Kenneth K. Kidd - Publications

Affiliations: 
Yale University, New Haven, CT 
Area:
Genetics, Health Care Management, Public Administration, Philosophy

385 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Mestiri S, Boussetta S, Pakstis AJ, Elkamel S, Elgaaied ABA, Kidd KK, Cherni L. Genetic diversity of the North African population revealed by the typing of SNPs in the DRD2/ANKK1 genomic region. Gene. 777: 145466. PMID 33524518 DOI: 10.1016/j.gene.2021.145466  0.36
2020 Kidd KK, Pakstis AJ, Donnelly MP, Bulbul O, Cherni L, Gurkan C, Kang L, Li H, Yun L, Paschou P, Meiklejohn KA, Haigh E, Speed WC. The distinctive geographic patterns of common pigmentation variants at the OCA2 gene. Scientific Reports. 10: 15433. PMID 32963319 DOI: 10.1038/s41598-020-72262-6  0.36
2020 Gandotra N, Speed WC, Qin W, Tang Y, Pakstis AJ, Kidd KK, Scharfe C. Validation of novel forensic DNA markers using multiplex microhaplotype sequencing. Forensic Science International. Genetics. 47: 102275. PMID 32305739 DOI: 10.1016/J.Fsigen.2020.102275  0.36
2020 Rajeevan H, Soundararajan U, Pakstis AJ, Kidd KK. FrogAncestryCalc: A standalone batch likelihood computation tool for ancestry inference panels catalogued in FROG-kb. Forensic Science International. Genetics. 46: 102237. PMID 31991337 DOI: 10.1016/J.Fsigen.2020.102237  0.36
2019 Pakstis AJ, Speed WC, Soundararajan U, Rajeevan H, Kidd JR, Li H, Kidd KK. Population relationships based on 170 ancestry SNPs from the combined Kidd and Seldin panels. Scientific Reports. 9: 18874. PMID 31827153 DOI: 10.1038/S41598-019-55175-X  0.6
2019 Pakstis AJ, Gurkan C, Dogan M, Balkaya HE, Dogan S, Neophytou PI, Cherni L, Boussetta S, Khodjet-El-Khil H, Ben Ammar ElGaaied A, Salvo NM, Janssen K, Olsen GH, Hadi S, Almohammed EK, ... ... Kidd KK, et al. Genetic relationships of European, Mediterranean, and SW Asian populations using a panel of 55 AISNPs. European Journal of Human Genetics : Ejhg. PMID 31285530 DOI: 10.1038/S41431-019-0466-6  0.6
2019 Drineas P, Tsetsos F, Plantinga A, Lazaridis I, Yannaki E, Razou A, Kanaki K, Michalodimitrakis M, Perez-Jimenez F, De Silvestro G, Renda MC, Stamatoyannopoulos JA, Kidd KK, Browning BL, Paschou P, et al. Genetic history of the population of Crete. Annals of Human Genetics. PMID 31192450 DOI: 10.1111/Ahg.12328  0.4
2019 Boussetta S, Cherni L, Pakstis AJ, Salem NB, Elkamel S, Khodjet-El-Khil H, Kidd KK, Elgaaied ABA. Usefulness of COMT gene polymorphisms in North African populations. Gene. PMID 30790653 DOI: 10.1016/J.Gene.2019.02.021  0.36
2018 Gu S, Li H, Pakstis AJ, Speed WC, Gurwitz D, Kidd JR, Kidd KK. Recent Selection on a Class I ADH Locus Distinguishes Southwest Asian Populations Including Ashkenazi Jews. Genes. 9. PMID 30205534 DOI: 10.3390/Genes9090452  0.6
2018 Kidd KK, Pakstis AJ, Speed WC, Lagace R, Wootton S, Chang J. Selecting microhaplotypes optimized for different purposes. Electrophoresis. PMID 29931757 DOI: 10.1002/Elps.201800092  0.36
2018 Bulbul O, Speed WC, Gurkan C, Soundararajan U, Rajeevan H, Pakstis AJ, Kidd KK. Improving ancestry distinctions among Southwest Asian populations. Forensic Science International. Genetics. 35: 14-20. PMID 29625264 DOI: 10.1016/J.Fsigen.2018.03.010  0.36
2017 Bulbul O, Pakstis AJ, Soundararajan U, Gurkan C, Brissenden JE, Roscoe JM, Evsanaa B, Togtokh A, Paschou P, Grigorenko EL, Gurwitz D, Wootton S, Lagace R, Chang J, Speed WC, ... Kidd KK, et al. Ancestry inference of 96 population samples using microhaplotypes. International Journal of Legal Medicine. PMID 29248957 DOI: 10.1007/S00414-017-1748-6  0.36
2017 Kidd KK, Soundararajan U, Rajeevan H, Pakstis AJ, Moore KN, Ropero-Miller JD. The redesigned Forensic Research/Reference on Genetics-knowledge base, FROG-kb. Forensic Science International. Genetics. 33: 33-37. PMID 29175726 DOI: 10.1016/J.Fsigen.2017.11.009  0.36
2017 Kidd KK, Speed WC, Pakstis AJ, Podini DS, Lagacé R, Chang J, Wootton S, Haigh E, Soundararajan U. Evaluating 130 microhaplotypes across a global set of 83 populations. Forensic Science International. Genetics. 29: 29-37. PMID 28359046 DOI: 10.1016/J.Fsigen.2017.03.014  0.36
2017 Stamatoyannopoulos G, Bose A, Teodosiadis A, Tsetsos F, Plantinga A, Psatha N, Zogas N, Yannaki E, Zalloua P, Kidd KK, Browning BL, Stamatoyannopoulos J, Paschou P, Drineas P. Genetics of the peloponnesean populations and the theory of extinction of the medieval peloponnesean Greeks. European Journal of Human Genetics : Ejhg. PMID 28272534 DOI: 10.1038/Ejhg.2017.18  0.4
2017 Nakagome S, Chinen H, Iraha A, Hokama A, Takeyama Y, Sakisaka S, Matsui T, Kidd JR, Kidd KK, Said HS, Suda W, Morita H, Hattori M, Hanihara T, Kimura R, et al. Confounding effects of microbiome on the susceptibility of TNFSF15 to Crohn's disease in the Ryukyu Islands. Human Genetics. PMID 28197769 DOI: 10.1007/S00439-017-1764-0  0.6
2017 Pakstis AJ, Kang L, Liu L, Zhang Z, Jin T, Grigorenko EL, Wendt FR, Budowle B, Hadi S, Al Qahtani MS, Morling N, Mogensen HS, Themudo GE, Soundararajan U, Rajeevan H, ... ... Kidd KK, et al. Increasing the reference populations for the 55 AISNP panel: the need and benefits. International Journal of Legal Medicine. PMID 28070634 DOI: 10.1007/S00414-016-1524-Z  0.6
2016 Cherni L, Pakstis AJ, Boussetta S, Elkamel S, Frigi S, Khodjet-El-Khil H, Barton A, Haigh E, Speed WC, Ben Ammar Elgaaied A, Kidd JR, Kidd KK. Genetic variation in Tunisia in the context of human diversity worldwide. American Journal of Physical Anthropology. PMID 27192181 DOI: 10.1002/Ajpa.23008  0.6
2016 Li CX, Pakstis AJ, Jiang L, Wei YL, Sun QF, Wu H, Bulbul O, Wang P, Kang LL, Kidd JR, Kidd KK. A panel of 74 AISNPs: Improved ancestry inference within Eastern Asia. Forensic Science International. Genetics. 23: 101-110. PMID 27077960 DOI: 10.1016/J.Fsigen.2016.04.002  0.92
2016 Soundararajan U, Yun L, Shi M, Kidd KK. Minimal SNP overlap among multiple panels of ancestry informative markers argues for more international collaboration. Forensic Science International. Genetics. 23: 25-32. PMID 26977931 DOI: 10.1016/J.Fsigen.2016.01.013  0.92
2016 Boyden SE, Desai A, Cruse G, Young ML, Bolan HC, Scott LM, Eisch AR, Long RD, Lee CR, Satorius CL, Pakstis AJ, Olivera A, Mullikin JC, Chouery E, Mégarbané A, ... ... Kidd KK, et al. Vibratory Urticaria Associated with a Missense Variant in ADGRE2. The New England Journal of Medicine. PMID 26841242 DOI: 10.1056/Nejmoa1500611  0.36
2015 Brissenden JE, Kidd JR, Evsanaa B, Togtokh AJ, Pakstis AJ, Friedlaender F, Kidd KK, Roscoe JM. Mongolians in the Genetic Landscape of Central Asia: Exploring the Genetic Relations among Mongolians and Other World Populations. Human Biology. 87: 73-91. PMID 26829292 DOI: 10.13110/Humanbiology.87.2.0005  0.6
2015 Pakstis AJ, Haigh E, Cherni L, ElGaaied AB, Barton A, Evsanaa B, Togtokh A, Brissenden J, Roscoe J, Bulbul O, Filoglu G, Gurkan C, Meiklejohn KA, Robertson JM, Li CX, ... ... Kidd KK, et al. 52 additional reference population samples for the 55 AISNP panel. Forensic Science International. Genetics. 19: 269-271. PMID 26355664 DOI: 10.1016/J.Fsigen.2015.08.003  0.6
2015 Kidd KK, Speed WC. Criteria for selecting microhaplotypes: mixture detection and deconvolution. Investigative Genetics. 6: 1. PMID 25750707 DOI: 10.1186/S13323-014-0018-3  0.92
2015 Xu H, Wang CC, Shrestha R, Wang LX, Zhang M, He Y, Kidd JR, Kidd KK, Jin L, Li H. Inferring population structure and demographic history using Y-STR data from worldwide populations. Molecular Genetics and Genomics : Mgg. 290: 141-50. PMID 25159112 DOI: 10.1007/S00438-014-0903-8  0.92
2015 Kidd KK, Speed WC, Wootton S, Lagace R, Langit R, Haigh E, Chang J, Pakstis AJ. Genetic markers for massively parallel sequencing in forensics Forensic Science International: Genetics Supplement Series. DOI: 10.1016/J.Fsigss.2015.12.004  0.92
2015 Pakstis AJ, Haigh E, Cherni L, Elgaaied ABA, Barton A, Evsanaa B, Togtokh A, Brissenden J, Roscoe J, Bulbul O, Filoglu G, Gurkan C, Meiklejohn KA, Robertson JM, Li CX, ... ... Kidd KK, et al. 52 additional reference population samples for the 55 AISNP panel Forensic Science International: Genetics. 19: 269-271. DOI: 10.1016/j.fsigen.2015.08.003  0.6
2014 Kidd KK, Pakstis AJ, Speed WC, Lagacé R, Chang J, Wootton S, Haigh E, Kidd JR. Current sequencing technology makes microhaplotypes a powerful new type of genetic marker for forensics. Forensic Science International. Genetics. 12: 215-24. PMID 25038325 DOI: 10.1016/J.Fsigen.2014.06.014  0.92
2014 Paschou P, Drineas P, Yannaki E, Razou A, Kanaki K, Tsetsos F, Padmanabhuni SS, Michalodimitrakis M, Renda MC, Pavlovic S, Anagnostopoulos A, Stamatoyannopoulos JA, Kidd KK, Stamatoyannopoulos G. Maritime route of colonization of Europe. Proceedings of the National Academy of Sciences of the United States of America. 111: 9211-6. PMID 24927591 DOI: 10.1073/Pnas.1320811111  0.92
2014 Keramati AR, Fathzadeh M, Go GW, Singh R, Choi M, Faramarzi S, Mane S, Kasaei M, Sarajzadeh-Fard K, Hwa J, Kidd KK, Babaee Bigi MA, Malekzadeh R, Hosseinian A, Babaei M, et al. A form of the metabolic syndrome associated with mutations in DYRK1B. The New England Journal of Medicine. 370: 1909-19. PMID 24827035 DOI: 10.1056/Nejmoa1301824  0.92
2014 Kim M, Chen X, Chin LJ, Paranjape T, Speed WC, Kidd KK, Zhao H, Weidhaas JB, Slack FJ. Extensive sequence variation in the 3' untranslated region of the KRAS gene in lung and ovarian cancer cases. Cell Cycle (Georgetown, Tex.). 13: 1030-40. PMID 24552817 DOI: 10.4161/Cc.27941  0.92
2014 Kidd KK, Speed WC, Pakstis AJ, Furtado MR, Fang R, Madbouly A, Maiers M, Middha M, Friedlaender FR, Kidd JR. Progress toward an efficient panel of SNPs for ancestry inference. Forensic Science International. Genetics. 10: 23-32. PMID 24508742 DOI: 10.1016/J.Fsigen.2014.01.002  0.92
2014 Yun L, Gu Y, Rajeevan H, Kidd KK. Application of six IrisPlex SNPs and comparison of two eye color prediction systems in diverse Eurasia populations. International Journal of Legal Medicine. 128: 447-53. PMID 24395150 DOI: 10.1007/S00414-013-0953-1  0.92
2014 Kidd KK, Pakstis AJ, Yun L. An historical perspective on "The world-wide distribution of allele frequencies at the human dopamine D4 receptor locus". Human Genetics. 133: 431-3. PMID 24162668 DOI: 10.1007/S00439-013-1386-0  0.92
2014 Heffelfinger C, Pakstis AJ, Speed WC, Clark AP, Haigh E, Fang R, Furtado MR, Kidd KK, Snyder MP. Haplotype structure and positive selection at TLR1. European Journal of Human Genetics : Ejhg. 22: 551-7. PMID 24002163 DOI: 10.1038/Ejhg.2013.194  0.92
2013 Nievergelt CM, Maihofer AX, Shekhtman T, Libiger O, Wang X, Kidd KK, Kidd JR. Inference of human continental origin and admixture proportions using a highly discriminative ancestry informative 41-SNP panel. Investigative Genetics. 4: 13. PMID 23815888 DOI: 10.1186/2041-2223-4-13  0.92
2013 Murdoch JD, Speed WC, Pakstis AJ, Heffelfinger CE, Kidd KK. Worldwide population variation and haplotype analysis at the serotonin transporter gene SLC6A4 and implications for association studies. Biological Psychiatry. 74: 879-89. PMID 23510579 DOI: 10.1016/J.Biopsych.2013.02.006  0.92
2013 Keating B, Bansal AT, Walsh S, Millman J, Newman J, Kidd K, Budowle B, Eisenberg A, Donfack J, Gasparini P, Budimlija Z, Henders AK, Chandrupatla H, Duffy DL, Gordon SD, et al. First all-in-one diagnostic tool for DNA intelligence: genome-wide inference of biogeographic ancestry, appearance, relatedness, and sex with the Identitas v1 Forensic Chip. International Journal of Legal Medicine. 127: 559-72. PMID 23149900 DOI: 10.1007/S00414-012-0788-1  0.92
