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Aravinda Chakravarti

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Disorders

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Chromosomes, Human, Pair 21

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Publications

TOP 3
Santhi K Ganesh; Ron T Gansevoort; Tom R Gaunt; Johannes M I H Gho; Christian Gieger; Yan Gong; John G Gums; Wei Guo; Yiran Guo; Hakon Hakonarson; Hans L Hillege; Marten H Hofker; G Kees Hovingh; Thomas Illig; Aaron Isaacs; Gail P Jarvik; Andrew D Johnson; Julie A Johnson; Toby Johnson; John J P Kastelein; Brendan J Keating; Susan A Kirkland; Marcus E Kleber; Wolfgang Koenig; Kandice Kottke-Marchant; Abdullah Kutlar; Andrea Z Lacroix; Taimour Y Langaee; Matthew B Lanktree; Daniel Levy; Yun R Li; Honghuang Lin; Kiang Liu; Steffi Maiwald; Rainer Malik; Winfried März; Irene Mateo Leach; Caitrin W McDonough; Matthijs F L Meijs; Olle Mellander; Braxton D Mitchell; Cliona M Molony; Patricia B Munroe; Sarah S Murray; Gurunathan Murugesan; Christopher Newton-Cheh; Ilja M Nolte; Jeffery R O'Connell; Albertine J Oldehinkel; N Charlotte Onland-Moret; Willem H Ouwehand; Sandosh Padmanabhan; Walter Palmas; Brenda W Penninx; Carl J Pepine; Mary Pettinger; Joseph F Polak; Tom S Price; Daniel J Rader; Ramakrishnan Rajagopalan; Vasan S Ramachandran; Jane Ranchalis; Susan Redline; Muredach P Reilly; Alex P Reiner; Paul M Ridker; Lynda M Rose; Nilesh J Samani; Eric E Schadt; Hubert Scharnag; Nicholas J Schork; Jonathan Shaffer; Sonia Shah; Haiqing Shen; Daichi Shimbo; Alan R Shuldiner; Roy L Silverstein; Erin N Smith; Harold Snieder; Nicole Soranzo; Sathanur R Srinivasan; Alice V Stanton; Ronald P Stolk; Herman A Taylor; Barbara Thorand; Vinicius Tragante; Mieke D Trip; André G Uitterlinden; Pim van der Harst; Peter J van der Most; Yvonne T van der Schouw; Cornelia M van Duijn; Erik P A Van Iperen; Jessic A Van Setten; W Monique Verschuren; Judith M Vonk; Cisca Wijmenga; Bernhard R Winkelmann; Sharon Wyatt; J Hunter Young; Li Zhang; Xiaofeng Zhu; John Barnard; Jens Baumert; Amber L Beitelshees; Gerald S Berenson; Deepak L Bhatt; Bernhard O Boehm; Jolanda M A Boer; Eric Boerwinkle; Ben Burkley; Amber Burt; Berta Almoguera Castillo; Mark J Caulfield; Aravinda Chakravarti; Yen-Pei C Chang; Daniel I Chasman; Wei Chen; Rhonda M Cooper-Dehoff; Sean P Curtis; Karina W Davidson; Paul I W de Bakker; Pieter A Doevendans; Albert Dreisbach; David Duggan; Georg Benedikt Ehret; Clara C Elbers; Richard R Fabsitz; Martin Farrall; Mary E Fischer; Garret A Fitzgerald; Myriam Fornage; Ervin Fox; Nora Franceschini; Clement E Furlong; Folkert W Asselbergs
Loci influencing blood pressure identified using a cardiovascular gene-centric array.
Ying Wu; Alicia M Young; Leena Moilanen; Narisu Narisu; Inger Njølstad; Kari E North; Ulrike Peters; Thomas Quertermous; Rainer Rauramaa; Jennifer G Robinson; Jerome I Rotter; Jouko Saramies; Fred Schumacher; Wayne H-H Sheu; Alena Stančáková; Jouko Sundvall; Yun-Ju Sung; Amy J Swift; Jaakko Tuomilehto; Matti Uusitupa; Lindsay L Waite; Tzung-Dau Wang; Wen-Chang Wang; Lynne Wilkens; Tom Wilsgaard; Devin Absher; Linda S Adair; Donna K Arnett; Themistocles L Assimes; Christie M Ballantyne; Michael Boehnke; Eric Boerwinkle; Lori L Bonnycastle; Steven Buyske; Petra Bůžková; Cara L Carty; Aravinda Chakravarti; Yii-Der I Chen; Iona Cheng; Barbara Cochran; Francis S Collins; Dana C Crawford; Damien C Croteau-Chonka; David Duggan; Logan Dumitrescu; Charles B Eaton; Alan B Feranil; Nora Franceschini; Xiuqing Guo; Christopher A Haiman; Brian E Henderson; Lucia A Hindorff; Low-Tone Ho; Chao A Hsiung; Yi-Jen Hung; Steven C Hunt; Kristian Hveem; Anne U Jackson; Jyh-Ming J Juang; Antero Y Kesäniemi; Eric Kim; Leena Kinnunen; Pirjo Komulainen; Charles Kooperberg; Johanna Kuusisto; Markku Laakso; Timo A Lakka; Loic Le Marchand; I-Te Lee; Wen-Jane Lee; Mark F Leppert; Yi Lin; Jaana Lindström; Oddgeir Lingaas-Holmen; Tara C Matise; Sabrina L Mitchell; Karen L Mohlke
Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained.
Khanh-Dung H Nguyen; Vasyl Pihur; Ankit Rakha; Eric Boerwinkle; Richard S Cooper; Josef Coresh; Georg Benedikt Ehret; Barry I Freedman; Santhi Ganesh; Steven C Hunt; WEN KAO; Alanna C Morrison; Aravinda Chakravarti
Effects of rare and common blood pressure gene variants on essential hypertension: results from the Family Blood Pressure Program, CLUE, and Atherosclerosis Risk in Communities studies.

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All Publications

2013: Santhi K Ganesh; Ron T Gansevoort; Tom R Gaunt; Johannes M I H Gho; Christian Gieger; Yan Gong; John G Gums; Wei Guo; Yiran Guo; Hakon Hakonarson; Hans L Hillege; Marten H Hofker; G Kees Hovingh; Thomas Illig; Aaron Isaacs; Gail P Jarvik; Andrew D Johnson; Julie A Johnson; Toby Johnson; John J P Kastelein; Brendan J Keating; Susan A Kirkland; Marcus E Kleber; Wolfgang Koenig; Kandice Kottke-Marchant; Abdullah Kutlar; Andrea Z Lacroix; Taimour Y Langaee; Matthew B Lanktree; Daniel Levy; Yun R Li; Honghuang Lin; Kiang Liu; Steffi Maiwald; Rainer Malik; Winfried März; Irene Mateo Leach; Caitrin W McDonough; Matthijs F L Meijs; Olle Mellander; Braxton D Mitchell; Cliona M Molony; Patricia B Munroe; Sarah S Murray; Gurunathan Murugesan; Christopher Newton-Cheh; Ilja M Nolte; Jeffery R O'Connell; Albertine J Oldehinkel; N Charlotte Onland-Moret; Willem H Ouwehand; Sandosh Padmanabhan; Walter Palmas; Brenda W Penninx; Carl J Pepine; Mary Pettinger; Joseph F Polak; Tom S Price; Daniel J Rader; Ramakrishnan Rajagopalan; Vasan S Ramachandran; Jane Ranchalis; Susan Redline; Muredach P Reilly; Alex P Reiner; Paul M Ridker; Lynda M Rose; Nilesh J Samani; Eric E Schadt; Hubert Scharnag; Nicholas J Schork; Jonathan Shaffer; Sonia Shah; Haiqing Shen; Daichi Shimbo; Alan R Shuldiner; Roy L Silverstein; Erin N Smith; Harold Snieder; Nicole Soranzo; Sathanur R Srinivasan; Alice V Stanton; Ronald P Stolk; Herman A Taylor; Barbara Thorand; Vinicius Tragante; Mieke D Trip; André G Uitterlinden; Pim van der Harst; Peter J van der Most; Yvonne T van der Schouw; Cornelia M van Duijn; Erik P A Van Iperen; Jessic A Van Setten; W Monique Verschuren; Judith M Vonk; Cisca Wijmenga; Bernhard R Winkelmann; Sharon Wyatt; J Hunter Young; Li Zhang; Xiaofeng Zhu; John Barnard; Jens Baumert; Amber L Beitelshees; Gerald S Berenson; Deepak L Bhatt; Bernhard O Boehm; Jolanda M A Boer; Eric Boerwinkle; Ben Burkley; Amber Burt; Berta Almoguera Castillo; Mark J Caulfield; Aravinda Chakravarti; Yen-Pei C Chang; Daniel I Chasman; Wei Chen; Rhonda M Cooper-Dehoff; Sean P Curtis; Karina W Davidson; Paul I W de Bakker; Pieter A Doevendans; Albert Dreisbach; David Duggan; Georg Benedikt Ehret; Clara C Elbers; Richard R Fabsitz; Martin Farrall; Mary E Fischer; Garret A Fitzgerald; Myriam Fornage; Ervin Fox; Nora Franceschini; Clement E Furlong; Folkert W Asselbergs
Loci influencing blood pressure identified using a cardiovascular gene-centric array.
Human molecular genetics 2013;22(8):1663-78.
2013: Ying Wu; Alicia M Young; Leena Moilanen; Narisu Narisu; Inger Njølstad; Kari E North; Ulrike Peters; Thomas Quertermous; Rainer Rauramaa; Jennifer G Robinson; Jerome I Rotter; Jouko Saramies; Fred Schumacher; Wayne H-H Sheu; Alena Stančáková; Jouko Sundvall; Yun-Ju Sung; Amy J Swift; Jaakko Tuomilehto; Matti Uusitupa; Lindsay L Waite; Tzung-Dau Wang; Wen-Chang Wang; Lynne Wilkens; Tom Wilsgaard; Devin Absher; Linda S Adair; Donna K Arnett; Themistocles L Assimes; Christie M Ballantyne; Michael Boehnke; Eric Boerwinkle; Lori L Bonnycastle; Steven Buyske; Petra Bůžková; Cara L Carty; Aravinda Chakravarti; Yii-Der I Chen; Iona Cheng; Barbara Cochran; Francis S Collins; Dana C Crawford; Damien C Croteau-Chonka; David Duggan; Logan Dumitrescu; Charles B Eaton; Alan B Feranil; Nora Franceschini; Xiuqing Guo; Christopher A Haiman; Brian E Henderson; Lucia A Hindorff; Low-Tone Ho; Chao A Hsiung; Yi-Jen Hung; Steven C Hunt; Kristian Hveem; Anne U Jackson; Jyh-Ming J Juang; Antero Y Kesäniemi; Eric Kim; Leena Kinnunen; Pirjo Komulainen; Charles Kooperberg; Johanna Kuusisto; Markku Laakso; Timo A Lakka; Loic Le Marchand; I-Te Lee; Wen-Jane Lee; Mark F Leppert; Yi Lin; Jaana Lindström; Oddgeir Lingaas-Holmen; Tara C Matise; Sabrina L Mitchell; Karen L Mohlke
Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained.
PLoS genetics 2013;9(3):e1003379.
2013: Khanh-Dung H Nguyen; Vasyl Pihur; Ankit Rakha; Eric Boerwinkle; Richard S Cooper; Josef Coresh; Georg Benedikt Ehret; Barry I Freedman; Santhi Ganesh; Steven C Hunt; WEN KAO; Alanna C Morrison; Aravinda Chakravarti
Effects of rare and common blood pressure gene variants on essential hypertension: results from the Family Blood Pressure Program, CLUE, and Atherosclerosis Risk in Communities studies.
Circulation research 2013;112(2):318-26.
2013: Anne-Sophie Jannot; Marine Masse-Morel; Arnold Munnich; Anna Pelet; Damien Sanlaville; Jeanne Amiel; Stacey Arnold; Nadege Bondurand; Salud Borrego; Isabella Ceccherini; Aravinda Chakravarti; Asma Chaoui; Françoise Clerget-Darpoux; Alexandra Henrion-Caude; Robert M W Hofstra; Stanislas LYONNET
Chromosome 21 Scan in Down Syndrome Reveals DSCAM as a Predisposing Locus in Hirschsprung Disease.
PloS one 2013;8(5):e62519.
2013: Sidharth A Shah; David S Siscovick; Gordon F Tomaselli; WEN KAO; Bruce M Psaty; Stephen S Rich; Donna K Arnett; Donald W Bowden; Greg L Burke; Aravinda Chakravarti; Jasmin Divers; Xiuqing Guo; David M Herrington; Timothy D Howard; João A C Lima; Wendy S Post
Associations between NOS1AP single nucleotide polymorphisms (SNPs) and QT interval duration in four racial/ethnic groups in the Multi-Ethnic Study of Atherosclerosis (MESA).
Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc 2013;18(1):29-40.
2012: N Amin; Y S Aulchenko; S Baumeister; R Biffar; D I Boomsma; L Broer; E Byrne; Aravinda Chakravarti; G Chenevix-Trench; N Dahmen; A Doering; H J Grabe; D F Gudbjartsson; V Gudnason; C J Hammond; A C Heath; A Hofman; J J Hottenga; A Ikram; A Isaacs; A C J W Janssens; J Johnson; J C Keers; L A Kiemeney; D Levy; M Mangino; N G Martin; G W Montgomery; I M Nolte; B A Oostra; A Petersmann; B M Psaty; R Rawal; F R Rivadeneira; S-Y Shin; H Snieder; T D Spector; K Stefansson; P Sulem; A Teumer; U Thorsteinsdottir; H Tiemeier; A G Uitterlinden; F J A van Rooij; G Verwoert; J M Vink; S Walter; E Wichmann; J C M Witteman; B H R Wolfenbuttel; N R Wray; C M van Duijn
Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM.
Molecular psychiatry 2012;17(11):1116-29.
2012: Anne-Sophie Jannot; Francesca Lantieri; Arnold Munnich; Anna Pelet; Paul K H Tam; Joke B G M Verheij; Jeanne Amiel; Stacey Marie Arnold; Salud Borrego; Isabella Ceccherini; Aravinda Chakravarti; Françoise Clerget-Darpoux; Raquel M Fernandez; Mercè Garcia-Barcelo; Robert M W Hofstra; Stanislas LYONNET
Male and female differential reproductive rate could explain parental transmission asymmetry of mutation origin in Hirschsprung disease.
European journal of human genetics : EJHG 2012;20(9):917-20.
2012: Patrick T Ellinor; Stephan B Felix; Karen L Furie; Tetsushi Furukawa; Nicole L Glazer; Michael H Gollob; Vilmundur Gudnason; Tamara B Harris; Susan R Heckbert; Albert Hofman; Christine M Albert; Alvaro Alonso; Dan E Arking; John Barnard; Emelia J Benjamin; Joshua C Bis; Eric Boerwinkle; Matthew Borkovich; Aravinda Chakravarti; Daniel I Chasman; Lin Y Chen; Mina K Chung; Sebastian Clauss; David Conen; Dawood Darbar; Robert W Davies; Jingzhong Ding; Marcus Dörr; Naoyuki Kamatani; WEN KAO; Sekar Kathiresan; Bouwe P Krijthe; Michiaki Kubo; Lenore J Launer; Daniel Levy; Guo Li; Honghuang Lin; Yongmei Liu; Kurt Lohman; Steven A Lubitz; Kathryn L Lunetta; Jared W Magnani; Saagar Mahida; Barbara McKnight; Thomas Meitinger; Olle Melander; David J Milan; Raafia Muhammad; Martina Müller-Nurasyid; Yusuke Nakamura; Anne B Newman; Kouichi Ozaki; Babar Parvez; Siegfried Perz; Arne Pfeufer; Bruce M Psaty; Kenneth M Rice; Paul M Ridker; Michiel Rienstra; Marylyn D Ritchie; Fernando Rivadeneira; Jason D Roberts; Dan M Roden; Jonathan Rosand; Lynda M Rose; Jerome I Rotter; Moritz F Sinner; Marketa Sjögren; Albert V Smith; Jonathan D Smith; J Gustav Smith; Nicholas L Smith; Elsayed Z Soliman; Nona Sotoodehnia; Gerhard Steinbeck; Bruno H Ch Stricker; Toshihiro Tanaka; Usha B Tedrow; Tatsuhiko Tsunoda; Andre G Uitterlinden; David Van Wagoner; Benjamin F Voight; Uwe Völker; Henry Völzke; Reza Wakili; H-Erich Wichmann; Jacqueline C M Witteman; Siyan Xu; Stefan Kääb
Meta-analysis identifies six new susceptibility loci for atrial fibrillation.
Nature genetics 2012;44(6):670-5.
2012: Aravinda Chakravarti
2011 introduction to Curt Stern Award.
American journal of human genetics 2012;90(3):405-6.
2012: Aravinda Chakravarti; Ashish Kapoor
Genetics. Mendelian puzzles.
Science (New York, N.Y.) 2012;335(6071):930-1.
2012: Maria Ximena Sosa; Pramila Tata; Vamsi Veeramachaneni; Georg Benedikt Ehret; Andrew B Feldman; Karin M Fredrikson; Ramesh Hariharan; Timothy T Harkins; Jeffrey Lin; Samantha Maragh; Minothi Parulekar; I K Ashok Sivakumar; Aravinda Chakravarti
Next-generation sequencing of human mitochondrial reference genomes uncovers high heteroplasmy frequency.
