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Kenneth Kidd

Research Profile

Physiology

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Genes & Molecular Sequences

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Genetics, Population

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Chromosomes, Human, Pair 10

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TOP 3
Michael Krauthammer; Richard P Lifton; Roger S Lo; Shuangge Ma; Shrikant M Mane; Miguel A Materin; James P McCusker; Deepak Narayan; Joseph Schlessinger; David F Stern; Mario Sznol; Stephan Ariyan; Antonella Bacchiocchi; Titus J Boggon; Marcus W Bosenberg; Douglas E Brash; Ana Capatana; Elaine Cheng; Murim Choi; Matthew J Davis; Ken Dutton-Regester; Perry Evans; Gerald Goh; Byung Hak Ha; Nicholas K Hayward; Edna C Holman; Kenneth K Kidd; Harriet M Kluger; Yong Kong; Ruth Halaban
Exome sequencing identifies recurrent somatic RAC1 mutations in melanoma.
Kenneth K Kidd; William C Speed; Rixun Fang; Manohar R Furtado; F C L Hyland; Judith R Kidd; Andrew J Pakstis
Expanding data and resources for forensic use of SNPs in individual identification.
Michael P Donnelly; Elena Grigorenko; David Gurwitz; Sylvester L B Kajuna; Judith R Kidd; Csaba Barta; Jong-Jin Kim; Hui Li; Ru-Band Lu; Vangelis G Manolopoulos; Maria New; Andrew J Pakstis; Peristera Paschou; Marcello Siniscalco; William C Speed; Olga V Zhukova; Kenneth K Kidd
A global view of the OCA2-HERC2 region and pigmentation.

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All Publications

2012: Michael Krauthammer; Richard P Lifton; Roger S Lo; Shuangge Ma; Shrikant M Mane; Miguel A Materin; James P McCusker; Deepak Narayan; Joseph Schlessinger; David F Stern; Mario Sznol; Stephan Ariyan; Antonella Bacchiocchi; Titus J Boggon; Marcus W Bosenberg; Douglas E Brash; Ana Capatana; Elaine Cheng; Murim Choi; Matthew J Davis; Ken Dutton-Regester; Perry Evans; Gerald Goh; Byung Hak Ha; Nicholas K Hayward; Edna C Holman; Kenneth K Kidd; Harriet M Kluger; Yong Kong; Ruth Halaban
Exome sequencing identifies recurrent somatic RAC1 mutations in melanoma.
Nature genetics 2012;44(9):1006-14.
2012: Kenneth K Kidd; William C Speed; Rixun Fang; Manohar R Furtado; F C L Hyland; Judith R Kidd; Andrew J Pakstis
Expanding data and resources for forensic use of SNPs in individual identification.
Forensic science international. Genetics 2012;6(5):646-52.
2012: Michael P Donnelly; Elena Grigorenko; David Gurwitz; Sylvester L B Kajuna; Judith R Kidd; Csaba Barta; Jong-Jin Kim; Hui Li; Ru-Band Lu; Vangelis G Manolopoulos; Maria New; Andrew J Pakstis; Peristera Paschou; Marcello Siniscalco; William C Speed; Olga V Zhukova; Kenneth K Kidd
A global view of the OCA2-HERC2 region and pigmentation.
Human genetics 2012;131(5):683-96.
2012: Haseena Rajeevan; Usha Soundararajan; Andrew J Pakstis; Kenneth K Kidd
Introducing the Forensic Research/Reference on Genetics knowledge base, FROG-kb.
Investigative genetics 2012;3(1):18.
2011: Judith R Kidd; Rixun Fang; Françoise R Friedlaender; Manohar R Furtado; Caroline M Nievergelt; Andrew J Pakstis; Xudong Wang; Kenneth K Kidd
Single nucleotide polymorphisms and haplotypes in Native American populations.
American journal of physical anthropology 2011;146(4):495-502.
2011: Hui Li; Andrew J Pakstis; Zhi Xu; Sheng Gu; Yi Han; Li Jin; Judith R Kidd; Kenneth K Kidd
Diversification of the ADH1B gene during expansion of modern humans.
Annals of human genetics 2011;75(4):497-507.
2011: Hui Li; Andrew J Pakstis; Judith R Kidd; Kenneth K Kidd
Selection on the human bitter taste gene, TAS2R16, in Eurasian populations.
Human biology 2011;83(3):363-77.
2011: Dean Palejev; Wookyeon Hwang; Nicole Landi; Maria Eastman; Stephen J Frost; Robert K Fulbright; Judith R Kidd; Kenneth K Kidd; Graeme F Mason; W Einar Mencl; Carolyn Yrigollen; Kenneth R Pugh; Elena L Grigorenko
An application of the elastic net for an endophenotype analysis.
Behavior genetics 2011;41(1):120-4.
2011: Judith R Kidd; Françoise R Friedlaender; William C Speed; Andrew J Pakstis; Francisco M De La Vega; Kenneth K Kidd
Analyses of a set of 128 ancestry informative single-nucleotide polymorphisms in a global set of 119 population samples.
Investigative genetics 2011;2(1):1.
2011: Cory Pelletier; William C Speed; Trupti Paranjape; Katie Keane; Rachel Blitzblau; Antoinette Hollestelle; Kyan Safavi; Ans van den Ouweland; Daniel Zelterman; Frank J Slack; Kenneth K Kidd; Joanne B Weidhaas
Rare BRCA1 haplotypes including 3'UTR SNPs associated with breast cancer risk.
Cell cycle (Georgetown, Tex.) 2011;10(1):90-9.
2010: Andrew J Pakstis; William C Speed; Rixun Fang; Fiona C L Hyland; Manohar R Furtado; Judith R Kidd; Kenneth K Kidd
SNPs for a universal individual identification panel.
Human genetics 2010;127(3):315-24.
