen Fagerness; David Altshuler; Mark J Daly; Johanna M Seddon
Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degeneration.
Nature genetics 2006;38(9):1055-9.
2006: Sheila A Fisher; Jochen Hampe; Clive M Onnie; Mark J Daly; Christine R Curley; Shaun Purcell; Jeremy Sanderson; John Mansfield; Vito Annese; Alastair Forbes; Cathryn M Lewis; Stefan Schreiber; John D Rioux; Christopher G Mathew
Direct or indirect association in a complex disease: the role of SLC22A4 and SLC22A5 functional variants in Crohn disease.
Human mutation 2006;27(8):778-85.
2006: Cosmas Giallourakis; Zhifang Cao; Todd Green; Heather Wachtel; Xiaohui Xie; Marco Lopez-Illasaca; Mark J Daly; John D Rioux; Ramnik Xavier
A molecular-properties-based approach to understanding PDZ domain proteins and PDZ ligands.
Genome research 2006;16(8):1056-72.
2006: Kazuhiro Ishiguro; Todd Green; Joseph Rapley; Heather Wachtel; Cosmas Giallourakis; Aimee Landry; Zhifang Cao; Naifang Lu; Ando Takafumi; Hidemi Goto; Mark J Daly; Ramnik Xavier
Ca2+/calmodulin-dependent protein kinase II is a modulator of CARMA1-mediated NF-kappaB activation.
Molecular and cellular biology 2006;26(14):5497-508.
2006: Richa Saxena; Paul I W de Bakker; Karyn Singer; Vamsi K Mootha; Noël P Burtt; Joel N Hirschhorn; Daniel Gaudet; Bo Isomaa; Mark J Daly; Leif Groop; Kristin G Ardlie; David Altshuler
Comprehensive association testing of common mitochondrial DNA variation in metabolic disease.
American journal of human genetics 2006;79(1):54-61.
2006: Itsik Pe'er; Paul I W de Bakker; Julian Maller; Roman Yelensky; David Altshuler; Mark J Daly
Evaluating and improving power in whole-genome association studies using fixed marker sets.
Nature genetics 2006;38(6):663-7.
2006: Marcela Karey Tello-Ruiz; Christine R Curley; Terrye Delmonte; Cosmas Giallourakis; Andrew Kirby; Kathryn Miller; Gary Wild; Albert Cohen; Diane Langelier; Anna Latiano; Neils Wedemeyer; Eric S Lander; Stefan Schreiber; Vito Annese; Mark J Daly; John D Rioux
Haplotype-based association analysis of 56 functional candidate genes in the IBD6 locus on chromosome 19.
European journal of human genetics : EJHG 2006;14(6):780-90.
2006: Robert R Graham; Sergey V Kozyrev; Emily C Baechler; M V Prasad Linga Reddy; Robert M Plenge; Jason W Bauer; Ward A Ortmann; Thearith Koeuth; María Francisca González-Escribano; Bernardo A Pons-Estel; Michelle Petri; Mark J Daly; Peter K Gregersen; Javier Martín; David Altshuler; timothy wayne behrens; Marta E Alarcón-Riquelme
A common haplotype of interferon regulatory factor 5 (IRF5) regulates splicing and expression and is associated with increased risk of systemic lupus erythematosus.
Nature genetics 2006;38(5):550-5.
2006: Itsik Pe'er; Yves R Chretien; Paul I W de Bakker; Jeffrey C Barrett; Mark J Daly; David Altshuler
Biases and reconciliation in estimates of linkage disequilibrium in the human genome.
American journal of human genetics 2006;78(4):588-603.
2006: Bo-Shiun Yan; A Kirby; Yuriy V Shebzukhov; Mark J Daly; Igor Kramnik
Genetic architecture of tuberculosis resistance in a mouse model of infection.
Genes and immunity 2006;7(3):201-10.
2006: Frauke Friedrichs; Sonia Brescianini; Vito Annese; Anna Latiano; Klaus Berger; Subra Kugathasan; Ulrich Broeckel; Susanna Nikolaus; Mark J Daly; Stefan Schreiber; John D Rioux; Monika Stoll
Evidence of transmission ratio distortion of DLG5 R30Q variant in general and implication of an association with Crohn disease in men.
Human genetics 2006;119(3):305-11.
2006: Maria W Sun; Jennifer Y Lee; Paul I W de Bakker; Noël P Burtt; Peter Almgren; Lennart Råstam; Tiinamaija Tuomi; Daniel Gaudet; Mark J Daly; Joel N Hirschhorn; David Altshuler; Leif Groop; Jose C Florez
Haplotype structures and large-scale association testing of the 5' AMP-activated protein kinase genes PRKAA2, PRKAB1, and PRKAB2 [corrected] with type 2 diabetes.
Diabetes 2006;55(3):849-55.
2006: Penelope E Bonnen; Itsik Pe'er; Robert M Plenge; Jacqueline Salit; Jennifer K Lowe; Michael H Shapero; Richard P Lifton; Jan L Breslow; Mark J Daly; David E Reich; Keith W Jones; Markus Stoffel; David Altshuler; Jeffrey M Friedman
Evaluating potential for whole-genome studies in Kosrae, an isolated population in Micronesia.
Nature genetics 2006;38(2):214-7.
2006: Steven A McCarroll; Tracy N Hadnott; George H Perry; Pardis C Sabeti; Michael C Zody; Jeffrey C Barrett; Stephanie Dallaire; Stacey B Gabriel; Charles Lee; Mark J Daly; David Altshuler
Common deletion polymorphisms in the human genome.
Nature genetics 2006;38(1):86-92.
2006: Jose C Florez; Steven Wiltshire; Christina M Agapakis; Noël P Burtt; Paul I W de Bakker; Peter Almgren; Kristina Bengtsson Boström; Tiinamaija Tuomi; Daniel Gaudet; Mark J Daly; Joel N Hirschhorn; Mark I McCarthy; David Altshuler; Leif Groop
High-density haplotype structure and association testing of the insulin-degrading enzyme (IDE) gene with type 2 diabetes in 4,206 people.
Diabetes 2006;55(1):128-35.
2006: Gregory E Crawford; Ingeborg E Holt; James Whittle; Bryn D Webb; Denise Tai; Sean Davis; Elliott H Margulies; Yidong Chen; John A Bernat; David Ginsburg; Daixing Zhou; Shujun Luo; thomas vasicek; Mark J Daly; Tyra G Wolfsberg; Francis S Collins
Genome-wide mapping of DNase hypersensitive sites using massively parallel signature sequencing (MPSS).
Genome research 2006;16(1):123-31.