PLoS computational biology 2012;8(10):e1002737.
2012: Qian Jiang; Tychele Turner; Ankit Rakha; Maria X Sosa; Stacey Marie Arnold; Aravinda Chakravarti
Rapid and efficient human mutation detection using a bench-top next-generation DNA sequencer.
Human mutation 2012;33(1):281-9.
2011: K S Benke; Michelle C Carlson; Aravinda Chakravarti; B Q Doan; Linda P Fried; A P Reiner; Jeremy Walston; Qian-Li Xue; Dan E Arking; MARGARET D FALLIN
The association of genetic variants in interleukin-1 genes with cognition: findings from the cardiovascular health study.
Experimental gerontology 2011;46(12):1010-9.
2011: Aravinda Chakravarti
Widespread promiscuous genetic information transfer from DNA to RNA.
Circulation research 2011;109(11):1202-3.
2011: Aravinda Chakravarti
Genomics is not enough.
Science (New York, N.Y.) 2011;334(6052):15.
2011: Mika Kähönen; Antti J Kangas; WEN KAO; Sharon L Kardia; Sekar Kathiresan; Johannes Kettunen; Kay-Tee Khaw; Hyung-Lae Kim; Sanjay Kinra; Yoshikuni Kita; Mika Kivimaki; Jaspal S Kooner; Anna Köttgen; Heyo K Kroemer; Diana Kuh; Smita R Kulkarni; M V Kranthi Kumar; Meena Kumari; Johanna Kuusisto; Tatiana Kuznetsova; Markku Laakso; Maris Laan; Jaana Laitinen; Edward G Lakatta; Carl D Langefeld; Martin G Larson; Mark Lathrop; Lenore Launer; Debbie A Lawlor; Robert W Lawrence; Jong-Young Lee; Nanette R Lee; Terho Lehtimäki; Daniel Levy; Yali Li; Yongmei Liu; Kurt K Lohman; W T Longstreth; Ruth J F Loos; Jian'an Luan; Gavin Lucas; Barbara Ludwig; Leo-Pekka Lyytikäinen; Massimo Mangino; K Radha Mani; Michael G Marmot; Francesco U S Mattace-Raso; Giuseppe Matullo; Wendy L McArdle; Colin A McKenzie; Thomas Meitinger; Olle Melander; Pierre Meneton; James F Meschia; Tetsuro Miki; Yuri Milaneschi; Karen L Mohlke; Vincent Mooser; Mario A Morken; Richard W Morris; Alanna C Morrison; Thomas H Mosley; Patricia B Munroe; Samer Najjar; Michael A Nalls; Narisu Narisu; Gerjan Navis; Christopher Newton-Cheh; Khanh-Dung H Nguyen; Peter Nilsson; Fredrik Nyberg; Jeffrey R O'Connell; Christopher J O'Donnell; Toshio Ogihara; Takayoshi Ohkubo; Tomonori Okamura; Matthias Olden; Rick Twee-Hee Ong; Halit Ongen; N Charlotte Onland-Moret; Ben A Oostra; Paul F O'Reilly; Elin Org; Marco Orru; Walter Palmas; Jutta Palmen; Lyle J Palmer; Nicholette D Palmer; Alex N Parker; Afshin Parsa; Cristian Pattaro; John F Peden; Leena Peltonen; Markus Perola; Vasyl Pihur; Carl G P Platou; Andrew Plump; Ozren Polasek; Dorairaj Prabhakaran; Peter P Pramstaller; Inga Prokopenko; Bruce M Psaty; Leslie J Raffel; Olli Raitakari; Dabeeru C Rao; Asif Rasheed; Rainer Rettig; Fulvio Ricceri; Kenneth M Rice; Paul M Ridker; Fernando Rivadeneira; Annika Rosengren; Charles Rotimi; Jerome I Rotter; Igor Rudan; Megan E Rudock; Tunde Salako; Danish Saleheen; Veikko Salomaa; Nilesh J Samani; Stephen M Schwartz; Peter E H Schwarz; James Scott; Laura J Scott; Angelo Scuteri; Joban S Sehmi; Mark Seielstad; Sudha Seshadri; Pankaj Sharma; Sue Shaw-Hawkins; Gang Shi; Nick R G Shrine; Daniel Shriner; Alan R Shuldiner; Eric J G Sijbrands; Xueling Sim; Andrew Singleton; Marketa Sjögren; Albert V Smith; George Davey Smith; Nicholas L Smith; Harold Snieder; Siim Sõber; Pasi Soininen; Nicole Soranzo; Tim D Spector; Jan A Staessen; Alena Stančáková; Nanette I Steinle; David P Strachan; Heather M Stringham; Yan V Sun; Amy J Swift; Yasuharu Tabara; E Shyong Tai; Philippa J Talmud; Toshiko Tanaka; Andrew Taylor; Bamidele Tayo; Janos Terzic; Alexander Teumer; Dag S Thelle; Martin D Tobin; Maciej Tomaszewski; Vikal Tripathy; Taru Tukiainen; Jaakko Tuomilehto; Ioanna Tzoulaki; Manuela Uda; Hirotsugu Ueshima; Cuno S P M Uiterwaal; Andre G Uitterlinden; Satoshi Umemura; Pim van der Harst; Yvonne T van der Schouw; Cornelia M van Duijn; Wiek H van Gilst; Erkki Vartiainen; Ramachandran S Vasan; Gudrun Veldre; Germaine C Verwoert; Margus Viigimaa; Jorma Viikari; D G Vinay; Paolo Vineis; Veronique Vitart; Benjamin F Voight; Uwe Völker; Peter Vollenweider; Henry Völzke; Lynne E Wagenknecht; Louise V Wain; Thomas J Wang; Xiaoling Wang; Nicholas J Wareham; Hugh Watkins; Alan B Weder; Peter H Whincup; H-Erich Wichmann; Kerri L Wiggins; Sarah H Wild; James F Wilson; Jacqueline C M Witteman; Andrew Wong; Tien Y Wong; Alan F Wright; Ying Wu; Peter Würtz; Chittaranjan S Yajnik; Jie Yao; J Hunter Young; Diana Zelenika; Guangju Zhai; Feng Zhang; Weihua Zhang; Jing Hua Zhao; Haidong Zhu; Xiaofeng Zhu; Paavo Zitting; Ewa Zukowska-Szczechowska; Maria Soler Artigas; Gonçalo R Abecasis; Linda S Adair; Adebowale Adeyemo; Mika Ala-Korpela; Myriam Alexander; David Altshuler; Najaf Amin; Dan E Arking; Pankaj Arora; Thor Aspelund; Yurii Aulchenko; Stephan J L Bakker; Stefania Bandinelli; Inês Barroso; Jacques Beckmann; John P Beilby; Richard N Bergman; Sven Bergmann; Joshua C Bis; Murielle Bochud; Michael Boehnke; Eric Boerwinkle; Judith A Hoffman Bolton; Lori L Bonnycastle; Stefan R Bornstein; Michiel L Bots; Jennifer L Bragg-Gresham; Eva Brand; Stefan-Martin Brand; Peter S Braund; Morris J Brown; Paul R Burton; Harry Campbell; Juan P Casas; Mark J Caulfield; Aravinda Chakravarti; John C Chambers; Giriraj R Chandak; Yen-Pei C Chang; Fadi J Charchar; Daniel I Chasman; Nish Chaturvedi; Ming-Huei Chen; Yoon Shin Cho; Robert Clarke; Francis S Collins; John M Connell; Jackie A Cooper; Matthew N Cooper; Richard S Cooper; Josef Coresh; Anna Maria Corsi; Santosh Dahgam; John Danesh; Ian N M Day; Abbas Dehghan; Panos Deloukas; Ayse Demirkan; Matthew Denniff; Anna F Dominiczak; Yanbin Dong; Marcus Dörr; Ayo Doumatey; Albert W Dreisbach; Georg Benedikt Ehret; Paul Elliott; Roberto Elosua; Valur Emilsson; Jeanette Erdmann; Susana Eyheramendy; Martin Farrall; Cristiano Fava; Luigi Ferrucci; Terrence Forrester; F Gerald R Fowkes; Ervin R Fox; Timothy M Frayling; Pilar Galan; Santhi Ganesh; Melissa Garcia; Tom R Gaunt; Christian Gieger; Nicole L Glazer; Min Jin Go; Anuj Goel; Jürgen Grässler; Diederick E Grobbee; Leif Groop; Simonetta Guarrera; Vilmundur Gudnason; Xiuqing Guo; Ulf B Gyllensten; David Hadley; Anders Hamsten; Bok-Ghee Han; Rebecca Hardy; Tamara B Harris; Anna-Liisa Hartikainen; Caroline Hayward; Simon Heath; Susan R Heckbert; Bo Hedblad; Serge Hercberg; Dena Hernandez; Andrew A Hicks; Gina Hilton; Aroon D Hingorani; Albert Hofman; Jemma C Hopewell; Philip Howard; Steve E Humphries; Steven C Hunt; Kristian Hveem; Shih-Jen Hwang; Wilmar Igl; M Arfan Ikram; Aaron Isaacs; Muhammad Islam; Naoharu Iwai; Anne U Jackson; Tazeen H Jafar; Charles S Janipalli; Marjo-Riitta Järvelin; Andrew D Johnson; Toby Johnson
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
Nature 2011;478(7367):103-9.
2011: Louise V Wain; Thomas J Wang; Nicholas J Wareham; Hugh Watkins; Rebecca J Webster; H-Erich Wichmann; Sarah H Wild; Gonneke Willemsen; James F Wilson; Jacqueline C M Witteman; Alan F Wright; Marion Zeginigg; Feng Zhang; Weihua Zhang; Jing Hua Zhao; Paavo Zitting; Fabiola M Del Greco; Ramachandran S Vasan; Germaine C Verwoert; Jorma Viikari; Veronique Vitart; Benjamin F Voight; Uwe Völker; Peter Vollenweider; Henry Völzke; Gérard Waeber; Goncalo R Abecasis; Helene Alavere; Behrooz Z Alizadeh; David Altshuler; Najaf Amin; Pankaj Arora; Thor Aspelund; Yurii Aulchenko; Stefania Bandinelli; Inês Barroso; Jacques Beckmann; John P Beilby; Richard N Bergman; Sven Bergmann; Joshua C Bis; Mladen Boban; Murielle Bochud; Michael Boehnke; Eric Boerwinkle; Dorret I Boomsma; Jennifer L Bragg-Gresham; Monique Breteler; Brendan Buckley; Gregory L Burke; Harry Campbell; Mark J Caulfield; Aravinda Chakravarti; John C Chambers; Daniel I Chasman; Yii-Der Ida Chen; Robert Clarke; Francis S Collins; Tanguy Corre; Anna Maria Corsi; Adamo Pio d'Adamo; Gail Davies; Eco J C de Geus; Ian J Deary; Stéphanie Debette; Anita L Destefano; Angela Döring; Marcus Dörr; Georg Benedikt Ehret; Paul Elliott; Valur Emilsson; Jeanette Erdmann; Tõnu Esko; Susana Eyheramendy; Antonella Fabretto; Maurizio Facheris; Flavio Faletra; Martin Farrall; Janine F Felix; Luigi Ferrucci; Myriam Fornage; Jingyuan Fu; Pilar Galan; Santhi Ganesh; Paolo Gasparini; Pierre Gider; Christian Gieger; Nicole L Glazer; Anuj Goel; Leif Groop; Vilmundur Gudnason; Xiuqing Guo; Ulf B Gyllensten; David Hadley; Toomas Haller; Anders Hamsten; Tamara B Harris; Caroline Hayward; Simon Heath; Peter Henneman; Serge Hercberg; Dena Hernandez; Peter A C 't Hoen; Albert Hofman; Hilma Holm; Jemma C Hopewell; Jouke-Jan Hottenga; Joseph Hung; Shih-Jen Hwang; Wilmar Igl; Anne U Jackson; A Cecile J W Janssens; Marjo-Riitta Jarvelin; Andrew D Johnson; Toby Johnson; J Wouter Jukema; Mika Kähönen; Aime Keis; Kay-Tee Khaw; Inke R König; Jaspal S Kooner; Heyo K Kroemer; Brigitte Kühnel; Suman Kundu; Maris Laan; Jaana Laitinen; Martin G Larson; Mark Lathrop; Lenore Launer; Terho Lehtimäki; Daniel Levy; Xinzhong Li; Jan H Lindeman; Marisa Loitfelder; Ruth J F Loos; Lorna M Lopez; Xiaowen Lu; Jian'an Luan; Gavin Lucas; Massimo Mangino; Corrado Masciullo; Francesco U S Mattace-Raso; Wendy L McArdle; Thomas Meitinger; Olle Melander; Pierre Meneton; Andres Metspalu; Yuri Milaneschi; Gary F Mitchell; Vincent Mooser; Alanna C Morrison; Patricia B Munroe; A William Musk; Samer S Najjar; Pau Navarro; Christopher P Nelson; Christopher Newton-Cheh; Ilja M Nolte; Christopher J O'Donnell; Halit Ongen; Ben A Oostra; Paul F O'Reilly; Elin Org; Marco Orru; Walter Palmas; Lyle J Palmer; Alex N Parker; John F Peden; Brenda W Penninx; Arne Pfeufer; Irene Pichler; Vasyl Pihur; Nicola Pirastu; Giorgio Pistis; Andrew Plump; Ozren Polašek; Anneli Pouta; Michael Preuss; Bruce M Psaty; Olli T Raitakari; Dabeeru C Rao; Rainer Rettig; Kenneth M Rice; Paul M Ridker; Fernando Rivadeneira; Lynda M Rose; Igor Rudan; Cinzia Sala; Veikko Salomaa; Nilesh J Samani; Helena Schmidt; Reinhold Schmidt; James Scott; Gang Shi; So-Youn Shin; Eric J G Sijbrands; Andrew Singleton; David Siscovick; Albert V Smith; Nicholas L Smith; Harold Snieder; Siim Sõber; Nicole Soranzo; Tim D Spector; John M Starr; Kari Stefansson; Ronald P Stolk; David Stott; David P Strachan; Mari-Liis Tammesoo; Toshiko Tanaka; Kent D Taylor; Gudmar Thorleifsson; Unnur Thorsteinsdottir; Martin D Tobin; Daniela Toniolo; Stella Trompet; Jaakko Tuomilehto; Manuela Uda; Andre G Uitterlinden; Sheila Ulivi; Melanie M van der Klauw; Ko Willems van Dijk; Cornelia M van Duijn
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.
Nature genetics 2011;43(10):1005-11.
2011: Yen-Yi Ho; Amy M Matteini; Qian-Li Xue; Dan E Arking; Brock A Beamer; Aravinda Chakravarti; MARGARET D FALLIN; Linda P Fried; Jeremy Walston
Exploring biologically relevant pathways in frailty.
The journals of gerontology. Series A, Biological sciences and medical sciences 2011;66(9):975-9.
2011: Dan E Arking; Abdennasser Bardai; Connie R Bezzina; Pallav Bhatnagar; Marieke T Blom; Eric Boerwinkle; Gabrielle Boucher; Greg L Burke; Naima Carter-Monroe; Aravinda Chakravarti; Christine M Albert; Josef Coresh; L Adrienne Cupples; Abbas Dehghan; Georg Benedikt Ehret; Mark Eijgelsheim; Philippe Goyette; Karen Gunson; Gina Hilton; Albert Hofman; Adriana Huertas-Vazquez; Heikki V Huikuri; Shih-Jen Hwang; Jonathan Jui; M Juhani Junttila; Kari S Kaikkonen; WEN KAO; Y Antero Kesäniemi; Frank Kolodgie; Marja-Leena Kortelainen; Rudolph W Koster; Anna Köttgen; Caroline Lagacé; Man Li; Eduardo Marban; Roos F Marsman; Anna Moes; Christopher Newton-Cheh; Christopher J O'Donnell; Raha Pazoki; Wendy S Post; Ronald J Prineas; Bruce M Psaty; Kyndaron Reinier; John D Rioux; Fernando Rivadeneira; David S Siscovick; Nona Sotoodehnia; PETER SPOONER; Bruno H C H Stricker; Hanno L Tan; Jean-Claude Tardif; Carmen Teodorescu; Gordon F Tomaselli; André G Uitterlinden; Audrey Uy-Evanado; Renu Virmani; Arthur A M Wilde; Jacqueline C M Witteman; XiaoQing Zhao; Sumeet S Chugh
Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals.
PLoS genetics 2011;7(6):e1002158.