2010: Michael P Donnelly; Peristera Paschou; Elena L Grigorenko; David Gurwitz; S Qasim Mehdi; Sylvester L B Kajuna; Csaba Barta; Selemani Kungulilo; N J Karoma; Ru-Band Lu; Olga V Zhukova; Jong-Jin Kim; David Comas; Marcello Siniscalco; Maria New; Peining Li; Hui Li; Vangelis G Manolopoulos; William C Speed; Haseena Rajeevan; Andrew J Pakstis; Judith R Kidd; Kenneth K Kidd
The distribution and most recent common ancestor of the 17q21 inversion in humans.
American journal of human genetics 2010;86(2):161-71.
2010: Namita Mukherjee; Kenneth K Kidd; Andrew J Pakstis; William C Speed; Hui Li; Z Tarnok; Csaba Barta; Sylvester L B Kajuna; Judith R Kidd
The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase.
Molecular psychiatry 2010;15(2):216-25.
2010: Laura F Mustavich; Perry Miller; Kenneth K Kidd; Hongyu Zhao
Using a pharmacokinetic model to relate an individual's susceptibility to alcohol dependence to genotypes.
Human heredity 2010;70(3):177-93.
2010: Wang Pei; Alice Y N Ha; Kenneth K Kidd; Michael S Koehle; Jim L Rupert
A variant of the endothelial nitric oxide synthase gene (NOS3) associated with AMS susceptibility is less common in the Quechua, a high altitude Native population.
High altitude medicine & biology 2010;11(1):27-30.
2009: William C Speed; Soonmo Peter Kang; David Tuck; Lyndsay N Harris; Kenneth K Kidd
Global variation in CYP2C8-CYP2C9 functional haplotypes.
The pharmacogenomics journal 2009;9(4):283-90.
2009: Hui Li; Svetlana Borinskaya; Kimio Yoshimura; Nina Kal'ina; Andrey Marusin; Vadim A Stepanov; Zhendong Qin; Shagufta Khaliq; Mi-Young Lee; Yajun Yang; Aisha Mohyuddin; David Gurwitz; S Qasim Mehdi; Evgeny I Rogaev; L Jin; Nikolay K Yankovsky; Judith R Kidd; Kenneth K Kidd
Refined geographic distribution of the oriental ALDH2*504Lys (nee 487Lys) variant.
Annals of human genetics 2009;73(Pt 3):335-45.
2009: Jennifer Yamtich; William C Speed; Eva Straka; Judith R Kidd; Joann B Sweasy; Kenneth K Kidd
Population-specific variation in haplotype composition and heterozygosity at the POLB locus.
DNA repair 2009;8(5):579-84.
2009: Matthew E Holford; Haseena Rajeevan; Hongyu Zhao; Kenneth K Kidd; Kei-Hoi Cheung
Semantic Web-based integration of cancer pathways and allele frequency data.
Cancer informatics 2009;8():19-30.
2008: Lena J Chin; Elena Ratner; Shuguang Leng; Rihong Zhai; Sunitha Nallur; Imran Babar; Roman-Ulrich Muller; Eva Straka; Li Su; Elizabeth A Burki; Richard E Crowell; Rajeshvari Patel; Trupti Kulkarni; Robert Homer; Daniel Zelterman; Kenneth K Kidd; Yong Zhu; David C Christiani; Steven A Belinsky; Frank J Slack; Joanne B Weidhaas
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: M-Y Lee; N Mukherjee; Andrew J Pakstis; Shagufta Khaliq; Aisha Mohyuddin; S Q Mehdi; William C Speed; Judith R Kidd; Kenneth K Kidd
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: William C Speed; Brian J O'Roak; Zsanett Tárnok; Csaba Barta; Andrew J Pakstis; Sate Matthew; Kenneth K Kidd
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: Hui Li; Sheng Gu; Xiaoyun Cai; William C Speed; Andrew J Pakstis; Efim I Golub; Judith R Kidd; Kenneth K Kidd
Ethnic related selection for an ADH Class I variant within East Asia.
PloS one 2008;3(4):e1881.
2008: Hussam Al-Kateb; Andrew P Boright; Lucia Mirea; Xinlei Xie; Rinku Sutradhar; Alireza Mowjoodi; Bhupinder Bharaj; Michelle Liu; Jean M Bucksa; Valerie L Arends; Michael W Steffes; Patricia A Cleary; Wanjie Sun; John M Lachin; Paul S Thorner; Michael Ho; Amy Jayne McKnight; A Peter Maxwell; David A Savage; Kenneth K Kidd; Judith R Kidd; William C Speed; Trevor J Orchard; Rachel G Miller; Lei Sun; Shelley B Bull; Andrew D Paterson
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.
2007: Hui Li; Namita Mukherjee; Usha Soundararajan; Zsanett Tarnok; Csaba Barta; Shagufta Khaliq; Aisha Mohyuddin; Sylvester L B Kajuna; S Qasim Mehdi; Judith R Kidd; Kenneth K Kidd
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: Andrew J Pakstis; William C Speed; Judith R Kidd; Kenneth K Kidd
Candidate SNPs for a universal individual identification panel.
Human genetics 2007;121(3-4):305-17.
2007: Hiroki Oota; Casey W Dunn; William C Speed; Andrew J Pakstis; Meg A Palmatier; Judith R Kidd; Kenneth K Kidd
Conservative evolution in duplicated genes of the primate Class I ADH cluster.
Gene 2007;392(1-2):64-76.
2007: Yi Han; Sheng Gu; Hiroki Oota; Michael V Osier; Andrew J Pakstis; William C Speed; Judith R Kidd; Kenneth K Kidd
Evidence of positive selection on a class I ADH locus.
American journal of human genetics 2007;80(3):441-56.
2007: Sheng Gu; Andrew J Pakstis; Hui Li; William C Speed; Judith R Kidd; Kenneth K Kidd
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: Kaori Nakamoto; Judith R Kidd; Robert D Jenison; Curtis D Klaassen; Yu-Jui Yvonne Wan; Kenneth K Kidd; Xiao-bo Zhong
Genotyping and haplotyping of CYP2C19 functional alleles on thin-film biosensor chips.
Pharmacogenetics and genomics 2007;17(2):103-14.