2013 Kidd KK, Pakstis AJ, Speed WC, Lagace R, Chang J, Wootton S, Ihuegbu N. Microhaplotype loci are a powerful new type of forensic marker Forensic Science International: Genetics Supplement Series. 4: e123-e124. DOI: 10.1016/J.Fsigss.2013.10.063  0.92
2012 Lu Y, Kang L, Hu K, Wang C, Sun X, Chen F, Kidd JR, Kidd KK, Li H. High diversity and no significant selection signal of human ADH1B gene in Tibet. Investigative Genetics. 3: 23. PMID 23176670 DOI: 10.1186/2041-2223-3-23  0.92
2012 Stathias V, Sotiris GR, Karagiannidis I, Bourikas G, Martinis G, Papazoglou D, Tavridou A, Papanas N, Maltezos E, Theodoridis M, Vargemezis V, Manolopoulos VG, Speed WC, Kidd JR, Kidd KK, et al. Exploring genomic structure differences and similarities between the Greek and European HapMap populations: implications for association studies. Annals of Human Genetics. 76: 472-83. PMID 23061745 DOI: 10.1111/J.1469-1809.2012.00730.X  0.92
2012 Rajeevan H, Soundararajan U, Pakstis AJ, Kidd KK. Introducing the Forensic Research/Reference on Genetics knowledge base, FROG-kb. Investigative Genetics. 3: 18. PMID 22938150 DOI: 10.1186/2041-2223-3-18  0.92
2012 Krauthammer M, Kong Y, Ha BH, Evans P, Bacchiocchi A, McCusker JP, Cheng E, Davis MJ, Goh G, Choi M, Ariyan S, Narayan D, Dutton-Regester K, Capatana A, Holman EC, ... ... Kidd KK, et al. Exome sequencing identifies recurrent somatic RAC1 mutations in melanoma. Nature Genetics. 44: 1006-14. PMID 22842228 DOI: 10.1038/Ng.2359  0.92
2012 Steinberg KM, Antonacci F, Sudmant PH, Kidd JM, Campbell CD, Vives L, Malig M, Scheinfeldt L, Beggs W, Ibrahim M, Lema G, Nyambo TB, Omar SA, Bodo JM, Froment A, ... ... Kidd KK, et al. Structural diversity and African origin of the 17q21.31 inversion polymorphism. Nature Genetics. 44: 872-80. PMID 22751100 DOI: 10.1038/Ng.2335  0.92
2012 Pakstis AJ, Fang R, Furtado MR, Kidd JR, Kidd KK. Mini-haplotypes as lineage informative SNPs and ancestry inference SNPs. European Journal of Human Genetics : Ejhg. 20: 1148-54. PMID 22535184 DOI: 10.1038/Ejhg.2012.69  0.92
2012 Kidd KK, Kidd JR, Speed WC, Fang R, Furtado MR, Hyland FC, Pakstis AJ. Expanding data and resources for forensic use of SNPs in individual identification. Forensic Science International. Genetics. 6: 646-52. PMID 22445421 DOI: 10.1016/J.Fsigen.2012.02.012  0.92
2012 Nakagome S, Mano S, Kozlowski L, Bujnicki JM, Shibata H, Fukumaki Y, Kidd JR, Kidd KK, Kawamura S, Oota H. Crohn's disease risk alleles on the NOD2 locus have been maintained by natural selection on standing variation. Molecular Biology and Evolution. 29: 1569-85. PMID 22319155 DOI: 10.1093/Molbev/Mss006  0.92
2012 Donnelly MP, Paschou P, Grigorenko E, Gurwitz D, Barta C, Lu RB, Zhukova OV, Kim JJ, Siniscalco M, New M, Li H, Kajuna SL, Manolopoulos VG, Speed WC, Pakstis AJ, ... ... Kidd KK, et al. A global view of the OCA2-HERC2 region and pigmentation. Human Genetics. 131: 683-96. PMID 22065085 DOI: 10.1007/S00439-011-1110-X  0.92
2012 Rajeevan H, Soundararajan U, Kidd JR, Pakstis AJ, Kidd KK. ALFRED: an allele frequency resource for research and teaching. Nucleic Acids Research. 40: D1010-5. PMID 22039151 DOI: 10.1093/Nar/Gkr924  0.92
2012 Pagani L, Ayub Q, MacArthur DG, Xue Y, Baillie JK, Chen Y, Kozarewa I, Turner DJ, Tofanelli S, Bulayeva K, Kidd K, Paoli G, Tyler-Smith C. High altitude adaptation in Daghestani populations from the Caucasus. Human Genetics. 131: 423-33. PMID 21904933 DOI: 10.1007/S00439-011-1084-8  0.92
2011 Kidd JR, Friedlaender F, Pakstis AJ, Furtado M, Fang R, Wang X, Nievergelt CM, Kidd KK. Single nucleotide polymorphisms and haplotypes in Native American populations. American Journal of Physical Anthropology. 146: 495-502. PMID 21913176 DOI: 10.1002/Ajpa.21560  0.92
2011 O'huigin C, Kulkarni S, Xu Y, Deng Z, Kidd J, Kidd K, Gao X, Carrington M. The molecular origin and consequences of escape from miRNA regulation by HLA-C alleles. American Journal of Human Genetics. 89: 424-31. PMID 21907013 DOI: 10.1016/J.Ajhg.2011.07.024  0.92
2011 Li H, Pakstis AJ, Kidd JR, Kidd KK. Selection on the human bitter taste gene, TAS2R16, in Eurasian populations. Human Biology. 83: 363-77. PMID 21740153 DOI: 10.3378/027.083.0303  0.92
2011 Sampson JN, Kidd KK, Kidd JR, Zhao H. Selecting SNPs to identify ancestry. Annals of Human Genetics. 75: 539-53. PMID 21668909 DOI: 10.1111/J.1469-1809.2011.00656.X  0.92
2011 Li H, Gu S, Han Y, Xu Z, Pakstis AJ, Jin L, Kidd JR, Kidd KK. Diversification of the ADH1B gene during expansion of modern humans. Annals of Human Genetics. 75: 497-507. PMID 21592108 DOI: 10.1111/J.1469-1809.2011.00651.X  0.92
2011 Henn BM, Gignoux CR, Jobin M, Granka JM, Macpherson JM, Kidd JM, Rodríguez-Botigué L, Ramachandran S, Hon L, Brisbin A, Lin AA, Underhill PA, Comas D, Kidd KK, Norman PJ, et al. Hunter-gatherer genomic diversity suggests a southern African origin for modern humans. Proceedings of the National Academy of Sciences of the United States of America. 108: 5154-62. PMID 21383195 DOI: 10.1073/Pnas.1017511108  0.92
2011 Palejev D, Hwang W, Landi N, Eastman M, Frost SJ, Fulbright RK, Kidd JR, Kidd KK, Mason GF, Mencl WE, Yrigollen C, Pugh KR, Grigorenko EL. An application of the elastic net for an endophenotype analysis. Behavior Genetics. 41: 120-4. PMID 21229297 DOI: 10.1007/S10519-011-9443-8  0.92
2011 Kidd JR, Friedlaender FR, Speed WC, Pakstis AJ, De La Vega FM, Kidd KK. Analyses of a set of 128 ancestry informative single-nucleotide polymorphisms in a global set of 119 population samples. Investigative Genetics. 2: 1. PMID 21208434 DOI: 10.1186/2041-2223-2-1  0.92
2011 Pelletier C, Speed WC, Paranjape T, Keane K, Blitzblau R, Hollestelle A, Safavi K, van den Ouweland A, Zelterman D, Slack FJ, Kidd KK, Weidhaas JB. Rare BRCA1 haplotypes including 3'UTR SNPs associated with breast cancer risk. Cell Cycle (Georgetown, Tex.). 10: 90-9. PMID 21191178 DOI: 10.4161/Cc.10.1.14359  0.92
2011 Godshalk SE, Paranjape T, Nallur S, Speed W, Chan E, Molinaro AM, Bacchiocchi A, Hoyt K, Tworkoski K, Stern DF, Sznol M, Ariyan S, Lazova R, Halaban R, Kidd KK, et al. A Variant in a MicroRNA complementary site in the 3' UTR of the KIT oncogene increases risk of acral melanoma. Oncogene. 30: 1542-50. PMID 21119596 DOI: 10.1038/Onc.2010.536  0.92
2010 Duffy VB, Hayes JE, Davidson AC, Kidd JR, Kidd KK, Bartoshuk LM. Vegetable Intake in College-Aged Adults Is Explained by Oral Sensory Phenotypes and TAS2R38 Genotype. Chemosensory Perception. 3: 137-148. PMID 21157576 DOI: 10.1007/S12078-010-9079-8  0.92
2010 Mustavich LF, Miller P, Kidd KK, Zhao H. Using a pharmacokinetic model to relate an individual's susceptibility to alcohol dependence to genotypes. Human Heredity. 70: 177-93. PMID 20714161 DOI: 10.1159/000317056  0.92
2010 Wang P, Ha AY, Kidd KK, Koehle MS, Rupert JL. 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. 11: 27-30. PMID 20367485 DOI: 10.1089/Ham.2009.1054  0.92
2010 O'Roak BJ, Morgan TM, Fishman DO, Saus E, Alonso P, Gratacòs M, Estivill X, Teltsh O, Kohn Y, Kidd KK, Cho J, Lifton RP, State MW. Additional support for the association of SLITRK1 var321 and Tourette syndrome. Molecular Psychiatry. 15: 447-50. PMID 20351724 DOI: 10.1038/Mp.2009.105  0.92
2010 Donnelly MP, Paschou P, Grigorenko E, Gurwitz D, Mehdi SQ, Kajuna SL, Barta C, Kungulilo S, Karoma NJ, Lu RB, Zhukova OV, Kim JJ, Comas D, Siniscalco M, New M, ... ... Kidd KK, et al. The distribution and most recent common ancestor of the 17q21 inversion in humans. American Journal of Human Genetics. 86: 161-71. PMID 20116045 DOI: 10.1016/J.Ajhg.2010.01.007  0.92
2010 Pakstis AJ, Speed WC, Fang R, Hyland FC, Furtado MR, Kidd JR, Kidd KK. SNPs for a universal individual identification panel. Human Genetics. 127: 315-24. PMID 19937056 DOI: 10.1007/S00439-009-0771-1  0.92
2010 Mukherjee N, Kidd KK, Pakstis AJ, Speed WC, Li H, Tarnok Z, Barta C, Kajuna SL, Kidd JR. The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase. Molecular Psychiatry. 15: 216-25. PMID 18574484 DOI: 10.1038/Mp.2008.64  0.92
2010 Kidd KK, Kidd JR. Human genetic variation of medical significance Evolution in Health and Disease. DOI: 10.1093/acprof:oso/9780199207466.003.0005  0.92
2009 Li H, Cho K, Kidd JR, Kidd KK. Genetic landscape of Eurasia and "admixture" in Uyghurs. American Journal of Human Genetics. 85: 934-7; author reply . PMID 20004770 DOI: 10.1016/J.Ajhg.2009.10.024  0.6
2009 Barreiro LB, Ben-Ali M, Quach H, Laval G, Patin E, Pickrell JK, Bouchier C, Tichit M, Neyrolles O, Gicquel B, Kidd JR, Kidd KK, Alcaïs A, Ragimbeau J, Pellegrini S, et al. Evolutionary dynamics of human Toll-like receptors and their different contributions to host defense. Plos Genetics. 5: e1000562. PMID 19609346 DOI: 10.1371/Journal.Pgen.1000562  0.92
2009 Holford ME, Rajeevan H, Zhao H, Kidd KK, Cheung KH. Semantic Web-based integration of cancer pathways and allele frequency data. Cancer Informatics. 8: 19-30. PMID 19458791 DOI: 10.4137/Cin.S1006  0.92
2009 Li H, Borinskaya S, Yoshimura K, Kal'ina N, Marusin A, Stepanov VA, Qin Z, Khaliq S, Lee MY, Yang Y, Mohyuddin A, Gurwitz D, Mehdi SQ, Rogaev E, Jin L, ... ... Kidd KK, et al. Refined geographic distribution of the oriental ALDH2*504Lys (nee 487Lys) variant. Annals of Human Genetics. 73: 335-45. PMID 19456322 DOI: 10.1111/J.1469-1809.2009.00517.X  0.92
2009 Luo HR, Wu GS, Pakstis AJ, Tong L, Oota H, Kidd KK, Zhang YP. Origin and dispersal of atypical aldehyde dehydrogenase ALDH2487Lys. Gene. 435: 96-103. PMID 19393179 DOI: 10.1016/J.Gene.2008.12.021  0.92
2009 Speed WC, Kang SP, Tuck DP, Harris LN, Kidd KK. Global variation in CYP2C8-CYP2C9 functional haplotypes. The Pharmacogenomics Journal. 9: 283-90. PMID 19381162 DOI: 10.1038/Tpj.2009.10  0.92
2009 Patin E, Laval G, Barreiro LB, Salas A, Semino O, Santachiara-Benerecetti S, Kidd KK, Kidd JR, Van der Veen L, Hombert JM, Gessain A, Froment A, Bahuchet S, Heyer E, Quintana-Murci L. Inferring the demographic history of African farmers and pygmy hunter-gatherers using a multilocus resequencing data set. Plos Genetics. 5: e1000448. PMID 19360089 DOI: 10.1371/Journal.Pgen.1000448  0.92
2009 Quach H, Barreiro LB, Laval G, Zidane N, Patin E, Kidd KK, Kidd JR, Bouchier C, Veuille M, Antoniewski C, Quintana-Murci L. Signatures of purifying and local positive selection in human miRNAs. American Journal of Human Genetics. 84: 316-27. PMID 19232555 DOI: 10.1016/J.Ajhg.2009.01.022  0.92
2009 Yamtich J, Speed WC, Straka E, Kidd JR, Sweasy JB, Kidd KK. Population-specific variation in haplotype composition and heterozygosity at the POLB locus. Dna Repair. 8: 579-84. PMID 19167932 DOI: 10.1016/J.Dnarep.2008.12.005  0.92
2009 Fang R, Pakstis AJ, Hyland F, Wang D, Shewale J, Kidd JR, Kidd KK, Furtado MR. Multiplexed SNP detection panels for human identification Forensic Science International: Genetics Supplement Series. 2: 538-539. DOI: 10.1016/J.Fsigss.2009.08.161  0.92
2009 Li H, Kidd KK. Low Allele Frequency of ADH1B*47His in West China and Different ADH1B Haplotypes in Western and Eastern Asia American Journal of Human Genetics. 84: 92-94. DOI: 10.1016/J.Ajhg.2008.12.006  0.92
2008 Chin LJ, Ratner E, Leng S, Zhai R, Nallur S, Babar I, Muller RU, Straka E, Su L, Burki EA, Crowell RE, Patel R, Kulkarni T, Homer R, Zelterman D, ... Kidd KK, et al. A SNP in a let-7 microRNA complementary site in the KRAS 3' untranslated region increases non-small cell lung cancer risk. Cancer Research. 68: 8535-40. PMID 18922928 DOI: 10.1158/0008-5472.Can-08-2129  0.92
2008 Lee MY, Mukherjee N, Pakstis AJ, Khaliq S, Mohyuddin A, Mehdi SQ, Speed WC, Kidd JR, Kidd KK. Global patterns of variation in allele and haplotype frequencies and linkage disequilibrium across the CYP2E1 gene. The Pharmacogenomics Journal. 8: 349-56. PMID 18663376 DOI: 10.1038/Tpj.2008.9  0.92