2006: Sapna Chadha; Katie Miller; Lisa Farwell; Steven Sacks; Mark J Daly; John D Rioux; Timothy J Vyse
Haplotype analysis of tumour necrosis factor receptor genes in 1p36: no evidence for association with systemic lupus erythematosus.
European journal of human genetics : EJHG 2006;14(1):69-78.
2005: Kerstin Lindblad-Toh; Claire M Wade; Tarjei S Mikkelsen; Elinor K. Karlsson; David B Jaffe; Michael Kamal; Michele Clamp; Jean L Chang; Edward J Kulbokas; Michael C Zody; Evan Mauceli; Xiaohui Xie; Matthew Breen; Robert K Wayne; Elaine A Ostrander; Chris P Ponting; Francis Galibert; Douglas R Smith; Pieter J DeJong; Ewen Kirkness; Pablo Alvarez; Tara Biagi; William Brockman; Jonathan Butler; Chee-Wye Chin; April Cook; James Cuff; Mark J Daly; David DeCaprio; Sante Gnerre; Manfred Grabherr; Manolis Kellis; Michael Kleber; Carolyne Bardeleben; Leo Goodstadt; Andreas Heger; Christophe Hitte; Lisa Kim; Klaus-Peter Koepfli; Heidi G Parker; John P Pollinger; Stephen M J Searle; Nathan B Sutter; Rachael Thomas; Caleb Webber; Jennifer Baldwin; Adal Abebe; Amr Abouelleil; Lynne Aftuck; Mostafa Ait-Zahra; Tyler Aldredge; Nicole Allen; Peter An; Scott Anderson; Claudel Antoine; Harindra Arachchi; Ali Aslam; Laura Ayotte; Pasang Bachantsang; Andrew Barry; Tashi Bayul; Mostafa Benamara; Aaron Berlin; Daniel Bessette; Berta Blitshteyn; Toby Bloom; Jason Blye; Leonid Boguslavskiy; Claude Bonnet; Boris Boukhgalter; Adam Brown; Patrick Cahill; Nadia Calixte; Jody Camarata; Yama Cheshatsang; Jeffrey Chu; Mieke Citroen; Alville Collymore; Patrick Cooke; Tenzin Dawoe; Riza Daza; Karin Decktor; Stuart DeGray; Norbu Dhargay; Kimberly Dooley; Kathleen Dooley; Passang Dorje; Kunsang Dorjee; Lester Dorris; Noah Duffey; Alan Dupes; Osebhajajeme Egbiremolen; Richard Elong; Jill Falk; Abderrahim Farina; Susan Faro; Diallo Ferguson; Patricia Ferreira; Sheila Fisher; Mike FitzGerald; Karen Foley; Chelsea Foley; Alicia Franke; Dennis Friedrich; Diane Gage; Manuel Garber; Gary Gearin; Georgia Giannoukos; Tina Goode; Audra Goyette; Joseph Graham; Edward Grandbois; Kunsang Gyaltsen; Nabil Hafez; Daniel Hagopian; Birhane Hagos; Jennifer Hall; Claire Healy; Ryan Hegarty; Tracey Honan; Andrea Horn; Nathan Houde; Leanne Hughes; Leigh Hunnicutt; M Husby; Benjamin Jester; Charlien Jones; Asha Kamat; Ben Kanga; Cristyn Kells; Dmitry Khazanovich; Alix Chinh Kieu; Peter Kisner; Mayank Kumar; Krista Lance; Thomas Landers; Marcia Lara; William Lee; Jean-Pierre Leger; Niall Lennon; Lisa Leuper; Sarah LeVine; Jinlei Liu; Xiaohong Liu; Yeshi Lokyitsang; Tashi Lokyitsang; Annie Lui; Jan Macdonald; John Major; Richard Marabella; Kebede Maru; Charles Matthews; Susan McDonough; Teena Mehta; James Meldrim; Alexandre Melnikov; Louis Meneus; Atanas Mihalev; Tanya Mihova; Karen Miller; Rachel Mittelman; Valentine Mlenga; Leonidas Mulrain; Glen Munson; Adam Navidi; Jerome Naylor; Tuyen Nguyen; Nga Nguyen; Cindy Nguyen; Thu Nguyen; Robert Nicol; Nyima Norbu; Choe Norbu; Nathaniel Novod; Tenchoe Nyima; Peter Olandt; Barry O'Neill; Keith O'Neill; Sahal Osman; Lucien Oyono; Christopher Patti; Danielle Perrin; Pema Phunkhang; Fritz Pierre; Margaret Priest; Anthony Rachupka; Sujaa Raghuraman; Rayale Rameau; Verneda Ray; Christina Raymond; Filip Rege; Cecil Rise; Julie Rogers; Peter Rogov; Julie Sahalie; Sampath Settipalli; Theodore Sharpe; Terrance Shea; Mechele Sheehan; Ngawang Sherpa; Jianying Shi; Diana Shih; Jessie Sloan; Cherylyn Smith; Todd Sparrow; John Stalker; Nicole Stange-Thomann; Sharon Stavropoulos; Catherine Stone; Sabrina Stone; Sean Sykes; Pierre Tchuinga; Pema Tenzing; Senait Tesfaye; Dawa Thoulutsang; Yama Thoulutsang; Kerri Topham; Ira Topping; Tsamla Tsamla; Helen Vassiliev; Vijay Venkataraman; Andy Vo; Tsering Wangchuk; Tsering Wangdi; Michael Weiand; Jane Wilkinson; Adam Wilson; Shailendra Yadav; Shuli Yang; Xiaoping Yang; Geneva Young; Qing Yu; Joanne Zainoun; Lisa Zembek; Andrew Zimmer; Eric S Lander
Genome sequence, comparative analysis and haplotype structure of the domestic dog.
Nature 2005;438(7069):803-19.
2005: Alienke J Monsuur; Paul I W de Bakker; Behrooz Alizadeh; Alexandra Zhernakova; Marianna R Bevova; Eric Strengman; Lude Franke; Ruben van't Slot; Martine J Van Belzen; Ineke C M Lavrijsen; Begoña Diosdado; Mark J Daly; Chris J J Mulder; M Luisa Mearin; Jos W R Meijer; Gerrit A Meijer; Erica van Oort; Martin C Wapenaar; Bobby P C Koeleman; Cisca Wijmenga
Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect.
Nature genetics 2005;37(12):1341-4.
