Torthaí cuardaigh - Michael Boehnke
- 1 - 20 toradh as 202 á dtaispeáint
- Téigh chuig an gcéad leathanach eile
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1
Quantifying and correcting for the winner's curse in genetic association studies de réir Rui Xiao, Michael Boehnke
Foilsithe / Cruthaithe 2009Artigo -
2
Methods for meta‐analysis of multiple traits using GWAS summary statistics de réir Debashree Ray, Michael Boehnke
Foilsithe / Cruthaithe 2017Artigo -
3
Recent advances in understanding the genetic architecture of type 2 diabetes de réir Karen L. Mohlke, Michael Boehnke
Foilsithe / Cruthaithe 2015Revisão -
4
Genetic Association Mapping Based on Discordant Sib Pairs: The Discordant-Alleles Test de réir Michael Boehnke, Carl D. Langefeld
Foilsithe / Cruthaithe 1998Artigo -
5
Accurate Inference of Relationships in Sib-Pair Linkage Studies de réir Michael Boehnke, Nancy J. Cox
Foilsithe / Cruthaithe 1997Artigo -
6
A Multipoint Method for Detecting Genotyping Errors and Mutations in Sibling-Pair Linkage Data de réir Julie A. Douglas, Michael Boehnke, Kenneth Lange
Foilsithe / Cruthaithe 2000Artigo -
7
Efficient Study Designs for Test of Genetic Association Using Sibship Data and Unrelated Cases and Controls de réir Mingyao Li, Michael Boehnke, Gonçalo R. Abecasis
Foilsithe / Cruthaithe 2006Artigo -
8
Joint Modeling of Linkage and Association: Identifying SNPs Responsible for a Linkage Signal de réir Mingyao Li, Michael Boehnke, Gonçalo R. Abecasis
Foilsithe / Cruthaithe 2005Artigo -
9
Metabolic and cardiovascular traits: an abundance of recently identified common genetic variants de réir Karen L. Mohlke, Michael Boehnke, Gonçalo R. Abecasis
Foilsithe / Cruthaithe 2008Artigo -
10
Improved Inference of Relationship for Pairs of Individuals de réir Michael P. Epstein, William L. Duren, Michael Boehnke
Foilsithe / Cruthaithe 2000Artigo -
11
Revisiting the genome-wide significance threshold for common variant GWAS de réir Zhongsheng Chen, Michael Boehnke, Xiaoquan Wen, Bhramar Mukherjee
Foilsithe / Cruthaithe 2021Revisão -
12
Rare-Variant Association Analysis: Study Designs and Statistical Tests de réir Seunggeung Lee, Gonçalo R. Abecasis, Michael Boehnke, Xihong Lin
Foilsithe / Cruthaithe 2014Revisão -
13
General Framework for Meta-analysis of Rare Variants in Sequencing Association Studies de réir Seunggeun Lee, Tanya M. Teslovich, Michael Boehnke, Xihong Lin
Foilsithe / Cruthaithe 2013Artigo -
14
Recommended Joint and Meta‐Analysis Strategies for Case‐Control Association Testing of Single Low‐Count Variants de réir Clement Ma, Tom Blackwell, Michael Boehnke, Laura J. Scott
Foilsithe / Cruthaithe 2013Artigo -
15
Multi‐SKAT: General framework to test for rare‐variant association with multiple phenotypes de réir Diptavo Dutta, Laura J. Scott, Michael Boehnke, Seunggeun Lee
Foilsithe / Cruthaithe 2018Artigo -
16
Affected-sib-pair interval mapping and exclusion for complex genetic traits: Sampling considerations de réir Elizabeth R. Hauser, Michael Boehnke, Sun‐Wei Guo, Neil Risch
Foilsithe / Cruthaithe 1996Artigo -
17
Statistical methods for polyploid radiation hybrid mapping. de réir Kenneth Lange, Michael Boehnke, David R. Cox, Kathryn L. Lunetta
Foilsithe / Cruthaithe 1995Artigo -
18
Optimal designs for two‐stage genome‐wide association studies de réir Andrew D. Skol, Laura J. Scott, Gonçalo R. Abecasis, Michael Boehnke
Foilsithe / Cruthaithe 2007Artigo -
19
Correcting for Sample Contamination in Genotype Calling of DNA Sequence Data de réir Matthew Flickinger, Goo Jun, Gonçalo R. Abecasis, Michael Boehnke, Hyun Min Kang
Foilsithe / Cruthaithe 2015Artigo -
20
Low-coverage sequencing: Implications for design of complex trait association studies de réir Yun Li, Carlo Sidore, Hyun Min Kang, Michael Boehnke, Gonçalo R. Abecasis
Foilsithe / Cruthaithe 2011Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Biology
Genetics
Gene
Genotype
Single-nucleotide polymorphism
Genome-wide association study
Medicine
Endocrinology
Computational biology
Genetic association
Internal medicine
Diabetes mellitus
Type 2 diabetes
Allele
Genome
Quantitative trait locus
Computer science
Bioinformatics
Phenotype
Population
Locus (genetics)
Environmental health
Evolutionary biology
Genotyping
Mathematics
Exome sequencing
Statistics
Exome
Psychology
Genetic architecture