2008 Ciarleglio CM, Ryckman KK, Servick SV, Hida A, Robbins S, Wells N, Hicks J, Larson SA, Wiedermann JP, Carver K, Hamilton N, Kidd KK, Kidd JR, Smith JR, Friedlaender J, et al. Genetic differences in human circadian clock genes among worldwide populations. Journal of Biological Rhythms. 23: 330-40. PMID 18663240 DOI: 10.1177/0748730408320284  0.92
2008 Li H, Gu S, Cai X, Speed WC, Pakstis AJ, Golub EI, Kidd JR, Kidd KK. Ethnic related selection for an ADH Class I variant within East Asia. Plos One. 3: e1881. PMID 18382665 DOI: 10.1371/Journal.Pone.0001881  0.92
2008 Quintana-Murci L, Quach H, Harmant C, Luca F, Massonnet B, Patin E, Sica L, Mouguiama-Daouda P, Comas D, Tzur S, Balanovsky O, Kidd KK, Kidd JR, van der Veen L, Hombert JM, et al. Maternal traces of deep common ancestry and asymmetric gene flow between Pygmy hunter-gatherers and Bantu-speaking farmers. Proceedings of the National Academy of Sciences of the United States of America. 105: 1596-601. PMID 18216239 DOI: 10.1073/Pnas.0711467105  0.92
2008 Friedlaender JS, Friedlaender FR, Reed FA, Kidd KK, Kidd JR, Chambers GK, Lea RA, Loo JH, Koki G, Hodgson JA, Merriwether DA, Weber JL. The genetic structure of Pacific Islanders. Plos Genetics. 4: e19. PMID 18208337 DOI: 10.1371/Journal.Pgen.0040019  0.92
2008 Speed WC, O'Roak BJ, Tárnok Z, Barta C, Pakstis AJ, State MW, Kidd KK. 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. 147: 463-6. PMID 18004766 DOI: 10.1002/Ajmg.B.30641  0.92
2008 Al-Kateb H, Boright AP, Mirea L, Xie X, Sutradhar R, Mowjoodi A, Bharaj B, Liu M, Bucksa JM, Arends VL, Steffes MW, Cleary PA, Sun W, Lachin JM, Thorner PS, ... ... Kidd KK, et al. 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. 57: 218-28. PMID 17914031 DOI: 10.2337/Db07-1059  0.92
2008 Niemann S, Landers JE, Churchill MJ, Hosler B, Sapp P, Speed WC, Lahn BT, Kidd KK, Brown RH, Hayashi Y. Motoneuron-specific NR3B gene: no association with ALS and evidence for a common null allele. Neurology. 70: 666-76. PMID 17687115 DOI: 10.1212/01.Wnl.0000271078.51280.17  0.92
2008 Pakstis AJ, Speed WC, Kidd JR, Kidd KK. SNPs for individual identification Forensic Science International: Genetics Supplement Series. 1: 479-481. DOI: 10.1016/J.Fsigss.2007.10.200  0.92
2008 Butler JM, Budowle B, Gill P, Kidd KK, Phillips C, Schneider PM, Vallone PM, Morling N. Report on ISFG SNP Panel Discussion Forensic Science International: Genetics Supplement Series. 1: 471-472. DOI: 10.1016/J.Fsigss.2007.10.159  0.92
2007 Li H, Mukherjee N, Soundararajan U, Tarnok Z, Barta C, Khaliq S, Mohyuddin A, Kajuna SL, Mehdi SQ, Kidd JR, Kidd KK. Geographically separate increases in the frequency of the derived ADH1B*47His allele in eastern and western Asia. American Journal of Human Genetics. 81: 842-6. PMID 17847010 DOI: 10.1086/521201  0.92
2007 Single RM, Martin MP, Gao X, Meyer D, Yeager M, Kidd JR, Kidd KK, Carrington M. Global diversity and evidence for coevolution of KIR and HLA. Nature Genetics. 39: 1114-9. PMID 17694058 DOI: 10.1038/Ng2077  0.92
2007 Pakstis AJ, Speed WC, Kidd JR, Kidd KK. Candidate SNPs for a universal individual identification panel. Human Genetics. 121: 305-17. PMID 17333283 DOI: 10.1007/S00439-007-0342-2  0.92
2007 Pauls D, Cath D, Heutink P, Grados M, Singer HS, Walkup JT, Illmann C, Scharf JM, Santangelo S, Stewart SE, Platko J, Pauls DL, Cox NJ, Robertson MM, Service S, ... ... Kidd KK, et al. Genome scan for tourette disorder in affected-sibling-pair and multigenerational families American Journal of Human Genetics. 80: 265-272. PMID 17304708 DOI: 10.1086/511052  0.92
2007 Nakamoto K, Kidd JR, Jenison RD, Klaassen CD, Wan YJ, Kidd KK, Zhong XB. Genotyping and haplotyping of CYP2C19 functional alleles on thin-film biosensor chips. Pharmacogenetics and Genomics. 17: 103-14. PMID 17301690 DOI: 10.1097/Fpc.0B013E32801152C2  0.6
2007 Han Y, Gu S, Oota H, Osier MV, Pakstis AJ, Speed WC, Kidd JR, Kidd KK. Evidence of positive selection on a class I ADH locus. American Journal of Human Genetics. 80: 441-56. PMID 17273965 DOI: 10.1086/512485  0.92
2007 Oota H, Dunn CW, Speed WC, Pakstis AJ, Palmatier MA, Kidd JR, Kidd KK. Conservative evolution in duplicated genes of the primate Class I ADH cluster. Gene. 392: 64-76. PMID 17204375 DOI: 10.1016/J.Gene.2006.11.008  0.92
2007 Gu S, Pakstis AJ, Li H, Speed WC, Kidd JR, Kidd KK. Significant variation in haplotype block structure but conservation in tagSNP patterns among global populations. European Journal of Human Genetics : Ejhg. 15: 302-12. PMID 17202997 DOI: 10.1038/Sj.Ejhg.5201751  0.92
2007 Paschou P, Mahoney MW, Javed A, Kidd JR, Pakstis AJ, Gu S, Kidd KK, Drineas P. Intra- and interpopulation genotype reconstruction from tagging SNPs. Genome Research. 17: 96-107. PMID 17151345 DOI: 10.1101/Gr.5741407  0.92
2006 Verdu P, Barreiro LB, Patin E, Gessain A, Cassar O, Kidd JR, Kidd KK, Behar DM, Froment A, Heyer E, Sica L, Casanova JL, Abel L, Quintana-Murci L. Evolutionary insights into the high worldwide prevalence of MBL2 deficiency alleles. Human Molecular Genetics. 15: 2650-8. PMID 16885193 DOI: 10.1093/Hmg/Ddl193  0.6
2006 Schulz LO, Bennett PH, Ravussin E, Kidd JR, Kidd KK, Esparza J, Valencia ME. Effects of traditional and western environments on prevalence of type 2 diabetes in Pima Indians in Mexico and the U.S. Diabetes Care. 29: 1866-71. PMID 16873794 DOI: 10.2337/Dc06-0138  0.6
2006 Fredman D, Sawyer SL, Strömqvist L, Mottagui-Tabar S, Kidd KK, Wahlestedt C, Chanock SJ, Brookes AJ. Nonsynonymous SNPs: validation characteristics, derived allele frequency patterns, and suggestive evidence for natural selection. Human Mutation. 27: 173-86. PMID 16429399 DOI: 10.1002/Humu.20289  0.92
2006 Kidd KK, Pakstis AJ, Speed WC, Grigorenko EL, Kajuna SL, Karoma NJ, Kungulilo S, Kim JJ, Lu RB, Odunsi A, Okonofua F, Parnas J, Schulz LO, Zhukova OV, Kidd JR. Developing a SNP panel for forensic identification of individuals. Forensic Science International. 164: 20-32. PMID 16360294 DOI: 10.1016/J.Forsciint.2005.11.017  0.6
2006 Sternberg RJ, Grigorenko EL, Kidd KK. Racing toward the finish line American Psychologist. 61: 178-179. DOI: 10.1037/0003-066X.61.2.178  0.92
2005 Rajeevan H, Cheung KH, Gadagkar R, Stein S, Soundararajan U, Kidd JR, Pakstis AJ, Miller PL, Kidd KK. ALFRED: an allele frequency database for microevolutionary studies. Evolutionary Bioinformatics Online. 1: 1-10. PMID 19325849 DOI: 10.4137/Ebo.S0  0.6
2005 Han Y, Oota H, Osier MV, Pakstis AJ, Speed WC, Odunsi A, Okonofua F, Kajuna SL, Karoma NJ, Kungulilo S, Grigorenko E, Zhukova OV, Bonne-Tamir B, Lu RB, Parnas J, ... ... Kidd KK, et al. Considerable haplotype diversity within the 23kb encompassing the ADH7 gene. Alcoholism, Clinical and Experimental Research. 29: 2091-100. PMID 16385178 DOI: 10.1097/01.Alc.0000191769.92667.04  0.92
2005 Biesecker LG, Bailey-Wilson JE, Ballantyne J, Baum H, Bieber FR, Brenner C, Budowle B, Butler JM, Carmody G, Conneally PM, Duceman B, Eisenberg A, Forman L, Kidd KK, Leclair B, et al. Epidemiology. DNA identifications after the 9/11 World Trade Center attack. Science (New York, N.Y.). 310: 1122-3. PMID 16293742 DOI: 10.1126/Science.1116608  0.92
2005 Gu S, Pakstis AJ, Kidd KK. HAPLOT: a graphical comparison of haplotype blocks, tagSNP sets and SNP variation for multiple populations. Bioinformatics (Oxford, England). 21: 3938-9. PMID 16131520 DOI: 10.1093/Bioinformatics/Bti649  0.92
2005 Kim JJ, Verdu P, Pakstis AJ, Speed WC, Kidd JR, Kidd KK. Use of autosomal loci for clustering individuals and populations of East Asian origin. Human Genetics. 117: 511-9. PMID 16028061 DOI: 10.1007/S00439-005-1334-8  0.6
2005 Sawyer SL, Mukherjee N, Pakstis AJ, Feuk L, Kidd JR, Brookes AJ, Kidd KK. Linkage disequilibrium patterns vary substantially among populations. European Journal of Human Genetics : Ejhg. 13: 677-86. PMID 15657612 DOI: 10.1038/Sj.Ejhg.5201368  0.92
2005 Sternberg RJ, Grigorenko EL, Kidd KK. Intelligence, race, and genetics. The American Psychologist. 60: 46-59. PMID 15641921 DOI: 10.1036/1097-8542.Yb071440  0.92
2004 Duffy VB, Davidson AC, Kidd JR, Kidd KK, Speed WC, Pakstis AJ, Reed DR, Snyder DJ, Bartoshuk LM. Bitter receptor gene (TAS2R38), 6-n-propylthiouracil (PROP) bitterness and alcohol intake. Alcoholism, Clinical and Experimental Research. 28: 1629-37. PMID 15547448 DOI: 10.1097/01.Alc.0000145789.55183.D4  0.92
2004 Tishkoff SA, Kidd KK. Implications of biogeography of human populations for 'race' and medicine. Nature Genetics. 36: S21-7. PMID 15507999 DOI: 10.1038/Ng1438  0.92
2004 Liu N, Sawyer SL, Mukherjee N, Pakstis AJ, Kidd JR, Kidd KK, Brookes AJ, Zhao H. Haplotype block structures show significant variation among populations. Genetic Epidemiology. 27: 385-400. PMID 15389924 DOI: 10.1002/Gepi.20026  0.92
2004 Kidd KK, Pakstis AJ, Speed WC, Kidd JR. Understanding human DNA sequence variation. The Journal of Heredity. 95: 406-20. PMID 15388768 DOI: 10.1093/Jhered/Esh060  0.92
2004 Paschou P, Feng Y, Pakstis AJ, Speed WC, DeMille MM, Kidd JR, Jaghori B, Kurlan R, Pauls DL, Sandor P, Barr CL, Kidd KK. 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. 75: 545-60. PMID 15303240 DOI: 10.1086/424389  0.92
2004 Jensen-Seaman MI, Sarmiento EE, Deinard AS, Kidd KK. Nuclear integrations of mitochondrial DNA in gorillas. American Journal of Primatology. 63: 139-47. PMID 15258958 DOI: 10.1002/Ajp.20047  0.92
2004 Palmatier MA, Pakstis AJ, Speed W, Paschou P, Goldman D, Odunsi A, Okonofua F, Kajuna S, Karoma N, Kungulilo S, Grigorenko E, Zhukova OV, Bonne-Tamir B, Lu RB, Parnas J, ... ... Kidd KK, et al. COMT haplotypes suggest P2 promoter region relevance for schizophrenia. Molecular Psychiatry. 9: 859-70. PMID 15098000 DOI: 10.1038/Sj.Mp.4001496  0.92
2004 Wang E, Ding YC, Flodman P, Kidd JR, Kidd KK, Grady DL, Ryder OA, Spence MA, Swanson JM, Moyzis RK. The genetic architecture of selection at the human dopamine receptor D4 (DRD4) gene locus. American Journal of Human Genetics. 74: 931-44. PMID 15077199 DOI: 10.1086/420854  0.92
2004 Osier MV, Lu RB, Pakstis AJ, Kidd JR, Huang SY, Kidd KK. 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. 126: 19-22. PMID 15048643 DOI: 10.1002/Ajmg.B.20136  0.92
2004 Oota H, Pakstis AJ, Bonne-Tamir B, Goldman D, Grigorenko E, Kajuna SL, Karoma NJ, Kungulilo S, Lu RB, Odunsi K, Okonofua F, Zhukova OV, Kidd JR, Kidd KK. The evolution and population genetics of the ALDH2 locus: random genetic drift, selection, and low levels of recombination. Annals of Human Genetics. 68: 93-109. PMID 15008789 DOI: 10.1046/J.1529-8817.2003.00060.X  0.6
2003 Horton R, Rosenberg NA, Pritchard JK, Weber JL, Cann HM, Kidd KK, Zhivotovsky LA, Feldman MW. Read all about it: The Lancet's Paper of the Year, 2003. Lancet. 362: 2101-3. PMID 14697815  0.92
2003 Chattopadhyay P, Pakstis AJ, Mukherjee N, Iyengar S, Odunsi A, Okonofua F, Bonne-Tamir B, Speed W, Kidd JR, Kidd KK. Global survey of haplotype frequencies and linkage disequilibrium at the RET locus. European Journal of Human Genetics : Ejhg. 11: 760-9. PMID 14512966 DOI: 10.1038/Sj.Ejhg.5201036  0.6
2003 Zhong XB, Reynolds R, Kidd JR, Kidd KK, Jenison R, Marlar RA, Ward DC. Single-nucleotide polymorphism genotyping on optical thin-film biosensor chips. Proceedings of the National Academy of Sciences of the United States of America. 100: 11559-64. PMID 12975525 DOI: 10.1073/Pnas.1934783100  0.92
2003 Rupert JL, Monsalve MV, Kidd KK, Tan C, Hochachka PW, Devine DV. Selective pressure has not acted against hypercoagulability alleles in high-altitude Amerindians. Annals of Human Genetics. 67: 426-32. PMID 12940916 DOI: 10.1046/J.1469-1809.2003.00043.X  0.92
