Published in Genomics on September 01, 1995
Computational and experimental analysis of microsatellites in rice (Oryza sativa L.): frequency, length variation, transposon associations, and genetic marker potential. Genome Res (2001) 9.95
The impact of retrotransposons on human genome evolution. Nat Rev Genet (2009) 8.08
Alu insertion polymorphisms and human evolution: evidence for a larger population size in Africa. Genome Res (1997) 3.73
Comparative genomics and molecular dynamics of DNA repeats in eukaryotes. Microbiol Mol Biol Rev (2008) 3.35
A comprehensive analysis of recently integrated human Ta L1 elements. Am J Hum Genet (2002) 2.47
LINE-1 elements in structural variation and disease. Annu Rev Genomics Hum Genet (2011) 2.42
Molecular archeology of L1 insertions in the human genome. Genome Biol (2002) 2.14
A systematic analysis of LINE-1 endonuclease-dependent retrotranspositional events causing human genetic disease. Hum Genet (2005) 2.10
Reading between the LINEs: human genomic variation induced by LINE-1 retrotransposition. Genome Res (2000) 2.09
Inviting instability: Transposable elements, double-strand breaks, and the maintenance of genome integrity. Mutat Res (2006) 2.00
Genomic characterization of recent human LINE-1 insertions: evidence supporting random insertion. Genome Res (2001) 1.98
Patterns of ancestral human diversity: an analysis of Alu-insertion and restriction-site polymorphisms. Am J Hum Genet (2001) 1.91
Active Alu element "A-tails": size does matter. Genome Res (2002) 1.79
Processed pseudogenes of human endogenous retroviruses generated by LINEs: their integration, stability, and distribution. Genome Res (2002) 1.54
Genome-wide sequence and functional analysis of early replicating DNA in normal human fibroblasts. BMC Genomics (2006) 1.39
Discovery of highly divergent repeat landscapes in snake genomes using high-throughput sequencing. Genome Biol Evol (2011) 1.39
A genome-wide analysis of common fragile sites: what features determine chromosomal instability in the human genome? Genome Res (2012) 1.37
Genome-wide analysis of the human Alu Yb-lineage. Hum Genomics (2004) 1.33
Widespread Alu repeat-driven expansion of consensus DR2 retinoic acid response elements during primate evolution. BMC Genomics (2007) 1.27
Diverse cis factors controlling Alu retrotransposition: what causes Alu elements to die? Genome Res (2009) 1.26
Biased distribution of microsatellite motifs in the rice genome. Mol Genet Genomics (2007) 1.19
Gene encoding human Ro-associated autoantigen Y5 RNA. Nucleic Acids Res (1996) 1.07
Comprehensive analysis of two Alu Yd subfamilies. J Mol Evol (2003) 1.06
Survey and analysis of simple sequence repeats in the Laccaria bicolor genome, with development of microsatellite markers. Curr Genet (2010) 1.02
A matter of life or death: how microsatellites emerge in and vanish from the human genome. Genome Res (2011) 1.02
Characterization of transposable elements in the ectomycorrhizal fungus Laccaria bicolor. PLoS One (2012) 0.99
A novel protein isoform of the multicopy human NAIP gene derives from intragenic Alu SINE promoters. PLoS One (2009) 0.98
Survey of microsatellite clustering in eight fully sequenced species sheds light on the origin of compound microsatellites. BMC Genomics (2008) 0.97
A helitron-like transposon superfamily from lepidoptera disrupts (GAAA)(n) microsatellites and is responsible for flanking sequence similarity within a microsatellite family. J Mol Evol (2010) 0.96
Expansion of microsatellites on evolutionary young Y chromosome. PLoS One (2013) 0.86
Detecting microsatellites in genome data: variance in definitions and bioinformatic approaches cause systematic bias. Evol Bioinform Online (2008) 0.86
LINE-1-derived poly(A) microsatellites undergo rapid shortening and create somatic and germline mosaicism in mice. Mol Biol Evol (2012) 0.86
Internal priming: an opportunistic pathway for L1 and Alu retrotransposition in hominins. Gene (2009) 0.85
