Username

Password

Preview

Sign-in free and Explore the Exciting World of BiomedExperts:

Over 1.500.000 Profiles
More than 1.800 Organizations worldwide
State of the Art Network Visualizations

Manage your own Profile
Locate Experts in your Country/Region
Locate Experts in your 1. and 2. Level Network
Connect to Experts Worldwide

NetworkView

Kenneth Kidd

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

Genes & Molecular Sequences

Physiology

Concepts & Ideas

Procedures

Disorders

Occupations

Population Genetics

Anatomy

Chromosomes, Human, Pair 10

Chemicals & Drugs

Phenomena

Molecular Evolution

Sign-in to see full Profile

Sign-in to see all Coauthors

Publications

TOP 3
Speed William C; Kang Soonmo Peter; Tuck David P; Harris Lyndsay N; Kidd Kenneth K
Global variation in CYP2C8-CYP2C9 functional haplotypes.
Li Hui; Borinskaya Svetlana; Yoshimura Kimio; Kal'ina Nina; Marusin Andrey; Stepanov Vadim A; Qin Zhendong; Khaliq Shagufta; Lee Mi-Young; Yang Yajun; Mohyuddin Aisha; Gurwitz David; Mehdi Syed Qasim; Rogaev Evgeny; Jin Li; Yankovsky Nikolay K; Kidd Judith R; Kidd Kenneth K
Refined geographic distribution of the oriental ALDH2*504Lys (nee 487Lys) variant.
Yamtich Jennifer; Speed William C; Straka Eva; Kidd Judith R; Sweasy Joann B; Kidd Kenneth K
Population-specific variation in haplotype composition and heterozygosity at the POLB locus.

Sign-in to see all Publications

Sign in free and see...

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the visualized research activity
of experts around the globe

Sign-in to see more

Geonetwork of Kenneth Kidd (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