2003 Yu N, Jensen-Seaman MI, Chemnick L, Kidd JR, Deinard AS, Ryder O, Kidd KK, Li WH. Low nucleotide diversity in chimpanzees and bonobos. Genetics. 164: 1511-8. PMID 12930756  0.92
2003 Rupert JL, Kidd KK, Norman LE, Monsalve MV, Hochachka PW, Devine DV. Genetic polymorphisms in the Renin-Angiotensin system in high-altitude and low-altitude Native American populations. Annals of Human Genetics. 67: 17-25. PMID 12556231 DOI: 10.1046/J.1469-1809.2003.00004.X  0.92
2003 Rajeevan H, Osier MV, Cheung KH, Deng H, Druskin L, Heinzen R, Kidd JR, Stein S, Pakstis AJ, Tosches NP, Yeh CC, Miller PL, Kidd KK. ALFRED: the ALelle FREquency Database. Update. Nucleic Acids Research. 31: 270-1. PMID 12519999 DOI: 10.1093/Nar/Gkg043  0.92
2003 Wang S, Kidd KK, Zhao H. On the use of DNA pooling to estimate haplotype frequencies. Genetic Epidemiology. 24: 74-82. PMID 12508258 DOI: 10.1002/Gepi.10195  0.92
2003 Leckman JF, Pauls DL, Zhang H, Rosario-Campos MC, Katsovich L, Kidd KK, Pakstis AJ, Alsobrook JP, Robertson MM, McMahon WM, Walkup JT, van de Wetering BJ, King RA, Cohen DJ. 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. 116: 60-8. PMID 12497616 DOI: 10.1002/Ajmg.B.10001  0.92
2002 Osier MV, Pakstis AJ, Goldman D, Edenberg HJ, Kidd JR, Kidd KK. A proline-threonine substitution in codon 351 of ADH1C is common in Native Americans. Alcoholism, Clinical and Experimental Research. 26: 1759-63. PMID 12500098 DOI: 10.1111/J.1530-0277.2002.Tb02481.X  0.92
2002 Rosenberg NA, Pritchard JK, Weber JL, Cann HM, Kidd KK, Zhivotovsky LA, Feldman MW. Genetic structure of human populations. Science (New York, N.Y.). 298: 2381-5. PMID 12493913 DOI: 10.1126/Science.1078311  0.92
2002 Whitfield JB, Kidd KK, Osier MV, Pakstis AJ, Kidd JR. Alcohol dehydrogenase and alcohol dependence: Variation in genotype-associated risk between populations [6] (multiple letters) American Journal of Human Genetics. 71: 1247-1251. PMID 12452180 DOI: 10.1086/344287  0.92
2002 DeMille MM, Kidd JR, Ruggeri V, Palmatier MA, Goldman D, Odunsi A, Okonofua F, Grigorenko E, Schulz LO, Bonne-Tamir B, Lu RB, Parnas J, Pakstis AJ, Kidd KK. Population variation in linkage disequilibrium across the COMT gene considering promoter region and coding region variation. Human Genetics. 111: 521-37. PMID 12436243 DOI: 10.1007/S00439-002-0809-0  0.6
2002 Osier MV, Cheung KH, Kidd JR, Pakstis AJ, Miller PL, Kidd KK. ALFRED: An allele frequency database for anthropology. American Journal of Physical Anthropology. 119: 77-83. PMID 12209575 DOI: 10.1002/Ajpa.10094  0.92
2002 Osier MV, Pakstis AJ, Soodyall H, Comas D, Goldman D, Odunsi A, Okonofua F, Parnas J, Schulz LO, Bertranpetit J, Bonne-Tamir B, Lu RB, Kidd JR, Kidd KK. A global perspective on genetic variation at the ADH genes reveals unusual patterns of linkage disequilibrium and diversity. American Journal of Human Genetics. 71: 84-99. PMID 12050823 DOI: 10.1086/341290  0.92
2002 Cann HM, de Toma C, Cazes L, Legrand MF, Morel V, Piouffre L, Bodmer J, Bodmer WF, Bonne-Tamir B, Cambon-Thomsen A, Chen Z, Chu J, Carcassi C, Contu L, Du R, ... ... Kidd KK, et al. A human genome diversity cell line panel. Science (New York, N.Y.). 296: 261-2. PMID 11954565 DOI: 10.1126/Science.296.5566.261B  0.92
2002 Fullerton SM, Bartoszewicz A, Ybazeta G, Horikawa Y, Bell GI, Kidd KK, Cox NJ, Hudson RR, Di Rienzo A. Geographic and haplotype structure of candidate type 2 diabetes susceptibility variants at the calpain-10 locus. American Journal of Human Genetics. 70: 1096-106. PMID 11891618 DOI: 10.1086/339930  0.92
2002 Ding YC, Chi HC, Grady DL, Morishima A, Kidd JR, Kidd KK, Flodman P, Spence MA, Schuck S, Swanson JM, Zhang YP, Moyzis RK. 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. 99: 309-14. PMID 11756666 DOI: 10.1073/Pnas.012464099  0.92
2002 Zhang S, Kidd KK, Zhao H. Detecting genetic association in case-control studies using similarity-based association tests Statistica Sinica. 12: 337-359.  0.92
2001 Jensen-Seaman MI, Deinard AS, Kidd KK. Modern African ape populations as genetic and demographic models of the last common ancestor of humans, chimpanzees, and gorillas. The Journal of Heredity. 92: 475-80. PMID 11948214 DOI: 10.1093/Jhered/92.6.475  0.92
2001 Turner G, Barbulescu M, Su M, Jensen-Seaman MI, Kidd KK, Lenz J. Insertional polymorphisms of full-length endogenous retroviruses in humans. Current Biology : Cb. 11: 1531-5. PMID 11591322 DOI: 10.1016/S0960-9822(01)00455-9  0.92
2001 Jensen-Seaman MI, Kidd KK. Mitochondrial DNA variation and biogeography of eastern gorillas. Molecular Ecology. 10: 2241-7. PMID 11555266 DOI: 10.1046/J.0962-1083.2001.01365.X  0.92
2001 Zhang S, Pakstis AJ, Kidd KK, Zhao H. Comparisons of two methods for haplotype reconstruction and haplotype frequency estimation from population data. American Journal of Human Genetics. 69: 906-14. PMID 11536083 DOI: 10.1086/323622  0.92
2001 Barbulescu M, Turner G, Su M, Kim R, Jensen-Seaman MI, Deinard AS, Kidd KK, Lenz J. A HERV-K provirus in chimpanzees, bonobos and gorillas, but not humans. Current Biology : Cb. 11: 779-83. PMID 11378389 DOI: 10.1016/S0960-9822(01)00227-5  0.92
2001 Osier MV, Cheung KH, Kidd JR, Pakstis AJ, Miller PL, Kidd KK. ALFRED: an allele frequency database for diverse populations and DNA polymorphisms--an update. Nucleic Acids Research. 29: 317-9. PMID 11125124 DOI: 10.1093/Nar/29.1.317  0.92
2001 Mateu E, Calafell F, Lao O, Bonné-Tamir B, Kidd JR, Pakstis A, Kidd KK, Bertranpetit J. Worldwide genetic analysis of the CFTR region. American Journal of Human Genetics. 68: 103-17. PMID 11104661 DOI: 10.1086/316940  0.6
2001 Calafell F, Grigorenko EL, Chikanian AA, Kidd KK. Haplotype evolution and linkage disequilibrium: A simulation study. Human Heredity. 51: 85-96. PMID 11096275 DOI: 10.1159/000022963  0.92
2001 Kidd K, Kidd JR, Pakstis AJ, Zhao H. Global patterns of linkage disequilibrium in Homo sapiens Pathologie Biologie. 49: 402-403. DOI: 10.1016/S0369-8114(01)00190-0  0.92
2000 Cheung KH, Miller PL, Kidd JR, Kidd KK, Osier MV, Pakstis AJ. ALFRED: a Web-accessible allele frequency database. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 639-50. PMID 10902212  0.92
2000 Tishkoff SA, Pakstis AJ, Ruano G, Kidd KK. The accuracy of statistical methods for estimation of haplotype frequencies: an example from the CD4 locus. American Journal of Human Genetics. 67: 518-22. PMID 10859209 DOI: 10.1086/303000  0.92
2000 Kidd JR, Pakstis AJ, Zhao H, Lu RB, Okonofua FE, Odunsi A, Grigorenko E, Tamir BB, Friedlaender J, Schulz LO, Parnas J, Kidd KK. Haplotypes and linkage disequilibrium at the phenylalanine hydroxylase locus, PAH, in a global representation of populations. American Journal of Human Genetics. 66: 1882-99. PMID 10788337 DOI: 10.1086/302952  0.92
2000 Seaman MI, Chang FM, Quiñones AT, Kidd KK. Evolution of exon 1 of the dopamine D4 receptor (DRD4) gene in primates. The Journal of Experimental Zoology. 288: 32-8. PMID 10750051 DOI: 10.1002/(Sici)1097-010X(20000415)288:1<32::Aid-Jez4>3.0.Co;2-G  0.92
2000 Deinard AS, Kidd K. Identifying conservation units within captive chimpanzee populations. American Journal of Physical Anthropology. 111: 25-44. PMID 10618587 DOI: 10.1002/(Sici)1096-8644(200001)111:1<25::Aid-Ajpa3>3.0.Co;2-R  0.92
2000 Cheung KH, Osier MV, Kidd JR, Pakstis AJ, Miller PL, Kidd KK. ALFRED: an allele frequency database for diverse populations and DNA polymorphisms. Nucleic Acids Research. 28: 361-3. PMID 10592274 DOI: 10.1093/Nar/28.1.361  0.92
2000 Kong A, Nicolae DL, Zhao H, Merikangas KR, Kidd KK. On a randomization procedure [1] (multiple letters) American Journal of Human Genetics. 67: 1352-1355.  0.92
1999 Zhao H, Pakstis AJ, Kidd JR, Kidd KK. Assessing linkage disequilibrium in a complex genetic system. I. Overall deviation from random association. Annals of Human Genetics. 63: 167-79. PMID 10738528 DOI: 10.1046/J.1469-1809.1999.6320167.X  0.92
1999 Quintana-Murci L, Semino O, Poloni ES, Liu A, Van Gijn M, Passarino G, Brega A, Nasidze IS, Maccioni L, Cossu G, al-Zahery N, Kidd JR, Kidd KK, Santachiara-Benerecetti AS. Y-chromosome specific YCAII, DYS19 and YAP polymorphisms in human populations: a comparative study. Annals of Human Genetics. 63: 153-66. PMID 10738527 DOI: 10.1046/J.1469-1809.1999.6320153.X  0.92
1999 Zhao H, Sheffield LJ, Pakstis AJ, Knauert MP, Kidd KK. A more powerful method to evaluate p-values in GENEHUNTER. Genetic Epidemiology. 17: S415-20. PMID 10597472 DOI: 10.1002/Gepi.1370170770  0.92
1999 Sheffield LJ, Knauert MP, Pakstis AJ, Zhao H, Kidd KK. Analyses of the COGA data set in one ethnic group with examinations of alternative definitions of alcoholism. Genetic Epidemiology. 17: S319-24. PMID 10597456 DOI: 10.1002/Gepi.1370170754  0.36
1999 Seaman MI, Fisher JB, Chang F, Kidd KK. Tandem duplication polymorphism upstream of the dopamine D4 receptor gene (DRD4). American Journal of Medical Genetics. 88: 705-9. PMID 10581493 DOI: 10.1002/(Sici)1096-8628(19991215)88:6<705::Aid-Ajmg22>3.0.Co;2-F  0.92
1999 Zhao H, Merikangas KR, Kidd KK. On a randomization procedure in linkage analysis. American Journal of Human Genetics. 65: 1449-56. PMID 10521312 DOI: 10.1086/302607  0.92
1999 Palmatier MA, Kang AM, Kidd KK. Global variation in the frequencies of functionally different catechol-O-methyltransferase alleles. Biological Psychiatry. 46: 557-67. PMID 10459407 DOI: 10.1016/S0006-3223(99)00098-0  0.92
1999 Deinard A, Dorit R, Castiglione C, Jiang Z, Becker D, Ruddle F, Schugart K, Kidd K. Evolution of the HOXB6 intergenic region: motif conservation at the lateral plate mesoderm (LPM) enhancer element. The Journal of Experimental Zoology. 285: 170-6. PMID 10440728 DOI: 10.1002/(Sici)1097-010X(19990815)285:2<170::Aid-Jez9>3.0.Co;2-J  0.92
1999 Kang AM, Palmatier MA, Kidd KK. Global variation of a 40-bp VNTR in the 3'-untranslated region of the dopamine transporter gene (SLC6A3). Biological Psychiatry. 46: 151-60. PMID 10418689 DOI: 10.1016/S0006-3223(99)00101-8  0.92
1999 Odunsi K, Kidd KK. A paradigm for finding genes for a complex human trait: polycystic ovary syndrome and follistatin. Proceedings of the National Academy of Sciences of the United States of America. 96: 8315-7. PMID 10411866 DOI: 10.1073/Pnas.96.15.8315  0.92
1999 Barr CL, Wigg KG, Pakstis AJ, Kurlan R, Pauls D, Kidd KK, Tsui LC, Sandor P. Genome scan for linkage to Gilles de la Tourette syndrome. American Journal of Medical Genetics. 88: 437-45. PMID 10402514 DOI: 10.1002/(Sici)1096-8628(19990820)88:4<437::Aid-Ajmg24>3.0.Co;2-E  0.36
1999 Deinard A, Kidd K. Evolution of a HOXB6 intergenic region within the great apes and humans. Journal of Human Evolution. 36: 687-703. PMID 10330333 DOI: 10.1006/Jhev.1999.0298  0.92
1999 Osier M, Pakstis AJ, Kidd JR, Lee JF, Yin SJ, Ko HC, Edenberg HJ, Lu RB, Kidd KK. Linkage disequilibrium at the ADH2 and ADH3 loci and risk of alcoholism. American Journal of Human Genetics. 64: 1147-57. PMID 10090900 DOI: 10.1086/302317  0.92
1999 Gelernter J, Cubells JF, Kidd JR, Pakstis AJ, Kidd KK. Population studies of polymorphisms of the serotonin transporter protein gene. American Journal of Medical Genetics. 88: 61-6. PMID 10050969 DOI: 10.1002/(Sici)1096-8628(19990205)88:1<61::Aid-Ajmg11>3.0.Co;2-K  0.92
1999 Calafell F, Shuster A, Speed WC, Kidd JR, Black FL, Kidd KK. Genealogy reconstruction from short tandem repeat genotypes in an Amazonian population. American Journal of Physical Anthropology. 108: 137-46. PMID 9988377 DOI: 10.1002/(Sici)1096-8644(199902)108:2<137::Aid-Ajpa1>3.0.Co;2-K  0.92
