
- Supplementary information for "Genetic structure of human populations" Sample, markers, and genotypes: The data set that we analyzed differs from the HGDP-CEPH Human
- 18 NOVEMBER 2005 VOL 310 SCIENCE www.sciencemag.org1122 efore the September 11, 2001, World
- Research article Report on ISFG SNP Panel Discussion
- Response to Comment on "Genetic Structure of Human
- RESEARCH ARTICLE Nuclear Integrations of Mitochondrial DNA in Gorillas
- Supplement Series Volume No. 21 and Metabolic Research
- Am. J. Hum. Genet. 64:11471157, 1999 Linkage Disequilibrium at the ADH2 and ADH3 Loci and Risk of
- The Molecular Origin and Consequences of Escape from miRNA Regulation by HLA-C Alleles
- DNA Sequence Polymorphism within Hominoid Species Exceeds the Number of Phylogenetically Informative
- DEVELOPMENTALDYNAMICS 2057341 (199s) Conserved Regulatory Element Involved in the Early Onset
- Additional Supporting Information for Ciarleglio et al.: "Genetic Differences in Human Circadian Clock Genes Among Worldwide Populations"
- Statistica Sinica 12(2002), 337-359 DETECTING GENETIC ASSOCIATION IN CASE-CONTROL
- Am. J. Hum. Genet. 47:946-951, 1990 The Mutation for Medullary Thyroid Carcinoma with
- 2001 The American Genetic Association 92:475480 Modern African Ape Populations as Genetic
- Bitter Receptor Gene (TAS2R38), 6-n-Propylthiouracil (PROP) Bitterness and Alcohol Intake
- HeinOnline ---33 Hous. L. Rev. 1431 (1996-1997) HeinOnline ---33 Hous. L. Rev. 1432 (1996-1997)
- Genealogy Reconstruction From Short Tandem Repeat Genotypes in an Amazonian Population
- Am. J. Hum. Genet. 46:950-955, 1990 Strong Linkage Disequilibrium Between the XY274
- A Variant of the Endothelial Nitric Oxide Synthase Gene (NOS3) Associated with AMS Susceptibility Is Less
- doi: 10.1111/j.1469-1809.2009.00517.x Refined Geographic Distribution of the Oriental
- MathematicsintheArchaeological andHistoricalSciences
- This article appeared in a journal published by Elsevier. The attached copy is furnished to the author for internal non-commercial research
- S E P T E M B E R 2 0 0 6 Lessons Learned From 9/11
- Latent Class Analysis of Gilles de la Tourette Syndrome Using Comorbidities: Clinical and Genetic Implications
- Considerable Haplotype Diversity within the 23kb Encompassing the ADH7 Gene
- Computer Notes 409 Made in United States of America
- Ann. Hum. Genet. (1999), 63, 167179 Printed in Great Britain
- GENOMICS 8,340-346 (1990) Genetic and Physical Mapping and Population Studies
- Evidence of positive selection acting at the human dopamine receptor D4 gene locus
- 204 BIOL PSYCHIATRY 1993;34:204-209
- Proc. Natl. Acad. Sci. USA Vol. 96, pp. 83158317, July 1999
- Intelligence, Race, and Genetics Robert J. Sternberg, Elena L. Grigorenko, and Kenneth K. Kidd
- Abstract A four-site haplotype system at the dopamine D2 receptor locus (DRD2) has been studied in a global sample
- www.ajhg.org The American Journal of Human Genetics Volume 80 February 2007 265 Genome Scan for Tourette Disorder in Affected-Sibling-Pair
- American Journal of Medical Genetics (Neuropsychiatric Genetics) 48:71-73 (1993) Associations of Disease With Genetic Markers
- The Journal of Pediatrics Gill et al. 459 Volume 129, Number 3
- 1993 3: 39-45Genome Res. S Zullo, J L Kennedy, J Gelernter, et al.