2007: Peristera Paschou; Michael W Mahoney; Asif Javed; Judith R Kidd; Andrew J Pakstis; Sheng Gu; Kenneth K Kidd; Petros Drineas
Intra- and interpopulation genotype reconstruction from tagging SNPs.
Genome research 2007;17(1):96-107.
2006: Kenneth K Kidd; Andrew J Pakstis; William C Speed; Elena L Grigorenko; Sylvester L B Kajuna; Nganyirwa J Karoma; Selemani Kungulilo; Jong-Jin Kim; Ru-Band Lu; Adekunle Odunsi; Friday Okonofua; Josef Parnas; Leslie O Schulz; Olga V Zhukova; Judith R Kidd
Developing a SNP panel for forensic identification of individuals.
Forensic science international 2006;164(1):20-32.
2006: Leslie O Schulz; Peter H Bennett; Eric Ravussin; Judith R Kidd; Kenneth K Kidd; Julian Esparza; Mauro E Valencia
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: David Fredman; Sarah L Sawyer; Linda Strömqvist; Salim Mottagui-Tabar; Kenneth K Kidd; Claes Wahlestedt; STEPHEN CHANOCK; Anthony J Brookes
Nonsynonymous SNPs: validation characteristics, derived allele frequency patterns, and suggestive evidence for natural selection.
Human mutation 2006;27(2):173-86.
2005: Yi Han; Hiroki Oota; Michael V Osier; Andrew J Pakstis; William C Speed; Adekunle Odunsi; Friday Okonofua; Sylvester L B Kajuna; Nganyirwa J Karoma; Selemani Kungulilo; Elena L Grigorenko; Olga V Zhukova; Batsheva Bonne-Tamir; Ru-Band Lu; Josef Parnas; Leslie O Schulz; Judith R Kidd; Kenneth K Kidd
Considerable haplotype diversity within the 23kb encompassing the ADH7 gene.
Alcoholism, clinical and experimental research 2005;29(12):2091-100.
2005: Sheng Gu; Andrew J Pakstis; Kenneth K Kidd
HAPLOT: a graphical comparison of haplotype blocks, tagSNP sets and SNP variation for multiple populations.
Bioinformatics (Oxford, England) 2005;21(20):3938-9.
2005: Jong-Jin Kim; Paul Verdu; Andrew J Pakstis; William C Speed; Judith R Kidd; Kenneth K Kidd
Use of autosomal loci for clustering individuals and populations of East Asian origin.
Human genetics 2005;117(6):511-9.
2005: Sarah L Sawyer; Namita Mukherjee; Andrew J Pakstis; Lars Feuk; Judith R Kidd; Anthony J Brookes; Kenneth K Kidd
Linkage disequilibrium patterns vary substantially among populations.
European journal of human genetics : EJHG 2005;13(5):677-86.
2005: Haseena Rajeevan; Kei-Hoi Cheung; Rohit Gadagkar; Shannon Stein; Usha Soundararajan; Judith R Kidd; Andrew J Pakstis; Perry L Miller; Kenneth K Kidd
ALFRED: an allele frequency database for microevolutionary studies.
Evolutionary bioinformatics online 2005;1():1-10.
2005: Robert J Sternberg; Elena L Grigorenko; Kenneth K Kidd
Intelligence, race, and genetics.
The American psychologist 2005;60(1):46-59.
2004: Nianjun Liu; Sarah L Sawyer; Namita Mukherjee; Andrew J Pakstis; Judith R Kidd; Kenneth K Kidd; Anthony J Brookes; Hongyu Zhao
Haplotype block structures show significant variation among populations.
Genetic epidemiology 2004;27(4):385-400.
2004: Valerie B Duffy; Andrew C Davidson; Judith R Kidd; Kenneth K Kidd; William C Speed; Andrew J Pakstis; Danielle R Reed; Derek J Snyder; Linda M Bartoshuk
Bitter receptor gene (TAS2R38), 6-n-propylthiouracil (PROP) bitterness and alcohol intake.
Alcoholism, clinical and experimental research 2004;28(11):1629-37.
2004: Sarah A Tishkoff; Kenneth K Kidd
Implications of biogeography of human populations for 'race' and medicine.
Nature genetics 2004;36(11 Suppl):S21-7.
2004: Peristera Paschou; Y Feng; Andrew J Pakstis; William C Speed; Mellissa M C DeMille; Judith R Kidd; B Jaghori; Roger Kurlan; David L Pauls; Paul Sandor; Cathy L Barr; Kenneth K Kidd
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: Kenneth K Kidd; Andrew J Pakstis; William C Speed; Judith R Kidd
Understanding human DNA sequence variation.
The Journal of heredity 2004;95(5):406-20.
2004: Meg A Palmatier; Andrew J Pakstis; William C Speed; Peristera Paschou; David Goldman; Adekunle Odunsi; Friday Okonofua; Sylvester L B Kajuna; Nganyirwa J Karoma; Selemani Kungulilo; Elena L Grigorenko; Olga V Zhukova; Batsheva Bonne-Tamir; Ru-Band Lu; Josef Parnas; Judith R Kidd; Mellissa M C DeMille; Kenneth K Kidd
COMT haplotypes suggest P2 promoter region relevance for schizophrenia.
Molecular psychiatry 2004;9(9):859-70.
2004: Michael I Jensen-Seaman; Esteban E Sarmiento; Amos S Deinard; Kenneth K Kidd
Nuclear integrations of mitochondrial DNA in gorillas.
American journal of primatology 2004;63(3):139-47.
