Related references
Note: Only part of the references are listed.Quantification and correction of bias in tagging SNPs caused by insufficient sample size and marker density by means of haplotype-dropping
Mark M. Iles
GENETIC EPIDEMIOLOGY (2008)
A genome-wide association study implicates diacylglycerol kinase η (DGKH) and several other genes in the etiology of bipolar disorder
A. E. Baum et al.
MOLECULAR PSYCHIATRY (2008)
Genetics of cardiovascular diseases - From single mutations to the whole genome
Francois Cambien et al.
CIRCULATION (2007)
Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma
Gudmar Thorleifsson et al.
SCIENCE (2007)
Risk alleles for multiple sclerosis identified by a genomewide study
David A. Hafler et al.
NEW ENGLAND JOURNAL OF MEDICINE (2007)
A genetic risk factor for periodic limb movements in sleep
Hreinn Stefansson et al.
NEW ENGLAND JOURNAL OF MEDICINE (2007)
Genomewide association analysis of coronary artery disease
Nilesh J. Samani et al.
NEW ENGLAND JOURNAL OF MEDICINE (2007)
Type 2 diabetes whole-genome association study in four populations:: The DiaGen consortium
Jukka T. Salonen et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
A common genetic risk factor for colorectal and prostate cancer
Christopher A. Haiman et al.
NATURE GENETICS (2007)
Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer
Simon N. Stacey et al.
NATURE GENETICS (2007)
A new multipoint method for genome-wide association studies by imputation of genotypes
Jonathan Marchini et al.
NATURE GENETICS (2007)
A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer
David J. Hunter et al.
NATURE GENETICS (2007)
Genome-wide association study identifies novel breast cancer susceptibility loci
Douglas F. Easton et al.
NATURE (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)
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
Paul R. Burton et al.
NATURE (2007)
Replicating genotype-phenotype associations
Stephen J. Chanock et al.
NATURE (2007)
A variant in CDKAL1 influences insulin response and risk of type 2 diabetes
Valgerdur Steinthorsdottir et al.
NATURE GENETICS (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)
A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity
Timothy M. Frayling et al.
SCIENCE (2007)
A genome-wide genotyping study in patients with ischaemic stroke:: initial analysis and data release
Mar Matarin et al.
LANCET NEUROLOGY (2007)
Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24
Julius Gudmundsson et al.
NATURE GENETICS (2007)
Upward bias in odds ratio estimates from genome-wide association studies
Chad Garner
GENETIC EPIDEMIOLOGY (2007)
Overcoming the winner's curse:: Estimating penetrance parameters from case-control data
Sebastian Zollner et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
A genome-wide association study identifies novel risk loci for type 2 diabetes
Robert Sladek et al.
NATURE (2007)
Simulations provide support for the common disease-common variant hypothesis
Bo Peng et al.
GENETICS (2007)
Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL
Stefano Romeo et al.
NATURE GENETICS (2007)
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes
Eleftheria Zeggini et al.
SCIENCE (2007)
Coverage and power in genomewide association studies
E Jorgenson et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
High-resolution whole-genome association study of Parkinson disease
DM Maraganore et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
Complement factor H polymorphism in age-related macular degeneration
RJ Klein et al.
SCIENCE (2005)
Genome-wide association studies: Theoretical and practical concerns
WYS Wang et al.
NATURE REVIEWS GENETICS (2005)
Multiple rare Alleles contribute to low plasma levels of HDL cholesterol
JC Cohen et al.
SCIENCE (2004)
Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease
KE Lohmueller et al.
NATURE GENETICS (2003)
Detecting disease associations due to linkage disequilibrium using haplotype tags: A class of tests and the determinants of statistical power
JM Chapman et al.
HUMAN HEREDITY (2003)
The allelic architecture of human disease genes: common disease - common variant ... or not?
JK Pritchard et al.
HUMAN MOLECULAR GENETICS (2002)
Sample size requirements for matched case-control studies of gene-environment interaction
WJ Gauderman
STATISTICS IN MEDICINE (2002)
Large upward bias in estimation of locus-specific effects from genomewide scans
HHH Göring et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2001)
On the allelic spectrum of human disease
DE Reich et al.
TRENDS IN GENETICS (2001)
Linkage disequilibrium in humans: Models and data
JK Pritchard et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2001)
Are rare variants responsible for susceptibility to complex diseases?
JK Pritchard
AMERICAN JOURNAL OF HUMAN GENETICS (2001)