- Evolutionary insights into the high worldwide prevalence of MBL2 deficiency alleles
- Am. J. Hum. Genet. 71:8499, 2002 A Global Perspective on Genetic Variation at the ADH Genes Reveals
- Am. J. Hum. Genet. 65:14281436, 1999 A Complete Genome Screen in Sib Pairs Affected by Gilles
- Hum Genet (1995) 95:677-680 9 Springer-Verlag 1995 J. Gelernter 9A. J. Pakstis 9K. K. Kidd
- Abstract We have investigated the frequency distribution, across a broad range of geographically dispersed popula-
- Am. J. Hum. Genet. 66:18821899, 2000 Haplotypes and Linkage Disequilibrium at the Phenylalanine Hydroxylase
- Amos Deinard* & Kenneth Kidd
- GENOMICS 13, 601-606 (19%) Isolation and High-Resolution Mapping of New DNA Markers
- Vegetable Intake in College-Aged Adults Is Explained by Oral Sensory Phenotypes and TAS2R38 Genotype
- 1716 Nucleic Acids Research, Vol. 19, No. 7 An Mspl polymorphism for the
- A Proline-Threonine Substitution in Codon 351 of ADH1C Is Common in Native Americans
- Fax +41 61 306 12 34 E-Mail karger@karger.ch
- 2011LandesBioscience. Donotdistribute.
- Long CAG/CTG repeats in mice Bonnie L. King,1
- GENOMICS 6.89-93 (1990) The Locus for the Medium-Chain Acyl-CoA Dehydrogenase Gene
- Brief Communication 779 A HERV-K provirus in chimpanzees, bonobos and gorillas, but not
- Effects of Traditional and Western Environments on Prevalence of Type 2
- 4956 Nucleic Acids Research, Vol. 18, No. 16 Polymorphism at the
- Supplemental Material Table S1. Descriptions of the populations and samples; links to more detail in ALFRED.
- 32 M.I. SEAMAN ET AL.JOURNAL OF EXPERIMENTAL ZOOLOGY (MOL DEV EVOL) 288:3238 (2000) 2000 WILEY-LISS, INC.
- Significant variation in haplotype block structure but conservation in tagSNP patterns among global
- Genetic variation in IL28B and spontaneous clearance of hepatitis C virus
- Hunter-gatherer genomic diversity suggests a southern African origin for modern humans
- Am. J. Hum. Genet. 75:545560, 2004 Indications of Linkage and Association of Gilles de la Tourette Syndrome
- OENOMICS 14, 1055-1063 (1992) The CEPH Consortium Linkage Map of Human Chromosome 2
- A SNP in a let-7 microRNA Complementary Site in the KRAS 3 Untranslated Region Increases NonSmall Cell Lung Cancer Risk
- Letters to the Editor Am. J. Hum. Genet. 67:13521355, 2000
- Vol. 21 no. 20 2005, pages 39383939 doi:10.1093/bioinformatics/bti649BIOINFORMATICSAPPLICATIONS NOTE
- Original article 103 Genotyping and haplotyping of CYP2C19 functional alleles
- Anim. Blood Grps biochem. Genet. 11 (1980) 21-38 Immunogenetic and population genetic analyses of
- American Journal of Medical Genetics (Neuropsychiatric Genetics) 54:51-58 (1994) Progress in a Genome Scan for Linkage
- Letters to the Editor Am. J. Hum. Genet. 63:648651, 1998
- American Journal of Medical Genetics Part B (Neuropsychiatric Genetics) 147B:463466 (2008) Haplotype Evolution of SLITRK1, a Candidate Gene
- Haplotype Block Structures Show Significant Variation Among Populations
- Introductory Review Normal DNA sequence variations
- Vol. 10 no. 4 1994 Pages 443-450
- 17 A nuclear perspective on human K. K. KIDD AND J. R. KIDD
- DNA Repair 8 (2009) 579584 Contents lists available at ScienceDirect
- Global Variation in the Frequencies of Functionally Different Catechol-O-Methyltransferase Alleles
- GENOMICS 25,44-58 (19%) The CEPH Consortium Linkage Map of Human Chromosome 16
- Am. J. Hum. Genet. 67:901925, 2000 Short Tandem-Repeat Polymorphism/Alu Haplotype Variation at the PLAT
- www.ajhg.org The American Journal of Human Genetics Volume 80 March 2007 441 Evidence of Positive Selection on a Class I ADH Locus
