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Gerard Schellenberg

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Wei Zhao; Thomas D Bird; Charles Y K Cheung; Elizabeth E Marchani; Gerard D Schellenberg; Ellen J Steinbart; Ellen M Wijsman
Genome scan in familial late-onset Alzheimer's disease: a locus on chromosome 6 contributes to age-at-onset.
Debby W Tsuang; Jia Y Wan; Randall L Woltjer; Dora Yearout; David A Bennett; Aron S Buchman; Paul K Crane; Karen L Edwards; Allison Fritts-Penniman; Douglas Galasko; Ronald L Hamilton; Haley Huston; Gregory A Jicha; Jeffrey A Kaye; Patricia Kramer; Walter Kukull; Eric B Larson; James B Leverenz; Oscar L Lopez; Eliezer Masliah; Ignacio Mata; Thomas J Montine; PETER NELSON; Janna H Neltner; Gerard D Schellenberg; Julie A Schneider; John Q Trojanowski; Cyrus Zabetian
GBA mutations increase risk for Lewy body disease with and without Alzheimer disease pathology.
Gyungah Jun; Eric B Larson; Kathryn L Lunetta; Richard Mayeux; Margaret A Pericak-Vance; Gerard D Schellenberg; Badri N Vardarajan; Chang-En Yu; Jacqueline Buros; Paul K Crane; Beth A Dombroski; Jonathan L Haines; Michele V Hawk; Lindsay A Farrer
Comprehensive search for Alzheimer disease susceptibility loci in the APOE region.

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2013: Wei Zhao; Thomas D Bird; Charles Y K Cheung; Elizabeth E Marchani; Gerard D Schellenberg; Ellen J Steinbart; Ellen M Wijsman
Genome scan in familial late-onset Alzheimer's disease: a locus on chromosome 6 contributes to age-at-onset.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2013;162B(2):201-12.
2012: Debby W Tsuang; Jia Y Wan; Randall L Woltjer; Dora Yearout; David A Bennett; Aron S Buchman; Paul K Crane; Karen L Edwards; Allison Fritts-Penniman; Douglas Galasko; Ronald L Hamilton; Haley Huston; Gregory A Jicha; Jeffrey A Kaye; Patricia Kramer; Walter Kukull; Eric B Larson; James B Leverenz; Oscar L Lopez; Eliezer Masliah; Ignacio Mata; Thomas J Montine; PETER NELSON; Janna H Neltner; Gerard D Schellenberg; Julie A Schneider; John Q Trojanowski; Cyrus Zabetian
GBA mutations increase risk for Lewy body disease with and without Alzheimer disease pathology.
Neurology 2012;79(19):1944-50.
2012: Gyungah Jun; Eric B Larson; Kathryn L Lunetta; Richard Mayeux; Margaret A Pericak-Vance; Gerard D Schellenberg; Badri N Vardarajan; Chang-En Yu; Jacqueline Buros; Paul K Crane; Beth A Dombroski; Jonathan L Haines; Michele V Hawk; Lindsay A Farrer
Comprehensive search for Alzheimer disease susceptibility loci in the APOE region.
Archives of neurology 2012;69(10):1270-9.
2012: Gerard D Schellenberg; Thomas J Montine
The genetics and neuropathology of Alzheimer's disease.
Acta neuropathologica 2012;124(3):305-23.
2011: Günter U Höglinger; Howard I Hurtig; Lambertus Klei; Andrew J Lees; Irene Litvan; Walter Maetzler; Nadine M Melhem; Ulrich Müller; Pau Pastor; Rosa Rademakers; Tamas Revesz; David E Riley; Andrew B Singleton; Patrick M A Sleiman; Eduardo Tolosa; Ryan J Uitti; Marcel P van der Brug; John C van Swieten; Jana Vandrovcova; Li-San Wang; Zbigniew K Wszolek; Chang-En Yu; Barbara Borroni; Laura B Cantwell; Mark R Cookson; Rohan de Silva; Bernie Devlin; dennis dickson; Allissa Dillman; Matthew J Farrer; J Raphael Gibbs; Lawrence I Golbe; Stefano Goldwurm; Rachel G Gross; Hakon Hakonarson; Mi Ryung Han; John Hardy; Dena G Hernandez; Peter Heutink; Gerard D Schellenberg
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.
Nature genetics 2011;43(7):699-705.
2011: Ruth Kohen; Jane B Shofer; O Korvatska; Eric C Petrie; L Y Wang; Gerard D Schellenberg; Elaine Peskind; Charles William Wilkinson
ABCB1 genotype and CSF beta-amyloid in Alzheimer disease.
Journal of geriatric psychiatry and neurology 2011;24(2):63-6.
2011: Adam C Naj; Gyungah Jun; Gary Beecham; Li-San Wang; Badri Narayan Vardarajan; Jacqueline Buros; Paul J Gallins; Joseph Buxbaum; Gail P Jarvik; Paul K Crane; Eric B Larson; Thomas D Bird; Bradley F Boeve; Neill R Graff-Radford; Philip L De Jager; Denis Evans; Julie A Schneider; Minerva M Carrasquillo; Nilufer Ertekin-Taner; Steven G Younkin; Carlos Cruchaga; John S K Kauwe; Petra Nowotny; Patricia Kramer; John Hardy; Matthew Huentelman; Amanda Myers; M. Michael Barmada; F Yesim Demirci; Clinton T Baldwin; Robert C Green; Ekaterina Rogaeva; Steven E Arnold; Robert C Barber; Thomas Beach; Eileen H Bigio; James D Bowen; Adam Boxer; James R Burke; Nigel J Cairns; Chris S Carlson; Regina M Carney; Steven L Carroll; Helena C Chui; David G Clark; Jason Corneveaux; Carl W Cotman; Jeffrey L Cummings; Charles DeCarli; Steven T DeKosky; Ramon Diaz-Arrastia; Malcolm Dick; dennis dickson; William G Ellis; Kelley M Faber; Kenneth B Fallon; Martin R Farlow; Steven Ferris; Matthew P Frosch; Douglas Galasko; Mary Ganguli; Marla Gearing; Daniel Geschwind; Bernardino Ghetti; John Gilbert; Sid Gilman; Bruno Giordani; Jonathan D Glass; John H Growdon; Ronald L Hamilton; Lindy E Harrell; Elizabeth Head; Lawrence Honig; Christine M Hulette; Bradley T Hyman; Gregory A Jicha; Lee-Way Jin; Nancy Johnson; Jason Karlawish; Anna Karydas; Jeffrey A Kaye; Ronald Kim; Edward H Koo; Neil W Kowall; James J Lah; Allan Levey; Andrew P Lieberman; Oscar L Lopez; Wendy J Mack; Daniel C Marson; Frank Martiniuk; Deborah C Mash; Eliezer Masliah; Wayne C McCormick; Susan M McCurry; Andrew N McDavid; Ann C McKee; Marsel Mesulam; Bruce L Miller; Carol A Miller; Joshua Miller; Joseph E Parisi; Daniel P Perl; Elaine Peskind; Ronald C. Petersen; Wayne W Poon; Joseph F Quinn; Ruchita A Rajbhandary; Murray Raskind; Barry Reisberg; John M Ringman; Erik D Roberson; Roger N Rosenberg; Mary Sano; Lon S Schneider; William Seeley; Michael L Shelanski; Michael Slifer; Charles D Smith; Joshua A Sonnen; Salvatore Spina; Robert A Stern; Rudolph E Tanzi; John Q Trojanowski; Juan C Troncoso; Vivianna M Van Deerlin; Harry V Vinters; Jean Paul Vonsattel; Sandra Weintraub; Kathleen A Welsh-Bohmer; Jennifer Williamson; Randall L Woltjer; Laura B Cantwell; Beth A Dombroski; Duane Beekly; Kathryn L Lunetta; Eden R Martin; M Ilyas Kamboh; Andrew J Saykin; Eric Reiman; David A Bennett; John C Morris; Thomas J Montine; Alison Goate; Deborah Blacker; Debby W Tsuang; Hakon Hakonarson; Walter A Kukull; Tatiana M Foroud; Jonathan L Haines; Richard Mayeux; Margaret Pericak-Vance; Lindsay A Farrer; Peter St George-Hyslop; Gerard D Schellenberg
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.
Nature genetics 2011;43(5):436-41.
2011: Alice S Chen-Plotkin; Maria Martinez-Lage; Patrick M A Sleiman; William Hu; Robert Greene; Elisabeth McCarty Wood; Shaoxu Bing; Murray Grossman; Gerard D Schellenberg; Kimmo J Hatanpaa; Myron F Weiner; Charles L White; William S Brooks; Glenda M Halliday; Jillian J Kril; Marla Gearing; Thomas Beach; Neill R Graff-Radford; dennis dickson; Rosa Rademakers; Bradley F Boeve; Stuart M Pickering-Brown; Julie Snowden; John C van Swieten; Peter Heutink; Harro Seelaar; Jill R Murrell; Bernardino Ghetti; Salvatore Spina; Jordan Grafman; Jeffrey A Kaye; Randall L Woltjer; Marsel Mesulam; Eileen Bigio; Albert Lladó; Bruce L Miller; Ainhoa Alzualde; Fermin Moreno; Jonathan D Rohrer; Ian R A Mackenzie; Howard H Feldman; Ronald L Hamilton; Marc Cruts; Sebastiaan Engelborghs; Peter P De Deyn; Christine Van Broeckhoven; Thomas D Bird; Nigel J Cairns; Alison Goate; Matthew P Frosch; Peter F Riederer; Nenad Bogdanovic; Virginia M-Y Lee; John Q Trojanowski; Vivianna M Van Deerlin
Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration.
Archives of neurology 2011;68(4):488-97.
2011: O Korvatska; Annette Estes; Jeffrey Munson; Geraldine Dawson; L M Bekris; R Kohen; Chang-En Yu; Gerard D Schellenberg; Wendy H Raskind
Mutations in the TSGA14 gene in families with autism spectrum disorders.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2011;156B(3):303-11.
2011: Suman Jayadev; David Nochlin; Parvoneh Poorkaj-Navas; Ellen J Steinbart; James A Mastrianni; Thomas J Montine; Bernardino Ghetti; Gerard D Schellenberg; Thomas D Bird; James B Leverenz
Familial prion disease with Alzheimer disease-like tau pathology and clinical phenotype.
Annals of neurology 2011;69(4):712-20.
2011: Lynn Bekris; N M Galloway; S Millard; David J Lockhart; Ge Li; Douglas Galasko; Martin R Farlow; Christopher M Clark; Joseph F Quinn; Jeffrey A Kaye; Gerard D Schellenberg; James B Leverenz; Peter Seubert; Debby W Tsuang; Elaine Peskind; Chang-En Yu
Amyloid precursor protein (APP) processing genes and cerebrospinal fluid APP cleavage product levels in Alzheimer's disease.
Neurobiology of aging 2011;32(3):556.e13-23.
2011: Nicola H Chapman; Annette Estes; Jeffrey Munson; Raphael Bernier; Sara Jane Webb; Joseph H Rothstein; Nancy J Minshew; Geraldine Dawson; Gerard D Schellenberg; Ellen M Wijsman
Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16.
Human genetics 2011;129(1):59-70.
2010: Gyungah Jun; Adam C Naj; Gary Beecham; Li-San Wang; Jacqueline Buros; Paul J Gallins; Joseph Buxbaum; Nilufer Ertekin-Taner; MARGARET D FALLIN; Robert Friedland; Rivka Inzelberg; Patricia Kramer; Ekaterina Rogaeva; Peter St George-Hyslop; Laura B Cantwell; Beth A Dombroski; Andrew J Saykin; Eric Reiman; David A Bennett; John C Morris; Kathryn L Lunetta; Eden R Martin; Thomas J Montine; Alison Goate; Deborah Blacker; Debby W Tsuang; Duane Beekly; L Adrienne Cupples; Hakon Hakonarson; Walter Kukull; Tatiana M Foroud; Jonathan Haines; Richard Mayeux; Lindsay A Farrer; Margaret Pericak-Vance; Gerard D Schellenberg
Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes.
Archives of neurology 2010;67(12):1473-84.
2010: Heather L Melrose; Justus C Dächsel; B Behrouz; Sarah J Lincoln; M Yue; Kelly M Hinkle; C B Kent; E Korvatska; Julie P Taylor; L Witten; Y-Q Liang; J E Beevers; Mona Boules; B N Dugger; V A Serna; A Gaukhman; X Yu; M Castanedes-Casey; A T Braithwaite; S Ogholikhan; N Yu; D Bass; Glenn M Tyndall; Gerard D Schellenberg; dennis dickson; C Janus; Matthew J Farrer
Impaired dopaminergic neurotransmission and microtubule-associated protein tau alterations in human LRRK2 transgenic mice.
Neurobiology of disease 2010;40(3):503-17.
