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Gail Jarvik
Gail Jarvik
Univ Washington, Seattle
Verified email at u.washington.edu
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Cited by
Cited by
Year
Heart disease and stroke statistics—2014 update: a report from the American Heart Association
AS Go, D Mozaffarian, VL Roger, EJ Benjamin, JD Berry, MJ Blaha, S Dai, ...
circulation 129 (3), e28-e292, 2014
77099*2014
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
BW Kunkle, B Grenier-Boley, R Sims, JC Bis, V Damotte, AC Naj, ...
Nature genetics 51 (3), 414-430, 2019
24862019
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
AC Naj, G Jun, GW Beecham, LS Wang, BN Vardarajan, J Buros, ...
Nature genetics 43 (5), 436-441, 2011
22242011
Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data
JC Denny, L Bastarache, MD Ritchie, RJ Carroll, R Zink, JD Mosley, ...
Nature biotechnology 31 (12), 1102-1111, 2013
10512013
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
R Sims, SJ Van Der Lee, AC Naj, C Bellenguez, N Badarinarayan, ...
Nature genetics 49 (9), 1373-1384, 2017
9652017
The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies
CA McCarty, RL Chisholm, CG Chute, IJ Kullo, GP Jarvik, EB Larson, R Li, ...
BMC medical genomics 4, 1-11, 2011
7902011
Presence of intraplaque hemorrhage stimulates progression of carotid atherosclerotic plaques: a high-resolution magnetic resonance imaging study
N Takaya, C Yuan, B Chu, T Saam, NL Polissar, GP Jarvik, C Isaac, ...
Circulation 111 (21), 2768-2775, 2005
6992005
Rare and low-frequency coding variants alter human adult height
E Marouli, M Graff, C Medina-Gomez, KS Lo, AR Wood, TR Kjaer, RS Fine, ...
Nature 542 (7640), 186-190, 2017
6792017
Detectable clonal mosaicism from birth to old age and its relationship to cancer
CC Laurie, CA Laurie, K Rice, KF Doheny, LR Zelnick, CP McHugh, ...
Nature genetics 44 (6), 642-650, 2012
6592012
Performance of ACMG-AMP variant-interpretation guidelines among nine laboratories in the clinical sequencing exploratory research consortium
LM Amendola, GP Jarvik, MC Leo, HM McLaughlin, Y Akkari, MD Amaral, ...
The American Journal of Human Genetics 98 (6), 1067-1076, 2016
6342016
The electronic medical records and genomics (eMERGE) network: past, present, and future
O Gottesman, H Kuivaniemi, G Tromp, WA Faucett, R Li, TA Manolio, ...
Genetics in Medicine 15 (10), 761-771, 2013
6222013
The power of genetic diversity in genome-wide association studies of lipids
SE Graham, SL Clarke, KHH Wu, S Kanoni, GJM Zajac, S Ramdas, ...
Nature 600 (7890), 675-679, 2021
5822021
Effects of 5′ regulatory-region polymorphisms on paraoxonase-gene (PON1) expression
VH Brophy, RL Jampsa, JB Clendenning, LA McKinstry, GP Jarvik, ...
The American journal of human genetics 68 (6), 1428-1436, 2001
5142001
Interactions of apolipoprotein E genotype, total cholesterol level, age, and sex in prediction of Alzheimer's disease: a case‐control study
GP Jarvik, EM Wijsman, WA Kukull, GD Schellenberg, C Yu, EB Larson
Neurology 45 (6), 1092-1096, 1995
4971995
Quality control procedures for genome‐wide association studies
S Turner, LL Armstrong, Y Bradford, CS Carlson, DC Crawford, ...
Current protocols in human genetics 68 (1), 1.19. 1-1.19. 18, 2011
4922011
Return of genomic results to research participants: the floor, the ceiling, and the choices in between
GP Jarvik, LM Amendola, JS Berg, K Brothers, EW Clayton, W Chung, ...
The American Journal of Human Genetics 94 (6), 818-826, 2014
4372014
Actionable, pathogenic incidental findings in 1,000 participants’ exomes
MO Dorschner, LM Amendola, EH Turner, PD Robertson, BH Shirts, ...
The American Journal of Human Genetics 93 (4), 631-640, 2013
4232013
Evidence for a rare prostate cancer–susceptibility locus at chromosome 1p36
M Gibbs, JL Stanford, RA McIndoe, GP Jarvik, S Kolb, EL Goode, ...
The American Journal of Human Genetics 64 (3), 776-787, 1999
4201999
Paraoxonase (PON1) Phenotype Is a Better Predictor of Vascular Disease Than Is PON1192 or PON155 Genotype
GP Jarvik, LS Rozek, VH Brophy, TS Hatsukami, RJ Richter, ...
Arteriosclerosis, thrombosis, and vascular biology 20 (11), 2441-2447, 2000
4092000
Actionable exomic incidental findings in 6503 participants: challenges of variant classification
LM Amendola, MO Dorschner, PD Robertson, JS Salama, R Hart, ...
Genome research 25 (3), 305-315, 2015
3972015
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