Nancy Cox
Nancy Cox
Vanderbilt University Medical Center
Verified email at
Cited by
Cited by
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-4α gene in maturity-onset diabetes of the young (MODY1)
K Yamagata, H Furuta, N Oda, PJ Kaisaki, S Menzel, NJ Cox, SS Fajans, ...
Nature 384 (6608), 458-460, 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
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
Genetic effects on gene expression across human tissues
GTEx Consortium
Nature 550 (7675), 204-213, 2017
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 Genet 6 (4), e1000888, 2010
Allele-sharing models: LOD scores and accurate linkage tests
A Kong, NJ Cox
The American Journal of Human Genetics 61 (5), 1179-1188, 1997
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
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
Allegro, a new computer program for multipoint linkage analysis
DF Gudbjartsson, K Jonasson, ML Frigge, A Kong
Nature genetics 25 (1), 12-13, 2000
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
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
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
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, 2015
The genetic architecture of type 2 diabetes
C Fuchsberger, J Flannick, TM Teslovich, A Mahajan, V Agarwala, ...
Nature 536 (7614), 41-47, 2016
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
Evidence of linkage between the serotonin transporter and autistic disorder
EH Cook Jr, R Courchesne, C Lord, NJ Cox, S Yan, A Lincoln, R Haas, ...
Molecular psychiatry 2 (3), 247-250, 1997
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