[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 | 8 | 1998 |
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 | 1 | 2018 |
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 | 67 | 2003 |
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 | 134 | 2019 |
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 | 594 | 2020 |
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 | 437 | 2000 |
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 | 236 | 1994 |
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 | 1628 | 2015 |
A genetic study of stuttering NJ Cox Yale University, 1982 | 4 | 1982 |
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 | 235 | 2007 |
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 | 125 | 2010 |
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 | 91 | 2013 |