2011: Michael A Nalls; Matthias Nauck; Christopher J O'Donnell; Yukinori Okada; Ben A Oostra; Willem H Ouwehand; Kushang V Patel; Nicola Pirastu; Giorgio Pistis; Holger Prokisch; Inga Prokopenko; Bruce M Psaty; Alex P Reiner; Augusto Rendon; Jennifer Sambrook; Andrew B Singleton; Albert V Smith; Nicole Soranzo; Tim D Spector; Jonathan Stephens; Michael Stumvoll; Atsushi Takahashi; Toshiko Tanaka; Toshihiro Tanaka; Kent Taylor; Alexander Teumer; Swee Lay Thein; Daniela Toniolo; Anke Tönjes; Tatsuhiko Tsunoda; André G Uitterlinden; Cornelia M van Duijn; Frank van Rooij; Uwe Völker; Henry Völzke; H-Erich Wichmann; Kerri L Wiggins; James G Wilson; Jacqueline C M Witteman; Andrew R Wood; Kazuhiko Yamamoto; Qiong Yang; Neil A Zakai; Sampath Arepalli; Stefania Bandinelli; Alessandro Biffi; Joshua C Bis; Eric Boerwinkle; Aravinda Chakravarti; Ming-Huei Chen; Sean Chong; Josef Coresh; David J Couper; L Adrienne Cupples; Abbas Dehghan; Angela Döring; Gudny Eiriksdottir; Janine F Felix; Luigi Ferrucci; Aaron R Folsom; Caroline S Fox; Timothy M Frayling; Melissa Garcia; Stephen F Garner; Paolo Gasparini; Christian Gieger; Nicole L Glazer; Natalia A Gouskova; Andreas Greinacher; Vilmundur Gudnason; Tamara B Harris; Dena G Hernandez; Albert Hofman; Thomas Illig; Naoyuki Kamatani; Yoichiro Kamatani; Michiaki Kubo; Brigitte Kuhnel; Vasiliki Lagou; Guillaume Lettre; Daniel Levy; JingPing Lin; Yongmei Liu; Dan L Longo; Thomas Lumley; Massimo Mangino; Koichi Matsuda; Christa Meisinger; David Melzer; Stephan Menzel; Matt Moore; Yusuke Nakamura; Santhi Ganesh
Multiple loci are associated with white blood cell phenotypes.
PLoS genetics 2011;7(6):e1002113.
2011: Xiaofeng Zhu; J Hunter Young; Ervin Fox; Brendan J Keating; Nora Franceschini; Sunjung Kang; Bamidele Tayo; Adebowale Adeyemo; Yun V Sun; Yali Li; Alanna Morrison; Christopher Newton-Cheh; Kiang Liu; Santhi Ganesh; Abdullah Kutlar; Ramachandran S Vasan; Albert Dreisbach; Sharon Wyatt; Joseph Polak; Walter Palmas; Solomon Musani; Herman Taylor; Richard Fabsitz; Raymond R Townsend; Daniel Dries; Joseph Glessner; Charleston W K Chiang; Thomas Mosley; Sharon Kardia; David Curb; Joel N Hirschhorn; Charles Rotimi; Alexander Reiner; Charles Eaton; Jerome I Rotter; Richard S Cooper; Susan Redline; Aravinda Chakravarti; Daniel Levy
Combined admixture mapping and association analysis identifies a novel blood pressure genetic locus on 5p13: contributions from the CARe consortium.
Human molecular genetics 2011;20(11):2285-95.
2011: Ervin R Fox; Nora Franceschini; Santhi Ganesh; Joel N Hirschorn; Toby Johnson; Sun J Kang; Sharon L R Kardia; Brendan J Keating; Abdullah Kutlar; Adebowale Adeyemo; Mark J Caulfield; Aravinda Chakravarti; Richard S Cooper; J David Curb; Ayo P Doumatey; Albert W Dreisbach; Daniel L Dries; Charles B Eaton; Georg Benedikt Ehret; Richard R Fabsitz; Deborah N Farlow; Yali Li; Kiang Liu; Helen N Lyon; Lisa W Martin; Alanna C Morrison; Thomas H Mosley; Solomon K Musani; Walter Palmas; Alan D Penman; Josef F Polak; Vasan S Ramachandran; Susan Redline; Charles N Rotimi; Jerome I Rotter; Yan V Sun; Herman A Taylor; Bamidele O Tayo; Raymond R Townsend; Sharon B Wyatt; J Hunter Young; Xiaofeng Zhu; Daniel Levy
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study.
Human molecular genetics 2011;20(11):2273-84.
2011: Aravinda Chakravarti
Genomic contributions to Mendelian disease.
Genome research 2011;21(5):643-4.
2011: Andrew D Johnson; Toby Johnson; Martin G Larson; Lenore J Launer; Daniel Levy; Patricia B Munroe; Christopher Newton-Cheh; Bruce M Psaty; Kenneth Rice; Paul M Ridker; Lynda Rose; Cornelia M van Duijn; Germaine C Verwoert; Mark Caulfield; Aravinda Chakravarti; Daniel I Chasman; Georg Benedikt Ehret; Vilmundur Gudnason
Association of hypertension drug target genes with blood pressure and hypertension in 86,588 individuals.
Hypertension 2011;57(5):903-10.
2011: Aldi T Kraja; Dhananjay Vaidya; James S Pankow; Mark O Goodarzi; Themistocles L Assimes; Iftikhar J Kullo; Ulla Sovio; Rasika A Mathias; Yan V Sun; Nora Franceschini; Devin Absher; Guo Li; Qunyuan Zhang; Mary F Feitosa; Nicole L Glazer; Talin Haritunians; Anna-Liisa Hartikainen; Joshua W Knowles; Kari E North; Carlos Iribarren; Brian G Kral; Lisa R Yanek; Paul F O'Reilly; Mark I McCarthy; Cashell Jaquish; David J Couper; Aravinda Chakravarti; Bruce M Psaty; Lewis C Becker; Michael A Province; Eric Boerwinkle; Thomas Quertermous; Leena Palotie; Marjo-Riitta Jarvelin; Diane M Becker; Sharon L R Kardia; Jerome I Rotter; Yii-Der Ida Chen; Ingrid B Borecki
A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.
Diabetes 2011;60(4):1329-39.
2011: Jeannette Simino; Gang Shi; Rezart Kume; Karen Schwander; Michael A Province; C Charles Gu; Sharon L R Kardia; Aravinda Chakravarti; Georg Benedikt Ehret; Richard A Olshen; Stephen T Turner; low-tone ho; Xiaofeng Zhu; Cashell E Jaquish; Dina Paltoo; Richard S Cooper; Alan B Weder; J David Curb; Eric Boerwinkle; Steven C Hunt; Dabeeru C Rao
Five blood pressure loci identified by an updated genome-wide linkage scan: meta-analysis of the Family Blood Pressure Program.
American journal of hypertension 2011;24(3):347-54.
2011: Gang Shi; Eric Boerwinkle; Alanna C Morrison; C Charles Gu; Aravinda Chakravarti; Dabeeru C Rao
Mining gold dust under the genome wide significance level: a two-stage approach to analysis of GWAS.
Genetic epidemiology 2011;35(2):111-8.
2011: Joong-Ho Won; Aravinda Chakravarti; Georg Benedikt Ehret; Richard A Olshen
SNPs and other features as they predispose to complex disease: genome-wide predictive analysis of a quantitative phenotype for hypertension.
PloS one 2011;6(11):e27891.
2011: Tychele Turner; Vasyl Pihur; Aravinda Chakravarti
Quantifying and modeling birth order effects in autism.
PloS one 2011;6(10):e26418.
2011: Qian Jiang; Courtney Nichols Berrios; Li Hao; Yen-Yi Ho; Aravinda Chakravarti
Copy number variants in candidate genes are genetic modifiers of Hirschsprung disease.
PloS one 2011;6(6):e21219.
2011: Kathleen HELEN Burns; Aravinda Chakravarti
Massively parallel rare disease genetics.
Genome medicine 2011;3(5):29.
2011: Guillaume Lettre; Cameron D Palmer; Taylor Young; Kenechi G Ejebe; Hooman Allayee; Emelia J Benjamin; Franklyn Bennett; Donald W Bowden; Aravinda Chakravarti; Al Dreisbach; Deborah N Farlow; Aaron R Folsom; Myriam Fornage; Terrence Forrester; Ervin Fox; Christopher A Haiman; Jaana Hartiala; Tamara B Harris; Stanley L Hazen; Susan R Heckbert; Brian E Henderson; Joel N Hirschhorn; Brendan J Keating; Stephen B Kritchevsky; Emma Larkin; Mingyao Li; Megan E Rudock; Colin A McKenzie; James B Meigs; Yang A Meng; Tom H Mosley; Anne B Newman; Christopher H Newton-Cheh; Dina N Paltoo; George J Papanicolaou; Nick Patterson; Wendy S Post; Bruce M Psaty; Atif N Qasim; Liming Qu; Daniel J Rader; Susan Redline; Muredach P Reilly; Alexander P Reiner; Stephen S Rich; Jerome I Rotter; Yongmei Liu; Peter Shrader; David S Siscovick; W H Wilson Tang; Herman A Taylor; Russell P Tracy; Ramachandran S Vasan; Kevin M Waters; Rainford Wilks; James G Wilson; Richard R Fabsitz; Stacey B Gabriel; Sekar Kathiresan; Eric Boerwinkle
Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.
PLoS genetics 2011;7(2):e1001300.
2011: Robert B Scharpf; Ingo Ruczinski; Benilton Carvalho; Betty Doan; Aravinda Chakravarti; Rafael A Irizarry
A multilevel model to address batch effects in copy number estimation using SNP arrays.
Biostatistics (Oxford, England) 2011;12(1):33-50.
2010: Nona Sotoodehnia; Aaron Isaacs; Paul I W de Bakker; Marcus Dörr; Christopher Newton-Cheh; Ilja M Nolte; Pim van der Harst; Martina Müller; Mark Eijgelsheim; Alvaro Alonso; Andrew A Hicks; Sandosh Padmanabhan; Caroline Hayward; Albert Vernon Smith; Ozren Polasek; Steven Giovannone; Jingyuan Fu; Jared W Magnani; Kristin D Marciante; Arne Pfeufer; Sina A Gharib; Alexander Teumer; Man Li; Joshua C Bis; Fernando Rivadeneira; Thor Aspelund; Anna Köttgen; Toby Johnson; Kenneth Rice; Mark P S Sie; Ying A Wang; Norman Klopp; Christian Fuchsberger; Sarah H Wild; Irene Mateo Leach; Karol Estrada; Uwe Völker; Alan F Wright; Folkert W Asselbergs; Jiaxiang Qu; Aravinda Chakravarti; Moritz F Sinner; Jan A Kors; Astrid Petersmann; Tamara B Harris; Elsayed Z Soliman; Patricia B Munroe; Bruce M Psaty; Ben A Oostra; L Adrienne Cupples; Siegfried Perz; Rudolf A de Boer; André G Uitterlinden; Henry Völzke; Timothy D Spector; Fang-Yu Liu; Eric Boerwinkle; Anna F Dominiczak; Jerome I Rotter; Gé van Herpen; Daniel Levy; H-Erich Wichmann; Wiek H van Gilst; Jacqueline C M Witteman; Heyo K Kroemer; WEN KAO; Susan R Heckbert; Thomas Meitinger; Albert Hofman; Harry Campbell; Aaron R Folsom; Dirk J van Veldhuisen; Christine Schwienbacher; Christopher J O'Donnell; Claudia Beu Volpato; Mark J Caulfield; John M Connell; Lenore Launer; Xiaowen Lu; Lude Franke; Rudolf S N Fehrmann; Gerard te Meerman; Harry J M Groen; Rinse K Weersma; Leonard H van den Berg; cisca wijmenga; Roel A Ophoff; Gerjan Navis; Igor Rudan; Harold Snieder; James F Wilson; Peter P Pramstaller; David S Siscovick; Thomas J Wang; Vilmundur Gudnason; Cornelia M van Duijn; Stephan B Felix; Glenn I Fishman; Yalda Jamshidi; Bruno H Ch Stricker; Nilesh J Samani; Stefan Kääb; Dan E Arking
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.
Nature genetics 2010;42(12):1068-76.
2010: Anna M Kucharska-Newton; David J Couper; James S Pankow; Ronald J Prineas; Thomas D Rea; Nona Sotoodehnia; Aravinda Chakravarti; Aaron R Folsom; David S Siscovick; Wayne D Rosamond
Diabetes and the risk of sudden cardiac death, the Atherosclerosis Risk in Communities study.
Acta diabetologica 2010;47 Suppl 1():161-8.
2010: Kari E North; Nora Franceschini; Christy L Avery; Lisa Baird; Mariaelisa Graff; Mark Leppert; Jay H Chung; Jinghui Zhang; Craig Hanis; Eric Boerwinkle; Kelly A Volcik; Megan L Grove; Thomas H Mosley; Charles Gu; Gerardo Heiss; James S Pankow; David J Couper; Christie M Ballantyne; W H Linda Kao; Alan B Weder; Richard S Cooper; Georg Benedikt Ehret; Ashley A O'Connor; Aravinda Chakravarti; Steven C Hunt
Variation in the checkpoint kinase 2 gene is associated with type 2 diabetes in multiple populations.
Acta diabetologica 2010;47 Suppl 1():199-207.
2010: Tamra E Meyer; Germaine C Verwoert; Shih-Jen Hwang; Nicole L Glazer; Albert V Smith; Frank van Rooij; Georg Benedikt Ehret; Eric Boerwinkle; Janine F Felix; Tennille S Leak; Tamara B Harris; Qiong Yang; Abbas Dehghan; Thor Aspelund; Ronit Katz; Georg Homuth; Thomas Kocher; Rainer Rettig; Janina S Ried; Christian Gieger; Hanna Prucha; Arne Pfeufer; Thomas Meitinger; Josef Coresh; Albert Hofman; Mark J Sarnak; Yii-Der Ida Chen; André G Uitterlinden; Aravinda Chakravarti; Bruce M Psaty; Cornelia M van Duijn; WEN KAO; Jacqueline C M Witteman; Vilmundur Gudnason; David S Siscovick; Caroline S Fox; Anna Köttgen
Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels.
PLoS genetics 2010;6(8):.
2010: Eileen Sproat Emison; Mercè Garcia-Barcelo; Elizabeth A Grice; Francesca Lantieri; Jeanne Amiel; Grzegorz Burzynski; Raquel M Fernandez; Li Hao; Carl S Kashuk; Kristen West; Xiaoping Miao; Paul K H Tam; Paola Griseri; Isabella Ceccherini; Anna Pelet; Anne-Sophie Jannot; Loïc de Pontual; Alexandra Henrion-Caude; Stanislas LYONNET; Joke B G M Verheij; Robert M W Hofstra; Guillermo Antiñolo; Salud Borrego; Andy McCallion; Aravinda Chakravarti
Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liability.
American journal of human genetics 2010;87(1):60-74.
2010: Marta Tomás; Carlo Napolitano; Luciana De Giuli; Raffaella Bloise; Isaac Subirana; Alberto Malovini; Riccardo Bellazzi; Dan E Arking; Eduardo Marban; Aravinda Chakravarti; PETER SPOONER; Silvia G Priori
Polymorphisms in the NOS1AP gene modulate QT interval duration and risk of arrhythmias in the long QT syndrome.
Journal of the American College of Cardiology 2010;55(24):2745-52.
2010: Stylianos E Antonarakis; Aravinda Chakravarti; Jonathan C Cohen; John Hardy
Mendelian disorders and multifactorial traits: the big divide or one for all?
Nature reviews. Genetics 2010;11(5):380-4.
2010: Aravinda Chakravarti
ASHG Awards and Addresses. 2008 Presidential address: Principia genetica: our future science.
American journal of human genetics 2010;86(3):302-8.
2010: Patrick T Ellinor; Kathryn L Lunetta; Nicole L Glazer; Arne Pfeufer; Alvaro Alonso; Mina K Chung; Moritz F Sinner; Paul I W de Bakker; Martina Mueller; Steven A Lubitz; Ervin Fox; Dawood Darbar; Nicholas L Smith; Jonathan D Smith; Renate B Schnabel; Elsayed Z Soliman; Kenneth M Rice; David Van Wagoner; britt beckmann; Charlotte van Noord; Ke Wang; Georg Benedikt Ehret; Jerome I Rotter; Stanley L Hazen; Gerhard Steinbeck; Albert Vernon Smith; Lenore J Launer; Tamara B Harris; Seiko Makino; Mari Nelis; David J Milan; Siegfried Perz; Tõnu Esko; Anna Köttgen; Susanne Moebus; Christopher Newton-Cheh; Man Li; Stefan Möhlenkamp; Thomas J Wang; WEN KAO; Ramachandran S Vasan; Markus M Nöthen; Calum A MacRae; Bruno H Ch Stricker; Albert Hofman; André G Uitterlinden; Daniel Levy; Eric Boerwinkle; Andres Metspalu; Eric J Topol; Aravinda Chakravarti; Vilmundur Gudnason; Bruce M Psaty; Dan Mark Roden; Thomas Meitinger; H-Erich Wichmann; Jacqueline C M Witteman; John Barnard; Dan E Arking; Emelia J Benjamin; Susan R Heckbert; Stefan Kääb
Common variants in KCNN3 are associated with lone atrial fibrillation.
Nature genetics 2010;42(3):240-4.
2010: A Y Chu; Josef Coresh; Dan E Arking; J S Pankow; Gordon F Tomaselli; Aravinda Chakravarti; Wendy S Post; P H Spooner; E Boerwinkle; WEN KAO
NOS1AP variant associated with incidence of type 2 diabetes in calcium channel blocker users in the Atherosclerosis Risk in Communities (ARIC) study.
Diabetologia 2010;53(3):510-6.
