| Year |
Citation |
Score |
| 2017 |
Li M, Carey J, Cristiano S, Susztak K, Coresh J, Boerwinkle E, Kao WH, Beaty TH, Köttgen A, Scharpf RB. Genome-Wide Association of Copy Number Polymorphisms and Kidney Function. Plos One. 12: e0170815. PMID 28135296 DOI: 10.1371/Journal.Pone.0170815 |
0.52 |
|
| 2016 |
Amin N, Allebrandt KV, van der Spek A, Müller-Myhsok B, Hek K, Teder-Laving M, Hayward C, Esko T, van Mill JG, Mbarek H, Watson NF, Melville SA, Del Greco FM, Byrne EM, Oole E, ... ... Kao WH, et al. Genetic variants in RBFOX3 are associated with sleep latency. European Journal of Human Genetics : Ejhg. PMID 27142678 DOI: 10.1038/Ejhg.2016.31 |
0.359 |
|
| 2016 |
Pattaro C, Teumer A, Gorski M, Chu AY, Li M, Mijatovic V, Garnaas M, Tin A, Sorice R, Li Y, Taliun D, Olden M, Foster M, Yang Q, Chen MH, ... ... Kao WH, et al. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nature Communications. 7: 10023. PMID 26831199 DOI: 10.1038/Ncomms10023 |
0.64 |
|
| 2015 |
Maruthur NM, Li M, Halushka MK, Astor BC, Pankow JS, Boerwinkle E, Coresh J, Selvin E, Kao WH. Genetics of Plasma Soluble Receptor for Advanced Glycation End-Products and Cardiovascular Outcomes in a Community-based Population: Results from the Atherosclerosis Risk in Communities Study. Plos One. 10: e0128452. PMID 26083729 DOI: 10.1371/Journal.Pone.0128452 |
0.576 |
|
| 2015 |
Tin A, Köttgen A, Folsom AR, Maruthur NM, Tajuddin SM, Nalls MA, Evans MK, Zonderman AB, Friedrich CA, Boerwinkle E, Coresh J, Kao WH. Genetic loci for serum magnesium among African-Americans and gene-environment interaction at MUC1 and TRPM6 in European-Americans: the Atherosclerosis Risk in Communities (ARIC) study. Bmc Genetics. 16: 56. PMID 26058915 DOI: 10.1186/S12863-015-0219-7 |
0.488 |
|
| 2015 |
Tin A, Grams ME, Maruthur NM, Astor BC, Couper D, Mosley TH, Fornage M, Parekh RS, Coresh J, Kao WH. Hemostatic Factors, APOL1 Risk Variants, and the Risk of ESRD in the Atherosclerosis Risk in Communities Study. Clinical Journal of the American Society of Nephrology : Cjasn. 10: 784-90. PMID 25887069 DOI: 10.2215/Cjn.08340814 |
0.427 |
|
| 2015 |
Huffman JE, Albrecht E, Teumer A, Mangino M, Kapur K, Johnson T, Kutalik Z, Pirastu N, Pistis G, Lopez LM, Haller T, Salo P, Goel A, Li M, Tanaka T, ... ... Kao WH, et al. Modulation of genetic associations with serum urate levels by body-mass-index in humans. Plos One. 10: e0119752. PMID 25811787 DOI: 10.1371/Journal.Pone.0119752 |
0.425 |
|
| 2015 |
Gorski M, Tin A, Garnaas M, McMahon GM, Chu AY, Tayo BO, Pattaro C, Teumer A, Chasman DI, Chalmers J, Hamet P, Tremblay J, Woodward M, Aspelund T, Eiriksdottir G, ... ... Kao WH, et al. Genome-wide association study of kidney function decline in individuals of European descent. Kidney International. 87: 1017-29. PMID 25493955 DOI: 10.1038/Ki.2014.361 |
0.601 |
|
| 2015 |
