Related references
Note: Only part of the references are listed.Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1α are associated with C-reactive protein
Alexander P. Reiner et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Loci related to metabolic-syndrome pathways including LEPR, HNF1A, IL6R, and GCKR associate with plasma C-reactive protein:: The women's genome health study
Paul M. Ridker et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Association of the TCF7L2 polymorphism with colorectal cancer and adenoma risk
Aditi Hazra et al.
CANCER CAUSES & CONTROL (2008)
Variation in TCF7L2 and increased risk of colon cancer -: The Atherosclerosis Risk in Communities (ARIC) Study
Aaron R. Folsom et al.
DIABETES CARE (2008)
Estimation of the multiple testing burden for genomewide association studies of nearly all common variants
Itsik Pe'er et al.
GENETIC EPIDEMIOLOGY (2008)
Association between microdeletion and microduplication at 16p11.2 and autism
Lauren A. Weiss et al.
NEW ENGLAND JOURNAL OF MEDICINE (2008)
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia
Tom Walsh et al.
SCIENCE (2008)
Psoriasis is associated with pleiotropic susceptibility loci identified in type II diabetes and Crohn disease
N. Wolf et al.
JOURNAL OF MEDICAL GENETICS (2008)
Direct selection of human genomic loci by microarray hybridization
Thomas J. Albert et al.
NATURE METHODS (2007)
Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma
Gudmar Thorleifsson et al.
SCIENCE (2007)
Genomewide association analysis of coronary artery disease
Nilesh J. Samani et al.
NEW ENGLAND JOURNAL OF MEDICINE (2007)
Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes
Julius Gudmundsson 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 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)
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)
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis
John D. Rioux et al.
NATURE GENETICS (2007)
Multiple regions within 8q24 independently affect risk for prostate cancer
Christopher A. Haiman et al.
NATURE GENETICS (2007)
Strong association of de novo copy number mutations with autism
Jonathan Sebat et al.
SCIENCE (2007)
Three functional variants of IFN regulatory factor 5 (IRF5) define risk and protective haplotypes for human lupus
Robert R. Graham et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
A large-scale genetic association study confirms IL12B and leads to the identification of IL23R as psoriasis-risk genes
Michele Cargill et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes
Eleftheria Zeggini et al.
SCIENCE (2007)
A genome-wide association study identifies IL23R as an inflammatory bowel disease gene
Richard H. Duerr et al.
SCIENCE (2006)
The connectivity map: Using gene-expression signatures to connect small molecules, genes, and disease
Justin Lamb et al.
SCIENCE (2006)
Admixture mapping identifies 8q24 as a prostate cancer risk locus in African-American men
Matthew L. Freedman et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration
Mingyao Li et al.
NATURE GENETICS (2006)
Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degeneration
Julian Maller et al.
NATURE GENETICS (2006)
Principal components analysis corrects for stratification in genome-wide association studies
Alkes L. Price et al.
NATURE GENETICS (2006)
Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome
Devin P. Locke et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
TCF7L2 polymorphisms and progression to diabetes in the Diabetes Prevention Program
Jose C. Florez et al.
NEW ENGLAND JOURNAL OF MEDICINE (2006)
A common variant associated with prostate cancer in European and African populations
Laufey T. Amundadottir et al.
NATURE GENETICS (2006)
Sequence variations in PCSK9, low LDL, and protection against coronary heart disease
JC Cohen et al.
NEW ENGLAND JOURNAL OF MEDICINE (2006)
A spectrum of PCSK9 Alleles contributes to plasma levels of low-density lipoprotein cholesterol
IK Kotowski et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes
SFA Grant et al.
NATURE GENETICS (2006)
Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk
A Rivera et al.
HUMAN MOLECULAR GENETICS (2005)
Efficiency and power in genetic association studies
PIW de Bakker et al.
NATURE GENETICS (2005)
Population structure, differential bias and genomic control in a large-scale, case-control association study
DG Clayton et al.
NATURE GENETICS (2005)
Fine-scale structural variation of the human genome
E Tuzun et al.
NATURE GENETICS (2005)
Complement factor H polymorphism in age-related macular degeneration
RJ Klein et al.
SCIENCE (2005)
Complement factor H polymorphism and age-related macular degeneration
AO Edwards et al.
SCIENCE (2005)
Complement factor H variant increases the risk of age-related macular degeneration
JL Haines et al.
SCIENCE (2005)
Whole-genome patterns of common DNA variation in three human populations
DA Hinds et al.
SCIENCE (2005)
Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9
C Jonathan et al.
NATURE GENETICS (2005)
The fine-scale structure of recombination rate variation in the human genome
GAT McVean et al.
SCIENCE (2004)
Detection of large-scale variation in the human genome
AJ Iafrate et al.
NATURE GENETICS (2004)
Multiple rare Alleles contribute to low plasma levels of HDL cholesterol
JC Cohen et al.
SCIENCE (2004)
Large-scale copy number polymorphism in the human genome
J Sebat et al.
SCIENCE (2004)
Evidence for substantial fine-scale variation in recombination rates across the human genome
DC Crawford et al.
NATURE GENETICS (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)
Human genome sequence variation and the influence of gene history, mutation and recombination
DE Reich et al.
NATURE GENETICS (2002)
The structure of haplotype blocks in the human genome
SB Gabriel et al.
SCIENCE (2002)
Patterns of linkage disequilibrium in the human genome
KG Ardlie et al.
NATURE REVIEWS GENETICS (2002)
Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21
N Patil et al.
SCIENCE (2001)
Haplotype tagging for the identification of common disease genes
GCL Johnson et al.
NATURE GENETICS (2001)
High-resolution haplotype structure in the human genome
MJ Daly et al.
NATURE GENETICS (2001)
On the allelic spectrum of human disease
DE Reich et al.
TRENDS IN GENETICS (2001)
BRCA1 and BRCA2 and the genetics of breast and ovarian cancer
PL Welcsh et al.
HUMAN MOLECULAR GENETICS (2001)
The HLA system - Second of two parts
J Klein et al.
NEW ENGLAND JOURNAL OF MEDICINE (2000)
The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes
D Altshuler et al.
NATURE GENETICS (2000)
Share Paper