Sign-in to see more

All Publications

2009: Speed William C; Kang Soonmo Peter; Tuck David P; Harris Lyndsay N; Kidd Kenneth K
Global variation in CYP2C8-CYP2C9 functional haplotypes.
The pharmacogenomics journal 2009;9(4):283-90.
2009: Li Hui; Borinskaya Svetlana; Yoshimura Kimio; Kal'ina Nina; Marusin Andrey; Stepanov Vadim A; Qin Zhendong; Khaliq Shagufta; Lee Mi-Young; Yang Yajun; Mohyuddin Aisha; Gurwitz David; Mehdi Syed Qasim; Rogaev Evgeny; Jin Li; Yankovsky Nikolay K; Kidd Judith R; Kidd Kenneth K
Refined geographic distribution of the oriental ALDH2*504Lys (nee 487Lys) variant.
Annals of human genetics 2009;73(Pt 3):335-45.
2009: Yamtich Jennifer; Speed William C; Straka Eva; Kidd Judith R; Sweasy Joann B; Kidd Kenneth K
Population-specific variation in haplotype composition and heterozygosity at the POLB locus.
DNA repair 2009;8(5):579-84.
2009: Holford Matthew E; Rajeevan Haseena; Zhao Hongyu; Kidd Kenneth K; Cheung Kei-Hoi
Semantic web-based integration of cancer pathways and allele frequency data.
Cancer informatics 2009;8():19-30.
2008: Chin Lena J; Ratner Elena; Leng Shuguang; Zhai Rihong; Nallur Sunitha; Babar Imran; Muller Roman-Ulrich; Straka Eva; Su Li; Burki Elizabeth A; Crowell Richard E; Patel Rajeshvari; Kulkarni Trupti; Homer Robert; Zelterman Daniel; Kidd Kenneth K; Zhu Yong; Christiani David C; Belinsky Steven A; Slack Frank J; Weidhaas Joanne B
A SNP in a let-7 microRNA complementary site in the KRAS 3' untranslated region increases non-small cell lung cancer risk.
Cancer research 2008;68(20):8535-40.
2008: Lee M-Y; Mukherjee N; Pakstis A J; Khaliq S; Mohyuddin A; Mehdi S Q; Speed W C; Kidd J R; Kidd K K
Global patterns of variation in allele and haplotype frequencies and linkage disequilibrium across the CYP2E1 gene.
The pharmacogenomics journal 2008;8(5):349-56.
2008: Speed William C; O'Roak Brian J; Tárnok Zsanett; Barta Csaba; Pakstis Andrew J; State Matthew W; Kidd Kenneth K
Haplotype evolution of SLITRK1, a candidate gene for Gilles de la Tourette syndrome.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008;147B(4):463-6.
2008: Al-Kateb Hussam; Boright Andrew P; Mirea Lucia; Xie Xinlei; Sutradhar Rinku; Mowjoodi Alireza; Bharaj Bhupinder; Liu Michelle; Bucksa Jean M; Arends Valerie L; Steffes Michael W; Cleary Patricia A; Sun Wanjie; Lachin John M; Thorner Paul S; Ho Michael; McKnight Amy Jayne; Maxwell A Peter; Savage David A; Kidd Kenneth K; Kidd Judith R; Speed William C; Orchard Trevor J; Miller Rachel G; Sun Lei; Bull Shelley B; Paterson Andrew D;
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 2008;57(1):218-28.
2008: Li Hui; Gu Sheng; Cai Xiaoyun; Speed William C; Pakstis Andrew J; Golub Efim I; Kidd Judith R; Kidd Kenneth K
Ethnic related selection for an ADH Class I variant within East Asia.
PloS one 2008;3(4):e1881.
2007: Li Hui; Mukherjee Namita; Soundararajan Usha; Tarnok Zsanett; Barta Csaba; Khaliq Shagufta; Mohyuddin Aisha; Kajuna Sylvester L B; Mehdi S Qasim; Kidd Judith R; Kidd Kenneth K
Geographically separate increases in the frequency of the derived ADH1B*47His allele in eastern and western Asia.
American journal of human genetics 2007;81(4):842-6.
2007: Pakstis Andrew J; Speed William C; Kidd Judith R; Kidd Kenneth K
Candidate SNPs for a universal individual identification panel.
Human genetics 2007;121(3-4):305-17.
2007: Oota Hiroki; Dunn Casey W; Speed William C; Pakstis Andrew J; Palmatier Meg A; Kidd Judith R; Kidd Kenneth K
Conservative evolution in duplicated genes of the primate Class I ADH cluster.
Gene 2007;392(1-2):64-76.
2007: Han Yi; Gu Sheng; Oota Hiroki; Osier Michael V; Pakstis Andrew J; Speed William C; Kidd Judith R; Kidd Kenneth K
Evidence of positive selection on a class I ADH locus.
American journal of human genetics 2007;80(3):441-56.
2007: Gu Sheng; Pakstis Andrew J; Li Hui; Speed William C; Kidd Judith R; Kidd Kenneth K
Significant variation in haplotype block structure but conservation in tagSNP patterns among global populations.
European journal of human genetics : EJHG 2007;15(3):302-12.
2007: Nakamoto Kaori; Kidd Judith R; Jenison Robert D; Klaassen Curtis D; Wan Yu-Jui Yvonne; Kidd Kenneth K; Zhong Xiao-Bo
Genotyping and haplotyping of CYP2C19 functional alleles on thin-film biosensor chips.
Pharmacogenetics and genomics 2007;17(2):103-14.
2007: Paschou Peristera; Mahoney Michael W; Javed Asif; Kidd Judith R; Pakstis Andrew J; Gu Sheng; Kidd Kenneth K; Drineas Petros
Intra- and interpopulation genotype reconstruction from tagging SNPs.
Genome research 2007;17(1):96-107.
2006: Kidd Kenneth K; Pakstis Andrew J; Speed William C; Grigorenko Elena L; Kajuna Sylvester L B; Karoma Nganyirwa J; Kungulilo Selemani; Kim Jong-Jin; Lu Ru-Band; Odunsi Adekunle; Okonofua Friday; Parnas Josef; Schulz Leslie O; Zhukova Olga V; Kidd Judith R
Developing a SNP panel for forensic identification of individuals.
Forensic science international 2006;164(1):20-32.
2006: Schulz Leslie O; Bennett Peter H; Ravussin Eric; Kidd Judith R; Kidd Kenneth K; Esparza Julian; Valencia Mauro E
Effects of traditional and western environments on prevalence of type 2 diabetes in Pima Indians in Mexico and the U.S.
Diabetes care 2006;29(8):1866-71.
2006: Fredman David; Sawyer Sarah L; Strömqvist Linda; Mottagui-Tabar Salim; Kidd Kenneth K; Wahlestedt Claes; Chanock Stephen J; Brookes Anthony J
Nonsynonymous SNPs: validation characteristics, derived allele frequency patterns, and suggestive evidence for natural selection.
Human mutation 2006;27(2):173-86.
2005: Han Yi; Oota Hiroki; Osier Michael V; Pakstis Andrew J; Speed William C; Odunsi Adekunle; Okonofua Friday; Kajuna Sylvester L B; Karoma Nganyirwa J; Kungulilo Selemani; Grigorenko Elena; Zhukova Olga V; Bonne-Tamir Batsheva; Lu Ru-B; Parnas Josef; Schulz Leslie O; Kidd Judith R; Kidd Kenneth K