2004: E Wang; Yuan-Chun Ding; Pamela Flodman; J R Kidd; Kenneth K Kidd; Deborah L Grady; Oliver Ryder; M Anne Spence; James M Swanson; Robert K Moyzis
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: Michael V Osier; Ru-Band Lu; Andrew J Pakstis; Judith R Kidd; S-Y Huang; Kenneth K Kidd
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: Hiroki Oota; Andrew J Pakstis; Batsheva Bonne-Tamir; David Goldman; Elena L Grigorenko; Sylvester L B Kajuna; Nganyirwa J Karoma; Selemani Kungulilo; Ru-Band Lu; Kunle Odunsi; Friday Okonofua; Olga V Zhukova; Judith R Kidd; Kenneth K Kidd
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: Pratima Chattopadhyay; Andrew J Pakstis; Namita Mukherjee; Sudha Iyengar; Adekunle Odunsi; Friday Okonofua; Batsheva Bonne-Tamir; William C Speed; Judith R Kidd; Kenneth K Kidd
Global survey of haplotype frequencies and linkage disequilibrium at the RET locus.
European journal of human genetics : EJHG 2003;11(10):760-9.
2003: Xiao-bo Zhong; Robert Reynolds; Judith R Kidd; Kenneth K Kidd; Robert D Jenison; Richard A Marlar; David C Ward
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: Ning Yu; Michael I Jensen-Seaman; Leona Chemnick; Judith R Kidd; Amos S Deinard; Oliver Ryder; Kenneth K Kidd; Wen-Hsiung Li
Low nucleotide diversity in chimpanzees and bonobos.
Genetics 2003;164(4):1511-8.
2003: H Rajeevan; Michael V Osier; Kei-Hoi Cheung; H Deng; L Druskin; R Heinzen; Judith R Kidd; S Stein; Andrew J Pakstis; Nick Tosches; C-C Yeh; Perry L Miller; Kenneth K Kidd
ALFRED: the ALelle FREquency Database. Update.
Nucleic acids research 2003;31(1):270-1.
2003: Shuang Wang; Kenneth K Kidd; Hongyu Zhao
On the use of DNA pooling to estimate haplotype frequencies.
Genetic epidemiology 2003;24(1):74-82.
2003: James F Leckman; David L Pauls; Heping Zhang; Maria Conceição Rosario-Campos; Liliya Katsovich; Kenneth K Kidd; Andrew J Pakstis; John Alsobrook; Mary M Robertson; William M McMahon; John T Walkup; Ben J M van de Wetering; Robert A King; Donald J Cohen
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: Michael V Osier; Andrew J Pakstis; David Goldman; Howard J Edenberg; Judith R Kidd; Kenneth K Kidd
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: Mellissa M C DeMille; Judith R Kidd; Valeria Ruggeri; Meg A Palmatier; David Goldman; Adekunle Odunsi; Friday Okonofua; Elena L Grigorenko; Leslie O Schulz; Batsheva Bonne-Tamir; Ru-Band Lu; Josef Parnas; Andrew J Pakstis; Kenneth K Kidd
Population variation in linkage disequilibrium across the COMT gene considering promoter region and coding region variation.
Human genetics 2002;111(6):521-37.
2002: Michael V Osier; Kei-Hoi Cheung; Judith R Kidd; Andrew J Pakstis; Perry L Miller; Kenneth K Kidd
ALFRED: An allele frequency database for anthropology.
American journal of physical anthropology 2002;119(1):77-83.
2002: Michael V Osier; Andrew J Pakstis; Himla Soodyall; David Comas; David Goldman; Adekunle Odunsi; Friday Okonofua; Josef Parnas; Leslie O Schulz; Jaume Bertranpetit; Batsheva Bonne-Tamir; Ru-Band Lu; Judith R Kidd; Kenneth K Kidd
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: Stephanie M Fullerton; Angelika Bartoszewicz; Gustavo Ybazeta; Yukio Horikawa; Graeme I Bell; Kenneth K Kidd; Nancy J Cox; Richard R Hudson; Anna Di Rienzo
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: Heping Zhang; James F Leckman; David L Pauls; Chin-Pei Tsai; Kenneth K Kidd; M Rosario Campos
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: Yuan-Chun Ding; Han-Chang Chi; Deborah L Grady; Atsuyuki Morishima; Judith R Kidd; Kenneth K Kidd; Pamela Flodman; M Anne Spence; Sabrina Schuck; James M Swanson; Ya-Ping Zhang; Robert K Moyzis
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: Michael I Jensen-Seaman; Amos S Deinard; Kenneth K Kidd
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: Geoffrey Turner; M Barbulescu; M Su; Michael I Jensen-Seaman; Kenneth K Kidd; Jack Lenz
Insertional polymorphisms of full-length endogenous retroviruses in humans.
Current biology : CB 2001;11(19):1531-5.
2001: Michael I Jensen-Seaman; Kenneth K Kidd
Mitochondrial DNA variation and biogeography of eastern gorillas.
Molecular ecology 2001;10(9):2241-7.
2001: M Barbulescu; Geoffrey Turner; M Su; R Kim; Michael I Jensen-Seaman; Amos S Deinard; Kenneth K Kidd; Jack Lenz
A HERV-K provirus in chimpanzees, bonobos and gorillas, but not humans.
Current biology : CB 2001;11(10):779-83.
2001: Michael V Osier; Kei-Hoi Cheung; Judith R Kidd; Andrew J Pakstis; Perry L Miller; Kenneth K Kidd
ALFRED: an allele frequency database for diverse populations and DNA polymorphisms--an update.
Nucleic acids research 2001;29(1):317-9.
2001: Francesc Calafell; Elena L Grigorenko; A A Chikanian; Kenneth K Kidd
Haplotype evolution and linkage disequilibrium: A simulation study.
Human heredity 2001;51(1-2):85-96.
2000: Sarah A Tishkoff; Andrew J Pakstis; M Stoneking; Judith R Kidd; Giovanni Destro-Bisol; A Sanjantila; Ru-Band Lu; Amos S Deinard; Giorgio Sirugo; T Jenkins; Kenneth K Kidd; andrew clark
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: Hongyu Zhao; S Zhang; Kathleen Ries Merikangas; Mátyás Trixler; Dieter B Wildenauer; F Sun; Kenneth K Kidd
Transmission/disequilibrium tests using multiple tightly linked markers.
American journal of human genetics 2000;67(4):936-46.
