Published in Am J Hum Genet on November 09, 2001
The effective mutation rate at Y chromosome short tandem repeats, with application to human population-divergence time. Am J Hum Genet (2003) 4.34
Prospects for admixture mapping of complex traits. Am J Hum Genet (2004) 2.73
The Genographic Project public participation mitochondrial DNA database. PLoS Genet (2007) 1.86
Contrasting patterns of Y chromosome variation in Ashkenazi Jewish and host non-Jewish European populations. Hum Genet (2004) 1.85
Analyses of genetic structure of Tibeto-Burman populations reveals sex-biased admixture in southern Tibeto-Burmans. Am J Hum Genet (2004) 1.57
Ancient DNA analysis of 8000 B.C. near eastern farmers supports an early neolithic pioneer maritime colonization of Mainland Europe through Cyprus and the Aegean Islands. PLoS Genet (2014) 1.37
Measurement of admixture proportions and description of admixture structure in different U.S. populations. Hum Mutat (2009) 1.33
Mutation history of the roma/gypsies. Am J Hum Genet (2004) 1.24
SNPSTRs: empirically derived, rapidly typed, autosomal haplotypes for inference of population history and mutational processes. Genome Res (2002) 1.16
Directional migration in the Hindu castes: inferences from mitochondrial, autosomal and Y-chromosomal data. Hum Genet (2004) 1.09
LTBP2 and CYP1B1 mutations and associated ocular phenotypes in the Roma/Gypsy founder population. Eur J Hum Genet (2010) 1.03
Reconstructing the Indian origin and dispersal of the European Roma: a maternal genetic perspective. PLoS One (2011) 1.00
Autosomal-recessive congenital cerebellar ataxia is caused by mutations in metabotropic glutamate receptor 1. Am J Hum Genet (2012) 0.98
Reconstructing Roma history from genome-wide data. PLoS One (2013) 0.96
Investigations of the Y chromosome, male founder structure and YSTR mutation rates in the Old Order Amish. Hum Hered (2007) 0.96
ANO10 c.1150_1151del is a founder mutation causing autosomal recessive cerebellar ataxia in Roma/Gypsies. J Neurol (2011) 0.92
The impact of recent events on human genetic diversity. Philos Trans R Soc Lond B Biol Sci (2012) 0.92
Integrin alpha 8 recessive mutations are responsible for bilateral renal agenesis in humans. Am J Hum Genet (2014) 0.92
Introducing the Algerian mitochondrial DNA and Y-chromosome profiles into the North African landscape. PLoS One (2013) 0.91
Bulgarians vs the other European populations: a mitochondrial DNA perspective. Int J Legal Med (2011) 0.91
Hungarian mtDNA population databases from Budapest and the Baranya county Roma. Int J Legal Med (2006) 0.90
Indian signatures in the westernmost edge of the European Romani diaspora: new insight from mitogenomes. PLoS One (2013) 0.88
The phylogeography of Y-chromosome haplogroup h1a1a-m82 reveals the likely Indian origin of the European Romani populations. PLoS One (2012) 0.86
Y-STR variation in Albanian populations: implications on the match probabilities and the genetic legacy of the minority claiming an Egyptian descent. Int J Legal Med (2010) 0.86
No evidence of association between 118A>G OPRM1 polymorphism and heroin dependence in a large Bulgarian case-control sample. Drug Alcohol Depend (2011) 0.84
Founder effect and estimation of the age of the French Gypsy mutation associated with Glanzmann thrombasthenia in Manouche families. Eur J Hum Genet (2011) 0.82
On the Etruscan mitochondrial DNA contribution to modern humans. Am J Hum Genet (2004) 0.82
Health and Roma People in Turkey. Balkan Med J (2016) 0.81
Origins, admixture and founder lineages in European Roma. Eur J Hum Genet (2015) 0.77
Carriers of human mitochondrial DNA macrohaplogroup M colonized India from southeastern Asia. BMC Evol Biol (2016) 0.76
Genetic and biochemical study of dual hereditary jaundice: Dubin-Johnson and Gilbert's syndromes. Haplotyping and founder effect of deletion in ABCC2. Eur J Hum Genet (2015) 0.75
A Romani mitochondrial haplotype in England 500 years before their recorded arrival in Britain. Biol Lett (2005) 0.75
Meta-Analysis of Mitochondrial DNA Variation in the Iberian Peninsula. PLoS One (2016) 0.75
Sequence and organization of the human mitochondrial genome. Nature (1981) 57.39
Analysis of molecular variance inferred from metric distances among DNA haplotypes: application to human mitochondrial DNA restriction data. Genetics (1992) 43.80
Mitochondrial portraits of human populations using median networks. Genetics (1995) 9.07
Y chromosome sequence variation and the history of human populations. Nat Genet (2000) 8.34