Tin A, Grams ME, Maruthur NM, Astor BC, Couper D, Mosley TH, Selvin E, Coresh J, Kao WH. Results from the Atherosclerosis Risk in Communities study suggest that low serum magnesium is associated with incident kidney disease. Kidney International. 87: 820-7. PMID 25272232 DOI: 10.1038/Ki.2014.331 |
0.6 |
|
| 2014 |
Holliday EG, Traylor M, Malik R, Bevan S, Maguire J, Koblar SA, Sturm J, Hankey GJ, Oldmeadow C, McEvoy M, Sudlow C, Rothwell PM, Coresh J, Hamet P, Tremblay J, ... ... Kao WH, et al. Polygenic overlap between kidney function and large artery atherosclerotic stroke. Stroke; a Journal of Cerebral Circulation. 45: 3508-13. PMID 25352485 DOI: 10.1161/Strokeaha.114.006609 |
0.378 |
|
| 2014 |
Arking DE, Pulit SL, Crotti L, van der Harst P, Munroe PB, Koopmann TT, Sotoodehnia N, Rossin EJ, Morley M, Wang X, Johnson AD, Lundby A, Gudbjartsson DF, Noseworthy PA, Eijgelsheim M, ... ... Kao WH, et al. Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. Nature Genetics. 46: 826-36. PMID 24952745 DOI: 10.1038/Ng.3014 |
0.432 |
|
| 2014 |
Cornes BK, Brody JA, Nikpoor N, Morrison AC, Dang HC, Ahn BS, Wang S, Dauriz M, Barzilay JI, Dupuis J, Florez JC, Coresh J, Gibbs RA, Kao WH, Liu CT, et al. Association of levels of fasting glucose and insulin with rare variants at the chromosome 11p11.2-MADD locus: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study. Circulation. Cardiovascular Genetics. 7: 374-82. PMID 24951664 DOI: 10.1161/Circgenetics.113.000169 |
0.398 |
|
| 2014 |
Grams ME, Matsushita K, Sang Y, Estrella MM, Foster MC, Tin A, Kao WH, Coresh J. Explaining the racial difference in AKI incidence. Journal of the American Society of Nephrology : Jasn. 25: 1834-41. PMID 24722442 DOI: 10.1681/Asn.2013080867 |
0.443 |
|
| 2014 |
Mahajan A, Go MJ, Zhang W, Below JE, Gaulton KJ, Ferreira T, Horikoshi M, Johnson AD, Ng MC, Prokopenko I, ... ... Kao WH, et al. Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. Nature Genetics. 46: 234-44. PMID 24509480 DOI: 10.1038/Ng.2897 |
0.375 |
|
| 2014 |
Scialla JJ, Kao WH, Crainiceanu C, Sozio SM, Oberai PC, Shafi T, Coresh J, Powe NR, Plantinga LC, Jaar BG, Parekh RS. Biomarkers of vascular calcification and mortality in patients with ESRD. Clinical Journal of the American Society of Nephrology : Cjasn. 9: 745-55. PMID 24458076 DOI: 10.2215/Cjn.05450513 |
0.31 |
|
| 2014 |
An P, Miljkovic I, Thyagarajan B, Kraja AT, Daw EW, Pankow JS, Selvin E, Kao WH, Maruthur NM, Nalls MA, Liu Y, Harris TB, Lee JH, Borecki IB, Christensen K, et al. Genome-wide association study identifies common loci influencing circulating glycated hemoglobin (HbA1c) levels in non-diabetic subjects: the Long Life Family Study (LLFS). Metabolism: Clinical and Experimental. 63: 461-8. PMID 24405752 DOI: 10.1016/J.Metabol.2013.11.018 |
0.613 |
|
| 2014 |
O'Seaghdha CM, Tin A, Yang Q, Katz R, Liu Y, Harris T, Astor B, Coresh J, Fox CS, Kao WH, Shlipak MG. Association of a cystatin C gene variant with cystatin C levels, CKD, and risk of incident cardiovascular disease and mortality. American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation. 63: 16-22. PMID 23932088 DOI: 10.1053/J.Ajkd.2013.06.015 |