Considerable haplotype diversity within the 23kb encompassing the ADH7 gene.
Alcoholism, clinical and experimental research 2005;29(12):2091-100.
2005: Gu Sheng; Pakstis Andrew J; Kidd Kenneth K
HAPLOT: a graphical comparison of haplotype blocks, tagSNP sets and SNP variation for multiple populations.
Bioinformatics (Oxford, England) 2005;21(20):3938-9.
2005: Kim Jong-Jin; Verdu Paul; Pakstis Andrew J; Speed William C; Kidd Judith R; Kidd Kenneth K
Use of autosomal loci for clustering individuals and populations of East Asian origin.
Human genetics 2005;117(6):511-9.
2005: Sawyer Sarah L; Mukherjee Namita; Pakstis Andrew J; Feuk Lars; Kidd Judith R; Brookes Anthony J; Kidd Kenneth K
Linkage disequilibrium patterns vary substantially among populations.
European journal of human genetics : EJHG 2005;13(5):677-86.
2005: Sternberg Robert J; Grigorenko Elena L; Kidd Kenneth K
Intelligence, race, and genetics.
The American psychologist 2005;60(1):46-59.
2005: Rajeevan Haseena; Cheung Kei-Hoi; Gadagkar Rohit; Stein Shannon; Soundararajan Usha; Kidd Judith R; Pakstis Andrew J; Miller Perry L; Kidd Kenneth K
ALFRED: An Allele Frequency Database for Microevolutionary Studies.
Evolutionary bioinformatics online 2005;1():1-10.
2004: Liu Nianjun; Sawyer Sarah L; Mukherjee Namita; Pakstis Andrew J; Kidd Judith R; Kidd Kenneth K; Brookes Anthony J; Zhao Hongyu
Haplotype block structures show significant variation among populations.
Genetic epidemiology 2004;27(4):385-400.
2004: Duffy Valerie B; Davidson Andrew C; Kidd Judith R; Kidd Kenneth K; Speed William C; Pakstis Andrew J; Reed Danielle R; Snyder Derek J; Bartoshuk Linda M
Bitter receptor gene (TAS2R38), 6-n-propylthiouracil (PROP) bitterness and alcohol intake.
Alcoholism, clinical and experimental research 2004;28(11):1629-37.
2004: Tishkoff Sarah A; Kidd Kenneth K
Implications of biogeography of human populations for 'race' and medicine.
Nature genetics 2004;36(11 Suppl):S21-7.
2004: Paschou P; Feng Y; Pakstis A J; Speed W C; DeMille M M; Kidd J R; Jaghori B; Kurlan R; Pauls D L; Sandor P; Barr C L; Kidd K K
Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility region.
American journal of human genetics 2004;75(4):545-60.
2004: Kidd K K; Pakstis A J; Speed W C; Kidd J R
Understanding human DNA sequence variation.
The Journal of heredity 2004;95(5):406-20.
2004: Palmatier M A; Pakstis A J; Speed W; Paschou P; Goldman D; Odunsi A; Okonofua F; Kajuna S; Karoma N; Kungulilo S; Grigorenko E; Zhukova O V; Bonne-Tamir B; Lu R-B; Parnas J; Kidd J R; DeMille M M C; Kidd K K
COMT haplotypes suggest P2 promoter region relevance for schizophrenia.
Molecular psychiatry 2004;9(9):859-70.
2004: Jensen-Seaman Michael I; Sarmiento Esteban E; Deinard Amos S; Kidd Kenneth K
Nuclear integrations of mitochondrial DNA in gorillas.
American journal of primatology 2004;63(3):139-47.
2004: Wang E; Ding Y-C; Flodman P; Kidd J R; Kidd K K; Grady D L; Ryder O A; Spence M A; Swanson J M; Moyzis R K
The genetic architecture of selection at the human dopamine receptor D4 (DRD4) gene locus.
American journal of human genetics 2004;74(5):931-44.
2004: Osier M V; Lu R-B; Pakstis A J; Kidd J R; Huang S-Y; Kidd Kenneth K
Possible epistatic role of ADH7 in the protection against alcoholism.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2004;126B(1):19-22.
2004: Oota Hiroki; Pakstis Andrew J; Bonne-Tamir Batsheva; Goldman David; Grigorenko Elena; Kajuna Sylvester L B; Karoma Nganyirwa J; Kungulilo Selemani; Lu Ru-Band; Odunsi Kunle; Okonofua Friday; Zhukova Olga V; Kidd Judith R; Kidd Kenneth K
The evolution and population genetics of the ALDH2 locus: random genetic drift, selection, and low levels of recombination.
Annals of human genetics 2004;68(Pt 2):93-109.
2003: Chattopadhyay Pratima; Pakstis Andrew J; Mukherjee Namita; Iyengar Sudha; Odunsi Adekunle; Okonofua Friday; Bonne-Tamir Batsheva; Speed William; Kidd Judith R; Kidd Kenneth K
Global survey of haplotype frequencies and linkage disequilibrium at the RET locus.
European journal of human genetics : EJHG 2003;11(10):760-9.
2003: Zhong Xiao-Bo; Reynolds Robert; Kidd Judith R; Kidd Kenneth K; Jenison Robert; Marlar Richard A; Ward David C
Single-nucleotide polymorphism genotyping on optical thin-film biosensor chips.
Proceedings of the National Academy of Sciences of the United States of America 2003;100(20):11559-64.
2003: Yu Ning; Jensen-Seaman Michael I; Chemnick Leona; Kidd Judith R; Deinard Amos S; Ryder Oliver; Kidd Kenneth K; Li Wen-Hsiung
Low nucleotide diversity in chimpanzees and bonobos.
Genetics 2003;164(4):1511-8.
2003: Rajeevan H; Osier M V; Cheung K-H; Deng H; Druskin L; Heinzen R; Kidd J R; Stein S; Pakstis A J; Tosches N P; Yeh C-C; Miller P L; Kidd K K
ALFRED: the ALelle FREquency Database. Update.
Nucleic acids research 2003;31(1):270-1.
2003: Wang Shuang; Kidd Kenneth K; Zhao Hongyu
On the use of DNA pooling to estimate haplotype frequencies.
Genetic epidemiology 2003;24(1):74-82.
2003: Leckman James F; Pauls David L; Zhang Heping; Rosario-Campos Maria C; Katsovich Liliya; Kidd Kenneth K; Pakstis Andrew J; Alsobrook John P; Robertson Mary M; McMahon William M; Walkup John T; van de Wetering Ben J M; King Robert A; Cohen Donald J;
Obsessive-compulsive symptom dimensions in affected sibling pairs diagnosed with Gilles de la Tourette syndrome.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003;116B(1):60-8.
2002: Osier Michael V; Pakstis Andrew J; Goldman David; Edenberg Howard J; Kidd Judith R; Kidd Kenneth K
A proline-threonine substitution in codon 351 of ADH1C is common in Native Americans.
Alcoholism, clinical and experimental research 2002;26(12):1759-63.
