Kenneth K Kidd

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Kenneth K



Publications in SciGraph latest 50 shown

  • 2018-05 Ancestry inference of 96 population samples using microhaplotypes in INTERNATIONAL JOURNAL OF LEGAL MEDICINE
  • 2017-07 Increasing the reference populations for the 55 AISNP panel: the need and benefits in INTERNATIONAL JOURNAL OF LEGAL MEDICINE
  • 2017-05 Genetics of the peloponnesean populations and the theory of extinction of the medieval peloponnesean Greeks in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2017-04 Confounding effects of microbiome on the susceptibility of TNFSF15 to Crohn’s disease in the Ryukyu Islands in HUMAN GENETICS
  • 2016-12 Proposed nomenclature for microhaplotypes in HUMAN GENOMICS
  • 2015-12 Criteria for selecting microhaplotypes: mixture detection and deconvolution in INVESTIGATIVE GENETICS
  • 2015-02 Inferring population structure and demographic history using Y-STR data from worldwide populations in MOLECULAR GENETICS AND GENOMICS
  • 2014-05 Application of six IrisPlex SNPs and comparison of two eye color prediction systems in diverse Eurasia populations in INTERNATIONAL JOURNAL OF LEGAL MEDICINE
  • 2014-04 Haplotype structure and positive selection at TLR1 in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2014-04 An historical perspective on “The world-wide distribution of allele frequencies at the human dopamine D4 receptor locus” in HUMAN GENETICS
  • 2013-12 Inference of human continental origin and admixture proportions using a highly discriminative ancestry informative 41-SNP panel in INVESTIGATIVE GENETICS
  • 2013-06 Genome-wide association study of Tourette's syndrome in MOLECULAR PSYCHIATRY
  • 2013-05 First all-in-one diagnostic tool for DNA intelligence: genome-wide inference of biogeographic ancestry, appearance, relatedness, and sex with the Identitas v1 Forensic Chip in INTERNATIONAL JOURNAL OF LEGAL MEDICINE
  • 2012-12 High diversity and no significant selection signal of human ADH1B gene in Tibet in INVESTIGATIVE GENETICS
  • 2012-12 Introducing the Forensic Research/Reference on Genetics knowledge base, FROG-kb in INVESTIGATIVE GENETICS
  • 2012-11 Mini-haplotypes as lineage informative SNPs and ancestry inference SNPs in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2012-09 Exome sequencing identifies recurrent somatic RAC1 mutations in melanoma in NATURE GENETICS
  • 2012-08 Reconstructing Native American population history in NATURE
  • 2012-08 Structural diversity and African origin of the 17q21.31 inversion polymorphism in NATURE GENETICS
  • 2012-05 A global view of the OCA2-HERC2 region and pigmentation in HUMAN GENETICS
  • 2012-03 High altitude adaptation in Daghestani populations from the Caucasus in HUMAN GENETICS
  • 2012 Duplicated Gene Evolution of the Primate Alcohol Dehydrogenase Family in POST-GENOME BIOLOGY OF PRIMATES
  • 2011-12 Analyses of a set of 128 ancestry informative single-nucleotide polymorphisms in a global set of 119 population samples in INVESTIGATIVE GENETICS
  • 2011-03 A Variant in a MicroRNA complementary site in the 3′ UTR of the KIT oncogene increases risk of acral melanoma in ONCOGENE
  • 2011-01 An Application of the Elastic Net for an Endophenotype Analysis in BEHAVIOR GENETICS
  • 2010-12 Vegetable Intake in College-Aged Adults Is Explained by Oral Sensory Phenotypes and TAS2R38 Genotype in CHEMOSENSORY PERCEPTION
  • 2010-05 Additional support for the association of SLITRK1 var321 and Tourette syndrome in MOLECULAR PSYCHIATRY
  • 2010-03 SNPs for a universal individual identification panel in HUMAN GENETICS
  • 2009-10-08 Genetic variation in IL28B and spontaneous clearance of hepatitis C virus in NATURE
  • 2009-08 Global variation in CYP2C8–CYP2C9 functional haplotypes in THE PHARMACOGENOMICS JOURNAL
  • 2007-09 Global diversity and evidence for coevolution of KIR and HLA in NATURE GENETICS
  • 2007-07 Significant variation in haplotype block structure but conservation in tagSNP patterns among global populations in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2007-05 Candidate SNPs for a universal individual identification panel in HUMAN GENETICS
  • 2007-03 Significant variation in haplotype block structure but conservation in tagSNP patterns among global populations in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2005-10 Use of autosomal loci for clustering individuals and populations of East Asian origin in HUMAN GENETICS
  • 2005-05 Linkage disequilibrium patterns vary substantially among populations in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2004-11 Implications of biogeography of human populations for 'race' and medicine in NATURE GENETICS
  • 2004-10 Positive selection in MAOA gene is human exclusive: determination of the putative amino acid change selected in the human lineage in HUMAN GENETICS
  • 2003-10 Global survey of haplotype frequencies and linkage disequilibrium at the RET locus in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2002-12 Population variation in linkage disequilibrium across the COMT gene considering promoter region and coding region variation in HUMAN GENETICS
  • 1998-09 A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus in HUMAN GENETICS
  • 1998-08 Genetic Structure of the Ancestral Population of Modern Humans in JOURNAL OF MOLECULAR EVOLUTION
  • 1998-05 Long CAG/CTG repeats in mice in MAMMALIAN GENOME
  • 1996-06 Distribution and frequency of a polymorphicAlu insertion at the plasminogen activator locus in humans in HUMAN GENETICS
  • 1996-02 Chromosomal localization of long trinucleotide repeats in the human genome by fluorescence in situ hybridization in NATURE GENETICS
  • 1995-06 Linkage mapping of serotonin transporter protein gene SLC6A4 on chromosome 17 in HUMAN GENETICS
  • 1993-01 A new polymorphic marker (D10S97) tightly linked to the multiple endocrine neoplasia type 2A (MEN2A) locus in HUMAN GENETICS
  • 1991-08 Status of the search for a major genetic locus for affective disorder in the Old Order Amish in HUMAN GENETICS
  • 1990-11 The Na+/H+ antiporter: a “melt” polymorphism allows regional mapping to the short arm of chromosome 1 in HUMAN GENETICS
  • 1990-02 Extensive sequence polymorphisms associated with chromosome 10 alpha satellite DNA and its close linkage to markers from the pericentromeric region in HUMAN GENETICS
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