PuSH - Publication Server of Helmholtz Zentrum München

10 Records found.
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1.
Lessard, S.* et al.: Testing the role of predicted gene knockouts in human anthropometric trait variation. Hum. Mol. Genet. 25, 2082-2092 (2016)
2.
Ma, C.* ; Boehnke, M.* ; Lee, S.* & GoT2D Consortium (Gieger, C. ; Grallert, H. ; Hrabě de Angelis, M. ; Huth, C. ; Kriebel, J. ; Meisinger, C. ; Meitinger, T. ; Müller-Nurasyid, M. ; Peters, A. ; Ried, J.S. ; Strauch, K. ; Strom, T.M.): Evaluating the calibration and power of three gene-based association tests of rare variants for the X chromosome. Genet. Epidemiol. 39, 499-508 (2015)
3.
Mahajan, A.* et al.: Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus. PLoS Genet. 11:e1004876 (2015)
4.
Moutsianas, L.* et al.: The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex disease. PLoS Genet. 11:e1005165 (2015)
5.
Flannick, J.* et al.: Loss-of-function mutations in SLC30A8 protect against type 2 diabetes. Nat. Genet. 46, 357-363 (2014)
6.
Majithia, A.R.* et al.: Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes. Proc. Natl. Acad. Sci. U.S.A. 111, 13127-13132 (2014)
7.
Wang, S.R.* et al.: Simulation of finnish population history, guided by empirical genetic data, to assess power of rare-variant tests in Finland. Am. J. Hum. Genet. 94, 710-720 (2014)
8.
Agarwala, V.* ; Flannick, J.* ; Sunyaev, S.R.* ; GoT2D Consortium (Gieger, C. ; Grallert, H. ; Hrabě de Angelis, M. ; Huth, C. ; Kriebel, J. ; Meisinger, C. ; Meitinger, T. ; Müller-Nurasyid, M. ; Peters, A. ; Rathmann, W. ; Ried, J.S. ; Strauch, K. ; Strom, T.M.) & Altshuler, D.*: Evaluating empirical bounds on complex disease genetic architecture. Nat. Genet. 45, 1418-1427 (2013)
9.
Ma, C.* ; Blackwell, T.* ; Boehnke, M.* ; Scott, L.J.* & GoT2D Consortium (Gieger, C. ; Grallert, H. ; Hrabě de Angelis, M. ; Huth, C. ; Kriebel, J. ; Meisinger, C. ; Meitinger, T. ; Müller-Nurasyid, M. ; Peters, A. ; Rathmann, W. ; Ried, J.S. ; Strauch, K. ; Strom, T.M.): Recommended joint and meta-analysis strategies for case-control association testing of single low-count variants. Genet. Epidemiol. 37, 539-550 (2013)
10.
Rivas, M.A.* et al.: Assessing association between protein truncating variants and quantitative traits. Bioinformatics 29, 2419-2426 (2013)