Published in Genomics on November 01, 1988
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Five polymorphic microsatellite VNTRs on the human X chromosome. Am J Hum Genet (1990) 5.38
Polymers of random short oligonucleotides detect polymorphic loci in the human genome. Nucleic Acids Res (1989) 2.57
Complex recombination events at the hypermutable minisatellite CEB1 (D2S90). EMBO J (1994) 1.79
The efficiency of multilocus DNA fingerprint probes for individualization and establishment of family relationships, determined from extensive casework. Am J Hum Genet (1991) 1.76
A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates. Am J Hum Genet (1991) 1.46
Sequences flanking the repeat arrays of human minisatellites: association with tandem and dispersed repeat elements. Nucleic Acids Res (1989) 1.41
Repeat instability at human minisatellites arising from meiotic recombination. EMBO J (1998) 1.40
Localization of the mutation in an extended family with Charcot-Marie-Tooth neuropathy (HMSN I). Am J Hum Genet (1989) 1.37
Molecular dissection of a contiguous gene syndrome: frequent submicroscopic deletions, evolutionarily conserved sequences, and a hypomethylated "island" in the Miller-Dieker chromosome region. Proc Natl Acad Sci U S A (1989) 1.33
Partial gene duplication involving exon-Alu interchange results in lipoprotein lipase deficiency. Am J Hum Genet (1990) 1.31
Role of the pseudoautosomal region in sex-chromosome pairing during male meiosis: meiotic studies in a man with a deletion of distal Xp. Am J Hum Genet (1992) 1.25
Mechanisms underlying telomere repeat turnover, revealed by hypervariable variant repeat distribution patterns in the human Xp/Yp telomere. EMBO J (1995) 1.23
Tandem amplification of a chromosomal segment harboring 5-enolpyruvylshikimate-3-phosphate synthase locus confers glyphosate resistance in Kochia scoparia. Plant Physiol (2014) 1.19
Characterization of a large deletion associated with a polymorphic block of repeated dinucleotides in the type III procollagen gene (COL3A1) of a patient with Ehlers-Danlos syndrome type IV. Am J Hum Genet (1991) 1.14
Possible role of natural selection in the formation of tandem-repetitive noncoding DNA. Genetics (1994) 1.09
Detection of cryptic chromosomal abnormalities in unexplained mental retardation: a general strategy using hypervariable subtelomeric DNA polymorphisms. Am J Hum Genet (1993) 1.09
Detection of a novel minisatellite-specific DNA-binding protein. Nucleic Acids Res (1990) 1.08
Narrowing the position of the Treacher Collins syndrome locus to a small interval between three new microsatellite markers at 5q32-33.1. Am J Hum Genet (1993) 1.07
Lack of effects of atomic bomb radiation on genetic instability of tandem-repetitive elements in human germ cells. Am J Hum Genet (1995) 1.07
Meiotic recombination and flanking marker exchange at the highly unstable human minisatellite CEB1 (D2S90). Am J Hum Genet (2000) 1.07
A highly polymorphic meiotic recombination mouse hot spot exhibits incomplete repair. Mol Cell Biol (2007) 1.05
Acquisition of telomere repeat sequences by transfected DNA integrated at the site of a chromosome break. Mol Cell Biol (1993) 1.03
Comparative sequence analysis of human minisatellites showing meiotic repeat instability. Genome Res (1999) 1.03
Asymmetry in chromosome pairing: a major factor in de novo mutation and the production of genetic disease in man. J Med Genet (1989) 1.02
The evolution of tandemly repetitive DNA: recombination rules. Genetics (1992) 1.01
Two modes of germline instability at human minisatellite MS1 (locus D1S7): complex rearrangements and paradoxical hyperdeletion. Am J Hum Genet (2003) 0.98
Genetic linkage map of 46 DNA markers on human chromosome 16. Proc Natl Acad Sci U S A (1990) 0.97
Minisatellite binding protein Msbp-1 is a sequence-specific single-stranded DNA-binding protein. Nucleic Acids Res (1991) 0.94
Characterisation of a novel minisatellite that provides multiple splice donor sites in an interferon-induced transcript. Nucleic Acids Res (1995) 0.92
