2009
13. Dupuis J et al.
Novel genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.
Nature Genetics in press.
[PDF]
12. Chambers JC, Zhang W, Li Y, Sehmi J, Wass MN, Zabaneh D,
Hoggart C, Bayele H, McCarthy MI, Peltonen L, Freimer NB, Srai SK, Maxwell PH,
Sternberg MJE, Ruokonen A, Abecasis G, Jarvelin MR, Scott J, Elliott P, Kooner JS.
Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels.
Nature Genetics 41(11): 1170-1172.
[PDF]
11-0.
Li Y, Willer CJ, Sanna S, Abecasis GR.
Genotype imputation.
Annual Review Genomics and Human Genetics 10: 387-406.
[PDF]
10-6.
Huang L, Li Y, Singleton AB, Hardy JA, Abecasis GR, Rosenberg NA, Scheet P.
Genotype imputation accuracy across worldwide human populations.
American Journal of Human Genetics 84(2): 235-50.
[PDF]
9-23.
Nair RP, Duffin KC, Helms C, Ding J, Stuard PE, Goldgar D, Gudjonsson JE, Li Y,
Tejasvi T, Feng BJ, Ruether A, Schreiber S, Weichenthal M, Gladman D, Rahman P, Schrodi SJ, Prahalad S,
Guthery SL, Fischer J, Liao W, Kwok P, Menter A, Lathrop GM, Wise C, Begovich AB, Voorhees JJ, Elder JT,
Krueger GG, Bowcock AM, Abecasis GR.
Genome-wide scan reveals association of psoriasis with IL-23 and NF-kB pathways.
Nature Genetics 41(2): 199-204.
[PDF]
8-38.
Kathiresan S, Willer CJ, Peloso G, Demissie S, Musunuru K, Schadt E, Kaplan L, Bennett D, Li Y,
Tanaka T, Voight BF, Bonnycastle LL, Jackson AU, Crawford G, Surti A, Guiducci C, Burtt N, Parish S, Clarke R,
Zelenika D, Kubalanza KA, Morken MA, Scott LJ, Stringham HM, Galan P, Swift AJ, Kuusisto J, Bergman RN,
Sundvall J, Laakso M, Ferrucci L, Scheet P, Sanna S, Uda M, Yang Q, Lunetta K, Dupuis J, deBakker PI,
O'Donnell CJ, Chambers JC, Kooner JS, Hercberg S, Meneton P, Lakatta EG, Scuteri A, Schlessinger D, Tuomilehto J,
Collins FS, Groop L, Altshuler D, Collins R, Lathrop GM, Melander O, Salomaa V, Peltonen L, Orho-Melander M,
Ordovas JM, Boehnke M, Abecasis GR, Mohlke KL, Cupples LA.
Common variants at 30 loci contribute to polygenic dyslipidemia.
Nature Genetics 41(1): 56-65.
[PDF]
2008
7-6.
Gaulton KJ, Willer CJ, Li Y, Scott LJ, Conneely KN, Jackson AU, Duren WL, Chines PS,
Narisu N, Bonnycastle LL, Luo J, Tong M, Sprau AG, Pugh EW, Doheny KF, Valle TT, Abecasis GR,
Tuomilehto J, Bergman RN, Collins FS, Boehnke M, Mohlke KL.
Comprehensive association study of type 2 diabetes and related quantitative traits with 222 candidate genes.
Diabetes 57: 3136-44.
[PDF]
6-36.
Chambers JC, Elliott P, Zabaneh D, Zhang W, Li Y, Froguel P, Balding D, Scott J, Kooner JS.
Common genetic variation near the melanocortin-4 receptor gene is associated with waist circumference and insulin resistance.
Nature Genetics 40(6):716-8.
[PDF]
5-222.
