Published in Ann Hum Genet on January 01, 1992
Incidence and origin of "null" alleles in the (AC)n microsatellite markers. Am J Hum Genet (1993) 3.18
Introgression through rare hybridization: A genetic study of a hybrid zone between red and sika deer (genus Cervus) in Argyll, Scotland. Genetics (1999) 2.31
Population genetics in the forensic DNA debate. Proc Natl Acad Sci U S A (1992) 1.46
Nondetectability of restriction fragments and independence of DNA fragment sizes within and between loci in RFLP typing of DNA. Am J Hum Genet (1994) 1.29
A novel approach for mining polymorphic microsatellite markers in silico. PLoS One (2011) 1.09
A White Campion (Silene latifolia) floral expressed sequence tag (EST) library: annotation, EST-SSR characterization, transferability, and utility for comparative mapping. BMC Genomics (2009) 1.08
Likelihood ratios for DNA identification. Proc Natl Acad Sci U S A (1994) 1.08
Null allele sequence structure at the DYS448 locus and implications for profile interpretation. Int J Legal Med (2008) 1.04
Characteristics of polymorphism at a VNTR locus 3' to the apolipoprotein B gene in five human populations. Am J Hum Genet (1992) 1.03
Physical properties of VNTR data, and their impact on a test of allelic independence. Am J Hum Genet (1993) 1.03
Microsatellite markers from the 'South American fruit fly' Anastrepha fraterculus: a valuable tool for population genetic analysis and SIT applications. BMC Genet (2014) 0.95
The genetic structure of Drosophila ananassae populations from Asia, Australia and Samoa. Genetics (2007) 0.90
Violations of the ceiling principle: exact conditions and statistical evidence. Am J Hum Genet (1993) 0.86
Spatial and temporal genetic structure of Anopheles arabiensis in Southern Zambia over consecutive wet and drought years. Am J Trop Med Hyg (2007) 0.85
Analysis of population genetic structure of Indian Anopheles culicifacies species A using microsatellite markers. Parasit Vectors (2013) 0.85
Similar evolutionary potentials in an obligate ant parasite and its two host species. J Evol Biol (2011) 0.84
On the use of excess homozygosity for subpopulation detection. Am J Hum Genet (1993) 0.82
Genetic diversity of Sitobion avenae (Homoptera: Aphididae) populations from different geographic regions in China. PLoS One (2014) 0.82
Genetic variation over space and time: analyses of extinct and remnant lake trout populations in the Upper Great Lakes. Proc Biol Sci (2003) 0.81
Evaluation of standard error and confidence interval of estimated multilocus genotype probabilities, and their implications in DNA forensics. Am J Hum Genet (1993) 0.80
Diversity of ethnic and racial VNTR RFLP fixed-bin frequency distributions. Am J Hum Genet (1994) 0.79
Reintroduction of the European Capercaillie from the Capercaillie Breeding Centre in Wisła Forest District: Genetic Assessments of Captive and Reintroduced Populations. PLoS One (2015) 0.78
Short alleles revealed by PCR demonstrate no heterozygote deficiency at minisatellite loci D1S7, D7S21, and D12S11. Am J Hum Genet (1997) 0.77
Assessment of power and accuracy of methods for detection and frequency-estimation of null alleles. Genetica (2007) 0.77
First evidence of inbreeding, relatedness and chaotic genetic patchiness in the holoplanktonic jellyfish Pelagia noctiluca (Scyphozoa, Cnidaria). PLoS One (2014) 0.77
Genetic divergence among sympatric colour morphs of the Dalmatian wall lizard (Podarcis melisellensis). Genetica (2010) 0.77
Genetic diversity and variability in endangered Pantesco and two other Sicilian donkey breeds assessed by microsatellite markers. ScientificWorldJournal (2012) 0.76
Microsatellite markers for characterization of native and introduced populations of Plasmopara viticola, the causal agent of grapevine downy mildew. Appl Environ Microbiol (2012) 0.76
Match probabilities in racially admixed populations. Am J Hum Genet (1993) 0.76
Discerning non-disjunction in Down syndrome patients by means of GluK1-(AGAT)(n) and D21S2055-(GATA)(n) microsatellites on chromosome 21. Indian J Hum Genet (2012) 0.75
Development of microsatellite loci of pod mahogany, Afzelia quanzensis (Fabaceae), by Illumina shotgun sequencing, and cross-amplification in A. africana. Appl Plant Sci (2016) 0.75
Microsatellite and Mitochondrial DNA Study of Native Eastern European Cattle Populations: The Case of the Romanian Grey. PLoS One (2015) 0.75
