Kenneth K Kidd

Author PubWeight™ 164.40‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Genetic structure of human populations. Science 2002 30.91
2 A human genome diversity cell line panel. Science 2002 14.11
3 Exome sequencing identifies recurrent somatic RAC1 mutations in melanoma. Nat Genet 2012 7.00
4 A SNP in a let-7 microRNA complementary site in the KRAS 3' untranslated region increases non-small cell lung cancer risk. Cancer Res 2008 5.05
5 Hunter-gatherer genomic diversity suggests a southern African origin for modern humans. Proc Natl Acad Sci U S A 2011 3.53
6 Implications of biogeography of human populations for 'race' and medicine. Nat Genet 2004 3.34
7 The genetic structure of Pacific Islanders. PLoS Genet 2008 3.31
8 Intelligence, race, and genetics. Am Psychol 2005 2.76
9 ALFRED: An allele frequency database for anthropology. Am J Phys Anthropol 2002 2.67
10 A global perspective on genetic variation at the ADH genes reveals unusual patterns of linkage disequilibrium and diversity. Am J Hum Genet 2002 2.60
11 Evidence of positive selection acting at the human dopamine receptor D4 gene locus. Proc Natl Acad Sci U S A 2001 2.48
12 Global diversity and evidence for coevolution of KIR and HLA. Nat Genet 2007 2.40
13 Evolutionary dynamics of human Toll-like receptors and their different contributions to host defense. PLoS Genet 2009 2.35
14 Bitter receptor gene (TAS2R38), 6-n-propylthiouracil (PROP) bitterness and alcohol intake. Alcohol Clin Exp Res 2004 2.26
15 Low nucleotide diversity in chimpanzees and bonobos. Genetics 2003 2.16
16 Vibratory Urticaria Associated with a Missense Variant in ADGRE2. N Engl J Med 2016 2.09
17 Inferring the demographic history of African farmers and pygmy hunter-gatherers using a multilocus resequencing data set. PLoS Genet 2009 2.07
18 Effects of traditional and western environments on prevalence of type 2 diabetes in Pima Indians in Mexico and the U.S. Diabetes Care 2006 1.96
19 Maternal traces of deep common ancestry and asymmetric gene flow between Pygmy hunter-gatherers and Bantu-speaking farmers. Proc Natl Acad Sci U S A 2008 1.96
20 Linkage disequilibrium patterns vary substantially among populations. Eur J Hum Genet 2005 1.73
21 Multiple superoxide dismutase 1/splicing factor serine alanine 15 variants are associated with the development and progression of diabetic nephropathy: the Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Genetics study. Diabetes 2007 1.65
22 Rare BRCA1 haplotypes including 3'UTR SNPs associated with breast cancer risk. Cell Cycle 2011 1.64
23 Structural diversity and African origin of the 17q21.31 inversion polymorphism. Nat Genet 2012 1.62
24 Geographic and haplotype structure of candidate type 2 diabetes susceptibility variants at the calpain-10 locus. Am J Hum Genet 2002 1.61
25 Refined geographic distribution of the oriental ALDH2*504Lys (nee 487Lys) variant. Ann Hum Genet 2009 1.49
26 Genotyping and haplotyping of CYP2C19 functional alleles on thin-film biosensor chips. Pharmacogenet Genomics 2007 1.49
27 The evolution and population genetics of the ALDH2 locus: random genetic drift, selection, and low levels of recombination. Ann Hum Genet 2004 1.49
28 Evidence of positive selection on a class I ADH locus. Am J Hum Genet 2007 1.48
29 SNPs for a universal individual identification panel. Hum Genet 2010 1.42
30 Candidate SNPs for a universal individual identification panel. Hum Genet 2007 1.39
31 Geographically separate increases in the frequency of the derived ADH1B*47His allele in eastern and western Asia. Am J Hum Genet 2007 1.37
32 On the use of DNA pooling to estimate haplotype frequencies. Genet Epidemiol 2003 1.33
33 Vegetable Intake in College-Aged Adults Is Explained by Oral Sensory Phenotypes and TAS2R38 Genotype. Chemosens Percept 2010 1.32
34 The distribution and most recent common ancestor of the 17q21 inversion in humans. Am J Hum Genet 2010 1.31
35 Haplotype block structures show significant variation among populations. Genet Epidemiol 2004 1.28
36 Genetic differences in human circadian clock genes among worldwide populations. J Biol Rhythms 2008 1.27
37 Significant variation in haplotype block structure but conservation in tagSNP patterns among global populations. Eur J Hum Genet 2007 1.26
38 Analyses of a set of 128 ancestry informative single-nucleotide polymorphisms in a global set of 119 population samples. Investig Genet 2011 1.22
39 Obsessive-compulsive symptom dimensions in affected sibling pairs diagnosed with Gilles de la Tourette syndrome. Am J Med Genet B Neuropsychiatr Genet 2003 1.21
40 Intra- and interpopulation genotype reconstruction from tagging SNPs. Genome Res 2006 1.21
41 Signatures of purifying and local positive selection in human miRNAs. Am J Hum Genet 2009 1.18