2005: Tracey L Petryshen; Frank A Middleton; A R Tahl; G N Rockwell; Shaun Purcell; K A Aldinger; Andrew Kirby; Christopher Morley; L McGann; Karen L Gentile; S G Waggoner; Helena Medeiros; C Carvalho; antonio macedo; Margot Albus; W Maier; Mátyás Trixler; P Eichhammer; Sibylle G Schwab; Dieter B Wildenauer; Maria H Azevedo; Michele T Pato; Carlos N Pato; Mark J Daly; Pamela Sklar
Genetic investigation of chromosome 5q GABAA receptor subunit genes in schizophrenia.
Molecular psychiatry 2005;10(12):1074-88, 1057.
2005: Tracey L Petryshen; Andrew Kirby; Ronald P Hammer; Shaun Purcell; Sinead B O'Leary; Jonathan Singer; Annie E Hill; Joseph H Nadeau; Mark J Daly; Pamela Sklar
Two quantitative trait loci for prepulse inhibition of startle identified on mouse chromosome 16 using chromosome substitution strains.
Genetics 2005;171(4):1895-904.
2005: Claire M Wade; Mark J Daly
Genetic variation in laboratory mice.
Nature genetics 2005;37(11):1175-80.
2005: Stephen F Schaffner; Catherine Foo; Stacey Gabriel; David Reich; Mark J Daly; David Altshuler
Calibrating a coalescent simulation of human genome sequence variation.
Genome research 2005;15(11):1576-83.
2005: Paul I W de Bakker; Roman Yelensky; Itsik Pe'er; Stacey B Gabriel; Mark J Daly; David Altshuler
Efficiency and power in genetic association studies.
Nature genetics 2005;37(11):1217-23.
2005: Matthew B McQueen; Bernie Devlin; Stephen Faraone; Vishwajit L Nimgaonkar; Pamela Sklar; Jordan W Smoller; Rami Abou Jamra; Margot Albus; Silviu-Alin Bacanu; Miron Baron; Thomas B Barrett; Wade Berrettini; Deborah Blacker; William Byerley; Sven Cichon; Willam Coryell; Nick Craddock; Mark J Daly; J. Raymond DePaulo; Howard J Edenberg; Tatiana Foroud; Michael Gill; T Conrad Gilliam; Marian Hamshere; Ian Jones; Lisa Jones; Suh-Hang Juo; John R Kelsoe; David Lambert; Christoph Lange; Bernard Lerer; Jianjun Liu; Wolfgang Maier; James D Mackinnon; Melvin G McInnis; Francis McMajon; Dennis L Murphy; Markus M Nothen; John I Nurnberger; Carlos N Pato; Michele T Pato; James B Potash; Peter Propping; Ann E Pulver; John P Rice; Marcella Rietschel; William Scheftner; Johannes Schumacher; Ricardo Segurado; Kristel Van Steen; Weiting Xie; Peter P Zandi; Nan M Laird
Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q.
American journal of human genetics 2005;77(4):582-95.
2005: Stephen Sawcer; Maria Ban; Mel Maranian; Tai Wai Yeo; Alastair Compston; Andrew Kirby; Mark J Daly; Philip De Jager; Emily Walsh; Eric S Lander; John D Rioux; David A Hafler; Adrian Ivinson; Jacqueline Rimmler; Simon G Gregory; Silke Schmidt; Margaret Pericak-Vance; Eva Akesson; Jan Hillert; Pameli Datta; Annette Oturai; lars peter ryder; Hanne F Harbo; Anne Spurkland; Kjell-Morten Myhr; Mikko Laaksonen; David Booth; Robert Heard; Graeme Stewart; Robin Lincoln; Lisa F Barcellos; Stephen L Hauser; Jorge R Oksenberg; Shannon J Kenealy; Jonathan L Haines
A high-density screen for linkage in multiple sclerosis.
American journal of human genetics 2005;77(3):454-67.
2005: Wendy Winckler; Noël P Burtt; Johan Holmkvist; Camilla Cervin; Paul I W de Bakker; Maria Sun; Peter Almgren; Tiinamaija Tuomi; Daniel Gaudet; Thomas J Hudson; Kristin G Ardlie; Mark J Daly; Joel N Hirschhorn; David Altshuler; Leif Groop
Association of common variation in the HNF1alpha gene region with risk of type 2 diabetes.
Diabetes 2005;54(8):2336-42.
2005: Mark J Daly; Alexandra V Pearce; Lisa Farwell; Sheila A Fisher; Anna Latiano; Natalie Prescott; Alastair Forbes; John Mansfield; Jeremy Sanderson; Diane Langelier; Albert Cohen; Alain Bitton; Gary Wild; Cathryn M Lewis; Vito Annese; Christopher G Mathew; John D Rioux
Association of DLG5 R30Q variant with inflammatory bowel disease.
European journal of human genetics : EJHG 2005;13(7):835-9.
2005: Jose C Florez; Christina M Agapakis; Noël P Burtt; Maria Sun; Peter Almgren; Lennart Råstam; Tiinamaija Tuomi; Daniel Gaudet; Thomas J Hudson; Mark J Daly; Kristin G Ardlie; Joel N Hirschhorn; Leif Groop; David Altshuler
Association testing of the protein tyrosine phosphatase 1B gene (PTPN1) with type 2 diabetes in 7,883 people.
Diabetes 2005;54(6):1884-91.
2005: Sapna Chadha; Katie Miller; Lisa Farwell; Liz Lightstone; Mark J Daly; John D Rioux; Timothy J Vyse
Haplotype structure of TNFRSF5-TNFSF5 (CD40-CD40L) and association analysis in systemic lupus erythematosus.
European journal of human genetics : EJHG 2005;13(5):669-76.
2005: Hui Pan; Bo-Shiun Yan; Mauricio Rojas; Yuriy V Shebzukhov; Hongwei Zhou; Lester Kobzik; Darren E Higgins; Mark J Daly; Barry R Bloom; Igor Kramnik
Ipr1 gene mediates innate immunity to tuberculosis.
Nature 2005;434(7034):767-72.
2005: Mark J Daly; David Altshuler
Partners in crime.
Nature genetics 2005;37(4):337-8.
2005: Tracey L Petryshen; Frank A Middleton; Andrew Kirby; K A Aldinger; Shaun Purcell; A R Tahl; Christopher Morley; L McGann; Karen L Gentile; G N Rockwell; Helena Medeiros; C Carvalho; antonio macedo; Ana Dourado; José Valente; CP Ferreira; Nick Patterson; Maria H Azevedo; Mark J Daly; Carlos N Pato; Michele T Pato; Pamela Sklar
Support for involvement of neuregulin 1 in schizophrenia pathophysiology.
Molecular psychiatry 2005;10(4):366-74, 328.