- Nucleic Acids Research, Vol. 18, No. 16 4965 PCR detection of the Tth Hincil polymorphism at the
- 820 Human Molecular Genetics, 1993, Vol. 2, No. 6 Unusual length polymorphism in
- DNA Sequence The Journal of Sequencing and Mapping, Vol. 8(5), pp. 317-327 Reprints available directly from the publisher
- Am. J. Hum. Genet. 57:1445-1456, 1995 Evolution of Haplotypes at the DRD2 Locus
- Nucleic Acids Research, Vol. 19, No. 24 6877-6882 Genotyping and haplotyping of polymorphisms directly
- 1997 Oxford University Press 18551863Human Molecular Genetics, 1997, Vol. 6, No. 11 A novel, heritable, expanding CTG repeat in an intron
- ALFRED: the ALelle FREquency Database. Update H. Rajeevan, M. V. Osier, K.-H. Cheung1
- Molecular Probes and Medical Applications
- 1314 Nucleic Acids Research, Vol. 18, No. 5 Monomorphism in humans and sequence differences
- Am. J. Hum. Genet. 74:931944, 2004 The Genetic Architecture of Selection at the Human Dopamine Receptor
- 1316 Nucleic Acids Research, Vol. 18, No. 5 An EcoRI polymorphism
- PCR Methods and Applications 2:112-1161992 by Cold Spring Harbor Laboratory ISSN 1054-9803/92 $3.00 Modeling of Heteroduplex Formation
- Nucleic Acids Research, Vol. 19, No. 20 5801 A Hincil RFLP in the human D4
- LETTERS TO THE EDITOR Additional support for the association of SLITRK1 var321
- HUMAN MUTATION Mutation and Polymorphism Report #238 (2001) Online Mutation and Polymorphism Report
- Copyright 2003 by the Genetics Society of America Low Nucleotide Diversity in Chimpanzees and Bonobos
- Am. J. Hum. Genet. 63:847860, 1998 Network Analyses of Y-Chromosomal Types in Europe, Northern Africa,
- Am. J. Hum. Genet. 65:14491456, 1999 On a Randomization Procedure in Linkage Analysis
- Am. J. Hum. Genet. 68:103117, 2001 Worldwide Genetic Analysis of the CFTR Region
- 3:225-231 1994 by Cold Spring Harbor Laboratory Press ISSN 1054-9803/94 $5.00 PCR Methods and Applications 225 Detection of DNA Sequence Variation via
- ORIGINAL ARTICLE Global patterns of variation in allele and
- For personal use. Only reproduce with permission from The Lancet publishing Group. PAPER OF THE YEAR
- Brief Communication 1531 Insertional polymorphisms of full-length endogenous retroviruses
- Identifying Conservation Units Within Captive Chimpanzee Populations
- BioOne sees sustainable scholarly publishing as an inherently collaborative enterprise connecting authors, nonprofit publishers, academic institutions, research libraries, and research funders in the common goal of
- Tandem Duplication Polymorphism Upstream of the Dopamine D4 Receptor Gene (DRD4)
- 906 Letters to the Editor Luiselli D, Simoni L, Tarazona-Santos E, Pastor S, Pettener D
- GENETICS OF AFFECTIVE DISORDERS 1 WENNER GREN CENTER
- ORIGINAL RESEARCH ARTICLE COMT haplotypes suggest P2 promoter region relevance
- Maternal traces of deep common ancestry and asymmetric gene flow between Pygmy
- ALFRED: A WEB-ACCESSIBLE ALLELE FREQUENCY DATABASE KEI-HOI CHEUNG*, PERRY L. MILLER
- HUMAN GENOME VARIATION: HAPLOTYPES, LINKAGE DISEQUILIBRIUM, AND POPULATIONS
- Genetic Landscape of Eurasia and ``Admixture'' in Uyghurs
- www.sciencemag.org SCIENCE VOL 296 12 APRIL 2002 261 A Human Genome
- Am. J. Hum. Genet. 67:936946, 2000 Transmission/Disequilibrium Tests Using Multiple Tightly Linked Markers
- BRIEF RESEARCH COMMUNICATION Family-Based Genetic Association Study of DLGAP3 in
- ORIGINAL RESEARCH An Application of the Elastic Net for an Endophenotype Analysis
- American Journal of Primatology 27:93-105 (1992) Variability in Nuclear DNA Among Nonhuman Primates
- Am. J. Hum. Genet. 62:800809, 1998 OA1 Mutations and Deletions in X-Linked Ocular Albinism
- HUMAN MUTATION 27(2),173^186, 2006 RESEARCH ARTICLE