Comparative analyses of human single- and multilocus tandem repeats. Genetics (2008) 0.91
Genetic analysis of children of atomic bomb survivors. Environ Health Perspect (1996) 0.91
Tandemly repeated transgenes of the human minisatellite MS32 (D1S8), with novel mouse gamma satellite integration. Nucleic Acids Res (1994) 0.90
A VNTR immediately adjacent to the human pseudoautosomal telomere. Nucleic Acids Res (1990) 0.90
Rare exonic minisatellite alleles in MUC2 influence susceptibility to gastric carcinoma. PLoS One (2007) 0.89
VNTR and microsatellite polymorphisms within the subtelomeric region of 7q. Am J Hum Genet (1993) 0.87
Genetic evidence that placental site trophoblastic tumours can originate from a hydatidiform mole or a normal conceptus. Br J Cancer (1992) 0.83
Variable germline and embryonic instability of the human minisatellite MS32 (D1S8) in transgenic mice. EMBO J (1994) 0.81
Simple human DNA-repeats associated with genomic hypervariability, flanking the genomic retroposons and similar to retroviral sites. Nucleic Acids Res (1990) 0.80
Schizophrenia-associated chromosome 11q21 translocation: identification of flanking markers and development of chromosome 11q fragment hybrids as cloning and mapping resources. Am J Hum Genet (1993) 0.80
CeRep25B forms chromosome-specific minisatellite arrays in Caenorhabditis elegans. Genome Res (1998) 0.79
Coherent somatic mutation in autoimmune disease. PLoS One (2014) 0.78
Complex germline and somatic mutation processes at a haploid human minisatellite shown by single-molecule analysis. Mutat Res (2008) 0.78
1992 William Allan Award address. Am J Hum Genet (1993) 0.78
Minisatellite MS32 alleles show population specificity among Thai, Chinese, and Japanese. J Mol Evol (2009) 0.78
Trisomy X in a female member of a family with X linked severe combined immunodeficiency: implications for carrier diagnosis. J Med Genet (1994) 0.75
Elevated frequency of microsatellite mutations in TK6 human lymphoblast clones selected for mutations at the thymidine kinase locus. Mol Cell Biol (1994) 0.75
Linkage of internal minisatellite loci on chromosome 1 and exclusion of autosomal dominant retinitis pigmentosa proximal to rhesus. J Med Genet (1990) 0.75
Hypervariable 'minisatellite' regions in human DNA. Nature (1985) 31.03
DNA sequence variants in the G gamma-, A gamma-, delta- and beta-globin genes of man. Cell (1979) 15.74
A physical map of the DNA regions flanking the rabbit beta-globin gene. Cell (1977) 12.96
Individual-specific 'fingerprints' of human DNA. Nature (1985) 10.38
Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA. Nature (1988) 9.47
Characterization of a panel of highly variable minisatellites cloned from human DNA. Ann Hum Genet (1987) 7.58
The rabbit beta-globin gene contains a large large insert in the coding sequence. Cell (1977) 6.45
Forensic application of DNA 'fingerprints'. Nature (1986) 5.19
Chromosome 5 allele loss in human colorectal carcinomas. Nature (1987) 4.46
Linkage of adult alpha- and beta-globin genes in X. laevis and gene duplication by tetraploidization. Cell (1980) 4.09
Identification of the skeletal remains of a murder victim by DNA analysis. Nature (1991) 3.73
Human minisatellite mutation rate after the Chernobyl accident. Nature (1996) 3.46
Systematic cloning of human minisatellites from ordered array charomid libraries. Genomics (1990) 3.21
DNA fingerprints of dogs and cats. Anim Genet (1987) 3.12
Positive identification of an immigration test-case using human DNA fingerprints. Nature (1985) 3.07
Cloning a selected fragment from a human DNA 'fingerprint': isolation of an extremely polymorphic minisatellite. Nucleic Acids Res (1986) 2.70
DNA fingerprints applied to gene introgression in breeding programs. Genetics (1990) 2.70
DNA "fingerprints" and segregation analysis of multiple markers in human pedigrees. Am J Hum Genet (1986) 2.55
Mouse DNA 'fingerprints': analysis of chromosome localization and germ-line stability of hypervariable loci in recombinant inbred strains. Nucleic Acids Res (1987) 2.47
