| Year |
Citation |
Score |
| 2022 |
Kidd KK, Pakstis AJ. State of the Art for Microhaplotypes. Genes. 13. PMID 35893059 DOI: 10.3390/genes13081322 |
0.317 |
|
| 2022 |
Kidd KK, Evsanaa B, Togtokh A, Brissenden JE, Roscoe JM, Dogan M, Neophytou PI, Gurkan C, Bulbul O, Cherni L, Speed WC, Murtha M, Kidd JR, Pakstis AJ. North Asian population relationships in a global context. Scientific Reports. 12: 7214. PMID 35508562 DOI: 10.1038/s41598-022-10706-x |
0.311 |
|
| 2022 |
Mestiri S, Boussetta S, Pakstis AJ, El Kamel S, Ben Ammar El Gaaied A, Kidd KK, Cherni L. New Insight into the human genetic diversity in North African populations by genotyping of SNPs in DRD3, CSMD1 and NRG1 genes. Molecular Genetics & Genomic Medicine. 10: e1871. PMID 35128830 DOI: 10.1002/mgg3.1871 |
0.354 |
|
| 2021 |
Pakstis AJ, Gandotra N, Speed WC, Murtha M, Scharfe C, Kidd KK. The population genetics characteristics of a 90 locus panel of microhaplotypes. Human Genetics. 140: 1753-1773. PMID 34643790 DOI: 10.1007/s00439-021-02382-0 |
0.362 |
|
| 2021 |
Kidd KK, Bulbul O, Gurkan C, Dogan M, Dogan S, Neophytou PI, Cherni L, Gurwitz D, Speed WC, Murtha M, Kidd JR, Pakstis AJ. Genetic relationships of Southwest Asian and Mediterranean populations. Forensic Science International. Genetics. 53: 102528. PMID 34020230 DOI: 10.1016/j.fsigen.2021.102528 |
0.316 |
|
| 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 |
0.355 |
|
| 2020 |
Oldoni F, Yoon L, Wootton SC, Lagacé R, Kidd KK, Podini D. Population genetic data of 74 microhaplotypes in four major U.S. population groups. Forensic Science International. Genetics. 49: 102398. PMID 33045522 DOI: 10.1016/j.fsigen.2020.102398 |
0.347 |
|
| 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 |
0.737 |
|
| 2020 |
Oldoni F, Bader D, Fantinato C, Wootton SC, Lagacé R, Kidd KK, Podini D. A sequence-based 74plex microhaplotype assay for analysis of forensic DNA mixtures. Forensic Science International. Genetics. 49: 102367. PMID 32919300 DOI: 10.1016/J.Fsigen.2020.102367 |
0.341 |
|
| 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 |
0.428 |
|
| 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 |
0.436 |
|
| 2020 |
Rogers J, Ruano G, Kidd KK. Variability in nuclear DNA among nonhuman primates: Application of molecular genetic techniques to intra- and inter-species genetic analyses. American Journal of Primatology. 27: 93-105. PMID 31948144 DOI: 10.1002/Ajp.1350270205 |
0.371 |
|
| 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 |
0.434 |
|
| 2019 |
Phillips C, McNevin D, Kidd KK, Lagacé R, Wootton S, de la Puente M, Freire-Aradas A, Mosquera-Miguel A, Eduardoff M, Gross T, Dagostino L, Power D, Olson S, Hashiyada M, Oz C, et al. MAPlex - A massively parallel sequencing ancestry analysis multiplex for Asia-Pacific populations. Forensic Science International. Genetics. 42: 213-226. PMID 31377479 DOI: 10.1016/J.Fsigen.2019.06.022 |
0.441 |
|
| 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 |
0.413 |
|
| 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 |
0.804 |
|
| 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 |
0.447 |
|
| 2019 |
Bennett L, Oldoni F, Long K, Cisana S, Madella K, Wootton S, Chang J, Hasegawa R, Lagacé R, Kidd KK, Podini D. Mixture deconvolution by massively parallel sequencing of microhaplotypes. International Journal of Legal Medicine. PMID 30758713 DOI: 10.1007/S00414-019-02010-7 |
0.412 |
|
| 2019 |
Oldoni F, Bader D, Fantinato C, Wootton SC, Lagacé R, Hasegawa R, Chang J, Kidd K, Podini D. A massively parallel sequencing assay of microhaplotypes for mixture deconvolution Forensic Science International: Genetics Supplement Series. 7: 522-524. DOI: 10.1016/J.Fsigss.2019.10.075 |
0.373 |
|
| 2018 |
Oldoni F, Kidd KK, Podini D. Microhaplotypes in forensic genetics. Forensic Science International. Genetics. 38: 54-69. PMID 30347322 DOI: 10.1016/J.Fsigen.2018.09.009 |
0.402 |
|
| 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 |
0.453 |
|
| 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 |
0.433 |
|
| 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 |
0.437 |
|
| 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 |
0.717 |
|
| 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 |
0.396 |
|
| 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 |
0.418 |
|
| 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 |
0.815 |
|
| 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 |
0.318 |
|
| 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 |
0.438 |
|
| 2017 |
Oldoni F, Hart R, Long K, Maddela K, Cisana S, Schanfield M, Wootton S, Chang J, Lagace R, Hasegawa R, Kidd K, Podini D. Microhaplotypes for ancestry prediction Forensic Science International: Genetics Supplement Series. 6: e513-e515. DOI: 10.1016/J.Fsigss.2017.09.209 |
0.428 |
|
| 2016 |
Kidd KK. Proposed nomenclature for microhaplotypes. Human Genomics. 10: 16. PMID 27316555 DOI: 10.1186/S40246-016-0078-Y |
0.409 |
|