- 842 The American Journal of Human Genetics Volume 81 October 2007 www.ajhg.org Geographically Separate Increases in the Frequency
- Pathol Biol 2001 ; 49 : 402, 403 2001 ditions scientifiques et mdicales Elsevier SAS. Tous droits rservs
- Am J Psychiatry 1 50:3, March 1993 449 Exclusion of Close Linkage of Tourette's Syndrome
- Recombination Breakpoints in the Human -Globin Gene Cluster By Rachelle A. Smith, P. Joy Ho, John B. Clegg, Judith R. Kidd, and Swee Lay Thein
- Proceedings from The Fourth International Symposium on Human Identification
- GENOMICS 11,968-973 (19%) A Linkage Map Spanning the Locus for Diastrophic Dysplasia (DTD)
- Anim. Blood Grps biochem. Genet. 5 (1974): 2128 The use of genetic relationships among cattle breeds in the
- 1997 Oxford University Press 403408Human Molecular Genetics, 1997, Vol. 6, No. 3 Survey of maximum CTG/CAG repeat lengths in
- Single Nucleotide Polymorphisms and Haplotypes in Native American Populations
- The EMBO Journal Vol.16 No.3 pp.588598, 1997 Concerted evolution of the tandemly repeated genes
- Am. J. Hum. Genet. 70:896904, 2002 Genomewide Scan of Hoarding in Sib Pairs in Which Both Sibs Have
- Ann. Hum. Genet. (1999), 63, 153166 Printed in Great Britain
- of Schizophrenia New Approaches to
- Nucleic Acids Research, Vol. 20, No. 5 1171 Two RFLPs near HOX2@/NGFR at
- A P P L I C A T I O N N O T E ALFRED: An Allele Frequency Database for Microevolutionary
- lst. WORLD CONGRESS ON GENETICS APPLIED TO LIVESTOCK PRODUCTION ler. CONGRES MONDIAL DE GENETIOUE APPLIQUEE A LIELEVAGE
- Single-nucleotide polymorphism genotyping on optical thin-film biosensor chips
- An Allele Frequency Database for Anthropology Michael V. Osier,1
- News and Views Hominoid phylogeny: inferences from a sub-terminal minisatellite analyzed by repeat
- ALFRED: an allele frequency resource for research and teaching
- ORIGINAL INVESTIGATION SNPs for a universal individual identification panel
- A Variant in a MicroRNA Complementary Site in the 3UTR of the KIT Oncogene Increases Risk of Acral Melanoma
- Conservative evolution in duplicated genes of the primate Class I ADH cluster
- Am. J. Hum. Genet. 61:719733, 1997 Differential Structuring of Human Populations for Homologous X and
- The Distribution and Most Recent Common Ancestor of the 17q21 Inversion in Humans
- Hum Genet (1991) 87 :475-483 9 Springer-Verlag 1991
- Journal of the American Medical Informatics Association Volume 2 Number 6 Nov / Dec 1995 Internet-based Support for
- Abstract Catechol-O-methyl transferase (COMT) cat-alyzes the first step in one of the major pathways in the
- Origin and dispersal of atypical aldehyde dehydrogenase ALDH2487Lys Huai-Rong Luo a,1
- Progress in W. B. SAUNDERS COMPANY
- Am. J. Hum. Genet. 62:13891402, 1998 A Global Haplotype Analysis of the Myotonic Dystrophy Locus
- Cancer Informatics 2009:8 1930 19 METHODOLOGY SPECIAL ISSUE
- Letter to the Editor Detection of a Large CTG/CAG Trinucleotide
- The Genetic Structure of Pacific Islanders Jonathan S. Friedlaender1*
- Genome Scan for Linkage to Gilles de la Tourette Syndrome
- Many human endogenous retrovirus K (HERV-K) proviruses are unique to humans
- American Journal of Medical Genetics Part B (Neuropsychiatric Genetics) 116B:6068 (2003) Obsessive-Compulsive Symptom Dimensions in
- Nucleic Acids Research, Vol. 19, No. 8 1957 Sequence tagged site (STS) Taql RFLP at dopamine fi-
- EUROPEAN SOCIETY FOR ANIMAL BLOOD GROUP RESEARCH
- Population Studies of Polymorphisms of the Serotonin Transporter Protein Gene
- Copyright0 1992 by the Genetics Society of America Human Population Genetic StudiesUsing Hypervariable Loci.