Tracing European founder lineages in the Near Eastern mtDNA pool. Am J Hum Genet (2000) 7.06
Detection of numerous Y chromosome biallelic polymorphisms by denaturing high-performance liquid chromatography. Genome Res (1997) 6.73
The genetic legacy of Paleolithic Homo sapiens sapiens in extant Europeans: a Y chromosome perspective. Science (2000) 6.57
The phylogeography of Y chromosome binary haplotypes and the origins of modern human populations. Ann Hum Genet (2001) 6.24
mtDNA variation among Greenland Eskimos: the edge of the Beringian expansion. Am J Hum Genet (2000) 5.17
The emerging tree of West Eurasian mtDNAs: a synthesis of control-region sequences and RFLPs. Am J Hum Genet (1999) 4.80
Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language. Am J Hum Genet (2000) 4.72
Y chromosomal DNA variation and the peopling of Japan. Am J Hum Genet (1995) 4.50
Genetic evidence of an early exit of Homo sapiens sapiens from Africa through eastern Africa. Nat Genet (1999) 4.12
Estimating Y chromosome specific microsatellite mutation frequencies using deep rooting pedigrees. Hum Mol Genet (1997) 3.78
Phylogeography of mitochondrial DNA in western Europe. Ann Hum Genet (1998) 3.54
Genetic evidence on the origins of Indian caste populations. Genome Res (2001) 3.25
Evaluation of Y-chromosomal STRs: a multicenter study. Int J Legal Med (1997) 3.19
Deep common ancestry of indian and western-Eurasian mitochondrial DNA lineages. Curr Biol (1999) 3.06
Origins of Old Testament priests. Nature (1998) 2.71
Population genetic implications from sequence variation in four Y chromosome genes. Proc Natl Acad Sci U S A (2000) 2.62
N-myc downstream-regulated gene 1 is mutated in hereditary motor and sensory neuropathy-Lom. Am J Hum Genet (2000) 2.47
Pattern of nucleotide substitution and rate heterogeneity in the hypervariable regions I and II of human mtDNA. Genetics (1999) 2.42
Dual origins of Finns revealed by Y chromosome haplotype variation. Am J Hum Genet (1998) 2.21
Geographic patterns of mtDNA diversity in Europe. Am J Hum Genet (2000) 2.18
From Asia to Europe: mitochondrial DNA sequence variability in Bulgarians and Turks. Ann Hum Genet (1996) 2.06
Hypervariable sites in the mtDNA control region are mutational hotspots. Am J Hum Genet (2000) 1.92
High-throughput multiplex SNP genotyping with MALDI-TOF mass spectrometry: practice, problems and promise. Hum Mutat (2001) 1.80
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
Gene mapping in Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24. Nat Genet (1996) 1.61
Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma. J Med Genet (1999) 1.55
Pre-Caucasoid and Caucasoid genetic features of the Indian population, revealed by mtDNA polymorphisms. Am J Hum Genet (1996) 1.46
Genetic studies of the Roma (Gypsies): a review. BMC Med Genet (2001) 1.28
Patterns of inter- and intra-group genetic diversity in the Vlax Roma as revealed by Y chromosome and mitochondrial DNA lineages. Eur J Hum Genet (2001) 1.24
A founder mutation in the gamma-sarcoglycan gene of gypsies possibly predating their migration out of India. Hum Mol Genet (1996) 1.10
A founder mutation in the GK1 gene is responsible for galactokinase deficiency in Roma (Gypsies). Am J Hum Genet (1999) 1.08
Polymorphism at the tetranucleotide repeat locus DYS389 in 10 populations reveals strong geographic clustering. Eur J Hum Genet (1999) 1.03
Congenital cataracts facial dysmorphism neuropathy (CCFDN) syndrome: a novel developmental disorder in Gypsies maps to 18qter. Eur J Hum Genet (1999) 1.03
A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic origin. Neurology (1999) 0.97
A novel locus for autosomal recessive peripheral neuropathy in the EGR2 region on 10q23. Am J Hum Genet (2000) 0.95
Hereditary motor and sensory neuropathy-russe: new autosomal recessive neuropathy in Balkan Gypsies. Ann Neurol (2001) 0.83
Peripheral nerve abnormalities in the congenital cataracts facial dysmorphism neuropathy (CCFDN) syndrome. Acta Neuropathol (1999) 0.81
Prevalence of Parkinson's disease in Bulgarian Gypsies. Neuroepidemiology (2000) 0.79
Sclerosis multiplex in gypsies. Acta Neurol Scand (1991) 0.78
A linkage study of affective disorders in two Bulgarian Gypsy families: results for candidate regions on chromosomes 18 and 21. Psychiatr Genet (1998) 0.78
Y chromosome sequence variation and the history of human populations. Nat Genet (2000) 8.34
Population growth of human Y chromosomes: a study of Y chromosome microsatellites. Mol Biol Evol (1999) 8.05