2010: Richard Anney; Lambertus Klei; Dalila Pinto; Regina Regan; Judith Conroy; Tiago R Magalhaes; Catarina Correia; Brett S. Abrahams; Nuala Sykes; Alistair T Pagnamenta; Joana Almeida; Elena Bacchelli; Anthony J Bailey; Gillian Baird; Agatino Battaglia; Tom Berney; Nadia Bolshakova; Sven Bölte; Patrick F Bolton; Thomas Bourgeron; Sean Brennan; Jessica Brian; Andrew R Carson; Guillermo Casallo; Jillian Casey; Su H Chu; Lynne Cochrane; Christina Corsello; Emily L Crawford; Andrew Crossett; Geraldine Dawson; Maretha de Jonge; Richard Delorme; Irene Drmic; Eftichia Duketis; Frederico Oliveira Duque; Annette Estes; Penny Farrar; Bridget A Fernandez; Susan E Folstein; Eric Fombonne; Christine M Freitag; John Gilbert; Christopher Gillberg; Joseph T Glessner; Jeremy Goldberg; Jonathan Green; Stephen J Guter; Hakon Hakonarson; Elizabeth A Heron; Matthew Hill; Richard Holt; Jennifer L Howe; Gillian Hughes; Vanessa Hus; Roberta Igliozzi; Cecilia Kim; Sabine M Klauck; Alexander Kolevzon; Olena Korvatska; Vlad Kustanovich; Clara M Lajonchere; Janine A Lamb; Magdalena Laskawiec; Marion Leboyer; Ann Le Couteur; Bennett L Leventhal; Anath C Lionel; Xiao-Qing Liu; Catherine Lord; Linda Lotspeich; Sabata C Lund; Elena Maestrini; William Mahoney; Carine Mantoulan; Christian R Marshall; Helen McConachie; Christopher J McDougle; Jane McGrath; William M McMahon; Nadine M Melhem; Alison Merikangas; Ohsuke Migita; Nancy J Minshew; Ghazala K Mirza; Jeffrey Munson; Stanley F Nelson; Carolyn Noakes; Abdul Noor; Gudrun Maria Nygren; Guiomar Oliveira; Katerina Papanikolaou; Jeremy R Parr; Barbara Parrini; Tara Paton; Andrew Pickles; Joseph Piven; David J Posey; Annemarie Poustka; Fritz Poustka; APARNA PRASAD; Jiannis Ragoussis; Katy Renshaw; Jessica Rickaby; Wendy Roberts; Kathryn Roeder; Bernadette Roge; Michael L Rutter; Laura J Bierut; John P Rice; Jeff Salt; Katherine Sansom; Daisuke Sato; Ricardo Segurado; Lili Senman; Naisha Shah; Val C Sheffield; Latha Soorya; Inês Sousa; Vera Stoppioni; Christina Strawbridge; Raffaella Tancredi; Katherine Tansey; Bhooma Thiruvahindrapduram; Ann P Thompson; Susanne Thomson; Ana Tryfon; John Tsiantis; Herman Van Engeland; John B Vincent; Fred Volkmar; Simon Wallace; Kai Wang; Zhouzhi Wang; Thomas H Wassink; Kirsty Wing; Kerstin Wittemeyer; Shawn Wood; Brian L Yaspan; Danielle Zurawiecki; Lonnie Zwaigenbaum; Catalina Betancur; Joseph Buxbaum; Rita M Cantor; Edwin H Cook; Hilary Coon; Michael Cuccaro; Louise Gallagher; Daniel Geschwind; Michael Gill; Jonathan L Haines; Judith Miller; Anthony P Monaco; John I Nurnberger; Andrew D Paterson; Margaret Pericak-Vance; Gerard D Schellenberg; Stephen W Scherer; James S Sutcliffe; Peter Szatmari; Astrid M Vicente; Veronica J Vieland; Ellen M Wijsman; Bernie Devlin; Sean Ennis; Joachim Hallmayer
A genome-wide scan for common alleles affecting risk for autism.
Human molecular genetics 2010;19(20):4072-82.
2010: Denise M Kay; C F Stevens; Taye H Hamza; Jennifer S Montimurro; Cyrus Zabetian; Stewart A Factor; Ali Samii; Alida Griffith; John W Roberts; E S Molho; Donald S Higgins; S Gancher; Lina Moses; S Zareparsi; Parvoneh Poorkaj-Navas; Thomas D Bird; John G Nutt; Gerard D Schellenberg; Haydeh Payami
A comprehensive analysis of deletions, multiplications, and copy number variations in PARK2.
Neurology 2010;75(13):1189-94.
2010: Abdul Noor; Annabel Whibley; Christian R Marshall; Peter J Gianakopoulos; Amelie Piton; Andrew R Carson; Marija Orlic-Milacic; Anath C Lionel; Daisuke Sato; Dalila Pinto; Irene Drmic; Carolyn Noakes; Lili Senman; Xiaoyun Zhang; Rong Mo; Julie Gauthier; Jennifer Crosbie; Alistair T Pagnamenta; Jeffrey Munson; Annette M Estes; Andreas Fiebig; Andre Franke; Stefan Schreiber; Alexandre Stewart; Robert Roberts; Ruth McPherson; Stephen J Guter; Edwin H Cook; Geraldine Dawson; Gerard D Schellenberg; Agatino Battaglia; Elena Maestrini; Linda Jeng; Terry Hutchison; Evica Rajcan-Separovic; Albert E Chudley; Suzanne M E Lewis; Xudong Liu; Jeanette J Holden; Bridget Fernandez; Lonnie Zwaigenbaum; Susan E Bryson; Wendy Roberts; Peter Szatmari; Louise Gallagher; Michael R Stratton; Jozef Gecz; Angela F Brady; Charles E Schwartz; Russell J Schachar; Anthony P Monaco; Guy A Rouleau; Chi-Chung Hui; F Lucy Raymond; Stephen W Scherer; John B Vincent
Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability.
Science translational medicine 2010;2(49):49ra68.
2010: Elena Maestrini; Alistair T Pagnamenta; Janine A Lamb; Elena Bacchelli; N H Sykes; I Sousa; Claudio Toma; Gabrielle Barnby; H Butler; L Winchester; Thomas Scerri; F Minopoli; J Reichert; G Cai; Joseph Buxbaum; O Korvatska; Gerard D Schellenberg; Geraldine Dawson; A de Bildt; Ruud B Minderaa; E J Mulder; Andrew P Morris; Anthony J Bailey; Anthony P Monaco
High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility.
Molecular psychiatry 2010;15(9):954-68.
2010: Kai Wang; Maja Bucan; Struan F A Grant; Gerard D Schellenberg; Hakon Hakonarson
Strategies for genetic studies of complex diseases.
Cell 2010;142(3):351-3; author reply 353-5.
2010: Dalila Pinto; Alistair T Pagnamenta; Lambertus Klei; Richard Anney; Daniele Merico; Regina Regan; Judith Conroy; Tiago R Magalhaes; Catarina Correia; Brett S. Abrahams; Joana Almeida; Elena Bacchelli; Gary D Bader; Anthony J Bailey; Gillian Baird; Agatino Battaglia; Tom Berney; Nadia Bolshakova; Sven Bölte; Patrick F Bolton; Thomas Bourgeron; Sean Brennan; Jessica Brian; Susan E Bryson; Andrew R Carson; Guillermo Casallo; Jillian Casey; Brian H Y Chung; Lynne Cochrane; Christina Corsello; Emily L Crawford; Andrew Crossett; Cheryl Cytrynbaum; Geraldine Dawson; Maretha de Jonge; Richard Delorme; Irene Drmic; Eftichia Duketis; Frederico Oliveira Duque; Annette Estes; Penny Farrar; Bridget A Fernandez; Susan E Folstein; Eric Fombonne; Christine M Freitag; John Gilbert; Christopher Gillberg; Joseph T Glessner; Jeremy Goldberg; Andrew Green; Jonathan Green; Stephen J Guter; Hakon Hakonarson; Elizabeth A Heron; Matthew Hill; Richard Holt; Jennifer L Howe; Gillian Hughes; Vanessa Hus; Roberta Igliozzi; Cecilia Kim; Sabine M Klauck; Alexander Kolevzon; Olena Korvatska; Vlad Kustanovich; Clara M Lajonchere; Janine A Lamb; Magdalena Laskawiec; Marion Leboyer; Ann Le Couteur; Bennett L Leventhal; Anath C Lionel; Xiao-Qing Liu; Catherine Lord; Linda Lotspeich; Sabata C Lund; Elena Maestrini; William Mahoney; Carine Mantoulan; Christian R Marshall; Helen McConachie; Christopher J McDougle; Jane McGrath; William M McMahon; Alison Merikangas; Ohsuke Migita; Nancy J Minshew; Ghazala K Mirza; Jeffrey Munson; Stanley F Nelson; Carolyn Noakes; Abdul Noor; Gudrun Maria Nygren; Guiomar Oliveira; Katerina Papanikolaou; Jeremy R Parr; Barbara Parrini; Tara Paton; Andrew Pickles; Marion Pilorge; Joseph Piven; Chris P Ponting; David J Posey; Annemarie Poustka; Fritz Poustka; APARNA PRASAD; Jiannis Ragoussis; Katy Renshaw; Jessica Rickaby; Wendy Roberts; Kathryn Roeder; Bernadette Roge; Michael L Rutter; Laura J Bierut; John P Rice; Jeff Salt; Katherine Sansom; Daisuke Sato; Ricardo Segurado; Ana F Sequeira; Lili Senman; Naisha Shah; Val C Sheffield; Latha Soorya; Inês Sousa; Olaf Stein; Nuala Sykes; Vera Stoppioni; Christina Strawbridge; Raffaella Tancredi; Katherine Tansey; Bhooma Thiruvahindrapduram; Ann P Thompson; Susanne Thomson; Ana Tryfon; John Tsiantis; Herman Van Engeland; John B Vincent; Fred Volkmar; Simon Wallace; Kai Wang; Zhouzhi Wang; Thomas H Wassink; Caleb Webber; Rosanna Weksberg; Kirsty Wing; Kerstin Wittemeyer; Shawn Wood; Jing Wu; Brian L Yaspan; Danielle Zurawiecki; Lonnie Zwaigenbaum; Joseph Buxbaum; Rita M Cantor; Edwin H Cook; Hilary Coon; Michael Cuccaro; Bernie Devlin; Sean Ennis; Louise Gallagher; Daniel Geschwind; Michael Gill; Jonathan L Haines; Joachim Hallmayer; Judith Miller; Anthony P Monaco; John I Nurnberger; Andrew D Paterson; Margaret Pericak-Vance; Gerard D Schellenberg; Peter Szatmari; Astrid M Vicente; Veronica J Vieland; Ellen M Wijsman; Stephen W Scherer; James S Sutcliffe; Catalina Betancur
Functional impact of global rare copy number variation in autism spectrum disorders.
Nature 2010;466(7304):368-72.
2010: Ge Li; Jane B Shofer; Isaac C Rhew; Walter A Kukull; Elaine Peskind; Wayne McCormick; James D Bowen; Gerard D Schellenberg; Paul K Crane; John C S Breitner; Eric B Larson
Age-varying association between statin use and incident Alzheimer's disease.
Journal of the American Geriatrics Society 2010;58(7):1311-7.
2010: Elizabeth E Marchani; Thomas D Bird; Ellen J Steinbart; Elisabeth Rosenthal; Chang-En Yu; Gerard D Schellenberg; Ellen M Wijsman
Evidence for three loci modifying age-at-onset of Alzheimer's disease in early-onset PSEN2 families.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010;153B(5):1031-41.
2010: David M Koelle; Amalia Magaret; Terri Warren; Gerard D Schellenberg; Anna Wald
APOE genotype is associated with oral herpetic lesions but not genital or oral herpes simplex virus shedding.
Sexually transmitted infections 2010;86(3):202-6.
2010: Amy R Borenstein; James A Mortimer; Gerard D Schellenberg; Charles DeCarli; Cathleen Copenhaver; Douglas Galasko; David P Salmon; Ronald C. Petersen
Effects of apolipoprotein E-epsilon4 and -epsilon2 in amnestic mild cognitive impairment and dementia in Shanghai: SCOBHI-P.
American journal of Alzheimer's disease and other dementias 2010;25(3):233-8.
2010: Brian C Kraemer; Theresa Schuck; Jeanna M Wheeler; Linda C Robinson; John Q Trojanowski; Virginia M-Y Lee; Gerard D Schellenberg
Loss of murine TDP-43 disrupts motor function and plays an essential role in embryogenesis.
Acta neuropathologica 2010;119(4):409-19.
2010: Lynn M Bekris; Nichole M Galloway; Thomas J Montine; Gerard D Schellenberg; Chang-En Yu
APOE mRNA and protein expression in postmortem brain are modulated by an extended haplotype structure.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010;153B(2):409-17.
2010: John Q Trojanowski; Steven E Arnold; Jason H Karlawish; Kurt Brunden; Mark Cary; Christos Davatzikos; John Detre; Glen Gaulton; Murray Grossman; Howard I Hurtig; Kathryn Jedrziewski; Leo McCluskey; Mary Naylor; Daniel Polsky; Gerard D Schellenberg; Andrew Siderowf; Leslie M Shaw; Vivianna Van Deerlin; Li-San Wang; Rachel Werner; Sharon X Xie; Virginia M-Y Lee
Design of comprehensive Alzheimer's disease centers to address unmet national needs.
Alzheimer's & dementia : the journal of the Alzheimer's Association 2010;6(2):150-5.
2010: ZAVEN KHACHATURIAN; Deborah Barnes; Richard Einstein; Sterling Johnson; Virginia M-Y Lee; Allen D Roses; Mark A Sager; William R Shankle; Peter J Snyder; Ronald C. Petersen; Gerard D Schellenberg; John Q Trojanowski; Paul Aisen; Marilyn S Albert; John C S Breitner; Neil Buckholtz; Maria Carrillo; Steven Ferris; Barry D Greenberg; Michael Grundman; Ara S Khachaturian; Lewis H Kuller; Oscar L Lopez; Paul Maruff; Richard C Mohs; Marcelle Morrison-Bogorad; Creighton Phelps; Eric Reiman; Marwan Sabbagh; Mary Sano; Lon S Schneider; Eric Siemers; Pierre Tariot; Jacques Touchon; Bruno Vellas; Lisa J Bain
Developing a national strategy to prevent dementia: Leon Thal Symposium 2009.
Alzheimer's & dementia : the journal of the Alzheimer's Association 2010;6(2):89-97.