0.59 |
|
| 2013 |
Gribble MO, Voruganti VS, Cropp CD, Francesconi KA, Goessler W, Umans JG, Silbergeld EK, Laston SL, Haack K, Kao WH, Fallin MD, Maccluer JW, Cole SA, Navas-Acien A. SLCO1B1 variants and urine arsenic metabolites in the Strong Heart Family Study. Toxicological Sciences : An Official Journal of the Society of Toxicology. 136: 19-25. PMID 23970802 DOI: 10.1093/Toxsci/Kft181 |
0.368 |
|
| 2013 |
Foster MC, Coresh J, Fornage M, Astor BC, Grams M, Franceschini N, Boerwinkle E, Parekh RS, Kao WH. APOL1 variants associate with increased risk of CKD among African Americans. Journal of the American Society of Nephrology : Jasn. 24: 1484-91. PMID 23766536 DOI: 10.1681/Asn.2013010113 |
0.491 |
|
| 2013 |
Tin A, Colantuoni E, Boerwinkle E, Kottgen A, Franceschini N, Astor BC, Coresh J, Kao WH. Using multiple measures for quantitative trait association analyses: application to estimated glomerular filtration rate. Journal of Human Genetics. 58: 461-6. PMID 23535967 DOI: 10.1038/Jhg.2013.23 |
0.395 |
|
| 2013 |
Olden M, Teumer A, Bochud M, Pattaro C, Köttgen A, Turner ST, Rettig R, Chen MH, Dehghan A, Bastardot F, Schmidt R, Vollenweider P, Schunkert H, Reilly MP, Fornage M, ... ... Kao WH, et al. Overlap between common genetic polymorphisms underpinning kidney traits and cardiovascular disease phenotypes: the CKDGen consortium. American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation. 61: 889-98. PMID 23474010 DOI: 10.1053/J.Ajkd.2012.12.024 |
0.496 |
|
| 2013 |
Tin A, Astor BC, Boerwinkle E, Hoogeveen RC, Coresh J, Kao WH. Genome-wide association study identified the human leukocyte antigen region as a novel locus for plasma beta-2 microglobulin. Human Genetics. 132: 619-27. PMID 23417110 DOI: 10.1007/S00439-013-1274-7 |
0.475 |
|
| 2013 |
Tin A, Astor BC, Boerwinkle E, Hoogeveen RC, Coresh J, Kao WH. Genome-wide significant locus of beta-trace protein, a novel kidney function biomarker, identified in European and African Americans. Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association. 28: 1497-504. PMID 23328707 DOI: 10.1093/Ndt/Gfs591 |
0.543 |
|
| 2013 |
Köttgen A, Albrecht E, Teumer A, Vitart V, Krumsiek J, Hundertmark C, Pistis G, Ruggiero D, O'Seaghdha CM, Haller T, Yang Q, Tanaka T, Johnson AD, Kutalik Z, Smith AV, ... ... Kao WH, et al. Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Nature Genetics. 45: 145-54. PMID 23263486 DOI: 10.1038/Ng.2500 |
0.455 |
|
| 2013 |
Nguyen KD, Pihur V, Ganesh SK, Rakha A, Cooper RS, Hunt SC, Freedman BI, Coresh J, Kao WH, Morrison AC, Boerwinkle E, Ehret GB, Chakravarti A. Effects of rare and common blood pressure gene variants on essential hypertension: results from the Family Blood Pressure Program, CLUE, and Atherosclerosis Risk in Communities studies. Circulation Research. 112: 318-26. PMID 23149595 DOI: 10.1161/Circresaha.112.276725 |
0.468 |
|
| 2012 |
