Agency
National Institute of Health (NIH)
Institute
National Human Genome Research Institute (NHGRI)
Type
Research Project (R01)
Project #
3R01HG000376-08S1
Application #
2208791
Study Section
Genome Study Section (GNM)
Project Start
1988-09-28
Project End
1998-08-31
Budget Start
1995-09-01
Budget End
1996-08-31
Support Year
8
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Biostatistics & Other Math Sci
Type
Schools of Public Health
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Wojcik, Genevieve L; Fuchsberger, Christian; Taliun, Daniel et al. (2018) Imputation-Aware Tag SNP Selection To Improve Power for Large-Scale, Multi-ethnic Association Studies. G3 (Bethesda) 8:3255-3267
Reppell, M; Zöllner, S (2018) An efficient algorithm for generating the internal branches of a Kingman coalescent. Theor Popul Biol 122:57-66
Jiang, Yu; Chen, Sai; McGuire, Daniel et al. (2018) Proper conditional analysis in the presence of missing data: Application to large scale meta-analysis of tobacco use phenotypes. PLoS Genet 14:e1007452
Dutta, Diptavo; Scott, Laura; Boehnke, Michael et al. (2018) Multi-SKAT: General framework to test for rare-variant association with multiple phenotypes. Genet Epidemiol :
Ray, Debashree; Boehnke, Michael (2018) Methods for meta-analysis of multiple traits using GWAS summary statistics. Genet Epidemiol 42:134-145
Scott, Robert A; Scott, Laura J; Mägi, Reedik et al. (2017) An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans. Diabetes 66:2888-2902
Chiu, Chi-Yang; Jung, Jeesun; Chen, Wei et al. (2017) Meta-analysis of quantitative pleiotropic traits for next-generation sequencing with multivariate functional linear models. Eur J Hum Genet 25:350-359
Chiu, Chi-Yang; Jung, Jeesun; Wang, Yifan et al. (2017) A comparison study of multivariate fixed models and Gene Association with Multiple Traits (GAMuT) for next-generation sequencing. Genet Epidemiol 41:18-34
Taliun, Daniel; Chothani, Sonia P; Schönherr, Sebastian et al. (2017) LASER server: ancestry tracing with genotypes or sequence reads. Bioinformatics 33:2056-2058
McCarthy, Shane; Das, Sayantan; Kretzschmar, Warren et al. (2016) A reference panel of 64,976 haplotypes for genotype imputation. Nat Genet 48:1279-83

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