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RNA interference knockdown of DNA methyl-transferase 3 affects gene alternative splicing in the honey bee., Li-Byarlay, Hongmei, Li Yang, Stroud Hume, Feng Suhua, Newman Thomas C., Kaneda Megan, Hou Kirk K., Worley Kim C., Elsik Christine G., Wickline Samuel A., et al. , Proceedings of the National Academy of Sciences of the United States of America, 2013 Jul 30, Volume 110, Issue 31, p.12750-5, (2013) Abstract
Risk of type 2 diabetes and obesity is differentially associated with variation in FTO in whites and African-Americans in the ARIC study., Bressler, Jan, Kao Linda W. H., Pankow James S., and Boerwinkle Eric , PloS one, 2010, Volume 5, Issue 5, p.e10521, (2010) Abstract
Resources for genetic management and genomics research on non-human primates at the National Primate Research Centers (NPRCs)., Kanthaswamy, S., Capitanio J. P., Dubay C. J., Ferguson B., Folks T., Ha J. C., Hotchkiss C. E., Johnson Z. P., Katze M. G., Kean L. S., et al. , Journal of medical primatology, 2009 Oct, Volume 38 Suppl 1, p.17-23, (2009) Abstract
Replication of long-bone length QTL in the F9-F10 LG,SM advanced intercross., Norgard, Elizabeth A., Jarvis Joseph P., Roseman Charles C., Maxwell Taylor J., Kenney-Hunt Jane P., Samocha Kaitlin E., Pletscher Susan L., Wang Bing, Fawcett Gloria L., Leatherwood Christopher J., et al. , Mammalian genome : official journal of the International Mammalian Genome Society, 2009 Apr, Volume 20, Issue 4, p.224-35, (2009) Abstract
Reorganization and expansion of the nidoviral family Arteriviridae., Kuhn, Jens H., Lauck Michael, Bailey Adam L., Shchetinin Alexey M., Vishnevskaya Tatyana V., Bào Yīmíng, Ng Terry Fei Fan, LeBreton Matthew, Schneider Bradley S., Gillis Amethyst, et al. , Archives of virology, 2015 Nov 25, (2015) Abstract
The relationship of JAK2(V617F) and acquired UPD at chromosome 9p in polycythemia vera., Wang, L., Swierczek S. I., Lanikova L., Kim Sj, Hickman K., Walker K., Wang K., Drummond J., Doddapaneni H., Reid J. G., et al. , Leukemia, 2014 Apr, Volume 28, Issue 4, p.938-41, (2014)
Regulation of Drosophila eye development by the transcription factor Sine oculis., Jusiak, Barbara, Karandikar Umesh C., Kwak Su-Jin, Wang Feng, Wang Hui, Chen Rui, and Mardon Graeme , PloS one, 2014, Volume 9, Issue 2, p.e89695, (2014) Abstract
Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia due to Bi-allelic TANGO2 Mutations., Lalani, Seema R., Liu Pengfei, Rosenfeld Jill A., Watkin Levi B., Chiang Theodore, Leduc Magalie S., Zhu Wenmiao, Ding Yan, Pan Shujuan, Vetrini Francesco, et al. , American journal of human genetics, 2016 Jan 19, (2016) Abstract
Recurrent internal tandem duplications of BCOR in clear cell sarcoma of the kidney., Roy, Angshumoy, Kumar Vijetha, Zorman Barry, Fang Erica, Haines Katherine M., Doddapaneni Harshavardhan, Hampton Oliver A., White Simon, Bavle Abhishek A., Patel Nimesh R., et al. , Nature communications, 2015, Volume 6, p.8891, (2015) Abstract
A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia., Shah, Sohela, Schrader Kasmintan A., Waanders Esmé, Timms Andrew E., Vijai Joseph, Miething Cornelius, Wechsler Jeremy, Yang Jun, Hayes James, Klein Robert J., et al. , Nature genetics, 2013 Oct, Volume 45, Issue 10, p.1226-31, (2013) Abstract
Recurrent CNVs and SNVs at the NPHP1 Locus Contribute Pathogenic Alleles to Bardet-Biedl Syndrome, Lindstrand, Anna, Davis Erica E., Carvalho Claudia M.B., Pehlivan Davut, Willer Jason R., Tsai I-Chun, Ramanathan Subhadra, Zuppan Craig, Sabo Aniko, Muzny Donna, et al. , The American Journal of Human Genetics, 05/2014, Volume 94, Issue 5, p.745 - 754, (2014)
Recurrent chromosome 16p13.1 duplications are a risk factor for aortic dissections., Kuang, Shao-Qing, Guo Dong-Chuan, Prakash Siddharth K., McDonald Merry-Lynn N., Johnson Ralph J., Wang Min, Regalado Ellen S., Russell Ludivine, Cao Jiu-Mei, Kwartler Callie, et al. , PLoS genetics, 2011 Jun, Volume 7, Issue 6, p.e1002118, (2011) Abstract
Recurrent BCAM-AKT2 fusion gene leads to a constitutively activated AKT2 fusion kinase in high-grade serous ovarian carcinoma., Kannan, Kalpana, Coarfa Cristian, Chao Pei-Wen, Luo Liming, Wang Yan, Brinegar Amy E., Hawkins Shannon M., Milosavljevic Aleksandar, Matzuk Martin M., and Yen Laising , Proceedings of the National Academy of Sciences of the United States of America, 2015 Mar 17, Volume 112, Issue 11, p.E1272-7, (2015) Abstract
