The population genetics of structural variation.

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. Genome Res (2007) 19.07

Human genetic variation and its contribution to complex traits. Nat Rev Genet (2009) 12.11

Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease. Nat Genet (2008) 9.52

African genetic diversity: implications for human demographic history, modern human origins, and complex disease mapping. Annu Rev Genomics Hum Genet (2008) 6.06

Challenges and standards in integrating surveys of structural variation. Nat Genet (2007) 6.05

The fine-scale and complex architecture of human copy-number variation. Am J Hum Genet (2008) 5.08

Copy number variation and evolution in humans and chimpanzees. Genome Res (2008) 2.69

Analysis of copy number variants and segmental duplications in the human genome: Evidence for a change in the process of formation in recent evolutionary history. Genome Res (2008) 2.17

Genetic association analysis of copy-number variation (CNV) in human disease pathogenesis. Genomics (2008) 1.76

Natural selection and the distribution of identity-by-descent in the human genome. Genetics (2010) 1.52

High resolution discovery and confirmation of copy number variants in 90 Yoruba Nigerians. Genome Biol (2009) 1.49

Copy number variation in the porcine genome inferred from a 60 k SNP BeadChip. BMC Genomics (2010) 1.43

From microscopes to microarrays: dissecting recurrent chromosomal rearrangements. Nat Rev Genet (2007) 1.37

Quantifying the mechanisms of domain gain in animal proteins. Genome Biol (2010) 1.32

Dosage sensitivity shapes the evolution of copy-number varied regions. PLoS One (2010) 1.30

Copy number variation in the genomes of twelve natural isolates of Caenorhabditis elegans. BMC Genomics (2010) 1.20

A genome-wide detection of copy number variations using SNP genotyping arrays in swine. BMC Genomics (2012) 1.18

Combinatorial content of CCL3L and CCL4L gene copy numbers influence HIV-AIDS susceptibility in Ukrainian children. AIDS (2009) 1.17

Recent findings in the genetics of blood pressure and hypertension traits. Am J Hypertens (2010) 1.14

Population-genetic nature of copy number variations in the human genome. Hum Mol Genet (2009) 1.12

A framework for assessing the risk of resistance for anti-malarials in development. Malar J (2012) 1.09

Whole genome distribution and ethnic differentiation of copy number variation in Caucasian and Asian populations. PLoS One (2009) 1.06

Gene copy number variation throughout the Plasmodium falciparum genome. BMC Genomics (2009) 1.03

An algorithm for inferring complex haplotypes in a region of copy-number variation. Am J Hum Genet (2008) 1.02

Copy number variation in the domestic dog. Mamm Genome (2011) 1.01

The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation. Front Genet (2013) 0.96

MOCSphaser: a haplotype inference tool from a mixture of copy number variation and single nucleotide polymorphism data. Bioinformatics (2008) 0.95

Olfactory copy number association with age at onset of Alzheimer disease. Neurology (2011) 0.95

Refined QTLs of osteoporosis-related traits by linkage analysis with genome-wide SNPs: Framingham SHARe. Bone (2010) 0.95

Osteoporosis: an evolutionary perspective. Hum Genet (2008) 0.94

Copy number variation in the cattle genome. Funct Integr Genomics (2012) 0.92

Haploinsufficiency of DNA Damage Response Genes and their Potential Influence in Human Genomic Disorders. Curr Genomics (2008) 0.91

Copy number variants (CNVs) in primate species using array-based comparative genomic hybridization. Methods (2009) 0.91

cn.FARMS: a latent variable model to detect copy number variations in microarray data with a low false discovery rate. Nucleic Acids Res (2011) 0.89

The evolutionary significance of copy number variation in the human genome. Cytogenet Genome Res (2009) 0.89

Submicroscopic chromosome imbalance in patients with developmental delay and/or dysmorphism referred specifically for Fragile X testing and karyotype analysis. Mol Cytogenet (2008) 0.88

Lower linkage disequilibrium at CNVs is due to both recurrent mutation and transposing duplications. Mol Biol Evol (2010) 0.88

