相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。9p21 DNA variants associated with coronary artery disease impair interferon-γ signalling response
Olivier Harismendy et al.
NATURE (2011)
A framework for variation discovery and genotyping using next-generation DNA sequencing data
Mark A. DePristo et al.
NATURE GENETICS (2011)
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
Aaron McKenna et al.
GENOME RESEARCH (2010)
Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice
Axel Visel et al.
NATURE (2010)
Integrating common and rare genetic variation in diverse human populations
David M. Altshuler et al.
NATURE (2010)
A map of human genome variation from population-scale sequencing
David Altshuler et al.
NATURE (2010)
Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk
Amy L. Sherborne et al.
NATURE GENETICS (2010)
Genome-wide association study identifies five new breast cancer susceptibility loci
Clare Turnbull et al.
NATURE GENETICS (2010)
A Genome-Wide Association Study of Optic Disc Parameters
Wishal D. Ramdas et al.
PLOS GENETICS (2010)
Genotype Imputation
Yun Li et al.
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS (2009)
Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing
Andreas Gnirke et al.
NATURE BIOTECHNOLOGY (2009)
New common variants affecting susceptibility to basal cell carcinoma
Simon N. Stacey et al.
NATURE GENETICS (2009)
Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility
Margaret Wrensch et al.
NATURE GENETICS (2009)
Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi
Mario Falchi et al.
NATURE GENETICS (2009)
Genome-wide association study identifies three loci associated with melanoma risk
D. Timothy Bishop et al.
NATURE GENETICS (2009)
Genome-wide association study identifies five susceptibility loci for glioma
Sanjay Shete et al.
NATURE GENETICS (2009)
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
Sekar Kathiresan et al.
NATURE GENETICS (2009)
The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm
Anna Helgadottir et al.
NATURE GENETICS (2008)
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
Eleftheria Zeggini et al.
NATURE GENETICS (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)
A common variant on chromosome 9p21 affects the risk of myocardial infarction
Anna Helgadottir et al.
SCIENCE (2007)
A common allele on chromosome 9 associated with coronary heart disease
Ruth McPherson et al.
SCIENCE (2007)
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants
Laura J. Scott et al.
SCIENCE (2007)
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
Richa Saxena et al.
SCIENCE (2007)
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes
Eleftheria Zeggini et al.
SCIENCE (2007)
Principal components analysis corrects for stratification in genome-wide association studies
Alkes L. Price et al.
NATURE GENETICS (2006)
Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputation
M Stephens et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
A new statistical method for haplotype reconstruction from population data
M Stephens et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2001)