Kenneth Kidd | Academic Influence

Kenneth Kidd's AcademicInfluence.com Rankings

Kenneth Kidd

Computer Science

#3417

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#3585

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Computational Linguistics

#216

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#220

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Machine Learning

#472

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#478

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Artificial Intelligence

#684

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#695

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computer-science Degrees

Kenneth Kidd

Engineering

#2638

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#3597

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Electrical Engineering

#496

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#550

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engineering Degrees

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Computer Science
Engineering

Kenneth Kidd's Degrees

PhD Computer Science Stanford University
Masters Electrical Engineering University of California, Berkeley

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Why Is Kenneth Kidd Influential?

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According to Wikipedia, Kenneth Kay Kidd is an American human geneticist and emeritus professor of genetics at Yale University School of Medicine. He is known for his work on the role of genetics in disorders such as manic depression and schizophrenia, on human genetic variation and its relationship to geography, and the Out of Africa theory of human evolution. He also helped discover the DRD4-7R gene that has been linked to exploratory behaviour.

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Kenneth Kidd's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Genetic Structure of Human Populations (2002) (2661)
Genetic variation in IL28B and spontaneous clearance of hepatitis C virus (2009) (2197)
Exome sequencing identifies recurrent somatic RAC1 mutations in melanoma (2012) (1047)
A Human Genome Diversity Cell Line Panel (2002) (987)
Bipolar affective disorders linked to DNA markers on chromosome 11 (1987) (771)
Reconstructing Native American Population History (2012) (688)
A SNP in a let-7 microRNA complementary site in the KRAS 3' untranslated region increases non-small cell lung cancer risk. (2008) (666)
Global Patterns of Linkage Disequilibrium at the CD4 Locus and Modern Human Origins (1996) (579)
A hypervariable segment in the human dopamine receptor D4 (DRD4) gene. (1993) (575)
Evidence of positive selection acting at the human dopamine receptor D4 gene locus (2001) (489)
Implications of biogeography of human populations for 'race' and medicine (2004) (445)
The world-wide distribution of allele frequencies at the human dopamine D4 receptor locus (1996) (441)
Psychiatric disorders in the relatives of probands with affective disorders. The Yale University--National Institute of Mental Health Collaborative Study. (1984) (431)
Re-evaluation of the linkage relationship between chromosome 11p loci and the gene for bipolar affective disorder in the Old Order Amish (1989) (415)
Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage (1987) (413)
The genetic architecture of selection at the human dopamine receptor D4 (DRD4) gene locus. (2004) (396)
Hunter-gatherer genomic diversity suggests a southern African origin for modern humans (2011) (393)
An international two–stage genome–wide search for schizophrenia susceptibility genes (1995) (382)
Effects of Traditional and Western Environments on Prevalence of Type 2 Diabetes in Pima Indians in Mexico and the U.S. A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances. (2006) (377)
Global variation in the frequencies of functionally different catechol-O-methyltransferase alleles (1999) (376)
Evolutionary Dynamics of Human Toll-Like Receptors and Their Different Contributions to Host Defense (2009) (370)
Drift, admixture, and selection in human evolution: a study with DNA polymorphisms. (1991) (370)
Insertional polymorphisms of full-length endogenous retroviruses in humans (2001) (353)
Evidence against linkage of schizophrenia to markers on chromosome 5 in a northern Swedish pedigree (1988) (348)
HAPLO: a program using the EM algorithm to estimate the frequencies of multi-site haplotypes. (1995) (347)
Bitter receptor gene (TAS2R38), 6-n-propylthiouracil (PROP) bitterness and alcohol intake. (2004) (342)
Onset of major depression in early adulthood. Increased familial loading and specificity. (1984) (330)
A twin study of Tourette syndrome. (1985) (325)
Report of the Committee on Methods of Linkage Analysis and Reporting. (1985) (314)
The Genetic Structure of Pacific Islanders (2008) (302)
Sequence variability and candidate gene analysis in complex disease: association of mu opioid receptor gene variation with substance dependence. (2000) (294)
No association between an allele at the D2 dopamine receptor gene (DRD2) and alcoholism. (1991) (285)
An evaluation of the family history method for ascertaining psychiatric disorders. (1982) (284)
Psychopathology in the children (ages 6-18) of depressed and normal parents. (1984) (278)
Population studies of polymorphisms of the serotonin transporter protein gene. (1999) (271)
A global perspective on genetic variation at the ADH genes reveals unusual patterns of linkage disequilibrium and diversity. (2002) (244)
Many human endogenous retrovirus K (HERV-K) proviruses are unique to humans (1999) (243)
Global diversity and evidence for coevolution of KIR and HLA (2007) (233)
Linkage disequilibrium at the ADH2 and ADH3 loci and risk of alcoholism. (1999) (230)
Refined Geographic Distribution of the Oriental ALDH2*504Lys (nee 487Lys) Variant (2009) (222)
Phylogenetic analysis: concepts and methods. (1971) (216)
Developing a SNP panel for forensic identification of individuals. (2006) (215)
The utility of DNA typing in forensic work. (1991) (211)
Progress toward an efficient panel of SNPs for ancestry inference. (2014) (211)
A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus (1998) (201)
Variability in rates of affective disorders in relatives of depressed and normal probands. (1982) (199)
Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms. (1989) (198)
Eighth International Workshop on Human Gene Mapping (1984) (195)
Maternal traces of deep common ancestry and asymmetric gene flow between Pygmy hunter–gatherers and Bantu-speaking farmers (2008) (194)
Global variation of a 40-bp VNTR in the 3′-untranslated region of the dopamine transporter gene (SLC6A3) (1999) (193)
Intelligence, race, and genetics. (2005) (191)
SNPs for a universal individual identification panel (2010) (187)
Genomewide scan of hoarding in sib pairs in which both sibs have Gilles de la Tourette syndrome. (2002) (183)
Minisatellite diversity supports a recent African origin for modern humans (1996) (182)
Inferring the Demographic History of African Farmers and Pygmy Hunter–Gatherers Using a Multilocus Resequencing Data Set (2009) (179)
A global haplotype analysis of the myotonic dystrophy locus: implications for the evolution of modern humans and for the origin of myotonic dystrophy mutations. (1998) (173)
Analyses of a set of 128 ancestry informative single-nucleotide polymorphisms in a global set of 119 population samples (2011) (172)
Vegetable Intake in College-Aged Adults Is Explained by Oral Sensory Phenotypes and TAS2R38 Genotype (2010) (172)
Family-genetic studies of psychiatric disorders. Developing technologies. (1986) (170)
The human "interferon-beta 2/hepatocyte stimulating factor/interleukin-6" gene: DNA polymorphism studies and localization to chromosome 7p21. (1988) (168)
The epidemiology of Tourette's syndrome: a pilot study. (1982) (168)
Transmission/disequilibrium tests using multiple tightly linked markers. (2000) (168)
Associations of disease with genetic markers: déjà vu all over again. (1993) (163)
Low nucleotide diversity in chimpanzees and bonobos. (2003) (160)
Gilles de la Tourette's syndrome and attention deficit disorder with hyperactivity. Evidence against a genetic relationship. (1986) (158)
