Published in Am J Hum Genet on April 06, 2000
Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language. Am J Hum Genet (2000) 4.72
The effective mutation rate at Y chromosome short tandem repeats, with application to human population-divergence time. Am J Hum Genet (2003) 4.34
A back migration from Asia to sub-Saharan Africa is supported by high-resolution analysis of human Y-chromosome haplotypes. Am J Hum Genet (2002) 3.71
Y-chromosomal DNA variation in Pakistan. Am J Hum Genet (2002) 3.35
Admixture dynamics in Hispanics: a shift in the nuclear genetic ancestry of a South American population isolate. Proc Natl Acad Sci U S A (2006) 2.65
The pedigree rate of sequence divergence in the human mitochondrial genome: there is a difference between phylogenetic and pedigree rates. Am J Hum Genet (2003) 2.23
Estimating Scandinavian and Gaelic ancestry in the male settlers of Iceland. Am J Hum Genet (2000) 2.22
A genetic landscape reshaped by recent events: Y-chromosomal insights into central Asia. Am J Hum Genet (2002) 2.21
Y chromosomal haplogroup J as a signature of the post-neolithic colonization of Europe. Hum Genet (2004) 2.21
Y-chromosome lineages trace diffusion of people and languages in southwestern Asia. Am J Hum Genet (2000) 2.05
A predominantly neolithic origin for Y-chromosomal DNA variation in North Africa. Am J Hum Genet (2004) 2.02
DNA Commission of the International Society of Forensic Genetics (ISFG): an update of the recommendations on the use of Y-STRs in forensic analysis. Int J Legal Med (2006) 2.00
A comprehensive survey of human Y-chromosomal microsatellites. Am J Hum Genet (2004) 1.97
Mutability of Y-chromosomal microsatellites: rates, characteristics, molecular bases, and forensic implications. Am J Hum Genet (2010) 1.88
Y-chromosome evidence of southern origin of the East Asian-specific haplogroup O3-M122. Am J Hum Genet (2005) 1.86
Reduced Y-chromosome, but not mitochondrial DNA, diversity in human populations from West New Guinea. Am J Hum Genet (2002) 1.86
Y-chromosome evidence for differing ancient demographic histories in the Americas. Am J Hum Genet (2003) 1.84
Y chromosomal evidence for the origins of oceanic-speaking peoples. Genetics (2002) 1.81
Likelihood-based estimation of microsatellite mutation rates. Genetics (2003) 1.77
Proportioning whole-genome single-nucleotide-polymorphism diversity for the identification of geographic population structure and genetic ancestry. Am J Hum Genet (2006) 1.76
Phylogeographic analysis of haplogroup E3b (E-M215) y chromosomes reveals multiple migratory events within and out of Africa. Am J Hum Genet (2004) 1.76
A predominantly indigenous paternal heritage for the Austronesian-speaking peoples of insular Southeast Asia and Oceania. Am J Hum Genet (2001) 1.76
Mutation patterns at dinucleotide microsatellite loci in humans. Am J Hum Genet (2002) 1.71
An extensive analysis of Y-chromosomal microsatellite haplotypes in globally dispersed human populations. Am J Hum Genet (2001) 1.70
How homologous recombination generates a mutable genome. Hum Genomics (2005) 1.67
Messages through bottlenecks: on the combined use of slow and fast evolving polymorphic markers on the human Y chromosome. Am J Hum Genet (2000) 1.65
High-resolution Y chromosome haplotypes of Israeli and Palestinian Arabs reveal geographic substructure and substantial overlap with haplotypes of Jews. Hum Genet (2000) 1.61
Microsatellite evolution inferred from human-chimpanzee genomic sequence alignments. Proc Natl Acad Sci U S A (2002) 1.59
Independent histories of human Y chromosomes from Melanesia and Australia. Am J Hum Genet (2000) 1.58
Signature of recent historical events in the European Y-chromosomal STR haplotype distribution. Hum Genet (2005) 1.54
