Related references
Note: Only part of the references are listed.Genotype Imputation of Metabochip SNPs Using a Study-Specific Reference Panel of ∼4,000 Haplotypes in African Americans From the Women's Health Initiative
Eric Yi Liu et al.
GENETIC EPIDEMIOLOGY (2012)
Performance of Genotype Imputations Using Data from the 1000 Genomes Project
Yun Ju Sung et al.
HUMAN HEREDITY (2012)
Comparing genotyping algorithms for Illumina's Infinium whole-genome SNP BeadChips
Matthew E. Ritchie et al.
BMC BIOINFORMATICS (2011)
Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association
Andrew R. Wood et al.
HUMAN MOLECULAR GENETICS (2011)
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
Gosia Trynka et al.
NATURE GENETICS (2011)
Promise and pitfalls of the Immunochip
Adrian Cortes et al.
ARTHRITIS RESEARCH & THERAPY (2011)
Multiple Common Susceptibility Variants near BMP Pathway Loci GREM1, BMP4, and BMP2 Explain Part of the Missing Heritability of Colorectal Cancer
Ian P. M. Tomlinson et al.
PLOS GENETICS (2011)
Genetic Determinants of Lipid Traits in Diverse Populations from the Population Architecture using Genomics and Epidemiology (PAGE) Study
Logan Dumitrescu et al.
PLOS GENETICS (2011)
Fine Mapping of Five Loci Associated with Low-Density Lipoprotein Cholesterol Detects Variants That Double the Explained Heritability
Serena Sanna et al.
PLOS GENETICS (2011)
Genome-Wide Association Study of Coronary Heart Disease and Its Risk Factors in 8,090 African Americans: The NHLBI CARe Project
Guillaume Lettre et al.
PLOS GENETICS (2011)
LocusZoom: regional visualization of genome-wide association scan results
Randall J. Pruim et al.
BIOINFORMATICS (2010)
METAL: fast and efficient meta-analysis of genomewide association scans
Cristen J. Willer et al.
BIOINFORMATICS (2010)
From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus
Kiran Musunuru et al.
NATURE (2010)
Integrating common and rare genetic variation in diverse human populations
David M. Altshuler et al.
NATURE (2010)
Biological, clinical and population relevance of 95 loci for blood lipids
Tanya M. Teslovich et al.
NATURE (2010)
A map of human genome variation from population-scale sequencing
David Altshuler et al.
NATURE (2010)
A method and server for predicting damaging missense mutations
Ivan A. Adzhubei et al.
NATURE METHODS (2010)
Genome-wide association studies in diverse populations
Noah A. Rosenberg et al.
NATURE REVIEWS GENETICS (2010)
Methodological challenges of genome-wide association analysis in Africa
Yik-Ying Teo et al.
NATURE REVIEWS GENETICS (2010)
Genotype imputation for genome-wide association studies
Jonathan Marchini et al.
NATURE REVIEWS GENETICS (2010)
Common variants at 30 loci contribute to polygenic dyslipidemia
Sekar Kathiresan et al.
NATURE GENETICS (2009)
SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap
Andrew D. Johnson et al.
BIOINFORMATICS (2008)
GenoSNP: a variational Bayes within-sample SNP genotyping algorithm that does not require a reference population
Eleni Giannoulatou et al.
BIOINFORMATICS (2008)
A second generation human haplotype map of over 3.1 million SNPs
Kelly A. Frazer et al.
NATURE (2007)
PLINK: A tool set for whole-genome association and population-based linkage analyses
Shaun Purcell et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Population structure and eigenanalysis
Nick Patterson et al.
PLOS GENETICS (2006)
Principal components analysis corrects for stratification in genome-wide association studies
Alkes L. Price et al.
NATURE GENETICS (2006)
GENCODE: producing a reference annotation for ENCODE
Jennifer Harrow et al.
GENOME BIOLOGY (2006)
Cholesteryl ester transfer protein promoter single-nucleotide polymorphisms in Sp1-binding sites affect transcription and are associated with high-density lipoprotein cholesterol
JF Thompson et al.
CLINICAL GENETICS (2004)
Measuring inconsistency in meta-analyses
JPT Higgins et al.
BMJ-BRITISH MEDICAL JOURNAL (2003)
Share Paper