Genome-wide copy number variations in Oryza sativa L. BMC Genomics (2013) 0.86

Large scale variation in DNA copy number in chicken breeds. BMC Genomics (2013) 0.86

Genome-wide copy number variation study and gene expression analysis identify ABI3BP as a susceptibility gene for Kashin-Beck disease. Hum Genet (2014) 0.86

A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum. Endocr Relat Cancer (2011) 0.84

Genetics of asthma: a molecular biologist perspective. Clin Mol Allergy (2009) 0.83

Inferring haplotypes of copy number variations from high-throughput data with uncertainty. G3 (Bethesda) (2011) 0.81

The 8p23 inversion polymorphism determines local recombination heterogeneity across human populations. Genome Biol Evol (2014) 0.81

Association between reduced copy-number at T-cell receptor gamma (TCRgamma) and childhood allergic asthma: A possible role for somatic mosaicism. Mutat Res (2010) 0.81

Systematic identification of balanced transposition polymorphisms in Saccharomyces cerevisiae. PLoS Genet (2009) 0.81

The comparative landscape of duplications in Heliconius melpomene and Heliconius cydno. Heredity (Edinb) (2016) 0.81

Microbial variome database: point mutations, adaptive or not, in bacterial core genomes. Mol Biol Evol (2013) 0.80

Detection of genome-wide copy number variations in two chicken lines divergently selected for abdominal fat content. BMC Genomics (2014) 0.80

Biological relevance of CNV calling methods using familial relatedness including monozygotic twins. BMC Bioinformatics (2014) 0.80

Genome-wide scan for copy number variation association with age at onset of Alzheimer's disease. J Alzheimers Dis (2013) 0.79

Diversity and population-genetic properties of copy number variations and multicopy genes in cattle. DNA Res (2016) 0.79

Plasmodium copy number variation scan: gene copy numbers evaluation in haploid genomes. Malar J (2016) 0.79

Structural conservation of a short, functional, peptide-sequence motif. Front Biosci (Landmark Ed) (2009) 0.78

Genome architecture and its roles in human copy number variation. Genomics Inform (2014) 0.77

Population-genetic properties of differentiated copy number variations in cattle. Sci Rep (2016) 0.77

Ordered subset analysis of copy number variation association with age at onset of Alzheimer's disease. J Alzheimers Dis (2014) 0.76

Extensive copy number variations in admixed Indian population of African ancestry: potential involvement in adaptation. Genome Biol Evol (2014) 0.76

Unexpected effects of different genetic backgrounds on identification of genomic rearrangements via whole-genome next generation sequencing. BMC Genomics (2016) 0.75

SeqCNV: a novel method for identification of copy number variations in targeted next-generation sequencing data. BMC Bioinformatics (2017) 0.75

A sequential Monte Carlo framework for haplotype inference in CNV/SNP genotype data. EURASIP J Bioinform Syst Biol (2014) 0.75

Segmentation and estimation for SNP microarrays: a Bayesian multiple change-point approach. Biometrics (2010) 0.75

Web-based database and viewer of East asian copy number variations. Genomics Inform (2012) 0.75

Fitness consequences of polymorphic inversions in the zebra finch genome. Genome Biol (2016) 0.75

Recurrent copy number variants associated with bronchopulmonary dysplasia. Pediatr Res (2016) 0.75

Medical case reports in the age of genomic medicine. Clin Transl Immunology (2015) 0.75

Enhanced copy number variants detection from whole-exome sequencing data using EXCAVATOR2. Nucleic Acids Res (2016) 0.75

Leveraging long read sequencing from a single individual to provide a comprehensive resource for benchmarking variant calling methods. Sci Rep (2015) 0.75

Identification of Copy Number Variations in Xiang and Kele Pigs. PLoS One (2016) 0.75

Worldwide population distribution of the common LCE3C-LCE3B deletion associated with psoriasis and other autoimmune disorders. BMC Genomics (2013) 0.75