2005: Wendy Winckler; Robert R Graham; Paul I W de Bakker; Maria Sun; Peter Almgren; Tiinamaija Tuomi; Daniel Gaudet; Thomas J Hudson; Kristin G Ardlie; Mark J Daly; Joel N Hirschhorn; Leif Groop; David Altshuler
Association testing of variants in the hepatocyte nuclear factor 4alpha gene with risk of type 2 diabetes in 7,883 people.
Diabetes 2005;54(3):886-92.
2005: Joel N Hirschhorn; Mark J Daly
Genome-wide association studies for common diseases and complex traits.
Nature reviews. Genetics 2005;6(2):95-108.
2005: Shaun Purcell; Pak Sham; Mark J Daly
Parental phenotypes in family-based association analysis.
American journal of human genetics 2005;76(2):249-59.
2005: J C Barrett; B Fry; J Maller; Mark J Daly
Haploview: analysis and visualization of LD and haplotype maps.
Bioinformatics (Oxford, England) 2005;21(2):263-5.
2005: Timothy J Vyse; Angela M Richardson; Emily Walsh; Lisa Farwell; Mark J Daly; Cox Terhorst; John D Rioux
Mapping autoimmune disease genes in humans: lessons from IBD and SLE.
Novartis Foundation symposium 2005;267():94-107; discussion 107-12.
2004: Elise Eller; Pnina Vardi; Mark J Daly; Sunanda Babu; Christine Roberts; Fan Yang; George S Eisenbarth; Pamela R Fain
IDDM17: polymorphisms in the AMACO gene are associated with dominant protection against type 1A diabetes in a Bedouin Arab family.
Annals of the New York Academy of Sciences 2004;1037():145-9.
2004: Jose C Florez; Marketa Sjögren; Noël P Burtt; Marju Orho-Melander; Steve Schayer; Maria Sun; Peter Almgren; Ulf Lindblad; Tiinamaija Tuomi; Daniel Gaudet; Thomas J Hudson; Mark J Daly; Kristin G Ardlie; Joel N Hirschhorn; David Altshuler; Leif Groop
Association testing in 9,000 people fails to confirm the association of the insulin receptor substrate-1 G972R polymorphism with type 2 diabetes.
Diabetes 2004;53(12):3313-8.
2004: John D Rioux; Hannele Karinen; Kerry Kocher; Sheila Guschwan McMahon; Päivi Kärkkäinen; Esko Janatuinen; Markku Heikkinen; Risto Julkunen; Jussi Pihlajamäki; Anita Naukkarinen; Veli-Matti Kosma; Mark J Daly; Eric S Lander; Markku Laakso
Genomewide search and association studies in a Finnish celiac disease population: Identification of a novel locus and replication of the HLA and CTLA4 loci.
American journal of medical genetics. Part A 2004;130A(4):345-50.
2004: Goncalo Abecasis; Nancy Cox; Mark J Daly; Leonid Kruglyak; Nan Laird; Kyriacos Markianos; Nick Patterson
No bias in linkage analysis.
American journal of human genetics 2004;75(4):722-3; author reply 723-7.
2004: Stephen Sawcer; Mel Maranian; Sara Singlehurst; Taiwai Yeo; Alastair Compston; Mark J Daly; Philip De Jager; Stacey Gabriel; David A Hafler; Adrian J Ivinson; Eric S Lander; John D Rioux; Emily Walsh; Simon G Gregory; Silke Schmidt; Margaret Pericak-Vance; Lisa F Barcellos; Stephen L Hauser; Jorge R Oksenberg; Shannon J Kenealy; Jonathan L Haines
Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping.
Human molecular genetics 2004;13(17):1943-9.
2004: Kelly A Frazer; Claire M Wade; David Hinds; Nila Patil; David R Cox; Mark J Daly
Segmental phylogenetic relationships of inbred mouse strains revealed by fine-scale analysis of sequence variation across 4.6 mb of mouse genome.
Genome research 2004;14(8):1493-500.
2004: Carlos N Pato; Michele T Pato; Andrew Kirby; Tracey L Petryshen; Helena Medeiros; C Carvalho; antonio macedo; Ana Dourado; Isabel Coelho; José Valente; Maria J Soares; CP Ferreira; M Lei; A Verner; Thomas J Hudson; Christopher Morley; James L Kennedy; Maria H Azevedo; Mark J Daly; Pamela Sklar
Genome-wide scan in Portuguese Island families implicates multiple loci in bipolar disorder: fine mapping adds support on chromosomes 6 and 11.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2004;127B(1):30-4.
2004: Mark J Daly; John D Rioux
New approaches to gene hunting in IBD.
Inflammatory bowel diseases 2004;10(3):312-7.
2004: Jose C Florez; Noël P Burtt; Paul I W de Bakker; Peter Almgren; Tiinamaija Tuomi; Johan Holmkvist; Daniel Gaudet; Thomas J Hudson; Stephen F Schaffner; Mark J Daly; Joel N Hirschhorn; Leif Groop; David Altshuler
Haplotype structure and genotype-phenotype correlations of the sulfonylurea receptor and the islet ATP-sensitive potassium channel gene region.
Diabetes 2004;53(5):1360-8.
2004: Nick Patterson; Neil Hattangadi; Barton Lane; Kirk E Lohmueller; David A Hafler; Jorge R Oksenberg; Stephen L Hauser; Michael W Smith; Stephen J O'Brien; David Altshuler; Mark J Daly; David Reich
Methods for high-density admixture mapping of disease genes.
American journal of human genetics 2004;74(5):979-1000.
2004: Frank A Middleton; Michele T Pato; Karen L Gentile; Christopher Morley; X Zhao; A F Eisener; A Brown; Tracey L Petryshen; A N Kirby; Helena Medeiros; C Carvalho; antonio macedo; Ana Dourado; Isabel Coelho; José Valente; Maria J Soares; CP Ferreira; M Lei; Maria H Azevedo; James L Kennedy; Mark J Daly; Pamela Sklar; Carlos N Pato
Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: a comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22.
American journal of human genetics 2004;74(5):886-97.
2004: David A van Heel; Sheila A Fisher; Andrew Kirby; Mark J Daly; John D Rioux; Cathryn M Lewis
Inflammatory bowel disease susceptibility loci defined by genome scan meta-analysis of 1952 affected relative pairs.
Human molecular genetics 2004;13(7):763-70.
2004: Pamela Sklar; Michele T Pato; Andrew Kirby; Tracey L Petryshen; Helena Medeiros; C Carvalho; antonio macedo; Ana Dourado; Isabel Coelho; José Valente; M J Soares; CP Ferreira; M Lei; A Verner; Thomas J Hudson; Christopher Morley; James L Kennedy; Maria H Azevedo; Eric S Lander; Mark J Daly; Carlos N Pato
Genome-wide scan in Portuguese Island families identifies 5q31-5q35 as a susceptibility locus for schizophrenia and psychosis.