Three sympatric clusters of the malaria vector Anopheles culicifacies E (Diptera: Culicidae) detected in Sri Lanka. Parasit Vectors (2016) 0.75
Microsatellite variation and differentiation among local populations of Castanopsis species in Japan. J Plant Res (2005) 0.75
Demographic expansion and subtle differentiation in the long-tailed hake Macruronus magellanicus: evidence from microsatellite data. Mar Biotechnol (NY) (2006) 0.75
Admixture as a tool for finding linked genes and detecting that difference from allelic association between loci. Proc Natl Acad Sci U S A (1988) 8.22
DNA fingerprinting dispute laid to rest. Nature (1994) 5.37
Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8. Genomics (1991) 3.93
Caucasian genes in American blacks: new data. Am J Hum Genet (1992) 3.78
Extensive restriction site polymorphism at the human phenylalanine hydroxylase locus and application in prenatal diagnosis of phenylketonuria. Am J Hum Genet (1985) 3.77
Mitochondrial DNA polymorphism reveals hidden heterogeneity within some Asian populations. Am J Hum Genet (1990) 3.64
Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies. Hum Mutat (2001) 3.07
Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis. Nat Genet (2000) 2.85
Parentage analysis with genetic markers in natural populations. I. The expected proportion of offspring with unambiguous paternity. Genetics (1988) 2.78
Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuria. Hum Genet (1987) 2.73
DNA recommendations. Further report of the DNA Commission of the ISFH regarding the use of short tandem repeat systems. International Society for Forensic Haemogenetics. Int J Legal Med (1997) 2.35
The utility of DNA typing in forensic work. Science (1991) 2.34
A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene. Am J Hum Genet (1998) 2.29
Determination of relatedness between individuals using DNA fingerprinting. Hum Biol (1993) 2.23
Polymerase chain reaction amplification products separated on rehydratable polyacrylamide gels and stained with silver. Biotechniques (1990) 2.23
Recombination of haplotypes leads to biased estimates of admixture proportions in human populations. Proc Natl Acad Sci U S A (1988) 2.16
Population amalgamation and genetic variation: observations on artificially agglomerated tribal populations of Central and South America. Am J Hum Genet (1988) 2.13
Detection of genetic variation with radioactive ligands. III. genetic polymorphism of transcobalamin II in human plasma. Am J Hum Genet (1978) 2.13
Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosa. Nat Genet (1999) 2.13
'Unique' alleles in admixed populations: a strategy for determining 'hereditary' population differences of disease frequencies. Ethn Dis (1991) 2.11
Prevalence of AIPL1 mutations in inherited retinal degenerative disease. Mol Genet Metab (2000) 2.07
Heterozygote deficiency, population substructure and their implications in DNA fingerprinting. Hum Genet (1992) 2.06
Genetic variation of the mitochondrial DNA genome in American Indians is at mutation-drift equilibrium. Am J Phys Anthropol (1991) 2.04
Description and validation of a method for simultaneous estimation of effective population size and mutation rate from human population data. Proc Natl Acad Sci U S A (1989) 2.02
Cleft lip and palate: no evidence of linkage to transforming growth factor alpha. Am J Hum Genet (1991) 1.94
Validation of mitochondrial DNA sequencing for forensic casework analysis. Int J Legal Med (1995) 1.91
Localization of two genes for Usher syndrome type I to chromosome 11. Genomics (1992) 1.90
Autosomal dominant sectoral retinitis pigmentosa. Two families with transversion mutation in codon 23 of rhodopsin. Arch Ophthalmol (1991) 1.81
Group-specific component (Gc) proteins bind vitamin D and 25-hydroxyvitamin D. Proc Natl Acad Sci U S A (1975) 1.77
The utility of short tandem repeat loci beyond human identification: implications for development of new DNA typing systems. Electrophoresis (1999) 1.57
Spinocerebellar ataxia: variable age of onset and linkage to human leukocyte antigen in a large kindred. Ann Neurol (1988) 1.54
Association of APOE polymorphisms with disease severity in MS is limited to women. Neurology (2004) 1.51
X-linked dominant cone-rod degeneration: linkage mapping of a new locus for retinitis pigmentosa (RP 15) to Xp22.13-p22.11. Am J Hum Genet (1995) 1.49
