Nancy Cox
Nancy Cox
Vanderbilt University Medical Center
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Cytowane przez
Cytowane przez
Finding the missing heritability of complex diseases
TA Manolio, FS Collins, NJ Cox, DB Goldstein, LA Hindorff, DJ Hunter, ...
Nature 461 (7265), 747-753, 2009
The genotype-tissue expression (GTEx) project
J Lonsdale, J Thomas, M Salvatore, R Phillips, E Lo, S Shad, R Hasz, ...
Nature genetics 45 (6), 580-585, 2013
The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans
GTEx Consortium
Science 348 (6235), 648-660, 2015
Mutations in the hepatocyte nuclear factor-1α gene in maturity-onset diabetes of the young (MODY3)
K Yamagata, N Oda, PJ Kaisaki, S Menzel, H Furuta, M Vaxillaire, ...
Nature 384 (6608), 455-458, 1996
Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus
Y Horikawa, N Oda, NJ Cox, X Li, M Orho-Melander, M Hara, Y Hinokio, ...
Nature genetics 26 (2), 163-175, 2000
Genetic effects on gene expression across human tissues.
A Battle, CD Brown, BE Engelhardt, SB Montgomery
Nature 550 (7675), 204-213, 2017
Association of attention-deficit disorder and the dopamine transporter gene.
EH Cook Jr, MA Stein, MD Krasowski, NJ Cox, DM Olkon, JE Kieffer, ...
American journal of human genetics 56 (4), 993, 1995
Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS
DL Nicolae, E Gamazon, W Zhang, S Duan, ME Dolan, NJ Cox
PLoS genetics 6 (4), e1000888, 2010
Guidelines for investigating causality of sequence variants in human disease
DG MacArthur, TA Manolio, DP Dimmock, HL Rehm, J Shendure, ...
Nature 508 (7497), 469-476, 2014
Allele-sharing models: LOD scores and accurate linkage tests
A Kong, NJ Cox
The American Journal of Human Genetics 61 (5), 1179-1188, 1997
Obesity-associated variants within FTO form long-range functional connections with IRX3
S Smemo, JJ Tena, KH Kim, ER Gamazon, NJ Sakabe, C Gómez-Marín, ...
Nature 507 (7492), 371-375, 2014
A gene-based association method for mapping traits using reference transcriptome data
ER Gamazon, HE Wheeler, KP Shah, SV Mozaffari, K Aquino-Michaels, ...
Nature genetics 47 (9), 1091-1098, 2015
Allegro, a new computer program for multipoint linkage analysis
DF Gudbjartsson, K Jonasson, ML Frigge, A Kong
Nature genetics 25 (1), 12-13, 2000
Germline BAP1 mutations predispose to malignant mesothelioma
JR Testa, M Cheung, J Pei, JE Below, Y Tan, E Sementino, NJ Cox, ...
Nature genetics 43 (10), 1022-1025, 2011
The genetic architecture of type 2 diabetes
C Fuchsberger, J Flannick, TM Teslovich, A Mahajan, V Agarwala, ...
Nature 536 (7614), 41-47, 2016
The allelic architecture of human disease genes: common disease–common variant… or not?
JK Pritchard, NJ Cox
Human molecular genetics 11 (20), 2417-2423, 2002
A genome–wide search for human non–insulin–dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2
CL Hanis, E Boerwinkle, R Chakraborty, DL Ellsworth, P Concannon, ...
Nature genetics 13 (2), 161-166, 1996
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
A Mahajan, MJ Go, W Zhang, JE Below, KJ Gaulton, T Ferreira, ...
Nature genetics 46 (3), 234-244, 2014
National Institutes of Health State-of-the-Science Conference statement: preventing alzheimer disease and cognitive decline
ML Daviglus, CC Bell, W Berrettini, PE Bowen, ES Connolly Jr, NJ Cox, ...
Annals of internal medicine 153 (3), 176-181, 2010
Insulin gene mutations as a cause of permanent neonatal diabetes
J Støy, EL Edghill, SE Flanagan, H Ye, VP Paz, A Pluzhnikov, JE Below, ...
Proceedings of the National Academy of Sciences 104 (38), 15040-15044, 2007
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