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David R. Cox - Publications

Affiliations: 
Genetics Stanford University, Palo Alto, CA 
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26 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2014 Cerhan JR, Berndt SI, Vijai J, Ghesquières H, McKay J, Wang SS, Wang Z, Yeager M, Conde L, de Bakker PI, Nieters A, Cox D, Burdett L, Monnereau A, Flowers CR, et al. Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma. Nature Genetics. 46: 1233-8. PMID 25261932 DOI: 10.1038/Ng.3105  0.363
2013 Deloukas P, Kanoni S, Willenborg C, Farrall M, Assimes TL, Thompson JR, Ingelsson E, Saleheen D, Erdmann J, Goldstein BA, Stirrups K, König IR, Cazier JB, Johansson A, ... ... Cox D, et al. Large-scale association analysis identifies new risk loci for coronary artery disease. Nature Genetics. 45: 25-33. PMID 23202125 DOI: 10.1038/Ng.2480  0.306
2011 Huang Y, Ballinger DG, Dai JY, Peters U, Hinds DA, Cox DR, Beilharz E, Chlebowski RT, Rossouw JE, McTiernan A, Rohan T, Prentice RL. Genetic variants in the MRPS30 region and postmenopausal breast cancer risk. Genome Medicine. 3: 42. PMID 21702935 DOI: 10.1186/Gm258  0.358
2010 Kirby A, Kang HM, Wade CM, Cotsapas C, Kostem E, Han B, Furlotte N, Kang EY, Rivas M, Bogue MA, Frazer KA, Johnson FM, Beilharz EJ, Cox DR, Eskin E, et al. Fine mapping in 94 inbred mouse strains using a high-density haplotype resource. Genetics. 185: 1081-95. PMID 20439770 DOI: 10.1534/Genetics.110.115014  0.316
2009 McNally KL, Childs KL, Bohnert R, Davidson RM, Zhao K, Ulat VJ, Zeller G, Clark RM, Hoen DR, Bureau TE, Stokowski R, Ballinger DG, Frazer KA, Cox DR, Padhukasahasram B, et al. Genomewide SNP variation reveals relationships among landraces and modern varieties of rice. Proceedings of the National Academy of Sciences of the United States of America. 106: 12273-8. PMID 19597147 DOI: 10.1073/Pnas.0900992106  0.695
2008 Thompson DJ, Healey CS, Baynes C, Kalmyrzaev B, Ahmed S, Dowsett M, Folkerd E, Luben RN, Cox D, Ballinger D, Pharoah PD, Ponder BA, Dunning AM, Easton DF. Identification of common variants in the SHBG gene affecting sex hormone-binding globulin levels and breast cancer risk in postmenopausal women. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 17: 3490-8. PMID 19064566 DOI: 10.1158/1055-9965.Epi-08-0734  0.328
2008 Nyholt DR, LaForge KS, Kallela M, Alakurtti K, Anttila V, Färkkilä M, Hämaläinen E, Kaprio J, Kaunisto MA, Heath AC, Montgomery GW, Göbel H, Todt U, Ferrari MD, Launer LJ, ... ... Cox DR, et al. A high-density association screen of 155 ion transport genes for involvement with common migraine. Human Molecular Genetics. 17: 3318-31. PMID 18676988 DOI: 10.1093/Hmg/Ddn227  0.313
2008 Kooner JS, Chambers JC, Aguilar-Salinas CA, Hinds DA, Hyde CL, Warnes GR, Gómez Pérez FJ, Frazer KA, Elliott P, Scott J, Milos PM, Cox DR, Thompson JF. Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides. Nature Genetics. 40: 149-51. PMID 18193046 DOI: 10.1038/Ng.2007.61  0.337
2007 Stokowski RP, Pant PV, Dadd T, Fereday A, Hinds DA, Jarman C, Filsell W, Ginger RS, Green MR, van der Ouderaa FJ, Cox DR. A genomewide association study of skin pigmentation in a South Asian population. American Journal of Human Genetics. 81: 1119-32. PMID 17999355 DOI: 10.1086/522235  0.682
2007 Sabeti PC, Varilly P, Fry B, Lohmueller J, Hostetter E, Cotsapas C, Xie X, Byrne EH, McCarroll SA, Gaudet R, Schaffner SF, Lander ES, Frazer KA, Ballinger DG, ... Cox DR, et al. Genome-wide detection and characterization of positive selection in human populations. Nature. 449: 913-8. PMID 17943131 DOI: 10.1038/Nature06250  0.43
2007 Frazer KA, Ballinger DG, Cox DR, Hinds DA, Stuve LL, Gibbs RA, Belmont JW, Boudreau A, Hardenbol P, Leal SM, Pasternak S, Wheeler DA, Willis TD, Yu F, et al. A second generation human haplotype map of over 3.1 million SNPs. Nature. 449: 851-61. PMID 17943122 DOI: 10.1038/Nature06258  0.499
2007 Frazer KA, Eskin E, Kang HM, Bogue MA, Hinds DA, Beilharz EJ, Gupta RV, Montgomery J, Morenzoni MM, Nilsen GB, Pethiyagoda CL, Stuve LL, Johnson FM, Daly MJ, Wade CM, ... Cox DR, et al. A sequence-based variation map of 8.27 million SNPs in inbred mouse strains. Nature. 448: 1050-3. PMID 17660834 DOI: 10.1038/Nature06067  0.326
