Evaluation of Y-chromosomal STRs: a multicenter study.

PubWeight™: 3.19‹?› | Rank: Top 1%

🔗 View Article (PMID 9228563)

Published in Int J Legal Med on January 01, 1997

Authors

M Kayser1, A Caglià, D Corach, N Fretwell, C Gehrig, G Graziosi, F Heidorn, S Herrmann, B Herzog, M Hidding, K Honda, M Jobling, M Krawczak, K Leim, S Meuser, E Meyer, W Oesterreich, A Pandya, W Parson, G Penacino, A Perez-Lezaun, A Piccinini, M Prinz, C Schmitt, L Roewer

Author Affiliations

1: Institut für Gerichtliche Medizin, Berlin, Germany.

Articles citing this

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-Chromosome evidence for a northward migration of modern humans into Eastern Asia during the last Ice Age. Am J Hum Genet (1999) 3.60

Characteristics and frequency of germline mutations at microsatellite loci from the human Y chromosome, as revealed by direct observation in father/son pairs. Am J Hum Genet (2000) 3.59

Excavating Y-chromosome haplotype strata in Anatolia. Hum Genet (2003) 3.15

The distribution of human genetic diversity: a comparison of mitochondrial, autosomal, and Y-chromosome data. Am J Hum Genet (2000) 2.91

Estimating Scandinavian and Gaelic ancestry in the male settlers of Iceland. Am J Hum Genet (2000) 2.22

The Levant versus the Horn of Africa: evidence for bidirectional corridors of human migrations. Am J Hum Genet (2004) 2.20

Y chromosomes traveling south: the cohen modal haplotype and the origins of the Lemba--the "Black Jews of Southern Africa". Am J Hum Genet (2000) 2.11

Genetic differentiation in South Amerindians is related to environmental and cultural diversity: evidence from the Y chromosome. Am J Hum Genet (2001) 2.00

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

Y chromosome haplotypes reveal prehistorical migrations to the Himalayas. Hum Genet (2000) 1.95

Strong Amerind/white sex bias and a possible Sephardic contribution among the founders of a population in northwest Colombia. Am J Hum Genet (2000) 1.94

Characterization of ancestral and derived Y-chromosome haplotypes of New World native populations. Am J Hum Genet (1998) 1.94

Use of X-linked markers for forensic purposes. Int J Legal Med (2003) 1.91

Mutability of Y-chromosomal microsatellites: rates, characteristics, molecular bases, and forensic implications. Am J Hum Genet (2010) 1.88

An extensive analysis of Y-chromosomal microsatellite haplotypes in globally dispersed human populations. Am J Hum Genet (2001) 1.70

Recent male-mediated gene flow over a linguistic barrier in Iberia, suggested by analysis of a Y-chromosomal DNA polymorphism. Am J Hum Genet (1999) 1.68

The dual origin and Siberian affinities of Native American Y chromosomes. Am J Hum Genet (2001) 1.65

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

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

Independent histories of human Y chromosomes from Melanesia and Australia. Am J Hum Genet (2000) 1.58

A short tandem repeat-based phylogeny for the human Y chromosome. Am J Hum Genet (2000) 1.58

Rare failures in the amelogenin sex test. Int J Legal Med (2002) 1.57

Signature of recent historical events in the European Y-chromosomal STR haplotype distribution. Hum Genet (2005) 1.54

Origins and divergence of the Roma (gypsies). Am J Hum Genet (2001) 1.53

Toward male individualization with rapidly mutating y-chromosomal short tandem repeats. Hum Mutat (2014) 1.53

Identification and characterisation of novel human Y-chromosomal microsatellites from sequence database information. Nucleic Acids Res (2000) 1.53

Investigating the effects of prehistoric migrations in Siberia: genetic variation and the origins of Yakuts. Hum Genet (2006) 1.51

Autosomal, mtDNA, and Y-chromosome diversity in Amerinds: pre- and post-Columbian patterns of gene flow in South America. Am J Hum Genet (2000) 1.45

Software for Y-haplogroup predictions: a word of caution. Int J Legal Med (2010) 1.45

A view of modern human origins from Y chromosome microsatellite variation. Genome Res (1999) 1.45

Variation in short tandem repeats is deeply structured by genetic background on the human Y chromosome. Am J Hum Genet (1999) 1.42

Paternal genetic affinity between Western Austronesians and Daic populations. BMC Evol Biol (2008) 1.33

Microsatellites provide evidence for Y chromosome diversity among the founders of the New World. Proc Natl Acad Sci U S A (1999) 1.33

Y chromosome STR haplotypes and the genetic structure of U.S. populations of African, European, and Hispanic ancestry. Genome Res (2003) 1.30

Y-chromosomal DNA haplogroups and their implications for the dual origins of the Koreans. Hum Genet (2003) 1.24

