{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,7]],"date-time":"2026-08-07T20:00:56Z","timestamp":1786132856335,"version":"build-2736575974"},"reference-count":23,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"5","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2015,5]]},"DOI":"10.1681\/asn.2014050444","type":"journal-article","created":{"date-parts":[[2014,9,24]],"date-time":"2014-09-24T01:44:10Z","timestamp":1411523050000},"page":"1021-1025","source":"Crossref","is-referenced-by-count":6,"title":["Lack of Association of the APOL1 G3 Haplotype in African Americans with ESRD"],"prefix":"10.1681","volume":"26","author":[{"given":"Nicholette D.","family":"Palmer","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Maggie C.Y.","family":"Ng","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Carl D.","family":"Langefeld","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jasmin","family":"Divers","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Janice P.","family":"Lea","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mark D.","family":"Okusa","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Robert P.","family":"Kimberly","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Donald W.","family":"Bowden","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Barry I.","family":"Freedman","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","reference":[{"key":"R1-8-20230208","doi-asserted-by":"crossref","first-page":"386","DOI":"10.1111\/j.1365-2141.2011.08832.x","article-title":"MYH9 and APOL1 are both associated with sickle cell disease nephropathy.","volume":"155","author":"Ashley-Koch","year":"2011","journal-title":"Br J Haematol"},{"key":"R2-8-20230208","doi-asserted-by":"crossref","first-page":"390","DOI":"10.1002\/art.38220","article-title":"End-stage renal disease in African Americans with lupus nephritis is associated with APOL1.","volume":"66","author":"Freedman","year":"2014","journal-title":"Arthritis Rheum (Munch"},{"key":"R3-8-20230208","doi-asserted-by":"crossref","first-page":"841","DOI":"10.1126\/science.1193032","article-title":"Association of trypanolytic ApoL1 variants with kidney disease in African Americans.","volume":"329","author":"Genovese","year":"2010","journal-title":"Science"},{"key":"R4-8-20230208","doi-asserted-by":"crossref","first-page":"2129","DOI":"10.1681\/ASN.2011040388","article-title":"APOL1 genetic variants in focal segmental glomerulosclerosis and HIV-associated nephropathy.","volume":"22","author":"Kopp","year":"2011","journal-title":"J Am Soc Nephrol"},{"key":"R5-8-20230208","doi-asserted-by":"crossref","first-page":"722","DOI":"10.1681\/ASN.2012121180","article-title":"Apolipoprotein L1 risk variants associate with systemic lupus erythematosus-associated collapsing glomerulopathy.","volume":"24","author":"Larsen","year":"2013","journal-title":"J Am Soc Nephrol"},{"key":"R6-8-20230208","doi-asserted-by":"crossref","first-page":"114","DOI":"10.1038\/ki.2012.263","article-title":"Apolipoprotein L1 gene variants associate with hypertension-attributed nephropathy and the rate of kidney function decline in African Americans.","volume":"83","author":"Lipkowitz","year":"2013","journal-title":"Kidney Int"},{"key":"R7-8-20230208","doi-asserted-by":"crossref","first-page":"2183","DOI":"10.1056\/NEJMoa1310345","article-title":"APOL1 risk variants, race, and progression of chronic kidney disease.","volume":"369","author":"Parsa","year":"2013","journal-title":"N Engl J Med"},{"key":"R8-8-20230208","doi-asserted-by":"crossref","first-page":"345","DOI":"10.1007\/s00439-010-0861-0","article-title":"Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene.","volume":"128","author":"Tzur","year":"2010","journal-title":"Hum Genet"},{"key":"R9-8-20230208","doi-asserted-by":"crossref","first-page":"54","DOI":"10.1016\/j.ajhg.2013.05.014","article-title":"Identifying Darwinian selection acting on different human APOL1 variants among diverse African populations.","volume":"93","author":"Ko","year":"2013","journal-title":"Am J Hum Genet"},{"key":"R10-8-20230208","doi-asserted-by":"crossref","first-page":"1505","DOI":"10.1093\/ndt\/gfr522","article-title":"Polymorphisms in MYH9 are associated with diabetic nephropathy in European Americans.","volume":"27","author":"Cooke","year":"2012","journal-title":"Nephrol Dial