Understanding the clinical heterogeneity of major depression using family data. (1986) (155)
Migraine and depression: association and familial transmission. (1988) (151)
Obsessive‐compulsive symptom dimensions in affected sibling pairs diagnosed with Gilles de la Tourette syndrome (2003) (150)
Comparison of the family history method to direct interview. Factors affecting the diagnosis of depression. (1982) (144)
Haplotypes and linkage disequilibrium at the phenylalanine hydroxylase locus, PAH, in a global representation of populations. (2000) (144)
The evolution and population genetics of the ALDH2 locus: random genetic drift, selection, and low levels of recombination (2004) (144)
Children and depression--the children of depressed parents; the childhood of depressed patients; depression in children. (1980) (140)
Familial pattern and transmission of Gilles de la Tourette syndrome and multiple tics. (1981) (138)
The accuracy of statistical methods for estimation of haplotype frequencies: an example from the CD4 locus. (2000) (135)
DNA Identifications After the 9/11 World Trade Center Attack (2005) (133)
The D4 dopamine receptor (DRD4) maps to distal 11p close to HRAS. (1992) (131)
Current sequencing technology makes microhaplotypes a powerful new type of genetic marker for forensics. (2014) (131)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (1991) (129)
Molecular haplotyping of genetic markers 10 kb apart by allele-specific long-range PCR. (1996) (128)
Structural Diversity and African Origin of the 17q21.31 Inversion Polymorphism (2012) (124)
No linkage between D2 dopamine receptor gene region and schizophrenia. (1991) (123)
Geographic and haplotype structure of candidate type 2 diabetes susceptibility variants at the calpain-10 locus. (2002) (122)
Haplotype of multiple polymorphisms resolved by enzymatic amplification of single DNA molecules. (1990) (122)
Vibratory Urticaria Associated with a Missense Variant in ADGRE2. (2016) (121)
Evolutionary insights into the high worldwide prevalence of MBL2 deficiency alleles. (2006) (121)
Population frequencies of the A1 allele at the dopamine D2 receptor locus (1993) (121)
Subtypes of depression. Family study perspective. (1984) (120)
Linkage disequilibrium patterns vary substantially among populations (2005) (120)
Report of the committee on human gene mapping by recombinant DNA techniques. (1987) (120)
A global view of the OCA2-HERC2 region and pigmentation (2011) (119)
Genome scan for Tourette disorder in affected-sibling-pair and multigenerational families. (2007) (119)
Linkage disequilibrium between an allele at the dopamine D4 receptor locus and Tourette syndrome, by the transmission-disequilibrium test. (1996) (118)
Population genetics of a functional variant of the dopamine beta-hydroxylase gene (DBH). (1997) (116)
Familial pattern of Gilles de la Tourette syndrome. (1980) (114)
Genetic Differences in Human Circadian Clock Genes among Worldwide Populations (2008) (109)
Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population. (1995) (108)
A form of the metabolic syndrome associated with mutations in DYRK1B. (2014) (105)
A novel, heritable, expanding CTG repeat in an intron of the SEF2-1 gene on chromosome 18q21.1. (1997) (105)
Studies of three Amerindian populations using nuclear DNA polymorphisms. (1991) (105)
Segregation and linkage analyses of Tourette's syndrome and related disorders. (1990) (105)
Tandem duplication polymorphism upstream of the dopamine D4 receptor gene (DRD4). (1999) (104)
Multiple Superoxide Dismutase 1/Splicing Factor Serine Alanine 15 Variants Are Associated With the Development and Progression of Diabetic Nephropathy (2008) (103)
Exome sequencing identifies recurrent somatic RAC 1 mutations in melanoma (2016) (103)
Genome-wide association study of Tourette Syndrome (2012) (102)
Genetic Structure of the Ancestral Population of Modern Humans (1998) (101)
Candidate SNPs for a universal individual identification panel (2007) (101)
Inference of human continental origin and admixture proportions using a highly discriminative ancestry informative 41-SNP panel (2013) (100)
Mitochondrial DNA variation and biogeography of eastern gorillas (2001) (97)
Evaluating 130 microhaplotypes across a global set of 83 populations. (2017) (97)
Genome scan for linkage to Gilles de la Tourette syndrome. (1994) (95)
ALFRED: the ALelle FREquency Database. Update (2003) (95)
Criteria for selecting microhaplotypes: mixture detection and deconvolution (2015) (94)
Short tandem-repeat polymorphism/alu haplotype variation at the PLAT locus: implications for modern human origins. (2000) (92)
ALFRED: an allele frequency resource for research and teaching (2011) (92)
ALFRED: an allele frequency database for diverse populations and DNA polymorphisms (2000) (91)
Biphasic amplification of very dilute DNA samples via 'booster' PCR. (1989) (90)
The human gene mapping workshops in transition. (1989) (90)
Estimating the genetic contribution to schizophrenia. (1976) (89)
Early presentation of metastatic medullary carcinoma in multiple endocrine neoplasia, type IIA: implications for therapy. (1996) (89)
Microhaplotypes in forensic genetics. (2019) (89)
Geographically separate increases in the frequency of the derived ADH1B*47His allele in eastern and western Asia. (2007) (89)
Nuclear DNA diversity in worldwide distributed human populations. (1997) (88)
Understanding human DNA sequence variation. (2004) (87)
An analysis of the genetics of schizophrenia. (1973) (87)
Coupled amplification and sequencing of genomic DNA. (1991) (86)
Population variation in linkage disequilibrium across the COMT gene considering promoter region and coding region variation (2002) (85)
Report of the committee on human gene mapping by recombinant DNA techniques. (1988) (84)
Gilles de la Tourette's syndrome (1986) (83)
Evidence of positive selection on a class I ADH locus. (2007) (82)
No association between alcoholism and multiple polymorphisms at the dopamine D2 receptor gene (DRD2) in three distinct taiwanese populations (1996) (82)
Concerted evolution of the tandemly repeated genes encoding human U2 snRNA (the RNU2 locus) involves rapid intrachromosomal homogenization and rare interchromosomal gene conversion (1997) (82)
Signatures of purifying and local positive selection in human miRNAs. (2009) (81)
Comparisons of two methods for haplotype reconstruction and haplotype frequency estimation from population data. (2001) (78)
Assignment of the norepinephrine transporter protein (NET1) locus to chromosome 16. (1993) (78)
Linkage mapping of serotonin transporter protein gene SLC6A4 on chromosome 17 (1995) (77)
COMT haplotypes suggest P2 promoter region relevance for schizophrenia (2004) (77)
Vertical transmission of susceptibility to stuttering with sex-modified expression. (1981) (76)
Genetic hypotheses for Tourette syndrome. (1982) (76)
Single-nucleotide polymorphism genotyping on optical thin-film biosensor chips (2003) (76)
Sub‐Saharan African coding sequence variation and haplotype diversity at the NAT2 gene (2006) (74)
Microhaplotype loci are a powerful new type of forensic marker (2013) (74)
Mapping the human genome: current status. (1990) (73)
Outcomes on lithium treatment as a tool for genetic studies in affective disorders. (1984) (72)
Early onset (under age 30 years) and panic disorder as markers for etiologic homogeneity in major depression. (1987) (71)
Network analyses of Y-chromosomal types in Europe, northern Africa, and western Asia reveal specific patterns of geographic distribution. (1998) (71)
Gilles de la Tourette syndrome is not linked to D2-dopamine receptor. (1990) (71)
Hand usage in a colony of bonnett monkeys,Macaca radiata (1981) (69)
Genetic analyses of pyloric stenosis suggesting a specific maternal effect. (1976) (69)
Differential structuring of human populations for homologous X and Y microsatellite loci. (1997) (68)
Worldwide genetic analysis of the CFTR region. (2001) (68)
Modeling of heteroduplex formation during PCR from mixtures of DNA templates. (1992) (68)
DRD2 haplotypes containing the TaqI A1 allele: implications for alcoholism research. (1996) (68)
Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility region. (2004) (67)
Estimating age-of-onset distributions for disorders with variable onset. (1980) (66)
Severity of Tourette's syndrome in one large kindred. Implication for determination of disease prevalence rate. (1987) (66)
Evolution of a HOXB6 intergenic region within the great apes and humans. (1999) (65)
OA1 mutations and deletions in X-linked ocular albinism. (1998) (64)
Alleles at the dopamine D4 receptor locus do not contribute to the genetic susceptibility to schizophrenia in a large Swedish kindred. (1993) (63)
ALFRED: An allele frequency database for anthropology. (2002) (63)
The distribution and most recent common ancestor of the 17q21 inversion in humans. (2010) (63)
Origin and dispersal of atypical aldehyde dehydrogenase ALDH2487Lys. (2009) (63)
The genetics of a wild population of rhesus monkeys (Macaca mulatta). I. Genetic variability within and between social groups (1984) (63)
Maritime route of colonization of Europe (2014) (62)
Genetic models of stuttering (1980) (62)
Biological divergences in south-central Bougainville: an analysis of blood polymorphism gene frequencies and anthropometric measurements utilizing tree models, and a comparison of these variables with linguistic, geographic, and migrational "distances". (1971) (61)
The risk of Tourette's syndrome and chronic multiple tics among relatives of Tourette's syndrome patients obtained by direct interview. (1984) (60)
Assignment of the 5HT7 receptor gene (HTR7) to chromosome 10q and exclusion of genetic linkage with Tourette syndrome. (1995) (60)
Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13. (1987) (59)
The possible causes of the sex ratio in stuttering and its implications (1978) (59)
Worldwide Population Variation and Haplotype Analysis at the Serotonin Transporter Gene SLC6A4 and Implications for Association Studies (2013) (59)
Direct haplotyping of chromosomal segments from multiple heterozygotes via allele-specific PCR amplification. (1989) (58)
Amish study, IV: Genetic linkage study of pedigrees of bipolar probands. (1984) (58)
The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase (2010) (56)
Study of 47 DNA markers in five populations from four continents. (1987) (55)
Additional support for the association of SLITRK1 var321 and Tourette syndrome (2010) (55)
Immunogenetic and population genetic analyses of Iberian cattle. (2009) (55)
The genetic consequences of social group fission in a wild population of rhesus monkeys (Macaca mulatta) (1983) (54)
A Genetic Perspective on Stuttering (1977) (54)
Genetic landscape of Eurasia and "admixture" in Uyghurs. (2009) (53)
Tenth International Workshop on Human Gene Mapping (1988) (53)
Global variation in CYP2C8–CYP2C9 functional haplotypes (2009) (52)
A panel of 74 AISNPs: Improved ancestry inference within Eastern Asia. (2016) (52)
Intra- and interpopulation genotype reconstruction from tagging SNPs. (2006) (52)
The dopamine D4 receptor gene (DRD4) is not associated with alcoholism in three Taiwanese populations: Six polymorphisms tested separately and as haplotypes (1997) (51)
On the use of DNA pooling to estimate haplotype frequencies (2003) (51)
Rearrangement of the retinoic acid receptor gene in acute promyelocytic leukemia. (1991) (50)
Haplotype block structures show significant variation among populations (2004) (50)
Nuclear DNA polymorphisms in a wild population of yellow baboons (Papio hamadryas cynocephalus) from Mikumi National Park, Tanzania. (1993) (48)
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 (2012) (48)
Introducing the Forensic Research/Reference on Genetics knowledge base, FROG-kb (2012) (47)
Tourette syndrome and neuropsychiatric disorders: is there a genetic relationship? (1988) (47)
Ethnic Related Selection for an ADH Class I Variant within East Asia (2008) (47)
No association between DRD2 locus and alcoholism after controlling the ADH and ALDH genotypes in Chinese Han population. (1999) (47)
Modern African ape populations as genetic and demographic models of the last common ancestor of humans, chimpanzees, and gorillas. (2001) (47)
Research designs for the study of gene-environment interactions in psychiatric disorders. Report of a Foundations Fund for Research in Psychiatry Panel. (1978) (47)
HLA and disease susceptibility: a primer. (1977) (47)
Proposed model ethical protocol for collecting DNA samples. (1997) (47)
The molecular origin and consequences of escape from miRNA regulation by HLA-C alleles. (2011) (46)
Ancestry inference of 96 population samples using microhaplotypes (2017) (45)
Positive selection in MAOA gene is human exclusive: determination of the putative amino acid change selected in the human lineage (2004) (45)
Use of autosomal loci for clustering individuals and populations of East Asian origin (2005) (44)
Multiple threshold models for the affective disorders: the Yale-NIMH collaborative family study. (1985) (44)
D2 dopamine receptor alleles do not influence severity of Tourette's syndrome. Results from four large kindreds. (1994) (44)
Minimal SNP overlap among multiple panels of ancestry informative markers argues for more international collaboration. (2016) (43)
Mixture deconvolution by massively parallel sequencing of microhaplotypes (2019) (43)
Some environmental factors and hypotheses for stuttering in families with several stutterers. (1984) (43)
Extensive sequence variation in the 3′ untranslated region of the KRAS gene in lung and ovarian cancer cases (2014) (43)
The detection of major loci by segregation and linkage analysis: A simulation study (1984) (42)
A proline-threonine substitution in codon 351 of ADH1C is common in Native Americans. (2002) (42)
Expanding data and resources for forensic use of SNPs in individual identification. (2012) (42)
Identifying conservation units within captive chimpanzee populations. (2000) (42)
Possible epistatic role of ADH7 in the protection against alcoholism (2004) (41)
DNA markers and genetic variation in the human species. (1986) (41)
A Variant in a MicroRNA Complementary Site in the 3′UTR of the KIT Oncogene Increases Risk of Acral Melanoma (2010) (41)
A Primate Genome Project Deserves High Priority (2000) (41)
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 1 of 14) (1990) (41)
ALFRED: an allele frequency database for diverse populations and DNA polymorphisms - an update (2001) (40)
Segregation analyses of stuttering (1984) (40)
The effects of requisite assumptions on linkage analyses of manic-depressive illness with HLA. (1982) (40)
Significant variation in haplotype block structure but conservation in tagSNP patterns among global populations (2007) (40)
Mini-haplotypes as lineage informative SNPs and ancestry inference SNPs (2012) (40)
A HERV-K provirus in chimpanzees, bonobos and gorillas, but not humans (2001) (39)
MAPlex - A massively parallel sequencing ancestry analysis multiplex for Asia-Pacific populations. (2019) (39)
Proposed nomenclature for microhaplotypes (2016) (39)
DNA sequence polymorphism within hominoid species exceeds the number of phylogenetically informative characters for a HOX2 locus. (1992) (39)
The effects of variable age-of-onset and diagnostic criteria on the estimates of linkage: an example using manic-depressive illness and color blindness. (1980) (39)
Recovery and persistence of stuttering among relatives of stutterers. (1983) (38)
The CEPH consortium linkage map of human chromosome 16. (1994) (38)
Identification of a recent recombination event within the human beta-globin gene cluster. (1984) (38)
52 additional reference population samples for the 55 AISNP panel. (2015) (38)
Application of six IrisPlex SNPs and comparison of two eye color prediction systems in diverse Eurasia populations (2014) (37)
Linkage relationships of human arginine vasopressin-neurophysin-II and oxytocin-neurophysin-I to prodynorphin and other loci on chromosome 20. (1990) (37)
Increasing the reference populations for the 55 AISNP panel: the need and benefits (2017) (36)
Analyses of cross species polymerase chain reaction products to infer the ancestral state of human polymorphisms. (1998) (36)
Report on ISFG SNP Panel Discussion (2008) (36)
