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Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation., Lalani, Seema R., Safiullah Arsalan M., Fernbach Susan D., Harutyunyan Karine G., Thaller Christina, Peterson Leif E., McPherson John D., Gibbs Richard A., White Lisa D., Hefner Margaret, et al. , American journal of human genetics, 2006 Feb, Volume 78, Issue 2, p.303-14, (2006) Abstract
Specific P-selectin and P-selectin glycoprotein ligand-1 genotypes/haplotypes are associated with risk of incident CHD and ischemic stroke: the Atherosclerosis Risk in Communities (ARIC) study., Volcik, Kelly A., Ballantyne Christie M., Coresh Josef, Folsom Aaron R., and Boerwinkle Eric , Atherosclerosis, 2007 Nov, Volume 195, Issue 1, p.e76-82, (2007) Abstract
Source identification in two criminal cases using phylogenetic analysis of HIV-1 DNA sequences., Scaduto, Diane I., Brown Jeremy M., Haaland Wade C., Zwickl Derrick J., Hillis David M., and Metzker Michael L. , Proceedings of the National Academy of Sciences of the United States of America, 2010 Dec 14, Volume 107, Issue 50, p.21242-7, (2010) Abstract
Somatic sequence variation at the Friedreich ataxia locus includes complete contraction of the expanded GAA triplet repeat, significant length variation in serially passaged lymphoblasts and enhanced mutagenesis in the flanking sequence., Bidichandani, S. I., Purandare S. M., Taylor E. E., Gumin G., Machkhas H., Harati Y., Gibbs R. A., Ashizawa T., and Patel P. I. , Human molecular genetics, 1999 Dec, Volume 8, Issue 13, p.2425-36, (1999) Abstract
Somatic mutations affect key pathways in lung adenocarcinoma., Ding, Li, Getz Gad, Wheeler David A., Mardis Elaine R., McLellan Michael D., Cibulskis Kristian, Sougnez Carrie, Greulich Heidi, Muzny Donna M., Morgan Margaret B., et al. , Nature, 2008 Oct 23, Volume 455, Issue 7216, p.1069-75, (2008) Abstract
The Somatic Genomic Landscape of Chromophobe Renal Cell Carcinoma., Davis, Caleb F., Ricketts Christopher J., Wang Min, Yang Lixing, Cherniack Andrew D., Shen Hui, Buhay Christian, Kang Hyojin, Kim Sang Cheol, Fahey Catherine C., et al. , Cancer cell, 2014 Sep 8, Volume 26, Issue 3, p.319-330, (2014) Abstract
The soluble epoxide hydrolase gene harbors sequence variation associated with susceptibility to and protection from incident ischemic stroke., Fornage, Myriam, Lee Craig R., Doris Peter A., Bray Molly S., Heiss Gerardo, Zeldin Darryl C., and Boerwinkle Eric , Human molecular genetics, 2005 Oct 1, Volume 14, Issue 19, p.2829-37, (2005) Abstract
Software for automated analysis of DNA fingerprinting gels., Fuhrmann, Daniel R., Krzywinski Martin I., Chiu Readman, Saeedi Parvaneh, Schein Jacqueline E., Bosdet Ian E., Chinwalla Asif, Hillier Ladeana W., Waterston Robert H., McPherson John D., et al. , Genome research, 2003 May, Volume 13, Issue 5, p.940-53, (2003) Abstract
SNPdetector: a software tool for sensitive and accurate SNP detection., Zhang, Jinghui, Wheeler David A., Yakub Imtiaz, Wei Sharon, Sood Raman, Rowe William, Liu Paul P., Gibbs Richard A., and Buetow Kenneth H. , PLoS computational biology, 2005 Oct, Volume 1, Issue 5, p.e53, (2005) Abstract
Sixty-nine kilobases of contiguous human genomic sequence containing the alpha-galactosidase A and Bruton's tyrosine kinase loci., Oeltjen, J. C., Liu X., Lu J., Allen R. C., Muzny D., Belmont J. W., and Gibbs R. A. , Mammalian genome : official journal of the International Mammalian Genome Society, 1995 May, Volume 6, Issue 5, p.334-8, (1995) Abstract
Single nucleotide polymorphisms in genes for 2'-5'-oligoadenylate synthetase and RNase L inpatients hospitalized with West Nile virus infection., Yakub, Imtiaz, Lillibridge Kristy M., Moran Ana, Gonzalez Omar Y., Belmont John, Gibbs Richard A., and Tweardy David J. , The Journal of infectious diseases, 2005 Nov 15, Volume 192, Issue 10, p.1741-8, (2005) Abstract
Single nucleotide polymorphisms associated with coronary heart disease predict incident ischemic stroke in the atherosclerosis risk in communities study., Morrison, Alanna C., Bare Lance A., Luke May M., Pankow James S., Mosley Thomas H., Devlin James J., Willerson James T., and Boerwinkle Eric , Cerebrovascular diseases (Basel, Switzerland), 2008, Volume 26, Issue 4, p.420-4, (2008) Abstract