| 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 |
0.424 |
|
| 2016 |
Bulbul O, Cherni L, Khodjet-El-Khil H, Rajeevan H, Kidd KK. Evaluating a subset of ancestry informative SNPs for discriminating among Southwest Asian and circum-Mediterranean populations. Forensic Science International. Genetics. 23: 153-158. PMID 27160361 DOI: 10.1016/J.Fsigen.2016.04.010 |
0.425 |
|
| 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 |
0.415 |
|
| 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 |
0.427 |
|
| 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 |
0.461 |
|
| 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 |
0.417 |
|
| 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 |
0.336 |
|
| 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 |
0.423 |
|
| 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 |
0.356 |
|
| 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 |
0.454 |
|
| 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 |
0.797 |
|
| 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 |
0.301 |
|
| 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 |
0.397 |
|
| 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 |
0.369 |
|
| 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 |
0.47 |
|
| 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 |
0.333 |
|
| 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 |
0.409 |
|
| 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 |
0.333 |
|
| 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 |
0.329 |
|
| 2013 |
Scharf JM, Yu D, Mathews CA, Neale BM, Stewart SE, Fagerness JA, Evans P, Gamazon E, Edlund CK, Service SK, Tikhomirov A, Osiecki L, Illmann C, Pluzhnikov A, Konkashbaev A, ... ... Kidd KK, et al. Genome-wide association study of Tourette's syndrome. Molecular Psychiatry. 18: 721-8. PMID 22889924 DOI: 10.1038/Mp.2012.69 |
0.374 |
|
| 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 |
0.385 |
|
| 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 |
0.367 |
|
| 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 |
0.694 |
|
| 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 |
0.422 |
|
| 2012 |
Reich D, Patterson N, Campbell D, Tandon A, Mazieres S, Ray N, Parra MV, Rojas W, Duque C, Mesa N, GarcÃa LF, Triana O, Blair S, Maestre A, Dib JC, ... ... Kidd K, et al. Reconstructing Native American population history. Nature. 488: 370-4. PMID 22801491 DOI: 10.1038/Nature11258 |
0.391 |
|
| 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 |
0.695 |
|
| 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 |
0.423 |
|
| 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 |
0.405 |
|
| 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 |
0.413 |
|
| 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 |
0.728 |
|
| 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 |
0.422 |
|
| 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 |
0.405 |
|
| 2012 |
Reich D, Patterson N, Campbell D, Tandon A, Mazieres S, Ray N, Parra MV, Rojas W, Duque C, Mesa N, García LF, Triana O, Blair S, Maestre A, Dib JC, ... ... Kidd K, et al. Erratum: Corrigendum: Reconstructing Native American population history Nature. 491: 288-288. DOI: 10.1038/Nature11667 |
0.304 |
|
| 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 |
0.447 |
|
| 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 |
0.428 |
|
| 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 |
0.327 |
|
| 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 |
0.434 |
|
| 2011 |
Henn BM, Gignoux CR, Jobin M, Granka JM, Macpherson JM, Kidd JM, RodrÃguez-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 |
0.427 |
|
| 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 |
0.367 |
|
| 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 |
0.45 |
|
| 2011 |
Kidd KK. Abstract ED04-03: Genetic variation among populations Cancer Epidemiology, Biomarkers & Prevention. 20. DOI: 10.1158/1055-9965.Disp-11-Ed04-03 |
0.455 |
|
| 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 |
0.337 |
|
| 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 |
0.786 |
|
| 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 |
0.369 |
|
| 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 |
0.352 |
|
| 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 |
0.729 |
|
| 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 |
0.448 |
|
| 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 |
0.42 |
|
| 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 |
0.362 |
|
| 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 |
0.343 |
|
| 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 |
0.394 |
|
| 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 |
0.418 |
|
| 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 |
0.395 |
|
| 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 |
0.398 |
|
| 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 |
0.433 |
|
| 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 |