Human population genetic studies using hypervariable loci. I. Analysis of Assamese, Australian, Cambodian, Caucasian, Chinese and Melanesian populations. (1992) (36)
Chromosomal localization of long trinucleotide repeats in the human genome by fluorescence in situ hybridization (1996) (35)
Haplotype Evolution and Linkage Disequilibrium: A Simulation Study (2000) (35)
Nuclear integrations of mitochondrial DNA in gorillas (2004) (34)
Exclusion of linkage between the serotonin2 receptor and schizophrenia in a large Swedish kindred. (1992) (34)
Genetic variation in Tunisia in the context of human diversity worldwide (2016) (32)
A sequence-based 74plex microhaplotype assay for analysis of forensic DNA mixtures. (2020) (32)
Improving ancestry distinctions among Southwest Asian populations. (2018) (32)
Y‐chromosome specific YCAII, DYS19 and YAP polymorphisms in human populations: a comparative study (1999) (32)
High altitude adaptation in Daghestani populations from the Caucasus (2011) (31)
Rare BRCA1 haplotypes including 3’UTR SNPs associated with breast cancer risk (2011) (31)
Study of an additional 58 DNA markers in five human populations from four continents. (1991) (31)
Editorial: Can we find genes for schizophrenia? (1997) (31)
Genetic and evolutionary relationships among Asian Macaques (1985) (31)
Selecting microhaplotypes optimized for different purposes (2018) (30)
A Comparison of Methods for Reconstructing Evolutionary Trees (1981) (30)
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. (2010) (30)
The dopamine transporter protein gene (SLC6A3): primary linkage mapping and linkage studies in Tourette syndrome. (1995) (30)
Diversification of the ADH1B Gene during Expansion of Modern Humans (2011) (29)
Inferring population structure and demographic history using Y-STR data from worldwide populations (2015) (29)
HAPLOT: a graphical comparison of haplotype blocks, tagSNP sets and SNP variation for multiple populations (2005) (29)
Familial patterns and possible modes of inheritance of primary affective disorders. (1981) (29)
Survey of maximum CTG/CAG repeat lengths in humans and non-human primates: total genome scan in populations using the Repeat Expansion Detection method. (1997) (28)
Conserved regulatory element involved in the early onset of Hoxb6 gene expression (1996) (27)
Gorilla Biology: Mitochondrial and nuclear DNA estimates of divergence between western and eastern gorillas (2002) (27)
Evaluating a subset of ancestry informative SNPs for discriminating among Southwest Asian and circum-Mediterranean populations. (2016) (26)
Rapid molecular haplotyping of the first exon of the human dopamine D4 receptor gene by heteroduplex analysis. (1997) (26)
Glucocorticoid receptor maps to the distal long arm of chromosome 5. (1988) (26)
Parallelizing genetic linkage analysis: a case study for applying parallel computation in molecular biology. (1990) (25)
Linkage study of a susceptibility locus for schizophrenia in the pseudoautosomal region. (1994) (25)
Strong linkage disequilibrium between the XY274 polymorphism and the pseudoautosomal boundary. (1990) (25)
The use of genetic relationships among cattle breeds in the formulation of rational breeding policies: an example with South Devon (South Africa) and Gelbvieh (Germany). (2009) (24)
ALFRED: An Allele Frequency Database for Microevolutionary Studies (2005) (24)
Validation of novel forensic DNA markers using multiplex microhaplotype sequencing (2020) (24)
Response to Comment on "Genetic Structure of Human Populations" (2003) (24)
Considerable haplotype diversity within the 23kb encompassing the ADH7 gene. (2005) (24)
Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2A. (1985) (24)
Global patterns of variation in allele and haplotype frequencies and linkage disequilibrium across the CYP2E1 gene (2008) (24)
ALFRED: a Web-accessible allele frequency database. (1999) (23)
Abstracts of workshop presentations (Part 13 of 13) (1985) (23)
Single nucleotide polymorphisms and haplotypes in Native American populations. (2011) (23)
Haplotype structure and positive selection at TLR1 (2013) (23)
Localization and linkage of three polymorphic DNA sequences on human chromosome 20. (1987) (23)
A linkage group of five DNA markers on human chromosome 10. (1988) (23)
Genetic relationships of European, Mediterranean, and SW Asian populations using a panel of 55 AISNPs (2019) (22)
Amish study, V: Lithium-sodium countertransport and catechol O-methyltransferase in pedigrees of bipolar probands. (1984) (22)
NONRANDOM DISTRIBUTION OF LETHALS INDUCED BY TRITIATED THYMIDINE IN DROSOPHILA MELANOGASTER. (1964) (22)
Crohn's disease risk alleles on the NOD2 locus have been maintained by natural selection on standing variation. (2012) (22)
Evolution of exon 1 of the dopamine D4 receptor (DRD4) gene in primates. (2000) (21)
Abstracts for the committee on the genetic constitution of chromosome 1 (1991) (21)
DNA polymorphisms for the nerve growth factor receptor gene exclude its role in familial dysautonomia. (1986) (21)
Population-specific variation in haplotype composition and heterozygosity at the POLB locus. (2009) (21)
The redesigned Forensic Research/Reference on Genetics-knowledge base, FROG-kb. (2018) (21)
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms. (1990) (21)
Molecular biology and human diversity: A nuclear perspective on human evolution (1996) (21)
Dermo-distortive urticaria: an autosomal dominant dermatologic disorder. (1981) (20)
Familial stuttering patterns are not related to one measure of severity. (1980) (20)
Human genome diversity initiative. (1993) (20)
Genetics of propionic acidemia in a Mennonite-Amish kindred. (1980) (20)
Microhaplotypes for ancestry prediction (2017) (20)
Abstracts of workshop presentations (Part 2 of 16) (1987) (20)
On the possible magnitudes of selective forces maintaining schizophrenia in the population. (1975) (19)
Motoneuron-specific NR3B gene (2008) (19)
Increased frequency of heterozygotes for α1 antitrypsin variants in individuals with either sex chromosome mosaicism or trisomy 21 (1976) (19)
Haplotype evolution of SLITRK1, a candidate gene for Gilles de la Tourette Syndrome (2008) (19)
The human genome map 1990. (1990) (19)
Genotyping and haplotyping of CYP2C19 functional alleles on thin-film biosensor chips (2007) (19)
Abstracts of workshop presentations (Part 6 of 16) (1987) (19)
Population genetics of a disease (1987) (19)
Selection on the Human Bitter Taste Gene, TAS2R16, in Eurasian Populations (2011) (18)
A linkage map spanning the locus for diastrophic dysplasia (DTD). (1991) (18)
Tyrosine hydroxylase maps to the short arm of chromosome 11 proximal to the insulin and HRAS1 loci. (1988) (18)
Global survey of haplotype frequencies and linkage disequilibrium at the RET locus (2003) (17)
Some effects of selection strategies on linkage analysis (1988) (17)
Genotyping and haplotyping of polymorphisms directly from genomic DNA via coupled amplification and sequencing (CAS). (1991) (17)
Major depression and panic disorder: a family study perspective. (1985) (17)
Selecting SNPs to Identify Ancestry (2011) (17)
The locus for the medium-chain acyl-CoA dehydrogenase gene on chromosome 1 is highly polymorphic. (1990) (17)
Linkage analysis of multiple endocrine neoplasia type 2A (MEN-2A) and three DNA markers on chromosome 20: evidence against synteny. (1987) (17)
Nucleotide polymorphism, effective population size, and dispersal distances in the yellow baboons (Papio hamadryas cynocephalus) of Mikumi National Park, Tanzania (1996) (17)
Multiplexed SNP detection panels for human identification (2009) (17)
Detection of a large CTG/CAG trinucleotide repeat expansion in a Danish schizophrenia kindred. (1997) (17)
Application of Technology: Internet-based Support for Bioscience Research: A Collaborative Genome center for Human Chromosome 12 (1995) (17)
Genetics of a wild population of rhesus monkeys (Macaca mulatta): II. The Dunga Gali population in species-wide perspective. (1986) (17)
Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 782–806 (1989) (16)
Conservative evolution in duplicated genes of the primate Class I ADH cluster. (2007) (16)
Detection of DNA sequence variation via deliberate heteroduplex formation from genomic DNAs amplified en masse in "population tubes". (1994) (16)