2010: Arne Pfeufer; Charlotte van Noord; Kristin D Marciante; Dan E Arking; Martin G Larson; Albert Vernon Smith; Kirill V Tarasov; Martina Müller; Nona Sotoodehnia; Moritz F Sinner; Germaine C Verwoert; Man Li; WEN KAO; Anna Köttgen; Josef Coresh; Joshua C Bis; Bruce M Psaty; Kenneth Rice; Jerome I Rotter; Fernando Rivadeneira; Albert Hofman; Jan A Kors; Bruno H C Stricker; André G Uitterlinden; Cornelia M van Duijn; britt beckmann; Wiebke Sauter; Christian Gieger; Steven A Lubitz; Christopher Newton-Cheh; Thomas J Wang; Jared W Magnani; Renate B Schnabel; Mina K Chung; John Barnard; Jonathan D Smith; David Van Wagoner; Ramachandran S Vasan; Thor Aspelund; Gudny Eiriksdottir; Tamara B Harris; Lenore J Launer; Samer S Najjar; Edward Lakatta; David Schlessinger; Manuela Uda; Gonçalo R Abecasis; Bertram Müller-Myhsok; Georg Benedikt Ehret; Eric Boerwinkle; Aravinda Chakravarti; Elsayed Z Soliman; Kathryn L Lunetta; Siegfried Perz; H-Erich Wichmann; Thomas Meitinger; Daniel Levy; Vilmundur Gudnason; Patrick T Ellinor; Serena Sanna; Stefan Kääb; Jacqueline C M Witteman; Alvaro Alonso; Emelia J Benjamin; Susan R Heckbert
Genome-wide association study of PR interval.
Nature genetics 2010;42(2):153-9.
2010: Delphine Fradin; Keely Cheslack-Postava; Christine Ladd-Acosta; Craig J Newschaffer; Aravinda Chakravarti; Dan E Arking; Andrew P Feinberg; MARGARET D FALLIN
Parent-of-origin effects in autism identified through genome-wide linkage analysis of 16,000 SNPs.
PloS one 2010;5(9):.
2010: Ann Z Moore; Mary L Biggs; Amy Matteini; Ashley O'Connor; Sarah McGuire; Brock A Beamer; MARGARET D FALLIN; Linda P Fried; Jeremy Walston; Aravinda Chakravarti; Dan E Arking
Polymorphisms in the mitochondrial DNA control region and frailty in older adults.
PloS one 2010;5(6):e11069.
2010: Dan E Arking; Kyndaron Reinier; Wendy S Post; Jonathan Jui; Gina Hilton; Ashley O'Connor; Ronald J Prineas; Eric Boerwinkle; Bruce M Psaty; Gordon F Tomaselli; Thomas Rea; Nona Sotoodehnia; David S Siscovick; Gregory L Burke; Eduardo Marban; PETER SPOONER; Aravinda Chakravarti; Sumeet S Chugh
Genome-wide association study identifies GPC5 as a novel genetic locus protective against sudden cardiac arrest.
PloS one 2010;5(3):e9879.
2010: A M Matteini; Jeremy Walston; Karen Bandeen-Roche; Dan E Arking; Robert H Allen; Linda P Fried; Aravinda Chakravarti; S P Stabler; MARGARET D FALLIN
Transcobalamin-II variants, decreased vitamin B12 availability and increased risk of frailty.
The journal of nutrition, health & aging 2010;14(1):73-7.
2009: Anna M Kucharska-Newton; David J Couper; James S Pankow; Ronald J Prineas; Thomas D Rea; Nona Sotoodehnia; Aravinda Chakravarti; Aaron R Folsom; David S Siscovick; Wayne D Rosamond
Hemostasis, inflammation, and fatal and nonfatal coronary heart disease: long-term follow-up of the atherosclerosis risk in communities (ARIC) cohort.
Arteriosclerosis, thrombosis, and vascular biology 2009;29(12):2182-90.
2009: Georg Benedikt Ehret; Ashley A O'Connor; Alan B Weder; Richard S Cooper; Aravinda Chakravarti
Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study.
European journal of human genetics : EJHG 2009;17(12):1650-7.
2009: Santhi Ganesh; Neil A Zakai; Frank van Rooij; Nicole Soranzo; Albert Vernon Smith; Michael A Nalls; Ming-Huei Chen; Anna Kottgen; Nicole L Glazer; Abbas Dehghan; Brigitte Kuhnel; Thor Aspelund; Qiong Yang; Toshiko Tanaka; Andrew Jaffe; Joshua C M Bis; Germaine C Verwoert; Alexander Teumer; Caroline S Fox; Jack M Guralnik; Georg Benedikt Ehret; Kenneth Rice; Janine F Felix; Augusto Rendon; Gudny Eiriksdottir; Daniel Levy; Kushang V Patel; Eric Boerwinkle; Jerome I Rotter; Albert Hofman; Jennifer G Sambrook; Dena G Hernandez; Gang Zheng; Stefania Bandinelli; Andrew Singleton; Josef Coresh; Thomas Lumley; André G Uitterlinden; Janine M Vangils; Lenore J Launer; L Adrienne Cupples; Ben A Oostra; Jaap-Jan Zwaginga; Willem H Ouwehand; Swee-Lay Thein; Christa Meisinger; Panos Deloukas; Matthias Nauck; Tim D Spector; Christian Gieger; Vilmundur Gudnason; Cornelia M van Duijn; Bruce M Psaty; Luigi Ferrucci; Aravinda Chakravarti; Andreas Greinacher; Christopher J O'Donnell; Jacqueline C M Witteman; Susan L Furth; Mary Cushman; Tamara B Harris; Jing-Ping Lin
Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.
Nature genetics 2009;41(11):1191-8.
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: Teri A Manolio; Francis S Collins; Nancy J Cox; David B Goldstein; Lucia A Hindorff; David J Hunter; Mark I McCarthy; Erin M Ramos; Lon R Cardon; Aravinda Chakravarti; Judy H Cho; Alan E Guttmacher; Augustine Kong; Leonid Kruglyak; Elaine Mardis; Charles N Rotimi; Montgomery Slatkin; David Valle; Alice S Whittemore; Michael Boehnke; Andrew G Clark; Evan E Eichler; Greg Gibson; Jonathan L Haines; Trudy F C Mackay; Steven A McCarroll; Peter M Visscher
Finding the missing heritability of complex diseases.
Nature 2009;461(7265):747-53.
2009: Aravinda Chakravarti
Human genetics: Tracing India's invisible threads.
Nature 2009;461(7263):487-8.
2009: Dan E Arking; Aravinda Chakravarti
Understanding cardiovascular disease through the lens of genome-wide association studies.
Trends in genetics : TIG 2009;25(9):387-94.
2009: David J Milan; Albert M Kim; Jeffrey R Winterfield; Ian L Jones; Arne Pfeufer; Serena Sanna; Dan E Arking; Adam H Amsterdam; Khaled M Sabeh; John D Mably; David S Rosenbaum; Randall T Peterson; Aravinda Chakravarti; Stefan Kääb; Dan Mark Roden; Calum A MacRae
Drug-sensitized zebrafish screen identifies multiple genes, including GINS3, as regulators of myocardial repolarization.
Circulation 2009;120(7):553-9.
2009: Emelia Benjamin; Kenneth M Rice; Dan E Arking; Arne Pfeufer; Charlotte van Noord; Albert Vernon Smith; Renate B Schnabel; Joshua C Bis; Eric Boerwinkle; Moritz F Sinner; Abbas Dehghan; Steven A Lubitz; Ralph B D'Agostino; Thomas Lumley; Georg Benedikt Ehret; Jan Heeringa; Thor Aspelund; Christopher Newton-Cheh; Martin G Larson; Kristin D Marciante; Elsayed Z Soliman; Fernando Rivadeneira; Thomas J Wang; Gudny Eiríksdottir; Daniel Levy; Bruce M Psaty; Man Li; Alanna M Chamberlain; Albert Hofman; Ramachandran S Vasan; Tamara B Harris; Jerome I Rotter; WEN KAO; Sunil K Agarwal; Bruno H Ch Stricker; Ke Wang; Lenore J Launer; Nicholas L Smith; Aravinda Chakravarti; André G Uitterlinden; Philip A Wolf; Nona Sotoodehnia; Anna Köttgen; C.M. Duijn; Thomas Meitinger; Martina Mueller; Siegfried Perz; Gerhard Steinbeck; H-Erich Wichmann; Kathryn L Lunetta; Susan R Heckbert; Vilmundur Gudnason; Alvaro Alonso; Stefan Kääb; Patrick T Ellinor; Jacqueline C M Witteman
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.
Nature genetics 2009;41(8):879-81.
2009: bina joe; Yasser Saad; Norman H Lee; Bryan C Frank; Ovokeraye H Achinike; Truong V Luu; Kathirvel Gopalakrishnan; Edward J Toland; Phyllis Farms; Shane Yerga-Woolwine; Ezhilarasi Manickavasagam; John P Rapp; Michael R Garrett; David Coe; Suneel S Apte; Tuomo Rankinen; Louis Pérusse; Georg Benedikt Ehret; Santhi Ganesh; Richard S Cooper; Ashley O'Connor; Treva Rice; Alan B Weder; Aravinda Chakravarti; Dabeeru C Rao; Seema Dhindaw; Claude Bouchard
Positional identification of variants of Adamts16 linked to inherited hypertension.
Human molecular genetics 2009;18(15):2825-38.
2009: Daniel Levy; Georg Benedikt Ehret; Kenneth Rice; Germaine C Verwoert; Lenore J Launer; Abbas Dehghan; Nicole L Glazer; Alanna C Morrison; Andrew D Johnson; Thor Aspelund; Yurii Aulchenko; Thomas Lumley; Anna Köttgen; Ramachandran S Vasan; Fernando Rivadeneira; Gudny Eiriksdottir; Xiuqing Guo; Dan E Arking; Gary F Mitchell; Francesco U S Mattace-Raso; Albert V Smith; Kent Taylor; Robert B Scharpf; Shih-Jen Hwang; Eric J G Sijbrands; Joshua Bis; Tamara B Harris; Santhi Ganesh; Christopher J O'Donnell; Albert Hofman; Jerome I Rotter; Josef Coresh; Emelia J Benjamin; André G Uitterlinden; Gerardo Heiss; Caroline S Fox; Jacqueline C M Witteman; Eric Boerwinkle; Thomas J Wang; Vilmundur Gudnason; Martin G Larson; Aravinda Chakravarti; Bruce M Psaty; Cornelia M van Duijn
Genome-wide association study of blood pressure and hypertension.
Nature genetics 2009;41(6):677-87.
2009: Stacey Marie Arnold; Anna Pelet; Jeanne Amiel; Salud Borrego; Robert Hofstra; Paul Tam; Isabella Ceccherini; Stanislas Lyonnet; Stephanie L Sherman; Aravinda Chakravarti
Interaction between a chromosome 10 RET enhancer and chromosome 21 in the Down syndrome-Hirschsprung disease association.
Human mutation 2009;30(5):771-5.
2009: Nora Franceschini; Kari E North; Donna K Arnett; James S Pankow; Jay H Chung; Lisa Baird; Mark F Leppert; John H Eckfeldt; Eric Boerwinkle; C Charles Gu; Cora E Lewis; Richard H Myers; Stephen T Turner; Alan B Weder; WEN KAO; Thomas H Mosley; Aravinda Chakravarti; Holly Kramer; Jinghui Zhang; Steven C Hunt
The association of cell cycle checkpoint 2 variants and kidney function: findings of the Family Blood Pressure Program and the Atherosclerosis Risk In Communities study.
American journal of hypertension 2009;22(5):552-8.
2009: Arne Pfeufer; Serena Sanna; Dan E Arking; Martina Müller; Vesela Gateva; Christian Fuchsberger; Georg Benedikt Ehret; Marco Orrú; Cristian Pattaro; Anna Köttgen; Siegfried Perz; Gianluca Usala; Maja Barbalic; Man Li; Benno Pütz; ANGELO SCUTERI; Ronald J Prineas; Moritz F Sinner; Christian Gieger; Samer S Najjar; WEN KAO; Thomas W Mühleisen; Mariano Dei; Christine Happle; Stefan Möhlenkamp; Laura Crisponi; Raimund Erbel; Karl-Heinz Jöckel; Silvia Naitza; Gerhard Steinbeck; Fabio Marroni; Andrew A Hicks; Edward Lakatta; Bertram Müller-Myhsok; Peter P Pramstaller; H-Erich Wichmann; David Schlessinger; Eric Boerwinkle; Thomas Meitinger; Manuela Uda; Josef Coresh; Stefan Kääb; Gonçalo R Abecasis; Aravinda Chakravarti
Common variants at ten loci modulate the QT interval duration in the QTSCD Study.
Nature genetics 2009;41(4):407-14.
2009: WEN KAO; Dan E Arking; Wendy S Post; Thomas D Rea; Nona Sotoodehnia; Ronald J Prineas; Bryan Bishe; Betty Q Doan; Eric Boerwinkle; Bruce M Psaty; Gordon F Tomaselli; Josef Coresh; David S Siscovick; Eduardo Marban; PETER SPOONER; Gregory L Burke; Aravinda Chakravarti
Genetic variations in nitric oxide synthase 1 adaptor protein are associated with sudden cardiac death in US white community-based populations.
Circulation 2009;119(7):940-51.
2009: David A Dezentje; Dan E Arking; Madeline Kortenhorst; Kristen West; Aravinda Chakravarti; Scott E Kern
Hybrids of aneuploid human cancer cells permit complementation of simple and complex cancer defects.
Cancer biology & therapy 2009;8(4):347-55.
2009: Aravinda Chakravarti
Being human: kinship: race relations.
Nature 2009;457(7228):380-1.
2009: Ying Wang; Jeffrey R O'Connell; Patrick F McArdle; James B Wade; Sarah E Dorff; Sanjiv J Shah; Xiaolian Shi; Lin Pan; Evadnie Rampersaud; Haiqing Shen; James D Kim; Arohan R Subramanya; Nanette I Steinle; Afshin Parsa; Carole C Ober; Fang Liang; Aravinda Chakravarti; Alan B Weder; Richard S Cooper; Braxton D Mitchell; Alan R Shuldiner; Yen-Pei C Chang
From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene.
Proceedings of the National Academy of Sciences of the United States of America 2009;106(1):226-31.
2009: John Paul SanGiovanni; Dan E Arking; Sudha K Iyengar; Michael Elashoff; Traci E Clemons; George F Reed; Alice K Henning; Theru A Sivakumaran; Xuming Xu; Andrew DeWan; Elvira Agrón; Elena Rochtchina; Carolyn M Sue; Jie Jin Wang; Paul Mitchell; Josephine Hoh; Peter J Francis; Michael L Klein; Emily Y Chew; Aravinda Chakravarti
Mitochondrial DNA variants of respiratory complex I that uniquely characterize haplogroup T2 are associated with increased risk of age-related macular degeneration.
PloS one 2009;4(5):e5508.
2009: Dan E Arking; Amit Khera; Chao Xing; WEN KAO; Wendy S Post; Eric Boerwinkle; Aravinda Chakravarti
Multiple independent genetic factors at NOS1AP modulate the QT interval in a multi-ethnic population.
PloS one 2009;4(1):e4333.
2008: Georg Benedikt Ehret; Alanna C Morrison; Ashley A O'Connor; Megan L Grove; Lisa Baird; Karen Schwander; Alan B Weder; Richard S Cooper; Dabeeru C Rao; Steven C Hunt; Eric Boerwinkle; Aravinda Chakravarti
Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure Program.
European journal of human genetics : EJHG 2008;16(12):1507-11.
2008: Aravinda Chakravarti
Obituary: Victor Almon McKusick (1921-2008).
Nature 2008;455(7209):46.
2008: Wenyi Wang; Benilton Carvalho; Neil R Miller; Jonathan Pevsner; Aravinda Chakravarti; Rafael A Irizarry
Estimating genome-wide copy number using allele-specific mixture models.
Journal of computational biology : a journal of computational molecular cell biology 2008;15(7):857-66.
2008: Nick Hastie; Aravinda Chakravarti
Genetics of disease.
Current opinion in genetics & development 2008;18(3):227-8.
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: Shin Lin; Benilton Carvalho; David J Cutler; Dan E Arking; Aravinda Chakravarti; Rafael A Irizarry
Validation and extension of an empirical Bayes method for SNP calling on Affymetrix microarrays.
Genome biology 2008;9(4):R63.
2008: Dan E Arking; David J Cutler; Camille W. Brune; Tanya M Teslovich; Kristen West; Morna Ikeda; Alexis Rea; Moltu Guy; Shin Lin; Edwin H Cook; Aravinda Chakravarti
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism.
American journal of human genetics 2008;82(1):160-4.
2008: Aik Choon Tan; Jian-Bing Fan; Collins Karikari; Marina Bibikova; Eliza Wickham Garcia; Lixin Zhou; David Barker; david serre; Georg Feldmann; Ralph Hruban; Alison P Klein; Michael Goggins; Fergus J. Couch; Thomas J Hudson; Raimond L Winslow; Anirban Maitra; Aravinda Chakravarti
Allele-specific expression in the germline of patients with familial pancreatic cancer: an unbiased approach to cancer gene discovery.
Cancer biology & therapy 2008;7(1):135-44.
2008: Jeanne Amiel; E Sproat-Emison; Mercè Garcia-Barcelo; Francesca Lantieri; Grzegorz Burzynski; Salud Borrego; Anna Pelet; Stacey Marie Arnold; Xiaoping Miao; Paola Griseri; A S Brooks; Guillermo Antinolo; Loïc de Pontual; M Clement-Ziza; Arnold Munnich; Carl S Kashuk; K West; K K-Y Wong; Stanislas LYONNET; Aravinda Chakravarti; Paul K H Tam; Isabella Ceccherini; Robert M W Hofstra; R Fernandez
Hirschsprung disease, associated syndromes and genetics: a review.