2010: Vivianna M Van Deerlin; Patrick M A Sleiman; Maria Martinez-Lage; Alice Chen-Plotkin; Li-San Wang; Neill R Graff-Radford; dennis dickson; Rosa Rademakers; Bradley F Boeve; Murray Grossman; Steven E Arnold; D M A Mann; Stuart M Pickering-Brown; Harro Seelaar; Peter Heutink; John C van Swieten; Jill R Murrell; Bernardino Ghetti; Salvatore Spina; Jordan Grafman; John R Hodges; Maria Grazia Spillantini; Sid Gilman; Andrew P Lieberman; Jeffrey A Kaye; Randall L Woltjer; Eileen H Bigio; Marsel Mesulam; Safa Al-Sarraj; Claire Troakes; Roger N Rosenberg; Charles L White; Isidro Ferrer; Albert Lladó; Manuela Neumann; Hans A Kretzschmar; Christine Marie Hulette; Kathleen A Welsh-Bohmer; Bruce L Miller; Ainhoa Alzualde; Adolfo Lopez de Munain; Ann C McKee; Marla Gearing; Allan Levey; James J Lah; John Hardy; Jonathan D Rohrer; Tammaryn Lashley; Ian R A Mackenzie; Howard H Feldman; Ronald L Hamilton; Steven T DeKosky; Julie van der Zee; Samir Kumar-Singh; Christine Van Broeckhoven; Richard Mayeux; Jean Paul G Vonsattel; Juan C Troncoso; Jillian J Kril; John B J Kwok; Glenda M Halliday; Thomas D Bird; Paul Geoffrey Ince; Pamela J Shaw; Nigel J Cairns; John C Morris; Catriona Ann McLean; Charles DeCarli; William G Ellis; Stefanie H Freeman; Matthew P Frosch; John H Growdon; Daniel P Perl; Mary Sano; David A Bennett; Julie A Schneider; Thomas Beach; Eric Reiman; Bryan Woodruff; Jeffrey L Cummings; Harry V Vinters; Carol A Miller; Helena C Chui; Irina Alafuzoff; Päivi Hartikainen; Danielle Seilhean; Douglas Galasko; Eliezer Masliah; Carl W Cotman; M Teresa Tuñón; M Cristina Caballero Martínez; David G Munoz; Steven L Carroll; Daniel Marson; Peter F Riederer; Nenad Bogdanovic; Gerard D Schellenberg; Hakon Hakonarson; John Q Trojanowski; Virginia M-Y Lee
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions.
Nature genetics 2010;42(3):234-9.
2010: Chang-En Yu; Thomas D Bird; Lynn M Bekris; Thomas J Montine; James B Leverenz; Ellen Steinbart; Nichole M Galloway; Howard Feldman; Randall L Woltjer; Carol A Miller; Elisabeth McCarty Wood; Murray Grossman; Leo McCluskey; Christopher M Clark; Manuela Neumann; Adrian Danek; Douglas Galasko; Steven E Arnold; Alice Chen-Plotkin; Anna Karydas; Bruce L Miller; John Q Trojanowski; Virginia M-Y Lee; Gerard D Schellenberg; Vivianna M Van Deerlin
The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegeneration.
Archives of neurology 2010;67(2):161-70.
2010: Mi-Ryung Han; Gerard D Schellenberg; Li-San Wang
Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study.
BMC neurology 2010;10():90.
2010: Jerome Carayol; Gerard D Schellenberg; Frederic Tores; Jörg Hager; Andreas Ziegler; Geraldine Dawson
Assessing the impact of a combined analysis of four common low-risk genetic variants on autism risk.
Molecular autism 2010;1(1):4.
2010: Haydeh Payami; Denise M Kay; Cyrus Zabetian; Gerard D Schellenberg; Stewart A Factor; Colin C McCulloch
Visualizing disease associations: graphic analysis of frequency distributions as a function of age using moving average plots (MAP) with application to Alzheimer's and Parkinson's disease.
Genetic epidemiology 2010;34(1):92-9.
2009: Weiva Sieh; Yoonha Choi; Nicola H Chapman; Ulla-Katrina Craig; Ellen J Steinbart; Joseph H Rothstein; Kiyomitsu Oyanagi; Ralph M Garruto; Thomas D Bird; Douglas Galasko; Gerard D Schellenberg; Ellen M Wijsman
Identification of novel susceptibility loci for Guam neurodegenerative disease: challenges of genome scans in genetic isolates.
Human molecular genetics 2009;18(19):3725-38.
2009: ZAVEN KHACHATURIAN; Jordi Camí; Sandrine Andrieu; Jesús Avila; Mercè Boada Rovira; Monique Breteler; Lutz Froelich; S Gauthier; Teresa Gómez-Isla; Ara Khachaturian; Lewis H Kuller; Eric B Larson; Oscar L Lopez; José Manuel Martinez-Lage; Ronald C. Petersen; Gerard D Schellenberg; Jordi Sunyer; Bruno Vellas; Lisa J Bain
Creating a transatlantic research enterprise for preventing Alzheimer's disease.
Alzheimer's & dementia : the journal of the Alzheimer's Association 2009;5(4):361-6.
2009: Maja Bucan; Brett S. Abrahams; Kai Wang; Joseph T Glessner; Edward I Herman; Lisa I Sonnenblick; Ana I Alvarez Retuerto; Marcin Imielinski; Dexter Hadley; Jonathan P Bradfield; Cecilia Kim; Nicole B Gidaya; Ingrid Lindquist; Ted Hutman; Marian Sigman; Vlad Kustanovich; Clara M Lajonchere; Andrew Singleton; Junhyong Kim; Thomas H Wassink; William M McMahon; Thomas Owley; John A Sweeney; Hilary Coon; John I Nurnberger; Mingyao Li; Rita M Cantor; Nancy J Minshew; James S Sutcliffe; Edwin H Cook; Geraldine Dawson; Joseph Buxbaum; Struan F A Grant; Gerard D Schellenberg; Daniel Geschwind; Hakon Hakonarson
Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes.
PLoS genetics 2009;5(6):e1000536.
2009: Joseph T Glessner; Kai Wang; Guiqing Cai; Olena Korvatska; Cecilia E Kim; Shawn Wood; Haitao Zhang; Annette Estes; Camille W. Brune; Jonathan P Bradfield; Marcin Imielinski; Edward C Frackelton; Jennifer Reichert; Emily L Crawford; Jeffrey Munson; Patrick M A Sleiman; Rosetta Chiavacci; Kiran Annaiah; Kelly Thomas; Cuiping Hou; Wendy Glaberson; James Flory; Frederick Otieno; Maria Garris; Latha Soorya; Lambertus Klei; Joseph Piven; Kacie J Meyer; Evdokia Anagnostou; Takeshi Sakurai; Rachel M Game; Danielle S Rudd; Danielle Zurawiecki; Christopher J McDougle; Lea Davis; Judith Miller; David J Posey; Shana Michaels; Alexander Kolevzon; Jeremy Silverman; Raphael Bernier; Susan E Levy; Robert T Schultz; Geraldine Dawson; Thomas Owley; William M McMahon; Thomas H Wassink; John A Sweeney; John I Nurnberger; Hilary Coon; James S Sutcliffe; Nancy J Minshew; Struan F A Grant; Maja Bucan; Edwin H Cook; Joseph Buxbaum; Bernie Devlin; Gerard D Schellenberg; Hakon Hakonarson
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
Nature 2009;459(7246):569-73.
2009: Kai Wang; Haitao Zhang; Deqiong Ma; Maja Bucan; Joseph T Glessner; Brett S. Abrahams; Daria Salyakina; Marcin Imielinski; Jonathan P Bradfield; Patrick M A Sleiman; Cecilia E Kim; Cuiping Hou; Edward Frackelton; Rosetta Chiavacci; Nagahide Takahashi; Takeshi Sakurai; Eric Rappaport; Clara M Lajonchere; Jeffrey Munson; Annette Estes; Olena Korvatska; Joseph Piven; Lisa I Sonnenblick; Ana I Alvarez Retuerto; Edward I Herman; Hongmei Dong; Ted Hutman; Marian Sigman; Sally Ozonoff; Ami Klin; Thomas Owley; John A Sweeney; Camille W. Brune; Rita M Cantor; Raphael Bernier; John Gilbert; Michael Cuccaro; William M McMahon; Judith Miller; Sate Matthew; Thomas H Wassink; Hilary Coon; Susan E Levy; Robert T Schultz; John I Nurnberger; Jonathan L Haines; James S Sutcliffe; Edwin H Cook; Nancy J Minshew; Joseph Buxbaum; Geraldine Dawson; Struan F A Grant; Daniel Geschwind; Margaret Pericak-Vance; Gerard D Schellenberg; Hakon Hakonarson
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
Nature 2009;459(7246):528-33.
2009: Cyrus Zabetian; Mitsutoshi Yamamoto; Alexis N Lopez; Hiroshi Ujike; Ignacio F Mata; Yuishin Izumi; Ryuji Kaji; Hirofumi Maruyama; Hiroyuki Morino; Masaya Oda; Carolyn M Hutter; Karen L Edwards; Gerard D Schellenberg; Debby W Tsuang; Dora Yearout; Eric B Larson; Hideshi Kawakami
LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2009;24(7):1034-41.
2009: Chris R Guthrie; Gerard D Schellenberg; Brian C. Kraemer
SUT-2 potentiates tau-induced neurotoxicity in Caenorhabditis elegans.
Human molecular genetics 2009;18(10):1825-38.
2009: Eric C Petrie; Donna J Cross; Douglas Galasko; Gerard D Schellenberg; Murray A Raskind; Elaine Peskind; Satoshi Minoshima
Preclinical evidence of Alzheimer changes: convergent cerebrospinal fluid biomarker and fluorodeoxyglucose positron emission tomography findings.
Archives of neurology 2009;66(5):632-7.
2009: Amy R Borenstein; James A Mortimer; Gerard D Schellenberg; Douglas Galasko; Patrick L McGeer; John C Steele
The ALS/PDC syndrome of Guam and the cycad hypothesis.
Neurology 2009;72(5):473, 476; author reply 475-6.
2009: Deborah M Little; Valerie C Crooks; Diana B Petitti; Vicki Chiu; Gerard D Schellenberg; Jeff M Slezak; Steven J Jacobsen
Mortality, dementia, and apolipoprotein E genotype in elderly white women in the United States.
Journal of the American Geriatrics Society 2009;57(2):231-6.
2009: G Stennis Watson; Laura D Baker; Brenna Cholerton; Kristoffer W Rhoads; George R Merriam; Gerard D Schellenberg; Sanjay Asthana; Monique M Cherrier; Suzanne Craft
Effects of insulin and octreotide on memory and growth hormone in Alzheimer's disease.
Journal of Alzheimer's disease : JAD 2009;18(3):595-602.
2008: Pamela J McMillan; Elena Korvatska; Parvoneh Poorkaj-Navas; Zana Evstafjeva; Linda Robinson; Lynne Greenup; James B Leverenz; Gerard D Schellenberg; Ian D'Souza
Tau isoform regulation is region- and cell-specific in mouse brain.
The Journal of comparative neurology 2008;511(6):788-803.
2008: Simona Vuletic; Ge Li; Elaine Peskind; Hal Kennedy; Santica M Marcovina; James B Leverenz; Eric C Petrie; Virginia M-Y Lee; Douglas Galasko; Gerard D Schellenberg; John J Albers
Apolipoprotein E highly correlates with AbetaPP- and tau-related markers in human cerebrospinal fluid.
Journal of Alzheimer's disease : JAD 2008;15(3):409-17.
2008: Paul R Borghesani; L Clark Johnson; Amy L Shelton; Elaine Peskind; Elizabeth H Aylward; Gerard D Schellenberg; Monique M Cherrier
Altered medial temporal lobe responses during visuospatial encoding in healthy APOE*4 carriers.
Neurobiology of aging 2008;29(7):981-91.
2008: Matthew J Winton; Vivianna M Van Deerlin; Linda K Kwong; Wuxing Yuan; Elisabeth McCarty Wood; Chang-En Yu; Gerard D Schellenberg; Rosa Rademakers; Richard Caselli; Anna Karydas; John Q Trojanowski; Bruce L Miller; Virginia M-Y Lee
A90V TDP-43 variant results in the aberrant localization of TDP-43 in vitro.
FEBS letters 2008;582(15):2252-6.
2008: M R Schultz; Michael J Lyons; Carol E Franz; Michael D Grant; C Boake; Kristen C Jacobson; H Xian; Gerard D Schellenberg; Seth A Eisen; W S Kremen
Apolipoprotein E genotype and memory in the sixth decade of life.
Neurology 2008;70(19 Pt 2):1771-7.
2008: Vivianna M Van Deerlin; James B Leverenz; Lynn M Bekris; Thomas D Bird; Wuxing Yuan; Lauren B Elman; Dana Clay; Elisabeth McCarty Wood; Alice S Chen-Plotkin; Maria Martinez-Lage; Ellen Steinbart; Leo McCluskey; Murray Grossman; Manuela Neumann; I-Lin Wu; Wei-Shiung Yang; Robert Kalb; Douglas Galasko; Thomas J Montine; John Q Trojanowski; Virginia M-Y Lee; Gerard D Schellenberg; Chang-En Yu
TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis.
Lancet neurology 2008;7(5):409-16.
2008: Mark Reger; G Stennis Watson; Pattie Green; Laura D Baker; Brenna Cholerton; Mark A Fishel; Stephen R Plymate; Monique M Cherrier; Gerard D Schellenberg; William H Frey; Suzanne Craft
Intranasal insulin administration dose-dependently modulates verbal memory and plasma amyloid-beta in memory-impaired older adults.
Journal of Alzheimer's disease : JAD 2008;13(3):323-31.
2008: Lynn M Bekris; Steven P Millard; Nichole M Galloway; Simona Vuletic; John J Albers; Ge Li; Douglas Galasko; Charles DeCarli; Martin R Farlow; Chris M Clark; Joseph F Quinn; Jeffrey A Kaye; Gerard D Schellenberg; Debby W Tsuang; Elaine Peskind; Chang-En Yu
Multiple SNPs within and surrounding the apolipoprotein E gene influence cerebrospinal fluid apolipoprotein E protein levels.
