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Rapid characterization of HIV-1 sequence diversity using denaturing gradient gel electrophoresis and direct automated DNA sequencing of PCR products., Andersson, B., Ying J. H., Lewis D. E., and Gibbs R. A. , PCR methods and applications, 1993 May, Volume 2, Issue 4, p.293-300, (1993) Abstract
B
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
Reactivity of antibodies from syphilis patients to a protein array representing the Treponema pallidum proteome., Brinkman, Mary Beth, McKevitt Matthew, McLoughlin Melanie, Perez Carla, Howell Jerrilyn, Weinstock George M., Norris Steven J., and Palzkill Timothy , Journal of clinical microbiology, 2006 Mar, Volume 44, Issue 3, p.888-91, (2006) Abstract
Resequencing of IRS2 reveals rare variants for obesity but not fasting glucose homeostasis in Hispanic children., Butte, Nancy F., Voruganti Saroja V., Cole Shelley A., Haack Karin, Comuzzie Anthony G., Muzny Donna M., Wheeler David A., Chang Kyle, Hawes Alicia, and Gibbs Richard A. , Physiological genomics, 2011 Sep 22, Volume 43, Issue 18, p.1029-37, (2011) Abstract
C
Replicative mechanisms for CNV formation are error prone., Carvalho, Claudia M. B., Pehlivan Davut, Ramocki Melissa B., Fang Ping, Alleva Benjamin, Franco Luis M., Belmont John W., Hastings P. J., and Lupski James R. , Nature genetics, 2013 Nov, Volume 45, Issue 11, p.1319-26, (2013) Abstract
The Red-R Framework for Integrated Discovery, Covington, Kyle R., and Parikh Anup , The Red-R Journal, Number 1-08/08/2011, (2011)
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Reporting genomic sequencing results to ordering clinicians: incidental, but not exceptional., Green, Robert C., Lupski James R., and Biesecker Leslie G. , JAMA : the journal of the American Medical Association, 2013 Jul 24, Volume 310, Issue 4, p.365-6, (2013)
Relationship of HIV testing and high-risk behaviors among clients in methadone maintenance treatment., Grella, C. E., Campos M., and Anglin M. D. , AIDS education and prevention : official publication of the International Society for AIDS Education, 1998 Oct, Volume 10, Issue 5, p.403-16, (1998) Abstract
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Relationship between low-density lipoprotein subclasses and asymptomatic atherosclerosis in subjects from the Atherosclerosis Risk in Communities (ARIC) Study., Hallman, Michael D., Brown Spencer A., Ballantyne Christie M., Sharrett Richey A., and Boerwinkle Eric , Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals, 2004 Mar-Apr, Volume 9, Issue 2, p.190-202, (2004) Abstract
Relation of PCSK9 mutations to serum low-density lipoprotein cholesterol in childhood and adulthood (from The Bogalusa Heart Study)., Hallman, Michael D., Srinivasan Sathanur R., Chen Wei, Boerwinkle Eric, and Berenson Gerald S. , The American journal of cardiology, 2007 Jul 1, Volume 100, Issue 1, p.69-72, (2007) Abstract
REGγ is associated with multiple oncogenic pathways in human cancers., He, Jing, Cui Long, Zeng Yu, Wang Guangqiang, Zhou Ping, Yang Yuanyuan, Ji Lei, Zhao Yanyan, Chen Jiwu, Wang Zhuo, et al. , BMC cancer, 2012, Volume 12, p.75, (2012) Abstract
J
Recurrent duplication-driven transposition of DNA during hominoid evolution., Johnson, Matthew E., Cheng Ze, Morrison Anne V., Scherer Steven, Ventura Mario, Gibbs Richard A., Green Eric D., and Eichler Evan E. , Proceedings of the National Academy of Sciences of the United States of America, 2006 Nov 21, Volume 103, Issue 47, p.17626-31, (2006) Abstract
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
K
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
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
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
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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
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
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)
Residual plasmatic activity of ADAMTS13 is correlated with phenotype severity in congenital thrombotic thrombocytopenic purpura., Lotta, Luca A., Wu Haifeng M., Mackie Ian J., Noris Marina, Veyradier Agnes, Scully Marie A., Remuzzi Giuseppe, Coppo Paul, Liesner Ri, Donadelli Roberta, et al. , Blood, 2012 Jul 12, Volume 120, Issue 2, p.440-8, (2012) Abstract
M
Rise and fall of subclones from diagnosis to relapse in pediatric B-acute lymphoblastic leukaemia., Ma, Xiaotu, Edmonson Michael, Yergeau Donald, Muzny Donna M., Hampton Oliver A., Rusch Michael, Song Guangchun, Easton John, Harvey Richard C., Wheeler David A., et al. , Nature communications, 2015, Volume 6, p.6604, (2015) Abstract
Research ethics and the challenge of whole-genome sequencing., McGuire, Amy L., Caulfield Timothy, and Cho Mildred K. , Nature reviews. Genetics, 2008 Feb, Volume 9, Issue 2, p.152-6, (2008) Abstract
ReadDepth: a parallel R package for detecting copy number alterations from short sequencing reads., Miller, Christopher A., Hampton Oliver, Coarfa Cristian, and Milosavljevic Aleksandar , PloS one, 2011, Volume 6, Issue 1, p.e16327, (2011) Abstract
Regional association-based fine-mapping for sodium-lithium countertransport on chromosome 10., Morrison, Alanna C., Boerwinkle Eric, Turner Stephen T., and Ferrell Robert E. , American journal of hypertension, 2008 Jan, Volume 21, Issue 1, p.117-21, (2008) Abstract
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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


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