Homologous recombination in Escherichia coli: dependence on substrate length and homology. Genetics (1986) 7.97
Detection of numerous Y chromosome biallelic polymorphisms by denaturing high-performance liquid chromatography. Genome Res (1997) 6.73
The genetic legacy of Paleolithic Homo sapiens sapiens in extant Europeans: a Y chromosome perspective. Science (2000) 6.57
The phylogeography of Y chromosome binary haplotypes and the origins of modern human populations. Ann Hum Genet (2001) 6.24
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4. Cell (1996) 5.99
Dating the origin of the CCR5-Delta32 AIDS-resistance allele by the coalescence of haplotypes. Am J Hum Genet (1998) 5.24
A genomic screen of autism: evidence for a multilocus etiology. Am J Hum Genet (1999) 4.96
The origin of the major cystic fibrosis mutation (delta F508) in European populations. Nat Genet (1994) 4.94
Sindbis virus: an efficient, broad host range vector for gene expression in animal cells. Science (1989) 4.84
Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language. Am J Hum Genet (2000) 4.72
A pre-Columbian Y chromosome-specific transition and its implications for human evolutionary history. Proc Natl Acad Sci U S A (1996) 4.52
Cytoreductive surgery combined with perioperative intraperitoneal chemotherapy for the management of peritoneal carcinomatosis from colorectal cancer: a multi-institutional study. J Clin Oncol (2004) 4.15
Genetic evidence of an early exit of Homo sapiens sapiens from Africa through eastern Africa. Nat Genet (1999) 4.12
Synaptogenesis via dendritic filopodia in developing hippocampal area CA1. J Neurosci (1998) 3.78
Y-Chromosome evidence for a northward migration of modern humans into Eastern Asia during the last Ice Age. Am J Hum Genet (1999) 3.60
Denaturing high-performance liquid chromatography: A review. Hum Mutat (2001) 3.58
Demographic history of India and mtDNA-sequence diversity. Am J Hum Genet (1995) 3.47
Denaturing HPLC-identified novel FBN1 mutations, polymorphisms, and sequence variants in Marfan syndrome and related connective tissue disorders. Genet Test (1999) 3.42
The Eurasian heartland: a continental perspective on Y-chromosome diversity. Proc Natl Acad Sci U S A (2001) 3.38
Evaluation of Y-chromosomal STRs: a multicenter study. Int J Legal Med (1997) 3.19
Recent common ancestry of human Y chromosomes: evidence from DNA sequence data. Proc Natl Acad Sci U S A (2000) 3.14
The genetic heritage of the earliest settlers persists both in Indian tribal and caste populations. Am J Hum Genet (2003) 2.82
Variability of the SIRT3 gene, human silent information regulator Sir2 homologue, and survivorship in the elderly. Exp Gerontol (2003) 2.77
A view of the neolithic demic diffusion in Europe through two Y chromosome-specific markers. Am J Hum Genet (1996) 2.65
Evolutionary correlation between control region sequence and restriction polymorphisms in the mitochondrial genome of a large Senegalese Mandenka sample. Mol Biol Evol (1995) 2.62
Population genetic implications from sequence variation in four Y chromosome genes. Proc Natl Acad Sci U S A (2000) 2.62
Mitochondrial DNA inherited variants are associated with successful aging and longevity in humans. FASEB J (1999) 2.61
Human mitochondrial DNA variation and the origin of Basques. Ann Hum Genet (1995) 2.55
Initial experience with partial liquid ventilation in adult patients with the acute respiratory distress syndrome. JAMA (1996) 2.50
N-myc downstream-regulated gene 1 is mutated in hereditary motor and sensory neuropathy-Lom. Am J Hum Genet (2000) 2.47
Construction of human Y-chromosomal haplotypes using a new polymorphic A to G transition. Hum Mol Genet (1994) 2.47
Inactivating mutations in an SH2 domain-encoding gene in X-linked lymphoproliferative syndrome. Proc Natl Acad Sci U S A (1998) 2.46
A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus. Hum Genet (1998) 2.44
Genome-wide mapping with biallelic markers in Arabidopsis thaliana. Nat Genet (1999) 2.43
High-resolution analysis of human Y-chromosome variation shows a sharp discontinuity and limited gene flow between northwestern Africa and the Iberian Peninsula. Am J Hum Genet (2001) 2.32
Trading genes along the silk road: mtDNA sequences and the origin of central Asian populations. Am J Hum Genet (1998) 2.32
CENTRAL VENOUS PRESSURE IN RELATION TO CARDIAC "COMPETENCE," BLOOD VOLUME AND EXERCISE. J Clin Invest (1946) 2.29
Melanesian origin of Polynesian Y chromosomes. Curr Biol (2000) 2.27