Population relationships based on 170 ancestry SNPs from the combined Kidd and Seldin panels (2019) (16)
Presymptomatic testing using DNA markers for individuals at risk for familial multiple endocrine neoplasia 2A. (1992) (16)
PhenoDB: an integrated client/server database for linkage and population genetics. (1996) (16)
Linkage analyses of multiple endocrine neoplasia, type 2A (MEN-2A) with 20 DNA polymorphisms: 5% of the genome excluded. (1986) (16)
Can we find genes for schizophrenia? (1997) (16)
Centennial of Wilhelm Waldeyer’s introduction of the term “chromosome” (1988) (16)
Why We Do Not Yet Understand the Genetics of Affective Disorders (1978) (16)
Family-Genetic Studies and Identification of Valid Diagnostic Categories in Adult and Child Psychiatry (1987) (16)
On a randomization procedure in linkage analysis. (1999) (16)
Physical and genetic maps for chromosome 10. (1993) (15)
RECOMBINANT DNA METHODS IN GENETIC STUDIES OF AFFECTIVE DISORDERS (1984) (15)
Genetic markers for massively parallel sequencing in forensics (2015) (15)
Recurrence risks in schizophrenia: Are they model dependent? (1979) (15)
Confounding effects of microbiome on the susceptibility of TNFSF15 to Crohn’s disease in the Ryukyu Islands (2017) (15)
The mutation for medullary thyroid carcinoma with parathyroid tumors (MTC with PTs) is closely linked to the centromeric region of chromosome 10. (1990) (15)
Apparent monomorphism of ALDH2 in seven American Indian populations. (1995) (15)
Handedness and stuttering: A dead horse? (1977) (15)
Recombinant DNA approach to neurogenetic disorders (1982) (15)
A high-resolution meiotic mapping panel for the pericentromeric region of chromosome 10. (1992) (14)
A paradigm for finding genes for a complex human trait: polycystic ovary syndrome and follistatin. (1999) (14)
GENETIC LINKAGE MARKERS IN THE STUDY OF PSYCHIATRIC DISORDERS (1982) (14)
Molecular genetic studies in schizophrenia. (1989) (14)
Mongolians in the Genetic Landscape of Central Asia: Exploring the Genetic Relations among Mongolians and Other World Populations (2015) (14)
Isolation and high-resolution mapping of new DNA markers from the pericentromeric region of chromosome 10. (1992) (14)
Human genome diversity project (2005) (14)
Can recovery from stuttering be considered a genetically milder subtype of stuttering? (1983) (14)
Genetic Linkage and Hemochromatosis (1979) (14)
Population genetic data of 74 microhaplotypes in four major U.S. population groups. (2020) (14)
Report of the chromosome 5 workshop. (1991) (14)
A HincII RFLP in the human D4 dopamine receptor locus (DRD4). (1991) (14)
Close linkage of MT2P1 with GC on chromosome 4. (1986) (14)
Testing of Evolutionary Independence in Simulated Phylogenetic Trees (1978) (13)
An historical perspective on “The world-wide distribution of allele frequencies at the human dopamine D4 receptor locus” (2014) (13)
Allele Frequencies in a Worldwide Survey of a CA Repeat in the First Intron of the CFTR Gene (1999) (13)
Genetics of the peloponnesean populations and the theory of extinction of the medieval peloponnesean Greeks (2017) (13)
Abstracts of workshop presentations (Part 1 of 13) (1985) (13)
Error in The Reconstruction of Evolutionary Trees (1974) (13)
Human genetic variation of medical significance (2007) (12)
Language onset and concomitant speech and language problems in subgroups of stutterers and their siblings. (1982) (12)
Searching for a major genetic locus for affective disorder in the Old Order Amish. (1987) (12)
Correction: The Genetic Structure of Pacific Islanders (2008) (12)
A dinucleotide repeat polymorphism at the HOX2B locus. (1992) (12)
An efficient strategy for gene mapping using multipoint linkage analysis: exclusion of the multiple endocrine neoplasia 2A (MEN2A) locus from chromosome 13. (1987) (12)
Sequence tagged site (STS) TaqI RFLP at dopamine beta-hydroxylase (DBH). (1991) (12)
Semantic Web-Based Integration of Cancer Pathways and Allele Frequency Data (2009) (12)
Computer-assisted restriction mapping: an integrated approach to handling experimental uncertainty (1994) (12)
Linkage analyses of multiple endocrine neoplasia, type 2 (MEN-2) with 23 classical genetic polymorphisms. (1986) (11)
The ornithine aminotransferase (OAT) locus is linked and distal to D10S20 on the long arm of chromosome 10. (1988) (11)
Molecular genetics of an autosomal dominant form of torsion dystonia. (1988) (11)
Analysis of the sibship patterns of stutterers. (1981) (11)
Eliminating mitochondrial DNA competition for nuclear DNA primers. (1993) (11)
Report of the Committee on the Genetic Constitution of Chromosomes 3 and 4. (1985) (10)
Nonsynonymous SNPs: validation characteristics, derived allele frequency patterns, and suggestive evidence for natural selection (2006) (10)
Abstracts of workshop presentations (Part 9 of 13) (1985) (10)
Abstracts of meeting presentations (Part 11 of 11) (1984) (10)
Abstracts of workshop presentations (Part 12 of 16) (1987) (10)
The population genetics characteristics of a 90 locus panel of microhaplotypes (2021) (10)
First human gene mapping interim meeting – New Haven, 1988 (1988) (10)
Evolution of a D2 dopamine receptor intron within the great apes and humans. (1998) (10)
DETECTING GENETIC ASSOCIATION IN CASE-CONTROL STUDIES USING SIMILARITY-BASED ASSOCIATION TESTS (2002) (10)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 27 of 27) (1991) (9)
MSP RFLP for X-linked proteolipid protein gene (PLP) identified with either rat or human PLP cDNA clone. (1987) (9)
Trials and tribulations in the search for genes causing neuropsychiatric disorders. (1991) (9)
Detection of major genes underlying several quantitative traits associated with a common disease using different ascertainment schemes (1997) (9)
Abstracts of workshop presentations (Part 12 of 13) (1985) (9)
Alternative genetic models for the analysis of complex traits. (1980) (9)
A polymorphic DNA marker on chromosome 10 linked to RBP3 on the MEN2A side. (1988) (9)
Regular ArticleThe CEPH Consortium Linkage Map of Human Chromosome 11 (1995) (9)
Abstracts for the committee on comparative gene mapping (1991) (9)
Genetics for the Human Race (2004) (9)
Abstracts of workshop presentations (Part 15 of 16) (1987) (8)
Genetic strategies for the analysis of childhood behavioral traits. (1982) (8)
Recent Selection on a Class I ADH Locus Distinguishes Southwest Asian Populations Including Ashkenazi Jews (2018) (8)
Significant variation in haplotype block structure but conservation in tagSNP patterns among global populations (2007) (8)
TaqI RFLP at norepinephrine transporter protein (NET) locus. (1993) (8)
Localization of the gene for MEN 2A. (1992) (8)
SNPs for individual identification (2008) (8)
A multipurpose panel of microhaplotypes for use with STR markers in casework. (2022) (8)
The distinctive geographic patterns of common pigmentation variants at the OCA2 gene (2020) (8)
Identifying conservation units within captive chimpanzee populationsA previous version of this paper was awarded the 1995 Sherwood Washburn Prize for a studen-presented paper to A.S.D. (2000) (8)
Searching for major genes for psychiatric disorders. (1987) (8)
Review article: HCV ? STAT-C era of therapy (2010) (8)
Monomorphism in humans and sequence differences among higher primates for a sequence tagged site (STS) in homeo box cluster 2 as assayed by denaturing gradient electrophoresis. (1990) (8)
Evidence of HLA linkage in depressive disorders. (1981) (7)
The anonymous RFLP locus D11S16 is tightly linked to catalase on 11p. (1987) (7)
Exploring Genomic Structure Differences and Similarities between the Greek and European HapMap Populations: Implications for Association Studies (2012) (7)
A frequent polymorphism for the cytosolic thymidine kinase gene, TK1, (17q21-q22) detected by the enzyme TaqI. (1986) (7)
Genetic relationships of Austrian cattle breeds (2009) (7)
GENETIC RELATIONSHIPS AMONG CATTLE BREEDS (1972) (7)
The value of dual mating data in estimating genetic parameters (1978) (7)
The anonymous RFLP locus D1S2 is close to PGM1 on chromosome 1. (1988) (7)
Using a Pharmacokinetic Model to Relate an Individual’s Susceptibility to Alcohol Dependence to Genotypes (2010) (7)