1999 Mateu E, Calafell F, Bonné-Tamir B, Kidd JR, Casals T, Kidd KK, Bertranpetit J. Allele frequencies in a worldwide survey of a CA repeat in the first intron of the CFTR gene. Human Heredity. 49: 15-20. PMID 9858852 DOI: 10.1159/000022834  0.6
1999 Kidd KK, Kidd JR. Experience and preliminary results in human genome diversity research Politics and the Life Sciences. 18: 314-316.  0.92
1998 Iyengar S, Seaman M, Deinard AS, Rosenbaum HC, Sirugo G, Castiglione CM, Kidd JR, Kidd KK. 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. 8: 317-27. PMID 10993602 DOI: 10.3109/10425179809034076  0.92
1998 Deinard AS, Kidd KK. Evolution of a D2 dopamine receptor intron within the great apes and humans. Dna Sequence : the Journal of Dna Sequencing and Mapping. 8: 289-301. PMID 10993600 DOI: 10.3109/10425179809034074  0.92
1998 Calafell F, Shuster A, Speed WC, Kidd JR, Kidd KK. Short tandem repeat polymorphism evolution in humans. European Journal of Human Genetics : Ejhg. 6: 38-49. PMID 9781013 DOI: 10.1038/Sj.Ejhg.5200151  0.92
1998 Kidd KK, Morar B, Castiglione CM, Zhao H, Pakstis AJ, Speed WC, Bonne-Tamir B, Lu RB, Goldman D, Lee C, Nam YS, Grandy DK, Jenkins T, Kidd JR. A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus. Human Genetics. 103: 211-27. PMID 9760208 DOI: 10.1007/S004390050809  0.92
1998 Deinard AS, Sirugo G, Kidd KK. Hominoid phylogeny: inferences from a sub-terminal minisatellite analyzed by repeat expansion detection (RED) Journal of Human Evolution. 35: 313-7. PMID 9749409  0.92
1998 Zietkiewicz E, Yotova V, Jarnik M, Korab-Laskowska M, Kidd KK, Modiano D, Scozzari R, Stoneking M, Tishkoff S, Batzer M, Labuda D. Genetic structure of the ancestral population of modern humans. Journal of Molecular Evolution. 47: 146-55. PMID 9694663 DOI: 10.1007/Pl00006371  0.92
1998 Sirugo G, Kidd KK. Repeat expansion-detection analysis of telomeric uninterrupted (TTAGGG)n arrays. American Journal of Human Genetics. 63: 648-51. PMID 9683592 DOI: 10.1086/301961  0.92
1998 Goodman AB, Sirugo G, Pakstis AJ, Kidd KK. Is transthyretin (TTR) disrupted by a trinucleotide repeat expansion in a Schizophrenia kindred? [1] (multiple letters) American Journal of Medical Genetics - Neuropsychiatric Genetics. 81: 347-348. PMID 9674983 DOI: 10.1002/(SICI)1096-8628(19980710)81:4<347::AID-AJMG13>3.0.CO;2-L  0.92
1998 Tishkoff SA, Goldman A, Calafell F, Speed WC, Deinard AS, Bonne-Tamir B, Kidd JR, Pakstis AJ, Jenkins T, Kidd KK. 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. 62: 1389-402. PMID 9585589 DOI: 10.1086/301861  0.92
1998 King BL, Sirugo G, Nadeau JH, Hudson TJ, Kidd KK, Kacinski BM, Schalling M. Long CAG/CTG repeats in mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 9: 392-3. PMID 9545500 DOI: 10.1007/S003359900778  0.92
1998 Schnur RE, Gao M, Wick PA, Keller M, Benke PJ, Edwards MJ, Grix AW, Hockey A, Jung JH, Kidd KK, Kistenmacher M, Levin AV, Lewis RA, Musarella MA, Nowakowski RW, et al. OA1 mutations and deletions in X-linked ocular albinism. American Journal of Human Genetics. 62: 800-9. PMID 9529334 DOI: 10.1086/301776  0.92
1997 Zietkiewicz E, Yotova V, Jarnik M, Korab-Laskowska M, Kidd KK, Modiano D, Scozzari R, Stoneking M, Tishkoff S, Batzer M, Labuda D. Nuclear DNA diversity in worldwide distributed human populations. Gene. 205: 161-71. PMID 9461390 DOI: 10.1016/S0378-1119(97)00408-3  0.92
1997 Iyengar S, Calafell F, Kidd KK. Detection of major genes underlying several quantitative traits associated with a common disease using different ascertainment schemes. Genetic Epidemiology. 14: 809-14. PMID 9433582 DOI: 10.1002/(Sici)1098-2272(1997)14:6<809::Aid-Gepi41>3.0.Co;2-R  0.92
1997 Sirugo G, Pakstis AJ, Kidd KK, Matthysse S, Levy DL, Holzman PS, Párnas J, McInnis M, Breschel T, Ross CA. Detection of a large CTG/CAG trinucleotide repeat expansion in a Danish schizophrenia kindred. American Journal of Medical Genetics. 74: 546-8. PMID 9342210 DOI: 10.1002/(Sici)1096-8628(19970919)74:5<546::Aid-Ajmg19>3.0.Co;2-C  0.92
1997 Breschel TS, McInnis MG, Margolis RL, Sirugo G, Corneliussen B, Simpson SG, McMahon FJ, MacKinnon DF, Xu JF, Pleasant N, Huo Y, Ashworth RG, Grundstrom C, Grundstrom T, Kidd KK, et al. A novel, heritable, expanding CTG repeat in an intron of the SEF2-1 gene on chromosome 18q21.1. Human Molecular Genetics. 6: 1855-63. PMID 9302263 DOI: 10.1093/Hmg/6.11.1855  0.92
1997 Cubells JF, Kobayashi K, Nagatsu T, Kidd KK, Kidd JR, Calafell F, Kranzler HR, Ichinose H, Gelernter J. Population genetics of a functional variant of the dopamine beta-hydroxylase gene (DBH). American Journal of Medical Genetics. 74: 374-9. PMID 9259372 DOI: 10.1002/(Sici)1096-8628(19970725)74:4<374::Aid-Ajmg7>3.0.Co;2-P  0.6
1997 Sirugo G, Deinard AS, Kidd JR, Kidd KK. 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. 6: 403-8. PMID 9147643 DOI: 10.1093/Hmg/6.3.403  0.92
1997 Chang FM, Ko HC, Lu RB, Pakstis AJ, Kidd KK. The dopamine D4 receptor gene (DRD4) is not associated with alcoholism in three Taiwanese populations: six polymorphisms tested separately and as haplotypes. Biological Psychiatry. 41: 394-405. PMID 9034534 DOI: 10.1016/S0006-3223(96)00248-X  0.92
1997 Liao D, Pavelitz T, Kidd JR, Kidd KK, Weiner AM. 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. 16: 588-98. PMID 9034341 DOI: 10.1093/Emboj/16.3.588  0.92
1997 Kidd KK. Can we find genes for schizophrenia? American Journal of Medical Genetics. 74: 104-11. PMID 9034016 DOI: 10.1002/(Sici)1096-8628(19970221)74:1<104::Aid-Ajmg21>3.0.Co;2-U  0.92
1996 Risch N, Kidd KK, Tishkoff SA. Response: genetic data and the african origin of humans. Science (New York, N.Y.). 274: 1548b-9b. PMID 17816998 DOI: 10.1126/Science.274.5292.1548B  0.92
1996 Tishkoff SA, Kidd KK, Risch N. Response:interpretations of multiregional evolution. Science (New York, N.Y.). 274: 706-7. PMID 17735319 DOI: 10.1126/Science.274.5288.706  0.92
1996 Michalatos-Beloin S, Tishkoff SA, Bentley KL, Kidd KK, Ruano G. Molecular haplotyping of genetic markers 10 kb apart by allele-specific long-range PCR. Nucleic Acids Research. 24: 4841-3. PMID 8972876 DOI: 10.1093/Nar/24.23.4841  0.92
1996 Pritchard JK, Feldman MW. Genetic data and the African origin of humans. Science (New York, N.Y.). 274: 1548-9. PMID 8966621 DOI: 10.1126/science.274.5292.1548  0.92
1996 Wolpoff MH, Tishkoff SA, Kidd KK, Risch N. Interpretations of multiregional evolution [4] Science. 274: 704-707. PMID 8966550 DOI: 10.1126/SCIENCE.274.5288.704D  0.92
1996 Cheung KH, Nadkarni P, Silverstein S, Kidd JR, Pakstis AJ, Miller P, Kidd KK. PhenoDB: an integrated client/server database for linkage and population genetics. Computers and Biomedical Research, An International Journal. 29: 327-37. PMID 8812078 DOI: 10.1006/Cbmr.1996.0024  0.92
1996 Nadkarni P, Cheung KH, 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. 3: 319-29. PMID 8811490 DOI: 10.1089/Cmb.1996.3.319  0.32
1996 Gill JR, Reyes-Múgica M, Iyengar S, Kidd KK, Touloukian RJ, Smith C, Keller MS, Genel M. Early presentation of metastatic medullary carcinoma in multiple endocrine neoplasia, type IIA: implications for therapy. The Journal of Pediatrics. 129: 459-64. PMID 8804341 DOI: 10.1016/S0022-3476(96)70084-7  0.92
1996 Kidd KK, Pakstis AJ, Castiglione CM, Kidd JR, Speed WC, Goldman D, Knowler WC, Lu RB, Bonne-Tamir B. DRD2 haplotypes containing the TaqI A1 allele: implications for alcoholism research. Alcoholism, Clinical and Experimental Research. 20: 697-705. PMID 8800387 DOI: 10.1111/J.1530-0277.1996.Tb01674.X  0.6
1996 Becker D, Jiang Z, Knödler P, Deinard AS, Eid R, Kidd KK, Shashikant CS, Ruddle FH, Schughart K. Conserved regulatory element involved in the early onset of Hoxb6 gene expression. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 205: 73-81. PMID 8770553 DOI: 10.1002/(Sici)1097-0177(199601)205:1<73::Aid-Aja7>3.0.Co;2-2  0.92
1996 Chang FM, Kidd JR, Livak KJ, Pakstis AJ, Kidd KK. The world-wide distribution of allele frequencies at the human dopamine D4 receptor locus. Human Genetics. 98: 91-101. PMID 8682515 DOI: 10.1007/S004390050166  0.92
1996 Lu RB, Ko HC, Chang FM, Castiglione CM, Schoolfield G, Pakstis AJ, Kidd JR, Kidd KK. No association between alcoholism and multiple polymorphisms at the dopamine D2 receptor gene (DRD2) in three distinct Taiwanese populations. Biological Psychiatry. 39: 419-29. PMID 8679787 DOI: 10.1016/0006-3223(95)00182-4  0.6
1996 Tishkoff SA, Ruano G, Kidd JR, Kidd KK. Distribution and frequency of a polymorphic Alu insertion at the plasminogen activator locus in humans. Human Genetics. 97: 759-64. PMID 8641693 DOI: 10.1007/Bf02346186  0.92
1996 Armour JA, Anttinen T, May CA, Vega EE, Sajantila A, Kidd JR, Kidd KK, Bertranpetit J, Pääbo S, Jeffreys AJ. Minisatellite diversity supports a recent African origin for modern humans. Nature Genetics. 13: 154-60. PMID 8640220 DOI: 10.1038/Ng0696-154  0.6
1996 Haaf T, Sirugo G, Kidd KK, Ward DC. Chromosomal localization of long trinucleotide repeats in the human genome by fluorescence in situ hybridization. Nature Genetics. 12: 183-5. PMID 8563757 DOI: 10.1038/Ng0296-183  0.92
1996 Rogers J, Kidd KK. Nucleotide polymorphism, effective population size, and dispersal distances in the yellow baboons (Papio hamadryas cynocephalus) of Mikumi National Park, Tanzania American Journal of Primatology. 38: 157-168.  0.92
1996 Grigorenko EL, Shikanyan AA, Kidd JR, Dorit R, Kidd KK. Dynamics of Haplotype Frequencies in Populations: Study by the Monte Carlo Method Russian Journal of Genetics. 32: 1486-1493.  0.92
1995 Gelernter J, Vandenbergh D, Kruger SD, Pauls DL, Kurlan R, Pakstis AJ, Kidd KK, Uhl G. The dopamine transporter protein gene (SLC6A3): primary linkage mapping and linkage studies in Tourette syndrome. Genomics. 30: 459-63. PMID 8825631 DOI: 10.1006/Geno.1995.1265  0.92
1995 Miller PL, Nadkarni PM, Kidd KK, Cheung K, Ward DC, Banks A, Bray-Ward P, Cupelli L, Herdman V, Marondel I, Montgomery K, Renault B, Yoon SJ, Krauter KS, Kucherlapati R. Internet-based support for bioscience research: a collaborative genome center for human chromosome 12. Journal of the American Medical Informatics Association : Jamia. 2: 351-64. PMID 8581551 DOI: 10.1136/Jamia.1995.96157828  0.32
1995 Gelernter J, Pakstis AJ, Kidd KK. Linkage mapping of serotonin transporter protein gene SLC6A4 on chromosome 17. Human Genetics. 95: 677-80. PMID 7789954 DOI: 10.1007/Bf00209486  0.92
1995 Litt M, Kramer P, Kort E, Fain P, Cox S, Root D, White R, Weissenbach J, Donis-Keller H, Gatti R, Weber J, Nakamura Y, Julier C, Hayashi K, Spurr N, ... ... Kidd K, et al. The CEPH Consortium Linkage Map of Human Chromosome 11 Genomics. 27: 101-112. PMID 7665156 DOI: 10.1006/Geno.1995.1011  0.92
1995 Gelernter J, Rao PA, Pauls DL, Hamblin MW, Sibley DR, Kidd KK. Assignment of the 5HT7 receptor gene (HTR7) to chromosome 10q and exclusion of genetic linkage with Tourette syndrome. Genomics. 26: 207-9. PMID 7601444 DOI: 10.1016/0888-7543(95)80202-W  0.92
1995 Moises HW, Yang L, Kristbjarnarson H, Wiese C, Byerley W, Macciardi F, Arolt V, Blackwood D, Liu X, Sjögren B, Aschauer HN, Hwu HG, Jang K, Livesley WJ, Kennedy JL, ... ... Kidd KK, et al. An international two–stage genome–wide search for schizophrenia susceptibility genes Nature Genetics. 11: 321-324. PMID 7581457 DOI: 10.1038/Ng1195-321  0.36
1995 Hawley ME, Kidd KK. HAPLO: a program using the EM algorithm to estimate the frequencies of multi-site haplotypes. The Journal of Heredity. 86: 409-11. PMID 7560877 DOI: 10.1093/Oxfordjournals.Jhered.A111613  0.92
1994 Ruano G, Deinard AS, Tishkoff S, Kidd KK. Detection of DNA sequence variation via deliberate heteroduplex formation from genomic DNAs amplified en masse in "population tubes". Pcr Methods and Applications. 3: 225-31. PMID 8173512 DOI: 10.1101/Gr.3.4.225  0.92