2002: DeMille Mellissa M C; Kidd Judith R; Ruggeri Valeria; Palmatier Meg A; Goldman David; Odunsi Adekunle; Okonofua Friday; Grigorenko Elena; Schulz Leslie O; Bonne-Tamir Batsheva; Lu Ru-Band; Parnas Josef; Pakstis Andrew J; Kidd Kenneth K
Population variation in linkage disequilibrium across the COMT gene considering promoter region and coding region variation.
Human genetics 2002;111(6):521-37.
2002: Osier Michael V; Cheung Kei-Hoi; Kidd Judith R; Pakstis Andrew J; Miller Perry L; Kidd Kenneth K
ALFRED: An allele frequency database for anthropology.
American journal of physical anthropology 2002;119(1):77-83.
2002: Osier Michael V; Pakstis Andrew J; Soodyall Himla; Comas David; Goldman David; Odunsi Adekunle; Okonofua Friday; Parnas Josef; Schulz Leslie O; Bertranpetit Jaume; Bonne-Tamir Batsheva; Lu Ru-Band; Kidd Judith R; Kidd Kenneth K
A global perspective on genetic variation at the ADH genes reveals unusual patterns of linkage disequilibrium and diversity.
American journal of human genetics 2002;71(1):84-99.
2002: Fullerton Stephanie M; Bartoszewicz Angelika; Ybazeta Gustavo; Horikawa Yukio; Bell Graeme I; Kidd Kenneth K; Cox Nancy J; Hudson Richard R; Di Rienzo Anna
Geographic and haplotype structure of candidate type 2 diabetes susceptibility variants at the calpain-10 locus.
American journal of human genetics 2002;70(5):1096-106.
2002: Zhang Heping; Leckman James F; Pauls David L; Tsai Chin-Pei; Kidd Kenneth K; Campos M Rosario;
Genomewide scan of hoarding in sib pairs in which both sibs have Gilles de la Tourette syndrome.
American journal of human genetics 2002;70(4):896-904.
2002: Ding Yuan-Chun; Chi Han-Chang; Grady Deborah L; Morishima Atsuyuki; Kidd Judith R; Kidd Kenneth K; Flodman Pamela; Spence M Anne; Schuck Sabrina; Swanson James M; Zhang Ya-Ping; Moyzis Robert K
Evidence of positive selection acting at the human dopamine receptor D4 gene locus.
Proceedings of the National Academy of Sciences of the United States of America 2002;99(1):309-14.
2001: Jensen-Seaman M I; Deinard A S; Kidd K K
Modern African ape populations as genetic and demographic models of the last common ancestor of humans, chimpanzees, and gorillas.
The Journal of heredity 2001;92(6):475-80.
2001: Turner G; Barbulescu M; Su M; Jensen-Seaman M I; Kidd K K; Lenz J
Insertional polymorphisms of full-length endogenous retroviruses in humans.
Current biology : CB 2001;11(19):1531-5.
2001: Jensen-Seaman M I; Kidd K K
Mitochondrial DNA variation and biogeography of eastern gorillas.
Molecular ecology 2001;10(9):2241-7.
2001: Barbulescu M; Turner G; Su M; Kim R; Jensen-Seaman M I; Deinard A S; Kidd K K; Lenz J
A HERV-K provirus in chimpanzees, bonobos and gorillas, but not humans.
Current biology : CB 2001;11(10):779-83.
2001: Osier M V; Cheung K H; Kidd J R; Pakstis A J; Miller P L; Kidd K K
ALFRED: an allele frequency database for diverse populations and DNA polymorphisms--an update.
Nucleic acids research 2001;29(1):317-9.
2001: Calafell F; Grigorenko E L; Chikanian A A; Kidd K K
Haplotype evolution and linkage disequilibrium: A simulation study.
Human heredity 2001;51(1-2):85-96.
2000: Tishkoff S A; Pakstis A J; Stoneking M; Kidd J R; Destro-Bisol G; Sanjantila A; Lu R B; Deinard A S; Sirugo G; Jenkins T; Kidd K K; Clark A G
Short tandem-repeat polymorphism/alu haplotype variation at the PLAT locus: implications for modern human origins.
American journal of human genetics 2000;67(4):901-25.
2000: Zhao H; Zhang S; Merikangas K R; Trixler M; Wildenauer D B; Sun F; Kidd K K
Transmission/disequilibrium tests using multiple tightly linked markers.
American journal of human genetics 2000;67(4):936-46.
2000: Tishkoff S A; Pakstis A J; Ruano G; Kidd K K
The accuracy of statistical methods for estimation of haplotype frequencies: an example from the CD4 locus.
American journal of human genetics 2000;67(2):518-22.
2000: Kidd J R; Pakstis A J; Zhao H; Lu R B; Okonofua F E; Odunsi A; Grigorenko E; Tamir B B; Friedlaender J; Schulz L O; Parnas J; Kidd K K
Haplotypes and linkage disequilibrium at the phenylalanine hydroxylase locus, PAH, in a global representation of populations.
American journal of human genetics 2000;66(6):1882-99.
2000: Seaman M I; Chang F M; Quiñones A T; Kidd K K
Evolution of exon 1 of the dopamine D4 receptor (DRD4) gene in primates.
The Journal of experimental zoology 2000;288(1):32-8.
2000: Cheung K H; Osier M V; Kidd J R; Pakstis A J; Miller P L; Kidd K K
ALFRED: an allele frequency database for diverse populations and DNA polymorphisms.
Nucleic acids research 2000;28(1):361-3.
2000: Cheung K H; Miller P L; Kidd J R; Kidd K K; Osier M V; Pakstis A J
ALFRED: a Web-accessible allele frequency database.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing 2000;():639-50.
1999: Seaman M I; Fisher J B; Chang F; Kidd K K
Tandem duplication polymorphism upstream of the dopamine D4 receptor gene (DRD4).
American journal of medical genetics 1999;88(6):705-9.
1999: Zhao H; Merikangas K R; Kidd K K
On a randomization procedure in linkage analysis.
American journal of human genetics 1999;65(5):1449-56.
1999: Barbulescu M; Turner G; Seaman M I; Deinard A S; Kidd K K; Lenz J
Many human endogenous retrovirus K (HERV-K) proviruses are unique to humans.
Current biology : CB 1999;9(16):861-8.
1999: Palmatier M A; Kang A M; Kidd K K
Global variation in the frequencies of functionally different catechol-O-methyltransferase alleles.
Biological psychiatry 1999;46(4):557-67.
1999: Barr C L; Wigg K G; Pakstis A J; Kurlan R; Pauls D; Kidd K K; Tsui L C; Sandor P
Genome scan for linkage to Gilles de la Tourette syndrome.
American journal of medical genetics 1999;88(4):437-45.
1999: Kang A M; Palmatier M A; Kidd K K
Global variation of a 40-bp VNTR in the 3'-untranslated region of the dopamine transporter gene (SLC6A3).
Biological psychiatry 1999;46(2):151-60.