2000: Sarah A Tishkoff; Andrew J Pakstis; G Ruano; Kenneth K Kidd
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: Judith R Kidd; Andrew J Pakstis; Hongyu Zhao; Ru-Band Lu; Friday Okonofua; Adekunle Odunsi; Elena L Grigorenko; B B Tamir; J Friedlaender; Leslie O Schulz; Josef Parnas; Kenneth K Kidd
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: MI Seaman; F M Chang; A T Quiñones; Kenneth K Kidd
Evolution of exon 1 of the dopamine D4 receptor (DRD4) gene in primates.
The Journal of experimental zoology 2000;288(1):32-8.
2000: Kei-Hoi Cheung; Perry L Miller; Judith R Kidd; Kenneth K Kidd; Michael V Osier; Andrew J Pakstis
ALFRED: a Web-accessible allele frequency database.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing 2000;():639-50.
2000: Kei-Hoi Cheung; Michael V Osier; Judith R Kidd; Andrew J Pakstis; Perry L Miller; Kenneth K Kidd
ALFRED: an allele frequency database for diverse populations and DNA polymorphisms.
Nucleic acids research 2000;28(1):361-3.
1999: MI Seaman; J B Fisher; F Chang; Kenneth K Kidd
Tandem duplication polymorphism upstream of the dopamine D4 receptor gene (DRD4).
American journal of medical genetics 1999;88(6):705-9.
1999: Hongyu Zhao; Kathleen Ries Merikangas; Kenneth K Kidd
On a randomization procedure in linkage analysis.
American journal of human genetics 1999;65(5):1449-56.
1999: M Barbulescu; Geoffrey Turner; MI Seaman; Amos S Deinard; Kenneth K Kidd; Jack Lenz
Many human endogenous retrovirus K (HERV-K) proviruses are unique to humans.
Current biology : CB 1999;9(16):861-8.
1999: Cathy L Barr; Karen Wigg; Andrew J Pakstis; Roger Kurlan; David L Pauls; Kenneth K Kidd; Lap-Chee Tsui; Paul Sandor
Genome scan for linkage to Gilles de la Tourette syndrome.
American journal of medical genetics 1999;88(4):437-45.
1999: Meg A Palmatier; AM Kang; Kenneth K Kidd
Global variation in the frequencies of functionally different catechol-O-methyltransferase alleles.
Biological psychiatry 1999;46(4):557-67.
1999: AM Kang; Meg A Palmatier; Kenneth K Kidd
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: Michael V Osier; Andrew J Pakstis; Judith R Kidd; J F Lee; Shih-Jiun Yin; Huei-Chen Ko; Howard J Edenberg; Ru-Band Lu; Kenneth K Kidd
Linkage disequilibrium at the ADH2 and ADH3 loci and risk of alcoholism.
American journal of human genetics 1999;64(4):1147-57.
1999: Hongyu Zhao; Andrew J Pakstis; Judith R Kidd; Kenneth K Kidd
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: Francesc Calafell; A Shuster; William C Speed; Judith R Kidd; F L Black; Kenneth K Kidd
Genealogy reconstruction from short tandem repeat genotypes in an Amazonian population.
American journal of physical anthropology 1999;108(2):137-46.
1999: Hongyu Zhao; L J Sheffield; Andrew J Pakstis; Melissa P Knauert; Kenneth K Kidd
A more powerful method to evaluate p-values in GENEHUNTER.
Genetic epidemiology 1999;17 Suppl 1():S415-20.
1999: L J Sheffield; Melissa P Knauert; Andrew J Pakstis; Hongyu Zhao; Kenneth K Kidd
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: Amos S Deinard; Giorgio Sirugo; Kenneth K Kidd
Hominoid phylogeny: inferences from a sub-terminal minisatellite analyzed by repeat expansion detection (RED)
Journal of human evolution 1998;35(3):313-7.
1998: Kenneth K Kidd; Bharti Morar; CM Castiglione; H Zhao; Andrew J Pakstis; William C Speed; Batsheva Bonne-Tamir; Ru-Band Lu; David Goldman; C Lee; Y S Nam; David K Grandy; T Jenkins; Judith R Kidd
A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus.
Human genetics 1998;103(2):211-27.
1998: Sarah A Tishkoff; A Goldman; Francesc Calafell; William C Speed; Amos S Deinard; Batsheva Bonne-Tamir; Judith R Kidd; Andrew J Pakstis; T Jenkins; Kenneth K Kidd
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: S Iyengar; MI Seaman; Amos S Deinard; H C Rosenbaum; Giorgio Sirugo; CM Castiglione; Judith R Kidd; Kenneth K Kidd
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: Amos S Deinard; Kenneth K Kidd
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.
1998: Francesc Calafell; A Shuster; William C Speed; Judith R Kidd; Kenneth K Kidd
Short tandem repeat polymorphism evolution in humans.
European journal of human genetics : EJHG 1998;6(1):38-49.
1997: TS Breschel; Melvin G McInnis; Russell L Margolis; Giorgio Sirugo; B Corneliussen; Sylvia G Simpson; Francis McMajon; Dean F MacKinnon; Jianfeng Xu; N Pleasant; Yuqing Huo; Roxann Ashworth; C Grundstrom; T Grundstrom; Kenneth K Kidd; J. Raymond DePaulo; Christopher A Ross
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: Giorgio Sirugo; Andrew J Pakstis; Kenneth K Kidd; Steven Matthysse; Deborah L Levy; Philip S Holzman; J Párnas; Melvin G McInnis; TS Breschel; Christopher A Ross
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: S Iyengar; H Kalinsky; S Weiss; Michael Korostishevsky; M Sadeh; Y Zhao; Kenneth K Kidd; Batsheva Bonne-Tamir
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: Giorgio Sirugo; Amos S Deinard; Judith R Kidd; Kenneth K Kidd
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: F M Chang; Kenneth K Kidd
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: F M Chang; H C Ko; Ru-Band Lu; Andrew J Pakstis; Kenneth K Kidd
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: Daiqing Liao; T Pavelitz; Judith R Kidd; Kenneth K Kidd; Alan M Weiner
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: S Iyengar; Francesc Calafell; Kenneth K Kidd
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: S Michalatos-Beloin; S A Tishkoff; K L Bentley; Kenneth K Kidd; G Ruano
Molecular haplotyping of genetic markers 10 kb apart by allele-specific long-range PCR.