Single nucleotide polymorphism in RECQL and survival in resectable pancreatic adenocarcinoma., Cotton, Ronald T., Li Donghui, Scherer Steven E., Muzny Donna M., Hodges Sally E., Catania Robbi L., Witkiewicz Agnieszka K., Brody Jonathan R., Kennedy Eugene P., Yeo Charles J., et al. , HPB : the official journal of the International Hepato Pancreato Biliary Association, 2009 Aug, Volume 11, Issue 5, p.435-44, (2009) Abstract
Single nucleotide polymorphism (SNP) analysis of mouse pulmonary adenoma susceptibility loci 1-4 for identification of candidate genes., Lemon, W. J., Swinton C. H., Wang M., Berbari N., Wang Y., and You M. , Journal of medical genetics, 2003 Apr, Volume 40, Issue 4, p.e36, (2003)
Simian T-lymphotropic virus type 1 (STLV-1) infection in wild yellow baboons (Papio hamadryas cynocephalus) from Mikumi National Park, Tanzania., Voevodin, A., Samilchuk E., Allan J., Rogers J., and Broussard S. , Virology, 1997 Feb 17, Volume 228, Issue 2, p.350-9, (1997) Abstract
Shotgun sample sequence comparisons between mouse and human genomes., Bouck, J. B., Metzker M. L., and Gibbs R. A. , Nature genetics, 2000 May, Volume 25, Issue 1, p.31-3, (2000) Abstract
The sheep genome illuminates biology of the rumen and lipid metabolism., Jiang, Yu, Xie Min, Chen Wenbin, Talbot Richard, Maddox Jillian F., Faraut Thomas, Wu Chunhua, Muzny Donna M., Li Yuxiang, Zhang Wenguang, et al. , Science (New York, N.Y.), 2014 Jun 6, Volume 344, Issue 6188, p.1168-73, (2014) Abstract
A server architecture for ambulatory patient record systems., Dargahi, R., Fowler J., Moreau D. R., and Buffone G. J. , Medinfo. MEDINFO, 1995, Volume 8 Pt 1, p.219-22, (1995) Abstract
Serum prostate specific antigen changes in cynomolgus monkeys (Macaca fascicularis) on a high sugar high fat diet., Mubiru, James N., Garcia-Forey Magdalena, Cavazos Nicole, Hemmat Peggah, Dick Edward J., Owston Michael A., Bauer Cassondra A., Shade Robert E., and Rogers Jeffrey , The Prostate, 2012 Apr, Volume 72, Issue 5, p.469-75, (2012) Abstract
Serum Metabolomic Profiling and Incident CKD among African Americans., Yu, Bing, Zheng Yan, Nettleton Jennifer A., Alexander Danny, Coresh Josef, and Boerwinkle Eric , Clinical journal of the American Society of Nephrology : CJASN, 2014 Aug 7, Volume 9, Issue 8, p.1410-7, (2014) Abstract
Sequencing and functional analysis of the SNRPN promoter: in vitro methylation abolishes promoter activity., Huq, A. H., Sutcliffe J. S., Nakao M., Shen Y., Gibbs R. A., and Beaudet A. L. , Genome research, 1997 Jun, Volume 7, Issue 6, p.642-8, (1997) Abstract
Sequence variations in PCSK9, low LDL, and protection against coronary heart disease., Cohen, Jonathan C., Boerwinkle Eric, Mosley Thomas H., and Hobbs Helen H. , The New England journal of medicine, 2006 Mar 23, Volume 354, Issue 12, p.1264-72, (2006) Abstract
Sequence variation in the soluble epoxide hydrolase gene and subclinical coronary atherosclerosis: interaction with cigarette smoking., Wei, Qi, Doris Peter A., Pollizotto Martin V., Boerwinkle Eric, Jacobs David R., Siscovick David S., and Fornage Myriam , Atherosclerosis, 2007 Jan, Volume 190, Issue 1, p.26-34, (2007) Abstract
Sequence variation in telomerase reverse transcriptase (TERT) as a determinant of risk of cardiovascular disease: the Atherosclerosis Risk in Communities (ARIC) study., Bressler, Jan, Franceschini Nora, Demerath Ellen W., Mosley Thomas H., Folsom Aaron R., and Boerwinkle Eric , BMC medical genetics, 2015, Volume 16, p.52, (2015) Abstract
Sequence variation in DOCK9 and heterogeneity in bipolar disorder., Detera-Wadleigh, Sevilla D., Liu Chun-yu, Maheshwari Manjula, Cardona Imer, Corona Winston, Akula Nirmala, Steele C. J. M., Badner Judith A., Kundu Mukta, Kassem Layla, et al. , Psychiatric genetics, 2007 Oct, Volume 17, Issue 5, p.274-86, (2007) Abstract

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