Selective Pressure has not Acted Against Hypercoagulability Alleles in High‐Altitude Amerindians (2003) (7)
Genetic relationships of Southwest Asian and Mediterranean populations. (2021) (7)
Abstracts of workshop presentations (Part 10 of 16) (1987) (7)
Linkage data excluding a locus for multiple endocrine neoplasia type 2 syndromes from the distal part of the short arm of chromosome 11. (1984) (7)
FrogAncestryCalc: A standalone batch likelihood computation tool for ancestry inference panels catalogued in FROG-kb. (2020) (6)
Genetic structure of the HL-A system in a Nahua Indian population in Mexico. (2008) (6)
Usefulness of COMT gene polymorphisms in North African populations. (2019) (6)
Abstracts of workshop presentations pp. 1040-1056 (1989) (6)
Abstracts of workshop presentations pp. 1040-1056 (1989) (6)
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 6 of 14) (1990) (6)
Abstracts of meeting presentations (Part 2 of 11) (1982) (6)
A moderately frequent RFLP identified by both SacI and BanII with a probe from the HOX2 locus in man (17q11-17q22). (1987) (6)
Extensive sequence polymorphisms associated with chromosome 10 alpha satellite DNA and its close linkage to markers from the pericentromeric region (1990) (6)
Where is the locus for multiple endocrine neoplasia type 2A? (1987) (6)
Homozygosity by descent for a rare mutation in the myophosphorylase gene is associated with variable phenotypes in a Druze family with McArdle disease. (1997) (6)
A PvuII RFLP for the human liver arginase (ARG1) gene. (1986) (6)
An historical perspective on “The world-wide distribution of allele frequencies at the human dopamine D4 receptor locus” (2013) (6)
Progress toward resolving the possible linkage of multiple endocrine neoplasia type 2A to haptoglobin and group‐specific loci: Use of restriction fragment length polymorphisms extends exclusion region (1986) (6)
Progress towards completing the human linkage map. (1991) (6)
THE ROLE OF GENETIC DRIFT IN THE DIFFERENTIATION (2016) (6)
State of the Art for Microhaplotypes (2022) (6)
Phenylketonuria. Population genetics of a disease. (1987) (6)
Genomic and yeast artificial chromosome long-range physical maps linking six loci in 10q11.2 and spanning the multiple endocrine neoplasia type 2A (MEN2A) region. (1993) (6)
Biochemical polymorphisms, breed relationships, and germ plasm resources in domestic cattle. (1974) (6)
Abstracts of workshop presentations pp. 1023-1039 (1989) (5)
Two RFLPs near HOX2@/NGFR at locus D17S444E. (1992) (5)
The Genetics of Sex and Its Consequences (1979) (5)
Abstracts of meeting presentations (Part 8 of 11) (1984) (5)
The current status of linkage studies in schizophrenia. (1991) (5)
An anonymous single copy X-chromosome clone, DXS79, from Xq26-Xq28, identifies a moderately frequent RFLP [HGM8 provisional no. DXS79]. (1985) (5)
Abstracts of meeting presentations (Part 10 of 11) (1984) (5)
Genetic Data and the African Origin of Humans (1996) (5)
Abstracts for the committee on the genetic constitution of chromosome 17 (1991) (5)
Probable linkage between the human galactose-1-P uridyl transferase locus and 9qh. (1980) (5)
An Application of the Elastic Net for an Endophenotype Analysis (2011) (5)
Abstracts of workshop presentations pp. 1023-1039 (1989) (5)
An EcoRI polymorphism identified by KW6 (D10S97) on chromosome 10. (1990) (5)
Linkage Analysis in Psychiatry (1989) (5)
Linkage map of eight human chromosome 11q markers, including DRD2, spanning 60 cM. (1992) (5)
Estimation of segregation and linkage parameters in simulated data. I. Segregation analyses with different ascertainment schemes. (1989) (5)
Research design considerations for linkage studies of affective disorders using recombinant DNA markers. (1987) (5)
Human Gene Mapping 10: New Haven Conference 1989 10th International Workshop, New Haven, Conn., June 1989 (1989) (5)
Prospects for research on schizophrenia. IV. Genetic and environmental factors. Genetic models for schizophrenia. (1972) (5)
Abstracts for the committee on the genetic constitution of the X chromosome (Part 3 of 3) (1991) (5)
Abstracts of workshop presentations pp. 948-967 (1989) (5)
Molecular approaches to carrier detection and prenatal diagnosis of the fragile x syndrome (1988) (5)
Abstracts of workshop presentations pp. 948-967 (1989) (5)
Tourette's Syndrome and Attention Deficit Disorder With Hyperactivity-Reply (1987) (5)
Distribution of lethals induced by tritiated DNA precursors in Drosophila melanogaster. (1966) (5)
Estimation of segregation and linkage parameters in simulated data. II. Simultaneous estimation with one linked marker. (1989) (4)
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 14 of 14) (1990) (4)
Abstracts for the committee on the genetic constitution of chromosome 6 (1991) (4)
Abstracts for the committee on the genetic constitution of chromosome 2 (1991) (4)
Abstracts of workshop presentations (Part 1 of 16) (1987) (4)
The CEPH consortium linkage map of human chromosome 2. (1992) (4)
Development of a map of chromosome 11p (1986) (4)
Abstracts of workshop presentations pp. 1057-1074 (1989) (4)
Utilizing automated methods to improve estimates of recurrence risk with linked genetic markers. (1984) (4)
High diversity and no significant selection signal of human ADH1B gene in Tibet (2012) (4)
Predicting genotypes at loci for autosomal recessive disorders using linked genetic markers: application to Wilson's disease (1988) (4)
DNA Workbench: A Database Package to Manage Regional Physical Mapping (1996) (4)
Abstracts of workshop presentations (Part 7 of 16) (1987) (4)
Abstracts of workshop presentations (Part 3 of 16) (1987) (4)
Corrigendum: Reconstructing Native American population history (2012) (4)
Genetics of Childhood Behavior Disorders (1981) (4)
The search for the ultimate cause of maleness. (1985) (4)
Summary of Human Gene Map, New Haven, HGM – 1, 1973, ‘Data 1' (1989) (4)
Summary of Human Gene Map, New Haven, HGM – 1, 1973, ‘Data 1' (1989) (4)
Status of the search for a major genetic locus for affective disorder in the Old Order Amish (1991) (4)
A new human RFLP identified by 7D2 places D13S10 proximal to esterase D. (1987) (4)
Progress Toward an Accurate Human Linkage Map (1987) (4)
Abstracts of workshop presentations pp. 1057-1074 (1989) (4)
Reply to Whitfield (2002) (4)
Abstracts of workshop presentations (Part 4 of 16) (1987) (3)
A massively parallel sequencing assay of microhaplotypes for mixture deconvolution (2019) (3)
Haplotype Evolution of SLITRK 1 , a Candidate Gene for Gilles de la Tourette Syndrome (2008) (3)
Abstracts of workshop presentations pp. 1075-1091 (1989) (3)
Evolution of the HOXB6 intergenic region: motif conservation at the lateral plate mesoderm (LPM) enhancer element. (1999) (3)
A more powerful method to evaluate p‐values in GENEHUNTER (1999) (3)
Report of the Committee on the Genetic Constitution of Chromosomes 2, 3, 4, and 5. (1984) (3)
Abstracts for the committee on the genetic constitution of chromosome 15 (1991) (3)
Response:Interpretations of Multiregional Evolution (1996) (3)
Low Allele Frequency of ADH1B∗47His in West China and Different ADH1B Haplotypes in Western and Eastern Asia (2009) (3)
Linkage analysis approach to hereditary movement disorders. (1989) (3)
Correction to: Mixture deconvolution by massively parallel sequencing of microhaplotypes (2019) (3)
Search for the gene for multiple endocrine neoplasia type 2A. (1990) (3)
Abstracts of workshop presentations (Part 8 of 16) (1987) (3)
Abstracts of workshop presentations (Part 11 of 13) (1985) (3)
High frequency PvuII and PstI polymorphisms identified by KW31 (D10S96) on chromosome 10. (1990) (3)
Revealing associations between PTC/PROP gene, 6-n-propylthiouracil bitterness and vegetable intake (2004) (3)
An MspI polymorphism for the HOX2F gene. (1991) (3)
Global patterns of linkage disequilibrium in Homo sapiens (2001) (3)
A second useful polymorphism for the cytosolic thymidine kinase gene (TK1) with the enzyme BstEII which will allow haplotying at this locus on chromosome 17 (q21-q22). (1987) (3)
Abstracts of workshop presentations pp. 1075-1091 (1989) (3)
Repeat expansion-detection analysis of telomeric uninterrupted (TTAGGG)n arrays. (1998) (3)