Genetic studies of human diversity in East Asia. Philos Trans R Soc Lond B Biol Sci (2007) 1.19

Improving global and regional resolution of male lineage differentiation by simple single-copy Y-chromosomal short tandem repeat polymorphisms. Forensic Sci Int Genet (2009) 1.13

A global analysis of Y-chromosomal haplotype diversity for 23 STR loci. Forensic Sci Int Genet (2014) 1.11

Deletions in the Y-derived amelogenin gene fragment in the Indian population. BMC Med Genet (2006) 1.07

Molecular genetic evidence for the human settlement of the Pacific: analysis of mitochondrial DNA, Y chromosome and HLA markers. Philos Trans R Soc Lond B Biol Sci (1999) 1.04

The first peopling of South America: new evidence from Y-chromosome haplogroup Q. PLoS One (2013) 1.03

Little genetic differentiation as assessed by uniparental markers in the presence of substantial language variation in peoples of the Cross River region of Nigeria. BMC Evol Biol (2010) 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

Distinguishing the co-ancestries of haplogroup G Y-chromosomes in the populations of Europe and the Caucasus. Eur J Hum Genet (2012) 1.03

Autosomal and uniparental portraits of the native populations of Sakha (Yakutia): implications for the peopling of Northeast Eurasia. BMC Evol Biol (2013) 1.02

Y-chromosomal STR haplotypes and their applications to forensic and population studies in east Asia. Int J Legal Med (2005) 1.02

Mutations in 14 Y-STR loci among Japanese father-son haplotypes. Int J Legal Med (2004) 1.01

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

Evidence from Y-chromosome analysis for a late exclusively eastern expansion of the Bantu-speaking people. Eur J Hum Genet (2012) 0.95

Y-STR typing of an Austrian population sample using a 17-loci multiplex PCR assay. Int J Legal Med (2005) 0.94

Haplotypes and mutation analysis of 22 Y-chromosomal STRs in Korean father-son pairs. Int J Legal Med (2006) 0.93

Disclosing the genetic structure of Brazil through analysis of male lineages with highly discriminating haplotypes. PLoS One (2012) 0.92

Validation of the X-chromosomal STR DXS6809. Int J Legal Med (2003) 0.91

Sex-Specific Genetic Data Support One of Two Alternative Versions of the Foundation of the Ruling Dynasty of the Nso' in Cameroon. Curr Anthropol (2008) 0.89

Separate analysis of DYS385a and b versus conventional DYS385 typing: is there forensic relevance? Int J Legal Med (2004) 0.88

Y-chromosomal STR haplotypes in a Northeast Italian population sample using 17plex loci PCR assay. Int J Legal Med (2005) 0.87

Localization and characterization of nucleotide sequences from the canine Y chromosome. Chromosome Res (1999) 0.86

An ultra-high discrimination Y chromosome short tandem repeat multiplex DNA typing system. PLoS One (2007) 0.85

Spanish population data and forensic usefulness of a novel Y-STR set (DYS437, DYS438, DYS439, DYS460, DYS461, GATA A10, GATA C4, GATA H4). Int J Legal Med (2003) 0.84

Y-STR analysis for detection and objective confirmation of child sexual abuse. Int J Legal Med (2004) 0.84

Y-chromosomal STR haplotypes in a Romanian population sample. Int J Legal Med (2003) 0.84

Y-chromosomal STR haplotypes in Chinese Uigur ethnic group. Int J Legal Med (2005) 0.83

Haplotype frequencies of 17 Y-chromosomal short tandem repeat loci from the Cukurova region of Turkey. Croat Med J (2011) 0.83

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

Population study and evaluation of 20 Y-chromosome STR loci in Germans. Int J Legal Med (2006) 0.81

The effect of number of loci on geographical structuring and forensic applicability of Y-STR data in Finland. Int J Legal Med (2008) 0.81

Duplication of DYS19 flanking regions in other parts of the Y chromosome. Int J Legal Med (2004) 0.80

Mutations or exclusion: an unusual case in paternity testing. Int J Legal Med (2005) 0.80

Seventeen Y-chromosomal short tandem repeat haplotypes in seven groups of population living in Taiwan. Int J Legal Med (2010) 0.80

X-chromosome STR sequence variation, repeat structure, and nomenclature in humans and chimpanzees. Int J Legal Med (2008) 0.79

Forensic use of Y-chromosome DNA: a general overview. Hum Genet (2017) 0.79

Paleo-Balkan and Slavic contributions to the genetic pool of Moldavians: insights from the Y chromosome. PLoS One (2013) 0.79

Differential DNA extraction of challenging simulated sexual-assault samples: a Swiss collaborative study. Investig Genet (2011) 0.79

Haplotypes of 20 Y-chromosomal STRs in a population sample from southeast China (Chaoshan area). Int J Legal Med (2007) 0.78

