Interlocus gene conversion explains at least 2.7 % of single nucleotide variants in human segmental duplications

Correlation between frequency of non-allelic homologous recombination and homology properties: evidence from homology-mediated CNV mutations in the human genome

(2014) Zhen Peng et al.   HUMAN MOLECULAR GENETICS

Rapid and accurate large-scale genotyping of duplicated genes and discovery of interlocus gene conversions

(2013) Xander Nuttle et al.   NATURE METHODS

Signals of Historical Interlocus Gene Conversion in Human Segmental Duplications

(2013) Beth L. Dumont et al.   PLoS One

Evolution of Human-Specific Neural SRGAP2 Genes by Incomplete Segmental Duplication

(2012) Megan Y. Dennis et al.   CELL

Rate of de novo mutations and the importance of father’s age to disease risk

(2012) Augustine Kong et al.   NATURE

Estimating the human mutation rate using autozygosity in a founder population

(2012) Catarina D Campbell et al.   NATURE GENETICS

Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes

(2012) J. A. Tennessen et al.   SCIENCE

Recent Explosive Human Population Growth Has Resulted in an Excess of Rare Genetic Variants

(2012) A. Keinan et al.   SCIENCE

Interlocus gene conversion events introduce deleterious mutations into at least 1% of human genes associated with inherited disease

(2011) C. Casola et al.   GENOME RESEARCH

Variation in genome-wide mutation rates within and between human families

(2011) Donald F Conrad et al.   NATURE GENETICS

Testing the Ortholog Conjecture with Comparative Functional Genomic Data from Mammals

(2011) Nathan L. Nehrt et al.   PLoS Computational Biology

Neutral and Non-Neutral Evolution of Duplicated Genes with Gene Conversion

(2011) Jeffrey Fawcett et al.   Genes

Haplotype-resolved genome sequencing of a Gujarati Indian individual

(2010) Jacob O Kitzman et al.   NATURE BIOTECHNOLOGY

Rate, molecular spectrum, and consequences of human mutation

(2010) M. Lynch   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Diversity of Human Copy Number Variation and Multicopy Genes

(2010) Peter H. Sudmant et al.   SCIENCE

Haplotype-Sharing Analysis Implicates Chromosome 7q36 Harboring DPP6 in Familial Idiopathic Ventricular Fibrillation

(2009) Marielle Alders et al.   AMERICAN JOURNAL OF HUMAN GENETICS

The Sequence Alignment/Map format and SAMtools

(2009) H. Li et al.   BIOINFORMATICS

Fast and accurate short read alignment with Burrows-Wheeler transform

(2009) H. Li et al.   BIOINFORMATICS

Minimal Effect of Ectopic Gene Conversion Among Recent Duplicates in Four Mammalian Genomes

(2009) C. L. McGrath et al.   GENETICS

The Power of the Methods for Detecting Interlocus Gene Conversion

(2009) S. P. Mansai et al.   GENETICS

Adaptive evolution of young gene duplicates in mammals

(2009) M. V. Han et al.   GENOME RESEARCH

Serine racemase is associated with schizophrenia susceptibility in humans and in a mouse model

(2009) Viviane Labrie et al.   HUMAN MOLECULAR GENETICS

Human Genome Sequencing Using Unchained Base Reads on Self-Assembling DNA Nanoarrays

(2009) R. Drmanac et al.   SCIENCE

Coordinate expression of the human pregnancy-specific glycoprotein gene family during induced and replicative senescence

(2008) Morio Endoh et al.   BIOGERONTOLOGY

Preservation of a Pseudogene by Gene Conversion and Diversifying Selection

(2008) S. Takuno et al.   GENETICS

Neofunctionalization of Duplicated Genes Under the Pressure of Gene Conversion

(2008) K. M. Teshima et al.   GENETICS

Ectopic gene conversions in the human genome

(2008) David Benovoy et al.   GENOMICS

GC-biased gene conversion promotes the fixation of deleterious amino acid changes in primates

(2008) Nicolas Galtier et al.   TRENDS IN GENETICS