A recombination hotspot responsible for two inherited peripheral neuropathies is located near a mariner transposon-like element., Reiter, L. T., Murakami T., Koeuth T., Pentao L., Muzny D. M., Gibbs R. A., and Lupski J. R. , Nature genetics, 1996 Mar, Volume 12, Issue 3, p.288-97, (1996) Abstract
Rare variants in the notch signaling pathway describe a novel type of autosomal recessive Klippel-Feil syndrome., Karaca, Ender, Yuregir Ozge O., Bozdogan Sevcan T., Aslan Huseyin, Pehlivan Davut, Jhangiani Shalini N., Akdemir Zeynep C., Gambin Tomasz, Bayram Yavuz, Atik Mehmed M., et al. , American journal of medical genetics. Part A, 2015 Aug 4, (2015) Abstract
Rare loss-of-function mutations in ANGPTL family members contribute to plasma triglyceride levels in humans., Romeo, Stefano, Yin Wu, Kozlitina Julia, Pennacchio Len A., Boerwinkle Eric, Hobbs Helen H., and Cohen Jonathan C. , The Journal of clinical investigation, 2009 Jan, Volume 119, Issue 1, p.70-9, (2009) Abstract
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders., Lim, Elaine T., Raychaudhuri Soumya, Sanders Stephan J., Stevens Christine, Sabo Aniko, MacArthur Daniel G., Neale Benjamin M., Kirby Andrew, Ruderfer Douglas M., Fromer Menachem, et al. , Neuron, 2013 Jan 23, Volume 77, Issue 2, p.235-42, (2013) Abstract
Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF., Huffman, Jennifer E., de Vries Paul S., Morrison Alanna C., Sabater-Lleal Maria, Kacprowski Tim, Auer Paul L., Brody Jennifer A., Chasman Daniel I., Chen Ming-Huei, Guo Xiuqing, et al. , Blood, 2015 Sep 10, Volume 126, Issue 11, p.e19-29, (2015) Abstract
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Quantitative trait loci affecting liver fat content in mice., Minkina, Olga, Cheverud James M., Fawcett Gloria, Semenkovich Clay F., and Kenney-Hunt Jane P. , G3 (Bethesda, Md.), 2012 Sep, Volume 2, Issue 9, p.1019-25, (2012) Abstract
Quantitative Genetics of Response to Novelty and Other Stimuli by Infant Rhesus Macaques (Macaca mulatta) Across Three Behavioral Assessments., Fawcett, G. L., Dettmer A. M., Kay D., Raveendran M., Higley J. D., Ryan N. D., Cameron J. L., and Rogers J. , International journal of primatology, 2014 Feb 1, Volume 35, Issue 1, p.325-339, (2014) Abstract
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Prospective associations of coronary heart disease loci in African Americans using the MetaboChip: the PAGE study., Franceschini, Nora, Hu Yijuan, Reiner Alex P., Buyske Steven, Nalls Mike, Yanek Lisa R., Li Yun, Hindorff Lucia A., Cole Shelley A., Howard Barbara V., et al. , PloS one, 2014, Volume 9, Issue 12, p.e113203, (2014) Abstract
Progress and prospects in rat genetics: a community view., Aitman, Timothy J., Critser John K., Cuppen Edwin, Dominiczak Anna, Fernandez-Suarez Xose M., Flint Jonathan, Gauguier Dominique, Geurts Aron M., Gould Michael, Harris Peter C., et al. , Nature genetics, 2008 May, Volume 40, Issue 5, p.516-22, (2008) Abstract
Pretranscriptional regulation of Tgf-beta1 by PI polyamide prevents scarring and accelerates wound healing of the cornea after exposure to alkali., Chen, Min, Matsuda Hiroyuki, Wang Linghua, Watanabe Takayoshi, Kimura Makoto T., Igarashi Jun, Wang Xiaofei, Sakimoto Tohru, Fukuda Noboru, Sawa Mitsuru, et al. , Molecular therapy : the journal of the American Society of Gene Therapy, 2010 Mar, Volume 18, Issue 3, p.519-27, (2010) Abstract
Prepublication data sharing., Birney, Ewan, Hudson Thomas J., Green Eric D., Gunter Chris, Eddy Sean, Rogers Jane, Harris Jennifer R., Ehrlich Dusko S., Apweiler Rolf, Austin Christopher P., et al. , Nature, 2009 Sep 10, Volume 461, Issue 7261, p.168-70, (2009) Abstract
Prediction of coronary heart disease risk using a genetic risk score: the Atherosclerosis Risk in Communities Study., Morrison, Alanna C., Bare Lance A., Chambless Lloyd E., Ellis Stephen G., Malloy Mary, Kane John P., Pankow James S., Devlin James J., Willerson James T., and Boerwinkle Eric , American journal of epidemiology, 2007 Jul 1, Volume 166, Issue 1, p.28-35, (2007) Abstract


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