Journal of medical genetics 2008;45(1):1-14.
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: Gen Wen; Jennifer Wessel; Weidong Zhou; Georg Benedikt Ehret; Fangwen Rao; Mats Stridsberg; Sushil K Mahata; Peter M Gent; Madhusudan Das; Richard S Cooper; Aravinda Chakravarti; Huilin Zhou; Nicholas J Schork; Daniel O'Connor; Bruce A Hamilton
An ancestral variant of Secretogranin II confers regulation by PHOX2 transcription factors and association with hypertension.
Human molecular genetics 2007;16(14):1752-64.
2007: Adrian Gherman; Peter E Chen; Tanya M Teslovich; Pawel Stankiewicz; Marjorie Withers; Carl S Kashuk; Aravinda Chakravarti; James R Lupski; David J Cutler; Nicholas Katsanis
Population bottlenecks as a potential major shaping force of human genome architecture.
PLoS genetics 2007;3(7):e119.
2007: ANGELO SCUTERI; serena Sanna; Wei-Min Chen; Manuela Uda; Giuseppe Albai; James Strait; Samer S Najjar; Ramaiah Nagaraja; Marco Orrú; Gianluca Usala; Mariano Dei; Sandra Lai; Andrea Maschio; Fabio Busonero; Antonella Mulas; Georg Benedikt Ehret; Ashley A Fink; Alan B Weder; Richard S Cooper; Pilar Galan; Aravinda Chakravarti; David Schlessinger; Antonio Cao; Edward Lakatta; Goncalo Abecasis
Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits.
PLoS genetics 2007;3(7):e115.
2007: C Charles Gu; Steven C Hunt; Sharon L R Kardia; Stephen T Turner; Aravinda Chakravarti; Nicholas Schork; Richard A Olshen; David Curb; Cashell E Jaquish; Eric Boerwinkle; Dabeeru C Rao
An investigation of genome-wide associations of hypertension with microsatellite markers in the family blood pressure program (FBPP).
Human genetics 2007;121(5):577-90.
2007: Joël Zlotogora; Yasir Hujerat; Saleh Barges; Stavit A Shalev; Aravinda Chakravarti
The fate of 12 recessive mutations in a single village.
Annals of human genetics 2007;71(Pt 2):202-8.
2007: Yen-Pei C Chang; Xin Liu; James Dae-Ok Kim; Morna A Ikeda; Marnie R Layton; Alan B Weder; Richard S Cooper; Sharon L R Kardia; Dabeeru C Rao; Steven C Hunt; Amy Luke; Eric Boerwinkle; Aravinda Chakravarti
Multiple genes for essential-hypertension susceptibility on chromosome 1q.
American journal of human genetics 2007;80(2):253-64.
2007: Wendy S Post; Haiqing Shen; Coleen M Damcott; Dan E Arking; WEN KAO; Paul A Sack; Kathleen A Ryan; Aravinda Chakravarti; Braxton D Mitchell; Alan R Shuldiner
Associations between genetic variants in the NOS1AP (CAPON) gene and cardiac repolarization in the old order Amish.
Human heredity 2007;64(4):214-9.
2006: SCOTT BLACKMAN; Rebecca Deering-Brose; Rita McWilliams; Kathleen Naughton; Barbara Coleman; Teresa Lai; Marilyn Algire; Suzanne Beck; Julie E Hoover-Fong; Ada Hamosh; MARGARET D FALLIN; Kristen West; Dan E Arking; Aravinda Chakravarti; David J Cutler; Garry R Cutting
Relative contribution of genetic and nongenetic modifiers to intestinal obstruction in cystic fibrosis.
Gastroenterology 2006;131(4):1030-9.
2006: Marina Bibikova; Eugene Chudin; Bonnie Wu; Lixin Zhou; Eliza Wickham Garcia; Ying Liu; Soojung Shin; Todd W Plaia; Jonathan M Auerbach; Dan E Arking; Rodolfo Gonzalez; Jeremy Crook; Bruce Davidson; Thomas C Schulz; Allan J Robins; Aparna Khanna; Peter Sartipy; Johan Hyllner; P Vanguri; Smita Savant-Bhonsale; Alan K Smith; Aravinda Chakravarti; Anirban Maitra; Mahendra S Rao; David L Barker; Jeanne F Loring; Jian-Bing Fan
Human embryonic stem cells have a unique epigenetic signature.
Genome research 2006;16(9):1075-83.
2006: Eric S Calhoun; Tomas Hucl; Eike Gallmeier; Kristen M West; Dan E Arking; Anirban Maitra; Christine A Iacobuzio-Donahue; Aravinda Chakravarti; Ralph Hruban; Scott E Kern
Identifying allelic loss and homozygous deletions in pancreatic cancer without matched normals using high-density single-nucleotide polymorphism arrays.
Cancer research 2006;66(16):7920-8.
2006: Dan E Arking; Arne Pfeufer; Wendy S Post; WEN KAO; Christopher Newton-Cheh; Morna Ikeda; Kristen West; Carl S Kashuk; Mahmut Akyol; Siegfried Perz; Shapour Jalilzadeh; Thomas Illig; Christian Gieger; Chao-Yu Guo; Martin G Larson; H-Erich Wichmann; Eduardo Marban; Christopher J O'Donnell; Joel N Hirschhorn; Stefan Kääb; PETER SPOONER; Thomas Meitinger; Aravinda Chakravarti
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization.
Nature genetics 2006;38(6):644-51.
2006: Dan E Arking; Daniele Fallin; Linda P Fried; Tao Li; Brock A Beamer; Qian-Li Xue; Aravinda Chakravarti; Jeremy Walston
Variation in the ciliary neurotrophic factor gene and muscle strength in older Caucasian women.
Journal of the American Geriatrics Society 2006;54(5):823-6.
2006: Yen-Pei C Chang; James Dae-Ok Kim; Karen Schwander; Dabeeru C Rao; Mike B Miller; Alan B Weder; Richard S Cooper; Nicholas J Schork; Michael A Province; Alanna C Morrison; Sharon L R Kardia; Thomas Quertermous; Aravinda Chakravarti
The impact of data quality on the identification of complex disease genes: experience from the Family Blood Pressure Program.
European journal of human genetics : EJHG 2006;14(4):469-77.
2006: Joël Zlotogora; Minerva Carasquillo; Saleh Barges; Stavit A Shalev; Yasir Hujerat; Aravinda Chakravarti
High incidence of deafness from three frequent connexin 26 mutations in an isolated community.
Genetic testing 2006;10(1):40-3.
2006: Jason M Laramie; Jemma B Wilk; Steven C Hunt; R Curtis Ellison; Aravinda Chakravarti; Eric Boerwinkle; Richard H Myers
Evidence for a gene influencing heart rate on chromosome 5p13-14 in a meta-analysis of genome-wide scans from the NHLBI Family Blood Pressure Program.
BMC medical genetics 2006;7():17.
2005: Elizabeth A Grice; Erin S Rochelle; Eric Green; Aravinda Chakravarti; Andy McCallion
Evaluation of the RET regulatory landscape reveals the biological relevance of a HSCR-implicated enhancer.
Human molecular genetics 2005;14(24):3837-45.
2005: J Hunter Young; Yen-Pei C Chang; James Dae-Ok Kim; Jean-Paul Chretien; Michael J Klag; Michael Levine; Christopher B Ruff; Nae-Yuh Wang; Aravinda Chakravarti
Differential susceptibility to hypertension is due to selection during the out-of-Africa expansion.
PLoS genetics 2005;1(6):e82.
2005: Laura J Rasmussen-Torvik; Kari E North; C Charles Gu; Cora E Lewis; Jemma B Wilk; Aravinda Chakravarti; Yen-Pei C Chang; Michael B Miller; Na Li; Richard B Devereux; Donna K Arnett
A population association study of angiotensinogen polymorphisms and haplotypes with left ventricular phenotypes.
Hypertension 2005;46(6):1294-9.
2005: Mary Armanios; Jiunn-Liang Chen; Yen-Pei C Chang; Robert A Brodsky; Anita E Hawkins; Constance A Griffin; James R Eshleman; Alan R Cohen; Aravinda Chakravarti; Ada Hamosh; Carol W Greider
Haploinsufficiency of telomerase reverse transcriptase leads to anticipation in autosomal dominant dyskeratosis congenita.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(44):15960-4.
2005: Anirban Maitra; Dan E Arking; Narayan Shivapurkar; Morna Ikeda; Victor Stastny; Keyaunoosh Kassauei; Guoping Sui; David J Cutler; Ying Liu; Sandii N Brimble; Karin Noaksson; Johan Hyllner; Thomas C Schulz; Xianmin Zeng; William J Freed; Jeremy Crook; Suman Abraham; Alan Colman; Peter Sartipy; Sei-Ichi Matsui; Melissa Carpenter; Adi F Gazdar; Mahendra S Rao; Aravinda Chakravarti
Genomic alterations in cultured human embryonic stem cells.
Nature genetics 2005;37(10):1099-103.
2005: Joël Zlotogora; Yasir Hujerat; Lucia Zalman; Saleh Barges; Dvora Filon; Ariel Koren; Stavit A Shalev; Aravinda Chakravarti
Origin and expansion of four different beta globin mutations in a single Arab village.
American journal of human biology : the official journal of the Human Biology Council 2005;17(5):659-61.
2005: Adele A Mitchell; Aravinda Chakravarti; David J Cutler
On the probability that a novel variant is a disease-causing mutation.
Genome research 2005;15(7):960-6.
2005: Carl S Kashuk; Eric A Stone; Elizabeth A Grice; Matthew E Portnoy; Eric Green; Arend Sidow; Aravinda Chakravarti; Andy McCallion
Phenotype-genotype correlation in Hirschsprung disease is illuminated by comparative analysis of the RET protein sequence.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(25):8949-54.
2005: Jennifer Gladys Mulle; Kodavali V Chowdari; Vishwajit L Nimgaonkar; Aravinda Chakravarti
No evidence for association to the G72/G30 locus in an independent sample of schizophrenia families.
Molecular psychiatry 2005;10(5):431-3.
2005: Jennifer Gladys Mulle; J A McDonough; Kodavali V Chowdari; Vishwajit L Nimgaonkar; Aravinda Chakravarti
Evidence for linkage to chromosome 13q32 in an independent sample of schizophrenia families.
Molecular psychiatry 2005;10(5):429-31.
2005: Eileen Sproat Emison; Andy McCallion; Carl S Kashuk; Richard T Bush; Elizabeth A Grice; Shin Lin; Matthew E Portnoy; David J Cutler; Eric Green; Aravinda Chakravarti
A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk.
Nature 2005;434(7035):857-63.
2005: Jeremy Walston; Dan E Arking; Daniele Fallin; T Li; Brock A Beamer; Qian-Li Xue; Luigi Ferrucci; Linda P Fried; Aravinda Chakravarti
IL-6 gene variation is not associated with increased serum levels of IL-6, muscle, weakness, or frailty in older women.
Experimental gerontology 2005;40(4):344-52.
2005: C Charles Gu; Yen-Pei C Chang; Steven C Hunt; Karen Schwander; Donna K Arnett; Luc Djousse; Gerardo Heiss; Albert Oberman; Jean-Marc Lalouel; Michael A Province; Aravinda Chakravarti; Dabeeru C Rao
Haplotype association analysis of AGT variants with hypertension-related traits: the HyperGEN study.
Human heredity 2005;60(3):164-76.
2004: Shin Lin; Aravinda Chakravarti; David J Cutler
Exhaustive allelic transmission disequilibrium tests as a new approach to genome-wide association studies.
Nature genetics 2004;36(11):1181-8.
2004: Aravinda Chakravarti
Finding needles in haystacks--IRF6 gene variants in isolated cleft lip or cleft palate.
The New England journal of medicine 2004;351(8):822-4.
2004: Shin Lin; Aravinda Chakravarti; David J Cutler
Haplotype and missing data inference in nuclear families.
Genome research 2004;14(8):1624-32.
2004: Anirban Maitra; Yoram Cohen; Susannah E D Gillespie; Elizabeth Mambo; Noriyoshi Fukushima; Mohammad Hoque; Nila Shah; Michael Goggins; Joseph A Califano; David Sidransky; Aravinda Chakravarti
The Human MitoChip: a high-throughput sequencing microarray for mitochondrial mutation detection.
Genome research 2004;14(5):812-9.
2004: Adele A Mitchell; Zwick Michael; Aravinda Chakravarti; David J Cutler
Discrepancies in dbSNP confirmation rates and allele frequency distributions from varying genotyping error rates and patterns.
Bioinformatics (Oxford, England) 2004;20(7):1022-32.
2004: Dan E Arking; Sumeet S Chugh; Aravinda Chakravarti; PETER SPOONER
Genomics in sudden cardiac death.
Circulation research 2004;94(6):712-23.
2004: Hee-Kyung Hong; Aravinda Chakravarti; Joseph S Takahashi
The gene for soluble N-ethylmaleimide sensitive factor attachment protein alpha is mutated in hydrocephaly with hop gait (hyh) mice.
Proceedings of the National Academy of Sciences of the United States of America 2004;101(6):1748-53.
2004: Zhiying Xu; Kimberly Kerstann; Stephanie L Sherman; Aravinda Chakravarti; Eleanor Feingold
A trisomic transmission disequilibrium test.
Genetic epidemiology 2004;26(2):125-31.
2004: Ruth Ann Barkley; Aravinda Chakravarti; Richard S Cooper; R Curtis Ellison; Steven C Hunt; Michael A Province; Stephen T Turner; Alan B Weder; Eric Boerwinkle
Positional identification of hypertension susceptibility genes on chromosome 2.
Hypertension 2004;43(2):477-82.
2003: Ruth R Faden; Liza Dawson; Alison S Bateman-House; Dawn Mueller Agnew; Hilary Bok; Dan W Brock; Aravinda Chakravarti; Xiao-Jiang Gao; Mark Greene; John A Hansen; Patricia A King; Stephen J O'Brien; David H Sachs; Kathryn E Schill; Andrew Siegel; Davor Solter; Sonia M Suter; Catherine M Verfaillie; LeRoy B Walters; John D Gearhart
Public stem cell banks: considerations of justice in stem cell research and therapy.
The Hastings Center report 2003;33(6):13-27.
2003: Liza Dawson; Alison S Bateman-House; Dawn Mueller Agnew; Hilary Bok; Dan W Brock; Aravinda Chakravarti; Mark Greene; Patricia A King; Stephen J O'Brien; David H Sachs; Kathryn E Schill; Andrew Siegel; Davor Solter; Sonia M Suter; Catherine M Verfaillie; LeRoy B Walters; John D Gearhart; Ruth R Faden
Safety issues in cell-based intervention trials.
Fertility and sterility 2003;80(5):1077-85.
2003: Suraj Peri; J Daniel Navarro; Ramars Amanchy; Troels Z Kristiansen; Chandra Kiran Jonnalagadda; Vineeth Surendranath; Vidya Niranjan; Babylakshmi Muthusamy; T K B Gandhi; Mads Gronborg; Nieves Ibarrola; Nandan Deshpande; K Shanker; H N Shivashankar; Rashmi Prasad; M A Ramya; Zhixing Zhao; K N Chandrika; N Padma; H C Harsha; A J Yatish; M P Kavitha; Minal Menezes; Dipanwita Roy Choudhury; Shubha Suresh; Neelanjana Ghosh; R Saravana; Sreenath Chandran; Subhalakshmi Krishna; Mary Joy; Sanjeev K Anand; V Madavan; Ansamma Joseph; GUANG WILLIAM WONG; William P Schiemann; Stefan N Constantinescu; Lily J. Huang; Roya Khosravi-Far; Hanno Steen; Muneesh Tewari; Saghi Ghaffari; Gerard C Blobe; Chi Dang; Joe G. N. Garcia; Jonathan Pevsner; Ole N Jensen; Peter Roepstorff; Krishna S Deshpande; Arul M Chinnaiyan; Ada Hamosh; Aravinda Chakravarti; Akhilesh Pandey
Development of human protein reference database as an initial platform for approaching systems biology in humans.
Genome research 2003;13(10):2363-71.
2003: J W Thomas; J W Touchman; R W Blakesley; G G Bouffard; Stephen Beckstrom-Sternberg; E H Margulies; M Blanchette; A C Siepel; P J Thomas; J C McDowell; B Maskeri; N F Hansen; M S Schwartz; Richard J. Weber; W James Kent; D Karolchik; T C Bruen; R Bevan; D J Cutler; S Schwartz; L Elnitski; J R Idol; A B Prasad; S-Q Lee-Lin; V V B Maduro; T J Summers; M E Portnoy; N L Dietrich; N Akhter; K Ayele; B Benjamin; K Cariaga; C P Brinkley; S Y Brooks; S Granite; X Guan; J Gupta; P Haghighi; S-L Ho; M C Huang; E Karlins; P L Laric; R Legaspi; M J Lim; Q L Maduro; C A Masiello; S D Mastrian; J C McCloskey; R Pearson; S Stantripop; E E Tiongson; J T Tran; Cyruss Tsurgeon; J L Vogt; M A Walker; K D Wetherby; L S Wiggins; A C Young; L-H Zhang; K Osoegawa; B Zhu; B Zhao; C L Shu; P J De Jong; C E Lawrence; A F Smit; Aravinda Chakravarti; D Haussler; P Green; W Miller; Eric Green
Comparative analyses of multi-species sequences from targeted genomic regions.