1999: Osier M; Pakstis A J; Kidd J R; Lee J F; Yin S J; Ko H C; Edenberg H J; Lu R B; Kidd K K
Linkage disequilibrium at the ADH2 and ADH3 loci and risk of alcoholism.
American journal of human genetics 1999;64(4):1147-57.
1999: Zhao H; Pakstis A J; Kidd J R; Kidd K K
Assessing linkage disequilibrium in a complex genetic system. I. Overall deviation from random association.
Annals of human genetics 1999;63(Pt 2):167-79.
1999: Calafell F; Shuster A; Speed W C; Kidd J R; Black F L; Kidd K K
Genealogy reconstruction from short tandem repeat genotypes in an Amazonian population.
American journal of physical anthropology 1999;108(2):137-46.
1999: Zhao H; Sheffield L J; Pakstis A J; Knauert M P; Kidd K K
A more powerful method to evaluate p-values in GENEHUNTER.
Genetic epidemiology 1999;17 Suppl 1():S415-20.
1999: Sheffield L J; Knauert M P; Pakstis A J; Zhao H; Kidd K K
Analyses of the COGA data set in one ethnic group with examinations of alternative definitions of alcoholism.
Genetic epidemiology 1999;17 Suppl 1():S319-24.
1998: Deinard A S; Sirugo G; Kidd K K
Hominoid phylogeny: inferences from a sub-terminal minisatellite analyzed by repeat expansion detection (RED)
Journal of human evolution 1998;35(3):313-7.
1998: Kidd K K; Morar B; Castiglione C M; Zhao H; Pakstis A J; Speed W C; Bonne-Tamir B; Lu R B; Goldman D; Lee C; Nam Y S; Grandy D K; Jenkins T; Kidd J R
A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus.
Human genetics 1998;103(2):211-27.
1998: Tishkoff S A; Goldman A; Calafell F; Speed W C; Deinard A S; Bonne-Tamir B; Kidd J R; Pakstis A J; Jenkins T; Kidd K K
A global haplotype analysis of the myotonic dystrophy locus: implications for the evolution of modern humans and for the origin of myotonic dystrophy mutations.
American journal of human genetics 1998;62(6):1389-402.
1998: Calafell F; Shuster A; Speed W C; Kidd J R; Kidd K K
Short tandem repeat polymorphism evolution in humans.
European journal of human genetics : EJHG 1998;6(1):38-49.
1998: Iyengar S; Seaman M; Deinard A S; Rosenbaum H C; Sirugo G; Castiglione C M; Kidd J R; Kidd K K
Analyses of cross species polymerase chain reaction products to infer the ancestral state of human polymorphisms.
DNA sequence : the journal of DNA sequencing and mapping 1998;8(5):317-27.
1998: Deinard A S; Kidd K K
Evolution of a D2 dopamine receptor intron within the great apes and humans.
DNA sequence : the journal of DNA sequencing and mapping 1998;8(5):289-301.
1997: Breschel T S; McInnis M G; Margolis R L; Sirugo G; Corneliussen B; Simpson S G; McMahon F J; MacKinnon D F; Xu J F; Pleasant N; Huo Y; Ashworth R G; Grundstrom C; Grundstrom T; Kidd K K; DePaulo J R; Ross C A
A novel, heritable, expanding CTG repeat in an intron of the SEF2-1 gene on chromosome 18q21.1.
Human molecular genetics 1997;6(11):1855-63.
1997: Sirugo G; Pakstis A J; Kidd K K; Matthysse S; Levy D L; Holzman P S; Párnas J; McInnis M; Breschel T; Ross C A
Detection of a large CTG/CAG trinucleotide repeat expansion in a Danish schizophrenia kindred.
American journal of medical genetics 1997;74(5):546-8.
1997: Iyengar S; Kalinsky H; Weiss S; Korostishevsky M; Sadeh M; Zhao Y; Kidd K K; Bonne-Tamir B
Homozygosity by descent for a rare mutation in the myophosphorylase gene is associated with variable phenotypes in a Druze family with McArdle disease.
Journal of medical genetics 1997;34(5):391-4.
1997: Sirugo G; Deinard A S; Kidd J R; Kidd K K
Survey of maximum CTG/CAG repeat lengths in humans and non-human primates: total genome scan in populations using the Repeat Expansion Detection method.
Human molecular genetics 1997;6(3):403-8.
1997: Chang F M; Ko H C; Lu R B; Pakstis A J; Kidd K K
The dopamine D4 receptor gene (DRD4) is not associated with alcoholism in three Taiwanese populations: six polymorphisms tested separately and as haplotypes.
Biological psychiatry 1997;41(4):394-405.
1997: Liao D; Pavelitz T; Kidd J R; Kidd K K; Weiner A M
Concerted evolution of the tandemly repeated genes encoding human U2 snRNA (the RNU2 locus) involves rapid intrachromosomal homogenization and rare interchromosomal gene conversion.
The EMBO journal 1997;16(3):588-98.
1997: Chang F M; Kidd K K
Rapid molecular haplotyping of the first exon of the human dopamine D4 receptor gene by heteroduplex analysis.
American journal of medical genetics 1997;74(1):91-4.
1997: Iyengar S; Calafell F; Kidd K K
Detection of major genes underlying several quantitative traits associated with a common disease using different ascertainment schemes.
Genetic epidemiology 1997;14(6):809-14.
1996: Michalatos-Beloin S; Tishkoff S A; Bentley K L; Kidd K K; Ruano G
Molecular haplotyping of genetic markers 10 kb apart by allele-specific long-range PCR.
Nucleic acids research 1996;24(23):4841-3.
1996: Gill J R; Reyes-Múgica M; Iyengar S; Kidd K K; Touloukian R J; Smith C; Keller M S; Genel M
Early presentation of metastatic medullary carcinoma in multiple endocrine neoplasia, type IIA: implications for therapy.
The Journal of pediatrics 1996;129(3):459-64.
1996: Grice D E; Leckman J F; Pauls D L; Kurlan R; Kidd K K; Pakstis A J; Chang F M; Buxbaum J D; Cohen D J; Gelernter J
Linkage disequilibrium between an allele at the dopamine D4 receptor locus and Tourette syndrome, by the transmission-disequilibrium test.
American journal of human genetics 1996;59(3):644-52.
1996: Cheung K H; Nadkarni P; Silverstein S; Kidd J R; Pakstis A J; Miller P; Kidd K K
PhenoDB: an integrated client/server database for linkage and population genetics.
Computers and biomedical research, an international journal 1996;29(4):327-37.
1996: Chang F M; Kidd J R; Livak K J; Pakstis A J; Kidd K K
The world-wide distribution of allele frequencies at the human dopamine D4 receptor locus.
Human genetics 1996;98(1):91-101.