Molecular psychiatry 2004;9(2):213-8.
2003: Bard J Geesaman; Erica Benson; Stephanie J Brewster; Louis Kunkel; Hélène Blanché; Gilles Thomas; Thomas T Perls; Mark J Daly; Annibale Puca
Haplotype-based identification of a microsomal transfer protein marker associated with the human lifespan.
Proceedings of the National Academy of Sciences of the United States of America 2003;100(24):14115-20.
2003: Aleister J Saunders; Lars Bertram; Kristina Mullin; Andrew J Sampson; Khushal Latifzai; Sanjay Basu; Jennifer Jones; Devon Kinney; Laura MacKenzie-Ingano; Stephen Yu; Marilyn S Albert; Thomas J Moscarillo; Rodney C P Go; Susan S Bassett; Mark J Daly; Nan M Laird; Xin Wang; Gonul Velicelebi; Steven L Wagner; David K Becker; Rudolph E Tanzi; Deborah Blacker
Genetic association of Alzheimer's disease with multiple polymorphisms in alpha-2-macroglobulin.
Human molecular genetics 2003;12(21):2765-76.
2003: Emily C Walsh; Sheila Guschwan-McMahon; Mark J Daly; David A Hafler; John D Rioux
Genetic analysis of multiple sclerosis.
Journal of autoimmunity 2003;21(2):111-6.
2003: Emily C Walsh; Kristie A Mather; Stephen F Schaffner; Lisa Farwell; Mark J Daly; Nick Patterson; Michael Cullen; Mary Carrington; Teodorica L Bugawan; Henry A Erlich; Jay Campbell; Jeffrey Barrett; Katie Miller; Glenys Thomson; Eric S Lander; John D Rioux
An integrated haplotype map of the human major histocompatibility complex.
American journal of human genetics 2003;73(3):580-90.
2003: Vamsi K Mootha; Cecilia M Lindgren; Karl-Fredrik Eriksson; Aravind Subramanian; Smita Sihag; Joseph Lehar; Pere Puigserver; Emma Carlsson; Martin Ridderstråle; Esa Laurila; Nicholas Houstis; Mark J Daly; Nick Patterson; Jill P Mesirov; Todd R Golub; Pablo Tamayo; Bruce M Spiegelman; Eric S Lander; Joel N Hirschhorn; David Altshuler; Leif C Groop
PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes.
Nature genetics 2003;34(3):267-73.
2003: Cosmas Giallourakis; Monika Stoll; Katie Miller; Jochen Hampe; Eric S Lander; Mark J Daly; Stefan Schreiber; John D Rioux
IBD5 is a general risk factor for inflammatory bowel disease: replication of association with Crohn disease and identification of a novel association with ulcerative colitis.
American journal of human genetics 2003;73(1):205-11.
2002: Claire M Wade; Edward J Kulbokas; Andrew W Kirby; Michael C Zody; James C Mullikin; Eric S Lander; Kerstin Lindblad-Toh; Mark J Daly
The mosaic structure of variation in the laboratory mouse genome.
Nature 2002;420(6915):574-8.
2002: Robert H Waterston; Kerstin Lindblad-Toh; Ewan Birney; Jane Rogers; Josep F Abril; Pankaj Agarwal; Richa Agarwala; Rachel Ainscough; Marina Alexandersson; Peter An; Stylianos Antonarakis; John Attwood; Robert Baertsch; Jonathon Bailey; Karen Barlow; Stephan Beck; Eric Berry; Bruce Birren; Toby Bloom; Peer Bork; Marc Botcherby; Nicolas Bray; Michael R Brent; Daniel G Brown; Stephen D Brown; Carol Bult; John Burton; Jonathan Butler; Robert D Campbell; piero carninci; Simon Cawley; Francesca Chiaromonte; Asif T Chinwalla; Deanna M Church; Michele Clamp; Christopher Clee; Francis S Collins; Lisa L Cook; Richard R Copley; Alan Coulson; Olivier Couronne; James Cuff; Val Curwen; Tim Cutts; Mark J Daly; Robert David; Joy Davies; Kimberly D Delehaunty; Justin Deri; Emmanouil T Dermitzakis; Colin Dewey; Nicholas J Dickens; Mark Diekhans; Sheila Dodge; Inna Dubchak; Diane M Dunn; Sean R Eddy; Laura Elnitski; Richard Emes; Pallavi Eswara; Eduardo Eyras; Adam Felsenfeld; Ginger A Fewell; Paul Flicek; Karen Foley; Wayne N Frankel; Lucinda A Fulton; Robert S Fulton; Terrence S Furey; Diane Gage; Richard A Gibbs; Gustavo Glusman; Sante Gnerre; Nick Goldman; Leo Goodstadt; Darren Grafham; Tina A Graves; Eric Green; Simon Gregory; Roderic Guigó; Mark Guyer; Ross C Hardison; David Haussler; Yoshihide Hayashizaki; LaDeana W Hillier; Angela Hinrichs; Wratko Hlavina; Timothy Holzer; Fan Hsu; Axin Hua; Tim Hubbard; Adrienne Hunt; Ian Jackson; David B Jaffe; L Steven Johnson; Matthew Jones; Thomas A Jones; Ann Joy; Michael Kamal; Elinor K. Karlsson; Donna Karolchik; Arkadiusz Kasprzyk; Jun Kawai; Evan Keibler; Cristyn Kells; W James Kent; Andrew Kirby; Diana L Kolbe; Ian F Korf; Raju S Kucherlapati; Edward J Kulbokas; David Kulp; Tom Landers; J P Leger; Steven Leonard; Ivica Letunic; Rosie Levine; Jia Li; Ming Li; Christine Lloyd; Susan Lucas; Bin Ma; Donna R Maglott; Elaine R Mardis; Lucy Matthews; Evan Mauceli; John H Mayer; Megan McCarthy; W Richard McCombie; Stuart McLaren; Kirsten McLay; John D McPherson; Jim Meldrim; Beverley Meredith; Jill P Mesirov; Webb Miller; Tracie L Miner; Emmanuel Mongin; Kate T Montgomery; Michael Morgan; Richard Mott; James C Mullikin; Donna M Muzny; William E Nash; Joanne O Nelson; Michael N Nhan; Robert Nicol; Zemin Ning; Chad Nusbaum; Michael J O'Connor; Yasushi Okazaki; Karen Oliver; Emma Overton-Larty; Lior Pachter; Genís Parra; Kymberlie H Pepin; Jane Peterson; Pavel Pevzner; Robert Plumb; Craig S Pohl; Alex Poliakov; Tracy C Ponce; Chris P Ponting; Simon Potter; Michael Quail; Alexandre Reymond; Bruce A Roe; Krishna M Roskin; Edward M Rubin; Alistair G Rust; Ralph Santos; Victor Sapojnikov; Brian Schultz; Jörg Schultz; Matthias S Schwartz; Scott Schwartz; Carol Scott; Steven Seaman; Steve Searle; Ted Sharpe; Andrew Sheridan; Ratna Shownkeen; Sarah Sims; Jonathan B Singer; Guy Slater; Arian Smit; Douglas R Smith; Brian Spencer; Arne Stabenau; Nicole Stange-Thomann; Charles Sugnet; Mikita Suyama; Glenn Tesler; Johanna Thompson; David Torrents; Evanne Trevaskis; John Tromp; Catherine Ucla; Abel Ureta-Vidal; Jade P Vinson; Andrew C Von Niederhausern; Claire M Wade; Melanie Wall; Ryan J Weber; Robert B Weiss; Michael Wendl; Anthony P West; Kris Wetterstrand; Raymond Wheeler; Simon Whelan; Jamey Wierzbowski; David Willey; Sophie Williams; Richard K Wilson; Eitan Winter; Kim C Worley; Dudley Wyman; Shan Yang; Shiaw-Pyng Yang; Evgeny M Zdobnov; Michael C Zody; Eric S Lander
Initial sequencing and comparative analysis of the mouse genome.