The peopling of Europe and the cautionary tale of Y chromosome lineage R-M269. Proc Biol Sci (2011) 1.52
Investigating the effects of prehistoric migrations in Siberia: genetic variation and the origins of Yakuts. Hum Genet (2006) 1.51
Comprehensive mutation analysis of 17 Y-chromosomal short tandem repeat polymorphisms included in the AmpFlSTR Yfiler PCR amplification kit. Int J Legal Med (2009) 1.50
Significant genetic differentiation between Poland and Germany follows present-day political borders, as revealed by Y-chromosome analysis. Hum Genet (2005) 1.47
Recent spread of a Y-chromosomal lineage in northern China and Mongolia. Am J Hum Genet (2005) 1.46
Multiple origins of Ashkenazi Levites: Y chromosome evidence for both Near Eastern and European ancestries. Am J Hum Genet (2003) 1.44
Y-chromosomal evidence for a limited Greek contribution to the Pathan population of Pakistan. Eur J Hum Genet (2006) 1.37
The rate and spectrum of microsatellite mutation in Caenorhabditis elegans and Daphnia pulex. Genetics (2008) 1.35
Y chromosome STR haplotypes and the genetic structure of U.S. populations of African, European, and Hispanic ancestry. Genome Res (2003) 1.30
Every microsatellite is different: Intrinsic DNA features dictate mutagenesis of common microsatellites present in the human genome. Mol Carcinog (2009) 1.29
Inferential genotyping of Y chromosomes in Latter-Day Saints founders and comparison to Utah samples in the HapMap project. Am J Hum Genet (2009) 1.29
Estimating the time to the most recent common ancestor for the Y chromosome or mitochondrial DNA for a pair of individuals. Genetics (2001) 1.26
Genomic microsatellites as evolutionary chronometers: a test in wild cats. Genome Res (2002) 1.25
Y-chromosomal DNA haplogroups and their implications for the dual origins of the Koreans. Hum Genet (2003) 1.24
A genomic portrait of human microsatellite variation. Mol Biol Evol (2010) 1.21
Genetic studies of human diversity in East Asia. Philos Trans R Soc Lond B Biol Sci (2007) 1.19
Machine-learning approaches for classifying haplogroup from Y chromosome STR data. PLoS Comput Biol (2008) 1.17
A novel Y-chromosome variant puts an upper limit on the timing of first entry into the Americas. Am J Hum Genet (2003) 1.13
Y-chromosomal microsatellite mutation rates in a population sample from northwestern Germany. Int J Legal Med (2006) 1.07
Y-chromosome descent clusters and male differential reproductive success: young lineage expansions dominate Asian pastoral nomadic populations. Eur J Hum Genet (2015) 1.06
Genomic and expression analysis of multiple Sry loci from a single Rattus norvegicus Y chromosome. BMC Genet (2007) 1.03
Drawing the history of the Hutterite population on a genetic landscape: inference from Y-chromosome and mtDNA genotypes. Eur J Hum Genet (2009) 1.03
A matter of life or death: how microsatellites emerge in and vanish from the human genome. Genome Res (2011) 1.02
Mutations in 14 Y-STR loci among Japanese father-son haplotypes. Int J Legal Med (2004) 1.01
DXS10079, DXS10074 and DXS10075 are STRs located within a 280-kb region of Xq12 and provide stable haplotypes useful for complex kinship cases. Int J Legal Med (2005) 0.99
A brief review of short tandem repeat mutation. Genomics Proteomics Bioinformatics (2007) 0.98
The genetic or mythical ancestry of descent groups: lessons from the Y chromosome. Am J Hum Genet (2004) 0.97
Domain-level differences in microsatellite distribution and content result from different relative rates of insertion and deletion mutations. Genome Res (2002) 0.97
Sub-Saharan Africa descendents in Rio de Janeiro (Brazil): population and mutational data for 12 Y-STR loci. Int J Legal Med (2007) 0.96