Nucleic acids research 1996;24(23):4841-3.
1996: J R Gill; M Reyes-Múgica; S Iyengar; Kenneth K Kidd; Robert J Touloukian; C Smith; MS Keller; M Genel
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: D E Grice; James F Leckman; David L Pauls; Roger Kurlan; Kenneth K Kidd; Andrew J Pakstis; F M Chang; Joseph Buxbaum; D J Cohen; Joel Gelernter
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: Kei-Hoi Cheung; Prakash M Nadkarni; S Silverstein; J R Kidd; Andrew J Pakstis; Perry Miller; Kenneth K Kidd
PhenoDB: an integrated client/server database for linkage and population genetics.
Computers and biomedical research, an international journal 1996;29(4):327-37.
1996: F M Chang; Judith R Kidd; K J Livak; Andrew J Pakstis; Kenneth K Kidd
The world-wide distribution of allele frequencies at the human dopamine D4 receptor locus.
Human genetics 1996;98(1):91-101.
1996: Kenneth K Kidd; Andrew J Pakstis; C M Castiglione; Judith R Kidd; William C Speed; David Goldman; W C Knowler; Ru-Band Lu; Batsheva Bonne-Tamir
DRD2 haplotypes containing the TaqI A1 allele: implications for alcoholism research.
Alcoholism, clinical and experimental research 1996;20(4):697-705.
1996: S A Tishkoff; G Ruano; Judith R Kidd; Kenneth K Kidd
Distribution and frequency of a polymorphic Alu insertion at the plasminogen activator locus in humans.
Human genetics 1996;97(6):759-64.
1996: Ru-Band Lu; Huei-Chen Ko; F M Chang; C M Castiglione; G Schoolfield; Andrew J Pakstis; J R Kidd; Kenneth K Kidd
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: Prakash M Nadkarni; Kei-Hoi Cheung; C Castiglione; Perry Miller; Kenneth K Kidd
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: Joel Gelernter; D Vandenbergh; S D Kruger; David L Pauls; Roger Kurlan; Andrew J Pakstis; Kenneth K Kidd; George R. Uhl
The dopamine transporter protein gene (SLC6A3): primary linkage mapping and linkage studies in Tourette syndrome.
Genomics 1995;30(3):459-63.
1995: Perry L Miller; Prakash M Nadkarni; Kenneth K Kidd; K Cheung; David C Ward; A Banks; Patricia Bray-Ward; L Cupelli; V Herdman; I Marondel; K Montgomery; B Renault; S J Yoon; K S Krauter; Raju Kucherlapati
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: Clinton T Baldwin; S Weiss; Lindsay A Farrer; A L De Stefano; R Adair; B Franklyn; Kenneth K Kidd; Michael Korostishevsky; B Bonné-Tamir
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: Joel Gelernter; P A Rao; David L Pauls; M W Hamblin; David R Sibley; Kenneth K Kidd
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: L W Wright; Jay Lichter; John Reinitz; M A Shifman; Kenneth K Kidd; Perry L Miller
Computer-assisted restriction mapping: an integrated approach to handling experimental uncertainty.
Computer applications in the biosciences : CABIOS 1994;10(4):435-42.
1994: G Ruano; Amos S Deinard; S Tishkoff; Kenneth K Kidd
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: Cathy L Barr; James L Kennedy; Andrew J Pakstis; C M Castiglione; Judith R Kidd; L Wetterberg; Kenneth K Kidd
Linkage study of a susceptibility locus for schizophrenia in the pseudoautosomal region.
Schizophrenia bulletin 1994;20(2):277-86.
1993: Cathy L Barr; James L Kennedy; Jay Lichter; Hubert H M Van Tol; L Wetterberg; K J Livak; Kenneth K Kidd
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: Joel Gelernter; S Kruger; Andrew J Pakstis; T Pacholczyk; R S Sparkes; Kenneth K Kidd; Susan Amara
Assignment of the norepinephrine transporter protein (NET1) locus to chromosome 16.
Genomics 1993;18(3):690-2.
1993: A R Brooks-Wilson; Jay Lichter; David C Ward; Kenneth K Kidd; Paul J Goodfellow
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: Cathy L Barr; Kenneth K Kidd
Population frequencies of the A1 allele at the dopamine D2 receptor locus.
Biological psychiatry 1993;34(4):204-9.
1993: Jay Lichter; Cathy L Barr; James L Kennedy; Hubert H M Van Tol; Kenneth K Kidd; K J Livak
A hypervariable segment in the human dopamine receptor D4 (DRD4) gene.
Human molecular genetics 1993;2(6):767-73.
1993: Joel Gelernter; S Kruger; Kenneth K Kidd; Susan Amara
TaqI RFLP at norepinephrine transporter protein (NET) locus.
Human molecular genetics 1993;2(6):820.
1993: Jay Lichter; M J Difilippantonio; Andrew J Pakstis; Paul J Goodfellow; David C Ward; Kenneth K Kidd
Physical and genetic maps for chromosome 10.
Genomics 1993;16(2):320-4.
1993: J Rogers; Kenneth K Kidd
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: Jay Lichter; J Wu; A R Brooks-Wilson; M Difillipantonio; S Brewster; David C Ward; Paul J Goodfellow; Kenneth K Kidd
A new polymorphic marker (D10S97) tightly linked to the multiple endocrine neoplasia type 2A (MEN2A) locus.
Human genetics 1993;90(5):516-20.
1992: G Ruano; Kenneth K Kidd
Modeling of heteroduplex formation during PCR from mixtures of DNA templates.
PCR methods and applications 1992;2(2):112-6.
1992: Jay Lichter; J Wu; D Miller; Paul J Goodfellow; Kenneth K Kidd
A high-resolution meiotic mapping panel for the pericentromeric region of chromosome 10.