Nature 2002;420(6915):520-62.
2002: C Noel Williams; Kerry Kocher; Eric S Lander; Mark J Daly; John D Rioux
Using a genome-wide scan and meta-analysis to identify a novel IBD locus and confirm previously identified IBD loci.
Inflammatory bowel diseases 2002;8(6):375-81.
2002: David E Reich; Stephen F Schaffner; Mark J Daly; Gil McVean; James C Mullikin; John M Higgins; Daniel J Richter; Eric S Lander; David Altshuler
Human genome sequence variation and the influence of gene history, mutation and recombination.
Nature genetics 2002;32(1):135-42.
2002: R C Andrew Symons; Mark J Daly; Jane Fridlyand; Terence P Speed; Wendy D Cook; Steve Gerondakis; Alan W Harris; Simon J Foote
Multiple genetic loci modify susceptibility to plasmacytoma-related morbidity in E(mu)-v-abl transgenic mice.
Proceedings of the National Academy of Sciences of the United States of America 2002;99(17):11299-304.
2002: Severine Vermeire; Gary Wild; Kerry Kocher; Josee Cousineau; Line Dufresne; Alain Bitton; Diane Langelier; Pierre Pare; Gilles Lapointe; Albert Cohen; Mark J Daly; John D Rioux
CARD15 genetic variation in a Quebec population: prevalence, genotype-phenotype relationship, and haplotype structure.
American journal of human genetics 2002;71(1):74-83.
2002: Stacey B Gabriel; Stephen F Schaffner; Huy Nguyen; Jamie M Moore; Jessica Roy; Brendan Blumenstiel; John Higgins; Matthew DeFelice; Amy Lochner; Maura Faggart; Shau Neen Liu-Cordero; Charles N Rotimi; Adebowale Adeyemo; Richard Cooper; Ryk Ward; Eric S Lander; Mark J Daly; David Altshuler
The structure of haplotype blocks in the human genome.
Science (New York, N.Y.) 2002;296(5576):2225-9.
2002: Mark J Daly
Estimating the human gene count.
Cell 2002;109(3):283-4.
2002: Cecilia M Lindgren; Melanie M Mahtani; Elisabeth Widén; Mark I McCarthy; Mark J Daly; Andrew Kirby; Mary Reeve; L Kruglyak; A Parker; J Meyer; Peter Almgren; Markku Lehto; Timo Kanninen; Tiinamaija Tuomi; Leif C Groop; Eric S Lander
Genomewide search for type 2 diabetes mellitus susceptibility loci in Finnish families: the Botnia study.
American journal of human genetics 2002;70(2):509-16.
2001: Mark S Silverberg; Mark J Daly; David N Moskovitz; John D Rioux; Robin S McLeod; Zane Cohen; Gordon R Greenberg; Thomas J Hudson; Katherine A Siminovitch; A Hillary Steinhart
Diagnostic misclassification reduces the ability to detect linkage in inflammatory bowel disease genetic studies.
Gut 2001;49(6):773-6.
2001: Mark J Daly; John D Rioux; Stephen F Schaffner; Thomas J Hudson; Eric S Lander
High-resolution haplotype structure in the human genome.
Nature genetics 2001;29(2):229-32.
2001: J D Rioux; Mark J Daly; M S Silverberg; K Lindblad; H Steinhart; Z Cohen; T Delmonte; K Kocher; K Miller; S Guschwan; E J Kulbokas; S O'Leary; E Winchester; K Dewar; T Green; V Stone; C Chow; A Cohen; D Langelier; G Lapointe; D Gaudet; J Faith; N Branco; S B Bull; R S McLeod; A M Griffiths; A Bitton; G R Greenberg; E S Lander; K A Siminovitch; T J Hudson
Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease.
Nature genetics 2001;29(2):223-8.
2001: Kristin G Ardlie; S N Liu-Cordero; Michael A Eberle; Mark J Daly; J Barrett; E Winchester; Eric S Lander; Leonid Kruglyak
Lower-than-expected linkage disequilibrium between tightly linked markers in humans suggests a role for gene conversion.
American journal of human genetics 2001;69(3):582-9.
2001: Annibale Puca; Mark J Daly; Stephanie J Brewster; T C Matise; J Barrett; M Shea-Drinkwater; S Kang; Erin Joyce; J Nicoli; E Benson; Louis Kunkel; Thomas T Perls
A genome-wide scan for linkage to human exceptional longevity identifies a locus on chromosome 4.
Proceedings of the National Academy of Sciences of the United States of America 2001;98(18):10505-8.
2001: Joel N Hirschhorn; Cecilia M Lindgren; Mark J Daly; Andrew Kirby; Stephen F Schaffner; Noël P Burtt; David Altshuler; A Parker; John D Rioux; Jill Platko; Daniel Gaudet; Thomas J Hudson; Leif C Groop; Eric S Lander
Genomewide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult height.
American journal of human genetics 2001;69(1):106-16.