42 Single-nucleotide polymorphism genotyping on optical thin-film biosensor chips. Proc Natl Acad Sci U S A 2003 1.16
43 Possible epistatic role of ADH7 in the protection against alcoholism. Am J Med Genet B Neuropsychiatr Genet 2004 1.13
44 Use of autosomal loci for clustering individuals and populations of East Asian origin. Hum Genet 2005 1.13
45 Genomewide scan of hoarding in sib pairs in which both sibs have Gilles de la Tourette syndrome. Am J Hum Genet 2002 1.13
46 ALFRED: an allele frequency resource for research and teaching. Nucleic Acids Res 2011 1.12
47 HAPLOT: a graphical comparison of haplotype blocks, tagSNP sets and SNP variation for multiple populations. Bioinformatics 2005 1.10
48 Evolutionary insights into the high worldwide prevalence of MBL2 deficiency alleles. Hum Mol Genet 2006 1.09
49 Global variation in CYP2C8-CYP2C9 functional haplotypes. Pharmacogenomics J 2009 1.09
50 Epidemiology. DNA identifications after the 9/11 World Trade Center attack. Science 2005 1.09
51 A global view of the OCA2-HERC2 region and pigmentation. Hum Genet 2011 1.08
52 Considerable haplotype diversity within the 23kb encompassing the ADH7 gene. Alcohol Clin Exp Res 2005 1.05
53 Inference of human continental origin and admixture proportions using a highly discriminative ancestry informative 41-SNP panel. Investig Genet 2013 1.04
54 Population variation in linkage disequilibrium across the COMT gene considering promoter region and coding region variation. Hum Genet 2002 1.01
55 Haplotype evolution of SLITRK1, a candidate gene for Gilles de la Tourette syndrome. Am J Med Genet B Neuropsychiatr Genet 2008 0.99
56 Genetic landscape of Eurasia and "admixture" in Uyghurs. Am J Hum Genet 2009 0.98
57 Positive selection in MAOA gene is human exclusive: determination of the putative amino acid change selected in the human lineage. Hum Genet 2004 0.98
58 Population-specific variation in haplotype composition and heterozygosity at the POLB locus. DNA Repair (Amst) 2009 0.98
59 Selection on the human bitter taste gene, TAS2R16, in Eurasian populations. Hum Biol 2011 0.96
60 Ethnic related selection for an ADH Class I variant within East Asia. PLoS One 2008 0.96
61 Worldwide population variation and haplotype analysis at the serotonin transporter gene SLC6A4 and implications for association studies. Biol Psychiatry 2013 0.95
62 A proline-threonine substitution in codon 351 of ADH1C is common in Native Americans. Alcohol Clin Exp Res 2002 0.94
63 ALFRED: an allele frequency database for microevolutionary studies. Evol Bioinform Online 2007 0.89
64 Diversification of the ADH1B gene during expansion of modern humans. Ann Hum Genet 2011 0.88
65 Nuclear integrations of mitochondrial DNA in gorillas. Am J Primatol 2004 0.87
66 Origin and dispersal of atypical aldehyde dehydrogenase ALDH2487Lys. Gene 2009 0.85
67 Mini-haplotypes as lineage informative SNPs and ancestry inference SNPs. Eur J Hum Genet 2012 0.84
68 Single nucleotide polymorphisms and haplotypes in Native American populations. Am J Phys Anthropol 2011 0.84
69 Introducing the Forensic Research/Reference on Genetics knowledge base, FROG-kb. Investig Genet 2012 0.83
70 Semantic Web-based integration of cancer pathways and allele frequency data. Cancer Inform 2009 0.82
71 Nonsynonymous SNPs: validation characteristics, derived allele frequency patterns, and suggestive evidence for natural selection. Hum Mutat 2006 0.82
72 Exploring genomic structure differences and similarities between the Greek and European HapMap populations: implications for association studies. Ann Hum Genet 2012 0.81
73 Read all about it: The Lancet's Paper of the Year, 2003. Lancet 2003 0.79
74 Conservative evolution in duplicated genes of the primate Class I ADH cluster. Gene 2006 0.78
75 Global survey of haplotype frequencies and linkage disequilibrium at the RET locus. Eur J Hum Genet 2003 0.78
76 A variant of the endothelial nitric oxide synthase gene (NOS3) associated with AMS susceptibility is less common in the Quechua, a high altitude Native population. High Alt Med Biol 2010 0.78
77 Application of six IrisPlex SNPs and comparison of two eye color prediction systems in diverse Eurasia populations. Int J Legal Med 2014 0.78
78 Crohn's disease risk alleles on the NOD2 locus have been maintained by natural selection on standing variation. Mol Biol Evol 2012 0.78
79 Using a pharmacokinetic model to relate an individual's susceptibility to alcohol dependence to genotypes. Hum Hered 2010 0.77
80 Selecting SNPs to identify ancestry. Ann Hum Genet 2011 0.76
81 An application of the elastic net for an endophenotype analysis. Behav Genet 2011 0.75
82 Inferring population structure and demographic history using Y-STR data from worldwide populations. Mol Genet Genomics 2014 0.75