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Nancy Cox
Nancy Cox
Vanderbilt University Medical Center
Verified email at vanderbilt.edu
Title
Cited by
Year
[Multipoint Linkage Analysis Using Affected Relative Pairs and Partially Informative Markers]: Discussion
DL Nicolae, ML Frigge, NJ Cox, A Kong
Biometrics 54 (4), 1271-1274, 1998
81998
11 LEVERAGING PHENOTYPE DATA TO IDENTIFY POTENTIAL CARRIERS OF DELETERIOUS GENETIC VARIANTS
T Morley, L Bastarache, N Cox, D Ruderfer
European Neuropsychopharmacology 29, S64-S65, 2019
2019
11 Novel Systematic Method for Identifying Congenital Anomaly Cases in Electronic Health Record Databases
E Brokamp, L Bastarache, N Cox, R Hamid, NK Khanakari, G Hooker, ...
Journal of Clinical and Translational Science 8 (s1), 3-3, 2024
2024
12. SHARED GENETIC ARCHITECTURE AND EVOLUTION OF HUMAN LANGUAGE AND MUSICAL RHYTHM TRAITS
G Alagoez, E Eising, Y Mekki, G Bignardi, P Fontanillas, M Luciano, ...
European Neuropsychopharmacology 75, S62-S63, 2023
2023
2017 Presidential Address: Checking, Balancing, and Celebrating Diversity: Celebrating Some of the Women Who Paved the Way1
NJ Cox
The American Journal of Human Genetics 102 (3), 342-349, 2018
12018
2023 ASHG Leadership Award
NJ Cox
The American Journal of Human Genetics 111 (3), 429-432, 2024
2024
285 Genetic Variation in the SLC22A1-3 Genes Influence the Risk of Congenital Anomalies
E Brokamp, M Shuey, T Miller-Flemming, NJ Cox
Journal of Clinical and Translational Science 7 (s1), 85-85, 2023
2023
4 RFLPS OF THE HUMAN INSULIN-RECEPTOR GENE-PSTI, KPNI, RSAI (2 RFLPS)
NJ COX, RS SPIELMAN, CR KAHN, D MULLERWIELAND, ...
NUCLEIC ACIDS RESEARCH 16 (16), 8204-8204, 1988
1988
4 RFLPS OF THE HUMAN INSULIN-RECEPTOR GENE-PSTI, KPNI, RSAI (2 RFLPS)
NJ COX, RS SPIELMAN, CR KAHN, D MULLERWIELAND, ...
NUCLEIC ACIDS RESEARCH 17 (2), 820-820, 1989
1989
7 UNRAVELING THE GENETIC ARCHITECTURE OF HUMAN MUSIC RHYTHM ABILITY: FINDINGS FROM THE FIRST GENOME-WIDE ASSOCIATION STUDY OF A MUSICAL RHYTHM TRAIT IN 606,825 INDIVIDUALS
M Niarchou, JF Sathirapongsasuti, N Jacoby, JD McAuley, E Bell, ...
European Neuropsychopharmacology 29, S62, 2019
2019
A 48-hour exposure of pancreatic islets to calpain inhibitors impairs mitochondrial fuel metabolism and the exocytosis of insulin
YP Zhou, S Sreenan, CY Pan, KPM Currie, VP Bindokas, Y Horikawa, ...
Metabolism 52 (5), 528-534, 2003
672003
A Bayesian framework that integrates multi-omics data and gene networks predicts risk genes from schizophrenia GWAS data
Q Wang, R Chen, F Cheng, Q Wei, Y Ji, H Yang, X Zhong, R Tao, Z Wen, ...
Nature neuroscience 22 (5), 691-699, 2019
1342019
A brief history of human disease genetics
M Claussnitzer, JH Cho, R Collins, NJ Cox, ET Dermitzakis, ME Hurles, ...
Nature 577 (7789), 179-189, 2020
5942020
A calpain-10 gene polymorphism is associated with reduced muscle mRNA levels and insulin resistance
LJ Baier, PA Permana, X Yang, RE Pratley, RL Hanson, GQ Shen, D Mott, ...
The Journal of clinical investigation 106 (7), R69-R73, 2000
4372000
A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1–1q1
S Kass, C MacRae, HL Graber, EA Sparks, D McNamara, H Boudoulas, ...
Nature genetics 7 (4), 546-551, 1994
2361994
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
16282015
A genetic study of stuttering
NJ Cox
Yale University, 1982
41982
A genome-wide approach to identify genetic variants that contribute to etoposide-induced cytotoxicity
RS Huang, S Duan, WK Bleibel, EO Kistner, W Zhang, TA Clark, TX Chen, ...
Proceedings of the National Academy of Sciences 104 (23), 9758-9763, 2007
2352007
A genome-wide association study identifies a novel major locus for glycemic control in type 1 diabetes, as measured by both A1C and glucose
AD Paterson, D Waggott, AP Boright, SM Hosseini, E Shen, MP Sylvestre, ...
Diabetes 59 (2), 539-549, 2010
1252010
A genome-wide association study of breast cancer in women of African ancestry
F Chen, GK Chen, DO Stram, RC Millikan, CB Ambrosone, EM John, ...
Human genetics 132, 39-48, 2013
912013
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