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R
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 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
Q
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
P
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
Population genomic analysis of 962 whole genome sequences of humans reveals natural selection in non-coding regions., Yu, Fuli, Lu Jian, Liu Xiaoming, Gazave Elodie, Chang Diana, Raj Srilakshmi, Hunter-Zinck Haley, Blekhman Ran, Arbiza Leonardo, Van Hout Cris, et al. , PloS one, 2015, Volume 10, Issue 3, p.e0121644, (2015) Abstract
Pooled genomic indexing of rhesus macaque., Milosavljevic, Aleksandar, Harris Ronald A., Sodergren Erica J., Jackson Andrew R., Kalafus Ken J., Hodgson Anne, Cree Andrew, Dai Weilie, Csuros Miklos, Zhu Baoli, et al. , Genome research, 2005 Feb, Volume 15, Issue 2, p.292-301, (2005) Abstract
Pooled genomic indexing of rhesus macaque., Milosavljevic, Aleksandar, Harris Ronald A., Sodergren Erica J., Jackson Andrew R., Kalafus Ken J., Hodgson Anne, Cree Andrew, Dai Weilie, Csuros Miklos, Zhu Baoli, et al. , Genome research, 2005 Feb, Volume 15, Issue 2, p.292-301, (2005) Abstract
Pol iota is a candidate for the mouse pulmonary adenoma resistance 2 locus, a major modifier of chemically induced lung neoplasia., Wang, Min, Devereux Theodora R., Vikis Haris G., McCulloch Scott D., Holliday Wanda, Anna Colleen, Wang Yian, Bebenek Katarzyna, Kunkel Thomas A., Guan Kunliang, et al. , Cancer research, 2004 Mar 15, Volume 64, Issue 6, p.1924-31, (2004) Abstract
Pleiotropic patterns of quantitative trait loci for 70 murine skeletal traits., Kenney-Hunt, Jane P., Wang Bing, Norgard Elizabeth A., Fawcett Gloria, Falk Doug, Pletscher Susan L., Jarvis Joseph P., Roseman Charles, Wolf Jason, and Cheverud James M. , Genetics, 2008 Apr, Volume 178, Issue 4, p.2275-88, (2008) Abstract
A physical map of the human genome., McPherson, J. D., Marra M., Hillier L., Waterston R. H., Chinwalla A., Wallis J., Sekhon M., Wylie K., Mardis E. R., Wilson R. K., et al. , Nature, 2001 Feb 15, Volume 409, Issue 6822, p.934-41, (2001) Abstract
A physical map of the chicken genome., Wallis, John W., Aerts Jan, Groenen Martien A. M., Crooijmans Richard P. M. A., Layman Dan, Graves Tina A., Scheer Debra E., Kremitzki Colin, Fedele Mary J., Mudd Nancy K., et al. , Nature, 2004 Dec 9, Volume 432, Issue 7018, p.761-4, (2004) Abstract
Phylogeny of the macaques (Cercopithecidae: Macaca) based on Alu elements., Li, Jing, Han Kyudong, Xing Jinchuan, Kim Heui-Soo, Rogers Jeffrey, Ryder Oliver A., Disotell Todd, Yue Bisong, and Batzer Mark A. , Gene, 2009 Dec 15, Volume 448, Issue 2, p.242-9, (2009) Abstract
Phosphorylated and sumoylation-deficient progesterone receptors drive proliferative gene signatures during breast cancer progression., Knutson, Todd P., Daniel Andrea R., Fan Danhua, Silverstein Kevin At, Covington Kyle R., Fuqua Suzanne A. W., and Lange Carol A. , Breast cancer research : BCR, 2012, Volume 14, Issue 3, p.R95, (2012) Abstract
PGM3 Mutations Cause a Congenital Disorder of Glycosylation with Severe Immunodeficiency and Skeletal Dysplasia, Stray-Pedersen, Asbjørg, Backe Paul H., Sorte Hanne S., Mørkrid Lars, Chokshi Niti Y., Erichsen Hans Christian, Gambin Tomasz, Elgstøen Katja B.P., Bjørås Magnar, Wlodarski Marcin W., et al. , The American Journal of Human Genetics, 07/2014, Volume 95, Issue 1, p.96 - 107, (2014)
Personalized copy number and segmental duplication maps using next-generation sequencing., Alkan, Can, Kidd Jeffrey M., Marques-Bonet Tomas, Aksay Gozde, Antonacci Francesca, Hormozdiari Fereydoun, Kitzman Jacob O., Baker Carl, Malig Maika, Mutlu Onur, et al. , Nature genetics, 2009 Oct, Volume 41, Issue 10, p.1061-7, (2009) Abstract


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