Evolution of the beta-globin gene cluster in man and the primates. J Mol Biol (1981) 2.31
Deletion of genes on chromosome 1 in endocrine neoplasia. Nature (1987) 2.27
Uniparental paternal disomy in Angelman's syndrome. Lancet (1991) 2.26
The retinoblastoma gene is frequently altered leading to loss of expression in primary breast tumours. Oncogene (1989) 2.02
Unequal crossingover between homologous chromosomes is not the major mechanism involved in the generation of new alleles at VNTR loci. Genomics (1989) 1.93
Further evidence for elevated human minisatellite mutation rate in Belarus eight years after the Chernobyl accident. Mutat Res (1997) 1.92
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
The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis. N Engl J Med (1992) 1.78
Detection of somatic changes in human cancer DNA by DNA fingerprint analysis. Br J Cancer (1987) 1.74
Highly variable minisatellites and DNA fingerprints. Biochem Soc Trans (1987) 1.71
DNA fingerprinting Dolly. Nature (1998) 1.69
Spontaneous mutation at the hypervariable mouse minisatellite locus Ms6-hm: flanking DNA sequence and analysis of germline and early somatic mutation events. Proc Biol Sci (1991) 1.56
Induction of minisatellite mutations in the mouse germline by low-dose chronic exposure to gamma-radiation and fission neutrons. Mutat Res (2000) 1.54
Characterization of a highly unstable mouse minisatellite locus: evidence for somatic mutation during early development. Genomics (1989) 1.51
Minisatellite mutation rate variation associated with a flanking DNA sequence polymorphism. Nat Genet (1994) 1.50
Organization of the human myoglobin gene. EMBO J (1984) 1.49
The seal myoglobin gene: an unusually long globin gene. Nature (1983) 1.44
Sequences flanking the repeat arrays of human minisatellites: association with tandem and dispersed repeat elements. Nucleic Acids Res (1989) 1.41
Isolation of human simple repeat loci by hybridization selection. Hum Mol Genet (1994) 1.39
Digital DNA typing at a second hypervariable locus by minisatellite variant repeat mapping. Hum Mol Genet (1993) 1.38
Use of vectorette and subvectorette PCR to isolate transgene flanking DNA. PCR Methods Appl (1994) 1.38
Processes of gene duplication. Nature (1982) 1.33
Mutation rate heterogeneity and the generation of allele diversity at the human minisatellite MS205 (D16S309). Hum Mol Genet (1996) 1.33
Minisatellite instability and germline mutation. Cell Mol Life Sci (1999) 1.28
Analysis of somatic mutations at human minisatellite loci in tumors and cell lines. Genomics (1989) 1.28
Isolation and sequence analysis of a hybrid delta-globin pseudogene from the brown lemur. J Mol Biol (1982) 1.27
Influences of array size and homogeneity on minisatellite mutation. EMBO J (1998) 1.26
High-resolution sperm typing of meiotic recombination in the mouse MHC Ebeta gene. EMBO J (2003) 1.26
Extremely complex repeat shuffling during germline mutation at human minisatellite B6.7. Hum Mol Genet (1999) 1.23
Mechanisms underlying telomere repeat turnover, revealed by hypervariable variant repeat distribution patterns in the human Xp/Yp telomere. EMBO J (1995) 1.23
A comparison of vertebrate interferon gene families detected by hybridization with human interferon DNA. J Mol Biol (1983) 1.23
Crossover breakpoint mapping identifies a subtelomeric hotspot for male meiotic recombination. Hum Mol Genet (2000) 1.22
Biology and applications of human minisatellite loci. Curr Opin Genet Dev (1992) 1.20
Localisation of the G gamma-, A gamma-, delta- and beta-globin genes on the short arm of human chromosome 11. Nature (1979) 1.19
Allelic diversity at minisatellite MS205 (D16S309): evidence for polarized variability. Hum Mol Genet (1993) 1.19
Mouse minisatellite mutations induced by ionizing radiation. Nat Genet (1993) 1.18
A tetranucleotide repeat mouse minisatellite displaying substantial somatic instability during early preimplantation development. Genomics (1993) 1.16