0.387 |
|
| 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 |
0.343 |
|
| 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 |
0.319 |
|
| 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 |
0.476 |
|
| 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 |
0.432 |
|
| 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 |
0.39 |
|
| 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 |
0.387 |
|
| 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 |
0.81 |
|
| 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 |
0.417 |
|
| 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 |
0.307 |
|
| 2008 |
Friedlaender JS, Friedlaender FR, Reed FA, Kidd KK, Kidd JR, Chambers GK, Lea RA, Loo J, Koki G, Hodgson JA, Merriwether DA, Weber JL. Correction: The Genetic Structure of Pacific Islanders Plos Genetics. 4. DOI: 10.1371/Annotation/Cbdd11A0-4A29-4E7C-9E4E-C00A184C7777 |
0.768 |
|
| 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 |
0.435 |
|
| 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 |
0.337 |
|
| 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 |
0.419 |
|
| 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 |
0.372 |
|
| 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 |
0.445 |
|
| 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 |
0.311 |
|
| 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 |
0.355 |
|
| 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 |
0.759 |
|
| 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 |
0.312 |
|
| 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 |
0.439 |
|
| 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 |
0.664 |
|
| 2007 |
Single RM, Martin MP, Gao X, Meyer D, Yeager M, Kidd JR, Kidd KK, Carrington M. 4-OR: Global diversity of KIR and HLA: Population-level evidence for co-evolution, natural selection, and signatures of demographic history Human Immunology. 68: S10. DOI: 10.1016/J.Humimm.2007.08.009 |
0.35 |
|
| 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 |
0.396 |
|
| 2006 |
Patin E, Harmant C, Kidd KK, Kidd J, Froment A, Mehdi SQ, Sica L, Heyer E, Quintana-Murci L. Sub-Saharan African coding sequence variation and haplotype diversity at the NAT2 gene. Human Mutation. 27: 720. PMID 16786516 DOI: 10.1002/Humu.9438 |
0.425 |
|
| 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 |
0.438 |
|
| 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 |
0.462 |
|
| 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 |
0.419 |
|
| 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 |
0.765 |
|
| 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 |
0.427 |
|
| 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 |
0.418 |
|
| 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 |
0.445 |
|
| 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 |
0.331 |
|
| 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 |
0.641 |
|
| 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 |
0.437 |
|
| 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 |
0.469 |
|
| 2004 |
Andrés AM, Soldevila M, Navarro A, Kidd KK, Oliva B, Bertranpetit J. Positive selection in MAOA gene is human exclusive: determination of the putative amino acid change selected in the human lineage. Human Genetics. 115: 377-86. PMID 15349769 DOI: 10.1007/S00439-004-1179-6 |
0.337 |
|
| 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 |
0.686 |
|
| 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 |
0.722 |
|
| 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 |
0.665 |
|
| 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 |
0.344 |
|
| 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 |
0.721 |
|
| 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 |
0.451 |
|
| 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 |
0.463 |
|
| 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 |
0.363 |
|
| 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 |
0.373 |
|
| 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 |
0.772 |
|
| 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 |
0.428 |
|
| 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 |
0.716 |
|
| 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 |
0.39 |
|
| 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 |
0.736 |
|
| 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 |
0.439 |
|
| 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 |
0.689 |
|
| 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 |
0.444 |
|
| 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 |
0.752 |
|
| 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 |
0.757 |
|
| 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 |
0.563 |
|
| 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 |
0.422 |
|
| 2002 |
Zhang H, Leckman JF, Pauls DL, Tsai CP, Kidd KK, Campos MR. Genomewide scan of hoarding in sib pairs in which both sibs have Gilles de la Tourette syndrome. American Journal of Human Genetics. 70: 896-904. PMID 11840360 DOI: 10.1086/339520 |