1994 Gelernter J, Pauls DL, Leckman J, Kidd KK, Kurlan R. D2 dopamine receptor alleles do not influence severity of Tourette's syndrome. Results from four large kindreds. Archives of Neurology. 51: 397-400. PMID 8155017 DOI: 10.1001/Archneur.1994.00540160099012  0.92
1994 Barr CL, Kennedy JL, Pakstis AJ, Castiglione CM, Kidd JR, Wetterberg L, Kidd KK. Linkage study of a susceptibility locus for schizophrenia in the pseudoautosomal region. Schizophrenia Bulletin. 20: 277-86. PMID 8085132 DOI: 10.1093/Schbul/20.2.277  0.6
1994 Wright LW, Lichter JB, Reinitz J, Shifman MA, Kidd KK, Miller PL. Computer-assisted restriction mapping: an integrated approach to handling experimental uncertainty. Computer Applications in the Biosciences : Cabios. 10: 435-42. PMID 7804876 DOI: 10.1093/Bioinformatics/10.4.435  0.92
1994 Ruano G, Deinard AS, Tishkoff S, Kidd KK. Detection of DNA sequence variation via deliberate heteroduplex formation from genomic DNAs amplified en masse in "population tubes'' Genome Research. 3: 225-231.  0.92
1993 Kidd JR, Kidd KK, Weiss KM. Human genome diversity initiative. Human Biology. 65: 1-6. PMID 8436383  0.92
1993 Barr CL, Kidd KK. Population frequencies of the A1 allele at the dopamine D2 receptor locus. Biological Psychiatry. 34: 204-9. PMID 8399816 DOI: 10.1016/0006-3223(93)90073-M  0.92
1993 Kidd KK. Associations of disease with genetic markers: déjà vu all over again. American Journal of Medical Genetics. 48: 71-3. PMID 8362928 DOI: 10.1002/Ajmg.1320480202  0.92
1993 Lichter JB, Barr CL, Kennedy JL, Van Tol HH, Kidd KK, Livak KJ. A hypervariable segment in the human dopamine receptor D4 (DRD4) gene. Human Molecular Genetics. 2: 767-73. PMID 8353495 DOI: 10.1093/Hmg/2.6.767  0.92
1993 Lichter JB, Difilippantonio MJ, Pakstis AJ, Goodfellow PJ, Ward DC, Kidd KK. Physical and genetic maps for chromosome 10. Genomics. 16: 320-4. PMID 8314570 DOI: 10.1006/Geno.1993.1192  0.92
1993 Barr CL, Kennedy JL, Lichter JB, Van Tol HH, Wetterberg L, Livak KJ, Kidd KK. 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. 48: 218-22. PMID 8135305 DOI: 10.1002/Ajmg.1320480409  0.92
1993 Gelernter J, Kruger S, Kidd KK, Amara S. TaqI RFLP at norepinephrine transporter protein (NET) locus. Human Molecular Genetics. 2: 820. PMID 8102573 DOI: 10.1093/Hmg/2.6.820-A  0.92
1993 Rogers J, Kidd KK. Nuclear DNA polymorphisms in a wild population of yellow baboons (Papio hamadryas cynocephalus) from Mikumi National Park, Tanzania. American Journal of Physical Anthropology. 90: 477-86. PMID 8097371 DOI: 10.1002/Ajpa.1330900407  0.92
1993 Lichter JB, Wu J, Brooks-Wilson AR, Difillipantonio M, Brewster S, Ward DC, Goodfellow PJ, Kidd KK. A new polymorphic marker (D10S97) tightly linked to the multiple endocrine neoplasia type 2A (MEN2A) locus. Human Genetics. 90: 516-20. PMID 8094065 DOI: 10.1007/Bf00217451  0.92
1993 Gelernter J, Kruger S, Pakstis AJ, Pacholczyk T, Sparkes RS, Kidd KK, Amara S. Assignment of the norepinephrine transporter protein (NET1) locus to chromosome 16. Genomics. 18: 690-2. PMID 7905857 DOI: 10.1016/S0888-7543(05)80375-1  0.92
1993 Brooks-Wilson AR, Lichter JB, Ward DC, Kidd KK, Goodfellow PJ. 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. 17: 611-7. PMID 7902324 DOI: 10.1006/Geno.1993.1380  0.92
1993 Zullo S, Kennedy JL, Gelernter J, Polymeropoulos MH, Tallini G, Pakstis AJ, Shapiro MB, Merril CR, Kidd KK. Eliminating mitochondrial DNA competition for nuclear DNA primers. Pcr Methods and Applications. 3: 39-45. PMID 7693114 DOI: 10.1101/Gr.3.1.39  0.36
1992 Lichter JB, Wu J, Miller D, Goodfellow PJ, Kidd KK. A high-resolution meiotic mapping panel for the pericentromeric region of chromosome 10. Genomics. 13: 607-12. PMID 1353475 DOI: 10.1016/0888-7543(92)90131-B  0.92
1992 Miller DL, Dill FJ, Lichter JB, Kidd KK, Goodfellow PJ. Isolation and high-resolution mapping of new DNA markers from the pericentromeric region of chromosome 10. Genomics. 13: 601-6. PMID 1353474 DOI: 10.1016/0888-7543(92)90130-K  0.92
1992 Ruano G, Rogers J, Ferguson-Smith AC, Kidd KK. DNA sequence polymorphism within hominoid species exceeds the number of phylogenetically informative characters for a HOX2 locus Molecular Biology and Evolution. 9: 575-586. PMID 1352841 DOI: 10.1093/Oxfordjournals.Molbev.A040743  0.92
1992 Gelernter J, Pakstis AJ, Grandy D, Litt M, Retief AE, Kennedy JL, Hing-Loh A, Schoolfield G, Civelli O, Kidd KK. Linkage map of eight human chromosome 11q markers, including DRD2, spanning 60 cM. Cytogenetics and Cell Genetics. 60: 26-8. PMID 1349858 DOI: 10.1159/000133287  0.36
1992 Deinard AS, Ruano G, Kidd KK. A dinucleotide repeat polymorphism at the HOX2B locus Nucleic Acids Research. 20: 1171. PMID 1347934 DOI: 10.1093/Nar/20.5.1171-A  0.92
1992 Lichter JB, Wu JS, Genel M, Flynn SD, Pakstis AJ, Kidd JR, Kidd KK. Presymptomatic testing using DNA markers for individuals at risk for familial multiple endocrine neoplasia 2A. The Journal of Clinical Endocrinology and Metabolism. 74: 368-73. PMID 1346145 DOI: 10.1210/Jcem.74.2.1346145  0.92
1992 Ruano G, Kidd KK. Modeling of heteroduplex formation during PCR from mixtures of DNA templates Genome Research. 2: 112-116. DOI: 10.1101/Gr.2.2.112  0.92
1992 Chakraborty R, Kidd KK. Forensic DNA typing [7] Science. 255: 1053-1054.  0.92
1992 Ruano G, Kidd KK. Modeling of heteroduplex formation during PCR from mixtures of DNA templates Genome Research. 2: 112-116.  0.92
1991 Kidd KK, Simpson NE. Search for the gene for multiple endocrine neoplasia type 2A Recent Progress in Hormone Research. 46: 305-341. PMID 2281187 DOI: 10.1016/B978-0-12-571146-3.50015-8  0.92
1991 Moises HW, Gelernter J, Giuffra LA, Zarcone V, Wetterberg L, Civelli O, Kidd KK, Cavalli-Sforza LL, Grandy DK, Kennedy JL. No linkage between D2 dopamine receptor gene region and schizophrenia. Archives of General Psychiatry. 48: 643-7. PMID 2069495 DOI: 10.1001/Archpsyc.1991.01810310061011  0.92
1991 Gelernter J, Kidd KK. The current status of linkage studies in schizophrenia Research Publications - Association For Research in Nervous and Mental Disease. 69: 137-152. PMID 2003157  0.92
1991 Bowcock AM, Kidd JR, Mountain JL, Hebert JM, Carotenuto L, Kidd KK, Luca Cavalli-Sforza L. Drift, admixture, and selection in human evolution: A study with DNA polymorphisms Proceedings of the National Academy of Sciences of the United States of America. 88: 839-843. PMID 1992475 DOI: 10.1073/Pnas.88.3.839  0.92
1991 Pakstis AJ, Kidd JR, Castiglione CM, Kidd KK. Status of the search for a major genetic locus for affective disorder in the Old Order Amish Human Genetics. 87: 475-483. PMID 1879834 DOI: 10.1007/Bf00197172  0.92
1991 Kidd KK. Progress towards completing the human linkage map Current Opinion in Genetics and Development. 1: 99-104. PMID 1840885 DOI: 10.1016/0959-437X(91)80049-R  0.92
1991 Miller PL, Shifman MA, Kidd KK. 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. 409-413. PMID 1807633  0.92
1991 Kidd KK. Trials and tribulations in the search for genes causing neuropsychiatric disorders Social Biology. 38: 163-178. PMID 1801198 DOI: 10.1080/19485565.1991.9988785  0.92
1991 Chakraborty R, Kidd KK. The utility of DNA typing in forensic work Science. 254: 1735-1739. PMID 1763323 DOI: 10.1126/Science.1763323  0.92
1991 Ogura T, Castiglione CM, Pakstis AJ, Kidd KK. An Mspl polymorphism for the HOX2F gene Nucleic Acids Research. 19: 1716. PMID 1709280 DOI: 10.1093/Nar/19.7.1716  0.92
1991 Ruano G, Kidd KK. Genotyping and haplotyping of polymorphisms directly from genomic DNA via coupled amplification and sequencing(CAS) Nucleic Acids Research. 19: 6877-6882. PMID 1684844 DOI: 10.1093/Nar/19.24.6877  0.92
1991 Kidd JR, Black FL, Weiss KM, Balazs I, Kidd KK. Studies of three Amerindian populations using nuclear DNA polymorphisms Human Biology. 63: 775-794. PMID 1683642  0.92
1991 Gelernter J, Gejman PV, Bisighini S, Kidd KK. Sequence tagged site (STS) TaqI RFLP at dopamine beta-hydroxylase (DBH). Nucleic Acids Research. 19: 1957. PMID 1674371 DOI: 10.1093/Nar/19.8.1957  0.92
1991 Ogura T, Castiglione CM, Pakstis AJ, Kidd KK. Two RFLPs at the HOX2G locus Nucleic Acids Research. 19: 1716. PMID 1674132 DOI: 10.1093/Nar/19.7.1716-A  0.92
1991 Ruano G, Kidd KK. Coupled amplification and sequencing of genomic DNA Proceedings of the National Academy of Sciences of the United States of America. 88: 2815-2819. PMID 1672768 DOI: 10.1073/Pnas.88.7.2815  0.92
1990 Kidd KK. Letter to the editor: Chromosome plotbooks and diskettes available from the human gene mapping library American Journal of Medical Genetics. 37: 292. PMID 2248303 DOI: 10.1002/Ajmg.1320370231  0.92
1990 Stephens JC, Cavanaugh ML, Gradie MI, Mador ML, Kidd KK. Mapping the human genome: current status. Science (New York, N.Y.). 250: 237-44. PMID 2218527 DOI: 10.1126/Science.2218527  0.92
1990 Stephens JC, Mador ML, Cavanaugh ML, Gradie MI, Kidd KK. The human genome map 1990. Science (New York, N.Y.). 250: suppl 1-4. PMID 2218516 DOI: 10.1126/Science.2218516  0.92
1990 Dudley CRK, Giuffra LA, Tippett P, Kidd KK, Reeders ST. The Na+/H+ antiporter: a “melt” polymorphism allows regional mapping to the short arm of chromosome 1 Human Genetics. 86: 79-83. PMID 1979310 DOI: 10.1007/Bf00205179  0.92
1990 Gelernter J, Pakstis AJ, Pauls DL, Kurlan R, Gancher ST, Civelli O, Grandy D, Kidd KK. Gilles de la Tourette syndrome is not linked to D2-dopamine receptor. Archives of General Psychiatry. 47: 1073-7. PMID 1978653 DOI: 10.1001/Archpsyc.1990.01810230089014  0.36
1990 Carson NL, Wu JS, Jackson CE, Kidd KK, Simpson NE. 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. 47: 946-51. PMID 1978560  0.92
1990 Wu J, Kidd KK. A HaeIII polymorphism at the D10S101 locus Nucleic Acids Research. 18: 5577. PMID 1977118 DOI: 10.1093/Nar/18.18.5577-A  0.92
1990 Wu J, Kidd KK. Hincll polymorphism at the D10S95 locus Nucleic Acids Research. 18: 4965. PMID 1975682 DOI: 10.1093/Nar/18.16.4965-A  0.92
1990 Ruano G, Kidd KK, Stephens JC. 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. 87: 6296-300. PMID 1974719 DOI: 10.1073/Pnas.87.16.6296  0.92
1990 Wu J, Kidd KK. High frequency Pvull and Pstl polymorphisms identified by KW31 (D10S96) on chromosome 10 Nucleic Acids Research. 18: 1316. PMID 1969625 DOI: 10.1093/Nar/18.5.1316-A  0.92
1990 Wu J, Kidd KK. An EcoRI polymorphism identified by KW6 (D10S97) on chromosome 10 Nucleic Acids Research. 18: 1316. PMID 1969624 DOI: 10.1093/Nar/18.5.1316  0.92
1990 Ruano G, Gray MR, Miki T, Ferguson-Smith AC, Ruddle FH, Kidd KK. 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. 18: 1314. PMID 1969622 DOI: 10.1093/Nar/18.5.1314  0.92
1990 Kidd JR, Matsubara Y, Castiglione CM, Tanaka K, Kidd KK. The locus for the medium-chain acyl-CoA dehydrogenase gene on chromosome 1 is highly polymorphic Genomics. 6: 89-93. PMID 1968047 DOI: 10.1016/0888-7543(90)90451-Y  0.92
1990 Wu J, Kidd KK. Extensive sequence polymorphisms associated with chromosome 10 alpha satellite DNA and its close linkage to markers from the pericentromeric region Human Genetics. 84: 279-282. PMID 1968036 DOI: 10.1007/Bf00200575  0.92
1989 Mador ML, Cavanaugh ML, Chan HS, Alles WP, Hawley ME, Miller RL, Schiff GL, Ruddle FH, Kidd KK. The HGM10 information management system Cytogenetic and Genome Research. 51: 3-7. PMID 2791654 DOI: 10.1159/000132774  0.92
1989 Ruddle FH, Kidd KK. The human gene mapping workshops in transition Cytogenetics and Cell Genetics. 51: 1-2. PMID 2791652 DOI: 10.1159/000132773  0.92
1989 Ruano G, Fenton W, Kidd KK. Biphasic amplification of very dilute DNA samples via 'booster' PCR Nucleic Acids Research. 17: 5407. PMID 2762140 DOI: 10.1093/Nar/17.13.5407  0.92