Journal of Alzheimer's disease : JAD 2008;13(3):255-66.
2008: Hans Basun; Nenad Bogdanovic; Martin Ingelsson; Ove Almkvist; Jan Näslund; Karin Axelman; Thomas D Bird; David Nochlin; Gerard D Schellenberg; Lars-Olof Wahlund; Lars Lannfelt
Clinical and neuropathological features of the arctic APP gene mutation causing early-onset Alzheimer disease.
Archives of neurology 2008;65(4):499-505.
2008: Camille W. Brune; Elena Korvatska; Kristina Allen-Brady; Edwin H Cook; Geraldine Dawson; Bernie Devlin; Annette Estes; Meghann Hennelly; Susan L Hyman; William M McMahon; Jeffrey Munson; Patricia M Rodier; Gerard D Schellenberg; Stodgell Christopher; Hilary Coon
Heterogeneous association between engrailed-2 and autism in the CPEA network.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008;147B(2):187-93.
2008: Ignacio F Mata; Ali Samii; Seth H Schneer; John W Roberts; Alida Griffith; Berta C Leis; Gerard D Schellenberg; Ellen Sidransky; Thomas D Bird; James B Leverenz; Debby W Tsuang; Cyrus Zabetian
Glucocerebrosidase gene mutations: a risk factor for Lewy body disorders.
Archives of neurology 2008;65(3):379-82.
2008: Suman Jayadev; Ellen J Steinbart; Yueh-Yun Chi; Walter A Kukull; Gerard D Schellenberg; Thomas D Bird
Conjugal Alzheimer disease: risk in children when both parents have Alzheimer disease.
Archives of neurology 2008;65(3):373-8.
2008: Dana C Crawford; Alex S Nord; Michael D Badzioch; Jane Ranchalis; Laura A McKinstry; Magdalena Ahearn; Caterina Bertucci; Cynthia Shephard; Michelle Wong; Mark J Rieder; Gerard D Schellenberg; Deborah A Nickerson; Patrick J Heagerty; Ellen M Wijsman; Gail P Jarvik
A common VLDLR polymorphism interacts with APOE genotype in the prediction of carotid artery disease risk.
Journal of lipid research 2008;49(3):588-96.
2007: Joshua A Sonnen; Eric B Larson; Paul K Crane; Sebastien Haneuse; Ge Li; Gerard D Schellenberg; Suzanne Craft; James B Leverenz; Thomas J Montine
Pathological correlates of dementia in a longitudinal, population-based sample of aging.
Annals of neurology 2007;62(4):406-13.
2007: Rosa Rademakers; Matt Baker; Jennifer Gass; Jennifer Adamson; Edward D Huey; Parastoo Momeni; Salvatore Spina; Giovanni Coppola; Anna M Karydas; Heather Stewart; Nancy Johnson; Ging-Yuek Hsiung; Brendan Kelley; Karen Kuntz; Ellen Steinbart; Elisabeth McCarty Wood; Chang-En Yu; Keith A Josephs; Eric Sorenson; Kyle B Womack; Sandra Weintraub; Stuart M Pickering-Brown; Peter R Schofield; William S Brooks; Vivianna M Van Deerlin; Julie Snowden; Christopher M Clark; Andrew Kertesz; Kevin Boylan; Bernardino Ghetti; David Neary; Gerard D Schellenberg; Thomas Beach; Marek-Marsel Mesulam; D M A Mann; Jordan Grafman; Ian R Mackenzie; Howard Feldman; Thomas D Bird; Ronald C. Petersen; David S. Knopman; Bradley Boeve; Daniel Geschwind; Bruce L Miller; Zbigniew K Wszolek; Carol F Lippa; Eileen H Bigio; dennis dickson; Neill Graff-Radford; Michael Hutton
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative.
Lancet neurology 2007;6(10):857-68.
2007: Kiri L Brickell; James B Leverenz; Ellen J Steinbart; Malia Rumbaugh; Gerard D Schellenberg; David Nochlin; Thomas H Lampe; Ida E Holm; Vivianna M Van Deerlin; Wuxing Yuan; Thomas D Bird
Clinicopathological concordance and discordance in three monozygotic twin pairs with familial Alzheimer's disease.
Journal of neurology, neurosurgery, and psychiatry 2007;78(10):1050-5.
2007: Brian C. Kraemer; Gerard D Schellenberg
SUT-1 enables tau-induced neurotoxicity in C. elegans.
Human molecular genetics 2007;16(16):1959-71.
2007: Ge Li; Izabela Sokal; Joseph F Quinn; James B Leverenz; M Brodey; Gerard D Schellenberg; Jeffrey A Kaye; Murray A Raskind; Jing Zhang; Elaine Peskind; Thomas J Montine
CSF tau/Abeta42 ratio for increased risk of mild cognitive impairment: a follow-up study.
Neurology 2007;69(7):631-9.
2007: Thomas H Wassink; Heather Cody Hazlett; Eric A Epping; Stephan Arndt; Stephen R Dager; Gerard D Schellenberg; Geraldine Dawson; Joseph Piven
Cerebral cortical gray matter overgrowth and functional variation of the serotonin transporter gene in autism.
Archives of general psychiatry 2007;64(6):709-17.
2007: Chang-En Yu; Howard Seltman; Elaine Peskind; Nichole Galloway; Peter X Zhou; Elisabeth Rosenthal; Ellen M Wijsman; Debby W Tsuang; Bernie Devlin; Gerard D Schellenberg
Comprehensive analysis of APOE and selected proximate markers for late-onset Alzheimer's disease: patterns of linkage disequilibrium and disease/marker association.
Genomics 2007;89(6):655-65.
2007: Douglas Galasko; David P Salmon; Anthony Gamst; John M Olichney; Leon J Thal; Lisa Silbert; Jeffrey A Kaye; P Brooks; R Adonay; Ulla-Katrina Craig; Gerard D Schellenberg; Amy R Borenstein
Prevalence of dementia in Chamorros on Guam: relationship to age, gender, education, and APOE.
Neurology 2007;68(21):1772-81.
2007: Amy R Borenstein; James A Mortimer; E Schofield; Yougui Wu; David P Salmon; Anthony Gamst; John M Olichney; Leon J Thal; Lisa Silbert; Jeffrey A Kaye; U L Craig; Gerard D Schellenberg; Douglas Galasko
Cycad exposure and risk of dementia, MCI, and PDC in the Chamorro population of Guam.
Neurology 2007;68(21):1764-71.
2007: James B Leverenz; Chang-En Yu; Thomas J Montine; Ellen J Steinbart; L M Bekris; Cyrus Zabetian; L K Kwong; Virginia M-Y Lee; Gerard D Schellenberg; Thomas D Bird
A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathology.
Brain : a journal of neurology 2007;130(Pt 5):1360-74.
2007: Peter Szatmari; Andrew D Paterson; Lonnie Zwaigenbaum; Wendy Roberts; Jessica Brian; Xiao-Qing Liu; John B Vincent; Jennifer L Skaug; Ann P Thompson; Lili Senman; Lars Feuk; Cheng Qian; Susan E Bryson; Marshall B Jones; Christian R Marshall; Stephen W Scherer; Veronica J Vieland; Christopher Bartlett; La Vonne Mangin; Rhinda Goedken; Alberto Segre; Margaret Pericak-Vance; Michael Cuccaro; John Gilbert; Harry H Wright; Ruth K Abramson; Catalina Betancur; Thomas Bourgeron; Christopher Gillberg; Marion Leboyer; Joseph Buxbaum; Kenneth L Davis; Eric Hollander; Jeremy Silverman; Joachim Hallmayer; Linda Lotspeich; James S Sutcliffe; Jonathan L Haines; Susan E Folstein; Joseph Piven; Thomas H Wassink; Val Sheffield; Daniel Geschwind; Maja Bucan; W Ted Brown; Rita M Cantor; John N Constantino; T Conrad Gilliam; Martha Herbert; Clara Lajonchere; David Ledbetter; Christa Lese Martin; Janet Miller; Stan Nelson; Carol A Samango-Sprouse; Sarah J Spence; Sate Matthew; Rudolph E Tanzi; Hilary Coon; Geraldine Dawson; Bernie Devlin; Annette Estes; Pamela Flodman; Lambertus Klei; William M McMahon; Nancy J Minshew; Jeffrey Munson; Elena Korvatska; Patricia M Rodier; Gerard D Schellenberg; Moyra Smith; M Anne Spence; Chris Stodgell; Ping Guo Tepper; Ellen M Wijsman; Chang-En Yu; Bernadette Rogé; Carine Mantoulan; Kerstin Wittemeyer; Annemarie Poustka; Bärbel Felder; Sabine M Klauck; Claudia Schuster; Fritz Poustka; Sven Bölte; Sabine Feineis-Matthews; Evelyn Herbrecht; Gabi Schmötzer; John Tsiantis; Katerina Papanikolaou; Elena Maestrini; Elena Bacchelli; Francesca Blasi; Simona Carone; Claudio Toma; Herman Van Engeland; Maretha de Jonge; Chantal Kemner; Frederieke Koop; Frederike Koop; Marjolein Langemeijer; Marjolijn Langemeijer; Channa Hijmans; Channa Hijimans; Wouter G Staal; Gillian Baird; Patrick Bolton; Michael L Rutter; Emma Weisblatt; Jonathan Green; Catherine Aldred; Julie-Anne Wilkinson; Andrew Pickles; Ann Le Couteur; Tom Berney; Helen McConachie; Anthony J Bailey; Kostas Francis; Gemma Honeyman; Aislinn Hutchinson; Jeremy R Parr; Simon Wallace; Anthony P Monaco; Gabrielle Barnby; Kazuhiro Kobayashi; Janine A Lamb; Ines Sousa; Nuala Sykes; Edwin H Cook; Stephen J Guter; Bennett L Leventhal; Jeff Salt; Catherine Lord; Christina Corsello; Vanessa Hus; Daniel E Weeks; Fred Volkmar; Maïté Tauber; Eric Fombonne; Andy Shih; Kacie J Meyer
Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
Nature genetics 2007;39(3):319-28.
2007: Geraldine Dawson; Annette Estes; Jeffrey Munson; Gerard D Schellenberg; Raphael Bernier; Robert Abbott
Quantitative assessment of autism symptom-related traits in probands and parents: Broader Phenotype Autism Symptom Scale.
Journal of autism and developmental disorders 2007;37(3):523-36.
2007: Purnima Desai Sundar; Chang-En Yu; Weiva Sieh; Ellen J Steinbart; Ralph M Garruto; Kiyomitsu Oyanagi; Ulla-Katrina Craig; Thomas D Bird; Ellen M Wijsman; Douglas Galasko; Gerard D Schellenberg
Two sites in the MAPT region confer genetic risk for Guam ALS/PDC and dementia.
Human molecular genetics 2007;16(3):295-306.
2007: Weiva Sieh; Chang-En Yu; Thomas D Bird; Gerard D Schellenberg; Ellen M Wijsman
Accounting for linkage disequilibrium among markers in linkage analysis: impact of haplotype frequency estimation and molecular haplotypes for a gene in a candidate region for Alzheimer's disease.
Human heredity 2007;63(1):26-34.
2007: Denise M Kay; Dawn Moran; Lina Moses; Parvoneh Poorkaj-Navas; Cyrus Zabetian; John G Nutt; Stewart A Factor; Chang-En Yu; Jennifer S Montimurro; Robert G Keefe; Gerard D Schellenberg; Haydeh Payami
Heterozygous parkin point mutations are as common in control subjects as in Parkinson's patients.
Annals of neurology 2007;61(1):47-54.
2007: Brian C. Kraemer; Gerard D Schellenberg
Using Caenorhabditis elegans models of neurodegenerative disease to identify neuroprotective strategies.
International review of neurobiology 2007;77():219-46.
2006: Robert G Riekse; Ge Li; Eric C Petrie; James B Leverenz; Darcy Vavrek; Simona Vuletic; John J Albers; Thomas J Montine; Virginia M-Y Lee; Michael K Lee; Peter Seubert; Douglas Galasko; Gerard D Schellenberg; William R Hazzard; Elaine Peskind
Effect of statins on Alzheimer's disease biomarkers in cerebrospinal fluid.
Journal of Alzheimer's disease : JAD 2006;10(4):399-406.
2006: Gerard D Schellenberg; Geraldine Dawson; Yun Ju Sung; Annette Estes; Jeffrey Munson; E Rosenthal; J Rothstein; Pamela Flodman; Moyra Smith; Hilary Coon; L Leong; Chang-En Yu; Stodgell Christopher; Patricia M Rodier; M Anne Spence; Nancy J Minshew; William M McMahon; Ellen M Wijsman
Evidence for multiple loci from a genome scan of autism kindreds.
Molecular psychiatry 2006;11(11):1049-60, 979.
2006: Ge Li; Monique M Cherrier; Debby W Tsuang; Eric C Petrie; Elizabeth A Colasurdo; Suzanne Craft; Gerard D Schellenberg; Elaine Peskind; Murray A Raskind; Charles William Wilkinson
Salivary cortisol and memory function in human aging.
Neurobiology of aging 2006;27(11):1705-14.
2006: Kiri L Brickell; Ellen J Steinbart; Malia Rumbaugh; Haydeh Payami; Gerard D Schellenberg; Vivianna M Van Deerlin; Wuxing Yuan; Thomas D Bird
Early-onset Alzheimer disease in families with late-onset Alzheimer disease: a potential important subtype of familial Alzheimer disease.
Archives of neurology 2006;63(9):1307-11.
2006: Debby W Tsuang; Robert G Riekse; Kristina M Purganan; Andrew C David; Thomas J Montine; Gerard D Schellenberg; Ellen J Steinbart; Eric C Petrie; Thomas D Bird; James B Leverenz
Lewy body pathology in late-onset familial Alzheimer's disease: a clinicopathological case series.