0.314 |
|
| 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 |
0.387 |
|
| 2002 |
Kidd KK, Osier MV, Pakstis AJ, Kidd JR. Reply to Whitfield The American Journal of Human Genetics. 71: 1250-1251. DOI: 10.1086/344288 |
0.776 |
|
| 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 |
0.763 |
|
| 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 |
0.719 |
|
| 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 |
0.757 |
|
| 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 |
0.351 |
|
| 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 |
0.727 |
|
| 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 |
0.764 |
|
| 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 |
0.468 |
|
| 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 |
0.435 |
|
| 2000 |
Hoehe MR, Köpke K, Wendel B, Rohde K, Flachmeier C, Kidd KK, Berrettini WH, Church GM. Sequence variability and candidate gene analysis in complex disease: association of mu opioid receptor gene variation with substance dependence. Human Molecular Genetics. 9: 2895-908. PMID 11092766 DOI: 10.1093/Hmg/9.19.2895 |
0.35 |
|
| 2000 |
Tishkoff SA, Pakstis AJ, Stoneking M, Kidd JR, Destro-Bisol G, Sanjantila A, Lu RB, Deinard AS, Sirugo G, Jenkins T, Kidd KK, Clark AG. Short tandem-repeat polymorphism/alu haplotype variation at the PLAT locus: implications for modern human origins. American Journal of Human Genetics. 67: 901-25. PMID 10986042 DOI: 10.1086/303068 |
0.72 |
|
| 2000 |
Zhao H, Zhang S, Merikangas KR, Trixler M, Wildenauer DB, Sun F, Kidd KK. Transmission/disequilibrium tests using multiple tightly linked markers. American Journal of Human Genetics. 67: 936-46. PMID 10968775 DOI: 10.1086/303073 |
0.378 |
|
| 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 |
0.744 |
|
| 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 |
0.625 |
|
| 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 |
0.48 |
|
| 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 |
0.37 |
|
| 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 |
0.444 |
|
| 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 |
0.767 |
|
| 2000 |
Zhao H, Merikangas KR, Kidd KK. Reply to Kong and Nicolae The American Journal of Human Genetics. 67: 1355-1356. DOI: 10.1016/S0002-9297(07)62968-1 |
0.346 |
|
| 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 |
0.401 |
|
| 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 |
0.467 |
|
| 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 |
0.322 |
|
| 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 |
0.308 |
|
| 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 |
0.42 |
|
| 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 |
0.306 |
|
| 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 |
0.398 |
|
| 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 |
0.342 |
|
| 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 |
0.369 |
|
| 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 |
0.333 |
|
| 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 |
0.454 |
|
| 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 |
0.724 |
|
| 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 |
0.444 |
|
| 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 |
0.388 |
|
| 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 |
0.452 |
|
| 1999 |
Lee J, Lu R, Ko H, Chang F, Yin S, Pakstis AJ, Kidd KK. No Association Between DRD2 Locus and Alcoholism After Controlling the ADH and ALDH Genotypes in Chinese Han Population Alcoholism: Clinical and Experimental Research. 23: 592-599. DOI: 10.1111/J.1530-0277.1999.Tb04159.X |
0.351 |
|
| 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 |
0.446 |
|
| 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 |
0.34 |
|
| 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 |
0.472 |
|
| 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 |
0.462 |
|
| 1998 |
Malaspina P, Cruciani F, Ciminelli BM, Terrenato L, Santolamazza P, Alonso A, Banyko J, Brdicka R, GarcÃa O, Gaudiano C, Guanti G, Kidd KK, Lavinha J, Avila M, Mandich P, et al. Network analyses of Y-chromosomal types in Europe, northern Africa, and western Asia reveal specific patterns of geographic distribution. American Journal of Human Genetics. 63: 847-60. PMID 9718330 DOI: 10.1086/301999 |
0.345 |
|
| 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 |
0.685 |
|
| 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 |
0.66 |
|
| 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 |
0.67 |
|
| 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 |
0.329 |
|
| 1997 |
Scozzari R, Cruciani F, Malaspina P, Santolamazza P, Ciminelli BM, Torroni A, Modiano D, Wallace DC, Kidd KK, Olckers A, Moral P, Terrenato L, Akar N, Qamar R, Mansoor A, et al. Differential structuring of human populations for homologous X and Y microsatellite loci. American Journal of Human Genetics. 61: 719-33. PMID 9326337 DOI: 10.1086/515500 |