Sequences on the human Y chromosome homologous to the autosomal gene for argininosuccinate synthetase. Nature (1982) 1.46
Validation of short tandem repeats (STRs) for forensic usage: performance testing of fluorescent multiplex STR systems and analysis of authentic and simulated forensic samples. J Forensic Sci (2001) 1.41
DNA commission of the international society for forensic genetics: guidelines for mitochondrial DNA typing. Forensic Sci Int (2000) 1.37
Multilocus linkage analysis with the human argininosuccinate synthetase gene. Genomics (1989) 1.36
Localization of retina/pineal-expressed sequences: identification of novel candidate genes for inherited retinal disorders. Genomics (1999) 1.36
The human apolipoprotein B-100 gene: a highly polymorphic gene that maps to the short arm of chromosome 2. Biochem Biophys Res Commun (1985) 1.36
Mutations in the RP1 gene causing autosomal dominant retinitis pigmentosa. Hum Mol Genet (1999) 1.35
Sample size requirements for addressing the population genetic issues of forensic use of DNA typing. Hum Biol (1992) 1.29
Nondetectability of restriction fragments and independence of DNA fragment sizes within and between loci in RFLP typing of DNA. Am J Hum Genet (1994) 1.29
Evidence for a major gene (RP10) for autosomal dominant retinitis pigmentosa on chromosome 7q: linkage mapping in a second, unrelated family. Hum Genet (1995) 1.29
DNA commission of the International Society of Forensic Genetics: recommendations on forensic analysis using Y-chromosome STRs. Int J Legal Med (2001) 1.28
Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15. Am J Hum Genet (2000) 1.28
Polymorphisms at VNTR loci suggest homogeneity of the white population of Utah. Hum Biol (1991) 1.27
Exclusion of Usher syndrome gene from much of chromosome 4. Cytogenet Cell Genet (1989) 1.27
Evaluation of prostate-specific antigen (PSA) membrane test assays for the forensic identification of seminal fluid. J Forensic Sci (1999) 1.24
A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q. J Thromb Haemost (2012) 1.23
Nonsyndromic cleft lip and palate: no evidence of linkage to HLA or factor 13A. Am J Hum Genet (1993) 1.23
Enhancement of PCR amplification yield and specificity using AmpliTaq Gold DNA polymerase. Biotechniques (1998) 1.20
Irritable bowel syndrome aggregates strongly in families: a family-based case-control study. Neurogastroenterol Motil (2008) 1.19
Can molecular imprinting explain heterozygote deficiency and hybrid vigor? Genetics (1989) 1.18
DNA Commission of the International Society for Forensic Genetics: guidelines for mitochondrial DNA typing. Int J Legal Med (2000) 1.18
Haplotype distribution of the human phenylalanine hydroxylase locus in Scotland and Switzerland. Am J Hum Genet (1989) 1.17
Polymorphic DNA haplotypes at the phenylalanine hydroxylase locus in prenatal diagnosis of phenylketonuria. Lancet (1986) 1.15
Assignment of autosomal dominant spinocerebellar ataxia (SCA1) centromeric to the HLA region on the short arm of chromosome 6, using multilocus linkage analysis. Am J Hum Genet (1989) 1.14
PCR amplification of alleles at the DIS80 locus: comparison of a Finnish and a North American Caucasian population sample, and forensic casework evaluation. Am J Hum Genet (1992) 1.13
Human chromosome 8 linkage map based on short tandem repeat polymorphisms: effect of genotyping errors. Genomics (1992) 1.13
Familial aggregation of coronary heart disease and its relation to known genetic risk factors. Am J Cardiol (1982) 1.12
Plant pathogen forensics: capabilities, needs, and recommendations. Microbiol Mol Biol Rev (2006) 1.12
Sympathetic overactivity in tetanus: fatality associated with propranolol. Br Med J (1978) 1.11
The anonymous polymorphic DNA clone D1S1, previously mapped to human chromosome 1p36 by in situ hybridization, is from chromosome 3 and is duplicated on chromosome 1. Am J Hum Genet (1986) 1.11
Forensic validation of the STR systems SE 33 and TC 11. Int J Legal Med (1993) 1.09
Familial segregation of venous thromboembolism. J Thromb Haemost (2004) 1.08
Extraction, PCR amplification and sequencing of mitochondrial DNA from human hair shafts. Biotechniques (1995) 1.07
Evidence for genetic heterogeneity in tuberous sclerosis: one locus on chromosome 9 and at least one locus elsewhere. Am J Hum Genet (1992) 1.07