Chasman DI, Fuchsberger C, Pattaro C, Teumer A, Böger CA, Endlich K, Olden M, Chen MH, Tin A, Taliun D, Li M, Gao X, Gorski M, Yang Q, Hundertmark C, ... ... Kao WH, et al. Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function. Human Molecular Genetics. 21: 5329-43. PMID 22962313 DOI: 10.1093/Hmg/Dds369 |
0.579 |
|
| 2012 |
Liu CT, Ng MC, Rybin D, Adeyemo A, Bielinski SJ, Boerwinkle E, Borecki I, Cade B, Chen YD, Djousse L, Fornage M, Goodarzi MO, Grant SF, Guo X, Harris T, ... ... Kao WH, et al. Transferability and fine-mapping of glucose and insulin quantitative trait loci across populations: CARe, the Candidate Gene Association Resource. Diabetologia. 55: 2970-84. PMID 22893027 DOI: 10.1007/S00125-012-2656-4 |
0.543 |
|
| 2012 |
Köttgen A, Yang Q, Shimmin LC, Tin A, Schaeffer C, Coresh J, Liu X, Rampoldi L, Hwang SJ, Boerwinkle E, Hixson JE, Kao WH, Fox CS. Association of estimated glomerular filtration rate and urinary uromodulin concentrations with rare variants identified by UMOD gene region sequencing. Plos One. 7: e38311. PMID 22693617 DOI: 10.1371/Journal.Pone.0038311 |
0.502 |
|
| 2012 |
Manning AK, Hivert MF, Scott RA, Grimsby JL, Bouatia-Naji N, Chen H, Rybin D, Liu CT, Bielak LF, Prokopenko I, Amin N, Barnes D, Cadby G, Hottenga JJ, Ingelsson E, ... ... Kao WH, et al. A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. Nature Genetics. 44: 659-69. PMID 22581228 DOI: 10.1038/Ng.2274 |
0.428 |
|
| 2012 |
Dastani Z, Hivert MF, Timpson N, Perry JR, Yuan X, Scott RA, Henneman P, Heid IM, Kizer JR, Lyytikäinen LP, Fuchsberger C, Tanaka T, Morris AP, Small K, Isaacs A, ... Kao WH, ... Kao WH, et al. Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. Plos Genetics. 8: e1002607. PMID 22479202 DOI: 10.1371/Journal.Pgen.1002607 |
0.48 |
|
| 2012 |
Pattaro C, Köttgen A, Teumer A, Garnaas M, Böger CA, Fuchsberger C, Olden M, Chen MH, Tin A, Taliun D, Li M, Gao X, Gorski M, Yang Q, Hundertmark C, ... ... Kao WH, et al. Genome-wide association and functional follow-up reveals new loci for kidney function. Plos Genetics. 8: e1002584. PMID 22479191 DOI: 10.1371/Journal.Pgen.1002584 |
0.579 |
|
| 2012 |
Cheng CY, Reich D, Haiman CA, Tandon A, Patterson N, Selvin E, Elizabeth S, Akylbekova EL, Brancati FL, Coresh J, Boerwinkle E, Altshuler D, Taylor HA, Henderson BE, Wilson JG, ... Kao WH, et al. African ancestry and its correlation to type 2 diabetes in African Americans: a genetic admixture analysis in three U.S. population cohorts. Plos One. 7: e32840. PMID 22438884 DOI: 10.1371/Journal.Pone.0032840 |
0.562 |
|
| 2012 |
Palmer ND, McDonough CW, Hicks PJ, Roh BH, Wing MR, An SS, Hester JM, Cooke JN, Bostrom MA, Rudock ME, Talbert ME, Lewis JP, Ferrara A, ... Kao WH, ... Kao WH, et al. A genome-wide association search for type 2 diabetes genes in African Americans. Plos One. 7: e29202. PMID 22238593 DOI: 10.1371/Journal.Pone.0029202 |
0.412 |
|
| 2012 |