1996: Kidd K K; Pakstis A J; Castiglione C M; Kidd J R; Speed W C; Goldman D; Knowler W C; Lu R B; Bonne-Tamir B
DRD2 haplotypes containing the TaqI A1 allele: implications for alcoholism research.
Alcoholism, clinical and experimental research 1996;20(4):697-705.
1996: Tishkoff S A; Ruano G; Kidd J R; Kidd K K
Distribution and frequency of a polymorphic Alu insertion at the plasminogen activator locus in humans.
Human genetics 1996;97(6):759-64.
1996: Lu R B; Ko H C; Chang F M; Castiglione C M; Schoolfield G; Pakstis A J; Kidd J R; Kidd K K
No association between alcoholism and multiple polymorphisms at the dopamine D2 receptor gene (DRD2) in three distinct Taiwanese populations.
Biological psychiatry 1996;39(6):419-29.
1996: Nadkarni P; Cheung K H; Castiglione C; Miller P; Kidd K
DNA workbench: a database package to manage regional physical mapping.
Journal of computational biology : a journal of computational molecular cell biology 1996;3(2):319-29.
1995: Gelernter J; Vandenbergh D; Kruger S D; Pauls D L; Kurlan R; Pakstis A J; Kidd K K; Uhl G
The dopamine transporter protein gene (SLC6A3): primary linkage mapping and linkage studies in Tourette syndrome.
Genomics 1995;30(3):459-63.
1995: Miller P L; Nadkarni P M; Kidd K K; Cheung K; Ward D C; Banks A; Bray-Ward P; Cupelli L; Herdman V; Marondel I; Montgomery K; Renault B; Yoon S J; Krauter K S; Kucherlapati R
Internet-based support for bioscience research: a collaborative genome center for human chromosome 12.
Journal of the American Medical Informatics Association : JAMIA 1995;2(6):351-64.
1995: Baldwin C T; Weiss S; Farrer L A; De Stefano A L; Adair R; Franklyn B; Kidd K K; Korostishevsky M; Bonné-Tamir B
Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population.
Human molecular genetics 1995;4(9):1637-42.
1995: Gelernter J; Rao P A; Pauls D L; Hamblin M W; Sibley D R; Kidd K K
Assignment of the 5HT7 receptor gene (HTR7) to chromosome 10q and exclusion of genetic linkage with Tourette syndrome.
Genomics 1995;26(2):207-9.
1994: Wright L W; Lichter J B; Reinitz J; Shifman M A; Kidd K K; Miller P L
Computer-assisted restriction mapping: an integrated approach to handling experimental uncertainty.
Computer applications in the biosciences : CABIOS 1994;10(4):435-42.
1994: Ruano G; Deinard A S; Tishkoff S; Kidd K K
Detection of DNA sequence variation via deliberate heteroduplex formation from genomic DNAs amplified en masse in "population tubes".
PCR methods and applications 1994;3(4):225-31.
1994: Barr C L; Kennedy J L; Pakstis A J; Castiglione C M; Kidd J R; Wetterberg L; Kidd K K
Linkage study of a susceptibility locus for schizophrenia in the pseudoautosomal region.
Schizophrenia bulletin 1994;20(2):277-86.
1993: Barr C L; Kennedy J L; Lichter J B; Van Tol H H; Wetterberg L; Livak K J; Kidd K K
Alleles at the dopamine D4 receptor locus do not contribute to the genetic susceptibility to schizophrenia in a large Swedish kindred.
American journal of medical genetics 1993;48(4):218-22.
1993: Gelernter J; Kruger S; Pakstis A J; Pacholczyk T; Sparkes R S; Kidd K K; Amara S
Assignment of the norepinephrine transporter protein (NET1) locus to chromosome 16.
Genomics 1993;18(3):690-2.
1993: Brooks-Wilson A R; Lichter J B; Ward D C; Kidd K K; Goodfellow P J
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.
Genomics 1993;17(3):611-7.
1993: Barr C L; Kidd K K
Population frequencies of the A1 allele at the dopamine D2 receptor locus.
Biological psychiatry 1993;34(4):204-9.
1993: Lichter J B; Barr C L; Kennedy J L; Van Tol H H; Kidd K K; Livak K J
A hypervariable segment in the human dopamine receptor D4 (DRD4) gene.
Human molecular genetics 1993;2(6):767-73.
1993: Gelernter J; Kruger S; Kidd K K; Amara S
TaqI RFLP at norepinephrine transporter protein (NET) locus.
Human molecular genetics 1993;2(6):820.
1993: Lichter J B; Difilippantonio M J; Pakstis A J; Goodfellow P J; Ward D C; Kidd K K
Physical and genetic maps for chromosome 10.
Genomics 1993;16(2):320-4.
1993: Rogers J; Kidd K K
Nuclear DNA polymorphisms in a wild population of yellow baboons (Papio hamadryas cynocephalus) from Mikumi National Park, Tanzania.
American journal of physical anthropology 1993;90(4):477-86.
1993: Lichter J B; Wu J; Brooks-Wilson A R; Difillipantonio M; Brewster S; Ward D C; Goodfellow P J; Kidd K K
A new polymorphic marker (D10S97) tightly linked to the multiple endocrine neoplasia type 2A (MEN2A) locus.
Human genetics 1993;90(5):516-20.
1992: Ruano G; Kidd K K
Modeling of heteroduplex formation during PCR from mixtures of DNA templates.
PCR methods and applications 1992;2(2):112-6.
1992: Lichter J B; Wu J; Miller D; Goodfellow P J; Kidd K K
A high-resolution meiotic mapping panel for the pericentromeric region of chromosome 10.
Genomics 1992;13(3):607-12.
1992: Miller D L; Dill F J; Lichter J B; Kidd K K; Goodfellow P J
Isolation and high-resolution mapping of new DNA markers from the pericentromeric region of chromosome 10.
Genomics 1992;13(3):601-6.
1992: Ruano G; Rogers J; Ferguson-Smith A C; Kidd K K
DNA sequence polymorphism within hominoid species exceeds the number of phylogenetically informative characters for a HOX2 locus.
Molecular biology and evolution 1992;9(4):575-86.
1992: Gelernter J; Kennedy J L; van Tol H H; Civelli O; Kidd K K
The D4 dopamine receptor (DRD4) maps to distal 11p close to HRAS.
Genomics 1992;13(1):208-10.
1992: Deinard A S; Ruano G; Kidd K K
A dinucleotide repeat polymorphism at the HOX2B locus.
Nucleic acids research 1992;20(5):1171.
1992: Lichter J B; Wu J S; Genel M; Flynn S D; Pakstis A J; Kidd J R; Kidd K K
Presymptomatic testing using DNA markers for individuals at risk for familial multiple endocrine neoplasia 2A.
The Journal of clinical endocrinology and metabolism 1992;74(2):368-73.