- SHORT COMMUNICATION The D4 Dopamine Receptor (DRD4) Maps to Distal 11 p Close to HRAS
- HUMAN MUTATION Mutation in Brief #909 (2006) Online MUTATION IN BRIEF
- Multiple Superoxide Dismutase 1/Splicing Factor Serine Alanine 15 Variants Are Associated With the
- Linkage Analysis of Tourette Syndrome in a Large Utah Pedigree Stacey Knight1, Hilary Coon2, Michael Johnson2, Mark F Leppert3, Nicola J Camp1,,
- Evolutionary Dynamics of Human Toll-Like Receptors and Their Different Contributions to Host Defense
- Hum Genet (2007) 121:305317 DOI 10.1007/s00439-007-0342-2
- VOL 20, NO. 2, 1994 Linkage Study of a
- Tishkoff,S.A.,K.K.Kidd,and A.G.Clark,2000. Inferences of modern human origins from variation in CD4 haplotypes. Proceedings of the Trinational Workshop on Molecular Evolution (M.K.Uyenoyama and A.Von Haeseler,Eds.),
- DOI: 10.1212/01.wnl.0000271078.51280.17 2008;70;666-676; originally published online Aug 8, 2007;Neurology
- Signatures of Purifying and Local Positive Selection in Human miRNAs
- GENOMICS26, 207-209 (1995) Assignment of the 5HT7 Receptor Gene (HTR7) to Chromosome 10q
- GENOMICS 13,607-612 (19%) A High-Resolution Meiotic Mapping Panel for the Pericentromeric
- Hum Genet (2004) 115: 377386 DOI 10.1007/s00439-004-1179-6
- Am. J. Hum. Genet. 48:281-294, 1991 Progress in the Search for Genetic Linkage with Tourette
- Genetic Polymorphisms in the Renin-Angiotensin System in High-Altitude and Low-Altitude Native
- 1995 Oxford University Press Human Molecular Genetics, 1995, Vol. 4, No. 7 1137-1146 Evidence for inter-generational instability
- SHORT COMMUNICATION Assignment of the Norepinephrine Transporter Protein (NET1) Locus
- Letters to the Editor 1247 proaches for studying complex genetic traits: practical con-
- J. Med Genet 1997;34:391-394 391 Homozygosity by descent for a rare mutation in the
- 170 A. DEINARD ET AL.JOURNAL OF EXPERIMENTAL ZOOLOGY (MOL DEV EVOL) 285:170176 (1999) 1999 WILEY-LISS, INC.
