Recently integrated Alu elements and human genomic diversity.

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Alu-directed transcriptional regulation of some novel miRNAs. BMC Genomics (2009) 1.00

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Detecting Alu insertions from high-throughput sequencing data. Nucleic Acids Res (2013) 0.93

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The role of recombination in the origin and evolution of Alu subfamilies. PLoS One (2013) 0.78

Genome-wide evolutionary and functional analysis of the Equine Repetitive Element 1: an insertion in the myostatin promoter affects gene expression. BMC Genet (2015) 0.78

Analysis of the features and source gene composition of the AluYg6 subfamily of human retrotransposons. BMC Evol Biol (2007) 0.76

Insertion and deletion polymorphisms of the ancient AluS family in the human genome. Mob DNA (2017) 0.75

Laboratory methods for the analysis of primate mobile elements. Methods Mol Biol (2010) 0.75

Discovery of rare, diagnostic AluYb8/9 elements in diverse human populations. Mob DNA (2017) 0.75

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The impact of retrotransposons on human genome evolution. Nat Rev Genet (2009) 8.08

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Mobile elements create structural variation: analysis of a complete human genome. Genome Res (2009) 7.06

The genome of a songbird. Nature (2010) 5.90

Genome analysis of the platypus reveals unique signatures of evolution. Nature (2008) 5.74

Genetic evidence for high-altitude adaptation in Tibet. Science (2010) 5.37

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Comparative and demographic analysis of orang-utan genomes. Nature (2011) 3.83

Large-scale SNP analysis reveals clustered and continuous patterns of human genetic variation. Hum Genomics (2005) 3.77

Repetitive elements may comprise over two-thirds of the human genome. PLoS Genet (2011) 3.70

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Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency. Am J Hum Genet (2011) 3.43

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Human genomic deletions mediated by recombination between Alu elements. Am J Hum Genet (2006) 3.15

A comprehensive map of mobile element insertion polymorphisms in humans. PLoS Genet (2011) 3.14

Birth of a chimeric primate gene by capture of the transposase gene from a mobile element. Proc Natl Acad Sci U S A (2006) 2.81

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

A comprehensive analysis of recently integrated human Ta L1 elements. Am J Hum Genet (2002) 2.47

SVA elements: a hominid-specific retroposon family. J Mol Biol (2005) 2.39

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood. Nat Genet (2012) 2.34

Natural selection and molecular evolution in PTC, a bitter-taste receptor gene. Am J Hum Genet (2004) 2.33

Mutations in genes encoding fast-twitch contractile proteins cause distal arthrogryposis syndromes. Am J Hum Genet (2003) 2.11

Microsatellites as EWS/FLI response elements in Ewing's sarcoma. Proc Natl Acad Sci U S A (2008) 2.06

Maximum-likelihood estimation of recent shared ancestry (ERSA). Genome Res (2011) 1.88

Estimating the retrotransposition rate of human Alu elements. Gene (2006) 1.85

Methodological Considerations in Studying Centenarians: Lessons Learned From the Georgia Centenarian Studies. Annu Rev Gerontol Geriatr (2007) 1.85

Alu elements and hominid phylogenetics. Proc Natl Acad Sci U S A (2003) 1.81

L1 recombination-associated deletions generate human genomic variation. Proc Natl Acad Sci U S A (2008) 1.79

Active Alu element "A-tails": size does matter. Genome Res (2002) 1.79

Evolutionary dynamics of transposable elements in the short-tailed opossum Monodelphis domestica. Genome Res (2007) 1.79

Alu retrotransposition-mediated deletion. J Mol Biol (2005) 1.79

A strong signature of balancing selection in the 5' cis-regulatory region of CCR5. Proc Natl Acad Sci U S A (2002) 1.78

Patterns of human diversity, within and among continents, inferred from biallelic DNA polymorphisms. Genome Res (2002) 1.78

Differential alu mobilization and polymorphism among the human and chimpanzee lineages. Genome Res (2004) 1.77

Retrotransposition of Alu elements: how many sources? Trends Genet (2004) 1.73

Genomic rearrangements by LINE-1 insertion-mediated deletion in the human and chimpanzee lineages. Nucleic Acids Res (2005) 1.73