Nature 2003;424(6950):788-93.
2003: Xiaofeng Zhu; Yen-Pei C Chang; Denise Yan; Alan B Weder; Richard Cooper; Amy Luke; Donghui Kan; Aravinda Chakravarti
Associations between hypertension and genes in the renin-angiotensin system.
Hypertension 2003;41(5):1027-34.
2003: Wendy R Uhlmann; Robin Bennett; Jeffrey R Botkin; David Botstein; Joann Boughman; Aravinda Chakravarti; Ellen Wright Clayton; Jeffrey Kahn; Barbara Koenig; Thomas H Murray; Maynard V Olson; Janet Rowley; Sharon Terry; David Valle
Planning the genome institute's future.
Science (New York, N.Y.) 2003;299(5612):1515; author reply 1515.
2003: Alan B Weder; Maria Carolina Delgado; Xiaofeng Zhu; Lillian Gleiberman; Donghui Kan; Aravinda Chakravarti
Erythrocyte sodium-lithium countertransport and blood pressure: a genome-wide linkage study.
Hypertension 2003;41(3 Pt 2):842-6.
2003: Adele A Mitchell; David J Cutler; Aravinda Chakravarti
Undetected genotyping errors cause apparent overtransmission of common alleles in the transmission/disequilibrium test.
American journal of human genetics 2003;72(3):598-610.
2003: Andy McCallion; Erine Stames; Ronald A Conlon; Aravinda Chakravarti
Phenotype variation in two-locus mouse models of Hirschsprung disease: tissue-specific interaction between Ret and Ednrb.
Proceedings of the National Academy of Sciences of the United States of America 2003;100(4):1826-31.
2003: Srijan Sen; Randolph M Nesse; Scott F Stoltenberg; Sheng Li; Lillian Gleiberman; Aravinda Chakravarti; Alan B Weder; Margit Burmeister
A BDNF coding variant is associated with the NEO personality inventory domain neuroticism, a risk factor for depression.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2003;28(2):397-401.
2003: Xiaofeng Zhu; Denise Yan; Richard S Cooper; Amy Luke; Morna A Ikeda; Yen-Pei C Chang; Alan B Weder; Aravinda Chakravarti
Linkage disequilibrium and haplotype diversity in the genes of the renin-angiotensin system: findings from the family blood pressure program.
Genome research 2003;13(2):173-81.
2003: Bonnie A Thiel; Aravinda Chakravarti; Richard S Cooper; Amy Luke; Sue Lewis; Audrey Lynn; Hemant K Tiwari; Nicholas J Schork; Alan B Weder
A genome-wide linkage analysis investigating the determinants of blood pressure in whites and African Americans.
American journal of hypertension 2003;16(2):151-3.
2003: Aravinda Chakravarti; Peter Little
Nature, nurture and human disease.
Nature 2003;421(6921):412-4.
2003: Gabor T Marth; Greg Schuler; Raymond Yeh; Ruth Davenport; Richa Agarwala; Deanna Church; Sarah J Wheelan; Jonathan Baker; Ming Ward; Michael Kholodov; Lon Phan; Eva Czabarka; Janos Murvai; David Cutler; Stephen Wooding; Alan Rogers; Aravinda Chakravarti; Henry Harpending; Pui-Yan Kwok; Stephen T Sherry
Sequence variations in the public human genome data reflect a bottlenecked population history.
Proceedings of the National Academy of Sciences of the United States of America 2003;100(1):376-81.
2003: Andy McCallion; Eileen Sproat Emison; Carl S Kashuk; R T Bush; M Kenton; Minerva M Carrasquillo; K W Jones; Giulia C Kennedy; Matthew E Portnoy; Eric Green; Aravinda Chakravarti
Genomic variation in multigenic traits: Hirschsprung disease.
Cold Spring Harbor symposia on quantitative biology 2003;68():373-81.
2002: Shin Lin; David J Cutler; Zwick Michael; Aravinda Chakravarti
Haplotype inference in random population samples.
American journal of human genetics 2002;71(5):1129-37.
2002: Minerva M Carrasquillo; Andy McCallion; Erik G Puffenberger; Carl S Kashuk; Nassim Nouri; Aravinda Chakravarti
Genome-wide association study and mouse model identify interaction between RET and EDNRB pathways in Hirschsprung disease.
Nature genetics 2002;32(2):237-44.
2002: Kathleen Ries Merikangas; Aravinda Chakravarti; Steven O Moldin; Houmam Araj; John C Blangero; Margit Burmeister; John C Crabbe; J. Raymond DePaulo; Edward Foulks; Nelson B Freimer; Doreen S Koretz; William Lichtenstein; Emmanuel Mignot; Allan L Reiss; Neil J Risch; Joseph S Takahashi
Future of genetics of mood disorders research.
Biological psychiatry 2002;52(6):457-77.
2002: Susan L Christian; Jennifer McDonough; Chun-yu Liu Cy; Sanober Shaikh; Vivian Vlamakis; Judith A Badner; Aravinda Chakravarti; Elliot S Gershon
An evaluation of the assembly of an approximately 15-Mb region on human chromosome 13q32-q33 linked to bipolar disorder and schizophrenia.
Genomics 2002;79(5):635-56.
2002: Stacey B Gabriel; Rémi Salomon; Anna Pelet; Misha Angrist; Jeanne Amiel; Myriam Fornage; Tania Attié-Bitach; Jane M Olson; Robert Hofstra; Charles Buys; Julie Steffann; Arnold Munnich; Stanislas LYONNET; Aravinda Chakravarti
Segregation at three loci explains familial and population risk in Hirschsprung disease.
Nature genetics 2002;31(1):89-93.
2002: Aravinda Chakravarti
A compelling genetic hypothesis for a complex disease: PRODH2/DGCR6 variation leads to schizophrenia susceptibility.
Proceedings of the National Academy of Sciences of the United States of America 2002;99(8):4755-6.
2002: Donald G Marshall; W A Meier-Ruge; Aravinda Chakravarti; Jacob C Langer
Chronic constipation due to Hirschsprung's disease and desmosis coli in a family.
Pediatric surgery international 2002;18(2-3):110-4.
2002: Blagoy Blagoev; Mogens M Nielsen; Misha Angrist; Aravinda Chakravarti; Akhilesh Pandey
Cloning of rat thymic stromal lymphopoietin receptor (TSLPR) and characterization of genomic structure of murine Tslpr gene.
Gene 2002;284(1-2):161-8.
2002: Swapan K Nath; Aravinda Chakravarti; Chien-Hsiun Chen; Richard Cooper; Alan B Weder; Nicholas J Schork
Segregation analysis of blood pressure and body mass index in a rural US community.
Human biology 2002;74(1):11-23.
2002: Debra E Weese-Mayer; Stacey Bolk; Jean M Silvestri; Aravinda Chakravarti
Idiopathic congenital central hypoventilation syndrome: evaluation of brain-derived neurotrophic factor genomic DNA sequence variation.
American journal of medical genetics 2002;107(4):306-10.
2002: Carl S Kashuk; Sanghamitra SenGupta; Evan E Eichler; Aravinda Chakravarti
ViewGene: a graphical tool for polymorphism visualization and characterization.
Genome research 2002;12(2):333-8.
2002: Xiaofeng Zhu; Richard S Cooper; Amy Luke; Guanjie Chen; Xiaodong Wu; Donghui Kan; Aravinda Chakravarti; Alan B Weder
A genome-wide scan for obesity in African-Americans.
Diabetes 2002;51(2):541-4.
2001: David J Cutler; Zwick Michael; Minerva M Carrasquillo; Chris T Yohn; K P Tobin; Carl S Kashuk; Debra J H Mathews; Nila A Shah; Evan E Eichler; J A Warrington; Aravinda Chakravarti
High-throughput variation detection and genotyping using microarrays.
Genome research 2001;11(11):1913-25.
2001: Debra J H Mathews; Carl S Kashuk; G Brightwell; Evan E Eichler; Aravinda Chakravarti
Sequence variation within the fragile X locus.
Genome research 2001;11(8):1382-91.
2001: Andy McCallion; Aravinda Chakravarti
EDNRB/EDN3 and Hirschsprung disease type II.
Pigment cell research / sponsored by the European Society for Pigment Cell Research and the International Pigment Cell Society 2001;14(3):161-9.
2001: Aravinda Chakravarti
Statistical analysis of radiation hybrid data.
Current protocols in human genetics / editorial board, Jonathan L. Haines ... [et al.] 2001;Chapter 3():Unit 3.4.
2001: Eric Green; Aravinda Chakravarti
The human genome sequence expedition: views from the "base camp".
Genome research 2001;11(5):645-51.
2001: Georgia L Wiesner; Petra Platzer; Sarah Buxbaum; Susan Lewis; M MacMillen; Joseph Olechnowicz; Joseph Willis; Aravinda Chakravarti; Robert C Elston; Sanford D Markowitz
Testing for colon neoplasia susceptibility variants at the human COX2 locus.
Journal of the National Cancer Institute 2001;93(8):635-9.
2001: H K Hong; Janice K Noveroske; Denis J Headon; T Liu; M S Sy; Monica J Justice; Aravinda Chakravarti
The winged helix/forkhead transcription factor Foxq1 regulates differentiation of hair in satin mice.
Genesis (New York, N.Y. : 2000) 2001;29(4):163-71.
2001: Aravinda Chakravarti
To a future of genetic medicine.
Nature 2001;409(6822):822-3.
2001: Subir K Chatterjee; S Banerjee; D Basak; Ashoke K Basu; Aravinda Chakravarti; Uttara Chatterjee; J Haque
Posterior urethral valves: the scenario in a developing center.
Pediatric surgery international 2001;17(1):2-7.
2000: Nicholas J Schork; S K Nath; Danielle Fallin; Aravinda Chakravarti
Linkage disequilibrium analysis of biallelic DNA markers, human quantitative trait loci, and threshold-defined case and control subjects.
American journal of human genetics 2000;67(5):1208-18.
2000: Audrey Lynn; Carl S Kashuk; M B Petersen; Jeffrey A Bailey; D R Cox; Stylianos Antonarakis; Aravinda Chakravarti
Patterns of meiotic recombination on the long arm of human chromosome 21.
Genome research 2000;10(9):1319-32.
2000: Michael A Province; Eric Boerwinkle; Aravinda Chakravarti; R Cooper; M Fornage; M Leppert; Neil Risch; Koustubh Ranade
Lack of association of the angiotensinogen-6 polymorphism with blood pressure levels in the comprehensive NHLBI Family Blood Pressure Program. National Heart, Lung and Blood Institute.
Journal of hypertension 2000;18(7):867-76.
2000: Jeffrey A Bailey; Laura Carrel; Aravinda Chakravarti; Evan E Eichler
Molecular evidence for a relationship between LINE-1 elements and X chromosome inactivation: the Lyon repeat hypothesis.
Proceedings of the National Academy of Sciences of the United States of America 2000;97(12):6634-9.
2000: Nicholas J Schork; Aravinda Chakravarti; Bonnie A Thiel; Myriam Fornage; H J Jacob; R Cai; Charles N Rotimi; Richard S Cooper; Alan B Weder
Lack of association between a biallelic polymorphism in the adducin gene and blood pressure in whites and African Americans.
American journal of hypertension 2000;13(6 Pt 1):693-8.
2000: Jian-Bing Fan; X Chen; Marc K Halushka; Anthony J Berno; X Huang; Thomas B Ryder; Rob Lipshutz; DJ Lockhart; Aravinda Chakravarti
Parallel genotyping of human SNPs using generic high-density oligonucleotide tag arrays.
Genome research 2000;10(6):853-60.
2000: MV Zaragoza; Urvashi Surti; Raymond W Redline; Elise A Millie; Aravinda Chakravarti; Terry J Hassold
Parental origin and phenotype of triploidy in spontaneous abortions: predominance of diandry and association with the partial hydatidiform mole.
American journal of human genetics 2000;66(6):1807-20.
2000: S Bolk; Anna Pelet; R M Hofstra; Misha Angrist; Rémi Salomon; D Croaker; C H Buys; Stanislas LYONNET; Aravinda Chakravarti
A human model for multigenic inheritance: phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus.
Proceedings of the National Academy of Sciences of the United States of America 2000;97(1):268-73.
2000: Zwick Michael; David J Cutler; Aravinda Chakravarti
Patterns of genetic variation in Mendelian and complex traits.
Annual review of genomics and human genetics 2000;1():387-407.
1999: S Bolk; Erik G Puffenberger; J Hudson; D Holmes Morton; Aravinda Chakravarti
Elevated frequency and allelic heterogeneity of congenital nephrotic syndrome, Finnish type, in the old order Mennonites.
American journal of human genetics 1999;65(6):1785-90.
1999: Marc K Halushka; Debra J H Mathews; J A Bailey; Aravinda Chakravarti
GIST: A web tool for collecting gene information.
Physiological genomics 1999;1(2):75-81.
1999: Erik G Jönsson; Vishwajit L Nimgaonkar; X R Zhang; S H Shaw; Edgar Burgert; Marc-Antoine Crocq; Aravinda Chakravarti; Göran C Sedvall
Trend for an association between schizophrenia and D3S1310, a marker in proximity to the dopamine D3 receptor gene.
American journal of medical genetics 1999;88(4):352-7.
1999: Marc K Halushka; Jian-Bing Fan; K Bentley; Linda Hsie; N Shen; Alan B Weder; R Cooper; Rob Lipshutz; Aravinda Chakravarti
Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis.
Nature genetics 1999;22(3):239-47.
1999: H K Hong; Jonathan H Lass; Aravinda Chakravarti
Pleiotropic skeletal and ocular phenotypes of the mouse mutation congenital hydrocephalus (ch/Mf1) arise from a winged helix/forkhead transcriptionfactor gene.
Human molecular genetics 1999;8(4):625-37.
1999: E Michelle Southard-Smith; M Angrist; J S Ellison; R Agarwala; Andreas D Baxevanis; Aravinda Chakravarti; William J Pavan
The Sox10(Dom) mouse: modeling the genetic variation of Waardenburg-Shah (WS4) syndrome.
Genome research 1999;9(3):215-25.
1999: Zoha Kibar; Ronald G Lafrenière; Aravinda Chakravarti; J C Wang; M Chevrette; Vazken M Der Kaloustian; Guy Rouleau
A radiation hybrid map of 48 loci including the clouston hidrotic ectodermal dysplasia locus in the pericentromeric region of chromosome 13q.
Genomics 1999;56(1):127-30.
1999: Aravinda Chakravarti
1998 ASHG Award for Excellence in Education. Professor Ching Chun Li, courageous scholar and educator.
American journal of human genetics 1999;64(1):14-5.
1999: Aravinda Chakravarti
Population genetics--making sense out of sequence.
Nature genetics 1999;21(1 Suppl):56-60.
1998: Misha Angrist; S Bolk; K Bentley; Sudha Nallasamy; Marc K Halushka; Aravinda Chakravarti
Genomic structure of the gene for the SH2 and pleckstrin homology domain-containing protein GRB10 and evaluation of its role in Hirschsprung disease.
Oncogene 1998;17(23):3065-70.
1998: Francis S Collins; Lisa D Brooks; Aravinda Chakravarti
A DNA polymorphism discovery resource for research on human genetic variation.
Genome research 1998;8(12):1229-31.
1998: Francis S Collins; A Patrinos; E Jordan; Aravinda Chakravarti; R Gesteland; L Walters
New goals for the U.S. Human Genome Project: 1998-2003.
Science (New York, N.Y.) 1998;282(5389):682-9.
1998: Jean-Louis Blouin; BA Dombroski; Swapan K Nath; Virginia K Lasseter; Paula S Wolyniec; Gerald Nestadt; Mary H Thornquist; G Ullrich; J McGrath; L Kasch; M Lamacz; M G Thomas; Corinne Gehrig; Uppala Radhakrishna; S E Snyder; K G Balk; Karin Neufeld; Karen L Swartz; N DeMarchi; G N Papadimitriou; Dimitris G Dikeos; C N Stefanis; Aravinda Chakravarti; Barton Childs; DE Housman; Haig Kazazian ; Stylianos E Antonarakis; Ann E Pulver
Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21.
Nature genetics 1998;20(1):70-3.
1998: Marie-Claude Potier; A Dutriaux; R Orti; Jürgen Groet; Nathalie Gibelin; GEORGIA KARADIMA; G Lutfalla; A Lynn; Christine Van Broeckhoven; Aravinda Chakravarti; M Petersen; Dean Nizetic; Jean-Maurice Delabar; Jean Rossier
Two sequence-ready contigs spanning the two copies of a 200-kb duplication on human 21q: partial sequence and polymorphisms.
Genomics 1998;51(3):417-26.
1998: Aravinda Chakravarti
It's raining SNPs, hallelujah?
Nature genetics 1998;19(3):216-7.
1998: D M Brown; T C Matise; G Koike; Jason Simon; E S Winer; S Zangen; M G McLaughlin; Masahide Shiozawa; O S Atkinson; J R Hudson; Aravinda Chakravarti; Eric S Lander; Howard J Jacob
An integrated genetic linkage map of the laboratory rat.
Mammalian genome : official journal of the International Mammalian Genome Society 1998;9(7):521-30.
1998: Misha Angrist; Shuqian Jing; S Bolk; K Bentley; Sudha Nallasamy; Marc K Halushka; GM Fox; Aravinda Chakravarti
Human GFRA1: cloning, mapping, genomic structure, and evaluation as a candidate gene for Hirschsprung disease susceptibility.