Bostrom MA, Kao WH, Li M, Abboud HE, Adler SG, Iyengar SK, Kimmel PL, Hanson RL, Nicholas SB, Rasooly RS, Sedor JR, Coresh J, Kohn OF, Leehey DJ, Thornley-Brown D, et al. Genetic association and gene-gene interaction analyses in African American dialysis patients with nondiabetic nephropathy. American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation. 59: 210-21. PMID 22119407 DOI: 10.1053/J.Ajkd.2011.09.020 |
0.492 |
|
| 2011 |
Böger CA, Gorski M, Li M, Hoffmann MM, Huang C, Yang Q, Teumer A, Krane V, O'Seaghdha CM, Kutalik Z, Wichmann HE, Haak T, Boes E, Coassin S, Coresh J, ... ... Kao WH, et al. Association of eGFR-Related Loci Identified by GWAS with Incident CKD and ESRD. Plos Genetics. 7: e1002292. PMID 21980298 DOI: 10.1371/Journal.Pgen.1002292 |
0.586 |
|
| 2011 |
Ehret GB, Munroe PB, Rice KM, Bochud M, Johnson AD, Chasman DI, Smith AV, Tobin MD, Verwoert GC, Hwang SJ, Pihur V, Vollenweider P, O'Reilly PF, Amin N, ... ... Kao WH, et al. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature. 478: 103-9. PMID 21909115 DOI: 10.1038/Nature10405 |
0.523 |
|
| 2011 |
McAdams DeMarco M, Coresh J, Woodward M, Butler KR, Kao WH, Mosley TH, Hindin M, Anderson CA. Hypertension status, treatment, and control among spousal pairs in a middle-aged adult cohort. American Journal of Epidemiology. 174: 790-6. PMID 21841158 DOI: 10.1093/Aje/Kwr167 |
0.679 |
|
| 2011 |
Tin A, Woodward OM, Kao WH, Liu CT, Lu X, Nalls MA, Shriner D, Semmo M, Akylbekova EL, Wyatt SB, Hwang SJ, Yang Q, Zonderman AB, Adeyemo AA, Palmer C, et al. Genome-wide association study for serum urate concentrations and gout among African Americans identifies genomic risk loci and a novel URAT1 loss-of-function allele. Human Molecular Genetics. 20: 4056-68. PMID 21768215 DOI: 10.1093/Hmg/Ddr307 |
0.387 |
|
| 2011 |
Arking DE, Junttila MJ, Goyette P, Huertas-Vazquez A, Eijgelsheim M, Blom MT, Newton-Cheh C, Reinier K, Teodorescu C, Uy-Evanado A, Carter-Monroe N, Kaikkonen KS, Kortelainen ML, Boucher G, Lagacé C, ... ... Kao WH, et al. Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals. Plos Genetics. 7: e1002158. PMID 21738491 DOI: 10.1371/Journal.Pgen.1002158 |
0.498 |
|
| 2011 |
O'Seaghdha CM, Parekh RS, Hwang SJ, Li M, Köttgen A, Coresh J, Yang Q, Fox CS, Kao WH. The MYH9/APOL1 region and chronic kidney disease in European-Americans. Human Molecular Genetics. 20: 2450-6. PMID 21429915 DOI: 10.1093/Hmg/Ddr118 |
0.554 |
|
| 2011 |
Speliotes EK, Yerges-Armstrong LM, Wu J, Hernaez R, Kim LJ, Palmer CD, Gudnason V, Eiriksdottir G, Garcia ME, Launer LJ, Nalls MA, Clark JM, Mitchell BD, Shuldiner AR, Butler JL, ... ... Kao WH, et al. Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits. Plos Genetics. 7: e1001324. PMID 21423719 DOI: 10.1371/Journal.Pgen.1001324 |
0.313 |
|
| 2011 |
Böger CA, Chen MH, Tin A, Olden M, Köttgen A, de Boer IH, Fuchsberger C, O'Seaghdha CM, Pattaro C, Teumer A, Liu CT, Glazer NL, Li M, O'Connell JR, Tanaka T, ... ... Kao WH, et al. CUBN is a gene locus for albuminuria. Journal of the American Society of Nephrology : Jasn. 22: 555-70. PMID 21355061 DOI: 10.1681/Asn.2010060598 |