1989 Price RA, Kramer PL, Pauls DL, Kidd KK. Estimation of segregation and linkage parameters in simulated data. II. Simultaneous estimation with one linked marker. American Journal of Human Genetics. 45: 95-105. PMID 2741954  0.92
1989 Kramer PL, Pauls DL, Price RA, Kidd KK. Estimation of segregation and linkage parameters in simulated data. I. Segregation analyses with different ascertainment schemes. American Journal of Human Genetics. 45: 83-94. PMID 2741953  0.92
1989 Kelsoe JR, Ginns EI, Egeland JA, Gerhard DS, Goldstein AM, Bale SJ, Pauls DL, Long RT, Kidd KK, Conte G, Housman DE, Paul SM. Re-evaluation of the linkage relationship between chromosome 11p loci and the gene for bipolar affective disorder in the Old Order Amish Nature. 342: 238-243. PMID 2682265 DOI: 10.1038/342238A0  0.92
1989 Simpson NE, Kidd KK. Closing in on the MEN2A locus Henry Ford Hospital Medical Journal. 37: 100-105. PMID 2576936  0.92
1989 Ruano G, Kidd KK. Direct haplotyping of chromosomal segments from multiple heterozygotes via allele-specific PCR amplification Nucleic Acids Research. 17: 8392. PMID 2573038 DOI: 10.1093/Nar/17.20.8392  0.92
1989 Wu J, Giuffra LA, Goodfellow PJ, Myers S, Carson NL, Anderson L, Hoyle LS, Simpson NE, Kidd KK. The β subunit locus of the human fibronectin receptor: DNA restriction fragment length polymorphism and linkage mapping studies Human Genetics. 83: 383-390. PMID 2572537 DOI: 10.1007/Bf00291386  0.92
1989 Simpson NE, Kidd KK. The mapping of the locus for multiple endocrine neoplasia type 2A by linkage with chromosome 10 markers Hormone and Metabolic Research. 21: 5-9. PMID 2572529  0.92
1989 Kurlan R, Kidd KK, Pauls D. Linkage analysis approach to hereditary movement disorders Journal of Neurogenetics. 5: 161-171. PMID 2569508 DOI: 10.3109/01677068909066206  0.92
1989 Giuffra LA, Kidd KK. Linkage analysis in psychiatry International Review of Psychiatry. 1: 231-242. DOI: 10.3109/09540268909089417  0.92
1988 Merikangas KR, Risch NJ, Merikangas JR, Weissman MM, Kidd KK. Migraine and depression: Association and familial transmission Journal of Psychiatric Research. 22: 119-129. PMID 3404480 DOI: 10.1016/0022-3956(88)90076-3  0.92
1988 Wu J, Ramesh V, Kidd JR, Castiglione CM, Myers S, Carson N, Anderson L, Gusella JF, Simpson NE, Kidd KK. The ornithine aminotransferase (OAT) locus is linked and distal to D10S20 on the long arm of chromosome 10 Cytogenetic and Genome Research. 48: 126-127. PMID 3197452 DOI: 10.1159/000132606  0.92
1988 Pauls DL, Cohen DJ, Kidd KK, Leckman JF. Tourette syndrome and neuropsychiatric disorders: is there a genetic relationship? American Journal of Human Genetics. 43: 206-217. PMID 3165247  0.92
1988 Cox NJ, Hodge SE, Marazita ML, Spence MA, Kidd KK. Some effects of selection strategies on linkage analysis Genetic Epidemiology. 5: 289-297. PMID 3049227 DOI: 10.1002/Gepi.1370050410  0.92
1988 Wu J, Cavenee WK, Miki T, Kidd KK. A polymorphic dna marker on chromosome 10 linked to rbp3 on the men2a side Cytogenetic and Genome Research. 48: 246-247. PMID 2907872 DOI: 10.1159/000132639  0.92
1988 Farrer LA, Castiglione CM, Kidd JR, Myers S, Carson N, Simpson NE, Kidd KK. A linkage group of five DNA markers on human chromosome 10 Genomics. 3: 72-77. PMID 2906045 DOI: 10.1016/0888-7543(88)90162-0  0.92
1988 Xue F, Kidd JR, Pakstis AJ, Castiglione CM, Mallet J, Kidd KK. Tyrosine hydroxylase maps to the short arm of chromosome 11 proximal to the insulin and HRAS1 loci Genomics. 2: 288-293. PMID 2906039 DOI: 10.1016/0888-7543(88)90016-X  0.92
1988 Wu J, Loren J, Sukhatme VP, Kidd KK. A hindIII polymorphism identified by the human early growth response gene 2 (EGR2) on chromosome 10 Nucleic Acids Research. 16: 11855. PMID 2905450 DOI: 10.1093/Nar/16.24.11855  0.92
1988 Miki T, Weil SC, Rosner GL, Reid MS, Kidd KK. An MPO cDNA clone identifies an RFLP with PstI. Nucleic Acids Research. 16: 1649. PMID 2894639 DOI: 10.1093/Nar/16.4.1649  0.92
1987 Kramer PL, Ozelius L, Gusella JF, Fahn S, Kidd KK, Breakefield XO. Exclusion of autosomal dominant dystonia gene from large regions of chromosomes 11p, 13q, and 21q by multi-point linkage analysis. Genetic Epidemiology. 4: 377-86. PMID 3692135 DOI: 10.1002/gepi.1370040506  0.92
1987 Pearson PL, Kidd KK, Willard HF. Human gene mapping by recombinant DNA techniques Cytogenetics and Cell Genetics. 46: 390-566. PMID 3507285 DOI: 10.1159/000132487  0.92
1987 Price RA, Kidd KK, Weissman MM. Early Onset (Under Age 30 Years) and Panic Disorder as Markers for Etiologic Homogeneity in Major Depression Archives of General Psychiatry. 44: 434-440. PMID 3472494 DOI: 10.1001/Archpsyc.1987.01800170048008  0.92
1987 Kidd KK. Research design considerations for linkage studies of affective disorders using recombinant DNA markers Journal of Psychiatric Research. 21: 551-557. PMID 3326941 DOI: 10.1016/0022-3956(87)90104-X  0.92
1987 Leckman JF, Weissman MM, Pauls DL, Kidd KK. Family-genetic studies and identification of valid diagnostic categories in adult and child psychiatry British Journal of Psychiatry. 151: 39-44. PMID 3315088 DOI: 10.1192/Bjp.151.1.39  0.92
1987 Kidd KK. Searching for major genes for psychiatric disorders Ciba Foundation Symposium. 130: 184-196. PMID 2894929  0.92
1987 Simpson NE, Kidd KK. Where is the locus for multiple endocrine neoplasia type 2A? Henry Ford Hospital Medical Journal. 35: 168-171. PMID 2891652  0.92
1987 Murphy PD, Lin PF, Ruddle FH, Kidd KK. 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. 15: 7212. PMID 2889186 DOI: 10.1093/Nar/15.17.7212  0.92
1987 Simpson NE, Kidd KK, Goodfellow PJ, McDermid H, Myers S, Kidd JR, Jackson CE, Duncan AM, Farrer LA, Brasch K. Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage. Nature. 328: 528-30. PMID 2886918 DOI: 10.1038/328528A0  0.92
1987 Kidd JR, Castiglione CM, Pakstis AJ, Kidd KK. The anonymous RFLP locus D11S16 is tightly linked to catalase on 11p Cytogenetic and Genome Research. 45: 63-64. PMID 2885154 DOI: 10.1159/000132428  0.92
1987 Farrer LA, Goodfellow PJ, White BN, Holden JJ, Kidd JR, Simpson NE, Kidd KK. Linkage analysis of multiple endocrine neoplasia type 2A (MEN-2A) and three DNA markers on chromosome 20: evidence against synteny. Cancer Genetics and Cytogenetics. 27: 327-34. PMID 2885081 DOI: 10.1016/0165-4608(87)90015-X  0.92
1987 Kidd KK. Population genetics of a disease Nature. 327: 282-283. PMID 2884567 DOI: 10.1038/327282A0  0.92
1987 Goodfellow PJ, Duncan AM, Farrer LA, Holden JJ, White BN, Kidd JR, Kidd KK, Simpson NE. Localization and linkage of three polymorphic DNA sequences on human chromosome 20. Cytogenetics and Cell Genetics. 44: 112-7. PMID 2882953 DOI: 10.1159/000132354  0.92
1987 Wu JS, Riordan JR, Willard HF, Milner R, Kidd KK. MSP RFLP for X-linked proteolipid protein gene (PLP) identified with either rat or human PLP cDNA clone Nucleic Acids Research. 15: 1882. PMID 2434933 DOI: 10.1093/Nar/15.4.1882  0.92
1987 Murphy PD, Ferguson-Smith AC, Miki T, Feinberg AA, Ruddle FH, Kidd KK. A moderately frequent RFLP identified by both saci and banii with a probe from the HOX2 locus in man (17q11-17q22) Nucleic Acids Research. 15: 6311. DOI: 10.1093/nar/15.15.6311  0.92
1986 Pakstis AJ, Kidd JR, Castiglione C, Sparkes RS, Kidd KK. Close linkage of MT2P1 with GC on chromosome 4 Cytogenetic and Genome Research. 41: 189-190. PMID 3956270 DOI: 10.1159/000132226  0.6
1986 Melnick DJ, Jolly CJ, Kidd KK. Genetics of a wild population of rhesus monkeys (Macaca mulatta): II. The Dunga Gali population in species-wide perspective. American Journal of Physical Anthropology. 71: 129-40. PMID 3799822 DOI: 10.1002/Ajpa.1330710202  0.92
1986 Weissman MM, Merikangas KR, John K, Wickramaratne P, Prusoff BA, Kidd KK. Family-Genetic Studies of Psychiatric Disorders: Developing Technologies Archives of General Psychiatry. 43: 1104-1116. PMID 3532996 DOI: 10.1001/Archpsyc.1986.01800110090012  0.92
1986 Kramer PL, Farrer LA, Pakstis AJ, Kidd KK. Development of a map of chromosome 11p. Genetic Epidemiology. Supplement. 1: 153-8. PMID 3471659 DOI: 10.1002/Gepi.1370030724  0.92
1986 Kendler KS, Kidd KK. Recurrence risks in an oligogenic threshold model: The effect of alterations in allele frequency Annals of Human Genetics. 50: 83-91. PMID 3426150 DOI: 10.1111/J.1469-1809.1986.Tb01941.X  0.92
1986 Murphy PD, Kidd JR, Castiglione CM, Lin PF, Ruddle FH, Kidd KK. A frequent polymorphism for the cytosolic thymidine kinase gene, TK1, (17q21-q22) detected by the enzyme TaqI. Nucleic Acids Research. 14: 4381. PMID 3012471 DOI: 10.1093/Nar/14.10.4381  0.92
1986 Cavalli-Sforza LL, Kidd JR, Kidd KK, Bucci C, Bowcock AM, Hewlett BS, Freidlaender JS. DNA markers and genetic variation in the human species Cold Spring Harbor Symposia On Quantitative Biology. 51: 411-417. PMID 2884067 DOI: 10.1101/Sqb.1986.051.01.049  0.92
1986 Kidd JR, Dizikes GJ, Grody WW, Cederbaum SD, Kidd KK. A pvuII RFLP for the human liver arginase (ARG1) gene Nucleic Acids Research. 14: 9544. PMID 2879271 DOI: 10.1093/Nar/14.23.9544  0.92
1986 Kidd KK, Kidd JR, Castiglione CM, Pakstis AJ, Sparkes RS. Progress toward resolving the possible linkage of multiple endocrine neoplasia type 2A to haptoglobin and group-specific loci: Use of restriction fragment length polymorphisms extends exclusion region Genetic Epidemiology. 3: 195-200. PMID 2873080 DOI: 10.1002/Gepi.1370030306  0.92
1985 Kidd KK. The search for the ultimate cause of maleness New England Journal of Medicine. 313: 260-261. PMID 4010729 DOI: 10.1056/Nejm198507253130410  0.92
1985 Murphy PD, Kidd JR, Breg WR, Ruddle FH, Kidd KK. An anonymous single copy X-chromosome clone, DXS79, from Xq26-Xq28, identifies a moderately frequent RFLP [HGM8 provisional no. DXS79]. Nucleic Acids Research. 13: 3015. PMID 4000970 DOI: 10.1093/Nar/13.8.3015  0.92
1985 Conneally PM, Edwards JH, Kidd KK, Lalouel JM, Morton NE, Ott J, White R. Report of the committee on methods of linkage analysis and reporting Cytogenetics and Cell Genetics. 40: 356-359. PMID 3864600 DOI: 10.1159/000132186  0.92
1985 Kidd KK, Gusella J. Report of the committee on the genetic constitution of chromosomes 3 and 4 Cytogenetics and Cell Genetics. 40: 107-127. PMID 3864591 DOI: 10.1159/000132171  0.92
1985 Prusoff BA, Weissman MM, Merikangas KR, Leckman JF, Kidd KK. Drug response as a predictor of transmission of non-bipolar major depression within families Journal of Affective Disorders. 8: 171-176. PMID 3157727 DOI: 10.1016/0165-0327(85)90041-2  0.92
1985 Melnick1 DJ, Kidd KK. Genetic and evolutionary relationships among Asian Macaques International Journal of Primatology. 6: 123-160. DOI: 10.1007/Bf02693650  0.92
1985 Arlen Price R, Kramer PL, Pakstis AJ, Kidd KK. Genetic analysis workshop III: Sampling considerations and assumptions in gene mapping Genetic Epidemiology. 2: 219-220. DOI: 10.1002/Gepi.1370020220  0.36
1984 Kramer PL, Altmann DB, Kidd KK. Genetic Analysis Workshop II: further consideration of segregation and linkage analyses in Problem 3. Genetic Epidemiology. 1: 189-93. PMID 14971372 DOI: 10.1002/Gepi.1370010213  0.92
1984 Miller RL, Partridge CW, Kidd KK, Ruddle FH. The Yale Human Gene Mapping Library Cytogenetics and Cell Genetics. 37: 394-397. PMID 6690233 DOI: 10.1159/000132015  0.92
1984 Egeland JA, Kidd JR, Frazer A, Kidd KK, Neuhauser VI. Amish study, V: Lithium-sodium countertransport and catechol O-methyltransferase in pedigrees of bipolar probands. The American Journal of Psychiatry. 141: 1049-54. PMID 6589966 DOI: 10.1176/Ajp.141.9.1049  0.92