- Comment on "Genetic Structure of Human Populations"
- Update to Chapter 77: Hyperphenylalaninemia: Phenylalanine Hydroxylase Deficiency The Population Genetics of PAH
- October 1991 Issue 7 PCR: The First Few Cycles
- ORIGINAL PAPER Short tandem repeat polymorphism evolution in
- Anim. Blood Grps biochem. Genet. 2 (1971) 145158 Present address: Genetics Department, Stanford University Medical Center, Stanford,
- Ethnic Related Selection for an ADH Class I Variant within , Sheng Gu1
- 0145-600819912304-0592$03.0010 ALCOHOLISM:CLINICALAND EXPERIMENTALRESEARCH
- 80 EvolutionaryAnthropology Human Genome Diversity Project
- PRIORITY COMMUNICATIONS Global Variation of a 40-bp VNTR in the
- ORIGINAL ARTICLE Global variation in CYP2C8CYP2C9 functional
- ORIGINAL ARTICLE The complex global pattern of genetic variation and
- Am. J. Hum. Genet. 59:644-652, 1996 Linkage Disequilibrium between an Allele at the Dopamine D4
- CUTANEOUS BIOLOGY DOI 10.1111/j.1365-2133.2005.06464.x PTCH codon 1315 polymorphism and risk for nonmelanoma
- AMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY 90:477-486 (1993) Nuclear DNA Polymorphisms in a Wild Population of Yellow
- On the Use of DNA Pooling to Estimate Haplotype Frequencies Shuang Wang,1
- GENOMICS 6,3%!-412 (1990) The CEPH' Consortium Primary Linkage Map
- ORIGINAL INVESTIGATION Jong-Jin Kim Paul Verdu Andrew J. Pakstis
- moneys spent on luxuries, or lost in affluent wastage. The monetary gains from basic scientific research may be invisi-
- Hum Genet (1990)86:79-83 9 Springer-Verlag1990
- Am. J. Hum. Genet. 67:518522, 2000 The Accuracy of Statistical Methods for Estimation of Haplotype
- Molecular Ecology (2001) 10, 22412247 2001 Blackwell Science Ltd
- 0021-972X/92/7402-0368$03.00/0 Journal of Clinical Endocrinology and Metabolism
- SPECIAL FEATURE-__---------~____ MEETING REPORT Genetic Mappint;
- American Journal of Medical Genetics (Neuropsychiatric Genetics) 74:9194 (1997) 1997 Wiley-Liss, Inc.
- Global survey of haplotype frequencies and linkage disequilibrium at the RET locus
- doi: 10.1111/j.1469-1809.2011.00651.x Diversification of the ADH1B Gene during Expansion
- Nucleic Acids Research, Vol. 18, No. 18 5577 Pvull polymorphism at the COL1A2 A HaeliI polymorphism at the
- 1993 Oxford University Press Human Molecular Genetics, 1993, Vol. 2, No. 6 767-773 A hypervariable segment in the human dopamine receptor
- Original Paper Hum Hered 1999;49:1520
- Research article SNPs for individual identification
- Intra-and interpopulation genotype reconstruction from tagging SNPs
- Original Paper Hum Hered 2001;51:8596
- 1. Li, H., Mukherjee, N., Soundararajan, U., Tarnok, Z., Barta, C., Khaliq, S., Mohyuddin, A., Kajuna, S.L.B., Mehdi, S.Q., et al.
- Am. J. Hum. Genet. 46:624-630, 1990 The Genetic Defect in Multiple Endocrine Neoplasia Type 2A
- Genetic Epidemiology 14:809!814 (1997) Detection of Major Genes Underlying
- RESEARCH Open Access Analyses of a set of 128 ancestry informative
- HLA and Disease Jean Dausset
- COMPUTERS AND BIOMEDICAL RESEARCH 29, 327337 (1996) ARTICLE NO. 0024
- Understanding Human DNA Sequence Variation
- http://jbr.sagepub.com Journal of Biological Rhythms
- Developing a SNP panel for forensic identification of individuals
- 1996 Oxford University Press 48414843Nucleic Acids Research, 1996, Vol. 24, No. 23 Molecular haplotyping of genetic markers 10 kb apart
- American Journal of Medical Genetics Part B (Neuropsychiatric Genetics) 126B:1922 (2004) Brief Research Communication
- Abstract The dopamine D4 receptor gene (DRD4) has an expressed polymorphism in the third exon that may
- DOI: 10.1212/01.wnl.0000296833.25484.bb 2008;70;1495-1496Neurology
- Population Genetics of a Functional Variant of the Dopamine -Hydroxylase Gene (DBH)
- Reprinted from EVOLUTION, Vol. 28, No. 3, October 22, 1974 pp. 38l395
- American Journal of Medical Genetics (Neuropsychiatric Genetics) 48:218-222 (1993) Alleles at the Dopamine D, Receptor Locus
- GENOMICS8,461-468 (1990) A Refined Linkage Map for DNA Markers around the
- Global diversity and evidence for coevolution of KIR and HLA
- Linkage disequilibrium patterns vary substantially among populations