Related references
Note: Only part of the references are listed.Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia
Christopher T. Johansen et al.
NATURE GENETICS (2010)
Common SNPs explain a large proportion of the heritability for human height
Jian Yang et al.
NATURE GENETICS (2010)
Rare Variants Create Synthetic Genome-Wide Associations
Samuel P. Dickson et al.
PLOS BIOLOGY (2010)
Finding the missing heritability of complex diseases
Teri A. Manolio et al.
NATURE (2009)
Parental origin of sequence variants associated with complex diseases
Augustine Kong et al.
NATURE (2009)
Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
Prateek Kumar et al.
NATURE PROTOCOLS (2009)
Rare Variants of IFIH1, a Gene Implicated in Antiviral Responses, Protect Against Type 1 Diabetes
Sergey Nejentsev et al.
SCIENCE (2009)
Common and rare variants in multifactorial susceptibility to common diseases
Walter Bodmer et al.
NATURE GENETICS (2008)
Rare independent mutations in renal salt handling genes contribute to blood pressure variation
Weizhen Ji et al.
NATURE GENETICS (2008)
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
Jeffrey C. Barrett et al.
NATURE GENETICS (2008)
The road to genome-wide association studies
Leonid Kruglyak
NATURE REVIEWS GENETICS (2008)
Genetic Mapping in Human Disease
David Altshuler et al.
SCIENCE (2008)
Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4
Cecile Libioulle et al.
PLOS GENETICS (2007)
A genome-wide association study identifies IL23R as an inflammatory bowel disease gene
Richard H. Duerr et al.
SCIENCE (2006)
Genome sequencing in microfabricated high-density picolitre reactors
M Margulies et al.
NATURE (2005)
Multiple rare Alleles contribute to low plasma levels of HDL cholesterol
JC Cohen et al.
SCIENCE (2004)
Multiple rare variants in different genes account for multifactorial inherited susceptibility to colorectal adenomas
NS Fearnhead et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
Functional variants of OCTN cation transporter genes are associated with Crohn disease
VD Peltekova et al.
NATURE GENETICS (2004)
Human non-synonymous SNPs: server and survey
V Ramensky et al.
NUCLEIC ACIDS RESEARCH (2002)
CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease
S Lesage et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2002)
Are rare variants responsible for susceptibility to complex diseases?
JK Pritchard
AMERICAN JOURNAL OF HUMAN GENETICS (2001)
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
JP Hugot et al.
NATURE (2001)
Share Paper