1984 Price RA, Kidd KK. Utilizing automated methods to improve estimates of recurrence risk with linked genetic markers American Journal of Medical Genetics. 17: 621-625. PMID 6585143 DOI: 10.1002/Ajmg.1320170311  0.92
1984 Cox NJ, Kramer PL, Kidd KK. Segregation analyses of stuttering. Genetic Epidemiology. 1: 245-53. PMID 6549563 DOI: 10.1002/Gepi.1370010304  0.92
1984 Cox NJ, Seider RA, Kidd KK. Some environmental factors and hypotheses for stuttering in families with several stutterers Journal of Speech and Hearing Research. 27: 543-548. PMID 6521460 DOI: 10.1044/Jshr.2704.543  0.92
1984 Weissman MM, Wickramaratne P, Merikangas KR, Leckman JF, Prusoff BA, Caruso KA, Kidd KK, Gammon GD. Onset of Major Depression in Early Adulthood: Increased Familial Loading and Specificity Archives of General Psychiatry. 41: 1136-1143. PMID 6508504 DOI: 10.1001/Archpsyc.1984.01790230022003  0.92
1984 Bootsma D, Kidd KK. Report of the committee on the genetic constitution of chromosomes 2, 3, 4, and 5 Cytogenetics and Cell Genetics. 37: 22-46. PMID 6360560 DOI: 10.1159/000132003  0.92
1984 Kidd KK, Krugen SD, Gerhard DS. Linkage data exclusing a locus for multiple endocrine neoplasia type 2 syndromes from the distal part of the short arm of chromosome 11 Henry Ford Hospital Medical Journal. 32: 262-265. PMID 6152463  0.92
1984 Gerhard DS, Kidd KK, Kidd JR, Egeland JA, Housman DE. Identification of a recent recombination event within the human β-globin gene cluster Proceedings of the National Academy of Sciences of the United States of America. 81: 7875-7879. PMID 6096866 DOI: 10.1073/Pnas.81.24.7875  0.92
1984 Melnick DJ, Jolly CJ, Kidd KK. The genetics of a wild population of rhesus monkeys (Macaca mulatta). I. Genetic variability within and between social groups American Journal of Physical Anthropology. 63: 341-360. DOI: 10.1002/Ajpa.1330630402  0.92
1984 Kramer PL, Altmann DB, Kidd KK. Genetic analysis workshop II: Further consideration of segregation and linkage analyses in problem 3 Genetic Epidemiology. 1: 189-193.  0.92
1983 Cox NJ, Kidd KK. Can recovery from stuttering be considered a genetically milder subtype of stuttering? Behavior Genetics. 13: 129-139. PMID 6860250 DOI: 10.1007/Bf01065662  0.92
1983 Seider RA, Gladstien KL, Kidd KK. Recovery and persistence of stuttering among relatives of stutterers Journal of Speech and Hearing Disorders. 48: 402-409. PMID 6645435 DOI: 10.1044/Jshd.4804.402  0.92
1983 Melnick DJ, Kidd KK. The genetic consequences of social group fission in a wild population of rhesus monkeys (Macaca mulatta) Behavioral Ecology and Sociobiology. 12: 229-236. DOI: 10.1007/Bf00290775  0.92
1982 Seider RA, Gladstien KL, Kidd KK. Language onset and concomitant speech and language problems in subgroups of stutterers and their siblings Journal of Speech and Hearing Research. 25: 482-486. PMID 7162147 DOI: 10.1044/Jshr.2504.482  0.92
1982 Weissman MM, Kidd KK, Prusoff BA. Variability in Rates of Affective Disorders in Relatives of Depressed and Normal Probands Archives of General Psychiatry. 39: 1397-1403. PMID 7149900 DOI: 10.1001/Archpsyc.1982.04290120033006  0.92
1982 Thompson WD, Orvaschel H, Prusoff BA, Kidd KK. An Evaluation of the Family History Method for Ascertaining Psychiatric Disorders Archives of General Psychiatry. 39: 53-58. PMID 7055408 DOI: 10.1001/Archpsyc.1982.04290010031006  0.92
1982 Kruger SD, Turner WJ, Kidd KK. The effects of requisite assumptions on linkage analyses of manic-depressive illness with HLA Biological Psychiatry. 17: 1081-1099. PMID 6959652  0.92
1982 Kidd KK, Pauls DL. Genetic hypotheses for Tourette syndrome Advances in Neurology. 35: 243-249. PMID 6959493  0.92
1982 Pauls DL, Kidd KK. Genetic strategies for the analysis of childhood behavioral traits Schizophrenia Bulletin. 8: 253-266. PMID 6955941 DOI: 10.1093/Schbul/8.2.253  0.92
1982 Orvaschel H, Thompson WD, Belanger A, Prusoff BA, Kidd KK. Comparison of the family history method to direct interview. Factors affecting the diagnosis of depression Journal of Affective Disorders. 4: 49-59. PMID 6461687 DOI: 10.1016/0165-0327(82)90019-2  0.92
1981 Gladstien KL, Seider RA, Kidd KK. Analysis of the sibship patterns of stutterers Journal of Speech and Hearing Research. 24: 460-462. PMID 7300289 DOI: 10.1044/Jshr.2403.460  0.92
1981 Epstein PA, Kidd KK. Dermo-distortive urticaria: An autosomal dominant dermatologic disorder American Journal of Medical Genetics. 9: 307-315. PMID 7294069 DOI: 10.1002/Ajmg.1320090407  0.92
1981 Gladstien K, Kidd KK. An easy-to-use maximum-likelihood method of estimating the ascertainment probability American Journal of Human Genetics. 33: 785-801. PMID 7294027  0.92
1981 Matthysse S, Kidd KK. Evidence of HLA linkage in depressive disorders New England Journal of Medicine. 305: 1340-1341. PMID 7290155 DOI: 10.1056/Nejm198111263052209  0.92
1981 Brooker RJ, Lehman RA, Heimbuch RC, Kidd KK. Hand usage in a colony of bonnet monkeys, Macaca radiata. Behavior Genetics. 11: 49-56. PMID 7259722 DOI: 10.1007/Bf01065827  0.92
1981 Pauls DL, Cohen DJ, Heimbuch R, Detlor J, Kidd KK. Familial Pattern and Transmission of Gilles de la Tourette Syndrome and Multiple Tics Archives of General Psychiatry. 38: 1091-1093. PMID 6945827 DOI: 10.1001/Archpsyc.1981.01780350025002  0.92
1981 Epstein PA, Kidd KK, Sparkes RS. Genetic linkage analysis of dermo-distortive urticaria American Journal of Medical Genetics. 9: 317-321. PMID 6945804 DOI: 10.1002/Ajmg.1320090408  0.92
1981 Kidd KK, Heimbuch RC, Records MA. Vertical transmission of susceptibility to stuttering with sex-modified expression Proceedings of the National Academy of Sciences of the United States of America. 78: 606-610. PMID 6941261 DOI: 10.1073/Pnas.78.1.606  0.92
1981 Smeraldi E, Negri F, Heimbuch RC, Kidd KK. Familial patterns and possible modes of inheritance of primary affective disorders Journal of Affective Disorders. 3: 173-182. PMID 6454711 DOI: 10.1016/0165-0327(81)90042-2  0.92
1980 Kidd KK, Heimbuch RC, Records MA, Oehlert G, Webster RL. Familial stuttering patterns are not related to one measure of severity. Journal of Speech and Hearing Research. 23: 539-45. PMID 7421157 DOI: 10.1044/Jshr.2303.539  0.92
1980 Heimbuch RC, Matthysse S, Kidd KK. Estimating age-of-onset distribution for disorders with variable onset American Journal of Human Genetics. 32: 564-574. PMID 7395869  0.92
1980 Kidd JR, Wolf B, Hsia YE, Kidd KK. Genetics of propionic acidemia in a Mennonite-Amish kindred American Journal of Human Genetics. 32: 236-245. PMID 7386459  0.92
1980 Gladstien K, Rushton AR, Kidd KK. Penetrance estimates and recurrence risks for fibromuscular dysplasia Clinical Genetics. 17: 115-116. PMID 7363496 DOI: 10.1111/J.1399-0004.1980.Tb00117.X  0.92
1980 Kidd KK, Gladstien K. Alternative genetic models for the analysis of complex traits Progress in Clinical and Biological Research. 46: 407-435. PMID 7022462  0.92
1980 Morton LA, Kidd KK. The effects of variable age-of-onset and diagnostic criteria on the estimates of linkage: An example using manic-depressive illness and color blindness Social Biology. 27: 1-10. PMID 6974894 DOI: 10.1080/19485565.1980.9988398  0.92
1980 Kidd KK, Prusoff BA, Cohen DJ. Familial Pattern of Gilles de la Tourette Syndrome Archives of General Psychiatry. 37: 1336-1339. PMID 6934712 DOI: 10.1001/Archpsyc.1980.01780250022001  0.92
1980 Orvaschel H, Weissman MM, Kidd KK. The children of depressed parents; the childhood of depressed patients; depression in children Journal of Affective Disorders. 2: 1-16. DOI: 10.1016/0165-0327(80)90017-8  0.92
1979 Morton LA, Kidd KK, Matthysse SW, Richards RL. Recurrence risks in schizophrenia: Are they model dependent? Behavior Genetics. 9: 389-406. PMID 539966 DOI: 10.1007/Bf01066977  0.92
1979 Kidd KK. Empiric recurrence risks and models of inheritance: part II Birth Defects: Original Article Series. 15: 51-65. PMID 526615  0.92
1979 Kidd KK. Genetic linkage and hemochromatosis New England Journal of Medicine. 301: 209-210. PMID 449978 DOI: 10.1056/Nejm197907263010409  0.92
1978 Kidd KK, Matthysee S. Research Designs for the Study of Gene-Environment Interactions in Psychiatric Disorders: Report of a Foundations Fund for Research in Psychiatry Panel Archives of General Psychiatry. 35: 925-932. PMID 678045 DOI: 10.1001/Archpsyc.1978.01770320019001  0.92
1978 Matthysse S, Kidd KK. The value of dual mating data in estimating genetic parameters Annals of Human Genetics. 41: 477-480. PMID 655637 DOI: 10.1111/J.1469-1809.1978.Tb00919.X  0.92
1978 Kidd KK, Kidd JR, Records MA. The possible causes of the sex ratio in stuttering and its implications Journal of Fluency Disorders. 3: 13-23. DOI: 10.1016/0094-730X(78)90003-7  0.92
1977 Rosenberg LE, Kidd KK. HLA and disease susceptibility: a primer New England Journal of Medicine. 297: 1060-1062. PMID 909551 DOI: 10.1056/Nejm197711102971909  0.92
1977 Records MA, Heimbuch RC, Kidd KK. Handedness and stuttering: A dead horse? Journal of Fluency Disorders. 2: 271-282. DOI: 10.1016/0094-730X(77)90031-6  0.92
1977 Kidd KK. A genetic perspective on stuttering Journal of Fluency Disorders. 2: 259-269. DOI: 10.1016/0094-730X(77)90030-4  0.92
1977 Hsia YE, Kidd KK, Williams ML. Did they ignore genetics? Pediatrics. 60: 938-939.  0.92
1976 Matthysse SW, Kidd KK. Estimating the genetic contribution to schizophrenia American Journal of Psychiatry. 133: 185-191. PMID 1251925 DOI: 10.1176/Ajp.133.2.185  0.92
1976 Fineman RM, Kidd KK, Johnson AM, Breg WR. Increased frequency of heterozygotes for α1 antitrypsin variants in individuals with either sex chromosome mosaicism or trisomy 21 Nature. 260: 320-321. PMID 1082990 DOI: 10.1038/260320A0  0.92
1976 Kidd KK, Spence MA. Genetic analyses of pyloric stensosis suggesting a specific maternal effect Journal of Medical Genetics. 13: 290-294. DOI: 10.1136/Jmg.13.4.290  0.92
1976 Kidd KK, Records MA, Kidd JR. Genetic analysis of stuttering Excerpta Med.,Amsterdam,I.C.S. 0.92
1976 Fineman RM, Johnson AM, Kidd KK, Breg WR. Increased frequency of heterozygotes for alpha 1 antitrypsin (AAT) variants in patients with Down syndrome associated with advanced maternal age Excerpta Med.,Amsterdam,I.C.S. 0.92
1975 Kidd KK. On the possible magnitudes of selective forces maintaining schizophrenia in the population Proceedings of the Annual Meeting of the American Psychopathological Association. 135-145. PMID 1242221 DOI: 10.1016/0010-440X(73)90068-0  0.92
1974 Kidd KK, Osterhoff D, Erhard L, Stone WH. The use of genetic relationships among cattle breeds in the formulation of rational breeding policies: an example with South Devon (South Africa) and Gelbvieh (Germany) Animal Blood Groups and Biochemical Genetics. 5: 21-28. PMID 4855145 DOI: 10.1111/J.1365-2052.1974.Tb01309.X  0.92
1974 Kidd KK, Cavalli Sforza LL. The role of genetic drift in the differentiation of Icelandic and Norwegian cattle Evolution. 28: 381-395. DOI: 10.1111/J.1558-5646.1974.Tb00759.X  0.92
1973 Cann HM, Kidd KK, Lisker R, Radvany R, Payne R. Genetic structure of the HL-A system in a Nahua Indian population in Mexico Tissue Antigens. 3: 364-372. PMID 4771177 DOI: 10.1111/J.1399-0039.1973.Tb00505.X  0.92
1973 Kidd KK, Cavalli Sforza LL. An analysis of the genetics of schizophrenia Social Biology. 20: 254-265. PMID 4763753 DOI: 10.1080/19485565.1973.9988051  0.92
1972 Cavalli-Sforza LL, Kidd KK. Prospects for research on schizophrenia. IV. Genetic and environmental factors. Genetic models for schizophrenia Neurosciences Research Program Bulletin. 10: 406-419. PMID 4663820  0.92
1971 Kidd KK, Sgaramella-Zonta LA. Phylogenetic analysis: concepts and methods American Journal of Human Genetics. 23: 235-252. PMID 5089842  0.92
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