Deriving evolutionary relationships among populations using microsatellites and (deltamu)(2): all loci are equal, but some are more equal than others... Genetics (2002) 0.96
Investigations of the Y chromosome, male founder structure and YSTR mutation rates in the Old Order Amish. Hum Hered (2007) 0.96
Population and mutation analysis of 17 Y-STR loci from Rio de Janeiro (Brazil). Int J Legal Med (2004) 0.95
Population and segregation data on 17 Y-STRs: results of a GEP-ISFG collaborative study. Int J Legal Med (2008) 0.94
Demographic estimates from Y chromosome microsatellite polymorphisms: analysis of a worldwide sample. Hum Genomics (2004) 0.93
Haplotypes and mutation analysis of 22 Y-chromosomal STRs in Korean father-son pairs. Int J Legal Med (2006) 0.93
Linkage disequilibrium between STRPs and SNPs across the human genome. Am J Hum Genet (2008) 0.91
High frequency of microsatellites in S. cerevisiae meiotic recombination hotspots. BMC Genomics (2008) 0.90
The origin of the isolated population of the Faroe Islands investigated using Y chromosomal markers. Hum Genet (2004) 0.90
Haplotype analysis of CYP11A1 identifies promoter variants associated with breast cancer risk. Cancer Res (2007) 0.89
On the evolutionary mutation rate at Y-chromosome STRs: comments on paper by Di Giacomo et al. (2004). Hum Genet (2005) 0.89
Human evolution in Siberia: from frozen bodies to ancient DNA. BMC Evol Biol (2010) 0.89
Y-chromosomal STR haplotypes in a Northeast Italian population sample using 17plex loci PCR assay. Int J Legal Med (2005) 0.87
Usefulness of SNPs as Supplementary Markers in a Paternity Case with 3 Genetic Incompatibilities at Autosomal and Y Chromosomal Loci. Transfus Med Hemother (2014) 0.85
Microsatellite length differences between humans and chimpanzees at autosomal Loci are not found at equivalent haploid Y chromosomal Loci. Genetics (2006) 0.85
Population-Scale Sequencing Data Enable Precise Estimates of Y-STR Mutation Rates. Am J Hum Genet (2016) 0.85
Haplotype data and mutation rates for the 23 Y-STR loci of PowerPlex® Y 23 System in a Northeast Italian population sample. Int J Legal Med (2014) 0.84
Gene conversion violates the stepwise mutation model for microsatellites in y-chromosomal palindromic repeats. Hum Mutat (2014) 0.82
Population genetic analysis of haplotypes based on 17 short tandem repeat loci on Y chromosome in population sample from eastern Croatia. Croat Med J (2010) 0.81
Distribution of polymorphic and non-polymorphic microsatellite repeats in Xenopus tropicalis. Bioinform Biol Insights (2008) 0.80
Widespread translocation from autosomes to sex chromosomes preserves genetic variability in an endangered lark. J Mol Evol (2010) 0.80
Haplotypes of 20 Y-chromosomal STRs in a population sample from southeast China (Chaoshan area). Int J Legal Med (2007) 0.78
Multistep microsatellite mutation in the maternally transmitted locus D13S317: a case of maternal allele mismatch in the child. Int J Legal Med (2006) 0.78
Empirical evaluation reveals best fit of a logistic mutation model for human Y-chromosomal microsatellites. Genetics (2011) 0.77
Bimodal allele frequency distribution at Y-STR loci DYS392 and DYS438: no evidence for a deviation from the stepwise mutation model. Int J Legal Med (2003) 0.77
The peopling of Europe from the maternal and paternal perspectives. Am J Hum Genet (2000) 0.77
A case of double alleles at three Y-STR loci: forensic implications. Int J Legal Med (2005) 0.76
Maximum likelihood estimation of locus-specific mutation rates in Y-chromosome short tandem repeats. Bioinformatics (2010) 0.76
Evolution of Nine Microsatellite Loci in the Fungus Fusarium oxysporum. J Mol Evol (2015) 0.76
Modular knowledge systems accelerate human migration in asymmetric random environments. J R Soc Interface (2016) 0.75