Dinucleotide repeat polymorphism at the human tissue plasminogen activator gene (PLAT). Nucleic Acids Res (1991) 1.06
DNA Commission of the International Society of Forensic Genetics: recommendations on forensic analysis using Y-chromosome STRs. Forensic Sci Int (2001) 1.04
Genetic mapping of RP1 on 8q11-q21 in an Australian family with autosomal dominant retinitis pigmentosa reduces the critical region to 4 cM between D8S601 and D8S285. Hum Genet (1996) 1.04
Identifying and mapping novel retinal-expressed ESTs from humans. Mol Vis (1999) 1.04
PCR-amplification and detection of the human D1S80 VNTR locus. Amplification conditions, population genetics and application in forensic analysis. Int J Legal Med (1993) 1.03
Inherited retinal degeneration: exceptional genetic and clinical heterogeneity. Mol Med Today (1996) 1.03
Extensive DNA polymorphism at the factor XIIIa (F13A) locus and linkage to HLA. Am J Hum Genet (1988) 0.99
Visual phenotype in patients with Arg41Gln and ala196+1bp mutations in the CRX gene. Ophthalmic Genet (2000) 0.98
A family exhibiting heteroplasmy in the human mitochondrial DNA control region reveals both somatic mosaicism and pronounced segregation of mitotypes. Hum Genet (1997) 0.98
Evidence for genetic admixture as a determinant in the occurrence of insulin-dependent diabetes mellitus in U.S. blacks. Diabetes (1982) 0.97
Splice site mutation in the peripherin/RDS gene associated with pattern dystrophy of the retina. Am J Ophthalmol (2001) 0.97
Mapping the RP10 locus for autosomal dominant retinitis pigmentosa on 7q: refined genetic positioning and localization within a well-defined YAC contig. Genome Res (1996) 0.96
Detection of genetic variation with radioactive ligands. I. Electrophoretic screening of plasma proteins with a selected panel of compounds. Am J Hum Genet (1977) 0.96
Human glutamate pyruvate transaminase (GPT): localization to 8q24.3, cDNA and genomic sequences, and polymorphic sites. Genomics (1997) 0.95
A simple and sensitive method for quantifying human genomic DNA in forensic specimen extracts. Biotechniques (1989) 0.95
DNA recommendations 1997 of the International Society for Forensic Genetics. Vox Sang (1998) 0.95
Clinical variability and genetic heterogeneity within the Acadian Usher population. Am J Med Genet (1992) 0.94
Men transmit MS more often to their children vs women: the Carter effect. Neurology (2006) 0.94
Linkage mapping of Thiel-Behnke corneal dystrophy (CDB2) to chromosome 10q23-q24. Genomics (1997) 0.93
Application of dual internal standards for precise sizing of polymerase chain reaction products using capillary electrophoresis. Electrophoresis (1995) 0.92
Population genetics and forensic efficiency data of 4 AMPFLP's. Int J Legal Med (1992) 0.92
Typing of deoxyribonucleic acid (DNA) extracted from compact bone from human remains. J Forensic Sci (1991) 0.91
Multiple, independent restriction site polymorphisms in human DNA detected with a cDNA probe to argininosuccinate synthetase (AS). Am J Hum Genet (1984) 0.91
Horizontal polyacrylamide gel electrophoresis for the separation of DNA fragments. Electrophoresis (1994) 0.91
The analysis of EDTA in dried bloodstains by electrospray LC-MS-MS and ion chromatography. J Anal Toxicol (1998) 0.90
Autosomal dominant retinal degeneration and bone loss in patients with a 12-bp deletion in the CRX gene. Invest Ophthalmol Vis Sci (2001) 0.90
PCR-based typing of DNA extracted from cigarette butts. Int J Legal Med (1991) 0.90
D1S80 allele frequencies in a Chinese population. Int J Legal Med (1994) 0.89
Detection of genetic variation with radioactive ligands. II. Genetic variants of vitamin D-labeled group-specific component (Gc) proteins. Am J Hum Genet (1977) 0.89
Report and abstracts of the First International Workshop on Human Chromosome 8 Mapping. Vancouver, British Columbia, May 2-4, 1993. Cytogenet Cell Genet (1993) 0.88
Validation studies on the analysis of the HLA DQ alpha locus using the polymerase chain reaction. J Forensic Sci (1991) 0.88
Czech population data on 10 short tandem repeat loci of SGM Plus STR system kit using DNA purified in FTA cards. Forensic Sci Int (2001) 0.88
Detection of genetic variation with radioactive ligands. IV. X-linked, polymorphic genetic variation of thyroxin-binding globulin (TBG). Am J Hum Genet (1981) 0.87