0.603 |
|
| 2011 |
Rasmussen-Torvik LJ, Li M, Kao WH, Couper D, Boerwinkle E, Bielinski SJ, Folsom AR, Pankow JS. Association of a fasting glucose genetic risk score with subclinical atherosclerosis: The Atherosclerosis Risk in Communities (ARIC) study. Diabetes. 60: 331-5. PMID 21036910 DOI: 10.2337/Db10-0839 |
0.322 |
|
| 2010 |
Yeung EH, Saudek CD, Jahren AH, Kao WH, Islas M, Kraft R, Coresh J, Anderson CA. Evaluation of a novel isotope biomarker for dietary consumption of sweets. American Journal of Epidemiology. 172: 1045-52. PMID 20817784 DOI: 10.1093/Aje/Kwq247 |
0.346 |
|
| 2010 |
Bi M, Kao WH, Boerwinkle E, Hoogeveen RC, Rasmussen-Torvik LJ, Astor BC, North KE, Coresh J, Köttgen A. Association of rs780094 in GCKR with metabolic traits and incident diabetes and cardiovascular disease: the ARIC Study. Plos One. 5: e11690. PMID 20661421 DOI: 10.1371/Journal.Pone.0011690 |
0.499 |
|
| 2010 |
Voight BF, Scott LJ, Steinthorsdottir V, Morris AP, Dina C, Welch RP, Zeggini E, Huth C, Aulchenko YS, Thorleifsson G, McCulloch LJ, Ferreira T, Grallert H, Amin N, Wu G, ... Kao WH, et al. Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nature Genetics. 42: 579-89. PMID 20581827 DOI: 10.1038/Ng.609 |
0.309 |
|
| 2010 |
Köttgen A, Pattaro C, Böger CA, Fuchsberger C, Olden M, Glazer NL, Parsa A, Gao X, Yang Q, Smith AV, O'Connell JR, Li M, Schmidt H, Tanaka T, Isaacs A, ... ... Kao WH, et al. New loci associated with kidney function and chronic kidney disease. Nature Genetics. 42: 376-84. PMID 20383146 DOI: 10.1038/Ng.568 |
0.578 |
|
| 2009 |
Chu AY, Parekh RS, Astor BC, Coresh J, Berthier-Schaad Y, Smith MW, Shuldiner AR, Kao WH. Association of APOE polymorphism with chronic kidney disease in a nationally representative sample: a Third National Health and Nutrition Examination Survey (NHANES III) Genetic Study. Bmc Medical Genetics. 10: 108. PMID 19852818 DOI: 10.1186/1471-2350-10-108 |
0.471 |
|
| 2009 |
Hsu CC, Brancati FL, Astor BC, Kao WH, Steffes MW, Folsom AR, Coresh J. Blood pressure, atherosclerosis, and albuminuria in 10,113 participants in the atherosclerosis risk in communities study. Journal of Hypertension. 27: 397-409. PMID 19226709 DOI: 10.1097/Hjh.0B013E32831Aede6 |
0.588 |
|
| 2007 |
Berthier-Schaad Y, Kao WH, Coresh J, Zhang L, Ingersoll RG, Stephens R, Smith MW. Reliability of high-throughput genotyping of whole genome amplified DNA in SNP genotyping studies. Electrophoresis. 28: 2812-7. PMID 17702060 DOI: 10.1002/Elps.200600674 |
0.375 |
|
| 2006 |
Liu Y, Berthier-Schaad Y, Plantinga L, Fink NE, Tracy RP, Kao WH, Klag MJ, Smith MW, Coresh J. Functional variants in the lymphotoxin-alpha gene predict cardiovascular disease in dialysis patients. Journal of the American Society of Nephrology : Jasn. 17: 3158-66. PMID 16988060 DOI: 10.1681/Asn.2006030299 |
0.552 |
|
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