Genomics 1992;13(3):607-12.
1992: D L Miller; F J Dill; Jay Lichter; Kenneth K Kidd; Paul J Goodfellow
Isolation and high-resolution mapping of new DNA markers from the pericentromeric region of chromosome 10.
Genomics 1992;13(3):601-6.
1992: G Ruano; J Rogers; A C Ferguson-Smith; Kenneth K Kidd
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: Joel Gelernter; James L Kennedy; Hubert H M Van Tol; Olivier Civelli; Kenneth K Kidd
The D4 dopamine receptor (DRD4) maps to distal 11p close to HRAS.
Genomics 1992;13(1):208-10.
1992: Amos S Deinard; G Ruano; Kenneth K Kidd
A dinucleotide repeat polymorphism at the HOX2B locus.
Nucleic acids research 1992;20(5):1171.
1992: Jay Lichter; J S Wu; M Genel; Stuart D Flynn; Andrew J Pakstis; Judith R Kidd; Kenneth K Kidd
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: Jay Lichter; M Difilippantonio; J Wu; D Miller; David C Ward; Paul J Goodfellow; Kenneth K Kidd
Localization of the gene for MEN 2A.
Henry Ford Hospital medical journal 1992;40(3-4):199-204.
1992: Joel Gelernter; Andrew J Pakstis; David K Grandy; M Litt; A E Retief; James L Kennedy; A Hing-Loh; G Schoolfield; Olivier Civelli; Kenneth K Kidd
Linkage map of eight human chromosome 11q markers, including DRD2, spanning 60 cM.
Cytogenetics and cell genetics 1992;60(1):26-8.
1991: G Ruano; Kenneth K Kidd
Genotyping and haplotyping of polymorphisms directly from genomic DNA via coupled amplification and sequencing (CAS).
Nucleic acids research 1991;19(24):6877-82.
1991: J Hästbacka; Pertti Sistonen; Ilkka Kaitila; B Weiffenbach; Kenneth K Kidd; Albert de La Chapelle
A linkage map spanning the locus for diastrophic dysplasia (DTD).
Genomics 1991;11(4):968-73.
1991: Joel Gelernter; Stephanie O'Malley; N Risch; H R Kranzler; John H Krystal; Kathleen Ries Merikangas; James L Kennedy; Kenneth K Kidd
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: Andrew J Pakstis; Judith R Kidd; C M Castiglione; Kenneth K Kidd
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: H W Moises; Joel Gelernter; L A Giuffra; V Zarcone; L Wetterberg; Olivier Civelli; Kenneth K Kidd; L L Cavalli-Sforza; David K Grandy; James L Kennedy
No linkage between D2 dopamine receptor gene region and schizophrenia.
Archives of general psychiatry 1991;48(7):643-7.
1991: Perry L Miller; Prakash M Nadkarni; Joel Gelernter; N Carriero; Andrew J Pakstis; Kenneth K Kidd
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: Joel Gelernter; Pablo V Gejman; S Bisighini; Kenneth K Kidd
Sequence tagged site (STS) TaqI RFLP at dopamine beta-hydroxylase (DBH).
Nucleic acids research 1991;19(8):1957.
1991: T Ogura; C M Castiglione; Andrew J Pakstis; Kenneth K Kidd
An MspI polymorphism for the HOX2F gene.
Nucleic acids research 1991;19(7):1716.
1991: T Ogura; C M Castiglione; Andrew J Pakstis; Kenneth K Kidd
Two RFLPs at the HOX2G locus.
Nucleic acids research 1991;19(7):1716.
1991: G Ruano; Kenneth K Kidd
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: Joel Gelernter; Kenneth K Kidd
The current status of linkage studies in schizophrenia.
Research publications - Association for Research in Nervous and Mental Disease 1991;69():137-52.
1991: Perry L Miller; M A Shifman; Kenneth K Kidd
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: N L Carson; J S Wu; C E Jackson; Kenneth K Kidd; N E Simpson
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: C R Dudley; L A Giuffra; P Tippett; Kenneth K Kidd; S T Reeders
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: Joel Gelernter; Andrew J Pakstis; David L Pauls; Roger Kurlan; S T Gancher; Olivier Civelli; David K Grandy; Kenneth K Kidd
Gilles de la Tourette syndrome is not linked to D2-dopamine receptor.
Archives of general psychiatry 1990;47(11):1073-7.
1990: J S Wu; Kenneth K Kidd
A HaeIII polymorphism at the D10S101 locus.
Nucleic acids research 1990;18(18):5577.
1990: J Wu; Kenneth K Kidd
HincII polymorphism at the D10S95 locus.
Nucleic acids research 1990;18(16):4965.
1990: G Ruano; Kenneth K Kidd; J C Stephens
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: J S Wu; Kenneth K Kidd
High frequency PvuII and PstI polymorphisms identified by KW31 (D10S96) on chromosome 10.
Nucleic acids research 1990;18(5):1316.
1990: J S Wu; Kenneth K Kidd
An EcoRI polymorphism identified by KW6 (D10S97) on chromosome 10.
Nucleic acids research 1990;18(5):1316.
1990: G Ruano; M R Gray; T Miki; A C Ferguson-Smith; Frank H Ruddle; Kenneth K Kidd
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: David L Pauls; Andrew J Pakstis; Roger Kurlan; Kenneth K Kidd; James F Leckman; D J Cohen; Judith R Kidd; P Como; R Sparkes
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: J S Wu; Kenneth K Kidd
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: Kenneth K Kidd; N E Simpson
Search for the gene for multiple endocrine neoplasia type 2A.
Recent progress in hormone research 1990;46():305-41; discussion 341-3.
1990: Judith R Kidd; Y Matsubara; C M Castiglione; K Tanaka; Kenneth K Kidd
The locus for the medium-chain acyl-CoA dehydrogenase gene on chromosome 1 is highly polymorphic.
Genomics 1990;6(1):89-93.