2001: Pamela Sklar; Sibylle G Schwab; Nigel M Williams; Mark J Daly; Stephen F Schaffner; W Maier; Margot Albus; Mátyás Trixler; P Eichhammer; Bernard Lerer; Joachim Hallmayer; Nadine Norton; H Williams; Stanley Zammit; Alastair G Cardno; S Jones; G McCarthy; vihra milanova; George Kirov; M C O'Donovan; Eric S Lander; Michael J Owen; Dieter B Wildenauer
Association analysis of NOTCH4 loci in schizophrenia using family and population-based controls.
Nature genetics 2001;28(2):126-8.
2001: Tarja Laitinen; Mark J Daly; JD Rioux; Pekka E Kauppi; C Laprise; Tuula Petäys; T Green; M Cargill; Tari Haahtela; Eric S Lander; Lauri A Laitinen; Thomas J Hudson; Juha Kere
A susceptibility locus for asthma-related traits on chromosome 7 revealed by genome-wide scan in a founder population.
Nature genetics 2001;28(1):87-91.
2001: Hanna T Gazda; Jeffrey Lipton; Thiebaut-Noel Willig; S Ball; Charlotte M Niemeyer; Gil Tchernia; Narla Mohandas; Mark J Daly; Anna Ploszynska; Karen A Orfali; Adrianna Vlachos; Bertil E Glader; R Rokicka-Milewska; A Ohara; D Baker; Dagmar Pospisilova; A Webber; David H Viskochil; David G Nathan; Alan H Beggs; Colin A Sieff
Evidence for linkage of familial Diamond-Blackfan anemia to chromosome 8p23.3-p22 and for non-19q non-8p disease.
Blood 2001;97(7):2145-50.
2001: Kyriacos Markianos; Mark J Daly; Leonid Kruglyak
Efficient multipoint linkage analysis through reduction of inheritance space.
American journal of human genetics 2001;68(4):963-77.
2001: R Sachidanandam; D Weissman; S C Schmidt; J M Kakol; L D Stein; G Marth; S Sherry; J C Mullikin; B J Mortimore; D L Willey; S E Hunt; C G Cole; P C Coggill; C M Rice; Z Ning; J Rogers; D R Bentley; P Y Kwok; E R Mardis; R T Yeh; B Schultz; L Cook; R Davenport; M Dante; L Fulton; L Hillier; R H Waterston; J D McPherson; B Gilman; S Schaffner; W J Van Etten; D Reich; J Higgins; Mark J Daly; B Blumenstiel; J Baldwin; N Stange-Thomann; M C Zody; L Linton; E S Lander; D Altshuler
A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms.
Nature 2001;409(6822):928-33.
2001: N Lee; Mark J Daly; Terrye Delmonte; Eric S Lander; Fenghao Xu; Thomas J Hudson; G A Mitchell; C C Morin; Brian H Robinson; John D Rioux
A genomewide linkage-disequilibrium scan localizes the Saguenay-Lac-Saint-Jean cytochrome oxidase deficiency to 2p16.
American journal of human genetics 2001;68(2):397-409.
2001: Peter Ianakiev; Mark J Daly; sergio toledo; M G Cavalcanti; J C Neto; Elizabeth Silveira; A Freire-Maia; Peter Heutink; Michael W Kilpatrick; Petros Tsipouras
Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 gene.
American journal of human genetics 2001;68(1):38-45.
2000: Päivi Pajukanta; M Cargill; Laura Viitanen; Ilpo Nuotio; Anu Kareinen; Markus Perola; Joseph D Terwilliger; E Kempas; Mark J Daly; Heidi E Lilja; JD Rioux; T Brettin; Jorma S A Viikari; T Rönnemaa; Markku Laakso; Eric S Lander; Leena Peltonen
Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland.
American journal of human genetics 2000;67(6):1481-93.
2000: David Altshuler; Joel N Hirschhorn; Mia Klannemark; Cecilia M Lindgren; M C Vohl; James Nemesh; C R Lane; Stephen F Schaffner; S Bolk; Carl G Brewer; Tiinamaija Tuomi; Daniel Gaudet; Thomas J Hudson; Mark J Daly; Leif Groop; Eric S Lander
The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes.
Nature genetics 2000;26(1):76-80.
2000: Kerstin Lindblad-Toh; David M Tanenbaum; Mark J Daly; E Winchester; Weng-Onn Lui; A Villapakkam; S E Stanton; Catharina Larsson; Thomas J Hudson; Bruce E Johnson; Eric S Lander; Matthew Meyerson
Loss-of-heterozygosity analysis of small-cell lung carcinomas using single-nucleotide polymorphism arrays.
Nature biotechnology 2000;18(9):1001-5.
2000: John D Rioux; Mark S Silverberg; Mark J Daly; A Hillary Steinhart; Robin S McLeod; Anne M Griffiths; T Green; T S Brettin; V Stone; Shelley B Bull; Alain Bitton; C Noel Williams; Gordon R Greenberg; Zane Cohen; Eric S Lander; Thomas J Hudson; Katherine A Siminovitch
Genomewide search in Canadian families with inflammatory bowel disease reveals two novel susceptibility loci.
American journal of human genetics 2000;66(6):1863-70.
2000: Daniel Gaudet; S Arsenault; Louis Pérusse; Marie-Claude Vohl; Julie St-Pierre; Jean Bergeron; Jean-Pierre Després; K Dewar; Mark J Daly; T Hudson; John D Rioux
Glycerol as a correlate of impaired glucose tolerance: dissection of a complex system by use of a simple genetic trait.
American journal of human genetics 2000;66(5):1558-68.
2000: Kerstin Lindblad-Toh; E Winchester; Mark J Daly; D G Wang; Joel N Hirschhorn; J P Laviolette; Kristin G Ardlie; David E Reich; E Robinson; Pamela Sklar; N Shah; D Thomas; Jian-Bing Fan; Thomas Gingeras; J Warrington; N Patil; Thomas J Hudson; Eric S Lander
Large-scale discovery and genotyping of single-nucleotide polymorphisms in the mouse.
Nature genetics 2000;24(4):381-6.
2000: Stephen C Pratt; Mark J Daly; Leonid Kruglyak
Exact multipoint quantitative-trait linkage analysis in pedigrees by variance components.
American journal of human genetics 2000;66(3):1153-7.
1999: Owen R White; Jonathan Eisen; J F Heidelberg; E K Hickey; J D Peterson; R J Dodson; D H Haft; Michelle G Giglio; W C Nelson; D L Richardson; K S Moffat; H Qin; L Jiang; W Pamphile; M Crosby; M Shen; J J Vamathevan; P Lam; L McDonald; T Utterback; C Zalewski; K S Makarova; L Aravind; Mark J Daly; K W Minton; R D Fleischmann; K A Ketchum; K E Nelson; Steven L Salzberg; Hamilton O Smith; J C Venter; Claire M Fraser-Liggett
Genome sequence of the radioresistant bacterium Deinococcus radiodurans R1.