A global haplotype analysis of the myotonic dystrophy locus: implications for the evolution of modern humans and for the origin of myotonic dystrophy mutations. Am J Hum Genet (1998) 2.23
Effect of spontaneous breathing trial duration on outcome of attempts to discontinue mechanical ventilation. Spanish Lung Failure Collaborative Group. Am J Respir Crit Care Med (1999) 2.22
The Levant versus the Horn of Africa: evidence for bidirectional corridors of human migrations. Am J Hum Genet (2004) 2.20
Microsatellite variation and the differentiation of modern humans. Hum Genet (1997) 2.19
Blind analysis of denaturing high-performance liquid chromatography as a tool for mutation detection. Genomics (1998) 2.19
Geographic patterns of mtDNA diversity in Europe. Am J Hum Genet (2000) 2.18
Population genetics of Y-chromosome short tandem repeats in humans. J Mol Evol (1997) 2.17
Cytoreductive surgery and hyperthermic intraperitoneal chemotherapy in the management of peritoneal surface malignancies of colonic origin: a consensus statement. Society of Surgical Oncology. Ann Surg Oncol (2006) 2.13
From Asia to Europe: mitochondrial DNA sequence variability in Bulgarians and Turks. Ann Hum Genet (1996) 2.06
Effects of cis arrangement of chromatin insulators on enhancer-blocking activity. Science (2001) 2.03
Chromosome Y microsatellites: population genetic and evolutionary aspects. Int J Legal Med (1997) 1.89
A simple procedure for the analysis of single nucleotide polymorphisms facilitates map-based cloning in Arabidopsis. Plant Physiol (2000) 1.89
Global analysis of ATM polymorphism reveals significant functional constraint. Am J Hum Genet (2001) 1.80
Sequence diversity of the control region of mitochondrial DNA in Tuscany and its implications for the peopling of Europe. Am J Phys Anthropol (1996) 1.79
Fluoride and casein phosphopeptide-amorphous calcium phosphate. J Dent Res (2008) 1.76
Geographic clustering of human Y-chromosome haplotypes. Ann Hum Genet (1996) 1.75
Time course of hemostatic abnormalities in sepsis and its relation to outcome. Chest (1993) 1.72
Potential transmission of human polyomaviruses through the gastrointestinal tract after exposure to virions or viral DNA. J Virol (2001) 1.69
Retention in plaque and remineralization of enamel lesions by various forms of calcium in a mouthrinse or sugar-free chewing gum. J Dent Res (2003) 1.69
Distribution of haplotypes from a chromosome 21 region distinguishes multiple prehistoric human migrations. Proc Natl Acad Sci U S A (1999) 1.68
Geographic variation in human mitochondrial DNA control region sequence: the population history of Turkey and its relationship to the European populations. Mol Biol Evol (1996) 1.68
Y-chromosome and mtDNA polymorphisms in Iraq, a crossroad of the early human dispersal and of post-Neolithic migrations. Mol Phylogenet Evol (2003) 1.62
Gene mapping in Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24. Nat Genet (1996) 1.61
Sex-specific migration patterns in Central Asian populations, revealed by analysis of Y-chromosome short tandem repeats and mtDNA. Am J Hum Genet (1999) 1.61
The common, Near-Eastern origin of Ashkenazi and Sephardi Jews supported by Y-chromosome similarity. Ann Hum Genet (1993) 1.59
Accuracy and clinical relevance of computed tomography scan interpretation of peritoneal cancer index in colorectal cancer peritoneal carcinomatosis: a multi-institutional study. J Surg Oncol (2010) 1.59
Human genetic affinities for Y-chromosome P49a,f/TaqI haplotypes show strong correspondence with linguistics. Am J Hum Genet (1997) 1.58
Independent histories of human Y chromosomes from Melanesia and Australia. Am J Hum Genet (2000) 1.58
Study of the mass and spin-parity of the Higgs boson candidate via its decays to Z boson pairs. Phys Rev Lett (2013) 1.56
Optimal temperature selection for mutation detection by denaturing HPLC and comparison to single-stranded conformation polymorphism and heteroduplex analysis. Clin Chem (1999) 1.53
Identification of a Drosophila brain-gut peptide related to the neuropeptide Y family. Peptides (1999) 1.52
Large cell neuroendocrine carcinoma of the gallbladder: report of two cases. Am J Surg Pathol (2000) 1.51
Genetic structure of north-west Africa revealed by STR analysis. Eur J Hum Genet (2000) 1.50
Intravenous iloprost infusion in patients with Raynaud phenomenon secondary to systemic sclerosis. A multicenter, placebo-controlled, double-blind study. Ann Intern Med (1994) 1.50
Mutation rates at Y chromosome specific microsatellites. Hum Mutat (2005) 1.48