Analysis of genetic admixture in Uyghur using the 26 Y-STR loci system. Sci Rep (2016) 0.75
Calculating expected DNA remnants from ancient founding events in human population genetics. BMC Genet (2008) 0.75
Malignant tumors and forensics--dilemmas and proposals. Croat Med J (2009) 0.75
Independent methods for evolutionary genetic dating provide insights into Y-chromosomal STR mutation rates confirming data from direct father-son transmissions. Hum Genet (2005) 0.75
The Genetic Legacy of Zoroastrianism in Iran and India: Insights into Population Structure, Gene Flow, and Selection. Am J Hum Genet (2017) 0.75
Mutation rates of 15 X chromosomal short tandem repeat markers. Int J Legal Med (2014) 0.75
Mutation of human short tandem repeats. Hum Mol Genet (1993) 14.03
A model of mutation appropriate to estimate the number of electrophoretically detectable alleles in a finite population. Genet Res (1973) 13.08
Mutational processes of simple-sequence repeat loci in human populations. Proc Natl Acad Sci U S A (1994) 11.84
Allele frequencies at microsatellite loci: the stepwise mutation model revisited. Genetics (1993) 8.60
The evolutionary dynamics of repetitive DNA in eukaryotes. Nature (1994) 7.15
Mutation rate in human microsatellites: influence of the structure and length of the tandem repeat. Am J Hum Genet (1998) 5.26
Slippage synthesis of simple sequence DNA. Nucleic Acids Res (1992) 5.18
A pre-Columbian Y chromosome-specific transition and its implications for human evolutionary history. Proc Natl Acad Sci U S A (1996) 4.52
Estimating Y chromosome specific microsatellite mutation frequencies using deep rooting pedigrees. Hum Mol Genet (1997) 3.78
Genetic relationships of Asians and Northern Europeans, revealed by Y-chromosomal DNA analysis. Am J Hum Genet (1997) 3.54
Microsatellite instability in yeast: dependence on the length of the microsatellite. Genetics (1997) 3.51
Relative mutation rates at di-, tri-, and tetranucleotide microsatellite loci. Proc Natl Acad Sci U S A (1997) 3.32
Evaluation of Y-chromosomal STRs: a multicenter study. Int J Legal Med (1997) 3.19
Microsatellite 'evolution': directionality or bias? Nat Genet (1995) 2.85
The human Y chromosome: overlapping DNA clones spanning the euchromatic region. Science (1992) 2.66
The Y chromosome in forensic analysis and paternity testing. Int J Legal Med (1997) 2.27
Microsatellites show mutational bias and heterozygote instability. Nat Genet (1996) 2.18
Mutation rate varies among alleles at a microsatellite locus: phylogenetic evidence. Proc Natl Acad Sci U S A (1996) 1.96
Characterization of ancestral and derived Y-chromosome haplotypes of New World native populations. Am J Hum Genet (1998) 1.94
High mutation rate of a long microsatellite allele in Drosophila melanogaster provides evidence for allele-specific mutation rates. Mol Biol Evol (1998) 1.92
Microsatellite variation in North American populations of Drosophila melanogaster. Nucleic Acids Res (1995) 1.63
Geographic differences in the allele frequencies of the human Y-linked tetranucleotide polymorphism DYS19. Hum Genet (1996) 1.52
Studying human mutations by sperm typing: instability of CAG trinucleotide repeats in the human androgen receptor gene. Nat Genet (1994) 1.45
North and South Amerindians may have the same major founder Y chromosome haplotype. Am J Hum Genet (1996) 1.35
Microsatellites provide evidence for Y chromosome diversity among the founders of the New World. Proc Natl Acad Sci U S A (1999) 1.33
The tetranucleotide repeat polymorphism D21S1245 demonstrates hypermutability in germline and somatic cells. Hum Mol Genet (1995) 1.23
Ascertainment bias cannot entirely account for human microsatellites being longer than their chimpanzee homologues. Hum Mol Genet (1998) 1.16