Transplant"},{"key":"R11-8-20230208","doi-asserted-by":"crossref","first-page":"1175","DOI":"10.1038\/ng.226","article-title":"MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis.","volume":"40","author":"Kopp","year":"2008","journal-title":"Nat Genet"},{"key":"R12-8-20230208","doi-asserted-by":"crossref","first-page":"2450","DOI":"10.1093\/hmg\/ddr118","article-title":"The MYH9\/APOL1 region and chronic kidney disease in European-Americans.","volume":"20","author":"O\u2019Seaghdha","year":"2011","journal-title":"Hum Mol Genet"},{"key":"R13-8-20230208","doi-asserted-by":"crossref","first-page":"297","DOI":"10.1038\/ki.2009.135","article-title":"Genome-wide linkage analysis of serum creatinine in three isolated European populations.","volume":"76","author":"Pattaro","year":"2009","journal-title":"Kidney Int"},{"key":"R14-8-20230208","doi-asserted-by":"crossref","first-page":"1207","DOI":"10.1038\/ki.2013.173","article-title":"JC polyoma virus interacts with APOL1 in African Americans with nondiabetic nephropathy.","volume":"84","author":"Divers","year":"2013","journal-title":"Kidney Int"},{"key":"R15-8-20230208","doi-asserted-by":"crossref","first-page":"587","DOI":"10.1093\/ndt\/gft423","article-title":"Gene-gene interactions in APOL1-associated nephropathy.","volume":"29","author":"Divers","year":"2014","journal-title":"Nephrol Dial Transplant"},{"key":"R16-8-20230208","doi-asserted-by":"crossref","first-page":"1069","DOI":"10.1038\/ki.2013.299","article-title":"JC viruria and kidney disease in APOL1 risk genotype individuals: Is this a clue to a gene \u00d7 environment interaction?","volume":"84","author":"Kopp","year":"2013","journal-title":"Kidney Int"},{"key":"R17-8-20230208","doi-asserted-by":"crossref","first-page":"240","DOI":"10.1038\/nrneph.2013.34","article-title":"APOL1 variants and kidney disease in people of recent African ancestry.","volume":"9","author":"Genovese","year":"2013","journal-title":"Nat Rev Nephrol"},{"key":"R18-8-20230208","doi-asserted-by":"crossref","first-page":"E2130","DOI":"10.1073\/pnas.1400699111","article-title":"Evolution of the primate trypanolytic factor APOL1.","volume":"111","author":"Thomson","year":"2014","journal-title":"Proc Natl Acad Sci U S A"},{"key":"R19-8-20230208","doi-asserted-by":"crossref","first-page":"563","DOI":"10.1038\/ki.2010.467","article-title":"A genome-wide association study for diabetic nephropathy genes in African Americans.","volume":"79","author":"McDonough","year":"2011","journal-title":"Kidney Int"},{"key":"R20-8-20230208","doi-asserted-by":"crossref","first-page":"e1000529","DOI":"10.1371\/journal.pgen.1000529","article-title":"A flexible and accurate genotype imputation method for the next generation of genome-wide association studies.","volume":"5","author":"Howie","year":"2009","journal-title":"PLoS Genet"},{"key":"R21-8-20230208","doi-asserted-by":"crossref","first-page":"559","DOI":"10.1086\/519795","article-title":"PLINK: A tool set for whole-genome association and population-based linkage analyses.","volume":"81","author":"Purcell","year":"2007","journal-title":"Am J Hum Genet"},{"key":"R22-8-20230208","doi-asserted-by":"crossref","first-page":"906","DOI":"10.1038\/ng2088","article-title":"A new multipoint method for genome-wide association studies by imputation of genotypes.","volume":"39","author":"Marchini","year":"2007","journal-title":"Nat Genet"},{"key":"R23-8-20230208","doi-asserted-by":"crossref","first-page":"289","DOI":"10.1002\/gepi.20064","article-title":"Estimation of individual admixture: Analytical and study design considerations.","volume":"28","author":"Tang","year":"2005","journal-title":"Genet Epidemiol"}],"container-title":["Journal of the American Society of Nephrology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.ovid.com\/00001751-201505000-00008","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,8,7]],"date-time":"2026-08-07T19:25:04Z","timestamp":1786130704000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ovid.com\/00001751-201505000-00008"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2015,5]]},"references-count":23,"journal-issue":{"issue":"5","published-print":{"date-parts":[[2015]]}},"URL":"https:\/\/doi.org\/10.1681\/asn.2014050444","relation":{},"ISSN":["1046-6673"],"issn-type":[{"value":"1046-6673","type":"print"}],"subject":[],"published":{"date-parts":[[2015,5]]}}}