A subterminal satellite located adjacent to telomeres in chimpanzees is absent from the human genome. Nat Genet (1994) 1.15
Stage specificity, dose response, and doubling dose for mouse minisatellite germ-line mutation induced by acute radiation. Proc Natl Acad Sci U S A (1998) 1.14
Molecular cloning of seal myoglobin mRNA. Nucleic Acids Res (1982) 1.14
A novel unstable mouse VNTR family expanded from SINE B1 elements. Genomics (1998) 1.11
Evolutionary transience of hypervariable minisatellites in man and the primates. Proc Biol Sci (1991) 1.10
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Detection of a novel minisatellite-specific DNA-binding protein. Nucleic Acids Res (1990) 1.08
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Meiotic recombination and flanking marker exchange at the highly unstable human minisatellite CEB1 (D2S90). Am J Hum Genet (2000) 1.07
Big, bad minisatellites. Nat Genet (1997) 1.06
Allele-specific MVR-PCR analysis at minisatellite D1S8. Hum Mol Genet (1993) 1.04
Use of minisatellite DNA probes for determination of twin zygosity at birth. Lancet (1986) 1.03
Comparative sequence analysis of human minisatellites showing meiotic repeat instability. Genome Res (1999) 1.03
Transgenerational mutation by radiation. Nature (2000) 1.03
Identification of post-transplant cell population by DNA fingerprint analysis. Lancet (1986) 1.03
The mouse myoglobin gene. Characterisation and sequence comparison with other mammalian myoglobin genes. Eur J Biochem (1986) 1.02
Minisatellite "isoallele" discrimination in pseudohomozygotes by single molecule PCR and variant repeat mapping. Genomics (1991) 0.99
Somatic versus germline mutation processes at minisatellite CEB1 (D2S90) in humans and transgenic mice. Genomics (2000) 0.99
Influence of allele lineage on the role of the insulin minisatellite in susceptibility to type 1 diabetes. Hum Mol Genet (2000) 0.98
STS for minisatellite MS607 (D22S163). Nucleic Acids Res (1991) 0.96
Minisatellite binding protein Msbp-1 is a sequence-specific single-stranded DNA-binding protein. Nucleic Acids Res (1991) 0.94
Gestational and nongestational trophoblastic tumors distinguished by DNA analysis. Cancer (1992) 0.93
Isolation of telomere junction fragments by anchored polymerase chain reaction. Proc Biol Sci (1992) 0.93
Myoglobin expression: early induction and subsequent modulation of myoglobin and myoglobin mRNA during myogenesis. Mol Cell Biol (1986) 0.91
Allele diversity and germline mutation at the insulin minisatellite. Hum Mol Genet (2000) 0.90
Tandemly repeated transgenes of the human minisatellite MS32 (D1S8), with novel mouse gamma satellite integration. Nucleic Acids Res (1994) 0.90
Isolation and characterization of mouse minisatellites. Genomics (1998) 0.89
Isolation and detailed characterization of human cell lines resistant to D-threo-chloramphenicol. Exp Cell Res (1976) 0.89
Interspecific variation in products of animal mitochondrial protein synthesis. Nature (1976) 0.89
Frequency of heterozygous complete hydatidiform moles, estimated by locus-specific minisatellite and Y chromosome-specific probes. Hum Genet (1989) 0.88
Minisatellite mutation frequency in human sperm following radiotherapy. Mutat Res (2000) 0.88
Recent advances in minisatellite biology. FEBS Lett (1992) 0.88
Use of DNA fingerprint analysis in identification of the sire. Vet Rec (1988) 0.87
Linkage analysis of British and Indian families with Von Recklinghausen neurofibromatosis. J Med Genet (1987) 0.87
Four-state MVR-PCR: increased discrimination of digital DNA typing by simultaneous analysis of two polymorphic sites within minisatellite variant repeats at D1S8. Hum Mol Genet (1993) 0.86
The primate psi beta 1 gene. An ancient beta-globin pseudogene. J Mol Biol (1984) 0.86
A hypervariable locus D16S309 located at the distal end of 16p. Nucleic Acids Res (1992) 0.86
No correlation between germline mutation at repeat DNA and meiotic crossover in male mice exposed to X-rays or cisplatin. Mutat Res (2000) 0.85