Non-LTR retrotransposons and microsatellites: Partners in genomic variation. Mob Genet Elements (2013) 0.84
The unstable CCTG repeat responsible for myotonic dystrophy type 2 originates from an AluSx element insertion into an early primate genome. PLoS One (2012) 0.83
An efficient method to find potentially universal population genetic markers, applied to metazoans. BMC Evol Biol (2010) 0.82
Analyses of carnivore microsatellites and their intimate association with tRNA-derived SINEs. BMC Genomics (2006) 0.81
Hormone-sensitive lipase (Lipe): sequence analysis of the 129Sv mouse Lipe gene. Mamm Genome (1997) 0.80
MapToGenome: a comparative genomic tool that aligns transcript maps to sequenced genomes. Evol Bioinform Online (2007) 0.79
Chromosomal localization and distribution of simple sequence repeats and the Arabidopsis-type telomere sequence in the genome of Cicer arietinum L. Chromosome Res (1998) 0.78
Transcriptome Analysis of ESTs from a Chaetognath Reveals a Deep-Branching Clade of Retrovirus-Like Retrotransposons. Open Virol J (2008) 0.77
Heads or tails: L1 insertion-associated 5' homopolymeric sequences. Mob DNA (2010) 0.76
Discovery of a new repeat family in the Callithrix jacchus genome. Genome Res (2016) 0.75
High-throughput sequencing and graph-based cluster analysis facilitate microsatellite development from a highly complex genome. Ecol Evol (2016) 0.75
Development of microsatellite markers and detection of genetic variation between Goniozus wasp populations. J Insect Sci (2014) 0.75
Local mutagenic impact of insertions of LTR retrotransposons on the mouse genome. J Mol Evol (2006) 0.75
The sequence of the human genome. Science (2001) 101.55
DNA sequence and expression of the B95-8 Epstein-Barr virus genome. Nature (1984) 27.05
Estimating African American admixture proportions by use of population-specific alleles. Am J Hum Genet (1998) 22.90
Comprehensive human genetic maps: individual and sex-specific variation in recombination. Am J Hum Genet (1998) 19.35
Random subcloning of sonicated DNA: application to shotgun DNA sequence analysis. Anal Biochem (1983) 13.88
The Biomolecular Interaction Network Database and related tools 2005 update. Nucleic Acids Res (2005) 12.94
Nonviral retroposons: genes, pseudogenes, and transposable elements generated by the reverse flow of genetic information. Annu Rev Biochem (1986) 11.03
Long homozygous chromosomal segments in reference families from the centre d'Etude du polymorphisme humain. Am J Hum Genet (1999) 10.94
Ubiquitous, interspersed repeated sequences in mammalian genomes. Proc Natl Acad Sci U S A (1980) 9.48
Pulmonary expression of interleukin-13 causes inflammation, mucus hypersecretion, subepithelial fibrosis, physiologic abnormalities, and eotaxin production. J Clin Invest (1999) 8.38
Cereal genome evolution. Grasses, line up and form a circle. Curr Biol (1995) 8.33
Structure of the gene encoding the immunodominant surface antigen on the sporozoite of the human malaria parasite Plasmodium falciparum. Science (1984) 8.18
Activation of cardiac gene expression by myocardin, a transcriptional cofactor for serum response factor. Cell (2001) 8.09
Base sequence studies of 300 nucleotide renatured repeated human DNA clones. J Mol Biol (1981) 7.94
Partial nucleotide sequence of the 300-nucleotide interspersed repeated human DNA sequences. Nature (1980) 7.92
Genetic basis and molecular mechanism for idiopathic ventricular fibrillation. Nature (1998) 7.26
Alu repeats and human disease. Mol Genet Metab (1999) 6.64
The Y-family of DNA polymerases. Mol Cell (2001) 6.49
Repeat sequence families derived from mammalian tRNA genes. Nature (1985) 6.10
Sequence organization of the human genome. Cell (1975) 5.67
Genetic traces of ancient demography. Proc Natl Acad Sci U S A (1998) 5.48
Genetic diversity and disease control in rice. Nature (2000) 5.34
A new bacteriophage P1-derived vector for the propagation of large human DNA fragments. Nat Genet (1994) 5.34
Comparison of human genetic and sequence-based physical maps. Nature (2001) 4.97
