Related references
Note: Only part of the references are listed.Genetic architecture of quantitative traits in mice, flies, and humans
Jonathan Flint et al.
GENOME RESEARCH (2009)
Finding the missing heritability of complex diseases
Teri A. Manolio et al.
NATURE (2009)
Common Genetic Variation and Human Traits
David B. Goldstein
NEW ENGLAND JOURNAL OF MEDICINE (2009)
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
Lucia A. Hindorff et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
Evolutionary Processes Acting on Candidate cis-Regulatory Regions in Humans Inferred from Patterns of Polymorphism and Divergence
Dara G. Torgerson et al.
PLOS GENETICS (2009)
Natural selection on genes that underlie human disease susceptibility
Ran Blekhman et al.
CURRENT BIOLOGY (2008)
Personal genomes: The case of the missing heritability
Brendan Maher
NATURE (2008)
Progress and challenges in genome-wide association studies in humans
Peter Donnelly
NATURE (2008)
Genome-wide association analysis identifies 20 loci that influence adult height
Michael N. Weedon et al.
NATURE GENETICS (2008)
Common and rare variants in multifactorial susceptibility to common diseases
Walter Bodmer et al.
NATURE GENETICS (2008)
Many sequence variants affecting diversity of adult human height
Daniel F. Gudbjartsson et al.
NATURE GENETICS (2008)
Identification of ten loci associated with height highlights new biological pathways in human growth
Guillaume Lettre et al.
NATURE GENETICS (2008)
Assessing the evolutionary impact of amino acid mutations in the human genome
Adam R. Boyko et al.
PLOS GENETICS (2008)
A second generation human haplotype map of over 3.1 million SNPs
Kelly A. Frazer et al.
NATURE (2007)
The distribution of fitness effects of new mutations
Adam Eyre-Walker et al.
NATURE REVIEWS GENETICS (2007)
Widely distributed noncoding purifying selection in the human genome
Saurabh Asthana et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Most rare missense alleles are deleterious in humans: Implications for complex disease and association studies
Gregory V. Kryukov et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Localizing recent adaptive evolution in the human genome
Scott H. Williamson et al.
PLOS GENETICS (2007)
Distribution of the strength of selection against amino acid replacements in human proteins
LY Yampolsky et al.
HUMAN MOLECULAR GENETICS (2005)
A haplotype map of the human genome
D Altshuler et al.
NATURE (2005)
Natural selection on protein-coding genes in the human genome
CD Bustamante et al.
NATURE (2005)
Evolutionary constraints in conserved nongenic sequences of mammals
PD Keightley et al.
GENOME RESEARCH (2005)
Small fitness effect of mutations in highly conserved non-coding regions
GV Kryukov et al.
HUMAN MOLECULAR GENETICS (2005)
Theoretical models of selection and mutation on quantitative traits
T Johnson et al.
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES (2005)
Whole-genome patterns of common DNA variation in three human populations
DA Hinds et al.
SCIENCE (2005)
Evidence for widespread degradation of gene control regions in hominid genomes
PD Keightley et al.
PLOS BIOLOGY (2005)
Population history and natural selection shape patterns of genetic variation in 132 genes
JM Akey et al.
PLOS BIOLOGY (2004)
Coding sing le-nucleotide polymorphisms associated with complex vs. Mendelian disease: Evolutionary evidence for differences in molecular effects
PD Thomas et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
Pattern of sequence variation across 213 environmental response genes
RJ Livingston et al.
GENOME RESEARCH (2004)
On the allelic spectrum of human disease
DE Reich et al.
TRENDS IN GENETICS (2001)
Are rare variants responsible for susceptibility to complex diseases?
JK Pritchard
AMERICAN JOURNAL OF HUMAN GENETICS (2001)
Share Paper