Journal of Alzheimer's disease : JAD 2006;9(3):235-42.
2006: Erin M Ramos; Ming-Tesh Lin; Eric B Larson; Izumi Maezawa; LH Tseng; Karen L Edwards; Gerard D Schellenberg; John A Hansen; Walter A Kukull; Lee-Way Jin
Tumor necrosis factor alpha and interleukin 10 promoter region polymorphisms and risk of late-onset Alzheimer disease.
Archives of neurology 2006;63(8):1165-9.
2006: Elaine Peskind; Ge Li; Jane B Shofer; Joseph F Quinn; Jeffrey A Kaye; Christopher M Clark; Martin R Farlow; Charles DeCarli; Murray A Raskind; Gerard D Schellenberg; Virginia M-Y Lee; Douglas Galasko
Age and apolipoprotein E*4 allele effects on cerebrospinal fluid beta-amyloid 42 in adults with normal cognition.
Archives of neurology 2006;63(7):936-9.
2006: Brian C. Kraemer; Jack K Burgess; Jin H Chen; James H Thomas; Gerard D Schellenberg
Molecular pathways that influence human tau-induced pathology in Caenorhabditis elegans.
Human molecular genetics 2006;15(9):1483-96.
2006: Roneil Malkani; Ian D'Souza; Katrina Gwinn-Hardy; Gerard D Schellenberg; John Hardy; Parastoo Momeni
A MAPT mutation in a regulatory element upstream of exon 10 causes frontotemporal dementia.
Neurobiology of disease 2006;22(2):401-3.
2006: Christopher S Carlson; Patrick J Heagerty; Thomas S Hatsukami; Rebecca J Richter; Jane Ranchalis; Julieann Lewis; Tamara J Bacus; Laura A McKinstry; Gerard D Schellenberg; Mark J Rieder; Deborah A Nickerson; Clement E Furlong; Alan Chait; Gail P Jarvik
TagSNP analyses of the PON gene cluster: effects on PON1 activity, LDL oxidative susceptibility, and vascular disease.
Journal of lipid research 2006;47(5):1014-24.
2006: James B Leverenz; Mark A Fishel; Elaine Peskind; Thomas J Montine; David Nochlin; Ellen J Steinbart; Murray A Raskind; Gerard D Schellenberg; Thomas D Bird; Debby W Tsuang
Lewy body pathology in familial Alzheimer disease: evidence for disease- and mutation-specific pathologic phenotype.
Archives of neurology 2006;63(3):370-6.
2006: Mark Reger; G Stennis Watson; W H Frey; Laura D Baker; Brenna Cholerton; M L Keeling; D A Belongia; Mark A Fishel; Stephen R Plymate; Gerard D Schellenberg; Monique M Cherrier; Suzanne Craft
Effects of intranasal insulin on cognition in memory-impaired older adults: modulation by APOE genotype.
Neurobiology of aging 2006;27(3):451-8.
2006: Ian D'Souza; Gerard D Schellenberg
Arginine/serine-rich protein interaction domain-dependent modulation of a tau exon 10 splicing enhancer: altered interactions and mechanisms for functionally antagonistic FTDP-17 mutations Delta280K AND N279K.
The Journal of biological chemistry 2006;281(5):2460-9.
2006: Gerard D Schellenberg
Early Alzheimer's disease genetics.
Journal of Alzheimer's disease : JAD 2006;9(3 Suppl):367-72.
2006: Cyrus Zabetian; Chris J Lauricella; Debby W Tsuang; James B Leverenz; Gerard D Schellenberg; Haydeh Payami
Analysis of the LRRK2 G2019S mutation in Alzheimer Disease.
Archives of neurology 2006;63(1):156-7.
2005: Xiaohong Li; Lewis P Rowland; Hiroshi Mitsumoto; Serge Przedborski; Thomas D Bird; Gerard D Schellenberg; Elaine Peskind; Nancy Johnson; Teepu Siddique; Marek-Marsel Mesulam; Sandra Weintraub; James A Mastrianni
Prion protein codon 129 genotype prevalence is altered in primary progressive aphasia.
Annals of neurology 2005;58(6):858-64.
2005: Gary E Swan; Christina N Lessov-Schlaggar; Dorit Carmelli; Gerard D Schellenberg; Asenath La Rue
Apolipoprotein E epsilon4 and change in cognitive functioning in community-dwelling older adults.
Journal of geriatric psychiatry and neurology 2005;18(4):196-201.
2005: Bernie Devlin; Edwin H Cook; Hilary Coon; Geraldine Dawson; Elena L Grigorenko; William M McMahon; Nancy J Minshew; David Pauls; Moyra Smith; M Anne Spence; Patricia M Rodier; Stodgell Christopher; Gerard D Schellenberg
Autism and the serotonin transporter: the long and short of it.
Molecular psychiatry 2005;10(12):1110-6.
2005: Stephen Faraone; Andrew D Skol; Debby W Tsuang; Keith A Young; Susan L Haverstock; Sarita Prabhudesai; Felicitas Mena; Aerath Sri Kumar Menon; L Leong; F Sautter; Charlene Baldwin; Stephen F Bingham; David Weiss; Joseph F Collins; Tim Keith; J L Vanden Eng; Michael Boehnke; Ming T Tsuang; Gerard D Schellenberg
Genome scan of schizophrenia families in a large Veterans Affairs Cooperative Study sample: evidence for linkage to 18p11.32 and for racial heterogeneity on chromosomes 6 and 14.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2005;139B(1):91-100.
2005: Rosa Rademakers; Stacey Melquist; Marc Cruts; Jessie Theuns; Jurgen Del-Favero; Parvoneh Poorkaj-Navas; Matt Baker; Kristel Sleegers; Richard Crook; Tim De Pooter; Samira Bel Kacem; Jennifer Adamson; Dirk Van den Bossche; Marleen Van den Broeck; Jennifer Gass; Ellen Corsmit; Peter De Rijk; Natalie Thomas; Sebastiaan Engelborghs; Michael G Heckman; Irene Litvan; Julia Crook; Peter Paul De Deyn; dennis dickson; Gerard D Schellenberg; Christine Van Broeckhoven; Michael Hutton
High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy.
Human molecular genetics 2005;14(21):3281-92.
2005: Ge Li; Jane B Shofer; Walter A Kukull; Elaine Peskind; Debby W Tsuang; John C S Breitner; Wayne C McCormick; James D Bowen; Linda Teri; Gerard D Schellenberg; Eric B Larson
Serum cholesterol and risk of Alzheimer disease: a community-based cohort study.
Neurology 2005;65(7):1045-50.
2005: Laura S Rozek; Thomas S Hatsukami; Rebecca J Richter; Jane Ranchalis; Karen Nakayama; Laura A McKinstry; David A Gortner; Edward Boyko; Gerard D Schellenberg; Clement E Furlong; Gail P Jarvik
The correlation of paraoxonase (PON1) activity with lipid and lipoprotein levels differs with vascular disease status.
Journal of lipid research 2005;46(9):1888-95.
2005: Deborah A Hall; Maureen A Leehey; Christopher M Filley; E Steinbart; Thomas J Montine; Gerard D Schellenberg; Patrick Bosque; R Nixon; Thomas D Bird
PRNP H187R mutation associated with neuropsychiatric disorders in childhood and dementia.
Neurology 2005;64(7):1304-6.
2005: Audrey Hendrickson; Laura A McKinstry; Julieann K Lewis; Jeremy Lum; Andy Louie; Gerard D Schellenberg; Thomas S Hatsukami; Alan Chait; Gail P Jarvik
Ex vivo measures of LDL oxidative susceptibility predict carotid artery disease.
Atherosclerosis 2005;179(1):147-53.
2005: Amy R Borenstein; Yougui Wu; James A Mortimer; Gerard D Schellenberg; Wayne C McCormick; James D Bowen; Susan M McCurry; Eric B Larson
Developmental and vascular risk factors for Alzheimer's disease.
Neurobiology of aging 2005;26(3):325-34.
2005: Parvoneh Poorkaj-Navas; Lina Moses; Jennifer S Montimurro; John G Nutt; Gerard D Schellenberg; Haydeh Payami
Parkin mutation dosage and the phenomenon of anticipation: a molecular genetic study of familial parkinsonism.
BMC neurology 2005;5(1):4.
2005: Ellen M Wijsman; E Warwick Daw; Xuesong Yu; Ellen J Steinbart; David Nochlin; Thomas D Bird; Gerard D Schellenberg
APOE and other loci affect age-at-onset in Alzheimer's disease families with PS2 mutation.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2005;132B(1):14-20.
2005: Ian D'Souza; Gerard D Schellenberg
Regulation of tau isoform expression and dementia.
Biochimica et biophysica acta 2005;1739(2-3):104-15.
2005: Geraldine Dawson; Sara Jane Webb; Ellen M Wijsman; Gerard D Schellenberg; Annette Estes; Jeffrey Munson; Susan Faja
Neurocognitive and electrophysiological evidence of altered face processing in parents of children with autism: implications for a model of abnormal development of social brain circuitry in autism.
Development and psychopathology 2005;17(3):679-97.
2005: Yun Ju Sung; Geraldine Dawson; Jeffrey Munson; Annette Estes; Gerard D Schellenberg; Ellen M Wijsman
Genetic investigation of quantitative traits related to autism: use of multivariate polygenic models with ascertainment adjustment.
American journal of human genetics 2005;76(1):68-81.
2004: Ge Li; Roger Higdon; Walter A Kukull; Elaine Peskind; K Van Valen Moore; Debby W Tsuang; Gerald van Belle; Wayne C McCormick; James D Bowen; Linda Teri; Gerard D Schellenberg; Eric B Larson
Statin therapy and risk of dementia in the elderly: a community-based prospective cohort study.
Neurology 2004;63(9):1624-8.
2004: Chang-En Yu; Bernie Devlin; Nichole Galloway; Elaine Loomis; Gerard D Schellenberg
ADLAPH: A molecular haplotyping method based on allele-discriminating long-range PCR.
Genomics 2004;84(3):600-12.
2004: Ellen M Wijsman; E Warwick Daw; Chang-En Yu; Haydeh Payami; Ellen J Steinbart; David Nochlin; Erin M Conlon; Thomas D Bird; Gerard D Schellenberg
Evidence for a novel late-onset Alzheimer disease locus on chromosome 19p13.2.
American journal of human genetics 2004;75(3):398-409.
2004: Parvoneh Poorkaj-Navas; John G Nutt; D James; Steven Gancher; Thomas D Bird; Ellen J Steinbart; Gerard D Schellenberg; Haydeh Payami
parkin mutation analysis in clinic patients with early-onset Parkinson [corrected] disease.
American journal of medical genetics. Part A 2004;129A(1):44-50.
2004: Bernie Devlin; Pamela Bennett; Geraldine Dawson; Denise A Figlewicz; Elena L Grigorenko; William M McMahon; Nancy J Minshew; David Pauls; Moyra Smith; M Anne Spence; Patricia M Rodier; Stodgell Christopher; Gerard D Schellenberg
Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA network.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2004;126B(1):46-50.
2003: Gerard D Schellenberg
Alzheimer disease genes: presenilin 2 mutation number 9 and still counting.
Archives of neurology 2003;60(11):1521-2.
2003: William T Longstreth; Gerard D Schellenberg; Carol E Fahrenbruch; Leonard A Cobb; Michael K Copass; D S Siscovick
Apolipoprotein E genotypes and outcome from out of hospital cardiac arrest.
Journal of neurology, neurosurgery, and psychiatry 2003;74(10):1441-3.
2003: Katsutoshi Furukawa; Yue Wang; Pamela J Yao; Weiming Fu; Mark P Mattson; Yasuto Itoyama; Hiroshi Onodera; Ian D'Souza; Parvoneh Poorkaj-Navas; Thomas D Bird; Gerard D Schellenberg
Alteration in calcium channel properties is responsible for the neurotoxic action of a familial frontotemporal dementia tau mutation.
Journal of neurochemistry 2003;87(2):427-36.
2003: Brian C. Kraemer; Bin Zhang; James B Leverenz; James H Thomas; John Q Trojanowski; Gerard D Schellenberg
Neurodegeneration and defective neurotransmission in a Caenorhabditis elegans model of tauopathy.
Proceedings of the National Academy of Sciences of the United States of America 2003;100(17):9980-5.
2003: Suzanne Craft; Sanjay Asthana; David G Cook; Laura D Baker; Monique M Cherrier; Kristina M Purganan; Colby Wait; Andreana Petrova; Shawn Latendresse; G Stennis Watson; John W Newcomer; Gerard D Schellenberg; Aaron J Krohn
Insulin dose-response effects on memory and plasma amyloid precursor protein in Alzheimer's disease: interactions with apolipoprotein E genotype.
Psychoneuroendocrinology 2003;28(6):809-22.
2003: Gail P Jarvik; Thomas S Hatsukami; Chris Carlson; Rebecca J Richter; Rachel Jampsa; Victoria H Brophy; Sadie Margolin; Mark J Rieder; Deborah A Nickerson; Gerard D Schellenberg; Patrick J Heagerty; Clement E Furlong
Paraoxonase activity, but not haplotype utilizing the linkage disequilibrium structure, predicts vascular disease.
Arteriosclerosis, thrombosis, and vascular biology 2003;23(8):1465-71.
2003: Andrew D Skol; Keith A Young; Debby W Tsuang; Stephen Faraone; Susan L Haverstock; Stephen F Bingham; Sarita Prabhudesai; Felicitas Mena; Aerath Sri Kumar Menon; Chang-En Yu; Paul Rundell; John Pepple; F Sauter; Charlene Baldwin; David Weiss; Joseph F Collins; Tim Keith; Michael Boehnke; Gerard D Schellenberg; Ming T Tsuang
Modest evidence for linkage and possible confirmation of association between NOTCH4 and schizophrenia in a large Veterans Affairs Cooperative Study sample.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003;118B(1):8-15.