Markov chain Monte Carlo analysis of human Y-chromosome microsatellites provides evidence of biased mutation. Proc Natl Acad Sci U S A (1999) 1.15
Y-chromosome-specific microsatellite mutation rates re-examined using a minisatellite, MSY1. Hum Mol Genet (1999) 1.10
Characterization of a small family (CAIII) of microsatellite-containing sequences with X-Y homology. J Mol Evol (1997) 1.09
Microsatellites are subject to directional evolution. Nat Genet (1996) 1.06
Y chromosomal polymorphisms reveal founding lineages in the Finns and the Saami. Eur J Hum Genet (1999) 1.04
Experimentally observed germline mutations at human micro- and minisatellite loci. Eur J Hum Genet (1999) 0.99
Tandem repeat structure of the duplicated Y-chromosomal STR locus DYS385 and frequency studies in the German and three Asian populations. Forensic Sci Int (1998) 0.99
Multiplex DNA typing of short-tandem-repeat loci on the Y chromosome. Biol Chem (1997) 0.99
SYNTHETIC DEOXYRIBO-OLIGONUCLEOTIDES AS TEMPLATES FOR THE DNA POLYMERASE OF ESCHERICHIA COLI: NEW DNA-LIKE L-POLYMERS CONTAINING REPEATING NUCLEOTIDE SEQUENCES. Proc Natl Acad Sci U S A (1965) 0.98
Mutation rate in human microsatellites. Am J Hum Genet (1999) 0.95
DNA analysis in disputed parentage: the occurrence of two apparently false exclusions of paternity, both at short tandem repeat (STR) loci, in the one child. Electrophoresis (1997) 0.94
A genetic factor model for the statistical analysis of multilocus DNA fingerprints. Electrophoresis (1992) 0.82
Mitochondrial DNA and human evolution. Nature (1987) 22.33
African populations and the evolution of human mitochondrial DNA. Science (1991) 18.08
Length mutations in human mitochondrial DNA: direct sequencing of enzymatically amplified DNA. Nucleic Acids Res (1987) 10.38
Predicting the probability for falls in community-dwelling older adults using the Timed Up & Go Test. Phys Ther (2000) 8.77
Neandertal DNA sequences and the origin of modern humans. Cell (1997) 8.45
Haplotype diversity and linkage disequilibrium at human G6PD: recent origin of alleles that confer malarial resistance. Science (2001) 7.87
Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations. Lancet (2001) 7.27
The human gene mutation database. Nucleic Acids Res (1998) 6.38
Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language. Am J Hum Genet (2000) 4.72
Mismatch distributions of mtDNA reveal recent human population expansions. Hum Biol (1994) 4.39
The role of a common variant of the cholesteryl ester transfer protein gene in the progression of coronary atherosclerosis. The Regression Growth Evaluation Statin Study Group. N Engl J Med (1998) 3.97
Jefferson fathered slave's last child. Nature (1998) 3.83
Estimating Y chromosome specific microsatellite mutation frequencies using deep rooting pedigrees. Hum Mol Genet (1997) 3.78
Genetic relationships of Asians and Northern Europeans, revealed by Y-chromosomal DNA analysis. Am J Hum Genet (1997) 3.54
Cytosine methylation and the fate of CpG dinucleotides in vertebrate genomes. Hum Genet (1989) 3.27
DNA commission of the International Society of Forensic Genetics: Recommendations on the interpretation of mixtures. Forensic Sci Int (2006) 3.20
Evaluation of Y-chromosomal STRs: a multicenter study. Int J Legal Med (1997) 3.19
Evolutionary history of the COII/tRNALys intergenic 9 base pair deletion in human mitochondrial DNAs from the Pacific. Mol Biol Evol (1995) 3.10
African origin of human-specific polymorphic Alu insertions. Proc Natl Acad Sci U S A (1994) 3.09
Nonneutral mitochondrial DNA variation in humans and chimpanzees. Genetics (1996) 2.93
Ancestral Asian source(s) of new world Y-chromosome founder haplotypes. Am J Hum Genet (1999) 2.89
