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2015
The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex disease.Moutsianas, L., Agarwala V., Fuchsberger C., Flannick J., Rivas MA, Gaulton KJ, Albers PK, GoT2D Consortium, McVean G., Boehnke M., Altshuler D., and McCarthy MI PLoS genetics, 2015/04/01, Volume 11, Issue 4, p.e1005165, (2015) Read More / View Supplemental Materials
Abstract
2014
Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes.Majithia, AR, Flannick J., Shahinian P., Guo M., Bray MA, Fontanillas P., Gabriel SB, GoT2D Consortium, NHGRI JHS/FHS Allelic Spectrum Project, SIGMA T2D Consortium, T2D-GENES Consortium, Rosen ED, Altshuler D., and GoT2D Consortium Proceedings of the National Academy of Sciences of the United States of America, 2014/08/25, (2014) Read More / View Supplemental Materials
Abstract
Simulation of finnish population history, guided by empirical genetic data, to assess power of rare-variant tests in Finland.Wang, SR, Agarwala V., Flannick J., Chiang CW, Altshuler D., GoT2D Consortium, and Hirschhorn JN American journal of human genetics, 2014/05/01, Volume 94, Issue 5, p.710-20, (2014) Read More / View Supplemental Materials
Abstract
2013
Evaluating empirical bounds on complex disease genetic architecture.Agarwala, V., Flannick J., Sunyaev S., GoT2D Consortium, and Altshuler D. Nature genetics, 2013/10/20, (2013) Read More / View Supplemental Materials
Abstract
  • Showing 1-4 of 4 Results