0.432 |
|
| 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 |
0.429 |
|
| 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 |
0.441 |
|
| 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 |
0.407 |
|
| 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 |
0.378 |
|
| 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 |
0.357 |
|
| 1997 |
Chang FM, Kidd KK. Rapid molecular haplotyping of the first exon of the human dopamine D4 receptor gene by heteroduplex analysis. American Journal of Medical Genetics. 74: 91-4. PMID 9034013 DOI: 10.1002/(Sici)1096-8628(19970221)74:1<91::Aid-Ajmg18>3.0.Co;2-M |
0.36 |
|
| 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. PMID 31918472 DOI: 10.1002/(Sici)1098-2345(1996)38:2<157::Aid-Ajp4>3.0.Co;2-Y |
0.466 |
|
| 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 |
0.596 |
|
| 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 |
0.513 |
|
| 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 |
0.65 |
|
| 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 |
0.492 |
|
| 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 |
0.407 |
|
| 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 |
0.467 |
|
| 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 |
0.432 |
|
| 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 |
0.356 |
|
| 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 |
0.668 |
|
| 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 |
0.432 |
|
| 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 |
0.344 |
|
| 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. |
0.36 |
|
| 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 |
0.34 |
|
| 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 |
0.3 |
|
| 1995 |
Baldwin CT, Weiss S, Farrer LA, De Stefano AL, Adair R, Franklyn B, Kidd KK, Korostishevsky M, Bonné-Tamir B. Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population. Human Molecular Genetics. 4: 1637-42. PMID 8541853 DOI: 10.1093/Hmg/4.9.1637 |
0.349 |
|
| 1995 |
Takiyama Y, Igasrashi S, Rogaeva EA, Endo K, Rogaev EI, Tanaka H, Sherrington R, Sanpei K, Liang Y, Saito M, Tsuda T, Takano H, Ikeda M, Lin C, Chi H, ... ... Kidd KK, et al. Evidence for inter-generational instability in the CAG repeat in the MJD1 gene and for conserved haplotypes at flanking markers amongst Japanese and Caucasian subjects with Machado-Joseph disease Human Molecular Genetics. 4: 1137-1146. PMID 8528200 DOI: 10.1093/Hmg/4.7.1137 |
0.388 |
|
| 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 |
0.32 |
|
| 1995 |
Kozman HM, Keith TP, Donis-Keller H, White RL, Weissenbach J, Dean M, Vergnaud G, Kidd K, Gusella J, Royle NJ. The CEPH consortium linkage map of human chromosome 16. Genomics. 25: 44-58. PMID 7774955 DOI: 10.1016/0888-7543(95)80108-X |
0.316 |
|
| 1995 |
Novoradovsky AG, Kidd J, Kidd K, Goldman D. Apparent monomorphism of ALDH2 in seven American Indian populations. Alcohol (Fayetteville, N.Y.). 12: 163-7. PMID 7772269 DOI: 10.1016/0741-8329(94)00086-7 |
0.436 |
|
| 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 |
0.31 |
|
| 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 |
0.374 |
|
| 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 |
0.332 |
|
| 1995 |
Gelernter J, Leckman J, Pauls D, Kidd KK, Kurlan R. Dopamine d2 Receptor and Tourette's Syndrome-Reply Archives of Neurology. 52: 442-443. DOI: 10.1001/Archneur.1995.00540290019005 |
0.348 |
|
| 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 |
0.652 |
|
| 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 |
0.308 |
|
| 1994 |
Barr CL, Kennedy JL, Pakstis AJ, Wetterberg L, Sjögren B, Bierut L, Wadelius C, Wahlström J, Martinsson T, Giuffra L, Gelernter J, Hallmayer J, Moises HW, Kurth J, Cavalli-Sforza LL, ... Kidd KK, et al. Progress in a genome scan for linkage in schizophrenia in a large Swedish kindred American Journal of Medical Genetics. 54: 51-58. PMID 7909991 DOI: 10.1002/Ajmg.1320540110 |
0.583 |
|
| 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. |
0.538 |
|
| 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 |
0.372 |
|
| 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 |
0.328 |
|
| 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 |
0.36 |
|
| 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 |
0.3 |
|
| 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 |
0.369 |
|
| 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 |
0.437 |
|
| 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 |
0.358 |
|
| 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 |
0.314 |
|
| 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 |
0.326 |
|
| 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 |
0.303 |
|
| 1992 |
Hästbacka J, Sistonen P, Kaitila I, Weiffenbach B, Kidd KK, de la Chapelle A. A linkage map spanning the locus for diastrophic dysplasia (DTD). Genomics. 11: 968-73. PMID 1783404 DOI: 10.1016/0888-7543(91)90021-6 |
