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。The genetics of speciation: are complex incompatibilities easier to evolve?
C. Fraisse et al.
JOURNAL OF EVOLUTIONARY BIOLOGY (2014)
ClinVar: public archive of relationships among sequence variation and human phenotype
Melissa J. Landrum et al.
NUCLEIC ACIDS RESEARCH (2014)
The UCSC Genome Browser database: 2014 update
Donna Karolchik et al.
NUCLEIC ACIDS RESEARCH (2014)
Ensembl 2014
Paul Flicek et al.
NUCLEIC ACIDS RESEARCH (2014)
Exonic Deletions in AUTS2 Cause a Syndromic Form of Intellectual Disability and Suggest a Critical Role for the C Terminus
Gea Beunders et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2013)
Should evolutionary geneticists worry about higher-order epistasis?
Daniel M. Weinreich et al.
CURRENT OPINION IN GENETICS & DEVELOPMENT (2013)
Comparative genomics as a tool to understand evolution and disease
Jessica Alfoeldi et al.
GENOME RESEARCH (2013)
The role of epistasis in protein evolution
David M. McCandlish et al.
NATURE (2013)
Genetic incompatibilities are widespread within species
Russell B. Corbett-Detig et al.
NATURE (2013)
Determinants of incomplete penetrance and variable expressivity in heritable cardiac arrhythmia syndromes
John R. Giudicessi et al.
TRANSLATIONAL RESEARCH (2013)
An integrative variant analysis suite for whole exome next-generation sequencing data
Danny Challis et al.
BMC BIOINFORMATICS (2012)
Estimating the Rate of Irreversibility in Protein Evolution
Onuralp Soylemez et al.
GENOME BIOLOGY AND EVOLUTION (2012)
Epistasis as the primary factor in molecular evolution
Michael S. Breen et al.
NATURE (2012)
Truncations of Titin Causing Dilated Cardiomyopathy
Daniel S. Herman et al.
NEW ENGLAND JOURNAL OF MEDICINE (2012)
SIFT web server: predicting effects of amino acid substitutions on proteins
Ngak-Leng Sim et al.
NUCLEIC ACIDS RESEARCH (2012)
Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes
Jacob A. Tennessen et al.
SCIENCE (2012)
Needles in stacks of needles: finding disease-causal variants in a wealth of genomic data
Gregory M. Cooper et al.
NATURE REVIEWS GENETICS (2011)
Diminishing Returns Epistasis Among Beneficial Mutations Decelerates Adaptation
Hsin-Hung Chou et al.
SCIENCE (2011)
Targeted enrichment beyond the consensus coding DNA sequence exome reveals exons with higher variant densities
Matthew N. Bainbridge et al.
GENOME BIOLOGY (2011)
Easy retrieval of single amino-acid polymorphisms and phenotype information using SwissVar
Anais Mottaz et al.
BIOINFORMATICS (2010)
Sequence space and the ongoing expansion of the protein universe
Inna S. Povolotskaya et al.
NATURE (2010)
A method and server for predicting damaging missense mutations
Ivan A. Adzhubei et al.
NATURE METHODS (2010)
A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies
Hemant Khanna et al.
NATURE GENETICS (2009)
Model-based prediction of sequence alignment quality
Virpi Ahola et al.
BIOINFORMATICS (2008)
Characterization of compensated mutations in terms of structural and physico-chemical properties
Carles Ferrer-Costa et al.
JOURNAL OF MOLECULAR BIOLOGY (2007)
Darwinian evolution can follow only very few mutational paths to fitter proteins
DM Weinreich et al.
SCIENCE (2006)
Compensated deleterious mutations in insect genomes
RJ Kulathinal et al.
SCIENCE (2004)
Why are some human disease-associated mutations fixed in mice?
LZ Gao et al.
TRENDS IN GENETICS (2003)
Initial sequencing and comparative analysis of the mouse genome
RH Waterston et al.
NATURE (2002)
Dobzhansky-Muller incompatibilities in protein evolution
AS Kondrashov et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
BBS4 is a minor contributor to Bardet-Biedl syndrome and may also participate in triallelic inheritance
N Katsanis et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2002)
分享论文
