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Use of wrapper algorithms coupled with a random forests classifier for variable selection in large-scale genomic association studies., Rodin, Andrei S., Litvinenko Anatoliy, Klos Kathy, Morrison Alanna C., Woodage Trevor, Coresh Josef, and Boerwinkle Eric , Journal of computational biology : a journal of computational molecular cell biology, 2009 Dec, Volume 16, Issue 12, p.1705-18, (2009) Abstract
The use of primers from highly conserved pol regions to identify uncharacterized retroviruses by the polymerase chain reaction., Donehower, L. A., Bohannon R. C., Ford R. J., and Gibbs R. A. , Journal of virological methods, 1990 Apr, Volume 28, Issue 1, p.33-46, (1990) Abstract
Untangling the influences of unmodeled evolutionary processes on phylogenetic signal in a forensically important HIV-1 transmission cluster., Doyle, Vinson P., Andersen John J., Nelson Bradley J., Metzker Michael L., and Brown Jeremy M. , Molecular phylogenetics and evolution, 2014 Feb 28, Volume 75C, p.126-137, (2014) Abstract
Unique features of a global human ectoparasite identified through sequencing of the bed bug genome., Benoit, Joshua B., Adelman Zach N., Reinhardt Klaus, Dolan Amanda, Poelchau Monica, Jennings Emily C., Szuter Elise M., Hagan Richard W., Gujar Hemant, Shukla Jayendra Nath, et al. , Nature communications, 2016, Volume 7, p.10165, (2016) Abstract
Union makes strength: a worldwide collaborative genetic and clinical study to provide a comprehensive survey of RD3 mutations and delineate the associated phenotype., Perrault, Isabelle, Estrada-Cuzcano Alejandro, Lopez Irma, Kohl Susanne, Li Shiqiang, Testa Francesco, Zekveld-Vroon Renate, Wang Xia, Pomares Esther, Andorf Jean, et al. , PloS one, 2013, Volume 8, Issue 1, p.e51622, (2013) Abstract
Understanding the development of human bladder cancer by using a whole-organ genomic mapping strategy., Majewski, Tadeusz, Lee Sangkyou, Jeong Joon, Yoon Dong-Sup, Kram Andrzej, Kim Mi-Sook, Tuziak Tomasz, Bondaruk Jolanta, Lee Sooyong, Park Weon-Seo, et al. , Laboratory investigation; a journal of technical methods and pathology, 2008 Jul, Volume 88, Issue 7, p.694-721, (2008) Abstract
Two Novel Simian Arteriviruses in Captive and Wild Baboons (Papio spp.)., Bailey, Adam L., Lauck Michael, Sibley Samuel D., Pecotte Jerilyn, Rice Karen, Weny Geoffrey, Tumukunde Alex, Hyeroba David, Greene Justin, Correll Michael, et al. , Journal of virology, 2014 Sep 3, (2014) Abstract
TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum., Davis, Erica E., Zhang Qi, Liu Qin, Diplas Bill H., Davey Lisa M., Hartley Jane, Stoetzel Corinne, Szymanska Katarzyna, Ramaswami Gokul, Logan Clare V., et al. , Nature genetics, 2011 Mar, Volume 43, Issue 3, p.189-96, (2011) Abstract
Trisomy 17 in a baboon (Papio hamadryas) with polydactyly, patent foramen ovale and pyelectasis., Moore, Charleen M., Hubbard Gene B., Dick Edward, Dunn Betty G., Raveendran Muthuswamy, Rogers Jeffrey, Williams Vick, Gomez Jeremiah J., Butler Stephanie D., Leland Michelle M., et al. , American journal of primatology, 2007 Oct, Volume 69, Issue 10, p.1105-18, (2007) Abstract
Treponema pallidum infection in the wild baboons of East Africa: distribution and genetic characterization of the strains responsible., Harper, Kristin N., Fyumagwa Robert D., Hoare Richard, Wambura Philemon N., Coppenhaver Dorian H., Sapolsky Robert M., Alberts Susan C., Tung Jenny, Rogers Jeffrey, Kilewo Morris, et al. , PloS one, 2012, Volume 7, Issue 12, p.e50882, (2012) Abstract
Transient alterations in the expression of protease and extracellular matrix genes during metastatic lung colonization by H-ras-transformed 10T1/2 fibroblasts., Gingras, M. C., Jarolim L., Finch J., Bowden G. T., Wright J. A., and Greenberg A. H. , Cancer research, 1990 Jul 1, Volume 50, Issue 13, p.4061-6, (1990) Abstract
Transethnic meta-analysis suggests genetic variation in the HEME pathway influences potassium response in patients treated with hydrochlorothiazide., Del-Aguila, J. L., Cooper-DeHoff R. M., Chapman A. B., Gums J. G., Beitelshees A. L., Bailey K., Turner S. T., Johnson J. A., and Boerwinkle E. , The pharmacogenomics journal, 2014 Sep 9, (2014) Abstract