2003: David G Cook; James B Leverenz; Pamela J McMillan; J Jacob Kulstad; Sasha Ericksen; Richard A Roth; Gerard D Schellenberg; Lee-Way Jin; Kristina S Kovacina; Suzanne Craft
Reduced hippocampal insulin-degrading enzyme in late-onset Alzheimer's disease is associated with the apolipoprotein E-epsilon4 allele.
The American journal of pathology 2003;162(1):313-9.
2002: Walter A Kukull; Roger Higdon; James D Bowen; Wayne C McCormick; Linda Teri; Gerard D Schellenberg; Gerald van Belle; Lance Jolley; Eric B Larson
Dementia and Alzheimer disease incidence: a prospective cohort study.
Archives of neurology 2002;59(11):1737-46.
2002: Parvoneh Poorkaj-Navas; Nancy A Muma; Victoria Zhukareva; Elizabeth J Cochran; Kathleen M Shannon; Howard I Hurtig; William Koller; Thomas D Bird; John Q Trojanowski; Virginia M-Y Lee; Gerard D Schellenberg
An R5L tau mutation in a subject with a progressive supranuclear palsy phenotype.
Annals of neurology 2002;52(4):511-6.
2002: Bernie Devlin; Pamela Bennett; Edwin H Cook; Geraldine Dawson; David Gonen; Elena L Grigorenko; William M McMahon; David Pauls; Moyra Smith; M Anne Spence; Gerard D Schellenberg
No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA network.
American journal of medical genetics 2002;114(6):667-72.
2002: Stephen Faraone; Andrew D Skol; Debby W Tsuang; Stephen F Bingham; Keith A Young; Sarita Prabhudesai; Susan L Haverstock; Felicitas Mena; Aerath Sri Kumar Menon; Darren Bisset; John Pepple; Fred Sautter; Charlene Baldwin; David Weiss; Joseph F Collins; Tim Keith; Michael Boehnke; Ming T Tsuang; Gerard D Schellenberg
Linkage of chromosome 13q32 to schizophrenia in a large veterans affairs cooperative study sample.
American journal of medical genetics 2002;114(6):598-604.
2002: Gail P Jarvik; Nancey Trevanian Tsai; Laura A McKinstry; Roohi Wani; Victoria H Brophy; Rebecca J Richter; Gerard D Schellenberg; Patrick J Heagerty; Thomas S Hatsukami; Clement E Furlong
Vitamin C and E intake is associated with increased paraoxonase activity.
Arteriosclerosis, thrombosis, and vascular biology 2002;22(8):1329-33.
2002: Razia Sultana; Chang-En Yu; Jun Yu; Jeffrey Munson; Donghui Chen; Wenhui Hua; Annette Estes; Fanny Cortes; Flora de la Barra; Dongmei Yu; Syed T Haider; Barbara J Trask; Eric Green; Wendy H Raskind; Christine M Disteche; Ellen M Wijsman; Geraldine Dawson; Daniel R Storm; Gerard D Schellenberg; Enrique C Villacres
Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins.
Genomics 2002;80(2):129-34.
2002: Ian D'Souza; Gerard D Schellenberg
tau Exon 10 expression involves a bipartite intron 10 regulatory sequence and weak 5' and 3' splice sites.
The Journal of biological chemistry 2002;277(29):26587-99.
2002: Chang-En Yu; Geraldine Dawson; Jeffrey Munson; Ian D'Souza; Julie Osterling; Annette Estes; Anne-Louise Leutenegger; Pamela Flodman; Moyra Smith; Wendy H Raskind; M Anne Spence; William M McMahon; Ellen M Wijsman; Gerard D Schellenberg
Presence of large deletions in kindreds with autism.
American journal of human genetics 2002;71(1):100-15.
2002: Sepideh Zareparsi; D M James; Jeffrey A Kaye; Thomas D Bird; Gerard D Schellenberg; Haydeh Payami
HLA-A2 homozygosity but not heterozygosity is associated with Alzheimer disease.
Neurology 2002;58(6):973-5.
2002: Douglas Galasko; David P Salmon; Ulla-Katrina Craig; Leon J Thal; Gerard D Schellenberg; Wigbert Wiederholt
Clinical features and changing patterns of neurodegenerative disorders on Guam, 1997-2000.
Neurology 2002;58(1):90-7.
2002: Geraldine Dawson; Sara Webb; Gerard D Schellenberg; Stephen R Dager; Seth Friedman; Elizabeth H Aylward; Todd Richards
Defining the broader phenotype of autism: genetic, brain, and behavioral perspectives.
Development and psychopathology 2002;14(3):581-611.
2002: Steven D Edland; Vincent O Tobe; Mark J Rieder; James D Bowen; Wayne C McCormick; Linda Teri; Gerard D Schellenberg; Eric B Larson; Deborah A Nickerson; Walter A Kukull
Mitochondrial genetic variants and Alzheimer disease: a case-control study of the T4336C and G5460A variants.
Alzheimer disease and associated disorders 2002;16(1):1-7.
2001: Debby W Tsuang; Andrew D Skol; Stephen Faraone; Stephen F Bingham; Keith A Young; Sarita Prabhudesai; Susan L Haverstock; Felicitas Mena; Aerath Sri Kumar Menon; D Bisset; John Pepple; F Sauter; Charlene Baldwin; David Weiss; Joseph F Collins; Michael Boehnke; Gerard D Schellenberg; Ming T Tsuang
Examination of genetic linkage of chromosome 15 to schizophrenia in a large Veterans Affairs Cooperative Study sample.
American journal of medical genetics 2001;105(8):662-8.
2001: Parvoneh Poorkaj-Navas; Debby W Tsuang; Ellen M Wijsman; Ellen J Steinbart; Ralph M Garruto; Ulla-Katrina Craig; N H Chapman; L Anderson; Thomas D Bird; Chris C Plato; Daniel P Perl; W Weiderholt; Douglas Galasko; Gerard D Schellenberg
TAU as a susceptibility gene for amyotropic lateral sclerosis-parkinsonism dementia complex of Guam.
Archives of neurology 2001;58(11):1871-8.
2001: Amy Borenstein-Graves; James A Mortimer; James D Bowen; Wayne C McCormick; Susan M McCurry; Gerard D Schellenberg; Eric B Larson
Head circumference and incident Alzheimer's disease: modification by apolipoprotein E.
Neurology 2001;57(8):1453-60.
2001: Parvoneh Poorkaj-Navas; Arnold Kas; Ian D'Souza; Y Zhou; Q Pham; M Stone; Maynard V Olson; Gerard D Schellenberg
A genomic sequence analysis of the mouse and human microtubule-associated protein tau.
Mammalian genome : official journal of the International Mammalian Genome Society 2001;12(9):700-12.
2001: Victoria Moceri; Walter A Kukull; I Emanual; Gerald van Belle; Jacqueline R Starr; Gerard D Schellenberg; Wayne C McCormick; James D Bowen; Linda Teri; Eric B Larson
Using census data and birth certificates to reconstruct the early-life socioeconomic environment and the relation to the development of Alzheimer's disease.
Epidemiology (Cambridge, Mass.) 2001;12(4):383-9.
2001: Elaine Peskind; Charles William Wilkinson; Eric C Petrie; Gerard D Schellenberg; Murray A Raskind
Increased CSF cortisol in AD is a function of APOE genotype.
Neurology 2001;56(8):1094-8.
2001: Parvoneh Poorkaj-Navas; Murray Grossman; Ellen J Steinbart; Haydeh Payami; A Sadovnick; David Nochlin; Takeshi Tabira; John Q Trojanowski; Soo Borson; Douglas Galasko; Stephen G Reich; B Quinn; Gerard D Schellenberg; Thomas D Bird
Frequency of tau gene mutations in familial and sporadic cases of non-Alzheimer dementia.
Archives of neurology 2001;58(3):383-7.
2001: Thomas D Bird; Gerard D Schellenberg
The case of the missing tau, or, why didn't the mRNA bark?
Annals of neurology 2001;49(2):144-5.
2001: Fred Baskin; Roger Rosenberg; L Iyer; Gerard D Schellenberg; Linda Hynan; L E Nee
Platelet APP isoform ratios in asymptomatic young adults expressing an AD-related presenilin-1 mutation.
Journal of the neurological sciences 2001;183(1):85-8.
2000: Gail P Jarvik; Laura S Rozek; Victoria H Brophy; Thomas S Hatsukami; Rebecca J Richter; Gerard D Schellenberg; Clement E Furlong
Paraoxonase (PON1) phenotype is a better predictor of vascular disease than is PON1(192) or PON1(55) genotype.
Arteriosclerosis, thrombosis, and vascular biology 2000;20(11):2441-7.
2000: Parvoneh Poorkaj-Navas; K R Peterson; Gerard D Schellenberg
Single-step conversion of P1 and P1 artificial chromosome clones into yeast artificial chromosomes.
Genomics 2000;68(1):106-10.
2000: Victoria H Brophy; Gail P Jarvik; Rebecca J Richter; Laura S Rozek; Gerard D Schellenberg; Clement E Furlong
Analysis of paraoxonase (PON1) L55M status requires both genotype and phenotype.
Pharmacogenetics 2000;10(5):453-60.
2000: Ian D'Souza; Gerard D Schellenberg
Determinants of 4-repeat tau expression. Coordination between enhancing and inhibitory splicing sequences for exon 10 inclusion.
The Journal of biological chemistry 2000;275(23):17700-9.
2000: I Litvan; dennis dickson; J A Buttner-Ennever; André Delacourte; Michael Hutton; Bruno Dubois; Lawrence I Golbe; Mark Hallett; Gerard D Schellenberg; D Standaert; David J Brooks; Donald L Price
Research goals in progressive supranuclear palsy. First International Brainstorming Conference on PSP.
Movement disorders : official journal of the Movement Disorder Society 2000;15(3):446-58.
2000: Gerard D Schellenberg; Ian D'Souza; Parvoneh Poorkaj-Navas
The genetics of Alzheimer's disease.
Current psychiatry reports 2000;2(2):158-64.
2000: Suzanne Craft; Sanjay Asthana; Gerard D Schellenberg; Laura D Baker; Monique M Cherrier; A A Boyt; Ralph N Martins; Murray A Raskind; Elaine Peskind; Stephen R Plymate
Insulin effects on glucose metabolism, memory, and plasma amyloid precursor protein in Alzheimer's disease differ according to apolipoprotein-E genotype.
Annals of the New York Academy of Sciences 2000;903():222-8.
2000: K Furukawa; Ian D'Souza; C H Crudder; H Onodera; Y Itoyama; Parvoneh Poorkaj-Navas; Thomas D Bird; Gerard D Schellenberg
Pro-apoptotic effects of tau mutations in chromosome 17 frontotemporal dementia and parkinsonism.
Neuroreport 2000;11(1):57-60.
2000: E Warwick Daw; Haydeh Payami; EJ Nemens; David Nochlin; Thomas D Bird; Gerard D Schellenberg; Ellen M Wijsman
The number of trait loci in late-onset Alzheimer disease.
American journal of human genetics 2000;66(1):196-204.
1999: Debby W Tsuang; Eric B Larson; J Bowen; Wayne C McCormick; Linda Teri; David Nochlin; James B Leverenz; Elaine Peskind; A Lim; Murray A Raskind; Mary Lou Thompson; Suzanne S Mirra; Marla Gearing; Gerard D Schellenberg; Walter A Kukull
The utility of apolipoprotein E genotyping in the diagnosis of Alzheimer disease in a community-based case series.
Archives of neurology 1999;56(12):1489-95.
1999: A B Graves; James D Bowen; Lakshminarayan Rajaram; Wayne C McCormick; Susan M McCurry; Gerard D Schellenberg; Eric B Larson
Impaired olfaction as a marker for cognitive decline: interaction with apolipoprotein E epsilon4 status.
Neurology 1999;53(7):1480-7.
1999: Gil Blander; Jonathan Kipnis; Juan Fernando Martinez Leal; Chang-En Yu; Gerard D Schellenberg; Moshe Oren
Physical and functional interaction between p53 and the Werner's syndrome protein.
The Journal of biological chemistry 1999;274(41):29463-9.
1999: Philip Bretsky; J Galen Buckwalter; Teresa Seeman; C A Miller; J Poirier; Gerard D Schellenberg; Caleb E Finch; Victor W. Henderson
Evidence for an interaction between apolipoprotein E genotype, gender, and Alzheimer disease.
Alzheimer disease and associated disorders 1999;13(4):216-21.
1999: Minoru Yasuda; Toshio Kawamata; Osamu Komure; S Kuno; Ian D'Souza; Parvoneh Poorkaj-Navas; J Kawai; Satoshi Tanimukai; Y Yamamoto; Hiroshi Hasegawa; Masakiyo Sasahara; F Hazama; Gerard D Schellenberg; Chikako Tanaka
A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration.
Neurology 1999;53(4):864-8.
1999: Suzanne Craft; Sanjay Asthana; Gerard D Schellenberg; Monique M Cherrier; Laura D Baker; John W Newcomer; Stephen R Plymate; Shawn Latendresse; Andreana Petrova; Murray A Raskind; Elaine Peskind; CP Lofgreen; K Grimwood
Insulin metabolism in Alzheimer's disease differs according to apolipoprotein E genotype and gender.
Neuroendocrinology 1999;70(2):146-52.
1999: Elisa A Spillare; Ana I Robles; Xin Wei Wang; Jiang Cheng Shen; Chang-En Yu; Gerard D Schellenberg; Curtis C Harris
p53-mediated apoptosis is attenuated in Werner syndrome cells.
Genes & development 1999;13(11):1355-60.
1999: Ian D'Souza; Parvoneh Poorkaj-Navas; M Hong; David Nochlin; Virginia M-Y Lee; Thomas D Bird; Gerard D Schellenberg
Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements.