Significance of micro-geographical population structure in forensic cases: a bayesian exploration. Int J Legal Med (2003) 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

Y-short tandem repeat haplotype and paternal lineage of the Ezhava population of Kerala, south India. Croat Med J (2011) 0.77

Divergence of East Asians and Europeans estimated using male- and female-specific genetic markers. Genome Biol Evol (2014) 0.77

Evaluation of miniY-STR multiplex PCR systems for extended 16 Y-STR loci. Int J Legal Med (2007) 0.77

Y-STR DNA analysis of 154 female child sexual assault cases in the Philippines. Int J Legal Med (2010) 0.77

DIP-STR: highly sensitive markers for the analysis of unbalanced genomic mixtures. Hum Mutat (2013) 0.77

Y-chromosomal STR haplotypes in a population sample from southwest Germany (Freiburg area). Int J Legal Med (2003) 0.77

Y-STR analysis of degraded DNA using reduced-size amplicons. Int J Legal Med (2006) 0.76

Detection of Y STR markers of male fetal dna in maternal circulation. Indian J Hum Genet (2007) 0.75

Y-chromosome diversity suggests southern origin and Paleolithic backwave migration of Austro-Asiatic speakers from eastern Asia to the Indian subcontinent. Sci Rep (2015) 0.75

Y chromosomal STRs haplotypes in two populations from Bolivia. Leg Med (Tokyo) (2006) 0.75

Analysis of genetic admixture in Uyghur using the 26 Y-STR loci system. Sci Rep (2016) 0.75

Iranian Azeri's Y-Chromosomal Diversity in the Context of Turkish-Speaking Populations of the Middle East. Iran J Public Health (2011) 0.75

Evaluation of DXS9902, DXS7132, DXS6809, DXS7133, and DXS7423 in humans and chimpanzees: sequence variation, repeat structure, and nomenclature. Int J Legal Med (2009) 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

Articles by these authors

Electrochemical photolysis of water at a semiconductor electrode. Nature (1972) 19.56

Population growth of human Y chromosomes: a study of Y chromosome microsatellites. Mol Biol Evol (1999) 8.05

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

A randomized comparison of antiplatelet and anticoagulant therapy after the placement of coronary-artery stents. N Engl J Med (1996) 6.05

TAP, the human homolog of Mex67p, mediates CTE-dependent RNA export from the nucleus. Mol Cell (1998) 5.85

Improved thermodynamic parameters and helix initiation factor to predict stability of DNA duplexes. Nucleic Acids Res (1996) 5.16

Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language. Am J Hum Genet (2000) 4.72

Translating biomolecular recognition into nanomechanics. Science (2000) 4.43

Competency development in public health leadership. Am J Public Health (2000) 3.84

Characteristics and frequency of germline mutations at microsatellite loci from the human Y chromosome, as revealed by direct observation in father/son pairs. Am J Hum Genet (2000) 3.59

Genetic relationships of Asians and Northern Europeans, revealed by Y-chromosomal DNA analysis. Am J Hum Genet (1997) 3.54

Lateralization of phonetic and pitch discrimination in speech processing. Science (1992) 3.43

Targeting gene-modified hematopoietic cells to the central nervous system: use of green fluorescent protein uncovers microglial engraftment. Nat Med (2001) 3.32

Cytosine methylation and the fate of CpG dinucleotides in vertebrate genomes. Hum Genet (1989) 3.27

Control of Photosynthetic Sucrose Synthesis by Fructose 2,6-Bisphosphate : I. Coordination of CO(2) Fixation and Sucrose Synthesis. Plant Physiol (1984) 3.27

DNA commission of the International Society of Forensic Genetics: Recommendations on the interpretation of mixtures. Forensic Sci Int (2006) 3.20

Mind reading: neural mechanisms of theory of mind and self-perspective. Neuroimage (2001) 3.03

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21. Nat Genet (1998) 3.00

Neural mechanisms underlying melodic perception and memory for pitch. J Neurosci (1994) 2.86

TAP binds to the constitutive transport element (CTE) through a novel RNA-binding motif that is sufficient to promote CTE-dependent RNA export from the nucleus. EMBO J (1999) 2.83

Multiple representations of pain in human cerebral cortex. Science (1991) 2.74

The DExH/D box protein HEL/UAP56 is essential for mRNA nuclear export in Drosophila. Curr Biol (2001) 2.70

Functional activation of the human frontal cortex during the performance of verbal working memory tasks. Proc Natl Acad Sci U S A (1993) 2.63

The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictions. Hum Genet (1990) 2.59

Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness. J Med Genet (2003) 2.52

Barrett's esophagus: a new look at surveillance based on emerging estimates of cancer risk. Am J Gastroenterol (1999) 2.50