Transcriptomic variation of pharmacogenes in multiple human tissues and lymphoblastoid cell lines., Chhibber, A., French C. E., Yee S. W., Gamazon E. R., Theusch E., Qin X., Webb A., Papp A. C., Wang A., Simmons C. Q., et al. , The pharmacogenomics journal, 2016 Feb 9, (2016) Abstract
Transcriptomic analysis supports similar functional roles for the two thymuses of the tammar wallaby., Wong, Emily S. W., Papenfuss Anthony T., Heger Andreas, Hsu Arthur L., Ponting Chris P., Miller Robert D., Fenelon Jane C., Renfree Marilyn B., Gibbs Richard A., and Belov Katherine , BMC genomics, 2011, Volume 12, p.420, (2011) Abstract
TM4SF20 Ancestral Deletion and Susceptibility to a Pediatric Disorder of Early Language Delay and Cerebral White Matter Hyperintensities., Wiszniewski, Wojciech, Hunter Jill V., Hanchard Neil A., Willer Jason R., Shaw Chad, Tian Qi, Illner Anna, Wang Xueqing, Cheung Sau W., Patel Ankita, et al. , American journal of human genetics, 2013 Aug 8, Volume 93, Issue 2, p.197-210, (2013) Abstract
Tissue-specific transcriptome sequencing analysis expands the non-human primate reference transcriptome resource (NHPRTR)., Peng, Xinxia, Thierry-Mieg Jean, Thierry-Mieg Danielle, Nishida Andrew, Pipes Lenore, Bozinoski Marjan, Thomas Matthew J., Kelly Sara, Weiss Jeffrey M., Raveendran Muthuswamy, et al. , Nucleic acids research, 2014 Nov 11, (2014) Abstract
TET2 and CSMD1 genes affect SBP response to hydrochlorothiazide in never-treated essential hypertensives., Chittani, Martina, Zaninello Roberta, Lanzani Chiara, Frau Francesca, Ortu Maria F., Salvi Erika, Fresu Giovanni, Citterio Lorena, Braga Daniele, Piras Daniela A., et al. , Journal of hypertension, 2015 Feb 18, (2015) Abstract
Test of the potential of a dATP surrogate for sequencing via MALDI-MS., Jacutin, S., Zhang A. J., Russell D. H., Gibbs R. A., and Burgess K. , Nucleic acids research, 1997 Dec 15, Volume 25, Issue 24, p.5072-6, (1997) Abstract
Termination of DNA synthesis by novel 3'-modified-deoxyribonucleoside 5'-triphosphates., Metzker, M. L., Raghavachari R., Richards S., Jacutin S. E., Civitello A., Burgess K., and Gibbs R. A. , Nucleic acids research, 1994 Oct 11, Volume 22, Issue 20, p.4259-67, (1994) Abstract
Targeted sequencing in chromosome 17q linkage region identifies familial glioma candidates in the Gliogene Consortium., Jalali, Ali, Amirian Susan E., Bainbridge Matthew N., Armstrong Georgina N., Liu Yanhong, Tsavachidis Spyros, Jhangiani Shalini N., Plon Sharon E., Lau Ching C., Claus Elizabeth B., et al. , Scientific reports, 2015, Volume 5, p.8278, (2015) Abstract
Targeted sequencing in candidate genes for atrial fibrillation: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Targeted Sequencing Study., Lin, Honghuang, Sinner Moritz F., Brody Jennifer A., Arking Dan E., Lunetta Kathryn L., Rienstra Michiel, Lubitz Steven A., Magnani Jared W., Sotoodehnia Nona, McKnight Barbara, et al. , Heart rhythm : the official journal of the Heart Rhythm Society, 2014 Mar, Volume 11, Issue 3, p.452-7, (2014) Abstract
Targeted enrichment beyond the consensus coding DNA sequence exome reveals exons with higher variant densities., Bainbridge, Matthew N., Wang Min, Wu Yuanqing, Newsham Irene, Muzny Donna M., Jefferies John L., Albert Thomas J., Burgess Daniel L., and Gibbs Richard A. , Genome biology, 2011, Volume 12, Issue 7, p.R68, (2011) Abstract
Systems biology data analysis methodology in pharmacogenomics., Rodin, Andrei S., Gogoshin Grigoriy, and Boerwinkle Eric , Pharmacogenomics, 2011 Sep, Volume 12, Issue 9, p.1349-60, (2011) Abstract
A systematic survey of loss-of-function variants in human protein-coding genes., MacArthur, Daniel G., Balasubramanian Suganthi, Frankish Adam, Huang Ni, Morris James, Walter Klaudia, Jostins Luke, Habegger Lukas, Pickrell Joseph K., Montgomery Stephen B., et al. , Science (New York, N.Y.), 2012 Feb 17, Volume 335, Issue 6070, p.823-8, (2012) Abstract
Successful diagnosis of HIBCH deficiency from exome sequencing and positive retrospective analysis of newborn screening cards in two siblings presenting with Leigh's disease., Stiles, Ashlee R., Ferdinandusse Sacha, Besse Arnaud, Appadurai Vivek, Leydiker Karen B., Cambray-Forker E. J., Bonnen Penelope E., and Abdenur Jose E. , Molecular genetics and metabolism, 2015 Aug, Volume 115, Issue 4, p.161-7, (2015) Abstract

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