Haplotype phasing and inheritance of copy number variants in nuclear families. PLoS One (2015) 0.75

Trans-oceanic genomic divergence of Atlantic cod ecotypes is associated with large inversions. Heredity (Edinb) (2017) 0.75

The most common technologies and tools for functional genome analysis. Acta Med Litu (2017) 0.75

CNV Analysis of Host Responses to Porcine Reproductive and Respiratory Syndrome Virus Infection. J Genomics (2017) 0.75

Analysis of copy number variation in the Abp gene regions of two house mouse subspecies suggests divergence during the gene family expansions. Genome Biol Evol (2017) 0.75

Inference of population structure using multilocus genotype data. Genetics (2000) 147.76

A haplotype map of the human genome. Nature (2005) 105.70

Global variation in copy number in the human genome. Nature (2006) 57.50

Detection of large-scale variation in the human genome. Nat Genet (2004) 49.18

THE NUMBER OF ALLELES THAT CAN BE MAINTAINED IN A FINITE POPULATION. Genetics (1964) 45.28

Large-scale copy number polymorphism in the human genome. Science (2004) 34.64

A map of recent positive selection in the human genome. PLoS Biol (2006) 29.19

High resolution of human evolutionary trees with polymorphic microsatellites. Nature (1994) 28.48

A fine-scale map of recombination rates and hotspots across the human genome. Science (2005) 26.82

Analysis of gene diversity in subdivided populations. Proc Natl Acad Sci U S A (1973) 26.31

Initial sequence of the chimpanzee genome and comparison with the human genome. Nature (2005) 25.67

Fine-scale structural variation of the human genome. Nat Genet (2005) 24.31

Are rare variants responsible for susceptibility to complex diseases? Am J Hum Genet (2001) 22.46

Detecting recent positive selection in the human genome from haplotype structure. Nature (2002) 22.00

Structural variation in the human genome. Nat Rev Genet (2006) 21.40

Recent segmental duplications in the human genome. Science (2002) 21.30

Modeling linkage disequilibrium and identifying recombination hotspots using single-nucleotide polymorphism data. Genetics (2003) 17.73

The fine-scale structure of recombination rate variation in the human genome. Science (2004) 17.05

The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility. Science (2005) 17.00

A high-resolution survey of deletion polymorphism in the human genome. Nat Genet (2005) 16.99

Common deletion polymorphisms in the human genome. Nat Genet (2006) 15.66

The genetical structure of populations. Ann Eugen (1951) 15.13

A common inversion under selection in Europeans. Nat Genet (2005) 13.66

Segmental duplications and copy-number variation in the human genome. Am J Hum Genet (2005) 13.33

A model of mutation appropriate to estimate the number of electrophoretically detectable alleles in a finite population. Genet Res (1973) 13.08

Positive natural selection in the human lineage. Science (2006) 12.55

Genome architecture, rearrangements and genomic disorders. Trends Genet (2002) 12.26

An initial map of insertion and deletion (INDEL) variation in the human genome. Genome Res (2006) 11.60

Common deletions and SNPs are in linkage disequilibrium in the human genome. Nat Genet (2005) 9.61

Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans. Nature (2006) 9.30

Allele frequencies at microsatellite loci: the stepwise mutation model revisited. Genetics (1993) 8.60

A worldwide survey of haplotype variation and linkage disequilibrium in the human genome. Nat Genet (2006) 8.46

Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome. Am J Hum Genet (2006) 7.70

Genome assembly comparison identifies structural variants in the human genome. Nat Genet (2006) 6.93

Ascertainment bias in studies of human genome-wide polymorphism. Genome Res (2005) 6.63

Complex SNP-related sequence variation in segmental genome duplications. Nat Genet (2004) 5.90

A genome-wide comparison of recent chimpanzee and human segmental duplications. Nature (2005) 5.51

Accurate and reliable high-throughput detection of copy number variation in the human genome. Genome Res (2006) 5.50

The complex interplay among factors that influence allelic association. Nat Rev Genet (2004) 5.26

