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2013
Health disparities in kidney disease--emerging data from the human genome.Williams, WW, and Pollak MR The New England journal of medicine, 2013/12/05, Volume 369, Issue 23, p.2260-1, (2013) Read More / View Supplemental Materials
Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing.Kirby, A., Gnirke A., Jaffe DB, Barešová V., Pochet N., Blumenstiel B., Ye C., Aird D., Stevens C., Robinson JT, Cabili MN, Gat-Viks I., Kelliher E., Daza R., DeFelice M., Hůlková H., Sovová J., Vylet'al P., Antignac C., Guttman M., et al. Nature genetics, 2013/03/01, Volume 45, Issue 3, p.299-303, (2013) Read More / View Supplemental Materials
Abstract
Using population admixture to help complete maps of the human genome.Genovese, G., Handsaker RE, Li H., Altemose N., Lindgren AM, Chambert K., Pasaniuc B., Price AL, Reich D., Morton CC, Pollak MR, Wilson JG, and McCarroll SA Nature genetics, 2013/02/24, (2013) Read More / View Supplemental Materials
Abstract
APOL1 variants and kidney disease in people of recent African ancestry.Genovese, G., Friedman DJ, and Pollak MR Nature reviews. Nephrology, 2013/02/12, Volume 9, Issue 4, p.240-4, (2013) Read More / View Supplemental Materials
Abstract
2010
Metabolite profiling identifies markers of uremia.Rhee, EP, Souza A., Farrell L., Pollak MR, Lewis GD, Steele DJ, Thadhani R., Clish CB, Greka A., and Gerszten RE Journal of the American Society of Nephrology : JASN, 2010/06/01, Volume 21, Issue 6, p.1041-1051, (2010) Read More / View Supplemental Materials
Abstract
  • Showing 1-5 of 5 Results