0.344 |
|
| 1992 |
Kennedy JL, Honer WG, Kaufmann CA, Martignetti JA, Brosius J, Kidd KK. Two RFLPs near HOX2@/NGFR at locus D17S444E. Nucleic Acids Research. 20: 1171. PMID 1372406 DOI: 10.1093/Nar/20.5.1171 |
0.357 |
|
| 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 |
0.336 |
|
| 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 |
0.341 |
|
| 1992 |
Gelernter J, Kennedy JL, van Tol HH, Civelli O, Kidd KK. The D4 dopamine receptor (DRD4) maps to distal 11p close to HRAS. Genomics. 13: 208-10. PMID 1349574 DOI: 10.1016/0888-7543(92)90222-E |
0.314 |
|
| 1992 |
Hallmayer J, Kennedy JL, Wetterberg L, Sjögren B, Kidd KK, Cavalli-Sforza LL. Exclusion of linkage between the serotonin2 receptor and schizophrenia in a large Swedish kindred. Archives of General Psychiatry. 49: 216-9. PMID 1348924 DOI: 10.1001/Archpsyc.1992.01820030048006 |
0.559 |
|
| 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 |
0.385 |
|
| 1991 |
Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Chan HS, Chipperfield M, Cooper DN, Hewitt J, Lewitter F. Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms. Cytogenetics and Cell Genetics. 55: 457-778. PMID 2073845 DOI: 10.1159/000133027 |
0.326 |
|
| 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 |
0.531 |
|
| 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 |
0.485 |
|
| 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 |
0.339 |
|
| 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 |
0.34 |
|
| 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 |
0.344 |
|
| 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 |
0.324 |
|
| 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 |
0.302 |
|
| 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 |
0.39 |
|
| 1991 |
Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, et al. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 8 of 27) Cytogenetic and Genome Research. 58: 1400-1439. DOI: 10.1159/000317214 |
0.335 |
|
| 1991 |
Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper D, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B, et al. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms Cytogenetic and Genome Research. 58: 1190-1832. DOI: 10.1159/000133727 |
0.335 |
|
| 1990 |
Pauls DL, Pakstis AJ, Kurlan R, Kidd KK, Leckman JF, Cohen DJ, Kidd JR, Como P, Sparkes R. Segregation and linkage analyses of Tourette's syndrome and related disorders. Journal of the American Academy of Child and Adolescent Psychiatry. 29: 195-203. PMID 2324061 DOI: 10.1097/00004583-199003000-00007 |
0.328 |
|
| 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 |
0.383 |
|
| 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 |
0.343 |
|
| 1990 |
Summar ML, Phillips JA, Battey J, Castiglione CM, Kidd KK, Maness KJ, Weiffenbach B, Gravius TC. Linkage relationships of human arginine vasopressin-neurophysin-II and oxytocin-neurophysin-I to prodynorphin and other loci on chromosome 20. Molecular Endocrinology (Baltimore, Md.). 4: 947-50. PMID 1978246 DOI: 10.1210/Mend-4-6-947 |
0.401 |
|
| 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 |
0.389 |
|
| 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 |
0.388 |
|
| 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 |
0.392 |
|
| 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 |
0.34 |
|
| 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 |
0.339 |
|
| 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 |
0.382 |
|
| 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 |
0.377 |
|
| 1990 |
Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Chan H, Chipperfield M, Cooper D, Hewitt J, Lewitter F, Maidak B, Quitt M, Ricciuti F, Track R, Tolley M, et al. Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 13 of 14) Cytogenetic and Genome Research. 55: 757-768. DOI: 10.1159/000317054 |
0.326 |
|
| 1989 |
Bowcock AM, Kidd JR, Lathrop GM, Daneshvar L, May LT, Ray A, Sehgal PB, Kidd KK, Cavalli-Sforza LL. The human "interferon-beta 2/hepatocyte stimulating factor/interleukin-6" gene: DNA polymorphism studies and localization to chromosome 7p21. Genomics. 3: 8-16. PMID 2906047 DOI: 10.1016/0888-7543(88)90152-8 |
0.625 |
|
| 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 |
0.312 |
|
| 1989 |
Kennedy JL, Giuffra LA, Moises HW, Wetterberg L, Sjögren B, Cavalli-Sforza LL, Pakstis AJ, Kidd JR, Kidd KK. Molecular genetic studies in schizophrenia. Schizophrenia Bulletin. 15: 383-91. PMID 2573149 DOI: 10.1093/Schbul/15.3.383 |
0.572 |
|
| 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 |
0.334 |
|
| 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 |
0.407 |
|
| 1989 |
Giuffra LA, Kidd KK. Linkage analysis in psychiatry International Review of Psychiatry. 1: 231-242. DOI: 10.3109/09540268909089417 |
0.313 |
|
| 1989 |
Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 922–947 Cytogenetic and Genome Research. 51: 922-947. DOI: 10.1159/000227799 |
0.327 |
|
| 1989 |
Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 892–921 Cytogenetic and Genome Research. 51: 892-921. DOI: 10.1159/000227798 |
0.327 |
|
| 1989 |
Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 862–891 Cytogenetic and Genome Research. 51: 862-891. DOI: 10.1159/000227797 |
0.327 |
|
| 1989 |
Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 832–861 Cytogenetic and Genome Research. 51: 832-861. DOI: 10.1159/000227796 |
0.327 |
|
| 1989 |
Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 807–831 Cytogenetic and Genome Research. 51: 807-831. DOI: 10.1159/000227795 |
0.327 |
|
| 1989 |
Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 782–806 Cytogenetic and Genome Research. 51: 782-806. DOI: 10.1159/000227794 |
0.327 |
|
| 1989 |
Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 758–781 Cytogenetic and Genome Research. 51: 758-781. DOI: 10.1159/000227793 |
0.327 |
|
| 1989 |
Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 732–757 Cytogenetic and Genome Research. 51: 732-757. DOI: 10.1159/000227792 |
0.327 |
|
| 1989 |
Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 702–731 Cytogenetic and Genome Research. 51: 702-731. DOI: 10.1159/000227791 |
0.327 |
|
| 1989 |
Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 677–701 Cytogenetic and Genome Research. 51: 677-701. DOI: 10.1159/000227790 |
0.327 |
|
| 1989 |
Kidd K, Bowcock A, Schmidtke J, Track R, Ricciuti F, Hutchings G, Bale A, Pearson P, Willard H, Gelernter J, Giuffra L, Kubzdela K. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 644–676 Cytogenetic and Genome Research. 51: 644-676. DOI: 10.1159/000227789 |
0.327 |
|
| 1988 |
Farrer LA, Bonne-Tamir B, Frydman M, Magazanik A, Kidd KK, Bowcock AM, Cavalli-Sforza LL. Predicting genotypes at loci for autosomal recessive disorders using linked genetic markers: application to Wilson's disease. Human Genetics. 79: 109-17. PMID 3164701 DOI: 10.1007/Bf00280547 |
0.583 |
|
| 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 |
0.348 |
|
| 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 |
0.343 |
|
| 1988 |
Miki T, Nishisho I, Tateishi H, Chen Y, Kidd JR, Wu J, Pravtcheva D, Pakstis AJ, Takai S, Ruddle FH, Kidd KK. D10S20, a previously unmapped RFLP (OS-3), is located on 10q near D10S4 Genomics. 3: 78-81. PMID 2906046 DOI: 10.1016/0888-7543(88)90163-2 |
0.36 |
|
| 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 |
0.341 |
|
| 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 |
0.334 |
|
| 1988 |
Kennedy JL, Giuffra LA, Moises HW, Cavalli-Sforza LL, Pakstis AJ, Kidd JR, Castiglione CM, Sjogren B, Wetterberg L, Kidd KK. Evidence against linkage of schizophrenia to markers on chromosome 5 in a northern Swedish pedigree. Nature. 336: 167-70. PMID 2903450 DOI: 10.1038/336167A0 |
0.589 |
|
| 1988 |
Kidd KK, Kidd JR, Castiglione CM, Sparkes RS, Egeland JA, Bakker E. The anonymous RFLP locus D1S2 is close to PGM1 on chromosome 1. Human Heredity. 38: 22-6. PMID 2895061 DOI: 10.1159/000153749 |
0.333 |
|
| 1988 |
Kidd JR, Egeland JA, Pakstis AJ, Castiglione CM, Pletcher BA, Morton LA, Kidd KK. Searching for a major genetic locus for affective disorder in the Old Order Amish. Journal of Psychiatric Research. 21: 577-80. PMID 2894461 DOI: 10.1016/0022-3956(87)90107-5 |
0.303 |
|
| 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 |
0.312 |
|
| 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 |
0.313 |
|
| 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 |
0.339 |
|
| 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 |
0.303 |
|
| 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 |
0.355 |
|
| 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 |
0.321 |
|
| 1987 |
Kidd KK. Population genetics of a disease Nature. 327: 282-283. PMID 2884567 DOI: 10.1038/327282A0 |
0.376 |
|
| 1987 |
Bowcock AM, Farrer LA, Hebert JM, Bonne-Tamir B, Frydman M, Kidd KK, Cavalli-Sforza LL. A new human RFLP identified by 7D2 places D13S10 proximal to esterase D. Cytogenetics and Cell Genetics. 44: 236-7. PMID 2884079 DOI: 10.1159/000132379 |
0.511 |
|
| 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 |
0.378 |
|
| 1987 |
Egeland JA, Gerhard DS, Pauls DL, Sussex JN, Kidd KK, Allen CR, Hostetter AM, Housman DE. Bipolar affective disorders linked to DNA markers on chromosome 11. Nature. 325: 783-7. PMID 2881209 DOI: 10.1038/325783A0 |
0.343 |
|
| 1987 |
Hoffee PA, Chiang J, Rowland P, Qumsiyeh MB, Hamilton MJ, Schlitter DA, Lialiaris T, Mourelatos D, Dozi-Vassiliades J, Braekeleer MD, Ambros PF, Sumner AT, Volleth M, Mayr B, Schellander K, ... ... Kidd KK, et al. Subject Index Vol. 44, 1987 Cytogenetic and Genome Research. 44: 239-240. DOI: 10.1159/000132381 |
0.479 |
|
| 1987 |
Hoffee PA, Chiang J, Rowland P, Qumsiyeh MB, Hamilton MJ, Schlitter DA, Lialiaris T, Mourelatos D, Dozi-Vassiliades J, Braekeleer MD, Ambros PF, Sumner AT, Volleth M, Mayr B, Schellander K, ... ... Kidd KK, et al. Contents, Vol. 44, 1987 Cytogenetic and Genome Research. 44. DOI: 10.1159/000132369 |
