Rapid screening of mtDNA coding region SNPs for the identification of west European Caucasian haplogroups

[1]  J. Haines,et al.  Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease. , 2003, American journal of human genetics.

[2]  W. Parson,et al.  Single nucleotide polymorphism genotyping by on-line liquid chromatography-mass spectrometry in forensic science of the Y-chromosomal locus M9. , 2002, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

[3]  A. González-Neira,et al.  Point mutations in the flanking regions of the Y-chromosome specific STRs DYS391, DYS437 and DYS438 , 2002, International Journal of Legal Medicine.

[4]  Ming-Tseh Lin,et al.  Simultaneous genotyping of single nucleotide polymorphisms in the IL-1 gene complex by multiplex polymerase chain reaction-restriction fragment length polymorphism. , 2002, Journal of immunological methods.

[5]  B. Malyarchuk,et al.  Mitochondrial DNA variability in Poles and Russians. , 2002, Annals of human genetics.

[6]  D. Turnbull,et al.  Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups. , 2002, American journal of human genetics.

[7]  Mostafa Ronaghi,et al.  Pyrosequencing™: An accurate detection platform for single nucleotide polymorphisms , 2002, Human mutation.

[8]  G. Kirov,et al.  Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools , 2002, Human Genetics.

[9]  N. Maca-Meyer,et al.  Major genomic mitochondrial lineages delineate early human expansions , 2001, BMC Genetics.

[10]  P. Laforêt,et al.  Functional characterization of novel mutations in the human cytochrome b gene , 2001, European Journal of Human Genetics.

[11]  M. Lehtonen,et al.  Phylogenetic network for European mtDNA. , 2001, American journal of human genetics.

[12]  T. Parsons,et al.  Increasing the forensic discrimination of mitochondrial DNA testing through analysis of the entire mitochondrial DNA genome. , 2001, Croatian medical journal.

[13]  M. N. Gabriel,et al.  Population variation of human mitochondrial DNA hypervariable regions I and II in 105 Croatian individuals demonstrated by immobilized sequence-specific oligonucleotide probe analysis. , 2001, Croatian medical journal.

[14]  M. Stoneking Single nucleotide polymorphisms: From the evolutionary past. . . , 2001, Nature.

[15]  S. Pääbo,et al.  Mitochondrial genome variation and the origin of modern humans , 2000, Nature.

[16]  A. Di Rienzo,et al.  Tracing European founder lineages in the Near Eastern mtDNA pool. , 2000, American journal of human genetics.

[17]  R. Villems,et al.  mtDNA haplogroups and frequency patterns in Europe. , 2000, American journal of human genetics.

[18]  D. Turnbull,et al.  Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA , 1999, Nature Genetics.

[19]  D. Wallace,et al.  Mitochondrial DNA variation in human evolution and disease. , 1999, Gene.

[20]  B. Sykes,et al.  Phylogeography of mitochondrial DNA in western Europe , 1998, Annals of human genetics.

[21]  J. SantaLucia,et al.  A unified view of polymer, dumbbell, and oligonucleotide DNA nearest-neighbor thermodynamics. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[22]  S. Pollak,et al.  A third hypervariable region in the human mitochondrial D-loop. , 1997, Human genetics.

[23]  W. Parson,et al.  Austrian Caucasian population data for the quadruplex plus amelogenin: refined mutation rate for HumvWFA31/A. , 1997, Journal of forensic sciences.

[24]  K. Gerbitz,et al.  Population genetics and disease susceptibility: characterization of central European haplogroups by mtDNA gene mutations, correlation with D loop variants and association with disease. , 1997, Human molecular genetics.

[25]  A. Torroni,et al.  Classification of European mtDNAs from an analysis of three European populations. , 1996, Genetics.

[26]  H. Bandelt,et al.  Paleolithic and neolithic lineages in the European mitochondrial gene pool. , 1996, American journal of human genetics.

[27]  M. Stoneking,et al.  Population variation of human mtDNA control region sequences detected by enzymatic amplification and sequence-specific oligonucleotide probes. , 1991, American journal of human genetics.

[28]  Peter Gill,et al.  An assessment of the utility of single nucleotide polymorphisms (SNPs) for forensic purposes , 2001, International Journal of Legal Medicine.

[29]  G. Tully,et al.  Validation of mitochondrial DNA minisequencing for forensic casework , 1999, International Journal of Legal Medicine.

[30]  Georg-August Spreadsheet Software for Thermodynamic Melting Point Prediction of Oligonucleotide Hybridization with and without Mismatches , 1999 .

[31]  S. Pollak,et al.  Location and frequency of polymorphic positions in the mtDNA control region of individuals from Germany , 1998, International Journal of Legal Medicine.