A prospective randomized comparison of endoscopic ultrasound- and computed tomography-guided celiac plexus block for managing chronic pancreatitis pain. Am J Gastroenterol (1999) 2.40

Dissociation of human mid-dorsolateral from posterior dorsolateral frontal cortex in memory processing. Proc Natl Acad Sci U S A (1993) 2.40

Role of the human anterior cingulate cortex in the control of oculomotor, manual, and speech responses: a positron emission tomography study. J Neurophysiol (1993) 2.37

Anatomical mapping of functional activation in stereotactic coordinate space. Neuroimage (1992) 2.37

Rescue of hybrid sterility in crosses between D. melanogaster and D. simulans. Nature (1996) 2.30

ECG changes in a 25-year-old woman with hypocalcemia due to hypoparathyroidism. Hypocalcemia mimicking acute myocardial infarction. Chest (2000) 2.28

Melanesian origin of Polynesian Y chromosomes. Curr Biol (2000) 2.27

The Y chromosome in forensic analysis and paternity testing. Int J Legal Med (1997) 2.27

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

Intra-atrial ECG is not a reliable method for positioning left internal jugular vein catheters. Br J Anaesth (2003) 2.21

A Y chromosome gene family with RNA-binding protein homology: candidates for the azoospermia factor AZF controlling human spermatogenesis. Cell (1993) 2.15

A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment. J Med Genet (2005) 2.11

Genetic variation among the Mapuche Indians from the Patagonian region of Argentina: mitochondrial DNA sequence variation and allele frequencies of several nuclear genes. EXS (1993) 2.09

Distributed processing of pain and vibration by the human brain. J Neurosci (1994) 2.08

Two genes that map to the STSL locus cause sitosterolemia: genomic structure and spectrum of mutations involving sterolin-1 and sterolin-2, encoded by ABCG5 and ABCG8, respectively. Am J Hum Genet (2001) 2.08

Maintenance of sinus rhythm after electrical cardioversion of persistent atrial fibrillation; sotalol vs bisoprolol. Eur Heart J (2001) 2.06

Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness. Nat Genet (2001) 2.06

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

Does Paramecium primaurelia use a different genetic code in its macronucleus? Nature (1985) 2.04

Adhesive retention dressings are more comfortable than alginate dressings on split-skin-graft donor sites. Br J Plast Surg (2003) 2.03

The central Siberian origin for native American Y chromosomes. Am J Hum Genet (1999) 2.03

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

Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity. Am J Hum Genet (1998) 1.98

Clinical implications of endoscopic ultrasound: the American Endosonography Club Study. Gastrointest Endosc (1996) 1.98

Long-term outcome of enzyme-replacement therapy in advanced Fabry disease: evidence for disease progression towards serious complications. J Intern Med (2013) 1.96

Sensitization for death receptor- or drug-induced apoptosis by re-expression of caspase-8 through demethylation or gene transfer. Oncogene (2001) 1.94

alpha 7 nicotinic receptor transduces signals to phosphatidylinositol 3-kinase to block A beta-amyloid-induced neurotoxicity. J Biol Chem (2001) 1.93

Chronic urticaria is not significantly associated with hepatitis C or hepatitis G infection: a case-control study. Arch Dermatol (1999) 1.93

High hepatitis C viraemia and impaired antibody response in patients coinfected with HIV. AIDS (1995) 1.93

IL-7 receptor alpha+ CD3(-) cells in the embryonic intestine induces the organizing center of Peyer's patches. Int Immunol (1999) 1.91

Use of X-linked markers for forensic purposes. Int J Legal Med (2003) 1.91

Epigenetic self-regulation of developmental excision of an internal eliminated sequence on Paramecium tetraurelia. Genes Dev (1995) 1.91

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

Nanometer resolution and coherent optical dipole coupling of two individual molecules. Science (2002) 1.89

Common variable immunodeficiency patient classification based on impaired B cell memory differentiation correlates with clinical aspects. J Clin Immunol (2003) 1.86

Recombinant maxi-K channels on transistor, a prototype of iono-electronic interfacing. Nat Biotechnol (2001) 1.86

Do current dual chamber cardioverter defibrillators have advantages over conventional single chamber cardioverter defibrillators in reducing inappropriate therapies? A randomized, prospective study. J Cardiovasc Electrophysiol (2001) 1.84

Analysis of molecular variance (AMOVA) of Y-chromosome-specific microsatellites in two closely related human populations. Hum Mol Genet (1996) 1.84

[4 years' experience with combined hormonal treatment of cryptorchism]. Z Kinderchir (1984) 1.83

Management of major biliary complications after laparoscopic cholecystectomy. Ann Surg (1993) 1.81

Functional localization and lateralization of human olfactory cortex. Nature (1992) 1.79

Human gene cloning: the storm before the lull? Nature (1986) 1.78