0.472 |
|
| 1986 |
Price RA, Kidd KK, Pauls DL, Gershon ES, Prusoff BA, Weissman MM, Goldin LR. Multiple threshold models for the affective disorders: the Yale-NIMH collaborative family study. Journal of Psychiatric Research. 19: 533-46. PMID 4078756 DOI: 10.1016/0022-3956(85)90071-8 |
0.305 |
|
| 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 |
0.43 |
|
| 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 |
0.301 |
|
| 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 |
0.312 |
|
| 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 |
0.588 |
|
| 1986 |
Kidd KK, Kidd JR, Castiglione CM, Genel M, Darby J, Cavalli-Sforza LL, Gusella JF. Linkage analyses of multiple endocrine neoplasia, type 2A (MEN-2A) with 20 DNA polymorphisms: 5% of the genome excluded. Human Heredity. 36: 243-9. PMID 2875939 DOI: 10.1159/000153634 |
0.588 |
|
| 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 |
0.301 |
|
| 1986 |
Kruger SD, Gertner JM, Sparkes RS, Haedt LE, Crist M, Sparkes MC, Genel M, Kidd KK. Linkage analyses of multiple endocrine neoplasia, type 2 (MEN-2) with 23 classical genetic polymorphisms. Human Heredity. 36: 6-11. PMID 2868987 DOI: 10.1159/000153592 |
0.368 |
|
| 1985 |
Goldin LR, Cox NJ, Pauls DL, Gershon ES, Kidd KK. The detection of major loci by segregation and linkage analysis: a simulation study. Genetic Epidemiology. 1: 285-96. PMID 6599402 DOI: 10.1002/Gepi.1370010307 |
0.37 |
|
| 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 |
0.31 |
|
| 1985 |
Melnick1 DJ, Kidd KK. Genetic and evolutionary relationships among Asian Macaques International Journal of Primatology. 6: 123-160. DOI: 10.1007/Bf02693650 |
0.408 |
|
| 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 |
0.374 |
|
| 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 |
0.349 |
|
| 1984 |
Cox NJ, Kramer PL, Kidd KK. Segregation analyses of stuttering. Genetic Epidemiology. 1: 245-53. PMID 6549563 DOI: 10.1002/Gepi.1370010304 |
0.316 |
|
| 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 |
0.332 |
|
| 1984 |
Kidd KK, Egeland JA, Molthan L, Pauls DL, Kruger SD, Messner KH. Amish study, IV: Genetic linkage study of pedigrees of bipolar probands. The American Journal of Psychiatry. 141: 1042-8. PMID 6331772 DOI: 10.1176/Ajp.141.9.1042 |
0.341 |
|
| 1984 |
Smeraldi E, Petroccione A, Gasperini M, Macciardi F, Orsini A, Kidd KK. Outcomes on lithium treatment as a tool for genetic studies in affective disorders. Journal of Affective Disorders. 6: 139-51. PMID 6233346 DOI: 10.1016/0165-0327(84)90019-3 |
0.308 |
|
| 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 |
0.338 |
|
| 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 |
0.389 |
|
| 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 |
0.335 |
|
| 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 |
0.382 |
|
| 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 |
0.321 |
|
| 1982 |
Housman D, Kidd K, Gusella JF. Recombinant DNA approach to neurogenetic disorders Trends in Neurosciences. 5: 320-323. DOI: 10.1016/0166-2236(82)90192-8 |
0.334 |
|
| 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 |
0.353 |
|
| 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 |
0.326 |
|
| 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 |
0.311 |
|
| 1981 |
Astolfi P, Kidd KK, Cavalli-Sforza LL. A Comparison of Methods for Reconstructing Evolutionary Trees Systematic Biology. 30: 156-169. DOI: 10.1093/Sysbio/30.2.156 |
0.57 |
|
| 1980 |
Kidd KK, Stone WH, Crimella C, Carenzi C, Casati M, Rognoni G. Immunogenetic and population genetic analyses of Iberian cattle. Animal Blood Groups and Biochemical Genetics. 11: 21-38. PMID 7396241 DOI: 10.1111/J.1365-2052.1980.Tb01489.X |
0.357 |
|
| 1980 |
Kidd KK. Genetic models of stuttering Journal of Fluency Disorders. 5: 187-201. DOI: 10.1016/0094-730X(80)90028-5 |
0.308 |
|
| 1979 |
Kidd KK. Genetic linkage and hemochromatosis New England Journal of Medicine. 301: 209-210. PMID 449978 DOI: 10.1056/Nejm197907263010409 |
0.342 |
|
| 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 |
0.355 |
|
| 1978 |
Astolfi P, Piazza A, Kidd KK. Testing of Evolutionary Independence in Simulated Phylogenetic Trees Systematic Biology. 27: 391-400. DOI: 10.1093/Sysbio/27.4.391 |
0.349 |
|
| 1977 |
Kidd KK. A genetic perspective on stuttering Journal of Fluency Disorders. 2: 259-269. DOI: 10.1016/0094-730X(77)90030-4 |
0.344 |
|
| 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 |
0.332 |
|
| 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 |
0.305 |
|
| 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 |
0.342 |
|
| 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 |
0.365 |
|
| 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 |
0.418 |
|
| 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 |
0.407 |
|
| 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 |
0.369 |
|
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