Genomics 1998;48(3):354-62.
1998: S H Shaw; Minerva M Carrasquillo; Carl S Kashuk; Erik G Puffenberger; Aravinda Chakravarti
Allele frequency distributions in pooled DNA samples: applications to mapping complex disease genes.
Genome research 1998;8(2):111-23.
1998: BP Chadwick; LA Helbling; M Angrist; Aravinda Chakravarti; James Gusella; Susan A Slaugenhaupt
Assignment of persephin (PSPN), a human neurotrophic factor, to chromosome 19p13.3 by radiation hybrid mapping and somatic cell hybrid PCR.
Cytogenetics and cell genetics 1998;83(3-4):236-7.
1997: Minerva M Carrasquillo; Joël Zlotogora; Saleh Barges; Aravinda Chakravarti
Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations.
Human molecular genetics 1997;6(12):2163-72.
1997: M B Petersen; C Tomasetto; A Lynn; Aravinda Chakravarti
A PvuII polymorphism detected by a cDNA clone of the gene encoding the human spasmolytic protein protein (SML1 gene), one of three members of the trefoil peptide gene family clustered on chromosome 21q22.3.
Clinical genetics 1997;52(4):247-8.
1997: H Chen; Colette Rossier; Y Nakamura; A Lynn; Aravinda Chakravarti; Stylianos E Antonarakis
Cloning of a novel homeobox-containing gene, PKNOX1, and mapping to human chromosome 21q22.3.
Genomics 1997;41(2):193-200.
1996: Vishwajit L Nimgaonkar; A R Sanders; Rohan Ganguli; X R Zhang; Jaspreet S Brar; W Allen Hogge; W E Fann; Pragna I Patel; Aravinda Chakravarti
Association study of schizophrenia and the dopamine D3 receptor gene locus in two independent samples.
American journal of medical genetics 1996;67(6):505-14.
1996: Misha Angrist; S Bolk; Marc K Halushka; P A Lapchak; Aravinda Chakravarti
Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient.
Nature genetics 1996;14(3):341-4.
1996: T Cohen; M Zeitune; B C McGillivray; J G Hall; A H Lynn; C E Aston; Aravinda Chakravarti
Segregation analysis of microcephaly.
American journal of medical genetics 1996;65(3):226-34.
1996: M Boguski; Aravinda Chakravarti; R Gibbs; Eric Green; Richard Myers
The end of the beginning: the race to begin human genome sequencing.
Genome research 1996;6(9):771-2.
1996: S Bolk; Misha Angrist; J Xie; M Yanagisawa; Jean M Silvestri; Debra E Weese-Mayer; Aravinda Chakravarti
Endothelin-3 frameshift mutation in congenital central hypoventilation syndrome.
Nature genetics 1996;13(4):395-6.
1996: H Chen; Colette Rossier; Maria D Lalioti; A Lynn; Aravinda Chakravarti; G Perrin; Stylianos Antonarakis
Cloning of the cDNA for a human homologue of the Drosophila white gene and mapping to chromosome 21q22.3.
American journal of human genetics 1996;59(1):66-75.
1996: C K Kwoh; C Venglish; A H Lynn; D M Whitley; E Young; Aravinda Chakravarti
Age, sex, and the familial risk of rheumatoid arthritis.
American journal of epidemiology 1996;144(1):15-24.
1996: S Bolk; Misha Angrist; Stuart Schwartz; Jean M Silvestri; Debra E Weese-Mayer; Aravinda Chakravarti
Congenital central hypoventilation syndrome: mutation analysis of the receptor tyrosine kinase RET.
American journal of medical genetics 1996;63(4):603-9.
1996: Robert M W Hofstra; Jan Osinga; G Tan-Sindhunata; Ying Wu; E J Kamsteeg; Rein P Stulp; Conny van Ravenswaaij-Arts; D Majoor-Krakauer; Misha Angrist; Aravinda Chakravarti; Carel Meijers; Charles H C M Buys
A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome).
Nature genetics 1996;12(4):445-7.
1996: Evan E Eichler; J N Macpherson; A Murray; P A Jacobs; Aravinda Chakravarti; David L Nelson
Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome.
Human molecular genetics 1996;5(3):319-30.
1996: Aravinda Chakravarti
Endothelin receptor-mediated signaling in hirschsprung disease.
Human molecular genetics 1996;5(3):303-7.
1995: Misha Angrist; D E Wells; Aravinda Chakravarti; Akhilesh Pandey
Chromosomal localization of the mouse Src-like adapter protein (Slap) gene and its putative human homolog SLA.
Genomics 1995;30(3):623-5.
1995: Aravinda Chakravarti
The CD4/CD8 ratio: message in a bottle?
Nature medicine 1995;1(12):1240-1.
1995: Vishwajit L Nimgaonkar; Z W Yang; X R Zhang; Jaspreet S Brar; Aravinda Chakravarti; Rohan Ganguli
Association study of schizophrenia and the IL-2 receptor beta chain gene.
American journal of medical genetics 1995;60(5):448-51.
1995: J L Blouin; D H Christie; A Gos; A Lynn; Michael Morris; David Ledbetter; Aravinda Chakravarti; Stylianos Antonarakis
A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination.
American journal of human genetics 1995;57(2):388-94.
1995: C Conover Talbot; Dimitrios Avramopoulos; S Gerken; Aravinda Chakravarti; J A Armour; Nori Matsunami; Raymond White; Stylianos Antonarakis
The tetranucleotide repeat polymorphism D21S1245 demonstrates hypermutability in germline and somatic cells.
Human molecular genetics 1995;4(7):1193-9.
1995: Susan L Christian; Wendy P Robinson; B Huang; A Mutirangura; M R Line; M Nakao; U Surti; Aravinda Chakravarti; David Ledbetter
Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients.
American journal of human genetics 1995;57(1):40-8.
1995: A H Lynn; C K Kwoh; C M Venglish; Christopher E Aston; Aravinda Chakravarti
Genetic epidemiology of rheumatoid arthritis.
American journal of human genetics 1995;57(1):150-9.
1995: Misha Angrist; S Bolk; Bonnie A Thiel; Erik G Puffenberger; Robert M W Hofstra; Charles H C M Buys; D T Cass; Aravinda Chakravarti
Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease.
Human molecular genetics 1995;4(5):821-30.
1995: J A Scott; Sharon L Wenger; M W Steele; Aravinda Chakravarti
Down syndrome consequent to a cryptic maternal 12p;21q chromosome translocation.
American journal of medical genetics 1995;56(1):67-71.
1995: S S Washington; D Warburton; Aravinda Chakravarti
Report and abstracts of the Second International Workshop on Human Chromosome 13 Mapping 1994.
Cytogenetics and cell genetics 1995;70(1-2):1-22.
1994: Aravinda Chakravarti
The behavior of meiosis in sperm.
American journal of human genetics 1994;55(3):421-2.
1994: T C Matise; Aravinda Chakravarti; Pragna I Patel; James R Lupski; Eva Nelis; Vincent Timmerman; Christine Van Broeckhoven; Daniel E Weeks
Detection of tandem duplications and implications for linkage analysis.
American journal of human genetics 1994;54(6):1110-21.
1994: L Hoffner; R Deka; Aravinda Chakravarti; Urvashi Surti
Cytogenetics and origins of pediatric germ cell tumors.
Cancer genetics and cytogenetics 1994;74(1):54-8.
1994: T C Matise; M Perlin; Aravinda Chakravarti
Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage map.
Nature genetics 1994;6(4):384-90.
1994: C C Li; Aravinda Chakravarti
DNA profile similarity in a subdivided population.
Human heredity 1994;44(2):100-9.
1994: S Zappata; Michael B Petersen; U König; J Blaschak; Aravinda Chakravarti; F Tassone; A Serra; Stylianos Antonarakis; Christina Brahe
Highly polymorphic repeat marker within the beta-amyloid precursor protein gene.
Human genetics 1994;93(1):85-6.
1994: S Samec; Stuart G Clarkson; J Blaschak; Aravinda Chakravarti; M A Morris; D Scherly; Stylianos Antonarakis
Dinucleotide repeat polymorphism within ERCC5 gene.
Human molecular genetics 1994;3(1):214.
1993: Vishwajit L Nimgaonkar; X R Zhang; J G Caldwell; Rohan Ganguli; Aravinda Chakravarti
Association study of schizophrenia with dopamine D3 receptor gene polymorphisms: probable effects of family history of schizophrenia?
American journal of medical genetics 1993;48(4):214-7.
1993: Jean-Maurice Delabar; Nicole Créau; Pierre-Marie Sinet; O Ritter; Stylianos Antonarakis; Margit Burmeister; Aravinda Chakravarti; Dean Nizetic; M Ohki; D Patterson
Report of the Fourth International Workshop on Human Chromosome 21.
Genomics 1993;18(3):735-45.
1993: S S Washington; Anne M Bowcock; S Gerken; Nori Matsunami; D Lesh; S L Osborne-Lawrence; John Kenneth Cowell; David Ledbetter; Raymond White; Aravinda Chakravarti
A somatic cell hybrid map of human chromosome 13.
Genomics 1993;18(3):486-95.
1993: M Perlin; Aravinda Chakravarti
Efficient construction of high-resolution physical maps from yeast artificial chromosomes using radiation hybrids: inner product mapping.
Genomics 1993;18(2):283-9.
1993: Vishwajit L Nimgaonkar; J A Scott; Jaspreet S Brar; Rohan Ganguli; Aravinda Chakravarti
Co-occurrence of schizophrenia and Treacher Collins syndrome.
American journal of medical genetics 1993;48(3):156-8.
1993: Sara T Winokur; Brian C Schutte; B Weiffenbach; S S Washington; D McElligott; Aravinda Chakravarti; J H Wasmuth; M R Altherr
A radiation hybrid map of 15 loci on the distal long arm of chromosome 4, the region containing the gene responsible for facioscapulohumeral muscular dystrophy (FSHD).
American journal of human genetics 1993;53(4):874-80.
1993: H K Hong; R Giorda; Massimo Trucco; Aravinda Chakravarti
Dinucleotide repeat polymorphism at the DXS1146 locus.
Human molecular genetics 1993;2(7):1078.
1993: Melvin G McInnis; Aravinda Chakravarti; J Blaschak; Michael B Petersen; V Sharma; Dimitrios Avramopoulos; Jean-Louis Blouin; U König; Christina Brahe; T C Matise
A linkage map of human chromosome 21:43 PCR markers at average intervals of 2.5 cM.
Genomics 1993;16(3):562-71.
1993: H K Hong; R Giorda; L M Yu; Massimo Trucco; Aravinda Chakravarti
Microsatellite repeat polymorphism at the D13S197 locus.
Human molecular genetics 1993;2(3):337.
1993: AC Warren; Melvin G McInnis; M Kalaitsidaki; T K Cox; J Blaschak; Aravinda Chakravarti; S E Antonarakis
D21S210: a highly polymorphic (GT)n marker closely linked to the beta-amyloid protein precursor (APP) gene.
Human genetics 1993;91(1):87-8.
1993: Apiwat Mutirangura; F Greenberg; M G Butler; S Malcolm; R D Nicholls; Aravinda Chakravarti; David Ledbetter
Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy.
Human molecular genetics 1993;2(2):143-51.
1993: Anne M Bowcock; S Osborne-Lawrence; Robert Barnes; Aravinda Chakravarti; S Washington; C Dunn
Microsatellite polymorphism linkage map of human chromosome 13q.
Genomics 1993;15(2):376-86.
1993: C C Li; D E Weeks; Aravinda Chakravarti
Similarity of DNA fingerprints due to chance and relatedness.
Human heredity 1993;43(1):45-52.
1993: H K Hong; R Giorda; Massimo Trucco; Aravinda Chakravarti
Dinucleotide repeat polymorphisms at the D13S192 and D13S193 loci.
Human molecular genetics 1993;2(1):86.
1993: Dimitrios Avramopoulos; Aravinda Chakravarti; S E Antonarakis
DNA polymorphisms in the 3' untranslated region of genes on human chromosome 21.
Genomics 1993;15(1):98-102.
1993: Dimitrios Avramopoulos; T Cox; J P Kraus; Aravinda Chakravarti; Stylianos Antonarakis
Linkage mapping of the cystathionine beta-synthase (CBS) gene on human chromosome 21 using a DNA polymorphism in the 3' untranslated region.
Human genetics 1993;90(5):566-8.
1993: T C Matise; M Perlin; Aravinda Chakravarti
MultiMap: an expert system for automated genetic linkage mapping.
Proceedings / ... International Conference on Intelligent Systems for Molecular Biology ; ISMB. International Conference on Intelligent Systems for Molecular Biology 1993;1():260-5.
1992: M Kalaitsidaki; T Cox; Aravinda Chakravarti; S E Antonarakis
Cloning and linkage mapping of three polymorphic tetranucleotide (TAAA)n repeats on human chromosome 21.
Genomics 1992;14(4):1071-5.
1992: AC Warren; Melvin G McInnis; J Blaschak; M Kaliatsidaki; Michael B Petersen; Aravinda Chakravarti; S E Antonarakis
Dinucleotide repeat (GT)n markers on chromosome 21.
Genomics 1992;14(3):818-9.
1992: Dimitrios Avramopoulos; T Cox; J E Blaschak; Aravinda Chakravarti; S E Antonarakis
Linkage mapping of the AML1 gene on human chromosome 21 using a DNA polymorphism in the 3' untranslated region.
Genomics 1992;14(2):506-7.
1992: Vishwajit L Nimgaonkar; Rohan Ganguli; S S Washington; Aravinda Chakravarti
Schizophrenia and porphobilinogen deaminase gene polymorphisms: an association study.
Schizophrenia research 1992;8(1):51-8.
1992: M B Peterson; M Frantzen; S E Antonarakis; AC Warren; Christine Van Broeckhoven; Aravinda Chakravarti; T K Cox; C Lund; B Olsen; H Poulsen
Comparative study of microsatellite and cytogenetic markers for detecting the origin of the nondisjoined chromosome 21 in Down syndrome.
American journal of human genetics 1992;51(3):516-25.
1992: L Hoffner; S Shen-Schwarz; R Deka; Aravinda Chakravarti; Urvashi Surti
Genetics and biology of human ovarian teratomas. III. Cytogenetics and origins of malignant ovarian germ cell tumors.
Cancer genetics and cytogenetics 1992;62(1):58-65.
1992: AC Warren; Michael B Petersen; Wim Van Hul; Melvin G McInnis; Christine Van Broeckhoven; T K Cox; Aravinda Chakravarti; S E Antonarakis
D21S215 is a (GT)n polymorphic marker close to centromeric alphoid sequences on chromosome 21.
Genomics 1992;13(4):1365-7.
1992: Aravinda Chakravarti
Fragile X founder effect?
Nature genetics 1992;1(4):237-8.
1992: Dimitrios Avramopoulos; T Cox; G L Forrest; Aravinda Chakravarti; S E Antonarakis
Linkage mapping of the carbonyl reductase (CBR) gene on human chromosome 21 using a DNA polymorphism in the 3' untranslated region.
Genomics 1992;13(2):447-8.
1992: H Spielvogel; H C Hennies; U Claussen; S S Washington; Aravinda Chakravarti; A Reis
Band-specific localization of the microsatellite at D13S71 by microdissection and enzymatic amplification.
American journal of human genetics 1992;50(5):1031-7.
1992: Aravinda Chakravarti; J E Reefer
A theory for radiation hybrid (Goss-Harris) mapping: application to proximal 21q markers.
Cytogenetics and cell genetics 1992;59(2-3):99-101.
1992: C E Aston; Aravinda Chakravarti
The gene order problem when using somatic cell hybrids.
Cytogenetics and cell genetics 1992;59(2-3):90-2.
1992: AC Warren; S E Antonarakis; Aravinda Chakravarti
Chromosome 21 genetic linkage data set based on CEPH pedigrees.
Cytogenetics and cell genetics 1992;59(2-3):86-7.
1991: Melvin G McInnis; Georges Lutfalla; Susan A Slaugenhaupt; Michael B Petersen; G Uze; Aravinda Chakravarti; S E Antonarakis
Linkage mapping of highly informative DNA polymorphisms within the human interferon-alpha receptor gene on chromosome 21.
Genomics 1991;11(3):573-6.
1991: Aravinda Chakravarti
Information content of the Centre d'Etude du Polymorphisme Humain (CEPH) family structures for linkage studies.
Human genetics 1991;87(6):721-4.
1991: Aravinda Chakravarti
A graphical representation of genetic and physical maps: the Marey map.
Genomics 1991;11(1):219-22.
1991: Michael B Petersen; J L Weber; Susan A Slaugenhaupt; A E Kwitek; Melvin G McInnis; Aravinda Chakravarti; S E Antonarakis
Linkage mapping of D21S171 to the distal long arm of human chromosome 21 using a polymorphic (AC)n dinucleotide repeat.
Human genetics 1991;87(4):401-4.
1991: James R Lupski; R M de Oca-Luna; S Slaugenhaupt; L Pentao; V Guzzetta; Barbara J Trask; O Saucedo-Cardenas; David Barker; J M Killian; C A Garcia; Aravinda Chakravarti; Pragna I Patel
DNA duplication associated with Charcot-Marie-Tooth disease type 1A.
Cell 1991;66(2):219-32.