Proceedings of the National Academy of Sciences of the United States of America 1999;96(10):5598-603.
1999: Shigeki Arawaka; M Usami; N Sahara; Gerard D Schellenberg; Gloria Lee; Hiroshi Mori
The tau mutation (val337met) disrupts cytoskeletal networks of microtubules.
Neuroreport 1999;10(5):993-7.
1999: Thomas D Bird; David Nochlin; Parvoneh Poorkaj-Navas; Monique M Cherrier; Jeffrey A Kaye; Haydeh Payami; Elaine Peskind; T H Lampe; EJ Nemens; P J Boyer; Gerard D Schellenberg
A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L)
Brain : a journal of neurology 1999;122 ( Pt 4)():741-56.
1999: M Iijima; Takeshi Tabira; Parvoneh Poorkaj-Navas; Gerard D Schellenberg; John Q Trojanowski; Virginia M-Y Lee; M L Schmidt; K Takahashi; T Nabika; T Matsumoto; Y Yamashita; S Yoshioka; H Ishino
A distinct familial presenile dementia with a novel missense mutation in the tau gene.
Neuroreport 1999;10(3):497-501.
1999: Dorit Carmelli; Gary E Swan; Terry Reed; Gerard D Schellenberg; J C Christian
The effect of apolipoprotein E epsilon4 in the relationships of smoking and drinking to cognitive function.
Neuroepidemiology 1999;18(3):125-33.
1999: Minoru Yasuda; K Maeda; M Hashimoto; H Yamashita; Yoshitaka Ikejiri; Thomas D Bird; Chikako Tanaka; Gerard D Schellenberg
A pedigree with a novel presenilin 1 mutation at a residue that is not conserved in presenilin 2.
Archives of neurology 1999;56(1):65-9.
1998: M Hong; Victoria Zhukareva; Vanessa Vogelsberg-Ragaglia; Zbigniew K Wszolek; L Reed; Bruce L Miller; Daniel Geschwind; Thomas D Bird; Daniel W McKeel; Alison Goate; John C Morris; Kirk Wilhelmsen; Gerard D Schellenberg; John Q Trojanowski; Virginia M-Y Lee
Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17.
Science (New York, N.Y.) 1998;282(5395):1914-7.
1998: LN Clark; Parvoneh Poorkaj-Navas; Zbigniew K Wszolek; Daniel Geschwind; Ziad S Nasreddine; Bruce L Miller; D Li; Haydeh Payami; F Awert; Katerina Markopoulou; A Andreadis; Ian D'Souza; Virginia M-Y Lee; L Reed; John Q Trojanowski; Victoria Zhukareva; Thomas D Bird; Gerard D Schellenberg; Kirk Wilhelmsen
Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17.
Proceedings of the National Academy of Sciences of the United States of America 1998;95(22):13103-7.
1998: James B Leverenz; Chang-En Yu; Gerard D Schellenberg
Aging-associated neuropathology in Werner syndrome.
Acta neuropathologica 1998;96(4):421-4.
1998: Fuki M Hisama; Oshima Junko; Chang-En Yu; Y H Fu; J Mulligan; Sherman M Weissman; Gerard D Schellenberg
Comparison of methods for identifying transcription units and transcription map of the Werner syndrome gene region.
Genomics 1998;52(3):352-7.
1998: Suzanne Craft; Linda Teri; Steven D Edland; Walter A Kukull; Gerard D Schellenberg; Wayne C McCormick; James D Bowen; Eric B Larson
Accelerated decline in apolipoprotein E-epsilon4 homozygotes with Alzheimer's disease.
Neurology 1998;51(1):149-53.
1998: Dorit Carmelli; Gary E Swan; Terry Reed; Bruce L Miller; Philip A Wolf; Gail P Jarvik; Gerard D Schellenberg
Midlife cardiovascular risk factors, ApoE, and cognitive decline in elderly male twins.
Neurology 1998;50(6):1580-5.
1998: K Furukawa; Qing Guo; Gerard D Schellenberg; Mark P Mattson
Presenilin-1 mutation alters NGF-induced neurite outgrowth, calcium homeostasis, and transcription factor (AP-1) activation in PC12 cells.
Journal of neuroscience research 1998;52(5):618-24.
1998: Parvoneh Poorkaj-Navas; Thomas D Bird; Ellen M Wijsman; EJ Nemens; Ralph M Garruto; L Anderson; A Andreadis; Wigbert Wiederholt; Murray A Raskind; Gerard D Schellenberg
Tau is a candidate gene for chromosome 17 frontotemporal dementia.
Annals of neurology 1998;43(6):815-25.
1998: Takeshi Ikeuchi; K Sanpei; H Takano; H Sasaki; K Tashiro; G Cancel; Alexis Brice; Thomas D Bird; Gerard D Schellenberg; Margaret Pericak-Vance; K A Welsh-Bohmer; L N Clark; Kirk Wilhelmsen; Shoji Tsuji
A novel long and unstable CAG/CTG trinucleotide repeat on chromosome 17q.
Genomics 1998;49(2):321-6.
1998: V Sharma; Parvoneh Poorkaj-Navas; Fuki M Hisama; L Bonnycastle; Chang-En Yu; H Massa; Barbara J Trask; Kevin Clancy; D Patterson; Sherman M Weissman; Gerard D Schellenberg
An expression map from human chromosome 14q24.3.
Genomics 1998;47(2):314-8.
1998: Jean P Hubble; J H Kurth; S L Glatt; M C Kurth; Gerard D Schellenberg; R E Hassanein; A Lieberman; William Koller
Gene-toxin interaction as a putative risk factor for Parkinson's disease with dementia.
Neuroepidemiology 1998;17(2):96-104.
1998: Parvoneh Poorkaj-Navas; V Sharma; L Anderson; EJ Nemens; M E Alonso; H Orr; J White; L Heston; Thomas D Bird; Gerard D Schellenberg
Missense mutations in the chromosome 14 familial Alzheimer's disease presenilin 1 gene.
Human mutation 1998;11(3):216-21.
1998: Suzanne Craft; Elaine Peskind; Michael W Schwartz; Gerard D Schellenberg; Murray A Raskind; Daniel Porte
Cerebrospinal fluid and plasma insulin levels in Alzheimer's disease: relationship to severity of dementia and apolipoprotein E genotype.
Neurology 1998;50(1):164-8.
1997: Elaine Peskind; James B Leverenz; Martin R Farlow; R K Ito; S A Provow; R S Siegel; M Cleveland; C H Morgan; M R Pandian; S Corbin; David Nochlin; Gerard D Schellenberg; Murray A Raskind; S L Wagner
Clinicopathologic correlations of soluble amyloid beta-protein precursor in cerebrospinal fluid in patients with Alzheimer disease and controls.
Alzheimer disease and associated disorders 1997;11(4):201-6.
1997: Sepideh Zareparsi; Jeffrey A Kaye; Richard Camicioli; H Grimslid; Barry S Oken; M Litt; John G Nutt; Thomas D Bird; Gerard D Schellenberg; Haydeh Payami
Modulation of the age at onset of Parkinson's disease by apolipoprotein E genotypes.
Annals of neurology 1997;42(4):655-8.
1997: Ellen S O'Meara; Walter A Kukull; Elizabeth A Sheppard; James D Bowen; W C McCormick; Linda Teri; M Pfanschmidt; J D Thompson; Gerard D Schellenberg; Eric B Larson
Head injury and risk of Alzheimer's disease by apolipoprotein E genotype.
American journal of epidemiology 1997;146(5):373-84.
1997: Haydeh Payami; Gerard D Schellenberg; Sepideh Zareparsi; Jeffrey A Kaye; Gary Sexton; M A Head; S S Matsuyama; Lissy Jarvik; Bruce L Miller; D Q McManus; Thomas D Bird; Robert Katzman; L Heston; Douglas J Norman; Gary W Small
Evidence for association of HLA-A2 allele with onset age of Alzheimer's disease.
Neurology 1997;49(2):512-8.
1997: Gail P Jarvik; Ellen L Goode; Melissa A Austin; J Auwerx; S Deeb; Gerard D Schellenberg; T Reed
Evidence that the apolipoprotein E-genotype effects on lipid levels can change with age in males: a longitudinal analysis.
American journal of human genetics 1997;61(1):171-81.
1997: Thomas D Bird; Ellen M Wijsman; David Nochlin; M Leehey; Shuzo M Sumi; Haydeh Payami; Parvoneh Poorkaj-Navas; EJ Nemens; M Rafkind; Gerard D Schellenberg
Chromosome 17 and hereditary dementia: linkage studies in three non-Alzheimer families and kindreds with late-onset FAD.
Neurology 1997;48(4):949-54.
1997: Chang-En Yu; Oshima Junko; Ellen M Wijsman; Jun Nakura; T Miki; C Piussan; S Matthews; Y H Fu; J Mulligan; George M Martin; Gerard D Schellenberg
Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group.
American journal of human genetics 1997;60(2):330-41.
1997: Debby W Tsuang; Murray A Raskind; James B Leverenz; Elaine Peskind; Gerard D Schellenberg; Thomas D Bird
The effect of apolipoprotein E genotype on expression of an autosomal dominant schizophreniform disorder with progressive dementia and neurofibrillary tangles.
Biological psychiatry 1997;41(2):191-5.
1997: Ellen S O'Meara; Walter A Kukull; Gerard D Schellenberg; James D Bowen; W C McCormick; Linda Teri; M Pfanschmidt; J D Thompson; Eric B Larson
Alzheimer's disease and history of blood transfusion by apolipoprotein-E genotype.
Neuroepidemiology 1997;16(2):86-93.
1996: Thomas D Bird; Ephrat Levy-Lahad; Parvoneh Poorkaj-Navas; V Sharma; EJ Nemens; Amnon Lahad; T H Lampe; Gerard D Schellenberg
Wide range in age of onset for chromosome 1--related familial Alzheimer's disease.
Annals of neurology 1996;40(6):932-6.
1996: Masaki Ikeda; V Sharma; Shuzo M Sumi; Ekaterina Rogaeva; Parvoneh Poorkaj-Navas; R Sherrington; Linda E Nee; T Tsuda; N Oda; M Watanabe; M Aoki; Mikio Shoji; K Abe; Y Itoyama; S Hirai; Gerard D Schellenberg; Thomas D Bird; Peter St George-Hyslop
The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patients.
Annals of neurology 1996;40(6):912-7.
1996: Oshima Junko; Chang-En Yu; C Piussan; G Klein; J Jabkowski; S Balci; T Miki; Jun Nakura; T Ogihara; J Ells; M Smith; M I Melaragno; M Fraccaro; Susi Scappaticci; J Matthews; S Ouais; A Jarzebowicz; Gerard D Schellenberg; George M Martin
Homozygous and compound heterozygous mutations at the Werner syndrome locus.
Human molecular genetics 1996;5(12):1909-13.
1996: Pamela J McMillan; James B Leverenz; Parvoneh Poorkaj-Navas; Gerard D Schellenberg; Daniel M Dorsa
Neuronal expression of STM2 mRNA in human brain is reduced in Alzheimer's disease.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 1996;44(11):1215-22.
1996: Roger Rosenberg; R W Richter; RC Risser; K Taubman; I Prado-Farmer; E Ebalo; J Posey; D Kingfisher; D Dean; Myron Weiner; Doris A Svetlik; P Adams; Lawrence Honig; C Munro Cullum; F V Schaefer; Gerard D Schellenberg
Genetic factors for the development of Alzheimer disease in the Cherokee Indian.
Archives of neurology 1996;53(10):997-1000.
1996: Walter A Kukull; Gerard D Schellenberg; James D Bowen; Wayne C McCormick; Chang-En Yu; Linda Teri; J D Thompson; Ellen S O'Meara; Eric B Larson
Apolipoprotein E in Alzheimer's disease risk and case detection: a case-control study.
Journal of clinical epidemiology 1996;49(10):1143-8.
1996: Jun Nakura; T Miki; L Ye; Noriaki Mitsuda; Y Zhao; K Kihara; Chang-En Yu; Oshima Junko; Ken-Ichiro Fukuchi; Ellen M Wijsman; Gerard D Schellenberg; George M Martin; S i Murano; Katsuyuki Hashimoto; Y Fujiwara; Toshio Ogihara
Narrowing the position of the Werner syndrome locus by homozygosity analysis-extension of homozygosity analysis.
Genomics 1996;36(1):130-41.
1996: Chang-En Yu; Oshima Junko; Fuki M Hisama; S Matthews; Barbara J Trask; Gerard D Schellenberg
A YAC, P1, and cosmid contig and 17 new polymorphic markers for the Werner syndrome region at 8p12-p21.
Genomics 1996;35(3):431-40.
1996: Oshima Junko; Gerard D Schellenberg
[STM-2, a candidate gene for the familial Alzheimer's disease on chromosome 1].
Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme 1996;41(10):1448-52.
1996: Donalyn Scheuner; Christopher B Eckman; M Jensen; X Song; Martin Citron; N Suzuki; Thomas D Bird; John Hardy; Michael Hutton; Walter A Kukull; Eric B Larson; Ephrat Levy-Lahad; Matti Viitanen; Elaine Peskind; Parvoneh Poorkaj-Navas; Gerard D Schellenberg; Rudolph E Tanzi; Wilma Wasco; Lars Lannfelt; Dennis J Selkoe; Steven G Younkin
Secreted amyloid beta-protein similar to that in the senile plaques of Alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease.
Nature medicine 1996;2(8):864-70.
1996: Ephrat Levy-Lahad; Parvoneh Poorkaj-Navas; K Wang; Y H Fu; Oshima Junko; J Mulligan; Gerard D Schellenberg
Genomic structure and expression of STM2, the chromosome 1 familial Alzheimer disease gene.
Genomics 1996;34(2):198-204.