2007 Johansson A, Vavruch-Nilsson V, Cox DR, Frazer KA, Gyllensten U. Evaluation of the SNP tagging approach in an independent population sample--array-based SNP discovery in Sami. Human Genetics. 122: 141-50. PMID 17554563 DOI: 10.1007/S00439-007-0379-2  0.507
2007 Bernardinelli L, Murgia SB, Bitti PP, Foco L, Ferrai R, Musu L, Prokopenko I, Pastorino R, Saddi V, Ticca A, Piras ML, Cox DR, Berzuini C. Association between the ACCN1 gene and multiple sclerosis in Central East Sardinia. Plos One. 2: e480. PMID 17534430 DOI: 10.1371/Journal.Pone.0000480  0.364
2007 Easton DF, Pooley KA, Dunning AM, Pharoah PD, Thompson D, Ballinger DG, Struewing JP, Morrison J, Field H, Luben R, Wareham N, Ahmed S, Healey CS, Bowman R, ... ... Cox DG, ... ... Cox DR, et al. Genome-wide association study identifies novel breast cancer susceptibility loci. Nature. 447: 1087-93. PMID 17529967 DOI: 10.1038/Nature05887  0.35
2006 Tao H, Cox DR, Frazer KA. Allele-specific KRT1 expression is a complex trait. Plos Genetics. 2: e93. PMID 16789827 DOI: 10.1371/Journal.Pgen.0020093  0.319
2006 Pant PV, Tao H, Beilharz EJ, Ballinger DG, Cox DR, Frazer KA. Analysis of allelic differential expression in human white blood cells. Genome Research. 16: 331-9. PMID 16467561 DOI: 10.1101/Gr.4559106  0.304
2005 Maraganore DM, de Andrade M, Lesnick TG, Strain KJ, Farrer MJ, Rocca WA, Pant PV, Frazer KA, Cox DR, Ballinger DG. High-resolution whole-genome association study of Parkinson disease. American Journal of Human Genetics. 77: 685-93. PMID 16252231 DOI: 10.1086/496902  0.327
2005 Kukita Y, Miyatake K, Stokowski R, Hinds D, Higasa K, Wake N, Hirakawa T, Kato H, Matsuda T, Pant K, Cox D, Tahira T, Hayashi K. Genome-wide definitive haplotypes determined using a collection of complete hydatidiform moles. Genome Research. 15: 1511-8. PMID 16251461 DOI: 10.1101/Gr.4371105  0.69
2005 Hinds DA, Stuve LL, Nilsen GB, Halperin E, Eskin E, Ballinger DG, Frazer KA, Cox DR. Whole-genome patterns of common DNA variation in three human populations. Science (New York, N.Y.). 307: 1072-9. PMID 15718463 DOI: 10.1126/Science.1105436  0.426
2004 Hinds DA, Seymour AB, Durham LK, Banerjee P, Ballinger DG, Milos PM, Cox DR, Thompson JF, Frazer KA. Application of pooled genotyping to scan candidate regions for association with HDL cholesterol levels. Human Genomics. 1: 421-34. PMID 15606997 DOI: 10.1186/1479-7364-1-6-421  0.416
2004 Olivier M, Hsiung CA, Chuang LM, Ho LT, Ting CT, Bustos VI, Lee TM, de Witte A, Chen YDI, Olshen R, Rodriquez B, Wen CC, Cox DR. Single nucleotide polymorphisms in protein tyrosine phosphatase 1β (PTPN1) are associated with essential hypertension and obesity Human Molecular Genetics. 13: 1885-1892. PMID 15229188 DOI: 10.1093/Hmg/Ddh196  0.613
2004 Olivier M, Brady S, Cox DR. Radiation hybrid mapping with BAC ends. Methods in Molecular Biology (Clifton, N.J.). 255: 163-9. PMID 15020823 DOI: 10.1385/1-59259-752-1:163  0.477
2004 Hinds DA, Stokowski RP, Patil N, Konvicka K, Kershenobich D, Cox DR, Ballinger DG. Matching strategies for genetic association studies in structured populations. American Journal of Human Genetics. 74: 317-25. PMID 14740319 DOI: 10.1086/381716  0.689
2003 Ranade K, Hinds D, Hsiung CA, Chuang LM, Chang MS, Chen YT, Pesich R, Hebert J, Chen YD, Dzau V, Olshen R, Curb D, Botstein D, Cox DR, Risch N. A genome scan for hypertension susceptibility loci in populations of Chinese and Japanese origins. American Journal of Hypertension. 16: 158-62. PMID 12559686 DOI: 10.1016/S0895-7061(02)03245-4  0.304
2002 Olivier M, Chuang LM, Chang MS, Chen YT, Pei D, Ranade K, de Witte A, Allen J, Tran N, Curb D, Pratt R, Neefs H, de Arruda Indig M, Law S, Neri B, ... ... Cox DR, et al. High-throughput genotyping of single nucleotide polymorphisms using new biplex invader technology Nucleic Acids Research. 30: e53. PMID 12060691 DOI: 10.1093/Nar/Gnf052  0.653
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