1992: Lichter J B; Difilippantonio M; Wu J; Miller D; Ward D C; Goodfellow P J; Kidd K K
Localization of the gene for MEN 2A.
Henry Ford Hospital medical journal 1992;40(3-4):199-204.
1992: Gelernter J; Pakstis A J; Grandy D; Litt M; Retief A E; Kennedy J L; Hing-Loh A; Schoolfield G; Civelli O; Kidd K K
Linkage map of eight human chromosome 11q markers, including DRD2, spanning 60 cM.
Cytogenetics and cell genetics 1992;60(1):26-8.
1991: Hästbacka J; Sistonen P; Kaitila I; Weiffenbach B; Kidd K K; de la Chapelle A
A linkage map spanning the locus for diastrophic dysplasia (DTD).
Genomics 1991;11(4):968-73.
1991: Ruano G; Kidd K K
Genotyping and haplotyping of polymorphisms directly from genomic DNA via coupled amplification and sequencing (CAS).
Nucleic acids research 1991;19(24):6877-82.
1991: Gelernter J; O'Malley S; Risch N; Kranzler H R; Krystal J; Merikangas K; Kennedy J L; Kidd K K
No association between an allele at the D2 dopamine receptor gene (DRD2) and alcoholism.
JAMA : the journal of the American Medical Association 1991;266(13):1801-7.
1991: Pakstis A J; Kidd J R; Castiglione C M; Kidd K K
Status of the search for a major genetic locus for affective disorder in the Old Order Amish.
Human genetics 1991;87(4):475-83.
1991: Moises H W; Gelernter J; Giuffra L A; Zarcone V; Wetterberg L; Civelli O; Kidd K K; Cavalli-Sforza L L; Grandy D K; Kennedy J L
No linkage between D2 dopamine receptor gene region and schizophrenia.
Archives of general psychiatry 1991;48(7):643-7.
1991: Miller P L; Nadkarni P; Gelernter J E; Carriero N; Pakstis A J; Kidd K K
Parallelizing genetic linkage analysis: a case study for applying parallel computation in molecular biology.
Computers and biomedical research, an international journal 1991;24(3):234-48.
1991: Ogura T; Castiglione C M; Pakstis A J; Kidd K K
An MspI polymorphism for the HOX2F gene.
Nucleic acids research 1991;19(7):1716.
1991: Gelernter J; Gejman P V; Bisighini S; Kidd K K
Sequence tagged site (STS) TaqI RFLP at dopamine beta-hydroxylase (DBH).
Nucleic acids research 1991;19(8):1957.
1991: Ogura T; Castiglione C M; Pakstis A J; Kidd K K
Two RFLPs at the HOX2G locus.
Nucleic acids research 1991;19(7):1716.
1991: Ruano G; Kidd K K
Coupled amplification and sequencing of genomic DNA.
Proceedings of the National Academy of Sciences of the United States of America 1991;88(7):2815-9.
1991: Gelernter J; Kidd K K
The current status of linkage studies in schizophrenia.
Research publications - Association for Research in Nervous and Mental Disease 1991;69():137-52.
1991: Miller P L; Shifman M A; Kidd K K
Modeling uncertainty in a database for physical gene mapping data.
Proceedings / the ... Annual Symposium on Computer Application [sic] in Medical Care. Symposium on Computer Applications in Medical Care 1991;():409-13.
1990: Carson N L; Wu J S; Jackson C E; Kidd K K; Simpson N E
The mutation for medullary thyroid carcinoma with parathyroid tumors (MTC with PTs) is closely linked to the centromeric region of chromosome 10.
American journal of human genetics 1990;47(6):946-51.
1990: Dudley C R; Giuffra L A; Tippett P; Kidd K K; Reeders S T
The Na+/H+ antiporter: a "melt" polymorphism allows regional mapping to the short arm of chromosome 1.
Human genetics 1990;86(1):79-83.
1990: Gelernter J; Pakstis A J; Pauls D L; Kurlan R; Gancher S T; Civelli O; Grandy D; Kidd K K
Gilles de la Tourette syndrome is not linked to D2-dopamine receptor.
Archives of general psychiatry 1990;47(11):1073-7.
1990: Wu J S; Kidd K K
A HaeIII polymorphism at the D10S101 locus.
Nucleic acids research 1990;18(18):5577.
1990: Wu J; Kidd K K
HincII polymorphism at the D10S95 locus.
Nucleic acids research 1990;18(16):4965.
1990: Ruano G; Kidd K K; Stephens J C
Haplotype of multiple polymorphisms resolved by enzymatic amplification of single DNA molecules.
Proceedings of the National Academy of Sciences of the United States of America 1990;87(16):6296-300.
1990: Pauls D L; Pakstis A J; Kurlan R; Kidd K K; Leckman J F; Cohen D J; Kidd J R; Como P; Sparkes R
Segregation and linkage analyses of Tourette's syndrome and related disorders.
Journal of the American Academy of Child and Adolescent Psychiatry 1990;29(2):195-203.
1990: Wu J S; Kidd K K
High frequency PvuII and PstI polymorphisms identified by KW31 (D10S96) on chromosome 10.
Nucleic acids research 1990;18(5):1316.
1990: Wu J S; Kidd K K
An EcoRI polymorphism identified by KW6 (D10S97) on chromosome 10.
Nucleic acids research 1990;18(5):1316.
1990: Ruano G; Gray M R; Miki T; Ferguson-Smith A C; Ruddle F H; Kidd K K
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.
Nucleic acids research 1990;18(5):1314.
1990: Wu J S; Kidd K K
Extensive sequence polymorphisms associated with chromosome 10 alpha satellite DNA and its close linkage to markers from the pericentromeric region.
Human genetics 1990;84(3):279-82.
1990: Kidd J R; Matsubara Y; Castiglione C M; Tanaka K; Kidd K K
The locus for the medium-chain acyl-CoA dehydrogenase gene on chromosome 1 is highly polymorphic.
Genomics 1990;6(1):89-93.
1990: Kidd K K; Simpson N E
Search for the gene for multiple endocrine neoplasia type 2A.
Recent progress in hormone research 1990;46():305-41; discussion 341-3.
1989: Wu J S; Giuffra L A; Goodfellow P J; Myers S; Carson N L; Anderson L; Hoyle L S; Simpson N E; Kidd K K
The beta subunit locus of the human fibronectin receptor: DNA restriction fragment length polymorphism and linkage mapping studies.
Human genetics 1989;83(4):383-90.
1989: Ruano G; Kidd K K
Direct haplotyping of chromosomal segments from multiple heterozygotes via allele-specific PCR amplification.
Nucleic acids research 1989;17(20):8392.
1989: Ruano G; Fenton W; Kidd K K
Biphasic amplification of very dilute DNA samples via 'booster' PCR.
Nucleic acids research 1989;17(13):5407.
