Wen H. Kao, Ph.D. - Publications

Affiliations: 
2000 Johns Hopkins University, Baltimore, MD 
Area:
Public Health, Pathology

38 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
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  0.48
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  0.48
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  0.48
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  0.32
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  0.48
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  0.48
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  0.48
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  0.48
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  0.32
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  0.32
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  0.48
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  0.48
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  0.48
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  0.32
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  0.32
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  0.48
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  0.48
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  0.48
2013 Tellez-Plaza M, Gribble MO, Voruganti VS, Francesconi KA, Goessler W, Umans JG, Silbergeld EK, Guallar E, Franceschini N, North KE, Kao WH, MacCluer JW, Cole SA, Navas-Acien A. Heritability and preliminary genome-wide linkage analysis of arsenic metabolites in urine. Environmental Health Perspectives. 121: 345-51. PMID 23322787 DOI: 10.1289/ehp.1205305  0.32
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  0.48
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  0.32
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  0.48
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  0.48
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  0.32
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  0.48
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  0.32
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  0.32
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  0.32
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  0.32
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  0.48
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  0.32
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  0.48
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  0.48
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  0.48
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  0.32
2010 Estrella MM, Sperati CJ, Kao WH, Parekh RS. Genetic epidemiology of chronic kidney disease. Current Opinion in Nephrology and Hypertension. 19: 283-91. PMID 20393286 DOI: 10.1097/MNH.0b013e328338185f  0.32
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  0.4
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  0.44
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