Magnetofection: enhancing and targeting gene delivery by magnetic force in vitro and in vivo. Gene Ther (2002) 2.86
mtDNA control-region sequence variation suggests multiple independent origins of an "Asian-specific" 9-bp deletion in sub-Saharan Africans. Am J Hum Genet (1996) 2.79
Polynesian genetic affinities with Southeast Asian populations as identified by mtDNA analysis. Am J Hum Genet (1995) 2.74
Apolipoprotein E4 allele in a population-based study of early-onset Alzheimer's disease. Nat Genet (1994) 2.65
The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictions. Hum Genet (1990) 2.59
Human mtDNA and Y-chromosome variation is correlated with matrilocal versus patrilocal residence. Nat Genet (2001) 2.57
Genetic variation of recent Alu insertions in human populations. J Mol Evol (1996) 2.56
Identification of individuals by analysis of biallelic DNA markers, using PCR and solid-phase minisequencing. Am J Hum Genet (1993) 2.46
Human origins and analysis of mitochondrial DNA sequences. Science (1992) 2.43
Evidence for variable selective pressures at MC1R. Am J Hum Genet (2000) 2.43
Melanesian origin of Polynesian Y chromosomes. Curr Biol (2000) 2.27
mtDNA analysis of Nile River Valley populations: A genetic corridor or a barrier to migration? Am J Hum Genet (1999) 2.25
DNA Commission of the International Society of Forensic Genetics (ISFG): an update of the recommendations on the use of Y-STRs in forensic analysis. Forensic Sci Int (2006) 2.22
DNA fingerprinting with the oligonucleotide probe (CAC)5/(GTG)5: somatic stability and germline mutations. Hum Genet (1989) 2.22
Is the 6-minute walk test a reliable substitute for peak oxygen uptake in patients with dilated cardiomyopathy? Eur Heart J (2000) 2.16
Large-scale analysis of the Alu Ya5 and Yb8 subfamilies and their contribution to human genomic diversity. J Mol Biol (2001) 2.16
Evaluation of the novel myocardial perfusion positron-emission tomography tracer 18F-BMS-747158-02: comparison to 13N-ammonia and validation with microspheres in a pig model. Circulation (2009) 2.15
Allelic variation in human mitochondrial genes based on patterns of restriction site polymorphism. Proc Natl Acad Sci U S A (1986) 2.13
Rate of sequence divergence estimated from restriction maps of mitochondrial DNAs from Papua New Guinea. Cold Spring Harb Symp Quant Biol (1986) 2.13
Reading between the LINEs: human genomic variation induced by LINE-1 retrotransposition. Genome Res (2000) 2.09
De novo rearrangements found in 2% of index patients with spinal muscular atrophy: mutational mechanisms, parental origin, mutation rate, and implications for genetic counseling. Am J Hum Genet (1997) 2.05
Alu evolution in human populations: using the coalescent to estimate effective population size. Genetics (1997) 2.03
In vitro translation of Drosophila heat-shock and non--heat-shock mRNAs in heterologous and homologous cell-free systems. Cell (1981) 2.03
mtDNA analysis of a prehistoric Oneota population: implications for the peopling of the New World. Am J Hum Genet (1998) 2.01
DNA Commission of the International Society of Forensic Genetics (ISFG): an update of the recommendations on the use of Y-STRs in forensic analysis. Int J Legal Med (2006) 2.00
Pseudolinkage of the duplicate loci for supernatant aspartate aminotransferase in brook trout, Salvelinus fontinalis. J Hered (1980) 1.97
Mitochondrial mutation rate revisited: hot spots and polymorphism. Nat Genet (1998) 1.94
Use of X-linked markers for forensic purposes. Int J Legal Med (2003) 1.91
Questioning evidence for recombination in human mitochondrial DNA. Science (2000) 1.90
Chromosome Y microsatellites: population genetic and evolutionary aspects. Int J Legal Med (1997) 1.89
