Skip to Content

Publications

Filters: First Letter Of Title is R  [Clear All Filters]
A B C D E F G H I J K L M N O P Q [R] S T U V W X Y Z   [Show ALL]
Y
Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk., Yu, Bing, Pulit Sara L., Hwang Shih-Jen, Brody Jennifer A., Amin Najaf, Auer Paul L., Bis Joshua C., Boerwinkle Eric, Burke Gregory L., Chakravarti Aravinda, et al. , Circulation. Cardiovascular genetics, 2015 Dec 11, (2015) Abstract
Rare variants analysis using penalization methods for whole genome sequence data., Yazdani, Akram, Yazdani Azam, and Boerwinkle Eric , BMC bioinformatics, 2015, Volume 16, p.405, (2015) Abstract
W
Rapid molecular cytogenetic analysis of X-chromosomal microdeletions: fluorescence in situ hybridization (FISH) for complex glycerol kinase deficiency., Worley, K. C., Lindsay E. A., Bailey W., Wise J., McCabe E. R., and Baldini A. , American journal of medical genetics, 1995 Jul 17, Volume 57, Issue 4, p.615-9, (1995) Abstract
Rats in the genomic era, Worley, K. C., Weinstock G. M., and Gibbs R. A. , Physiological Genomics, 11/2007, Volume 32, Issue 3, p.273 - 282, (2007)
Rats in the genomic era., Worley, K. C., Weinstock G. M., and Gibbs R. A. , Physiological genomics, 2008 Feb 19, Volume 32, Issue 3, p.273-82, (2008) Abstract
Rapid identification of heterozygous mutations in Drosophila melanogaster using genomic capture sequencing., Wang, Hui, Chattopadhyay Abanti, Li Zhe, Daines Bryce, Li Yumei, Gao Chunxu, Gibbs Richard, Zhang Kun, and Chen Rui , Genome research, 2010 Jul, Volume 20, Issue 7, p.981-8, (2010) 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)
Recurrent DGCR8, DROSHA, and SIX homeodomain mutations in favorable histology Wilms tumors., Walz, Amy L., Ooms Ariadne, Gadd Samantha, Gerhard Daniela S., Smith Malcolm A., Guidry Auvil Jamie M., Meerzaman Daoud, Chen Qing-Rong, Hsu Chih Hao, Yan Chunhua, et al. , Cancer cell, 2015 Feb 9, Volume 27, Issue 2, p.286-97, (2015) Abstract
V
Relationship of alcohol consumption and type of alcoholic beverage consumed with plasma lipid levels: differences between Whites and African Americans of the ARIC study., Volcik, Kelly A., Ballantyne Christie M., Fuchs Flavio D., Sharrett Richey A., and Boerwinkle Eric , Annals of epidemiology, 2008 Feb, Volume 18, Issue 2, p.101-7, (2008) Abstract
T
Reassessment of biochemically determined Hunter syndrome carrier status by DNA testing., Timms, K. M., Edwards F. J., Belmont J. W., Yates J. R., and Gibbs R. A. , Journal of medical genetics, 1998 Aug, Volume 35, Issue 8, p.646-9, (1998) Abstract
Rigid, conjugated, fluoresceinated thymidine triphosphates: syntheses and polymerase mediated incorporation into DNA analogues., Thoresen, Lars H., Jiao Guan-Sheng, Haaland Wade C., Metzker Michael L., and Burgess Kevin , Chemistry (Weinheim an der Bergstrasse, Germany), 2003 Oct 6, Volume 9, Issue 19, p.4603-10, (2003) Abstract
S
Recognition of pore-forming colicin Y by its cognate immunity protein., Smajs, David, Matejková Petra, and Weinstock George M. , FEMS microbiology letters, 2006 May, Volume 258, Issue 1, p.108-13, (2006) 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
R
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
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
Roger et Al. Respond to "future of population studies"., Roger, Véronique L., Boerwinkle Eric, Crapo James D., Douglas Pamela S., Epstein Jonathan A., Granger Christopher B., Greenland Philip, Kohane Isaac, and Psaty Bruce M. , American journal of epidemiology, 2015 Mar 15, Volume 181, Issue 6, p.372-3, (2015)
Requirement for homologous recombination functions for expression of the mutA mistranslator tRNA-induced mutator phenotype in Escherichia coli., Ren, L., Al Mamun A. A., and Humayun M. Z. , Journal of bacteriology, 2000 Mar, Volume 182, Issue 5, p.1427-31, (2000) 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
The role of drinking water sources, consumption of vegetables and seafood in relation to blood arsenic concentrations of Jamaican children with and without Autism Spectrum Disorders., Rahbar, Mohammad H., Samms-Vaughan Maureen, Ardjomand-Hessabi Manouchehr, Loveland Katherine A., Dickerson Aisha S., Chen Zhongxue, Bressler Jan, Shakespeare-Pellington Sydonnie, Grove Megan L., Bloom Kari, et al. , The Science of the total environment, 2012 Sep 1, Volume 433, p.362-70, (2012) Abstract
P
The role of combined SNV and CNV burden in patients with distal symmetric polyneuropathy., Pehlivan, Davut, Beck Christine R., Okamoto Yuji, Harel Tamar, Akdemir Zeynep H. C., Jhangiani Shalini N., Withers Marjorie A., Goksungur Meryem Tuba, Carvalho Claudia M. B., Czesnik Dirk, et al. , Genetics in medicine : official journal of the American College of Medical Genetics, 2015 Sep 17, (2015) Abstract
N
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
M
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
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
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
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


about seo