1989: J S Wu; L A Giuffra; Paul J Goodfellow; S Myers; N L Carson; L Anderson; L S Hoyle; N E Simpson; Kenneth K Kidd
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: G Ruano; Kenneth K Kidd
Direct haplotyping of chromosomal segments from multiple heterozygotes via allele-specific PCR amplification.
Nucleic acids research 1989;17(20):8392.
1989: G Ruano; W Fenton; Kenneth K Kidd
Biphasic amplification of very dilute DNA samples via 'booster' PCR.
Nucleic acids research 1989;17(13):5407.
1989: James L Kennedy; L A Giuffra; H W Moises; L Wetterberg; B Sjögren; L L Cavalli-Sforza; Andrew J Pakstis; Judith R Kidd; Kenneth K Kidd
Molecular genetic studies in schizophrenia.
Schizophrenia bulletin 1989;15(3):383-91.
1989: N E Simpson; Kenneth K Kidd
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: J Wu; L Joseph; V P Sukhatme; Kenneth K Kidd
A HindIII polymorphism identified by the human early growth response gene 2 (EGR2) on chromosome 10.
Nucleic acids research 1988;16(24):11855.
1988: James L Kennedy; L A Giuffra; H W Moises; L L Cavalli-Sforza; Andrew J Pakstis; Judith R Kidd; C M Castiglione; B Sjogren; L Wetterberg; Kenneth K Kidd
Evidence against linkage of schizophrenia to markers on chromosome 5 in a northern Swedish pedigree.
Nature 1988;336(6195):167-70.
1988: David L Pauls; D J Cohen; Kenneth K Kidd; James F Leckman
Tourette syndrome and neuropsychiatric disorders: is there a genetic relationship?
American journal of human genetics 1988;43(2):206-17.
1988: Lindsay A Farrer; C M Castiglione; Judith R Kidd; S Myers; N Carson; N E Simpson; Kenneth K Kidd
A linkage group of five DNA markers on human chromosome 10.
Genomics 1988;3(1):72-7.
1988: Lindsay A Farrer; B Bonne-Tamir; Moshe Frydman; A Magazanik; Kenneth K Kidd; Anne M Bowcock; L L Cavalli-Sforza
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: F Xue; Judith R Kidd; Andrew J Pakstis; C M Castiglione; J Mallet; Kenneth K Kidd
Tyrosine hydroxylase maps to the short arm of chromosome 11 proximal to the insulin and HRAS1 loci.
Genomics 1988;2(4):288-93.
1988: T Miki; S C Weil; G L Rosner; M S Reid; Kenneth K Kidd
An MPO cDNA clone identifies an RFLP with PstI.
Nucleic acids research 1988;16(4):1649.
1988: Kathleen Ries Merikangas; N J Risch; J R Merikangas; M M Weissman; Kenneth K Kidd
Migraine and depression: association and familial transmission.
Journal of psychiatric research 1988;22(2):119-29.
1988: J Wu; Vijaya Ramesh; Judith R Kidd; C M Castiglione; S Myers; N Carson; L Anderson; James Gusella; N E Simpson; Kenneth K Kidd
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: L A Giuffra; James L Kennedy; C M Castiglione; R M Evans; J J Wasmuth; Kenneth K Kidd
Glucocorticoid receptor maps to the distal long arm of chromosome 5.
Cytogenetics and cell genetics 1988;49(4):313-4.
1988: J Wu; W K Cavenee; T Miki; Kenneth K Kidd
A polymorphic DNA marker on chromosome 10 linked to RBP3 on the MEN2A side.
Cytogenetics and cell genetics 1988;48(4):246-7.
1988: Patricia L Kramer; Laurie J Ozelius; Mitchell F Brin; Stanley Fahn; Kenneth K Kidd; James Gusella; X O Breakefield
Molecular genetics of an autosomal dominant form of torsion dystonia.
Advances in neurology 1988;50():57-66.
1988: Kenneth K Kidd; Judith R Kidd; C M Castiglione; R S Sparkes; Janice A Egeland; E Bakker
The anonymous RFLP locus D1S2 is close to PGM1 on chromosome 1.
Human heredity 1988;38(1):22-6.
1987: P D Murphy; P F Lin; Frank H Ruddle; Kenneth K Kidd
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: Anne M Bowcock; Lindsay A Farrer; L L Cavalli-Sforza; J M Hebert; Kenneth K Kidd; Moshe Frydman; B Bonne-Tamir
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: Patricia L Kramer; Laurie J Ozelius; James Gusella; Stanley Fahn; Kenneth K Kidd; X O Breakefield
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: Kenneth K Kidd
Research design considerations for linkage studies of affective disorders using recombinant DNA markers.
Journal of psychiatric research 1987;21(4):551-7.
1987: Kenneth K Kidd
Searching for major genes for psychiatric disorders.
Ciba Foundation symposium 1987;130():184-96.
1987: Judith R Kidd; Janice A Egeland; Andrew J Pakstis; C M Castiglione; B A Pletcher; L A Morton; Kenneth K Kidd
Searching for a major genetic locus for affective disorder in the Old Order Amish.
Journal of psychiatric research 1987;21(4):577-80.
1987: Andrew J Pakstis; Judith R Kidd; C M Castiglione; B A Pletcher; P D Murphy; Lindsay A Farrer; M Genel; Kenneth K Kidd
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: Anne M Bowcock; Lindsay A Farrer; J M Hebert; B Bonne-Tamir; Moshe Frydman; Kenneth K Kidd; L L Cavalli-Sforza
A new human RFLP identified by 7D2 places D13S10 proximal to esterase D.
Cytogenetics and cell genetics 1987;44(4):236-7.
1986: P D Murphy; Judith R Kidd; C M Castiglione; P F Lin; Frank H Ruddle; Kenneth K Kidd
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: Kenneth K Kidd; Judith R Kidd; C M Castiglione; M Genel; J Darby; L L Cavalli-Sforza; James Gusella
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: P D Murphy; Judith R Kidd; W R Breg; Frank H Ruddle; Kenneth K Kidd
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.