Interrogating multiple aspects of variation in a full resequencing data set to infer human population size changes. Proc Natl Acad Sci U S A (2005) 5.21

Evidence for positive selection in the superoxide dismutase (Sod) region of Drosophila melanogaster. Genetics (1994) 5.05

The rate of molecular evolution considered from the standpoint of population genetics. Proc Natl Acad Sci U S A (1969) 4.75

Adjusting the focus on human variation. Trends Genet (2000) 4.44

Human diallelic insertion/deletion polymorphisms. Am J Hum Genet (2002) 4.44

Bias of selection on human copy-number variants. PLoS Genet (2006) 4.44

Human subtelomeres are hot spots of interchromosomal recombination and segmental duplication. Nature (2005) 4.30

De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints. Am J Hum Genet (1991) 4.04

Mutational mechanisms of Williams-Beuren syndrome deletions. Am J Hum Genet (2003) 3.76

Positive selection of a gene family during the emergence of humans and African apes. Nature (2001) 3.68

Hotspots for copy number variation in chimpanzees and humans. Proc Natl Acad Sci U S A (2006) 3.68

Pseudogenes: are they "junk" or functional DNA? Annu Rev Genet (2003) 3.47

High mutation rates have driven extensive structural polymorphism among human Y chromosomes. Nat Genet (2006) 3.46

Estimating allele age. Annu Rev Genomics Hum Genet (2000) 3.30

An apportionment of human DNA diversity. Proc Natl Acad Sci U S A (1997) 3.15

Molecular mechanisms for constitutional chromosomal rearrangements in humans. Annu Rev Genet (2000) 2.82

The effect of gene conversion on intralocus associations. Genetics (1998) 2.77

Correcting for ascertainment biases when analyzing SNP data: applications to the estimation of linkage disequilibrium. Theor Popul Biol (2003) 2.73

High frequencies of alpha-thalassaemia are the result of natural selection by malaria. Nature (1986) 2.68

Genetic variation among world populations: inferences from 100 Alu insertion polymorphisms. Genome Res (2003) 2.47

Human lineage-specific amplification, selection, and neuronal expression of DUF1220 domains. Science (2006) 2.18

A chromosomal duplication map of malformations: regions of suspected haplo- and triplolethality--and tolerance of segmental aneuploidy--in humans. Am J Hum Genet (1999) 2.15

Breakpoints of gross deletions coincide with non-B DNA conformations. Proc Natl Acad Sci U S A (2004) 2.13

Discovery of human inversion polymorphisms by comparative analysis of human and chimpanzee DNA sequence assemblies. PLoS Genet (2005) 2.05

A novel human DNA polymorphism resulting from transfer of DNA from chromosome 6 to chromosome 16. Genomics (1990) 1.84

Minisatellite diversity supports a recent African origin for modern humans. Nat Genet (1996) 1.84

Scan of human genome reveals no new Loci under ancient balancing selection. Genetics (2006) 1.68

Recurrent duplication and deletion polymorphisms on the long arm of the Y chromosome in normal males. Hum Mol Genet (1996) 1.68

Unexpectedly high rate of de novo constitutional t(11;22) translocations in sperm from normal males. Nat Genet (2001) 1.66

A large AZFc deletion removes DAZ3/DAZ4 and nearby genes from men in Y haplogroup N. Am J Hum Genet (2003) 1.62

The DNA sequence and comparative analysis of human chromosome 5. Nature (2004) 1.62

High-throughput genotyping of intermediate-size structural variation. Hum Mol Genet (2006) 1.61

Recurrent duplication-driven transposition of DNA during hominoid evolution. Proc Natl Acad Sci U S A (2006) 1.47

Assaying chromosomal inversions by single-molecule haplotyping. Nat Methods (2006) 1.34

Unequal exchange at the Charcot-Marie-Tooth disease type 1A recombination hot-spot is not elevated above the genome average rate. Hum Mol Genet (2000) 1.21

Accurate whole human genome sequencing using reversible terminator chemistry. Nature (2008) 90.20