1989: Kennedy J L; Giuffra L A; Moises H W; Wetterberg L; Sjögren B; Cavalli-Sforza L L; Pakstis A J; Kidd J R; Kidd K K
Molecular genetic studies in schizophrenia.
Schizophrenia bulletin 1989;15(3):383-91.
1989: Simpson N E; Kidd K K
The mapping of the locus for multiple endocrine neoplasia type 2A by linkage with chromosome 10 markers.
Hormone and metabolic research. Supplement series 1989;21():5-9.
1988: Wu J; Joseph L; Sukhatme V P; Kidd K K
A HindIII polymorphism identified by the human early growth response gene 2 (EGR2) on chromosome 10.
Nucleic acids research 1988;16(24):11855.
1988: Kennedy J L; Giuffra L A; Moises H W; Cavalli-Sforza L L; Pakstis A J; Kidd J R; Castiglione C M; Sjogren B; Wetterberg L; Kidd K K
Evidence against linkage of schizophrenia to markers on chromosome 5 in a northern Swedish pedigree.
Nature 1988;336(6195):167-70.
1988: Pauls D L; Cohen D J; Kidd K K; Leckman J F
Tourette syndrome and neuropsychiatric disorders: is there a genetic relationship?
American journal of human genetics 1988;43(2):206-17.
1988: Farrer L A; Castiglione C M; Kidd J R; Myers S; Carson N; Simpson N E; Kidd K K
A linkage group of five DNA markers on human chromosome 10.
Genomics 1988;3(1):72-7.
1988: Farrer L A; Bonne-Tamir B; Frydman M; Magazanik A; Kidd K K; Bowcock A M; Cavalli-Sforza L L
Predicting genotypes at loci for autosomal recessive disorders using linked genetic markers: application to Wilson's disease.
Human genetics 1988;79(2):109-17.
1988: Xue F; Kidd J R; Pakstis A J; Castiglione C M; Mallet J; Kidd K K
Tyrosine hydroxylase maps to the short arm of chromosome 11 proximal to the insulin and HRAS1 loci.
Genomics 1988;2(4):288-93.
1988: Miki T; Weil S C; Rosner G L; Reid M S; Kidd K K
An MPO cDNA clone identifies an RFLP with PstI.
Nucleic acids research 1988;16(4):1649.
1988: Merikangas K R; Risch N J; Merikangas J R; Weissman M M; Kidd K K
Migraine and depression: association and familial transmission.
Journal of psychiatric research 1988;22(2):119-29.
1988: Wu J; Ramesh V; Kidd J R; Castiglione C M; Myers S; Carson N; Anderson L; Gusella J F; Simpson N E; Kidd K K
The ornithine aminotransferase (OAT) locus is linked and distal to D10S20 on the long arm of chromosome 10.
Cytogenetics and cell genetics 1988;48(2):126-7.
1988: Giuffra L A; Kennedy J L; Castiglione C M; Evans R M; Wasmuth J J; Kidd K K
Glucocorticoid receptor maps to the distal long arm of chromosome 5.
Cytogenetics and cell genetics 1988;49(4):313-4.
1988: Wu J; Cavenee W K; Miki T; Kidd K K
A polymorphic DNA marker on chromosome 10 linked to RBP3 on the MEN2A side.
Cytogenetics and cell genetics 1988;48(4):246-7.
1988: Kramer P L; Ozelius L; Brin M F; Fahn S; Kidd K K; Gusella J; Breakefield X O
Molecular genetics of an autosomal dominant form of torsion dystonia.
Advances in neurology 1988;50():57-66.
1988: Kidd K K; Kidd J R; Castiglione C M; Sparkes R S; Egeland J A; Bakker E
The anonymous RFLP locus D1S2 is close to PGM1 on chromosome 1.
Human heredity 1988;38(1):22-6.
1987: Murphy P D; Lin P F; Ruddle F H; Kidd K K
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).
Nucleic acids research 1987;15(17):7212.
1987: Bowcock A M; Farrer L A; Cavalli-Sforza L L; Hebert J M; Kidd K K; Frydman M; Bonne-Tamir B
Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13.
American journal of human genetics 1987;41(1):27-35.
1987: Kramer P L; Ozelius L; Gusella J F; Fahn S; Kidd K K; Breakefield X O
Exclusion of autosomal dominant dystonia gene from large regions of chromosomes 11p, 13q, and 21q by multi-point linkage analysis.
Genetic epidemiology 1987;4(5):377-86.
1987: Kidd K K
Research design considerations for linkage studies of affective disorders using recombinant DNA markers.
Journal of psychiatric research 1987;21(4):551-7.
1987: Kidd K K
Searching for major genes for psychiatric disorders.
Ciba Foundation symposium 1987;130():184-96.
1987: Kidd J R; Egeland J A; Pakstis A J; Castiglione C M; Pletcher B A; Morton L A; Kidd K K
Searching for a major genetic locus for affective disorder in the Old Order Amish.
Journal of psychiatric research 1987;21(4):577-80.
1987: Pakstis A J; Kidd J R; Castiglione C M; Pletcher B A; Murphy P D; Farrer L A; Genel M; Kidd K K
One large kindred excludes a locus for multiple endocrine neoplasia type 2A from about 25% of the human autosomal genetic map.
Henry Ford Hospital medical journal 1987;35(2-3):164-7.
1987: Bowcock A M; Farrer L A; Hebert J M; Bonne-Tamir B; Frydman M; Kidd K K; Cavalli-Sforza L L
A new human RFLP identified by 7D2 places D13S10 proximal to esterase D.
Cytogenetics and cell genetics 1987;44(4):236-7.
1986: Murphy P D; Kidd J R; Castiglione C M; Lin P F; Ruddle F H; Kidd K K
A frequent polymorphism for the cytosolic thymidine kinase gene, TK1, (17q21-q22) detected by the enzyme TaqI.
Nucleic acids research 1986;14(10):4381.
1986: Kidd K K; Kidd J R; Castiglione C M; Genel M; Darby J; Cavalli-Sforza L L; Gusella J F
Linkage analyses of multiple endocrine neoplasia, type 2A (MEN-2A) with 20 DNA polymorphisms: 5% of the genome excluded.
Human heredity 1986;36(4):243-9.
1985: Murphy P D; Kidd J R; Breg W R; Ruddle F H; Kidd K K
An anonymous single copy X-chromosome clone, DXS79, from Xq26-Xq28, identifies a moderately frequent RFLP [HGM8 provisional no. DXS79].
Nucleic acids research 1985;13(8):3015.

Sign-in to see more

Sign-in free and Explore the Exciting World of BiomedExperts:

NetworkView

Kenneth Kidd

Research Profile (preview)

Genes & Molecular Sequences

Physiology

Concepts & Ideas

Procedures

Disorders

Occupations

Anatomy

Chemicals & Drugs

Phenomena

Network (preview)

Publications

Sign in free and see...

Visualized networks:

GeoTargeted Searches:

Research Profiles:

Geonetwork of Kenneth Kidd (preview)

All Publications