An internal control for routine diagnostic PCR: design, properties, and effect on clinical performance. J Clin Microbiol (1998) 4.58
Inducible targeting of IL-13 to the adult lung causes matrix metalloproteinase- and cathepsin-dependent emphysema. J Clin Invest (2000) 4.16
Genetic mapping of a locus predisposing to human colorectal cancer. Science (1993) 4.12
A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC). Science (1994) 4.02
Closing in on a breast cancer gene on chromosome 17q. Am J Hum Genet (1992) 3.89
Cutting edge: a role for B lymphocyte stimulator in systemic lupus erythematosus. J Immunol (2001) 3.87
Cardiac hypertrophy is not a required compensatory response to short-term pressure overload. Circulation (2000) 3.82
Alu insertion polymorphisms and human evolution: evidence for a larger population size in Africa. Genome Res (1997) 3.73
Germline mutations in the ribonuclease L gene in families showing linkage with HPC1. Nat Genet (2002) 3.67
Organ-tissue mass measurement allows modeling of REE and metabolically active tissue mass. Am J Physiol (1998) 3.65
Mutation near the polyoma DNA replication origin permits productive infection of F9 embryonal carcinoma cells. Cell (1981) 3.61
Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements. Am J Hum Genet (2001) 3.57
A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps. Hum Mol Genet (1995) 3.44
Estimation of pairwise relationships in the presence of genotyping errors. Am J Hum Genet (1998) 3.37
Safety and immunogenicity trial in adult volunteers of a human papillomavirus 16 L1 virus-like particle vaccine. J Natl Cancer Inst (2001) 3.28
Genetic evidence on the origins of Indian caste populations. Genome Res (2001) 3.25
A familial Alzheimer's disease locus on chromosome 1. Science (1995) 3.14
Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14. Science (1992) 3.14
Regulation of imprinted X-chromosome inactivation in mice by Tsix. Development (2001) 3.12
Master genes in mammalian repetitive DNA amplification. Trends Genet (1992) 3.11
Integrated human genome-wide maps constructed using the CEPH reference panel. Nat Genet (1994) 3.06
Survey of human and rat microsatellites. Genomics (1992) 2.92
The distribution of human genetic diversity: a comparison of mitochondrial, autosomal, and Y-chromosome data. Am J Hum Genet (2000) 2.91
Tumoricidal activity of a novel anti-human DR5 monoclonal antibody without hepatocyte cytotoxicity. Nat Med (2001) 2.87
Phenobarbital compared with phenytoin for the treatment of neonatal seizures. N Engl J Med (1999) 2.84
HMGB1-induced autophagy promotes chemotherapy resistance in leukemia cells. Leukemia (2010) 2.83
Rho GTPase function in tumorigenesis. Biochim Biophys Acta (2009) 2.81
Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP. Nat Genet (2001) 2.75
Total-body skeletal muscle mass: development and cross-validation of anthropometric prediction models. Am J Clin Nutr (2000) 2.71
Localization of a domain on the paramyxovirus attachment protein required for the promotion of cellular fusion by its homologous fusion protein spike. Virology (1995) 2.67
Evolution of the master Alu gene(s). J Mol Evol (1991) 2.65
Genetic analysis of indefinite division in human cells: evidence for a cell senescence-related gene(s) on human chromosome 4. Proc Natl Acad Sci U S A (1991) 2.64
Different forms of TFIIH for transcription and DNA repair: holo-TFIIH and a nucleotide excision repairosome. Cell (1995) 2.58
The retinoblastoma gene product protects E2F-1 from degradation by the ubiquitin-proteasome pathway. Genes Dev (1996) 2.58
Genetic variation of recent Alu insertions in human populations. J Mol Evol (1996) 2.56
Unique TATA-binding protein-containing complexes and cofactors involved in transcription by RNA polymerases II and III. EMBO J (1993) 2.56
Hormonal changes in the grains of rice subjected to water stress during grain filling. Plant Physiol (2001) 2.52
Autophagy and chemotherapy resistance: a promising therapeutic target for cancer treatment. Cell Death Dis (2013) 2.52