Global variation in copy number in the human genome. Nature (2006) 57.50

Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing. Nat Genet (2008) 43.63

Paired-end mapping reveals extensive structural variation in the human genome. Science (2007) 30.46

Origins and functional impact of copy number variation in the human genome. Nature (2009) 23.63

Relative impact of nucleotide and copy number variation on gene expression phenotypes. Science (2007) 23.38

A high-resolution survey of deletion polymorphism in the human genome. Nat Genet (2005) 16.99

Mapping copy number variation by population-scale genome sequencing. Nature (2011) 12.55

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls. Nature (2010) 12.27

A systematic survey of loss-of-function variants in human protein-coding genes. Science (2012) 12.25

Cerebral organoids model human brain development and microcephaly. Nature (2013) 9.07

Variation in genome-wide mutation rates within and between human families. Nat Genet (2011) 8.84

Copy number variation: new insights in genome diversity. Genome Res (2006) 8.66

Copy number variation in human health, disease, and evolution. Annu Rev Genomics Hum Genet (2009) 7.64

The DNA sequence of the human X chromosome. Nature (2005) 6.97

Challenges and standards in integrating surveys of structural variation. Nat Genet (2007) 6.05

Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays. Genome Res (2006) 5.97

Accurate and reliable high-throughput detection of copy number variation in the human genome. Genome Res (2006) 5.50

Large, rare chromosomal deletions associated with severe early-onset obesity. Nature (2009) 5.20

Characterising and predicting haploinsufficiency in the human genome. PLoS Genet (2010) 4.85

A robust statistical method for case-control association testing with copy number variation. Nat Genet (2008) 4.78

Germline rates of de novo meiotic deletions and duplications causing several genomic disorders. Nat Genet (2007) 4.59

Genome-wide mapping and assembly of structural variant breakpoints in the mouse genome. Genome Res (2010) 4.22

The UK10K project identifies rare variants in health and disease. Nature (2015) 3.89

The genetic legacy of the Mongols. Am J Hum Genet (2003) 3.84

Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridization. Genome Biol (2007) 3.54

Mutation spectrum revealed by breakpoint sequencing of human germline CNVs. Nat Genet (2010) 3.52

Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing. Nat Genet (2010) 3.49

Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants. Nat Biotechnol (2011) 3.25

Genetic analysis of completely sequenced disease-associated MHC haplotypes identifies shuffling of segments in recent human history. PLoS Genet (2006) 2.80

Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome. Nat Genet (2012) 2.80

Towards a comprehensive structural variation map of an individual human genome. Genome Biol (2010) 2.79

Copy number variation and evolution in humans and chimpanzees. Genome Res (2008) 2.69

Adaptive evolution of UGT2B17 copy-number variation. Am J Hum Genet (2008) 2.58

Male demography in East Asia: a north-south contrast in human population expansion times. Genetics (2006) 2.30

Recessive HYDIN mutations cause primary ciliary dyskinesia without randomization of left-right body asymmetry. Am J Hum Genet (2012) 1.91

A chromosomal rearrangement hotspot can be identified from population genetic variation and is coincident with a hotspot for allelic recombination. Am J Hum Genet (2006) 1.86

A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism. Proc Natl Acad Sci U S A (2012) 1.85

DECIPHER: database for the interpretation of phenotype-linked plausibly pathogenic sequence and copy-number variation. Nucleic Acids Res (2013) 1.83

Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity. Nat Genet (2013) 1.72

DeNovoGear: de novo indel and point mutation discovery and phasing. Nat Methods (2013) 1.65

Fast-evolving noncoding sequences in the human genome. Genome Biol (2007) 1.64

Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits. Circ Cardiovasc Genet (2012) 1.60

Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders. Am J Hum Genet (2012) 1.52

Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycan. Am J Hum Genet (2013) 1.50

DECIPHER: web-based, community resource for clinical interpretation of rare variants in developmental disorders. Hum Mol Genet (2012) 1.50

Deciphering past human population movements in Oceania: provably optimal trees of 127 mtDNA genomes. Mol Biol Evol (2006) 1.49