The Genetics of Affective Disorders (1989) (3)
An MPO cDNA clone identifies an RFLP with PstI. (1988) (3)
Abstracts for the committee on chromosomal changes in neoplasia (1991) (3)
Abstracts for the committee on the genetic constitution of chromosome 12 (1991) (3)
Drug response as a predictor of transmission of non-bipolar major depression within families. (1985) (3)
Abstracts of workshop presentations (Part 11 of 16) (1987) (2)
THE SEARCH FOR BETTER MARKERS FOR FORENSIC ANCESTRY INFERENCE (2011) (2)
Abstracts of workshop presentations pp. 1106-1116 (1989) (2)
The Na+/H+ antiporter: a “melt” polymorphism allows regional mapping to the short arm of chromosome 1 (1990) (2)
A HindIII polymorphism identified by the human early growth response gene 2 (EGR2) on chromosome 10. (1988) (2)
Exclusion of autosomal dominant dystonia gene from large regions of chromosomes 11p, 13q, and 21q by multi‐point linkage analysis (1987) (2)
The HGM10 information management system. (1989) (2)
The mapping of the locus for multiple endocrine neoplasia type 2A by linkage with chromosome 10 markers. (1989) (2)
Genetic linkage analysis of dermo-distortive urticaria. (1981) (2)
Experience and Preliminary Results in Human Genome Diversity Research (1999) (2)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 24 of 27) (1991) (2)
North Asian population relationships in a global context (2022) (2)
Abstracts of workshop presentations (Part 14 of 16) (1987) (2)
Document Title: Population Genetics of SNPs for Forensic Purposes (Updated) (2008) (2)
Abstracts of workshop presentations (Part 5 of 16) (1987) (2)
Abstracts for the committee on the genetic constitution of chromosome 16 (1991) (2)
Abstracts for the committee on the genetic constitution of chromosome 11 (1991) (2)
Duplicated Gene Evolution of the Primate Alcohol Dehydrogenase Family (2012) (2)
4-OR: Global diversity of KIR and HLA: Population-level evidence for co-evolution, natural selection, and signatures of demographic history (2007) (2)
Hominoid phylogeny: inferences from a sub-terminal minisatellite analyzed by repeat expansion detection (RED) (1998) (2)
An expanded , nearly universal , panel of SNPs for individual identification (2007) (2)
DESIGN AND ANALYSIS OF GENETIC STUDIES AFTER THE HAPMAP PROJECT: SESSION INTRODUCTION (2005) (2)
An easy-to-use maximum-likelihood method of estimating the ascertainment probability. (1981) (2)
Abstracts of workshop presentations (Part 4 of 13) (1985) (2)
Closing in on the MEN2A locus. (1989) (2)
The β subunit locus of the human fibronectin receptor: DNA restriction fragment length polymorphism and linkage mapping studies (1989) (2)
Dopamine D2 Receptor and Tourette's Syndrome-Reply (1995) (2)
Abstracts for the committee on the genetic constitution of chromosome 22 (1991) (2)
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 9 of 14) (1990) (2)
Genetic diversity of the North African population revealed by the typing of SNPs in the DRD2/ANKK1 genomic region. (2021) (2)
Response: genetic data and the african origin of humans. (1996) (2)
Thoughts on Estimating Ancestry (2016) (2)
Empiric recurrence risks and models of inheritance: part II. (1979) (2)
EDIT10: a database interface for HGM10. (1989) (2)
Abstracts of workshop presentations pp. 1106-1116 (1989) (2)
Abstracts for the committee on the genetic constitution of chromosome 4 (1991) (1)
Editorial: Current and Emerging Trends in Human Identification and Molecular Anthropology (2021) (1)
One Form of Bipolar Affective Disorder is Mapped to Chromosome 11 (1989) (1)
Abstracts of workshop presentations (Part 16 of 16) (1987) (1)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 16 of 27) (1991) (1)
Genetic history of the population of Crete (2019) (1)
Contents Vol. 55, 1990 (1990) (1)
Abstracts of workshop presentations (Part 9 of 16) (1987) (1)
Human Gene Mapping 9.5: New Haven Conference 1988 Update to the 9th International Workshop, New Haven, Conn., August 1988 (1988) (1)
Forensic Ancestry Inference: Data Requirements, Analysis Methods, and Interpretation of Results (2021) (1)
Racing toward the Finish Line. (2006) (1)
The Human Gene Mapping Library Database: Representational Challenges Posed by New Bioscience Technologies and by Evolving Biomedical Knowledge (1989) (1)
Genetic counselling for schizophrenic patients and their families (1978) (1)
Genetic Linkage Studies of Schizophrenia (1989) (1)
Yu, N. et al. Low nucleotide diversity in chimpanzees and bonobos. Genetics 164, 1511-1518 (2003) (1)
Abstracts of workshop presentations (Part 5 of 13) (1985) (1)
Cancer Risk Small Cell Lung − Untranslated Region Increases Non ′ 3 KRAS microRNA Complementary Site in the let-7 A SNP in a (2008) (1)
Abstracts for the committee on the genetic constitution of chromosome 13 (1991) (1)
Anthropology's Role in the HGDP (1996) (1)
Abstracts for the committee on the genetic constitution of chromosome 7 (2004) (1)
Abstracts of meeting presentations (Part 9 of 11) (1984) (1)
Linkage studies of two new genes of neuropsychiatric interest (1991) (1)
Response : Forensic DNA Typing (1992) (1)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 21 of 27) (1991) (1)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 22 of 27) (1991) (1)
Network-based informatics support of research collaborations in the Human Genome Project and the Human Brain Project. (1995) (1)
Abstracts for the committee on the genetic constitution of chromosome 9 (1991) (1)
One large kindred excludes a locus for multiple endocrine neoplasia type 2A from about 25% of the human autosomal genetic map. (1987) (1)
Normal DNA sequence variation: detection technologies and implications. (1993) (1)
Two RFLPs at the HOX2G locus. (1991) (1)
Validity of RDC and DSM-III-Reply (1985) (1)
Abstracts of meeting presentations (Part 6 of 11) (1984) (1)
Abstracts of workshop presentations (Part 2 of 13) (1985) (1)
The Yale Human Gene Mapping Library. (1984) (1)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 23 of 27) (1991) (1)
Scanning for unstable trinucleotide repeats in neuropsychiatric disorders: Detection of a large CTG expansion in a schizophrenic patient (1994) (1)
Abstracts of workshop presentations (Part 6 of 13) (1985) (1)
Inheritance and Segregation Pattern of Tourette's Syndrome (1987) (1)
Abstracts for the committee on the genetic constitution of the Y chromosome (1991) (1)
Abstracts of workshop presentations (Part 7 of 13) (1985) (1)
Abstracts for the committee on the genetic constitution of chromosome 10 (1991) (1)
Race, Genes and Human Origins: How Genetically Diverse Are We? (2001) (1)
Abstracts of meeting presentations (Part 1 of 11) (1982) (0)
Genetic relationships of European, Mediterranean, and SW Asian populations using a panel of 55 AISNPs (2019) (0)
Subject Index Vol. 48, 1988 (1988) (0)
Reply to Dr. Goodman (1998) (0)
Contents, Vol. 46, 1987/ Title Page / Table of Contents (1987) (0)
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 12 of 14) (1990) (0)
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 8 of 14) (1990) (0)
Molecular analysis of a case with a non fluorescent y chromosome 45 x 46 xy non fluorescent (1985) (0)
Elim!nating M tOc hondrial DNA (1993) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 17 of 27) (1991) (0)
Metabolic diversity in human populations and correlation with genetic and ancestral geographic distances (2022) (0)
[Dynamics of the haplotype frequencies in populations: study using the Monte Carlo method]. (1996) (0)
Abstractsfor the informatics committee (1991) (0)
Abstracts for the committee on linkage and gene order (1991) (0)
Low linkage disequilibrium at the dopamine D4 receptor (DRD4) gene in the telomeric region of chromosome 11. (2000) (0)
Human gene mapping 10 : New Haven Conference (1989) : Tenth International Workshopon Human Gene Mapping (1989) (0)
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 5 of 14) (1990) (0)
RESEARCH ARTICLE Nuclear Integrations of Mitochondrial DNA in Gorillas (2004) (0)
Abstracts for the committee on the genetic constitution of chromosome 20 (1991) (0)
Importance of Studying Gene-Environment Interactions Psychiatric Disorders-Reply (1979) (0)
Genetic and evolutionary relationships among Asian Macaques (2007) (0)