Diabetes is related to cerebral infarction but not to AD pathology in older persons. Neurology (2006) 2.48
p53 modulation of TFIIH-associated nucleotide excision repair activity. Nat Genet (1995) 2.47
An electron microscope study of the DNA sequence organization of the human genome. J Mol Biol (1976) 2.45
Protection against Fas-dependent Th1-mediated apoptosis by antigen receptor engagement in B cells. Nature (1995) 2.43
Characterization of human crossover interference. Am J Hum Genet (2000) 2.42
A human-specific subfamily of Alu sequences. Genomics (1991) 2.40
Ionic remodeling underlying action potential changes in a canine model of atrial fibrillation. Circ Res (1997) 2.38
Fire and flood management of coastal swamp enabled first rice paddy cultivation in east China. Nature (2007) 2.36
Shedding of syndecan-1 and -4 ectodomains is regulated by multiple signaling pathways and mediated by a TIMP-3-sensitive metalloproteinase. J Cell Biol (2000) 2.33
Proximal sequence element-binding transcription factor (PTF) is a multisubunit complex required for transcription of both RNA polymerase II- and RNA polymerase III-dependent small nuclear RNA genes. Mol Cell Biol (1995) 2.33
Cloning, expression and chromosome locations of the human DNMT3 gene family. Gene (1999) 2.33
Mice devoid of all known thyroid hormone receptors are viable but exhibit disorders of the pituitary-thyroid axis, growth, and bone maturation. Genes Dev (1999) 2.31
Oxytocin is required for nursing but is not essential for parturition or reproductive behavior. Proc Natl Acad Sci U S A (1996) 2.31
Regional specialization in human nuclei: visualization of discrete sites of transcription by RNA polymerase III. EMBO J (1999) 2.28
Effects of angiotensin-converting enzyme inhibition on the development of the atrial fibrillation substrate in dogs with ventricular tachypacing-induced congestive heart failure. Circulation (2001) 2.27
Error-free and error-prone lesion bypass by human DNA polymerase kappa in vitro. Nucleic Acids Res (2000) 2.25
Activator-dependent transcription from chromatin in vitro involving targeted histone acetylation by p300. Mol Cell (2000) 2.25
Genomewide search for type 2 diabetes susceptibility genes in four American populations. Am J Hum Genet (2000) 2.19
Analysis of transcription of the human Alu family ubiquitous repeating element by eukaryotic RNA polymerase III. Nucleic Acids Res (1981) 2.18
Efficacy of murine malaria sporozoite vaccines: implications for human vaccine development. Science (1987) 2.17
Large-scale analysis of the Alu Ya5 and Yb8 subfamilies and their contribution to human genomic diversity. J Mol Biol (2001) 2.16
A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17. Nat Genet (1995) 2.16
Eukaryotic DNA polymerases: proposal for a revised nomenclature. J Biol Chem (2001) 2.15
Dual-energy X-ray absorptiometry body composition model: review of physical concepts. Am J Physiol (1996) 2.15
Specificity of DNA lesion bypass by the yeast DNA polymerase eta. J Biol Chem (2000) 2.12
Acquisition of sensitivity of stress-activated protein kinases to the p38 inhibitor, SB 203580, by alteration of one or more amino acids within the ATP binding pocket. J Biol Chem (1998) 2.12
Evolution of HIV-1 coreceptor usage through interactions with distinct CCR5 and CXCR4 domains. Proc Natl Acad Sci U S A (1997) 2.11
Renaturation rate studies of a single family of interspersed repeated sequences in human deoxyribonucleic acid. Biochemistry (1981) 2.10
The human REV1 gene codes for a DNA template-dependent dCMP transferase. Nucleic Acids Res (1999) 2.10
Expression of chemokine receptors by subsets of neurons in the central nervous system. J Immunol (1997) 2.10
Reading between the LINEs: human genomic variation induced by LINE-1 retrotransposition. Genome Res (2000) 2.09
A genomic-systems biology map for cardiovascular function. Science (2001) 2.09
Urokinase receptors promote beta1 integrin function through interactions with integrin alpha3beta1. Mol Biol Cell (2001) 2.09