Science (New York, N.Y.) 1999;286(5444):1571-7.
1999: AM Goodfellow; Wendy E Hoy; Kadaba S Sriprakash; Mark J Daly; Mary Reeve; John D Mathews
Proteinuria is associated with persistence of antibody to streptococcal M protein in Aboriginal Australians.
Epidemiology and infection 1999;122(1):67-75.
1998: John D Rioux; Mark J Daly; T Green; V Stone; Eric S Lander; Thomas J Hudson; A Hillary Steinhart; S Bull; Zane Cohen; Gordon Greenberg; A Griffiths; R McLeod; Mark S Silverberg; C Noel Williams; Katherine A Siminovitch
Absence of linkage between inflammatory bowel disease and selected loci on chromosomes 3, 7, 12, and 16.
Gastroenterology 1998;115(5):1062-5.
1998: JD Rioux; V A Stone; Mark J Daly; M Cargill; T Green; H Nguyen; T Nutman; Peter Zimmerman; M A Tucker; T Hudson; A M Goldstein; Eric S Lander; A Y Lin
Familial eosinophilia maps to the cytokine gene cluster on human chromosomal region 5q31-q33.
American journal of human genetics 1998;63(4):1086-94.
1998: Mark J Daly
Untangling the genetics of a complex disease.
JAMA : the journal of the American Medical Association 1998;280(7):652-3.
1998: Douglas F Levinson; Melanie M Mahtani; Derek J Nancarrow; D M Brown; L Kruglyak; Andrew Kirby; N K Hayward; Raymond R Crowe; N C Andreasen; Donald W Black; Jeremy Silverman; J Endicott; L Sharpe; Richard C Mohs; L J Siever; Marilyn K Walters; D P Lennon; HL Jones; Deborah A Nertney; Mark J Daly; Madeline Gladis; Bryan J Mowry
Genome scan of schizophrenia.
The American journal of psychiatry 1998;155(6):741-50.
1998: L Kruglyak; Mark J Daly
Linkage thresholds for two-stage genome scans.
American journal of human genetics 1998;62(4):994-7.
1997: Satu Kuokkanen; M Gschwend; JD Rioux; Mark J Daly; Joseph D Terwilliger; Pentti J Tienari; Juhani Wikström; Jukka U Palo; L D Stein; T J Hudson; Eric S Lander; Leena Peltonen
Genomewide scan of multiple sclerosis in Finnish multiplex families.
American journal of human genetics 1997;61(6):1379-87.
1997: Tarja Laitinen; Pekka E Kauppi; Jaakko Ignatius; T Ruotsalainen; Mark J Daly; Helena Kääriäinen; L Kruglyak; Harri Laitinen; ALBERT DE LA CHAPELLE; Eric S Lander; Lauri A Laitinen; Juha Kere
Genetic control of serum IgE levels and asthma: linkage and linkage disequilibrium studies in an isolated population.
Human molecular genetics 1997;6(12):2069-76.
1997: A Sidow; MS Bulotsky; AW Kerrebrock; RT Bronson; Mark J Daly; Mary Reeve; T L Hawkins; BW Birren; Rudolf Jaenisch; Eric S Lander
Serrate2 is disrupted in the mouse limb-development mutant syndactylism.
Nature 1997;389(6652):722-5.
1997: Augustine Kong; Michael L Frigge; G I Bell; E S Lander; Mark J Daly; N J Cox
Diabetes, dependence, asymptotics, selection and significance.
Nature genetics 1997;17(2):148.
1997: B A Hamilton; Desmond J Smith; K L Mueller; AW Kerrebrock; RT Bronson; V van Berkel; Mark J Daly; L Kruglyak; Mary Reeve; J L Nemhauser; T L Hawkins; E M Rubin; Eric S Lander
The vibrator mutation causes neurodegeneration via reduced expression of PITP alpha: positional complementation cloning and extragenic suppression.
Neuron 1997;18(5):711-22.
1997: Mark J Daly; A Kirby; Leonid Kruglyak
Do multiple data sets provide support for a bipolar illness susceptibility locus on chromosome 18?
Genetic epidemiology 1997;14(6):599-604.
1996: Mark J Daly; E S Lander
The importance of being independent: sib pair analysis in diabetes.
Nature genetics 1996;14(2):131-2.
1996: Melanie M Mahtani; Elisabeth Widén; Markku Lehto; J Thomas; M McCarthy; J Brayer; Bryant Barbara; G Chan; Mark J Daly; Carol Forsblom; Timo Kanninen; A Kirby; Leonid Kruglyak; K Munnelly; M Parkkonen; Mary Reeve; A Weaver; T Brettin; Geoffrey Duyk; Eric S Lander; Leif C Groop
Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish families.
Nature genetics 1996;14(1):90-4.
1996: Leonid Kruglyak; Mark J Daly; Mary Reeve; Eric S Lander
Parametric and nonparametric linkage analysis: a unified multipoint approach.
American journal of human genetics 1996;58(6):1347-63.
1996: W F Dietrich; J Miller; Robert Steen; M A Merchant; D Damron-Boles; Z Husain; R Dredge; Mark J Daly; K A Ingalls; T J O'Connor
A comprehensive genetic map of the mouse genome.
Nature 1996;380(6570):149-52.
1996: D M Brown; A P Provoost; Mark J Daly; Eric S Lander; Howard J Jacob
Renal disease susceptibility and hypertension are under independent genetic control in the fawn-hooded rat.
Nature genetics 1996;12(1):44-51.
1995: Mark J Daly
A visionary executive. Interview by Russell C. Coile, Jr..
The Healthcare Forum journal 1995;38(3):74-5.
1995: Leonid Kruglyak; Mark J Daly; Eric S Lander
Rapid multipoint linkage analysis of recessive traits in nuclear families, including homozygosity mapping.
American journal of human genetics 1995;56(2):519-27.
1994: J Hästbacka; Albert de La Chapelle; Melanie M Mahtani; GA Clines; Mary Reeve; Mark J Daly; B A Hamilton; K Kusumi; B Trivedi; A Weaver
The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping.
Cell 1994;78(6):1073-87.
1987: Eric S Lander; P Green; J Abrahamson; A Barlow; Mark J Daly; S E Lincoln; L A Newberg; L Newburg
MAPMAKER: an interactive computer package for constructing primary genetic linkage maps of experimental and natural populations.
Genomics 1987;1(2):174-81.