1991: Aravinda Chakravarti; L K Lasher; J E Reefer
A maximum likelihood method for estimating genome length using genetic linkage data.
Genetics 1991;128(1):175-82.
1991: Bronya J B Keats; Stephanie L Sherman; N E Morton; E B Robson; K H Buetow; P E Cartwright; Aravinda Chakravarti; U Francke; P P Green; J Ott
Guidelines for human linkage maps: an international system for human linkage maps (ISLM, 1990).
Genomics 1991;9(3):557-60.
1991: Michael B Petersen; Susan A Slaugenhaupt; J G Lewis; AC Warren; Aravinda Chakravarti; S E Antonarakis
A genetic linkage map of 27 markers on human chromosome 21.
Genomics 1991;9(3):407-19.
1991: Donald C Morizot; S A Slaugenhaupt; K D Kallman; Aravinda Chakravarti
Genetic linkage map of fishes of the genus Xiphophorus (Teleostei: Poeciliidae).
Genetics 1991;127(2):399-410.
1991: Bronya J B Keats; Stephanie L Sherman; N E Morton; E B Robson; K H Buetow; P E Cartwright; Aravinda Chakravarti; U Francke; P P Green; J Ott
Guidelines for human linkage maps. An International System for Human Linkage Maps (ISLM, 1990).
Annals of human genetics 1991;55(Pt 1):1-6.
1990: Pragna I Patel; C Garcia; R Montes de Oca-Luna; R I Malamut; Brunella Franco; S Slaugenhaupt; Aravinda Chakravarti; James R Lupski
Isolation of a marker linked to the Charcot-Marie-Tooth disease type IA gene by differential Alu-PCR of human chromosome 17-retaining hybrids.
American journal of human genetics 1990;47(6):926-34.
1990: Urvashi Surti; L Hoffner; Aravinda Chakravarti; R E Ferrell
Genetics and biology of human ovarian teratomas. I. Cytogenetic analysis and mechanism of origin.
American journal of human genetics 1990;47(4):635-43.
1990: J G Lewis; J L Weber; Michael B Petersen; Susan A Slaugenhaupt; A Kwitek; P E May; AC Warren; Aravinda Chakravarti; S E Antonarakis
Linkage mapping of the highly informative DNA marker D21S156 to human chromosome 21 using a polymorphic GT dinucleotide repeat.
Genomics 1990;8(2):400-2.
1990: Ranjan Deka; Aravinda Chakravarti; Urvashi Surti; E Hauselman; J Reefer; P P Majumder; Robert E Ferrell
Genetics and biology of human ovarian teratomas. II. Molecular analysis of origin of nondisjunction and gene-centromere mapping of chromosome I markers.
American journal of human genetics 1990;47(4):644-55.
1990: Katherine Neiswanger; S A Slaugenhaupt; Hugh B Hughes; Ellen Frank; D R Frankel; M J McCarty; Aravinda Chakravarti; George S Zubenko; David J Kupfer; Barry B Kaplan
Evidence against close linkage of unipolar affective illness to human chromosome 11p markers HRAS1 and INS and chromosome Xq marker DXS52.
Biological psychiatry 1990;28(1):63-72.
1990: Michael B Petersen; E P Economou; Susan A Slaugenhaupt; Aravinda Chakravarti; S E Antonarakis
Linkage analysis of the human HMG14 gene on chromosome 21 using a GT dinucleotide repeat as polymorphic marker.
Genomics 1990;7(1):136-8.
1990: Pragna I Patel; Brunella Franco; C Garcia; S A Slaugenhaupt; Y Nakamura; David Ledbetter; Aravinda Chakravarti; James R Lupski
Genetic mapping of autosomal dominant Charcot-Marie-Tooth disease in a large French-Acadian kindred: identification of new linked markers on chromosome 17.
American journal of human genetics 1990;46(4):801-9.
1990: J A Badner; W K Sieber; K L Garver; Aravinda Chakravarti
A genetic study of Hirschsprung disease.
American journal of human genetics 1990;46(3):568-80.
1990: J A Badner; Aravinda Chakravarti
Waardenburg syndrome and Hirschsprung disease: evidence for pleiotropic effects of a single dominant gene.
American journal of medical genetics 1990;35(1):100-4.
1990: J C Long; Aravinda Chakravarti; Corinne D Boehm; S Antonarakis; Haig Kazazian
Phylogeny of human beta-globin haplotypes and its implications for recent human evolution.
American journal of physical anthropology 1990;81(1):113-30.
1989: Batsheva Kerem; Johanna M Rommens; J A Buchanan; Danuta Markiewicz; T K Cox; Aravinda Chakravarti; Manuel Buchwald; Lap-Chee Tsui
Identification of the cystic fibrosis gene: genetic analysis.
Science (New York, N.Y.) 1989;245(4922):1073-80.
1989: Aravinda Chakravarti; Susan A Slaugenhaupt; George S Zubenko
Inheritance pattern of platelet membrane fluidity in Alzheimer disease.
American journal of human genetics 1989;44(6):799-805.
1989: Aravinda Chakravarti
The probability of detecting the origin of nondisjunction of autosomal trisomies.
American journal of human genetics 1989;44(5):639-45.
1989: AC Warren; Susan A Slaugenhaupt; J G Lewis; Aravinda Chakravarti; S E Antonarakis
A genetic linkage map of 17 markers on human chromosome 21.
Genomics 1989;4(4):579-91.
1989: E Leitersdorf; Aravinda Chakravarti; Helen H Hobbs
Polymorphic DNA haplotypes at the LDL receptor locus.
American journal of human genetics 1989;44(3):409-21.
1989: Aravinda Chakravarti; P P Majumder; Susan A Slaugenhaupt; Ranjan Deka; AC Warren; Urvashi Surti; Robert E Ferrell; S E Antonarakis
Gene-centromere mapping and the study of non-disjunction in autosomal trisomies and ovarian teratomas.
Progress in clinical and biological research 1989;311():45-79.
1989: S E Antonarakis; AC Warren; M K McCormick; J G Lewis; Philip Hieter; Aravinda Chakravarti
Molecular mapping of chromosome 21 and the region responsible for Down syndrome.
Progress in clinical and biological research 1989;311():29-43.
1989: S D Kittur; M M Bagdon; M L Lubs; J A Phillips; J C Murray; S A Slaugenhaupt; Aravinda Chakravarti; W H Adler
Linkage analysis of neurofibromatosis type I, using chromosome 17 DNA markers.
American journal of human genetics 1989;44(1):48-50.
1988: S E Antonarakis; P Oettgen; Aravinda Chakravarti; S Blanton; R R Hudson; L Feisee; Sotirios Karathanasis
DNA polymorphism haplotypes of the human apolipoprotein APOA1-APOC3-APOA4 gene cluster.
Human genetics 1988;80(3):265-73.
1988: Donald Cramer; Aravinda Chakravarti; O Arenas; J Humprieres; P A Mowery
Genetic diversity within and between natural populations of Rattus norvegicus.
The Journal of heredity 1988;79(5):319-24.
1988: C C Li; Aravinda Chakravarti
An expository review of two methods of calculating the paternity probability.
American journal of human genetics 1988;43(2):197-205.
1988: F J Huff; J Auerbach; Aravinda Chakravarti; François Boller
Risk of dementia in relatives of patients with Alzheimer's disease.
Neurology 1988;38(5):786-90.
1988: Jeffrey C Murray; K H Buetow; M Smith; Leon R Carlock; Aravinda Chakravarti; R F Ferrell; L Gedamu; C Gilliam; R Shiang; C R DeHaven
Pairwise linkage analysis of 11 loci on human chromosome 4.
American journal of human genetics 1988;42(3):490-7.
1988: S K Chatterjee; Aravinda Chakravarti; T K Deb Maulik; N De Majumdar; M K Sen
Staging the separation of ischiopagus twins.
Journal of pediatric surgery 1988;23(1 Pt 2):73-5.
1988: A Chidambaram; Aravinda Chakravarti; Robert E Ferrell; S Iyengar
Estimating the age-at-onset function using life-table methods.
Genetic epidemiology 1988;5(4):255-63.
1987: Aravinda Chakravarti; Susan A Slaugenhaupt
Methods for studying recombination on chromosomes that undergo nondisjunction.
Genomics 1987;1(1):35-42.
1987: S Blanton; Aravinda Chakravarti
DSLINK: a computer program for gene-centromere linkage analysis in families with a trisomic offspring.
American journal of human genetics 1987;41(3):350-5.
1987: S Kittur; M L Lubs; M Bauer; Aravinda Chakravarti; Haig Kazazian
Linkage analysis of neurofibromatosis.
Journal of medical genetics 1987;24(9):526-7.
1987: AC Warren; Aravinda Chakravarti; C Wong; Susan A Slaugenhaupt; S Blanton; P C Watkins; C Metaxotou; S E Antonarakis
Evidence for reduced recombination on the nondisjoined chromosomes 21 in Down syndrome.
Science (New York, N.Y.) 1987;237(4815):652-4.
1987: K H Buetow; Aravinda Chakravarti
Multipoint gene mapping using seriation. II. Analysis of simulated and empirical data.
American journal of human genetics 1987;41(2):189-201.
1987: K H Buetow; Aravinda Chakravarti
Multipoint gene mapping using seriation. I. General methods.
American journal of human genetics 1987;41(2):180-8.
1987: S J Bale; Aravinda Chakravarti
Evidence for autosomal dominance and pleiotropy of the cutaneous malignant melanoma (CMM)/Dysplastic nevus (DN) gene.
American journal of human genetics 1987;40(5):466-7.
1987: Aravinda Chakravarti; J A Badner; C C Li
Tests of linkage and heterogeneity in Mendelian diseases using identity by descent scores.
Genetic epidemiology 1987;4(4):255-66.
1987: C C Li; Aravinda Chakravarti; S Blanton
Estimation of segregation and ascertainment probabilities by discarding the single probands.
Genetic epidemiology 1987;4(3):185-91.
1986: Aravinda Chakravarti; K H Buetow; S E Antonarakis; P G Waber; Corinne D Boehm; Haig Kazazian
Nonuniform recombination within the human beta-globin gene cluster: A reply to B. S. Weir and W. G. Hill.
American journal of human genetics 1986;38(5):779-81.
1986: C C Li; Aravinda Chakravarti
Some fallacious thinking about the paternity index: A reply to Dr. Jack Valentin's comments.
American journal of human genetics 1986;38(4):586-9.
1986: S J Bale; Aravinda Chakravarti; M H Greene
Cutaneous malignant melanoma and familial dysplastic nevi: evidence for autosomal dominance and pleiotropy.
American journal of human genetics 1986;38(2):188-96.
1986: Aravinda Chakravarti; S C Elbein; M A Permutt
Evidence for increased recombination near the human insulin gene: implication for disease association studies.
Proceedings of the National Academy of Sciences of the United States of America 1986;83(4):1045-9.
1986: Aravinda Chakravarti; S Blanton; S J Bale; M A Tucker
Etiological heterogeneity in Hodgkin's disease: HLA linked and unlinked determinants of susceptibility independent of histological concordance.
Genetic epidemiology 1986;3(6):407-15.
1986: K H Buetow; Aravinda Chakravarti; S A Cole
A genetic map of human chromosome 11p.
Genetic epidemiology. Supplement 1986;1():135-40.
1986: S E Antonarakis; Aravinda Chakravarti; AC Warren; Susan A Slaugenhaupt; C Wong; S Blanton; C Metaxotou
Reduced recombination rate on chromosomes 21 that have undergone nondisjunction.
Cold Spring Harbor symposia on quantitative biology 1986;51 Pt 1():185-90.
1986: J A Badner; Aravinda Chakravarti; K H Buetow
Linkage analysis between Huntington disease and the G8 marker locus.
Genetic epidemiology. Supplement 1986;1():211-6.
1985: S D Kittur; S E Antonarakis; Rudolph E Tanzi; Deborah A Meyers; Aravinda Chakravarti; Y Groner; J A Phillips; P C Watkins; James Gusella; Haig Kazazian
A linkage map of three anonymous human DNA fragments and SOD-1 on chromosome 21.
The EMBO journal 1985;4(9):2257-60.
1985: Aravinda Chakravarti; K H Buetow
A strategy for using multiple linked markers for genetic counseling.
American journal of human genetics 1985;37(5):984-97.
1985: C C Li; Aravinda Chakravarti
Basic fallacies in the formulation of the paternity index.
American journal of human genetics 1985;37(4):809-18.
1985: K J Matteson; Harry Ostrer; Aravinda Chakravarti; K H Buetow; W E O'Brien; Arthur L Beaudet; J A Phillips
A study of restriction fragment length polymorphisms at the human alpha-1-antitrypsin locus.
Human genetics 1985;69(3):263-7.
1984: Aravinda Chakravarti; K H Buetow; S E Antonarakis; P G Waber; Corinne D Boehm; Haig Kazazian
Nonuniform recombination within the human beta-globin gene cluster.
American journal of human genetics 1984;36(6):1239-58.
1984: Aravinda Chakravarti; J A Phillips; K H Mellits; K H Buetow; P H Seeburg
Patterns of polymorphism and linkage disequilibrium suggest independent origins of the human growth hormone gene cluster.
Proceedings of the National Academy of Sciences of the United States of America 1984;81(19):6085-9.
1984: S J Bale; Aravinda Chakravarti; R E Ferrell; M A Spence
Possible heterogeneity in the phosphoglycolate phosphatase (PGP)-haptoglobin alpha (HPA) linkage.
American journal of human genetics 1984;36(4):808-14.
1984: Aravinda Chakravarti; C C Li
Estimating the prior probability of paternity from the results of exclusion tests.
Forensic science international 1984;24(2):143-7.
1984: J A Badner; Aravinda Chakravarti; D K Wagener
A test of nonrandom segregation.
Genetic epidemiology 1984;1(4):329-40.
1984: Aravinda Chakravarti
Aspects of linkage analysis using RFLP's.
Progress in clinical and biological research 1984;147():293-5.
1984: S J Bale; Aravinda Chakravarti; L C Strong
Aggregation of colon cancer in family data.
Genetic epidemiology 1984;1(1):53-61.
1984: Aravinda Chakravarti; C C Li; K H Buetow
Estimation of the marker gene frequency and linkage disequilibrium from conditional marker data.
American journal of human genetics 1984;36(1):177-86.
1983: Aravinda Chakravarti; S J Bale
Differences in the frequency of X-linked deleterious genes in human populations.
American journal of human genetics 1983;35(6):1252-7.
1983: Aravinda Chakravarti; C C Li
The probability of exclusion based on the HLA locus.
American journal of human genetics 1983;35(5):1048-52.
1983: R V Lebo; Aravinda Chakravarti; K H Buetow; M C Cheung; H Cann; B Cordell; H Goodman
Recombination within and between the human insulin and beta-globin gene loci.
Proceedings of the National Academy of Sciences of the United States of America 1983;80(15):4808-12.
1983: Aravinda Chakravarti
Utility and efficiency of linked marker genes for genetic counseling. III. Proportion of informative families under linkage disequilibrium.
American journal of human genetics 1983;35(4):592-610.
1983: S P Daiger; Aravinda Chakravarti
Deletion mapping of polymorphic loci by apparent parental exclusion.
American journal of medical genetics 1983;14(1):43-8.
1982: S E Antonarakis; Stuart H Orkin; Haig Kazazian ; S C Goff; Corinne D Boehm; P G Waber; J P Sexton; Harry Ostrer; V F Fairbanks; Aravinda Chakravarti
Evidence for multiple origins of the beta E-globin gene in Southeast Asia.
Proceedings of the National Academy of Sciences of the United States of America 1982;79(21):6608-11.
1982: Aravinda Chakravarti; M Nei
Utility and efficiency of linked marker genes for genetic counseling. II. Identification of linkage phase by offspring phenotypes.
American journal of human genetics 1982;34(4):531-51.
1981: R E Ferrell; H M Hittner; Aravinda Chakravarti
Autosomal dominant cone-rod dystrophy: a linkage study with 17 biochemical and serological markers.
American journal of medical genetics 1981;8(3):363-9.
1980: R E Ferrell; Aravinda Chakravarti; H M Hittner; V M Riccardi
Autosomal dominant aniridia: probable linkage to acid phosphatase-1 locus on chromosome 2.
Proceedings of the National Academy of Sciences of the United States of America 1980;77(3):1580-2.
1978: Aravinda Chakravarti; R Chakraborty
Elevated frequency of Tay-Sachs disease among Ashkenazic Jews unlikely by genetic drift alone.
American journal of human genetics 1978;30(3):256-61.
1978: K C Malhotra; R Chakraborty; Aravinda Chakravarti
Gene differentiation among the Dhangar caste-cluster of Maharashtra, India.
Human heredity 1978;28(1):26-36.
1977: M Nei; Aravinda Chakravarti
Drift variances of FST and GST statistics obtained from a finite number of isolated populations.
Theoretical population biology 1977;11(3):307-25.
1977: M Nei; Aravinda Chakravarti; Y Tateno
Mean and variance of FST in a finite number of incompletely isolated populations.
Theoretical population biology 1977;11(3):291-306.
1977: R Chakraborty; Aravinda Chakravarti; K C Malhotra
Variation in allele frequencies among caste groups of the Dhangars of Maharashtra, India: an analysis with Wright's Fst statistic.
Annals of human biology 1977;4(3):275-80.
1977: R Chakraborty; Aravinda Chakravarti
On consanguineous marriages and the genetic load.
Human genetics 1977;36(1):47-54.