Guidelines for interpreting abbreviations and specialized phrases in committee text and tables (1989) (0)
Index by Keyword (1989) (0)
Forensic DNA typing [7] (1992) (0)
A Distinctive Pattern of Diversity for the TAS2R38 Gene in North Africa (2021) (0)
Guidelines for interpreting abbreviations and specialized phrases in committee text and tables (1989) (0)
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 13 of 14) (1990) (0)
Human gene mapping 9.5 : New Haven Conference (1988) : update to the ninth International Workshop on Human Gene Mapping : at Yale University, New Haven, Conn., August 28 to 31, 1988 (1988) (0)
Abstracts for the committee on the genetic constitution of chromosome 18 (1991) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 14 of 27) (1991) (0)
New Insight into the human genetic diversity in North African populations by genotyping of SNPs in DRD3 , CSMD1 and NRG1 genes (2022) (0)
A Distinctive Pattern of Diversity for the TAS2R38 Gene in North Africa (2022) (0)
DataBase: Research and Evaluation Results (2008) (0)
Index by Keyword (1989) (0)
Abstracts dscribing resources, technological and other developments (1991) (0)
In Remembrance of: Luigi Luca Cavalli-Sforza (1922–2018) (2019) (0)
STAT3 polymorphisms in North Africa and its implication in breast cancer (2021) (0)
Index of GDB source ID numbers (1991) (0)
Abstractsfor the DNA committee (1991) (0)
A note on the use of HGML LIT literature file numbers (1989) (0)
A note on the use of HGML LIT literature file numbers (1989) (0)
Abstracts of meeting presentations (Part 7 of 11) (1984) (0)
Estimation ofSegregation andLinkage ParametersinSimulated Data. II.Simultaneous Estimation withOneLinked Marker (1989) (0)
Modeling uncertainty in a database for physical gene mapping data. (1991) (0)
Subject index Vol. 46, 1987 (1987) (0)
Chromosome plotbooks and diskettes available from the Human Gene Mapping Library. (1990) (0)
Contents, Vol. 37, 1984 (1984) (0)
Confounding effects of microbiome on the susceptibility of TNFSF15 to Crohn’s disease in the Ryukyu Islands (2017) (0)
Abstracts for the committee on the genetic constitution of chromosome 8 (1991) (0)
Abstracts for the committee on the genetic constitution of chromosome 21 (1991) (0)
Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 758–781 (1989) (0)
We thank M. Stoneking for his advice regarding the analysis of recombination, and (2000) (0)
Modeling Uncertainty ina Database forPhysical GeneMappingData (1992) (0)
Normal DNA sequence variations in humans (2005) (0)
A multipurpose panel of microhaplotypes for casework (2022) (0)
Psychopathology: Searching for major genes for schizophrenia (1996) (0)
Inferring population structure and demographic history using Y-STR data from worldwide populations (2014) (0)
High altitude adaptation in Daghestani populations from the Caucasus (2011) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 10 of 27) (1991) (0)
A new polymorphic marker (D10S97) tightly linked to the multiple endocrine neoplasia type 2A (MEN2A) locus (2004) (0)
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 7 of 14) (1990) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 18 of 27) (1991) (0)
Subject index Vol. 40, 1985 (1985) (0)
Abstracts for the comparative subcommittee on human and mouse homologies (1991) (0)
Abstracts for the committee on the genetic constitution of the X chromosome (Part 2 of 3) (2004) (0)
HincII polymorphism at the D10S95 locus. (1990) (0)
Long CAG/CTG repeats in mice (1998) (0)
Subject Index, Vol. 34, 1984 (1984) (0)
Abstracts of workshop presentations (Part 13 of 16) (1987) (0)
Abstracts of workshop presentations pp. 1006-1022 (1989) (0)
Abstracts of workshop presentations pp. 1006-1022 (1989) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 8 of 27) (1991) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 19 of 27) (1991) (0)
Vertical transmission of susceptibil sex-modified expression (2016) (0)
SNP panels for individual identification and for ancestry inference (2009) (0)
Reply to Kong and Nicolae (2000) (0)
Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 732–757 (1989) (0)
Book reviews (2008) (0)
Index by Abstract Number (1989) (0)
Computational Tools for Complex Trait Gene Mapping : Session Introduction (2004) (0)
Abstracts of workshop presentations (Part 10 of 13) (1985) (0)
Index by Abstract Number (1989) (0)
Author Index / Subject Index Vol. 49, 1988 (1988) (0)
Workshop on Human Behavior Genetics. (1982) (0)
A HaeIII polymorphism at the D10S101 locus. (1990) (0)
Human Genome Variation: Haplotypes, Linkage Disequilibrium, and Populations - Session Introduction (2003) (0)
Report of the third international workshop on human chromosome 18 mapping 1995 Prepared by J . Overhauser , 1 (2018) (0)
Abstracts for the committee on the genetic constitution of chromosome 5 (1991) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 5 of 27) (1991) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 13 of 27) (1991) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 3 of 27) (1991) (0)
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 3 of 14) (1990) (0)
DNA templates. Modeling of heteroduplex formation during PCR from mixtures of (2011) (0)
Genetic analyses ofpyloric stenosis suggesting aspecific maternal effect (1976) (0)
Subject Index Vol. 44, 1987 (1987) (0)
ALCOHOL DEHYDROGENASE (ADH) GENE CLUSTER IN PRIMATES (2010) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 25 of 27) (1991) (0)
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 4 of 14) (1990) (0)
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 2 of 14) (1990) (0)
Did They Ignore Genetics? (1977) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 4 of 27) (1991) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 20 of 27) (1991) (0)
Genetic analysis workshop III: Sampling considerations and assumptions in gene mapping (1985) (0)
Editorial Associations of Disease With Genetic Markers (1993) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 2 of 27) (1991) (0)
C OMP A SS LETTERS SCIENCE & SOCIETY POLICY FORUM BOOKS ET AL. PERSPECTIVES REVIEWS (2002) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 6 of 27) (1991) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 26 of 27) (1991) (0)
Abstracts for the committee on the genetic constitution of chromosome 14 (1991) (0)
Supplementary Material for: Using a Pharmacokinetic Model to Relate an Individual’s Susceptibility to Alcohol Dependence to Genotypes (2017) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 7 of 27) (1991) (0)
Research relevance of recent human evolution (2000) (0)
SNPsand interpopulation genotype reconstruction from tagging (2007) (0)
Abstracts of workshop presentations (Part 8 of 13) (1985) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 9 of 27) (1991) (0)
Internet-Based Support for a Collaborative Genome Center to Map Human Chromosome 12. (1995) (0)
Aripiprazole-Induced Tardive Dyskinesia: The Role of Tamoxifen (2007) (0)
Abstracts of meeting presentations (Part 4 of 11) (1979) (0)
Abstracts for the committee on the genetic constitution of chromosome 19 (1991) (0)
Genetic linkage and hemosiderosis. (1979) (0)
COMPUTATIONAL TOOLS FOR COMPLEX TRAIT GENE MAPPING (2003) (0)
HLA-linkage in affective disorder (1982) (0)
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 11 of 14) (1990) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 12 of 27) (1991) (0)
Contents, Vol. 44, 1987 (1987) (0)
A global view of the OCA2-HERC2 region and pigmentation (2011) (0)
Subject Index Vol. 58, 1991 (1991) (0)
Proposed nomenclature for microhaplotypes (2016) (0)
The Complexities of Linkage Studies for Neuropsychiatric Disorders (1992) (0)
Abstracts for the committee on the mitochondrial genome (1991) (0)
Xllth EUROPEAN CONFERENCE ON ANIMAL BLOOD GROUPS AND BIOCHEMICAL POLYMORPHISM (2009) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 15 of 27) (1991) (0)
Abstracts for the committee on clinical disorders and chromosomal deletion syndromes (1991) (0)
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 11 of 27) (1991) (0)
Abstract ED04-03: Genetic variation among populations (2011) (0)

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