Ancestry and disease in the age of genomic medicine. N Engl J Med (2010) 1.71

Promoter polymorphism of the erythropoietin gene in severe diabetic eye and kidney complications. Proc Natl Acad Sci U S A (2008) 1.70

Whole genome computational comparative genomics: A fruitful approach for ascertaining Alu insertion polymorphisms. Gene (2006) 1.68

Mobile element scanning (ME-Scan) identifies thousands of novel Alu insertions in diverse human populations. Genome Res (2013) 1.66

Emergence of primate genes by retrotransposon-mediated sequence transduction. Proc Natl Acad Sci U S A (2006) 1.66

Larger genetic differences within africans than between Africans and Eurasians. Genetics (2002) 1.62

Natural selection and population history in the human angiotensinogen gene (AGT): 736 complete AGT sequences in chromosomes from around the world. Am J Hum Genet (2004) 1.61

Alu recombination-mediated structural deletions in the chimpanzee genome. PLoS Genet (2007) 1.59

SINEs of a nearly perfect character. Syst Biol (2006) 1.59

A method for detecting recent selection in the human genome from allele age estimates. Genetics (2003) 1.55

Mobile element scanning (ME-Scan) by targeted high-throughput sequencing. BMC Genomics (2010) 1.54

Mutations in TNNT3 cause multiple congenital contractures: a second locus for distal arthrogryposis type 2B. Am J Hum Genet (2003) 1.52

Worldwide haplotype diversity and coding sequence variation at human bitter taste receptor loci. Hum Mutat (2005) 1.50

Alu insertion loci and platyrrhine primate phylogeny. Mol Phylogenet Evol (2005) 1.49

Fine-scaled human genetic structure revealed by SNP microarrays. Genome Res (2009) 1.48

Toward a more uniform sampling of human genetic diversity: a survey of worldwide populations by high-density genotyping. Genomics (2010) 1.47

Mobile DNA in Old World monkeys: a glimpse through the rhesus macaque genome. Science (2007) 1.47

Balinese Y-chromosome perspective on the peopling of Indonesia: genetic contributions from pre-neolithic hunter-gatherers, Austronesian farmers, and Indian traders. Hum Biol (2005) 1.45

5'-Transducing SVA retrotransposon groups spread efficiently throughout the human genome. Genome Res (2009) 1.43

AGT genetic variation, plasma AGT, and blood pressure: An analysis of the Utah Genetic Reference Project pedigrees. Am J Hypertens (2010) 1.43

Nucleotide diversity and haplotype structure of the human angiotensinogen gene in two populations. Am J Hum Genet (2001) 1.43

Insights into the demographic history of African Pygmies from complete mitochondrial genomes. Mol Biol Evol (2010) 1.43

Gene flow from the Indian subcontinent to Australia: evidence from the Y chromosome. Curr Biol (2002) 1.43

Alu element mutation spectra: molecular clocks and the effect of DNA methylation. J Mol Biol (2004) 1.41

Mobile DNA elements in primate and human evolution. Am J Phys Anthropol (2007) 1.38

From the margins of the genome: mobile elements shape primate evolution. Bioessays (2005) 1.36

A mobile threat to genome stability: The impact of non-LTR retrotransposons upon the human genome. Semin Cancer Biol (2010) 1.34

Genome-wide analysis of the human Alu Yb-lineage. Hum Genomics (2004) 1.33

Chromosomal inversions between human and chimpanzee lineages caused by retrotransposons. PLoS One (2008) 1.32

Extensive individual variation in L1 retrotransposition capability contributes to human genetic diversity. Proc Natl Acad Sci U S A (2006) 1.32

Under the genomic radar: the stealth model of Alu amplification. Genome Res (2005) 1.31

Recently integrated Alu retrotransposons are essentially neutral residents of the human genome. Gene (2006) 1.31

A novel mutation in FGFR3 causes camptodactyly, tall stature, and hearing loss (CATSHL) syndrome. Am J Hum Genet (2006) 1.31

Common variants on chromosome 2 and risk of primary open-angle glaucoma in the Afro-Caribbean population of Barbados. Proc Natl Acad Sci U S A (2009) 1.30