Examination of the current top candidate genes for AD in a genome-wide association study. Mol Psychiatry (2009) 1.89
Mitochondrial DNA sequences from Switzerland reveal striking homogeneity of European populations. Biol Chem Hoppe Seyler (1994) 1.87
Short tandem-repeat polymorphism/alu haplotype variation at the PLAT locus: implications for modern human origins. Am J Hum Genet (2000) 1.85
Analysis of molecular variance (AMOVA) of Y-chromosome-specific microsatellites in two closely related human populations. Hum Mol Genet (1996) 1.84
Minisatellite diversity supports a recent African origin for modern humans. Nat Genet (1996) 1.84
The STOR clinical information system. MD Comput (1989) 1.83
Effects of intraabdominally insufflated carbon dioxide and elevated intraabdominal pressure on splanchnic circulation: an experimental study in pigs. Anesthesiology (1998) 1.81
Genetic susceptibility to multiple sclerosis linked to myelin basic protein gene. Lancet (1992) 1.79
Human gene cloning: the storm before the lull? Nature (1986) 1.78
Aetiological monitor of congenital abnormalities: a case-control surveillance system. Acta Paediatr Hung (1983) 1.76
Malignant hyperthermia mutation Arg615Cys in the porcine ryanodine receptor alters voltage dependence of Ca2+ release. J Physiol (2000) 1.76
Familial aggregation in frontotemporal dementia. Neurology (1998) 1.76
Conformational mutation in human mtDNA detected by direct sequencing of enzymatically amplified DNA. Nucleic Acids Res (1988) 1.74
HLA-DQ alpha allele and genotype frequencies in various human populations, determined by using enzymatic amplification and oligonucleotide probes. Am J Hum Genet (1990) 1.72
An extensive analysis of Y-chromosomal microsatellite haplotypes in globally dispersed human populations. Am J Hum Genet (2001) 1.70
Genetic structure of the ancestral population of modern humans. J Mol Evol (1998) 1.70
Recurrent duplication and deletion polymorphisms on the long arm of the Y chromosome in normal males. Hum Mol Genet (1996) 1.68
Determination of allele frequencies at loci with length polymorphism by quantitative analysis of DNA amplified from pooled samples. PCR Methods Appl (1993) 1.67
Online reference database of European Y-chromosomal short tandem repeat (STR) haplotypes. Forensic Sci Int (2001) 1.67
Peopling of Sahul: mtDNA variation in aboriginal Australian and Papua New Guinean populations. Am J Hum Genet (1999) 1.67
A molecular basis for human hypersensitivity to aminoglycoside antibiotics. Nucleic Acids Res (1993) 1.67
Messages through bottlenecks: on the combined use of slow and fast evolving polymorphic markers on the human Y chromosome. Am J Hum Genet (2000) 1.65
Fetal spina bifida repair--current trends and prospects of intrauterine neurosurgery. Fetal Diagn Ther (2008) 1.64
Multivariate statistical approach to a data set of dioxin and furan contaminations in human milk. Bull Environ Contam Toxicol (1988) 1.64
Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location. Hum Mol Genet (2000) 1.61
Paternal relatedness and age proximity regulate social relationships among adult female rhesus macaques. Proc Natl Acad Sci U S A (2001) 1.61
Variants in the sulphonylurea receptor gene: association of the exon 16-3t variant with Type II diabetes mellitus in Dutch Caucasians. Diabetologia (1999) 1.59
Long-term treatment of trigeminal neuralgia with carbamazepine. Postgrad Med J (1981) 1.58
Independent histories of human Y chromosomes from Melanesia and Australia. Am J Hum Genet (2000) 1.58
Complete mitochondrial genome amplification. Nat Genet (1994) 1.58
Pulmonary and allergy subspecialty care in adults with asthma. Treatment, use of services, and health outcomes. West J Med (1997) 1.56