Deep short-read sequencing of chromosome 17 from the mouse strains A/J and CAST/Ei identifies significant germline variation and candidate genes that regulate liver triglyceride levels. Genome Biol (2009) 1.43

Genetic basis of Y-linked hearing impairment. Am J Hum Genet (2013) 1.42

Quantifying single nucleotide variant detection sensitivity in exome sequencing. BMC Bioinformatics (2013) 1.41

Dynamics of a human interparalog gene conversion hotspot. Genome Res (2004) 1.40

Structural variation on the short arm of the human Y chromosome: recurrent multigene deletions encompassing Amelogenin Y. Hum Mol Genet (2006) 1.36

Assaying chromosomal inversions by single-molecule haplotyping. Nat Methods (2006) 1.34

Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease. Hum Mol Genet (2010) 1.21

Mutations in the gene encoding IFT dynein complex component WDR34 cause Jeune asphyxiating thoracic dystrophy. Am J Hum Genet (2013) 1.16

The Y-chromosome landscape of the Philippines: extensive heterogeneity and varying genetic affinities of Negrito and non-Negrito groups. Eur J Hum Genet (2010) 1.15

Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1. PLoS Genet (2013) 1.08

Combined NGS approaches identify mutations in the intraflagellar transport gene IFT140 in skeletal ciliopathies with early progressive kidney Disease. Hum Mutat (2013) 1.07

Deletions of chromosomal regulatory boundaries are associated with congenital disease. Genome Biol (2014) 1.07

A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders. Genome Res (2013) 1.06

Genomic pathology of SLE-associated copy-number variation at the FCGR2C/FCGR3B/FCGR2B locus. Am J Hum Genet (2012) 1.02

High level of male-biased Scandinavian admixture in Greenlandic Inuit shown by Y-chromosomal analysis. Hum Genet (2003) 1.01

Evidence for widespread reticulate evolution within human duplicons. Am J Hum Genet (2005) 0.98

Mutations in B4GALNT1 (GM2 synthase) underlie a new disorder of ganglioside biosynthesis. Brain (2013) 0.93

Identification of a human synaptotagmin-1 mutation that perturbs synaptic vesicle cycling. J Clin Invest (2015) 0.91

Long-range, high-throughput haplotype determination via haplotype-fusion PCR and ligation haplotyping. Nucleic Acids Res (2008) 0.90

Empirical research on the ethics of genomic research. Am J Med Genet A (2013) 0.88

High-throughput haplotype determination over long distances by haplotype fusion PCR and ligation haplotyping. Nat Protoc (2009) 0.86

NDUFA4 mutations underlie dysfunction of a cytochrome c oxidase subunit linked to human neurological disease. Cell Rep (2013) 0.82

Mosaic structural variation in children with developmental disorders. Hum Mol Genet (2015) 0.81

Harnessing genomics to identify environmental determinants of heritable disease. Mutat Res (2012) 0.81

Global haplotype diversity in the human insulin gene region. Genome Res (2003) 0.81

A singular chromosome. Nat Genet (2003) 0.80

Validity of the family-based association test for copy number variant data in the case of non-linear intensity-genotype relationship. Genet Epidemiol (2012) 0.79

B56δ-related protein phosphatase 2A dysfunction identified in patients with intellectual disability. J Clin Invest (2015) 0.79

Shotgun haplotyping: a novel method for surveying allelic sequence variation. Nucleic Acids Res (2005) 0.78

Copy number variation in the human Y chromosome in the UK population. Hum Genet (2015) 0.77

Y chromosomal STRs haplotypes in two populations from Bolivia. Leg Med (Tokyo) (2006) 0.75

Don't mix radiocarbon and calendar years. Nature (2005) 0.75

Origins of the domestic horse. Proc Natl Acad Sci U S A (2012) 0.75

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans. Am J Hum Genet (2016) 0.75

Erratum to: Copy number variation in the human Y chromosome in the UK population. Hum Genet (2015) 0.75