Zeggini E, Scott LJ, Saxena R, Voight BF, Marchini JL, Hu T, de Bakker PI, Abecasis GR, Almgren P, Andersen G,
Ardlie K, Bostr?m KB, Bergman RN, Bonnycastle LL, Borch-Johnsen K, Burtt NP, Chen H,
Chines PS, Daly MJ, Deodhar P, Ding CJ, Doney AS, Duren WL, Elliott KS, Erdos MR,
Frayling TM, Freathy RM, Gianniny L, Grallert H, Grarup N, Groves CJ, Guiducci C, Hansen T,
Herder C, Hitman GA, Hughes TE, Isomaa B, Jackson AU, J?rgensen T, Kong A, Kubalanza K,
Kuruvilla FG, Kuusisto J, Langenberg C, Lango H, Lauritzen T, Li Y, Lindgren CM, Lyssenko V, Marvelle AF,
Meisinger C, Midthjell K, Mohlke KL, Morken MA, Morris AD, Narisu N, Nilsson P, Owen KR, Palmer CN,
Payne F, Perry JR, Pettersen E, Platou C, Prokopenko I, Qi L, Qin L, Rayner NW, Rees M, Roix JJ, Sandb?k A,
Shields B, Sj?gren M, Steinthorsdottir V, Stringham HM, Swift AJ, Thorleifsson G, Thorsteinsdottir U,
Timpson NJ, Tuomi T, Tuomilehto J, Walker M, Watanabe RM, Weedon MN, Willer CJ;
Wellcome Trust Case Control Consortium, Illig T, Hveem K, Hu FB, Laakso M, Stefansson K,
Pedersen O, Wareham NJ, Barroso I, Hattersley AT, Collins FS, Groop L, McCarthy MI, Boehnke M, Altshuler D.
Meta-analysis of genome-wide association data and large-scale replication identifies additional
susceptibility loci for type 2 diabetes.
Nature Genetics 40(5):638-45.
[PDF]
4-165.
Willer CJ, Sanna S, Jackson AU, Scuteri A, Bonnycastle LL, Clarke R, Heath SC, Timpson NJ,
Najjar SS, Stringham HM, Strait J, Duren WL, Maschio A, Busonero F, Mulas A, Albai G, Swift AJ,
Morken MA, Narisu N, Bennett D, Parish S, Shen H, Galan P, Meneton P, Hercberg S, Zelenika D,
Chen W, Li Y, Scott LJ, Scheet P, Sundvall J, Watanabe RM, Nagaraja R, Ebrahim S,
Lawlor DA, Ben-Shlomo Y, Davey-Smith G, Shuldiner AR, Collins R, Bergman RN, Uda M,
Tuomilehto J, Cao A, Collins FS, Lakatta E, Lathrop GM, Boehnke M, Schlessinger D, Mohlke KL, Abecasis GR.
Newly identified loci that influence lipid concentrations and risk of coronary artery disease.
Nature Genetics 40(2):161-9.
[PDF]
2007
3-556.
The International HapMap Consortium.
A second generation human haplotype map of over 3.1 million SNPs.
Nature 449:851-61.
[PDF]
2-560.
Scott JL, Mohlke KL, Bonnycastle LL, Willer CJ, Li Y, Duren WL, Erdos MR, Stringham HM, Chines PS,
Jackson AU, Prokunina-Olsson L, Ding CJ, Swift AJ, Narisu N, Hu T, Pruim R, Xiao R,
Li XY, Conneely KN, Riebow NL, Sprau AG, Tong M, White PP, Hetrick KN, Barnhart MW,
Bark CW, Goldstein JL, Watkins L, Xiang F, Saramies J, Buchanan TA, Watanabe RM, Valle TT,
Kinnunen L, Abecasis GR, Pugh EW, Doheny KF, Bergman RN, Tuomilehto J, Collins FS, Boehnke M.
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.
Science 316:1341-5.
[PDF]
2006
1-97.
Li M, Atmaca-Sonmez P, Othman M, Branham KE, Khanna R, Wade MS, Li Y, Liang L,
Zareparsi S, Swaroop A, Abecasis GR.
CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration.
Nature Genetics 38:1049-54.
[PDF]
|