1996: Katrina Goddard; Chang-En Yu; Oshima Junko; T Miki; Jun Nakura; C Piussan; George M Martin; Gerard D Schellenberg; Ellen M Wijsman
Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers.
American journal of human genetics 1996;58(6):1286-302.
1996: Debby W Tsuang; Walter A Kukull; Elizabeth A Sheppard; Ross L Barnhart; Elaine Peskind; Steven D Edland; Gerard D Schellenberg; Murray A Raskind; Eric B Larson
Impact of sample selection on APOE epsilon 4 allele frequency: a comparison of two Alzheimer's disease samples.
Journal of the American Geriatrics Society 1996;44(6):704-7.
1996: Chang-En Yu; Oshima Junko; Y H Fu; Ellen M Wijsman; Fuki M Hisama; R Alisch; S Matthews; Jun Nakura; T Miki; S Ouais; George M Martin; J Mulligan; Gerard D Schellenberg
Positional cloning of the Werner's syndrome gene.
Science (New York, N.Y.) 1996;272(5259):258-62.
1996: A Anouti; K Schmidt; Kelly E Lyons; Jean P Hubble; Gerard D Schellenberg; Lawrence I Golbe; Anthony E Lang; N Galvez-Jimenez; L Hershey; William Koller
Normal distribution of apolipoprotein E alleles in progressive supranuclear palsy.
Neurology 1996;46(4):1156-7.
1996: Haydeh Payami; Sepideh Zareparsi; K R Montee; Gary Sexton; Jeffrey A Kaye; Thomas D Bird; Chang-En Yu; Ellen M Wijsman; L L Heston; M Litt; Gerard D Schellenberg
Gender difference in apolipoprotein E-associated risk for familial Alzheimer disease: a possible clue to the higher incidence of Alzheimer disease in women.
American journal of human genetics 1996;58(4):803-11.
1996: Gail P Jarvik; Eric B Larson; Katrina Goddard; Gerard D Schellenberg; Ellen M Wijsman
Influence of apolipoprotein E genotype on the transmission of Alzheimer disease in a community-based sample.
American journal of human genetics 1996;58(1):191-200.
1995: Ephrat Levy-Lahad; Amnon Lahad; Ellen M Wijsman; Thomas D Bird; Gerard D Schellenberg
Apolipoprotein E genotypes and age of onset in early-onset familial Alzheimer's disease.
Annals of neurology 1995;38(4):678-80.
1995: Gerard D Schellenberg
Genetic dissection of Alzheimer disease, a heterogeneous disorder.
Proceedings of the National Academy of Sciences of the United States of America 1995;92(19):8552-9.
1995: Ephrat Levy-Lahad; Ellen M Wijsman; EJ Nemens; L Anderson; Katrina Goddard; J L Weber; Thomas D Bird; Gerard D Schellenberg
A familial Alzheimer's disease locus on chromosome 1.
Science (New York, N.Y.) 1995;269(5226):970-3.
1995: Gerard D Schellenberg
Progress in Alzheimer's disease genetics.
Current opinion in neurology 1995;8(4):262-7.
1995: Gail P Jarvik; Ellen M Wijsman; Walter A Kukull; Gerard D Schellenberg; Chang-En Yu; Eric B Larson
Interactions of apolipoprotein E genotype, total cholesterol level, age, and sex in prediction of Alzheimer's disease: a case-control study.
Neurology 1995;45(6):1092-6.
1995: Gerard D Schellenberg
Molecular genetics of familial Alzheimer's disease.
Arzneimittel-Forschung 1995;45(3A):418-24.
1994: L L Bonnycastle; Chang-En Yu; C R Hunt; Barbara J Trask; Kevin Clancy; J L Weber; D Patterson; Gerard D Schellenberg
Cloning, sequencing, and mapping of the human chromosome 14 heat shock protein gene (HSPA2).
Genomics 1994;23(1):85-93.
1994: Haydeh Payami; K R Montee; Jeffrey A Kaye; Thomas D Bird; Chang-En Yu; Ellen M Wijsman; Gerard D Schellenberg
Alzheimer's disease, apolipoprotein E4, and gender.
JAMA : the journal of the American Medical Association 1994;271(17):1316-7.
1994: Chang-En Yu; L Anderson; Oshima Junko; Gerard D Schellenberg
Dinucleotide repeat polymorphisms at the GSR gene.
Human molecular genetics 1994;3(1):212.
1994: Chang-En Yu; L Anderson; Oshima Junko; Gerard D Schellenberg
Dinucleotide repeat polymorphism at the FGFR1 gene.
Human molecular genetics 1994;3(1):212.
1994: Chang-En Yu; L Anderson; Oshima Junko; Gerard D Schellenberg
Dinucleotide repeat polymorphism at the D8S131 locus.
Human molecular genetics 1994;3(1):211.
1994: T R Hinds; Walter A Kukull; Gerald van Belle; Gerard D Schellenberg; E C Villacres; Eric B Larson
Relationship between serum alpha 1-antichymotrypsin and Alzheimer's disease.
Neurobiology of aging 1994;15(1):21-7.
1994: Gerard D Schellenberg
Alzheimer's disease: implications of genetic studies.
Neurobiology of aging 1994;15 Suppl 2():S141-4.
1993: C W Fu; L Anderson; Gerard D Schellenberg
Dinucleotide repeat polymorphism at the D14S294 locus.
Human molecular genetics 1993;2(10):1751.
1993: Haydeh Payami; Jeffrey A Kaye; L L Heston; Thomas D Bird; Gerard D Schellenberg
Apolipoprotein E genotype and Alzheimer's disease.
Lancet 1993;342(8873):738.
1993: Gerard D Schellenberg; Haydeh Payami; Ellen M Wijsman; H T Orr; Katrina Goddard; L Anderson; EJ Nemens; J A White; M E Alonso; Melvyn Ball
Chromosome 14 and late-onset familial Alzheimer disease (FAD).
American journal of human genetics 1993;53(3):619-28.
1993: A Cook; Wendy H Raskind; S Blanton; Richard M Pauli; R G Gregg; Clair A Francomano; E Puffenberger; E U Conrad; G Schmale; Gerard D Schellenberg
Genetic heterogeneity in families with hereditary multiple exostoses.
American journal of human genetics 1993;53(1):71-9.
1993: Ellen M Wijsman; Thomas D Bird; George M Martin; Gerard D Schellenberg
The Seattle Alzheimer's disease data set.
Genetic epidemiology 1993;10(6):365-9.
1992: Gerard D Schellenberg; Thomas D Bird; Ellen M Wijsman; H T Orr; L Anderson; EJ Nemens; J A White; L Bonnycastle; J L Weber; M E Alonso
Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14.
Science (New York, N.Y.) 1992;258(5082):668-71.
1992: Gerard D Schellenberg; George M Martin; E M Wijsman; Jun Nakura; T Miki; T Ogihara
Homozygosity mapping and Werner's syndrome.
Lancet 1992;339(8799):1002.
1992: Walter A Kukull; T R Hinds; Gerard D Schellenberg; Gerald van Belle; Eric B Larson
Increased platelet membrane fluidity as a diagnostic marker for Alzheimer's disease: a test in population-based cases and controls.
Neurology 1992;42(3 Pt 1):607-14.
1992: Gerard D Schellenberg; M Boehnke; Ellen M Wijsman; D K Moore; George M Martin; Thomas D Bird
Genetic association and linkage analysis of the apolipoprotein CII locus and familial Alzheimer's disease.
Annals of neurology 1992;31(2):223-7.
1992: Gerard D Schellenberg; K Kamino; E M Bryant; D Moore; Thomas D Bird
Genetic heterogeneity, Down syndrome, and Alzheimer disease.
Progress in clinical and biological research 1992;379():215-26.
1991: Gerard D Schellenberg; L Anderson; S O'dahl; E M Wisjman; A D Sadovnick; Melvyn Ball; Eric B Larson; Walter A Kukull; George M Martin; Allen D Roses
APP717, APP693, and PRIP gene mutations are rare in Alzheimer disease.
American journal of human genetics 1991;49(3):511-7.
1991: KK Hsiao; C Cass; Gerard D Schellenberg; Thomas D Bird; E Devine-Gage; Henryk M Wisniewski; Stanley B Prusiner
A prion protein variant in a family with the telencephalic form of Gerstmann-Sträussler-Scheinker syndrome.
Neurology 1991;41(5):681-4.
1991: Gerard D Schellenberg; Margaret Pericak-Vance; Ellen M Wijsman; D K Moore; Perry C Gaskell; L A Yamaoka; J L Bebout; L Anderson; K A Welsh; C M Clark
Linkage analysis of familial Alzheimer disease, using chromosome 21 markers.
American journal of human genetics 1991;48(3):563-83.
1990: George M Martin; Gerard D Schellenberg; E M Wijsman; Thomas D Bird
Alzheimer's disease. Dominant susceptibility genes.
Nature 1990;347(6289):124.
1990: K Eto; Shuzo M Sumi; Thomas D Bird; T McEvoy-Bush; M Boehnke; Gerard D Schellenberg
Family with dominantly inherited ataxia, amyotrophy, and peripheral sensory loss. Spinopontine atrophy or Machado-Joseph Azorean disease in another non-Portuguese family?
Archives of neurology 1990;47(9):968-74.
1989: Thomas D Bird; Gerard D Schellenberg; Ellen M Wijsman; George M Martin
Evidence for etiologic heterogeneity in Alzheimer's disease.
Neurobiology of aging 1989;10(5):432-4; discussion 446-8.
1989: Thomas D Bird; Shuzo M Sumi; EJ Nemens; David Nochlin; Gerard D Schellenberg; T H Lampe; A Sadovnick; H Chui; G W Miner; J Tinklenberg
Phenotypic heterogeneity in familial Alzheimer's disease: a study of 24 kindreds.
Annals of neurology 1989;25(1):12-25.
1989: Thomas D Bird; T H Lampe; EJ Nemens; Shuzo M Sumi; David Nochlin; Gerard D Schellenberg; Ellen M Wijsman
Characteristics of familial Alzheimer's disease in nine kindreds of Volga German ancestry.
Progress in clinical and biological research 1989;317():229-34.
1989: Gerard D Schellenberg; Thomas D Bird; Ellen M Wijsman; D K Moore; George M Martin
The genetics of Alzheimer's disease.
Biomedicine & pharmacotherapy = Biomédecine & pharmacothérapie 1989;43(7):463-8.
1988: Gerard D Schellenberg; Thomas D Bird; Ellen M Wijsman; D K Moore; M Boehnke; E M Bryant; T H Lampe; David Nochlin; Shuzo M Sumi; Samir S Deeb
Absence of linkage of chromosome 21q21 markers to familial Alzheimer's disease.
Science (New York, N.Y.) 1988;241(4872):1507-10.
1988: Thomas D Bird; T H Lampe; EJ Nemens; G W Miner; Shuzo M Sumi; Gerard D Schellenberg
Familial Alzheimer's disease in American descendants of the Volga Germans: probable genetic founder effect.
Annals of neurology 1988;23(1):25-31.
1987: Gerard D Schellenberg; Samir S Deeb; M Boehnke; E M Bryant; George M Martin; T H Lampe; Thomas D Bird
Association of an apolipoprotein CII allele with familial dementia of the Alzheimer type.
Journal of neurogenetics 1987;4(2-3):97-108.
1987: Thomas D Bird; M Boehnke; Gerard D Schellenberg; S S Deeb; H P Lipe
The use of apolipoprotein CII as a genetic marker for myotonic dystrophy.
Archives of neurology 1987;44(3):273-5.
1987: Thomas D Bird; M Boehnke; J Anderson; T H Lampe; Gerard D Schellenberg; Eric B Larson
The frequency of C4B variants of complement in familial and sporadic Alzheimer disease.
Alzheimer disease and associated disorders 1987;1(4):251-5.
1985: Gerard D Schellenberg; L Anderson; E J Cragoe; P D Swanson
Inhibition of brain mitochondrial Ca2+ transport by amiloride analogues.
Cell calcium 1985;6(5):431-47.
1985: Gerard D Schellenberg; L Anderson; E J Cragoe; P D Swanson
Inhibition of synaptosomal membrane Na+-Ca2+ exchange transport by amiloride and amiloride analogues.
Molecular pharmacology 1985;27(5):537-43.
1984: Gerard D Schellenberg; A Sarthy; A E Larson; M P Backer; J W Crabb; M Lidstrom; B D Hall; C E Furlong
Xylose isomerase from Escherichia coli. Characterization of the protein and the structural gene.
The Journal of biological chemistry 1984;259(11):6826-32.
1983: Gerard D Schellenberg; L Anderson; P D Swanson
Inhibition of Na+-Ca2+ exchange in rat brain by amiloride.
Molecular pharmacology 1983;24(2):251-8.
1982: Gerard D Schellenberg; P D Swanson
Solubilization and reconstitution of membranes containing the Na+ -Ca2+ exchange carrier from rat brain.
Biochimica et biophysica acta 1982;690(1):133-44.
1982: Gerard D Schellenberg; N M Wilson; B R Copeland; C E Furlong
Transketolase from human red blood cells.
Methods in enzymology 1982;90 Pt E():223-8.
1981: Gerard D Schellenberg; I V Pech; W L Stahl
Immunoreactivity of subunits of the (Na+ + K+)-ATPase. Cross-reactivity of the alpha, alpha + and beta forms in different organs and species.
Biochimica et biophysica acta 1981;649(3):691-700.
1981: Gerard D Schellenberg; P D Swanson
Sodium-dependent and calcium-dependent calcium transport by rat brain microsomes.
Biochimica et biophysica acta 1981;648(1):13-27.
1977: Gerard D Schellenberg; C E Furlong
Resolution of the multiplicity of the glutamate and aspartate transport systems of Escherichia coli.
The Journal of biological chemistry 1977;252(24):9055-64.