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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
Taking DNA from the dead., McGuire, Amy L., Majumder Mary A., Halpern Scott D., Swindell J. S., Yaeger Laura V., Gibbs Richard A., and Wheeler Thomas M. , Nature reviews. Genetics, 2010 May, Volume 11, Issue 5, p.318, (2010)
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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
Systematic cloning of Treponema pallidum open reading frames for protein expression and antigen discovery., McKevitt, Matthew, Patel Krupa, Smajs David, Marsh Michael, McLoughlin Melanie, Norris Steven J., Weinstock George M., and Palzkill Timothy , Genome research, 2003 Jul, Volume 13, Issue 7, p.1665-74, (2003) Abstract
A systematic approach to identify functional motifs within vertebrate developmental enhancers., Li, Qiang, Ritter Deborah, Yang Nan, Dong Zhiqiang, Li Hao, Chuang Jeffrey H., and Guo Su , Developmental biology, 2010 Jan 15, Volume 337, Issue 2, p.484-95, (2010) Abstract
Sweetness and light: illuminating the honey bee genome., Robinson, G. E., Evans J. D., Maleszka R., Robertson H. M., Weaver D. B., Worley K., Gibbs R. A., and Weinstock G. M. , Insect molecular biology, 2006 Oct, Volume 15, Issue 5, p.535-9, (2006)
Subtle genetic changes enhance virulence of methicillin resistant and sensitive Staphylococcus aureus., Highlander, Sarah K., Hultén Kristina G., Qin Xiang, Jiang Huaiyang, Yerrapragada Shailaja, Mason Edward O., Shang Yue, Williams Tiffany M., Fortunov Régine M., Liu Yamei, et al. , BMC microbiology, 2007, Volume 7, p.99, (2007) Abstract
Structure, function and diversity of the healthy human microbiome., , Nature, 2012 Jun 14, Volume 486, Issue 7402, p.207-14, (2012) Abstract
Strict evolutionary conservation followed rapid gene loss on human and rhesus Y chromosomes., Hughes, Jennifer F., Skaletsky Helen, Brown Laura G., Pyntikova Tatyana, Graves Tina, Fulton Robert S., Dugan Shannon, Ding Yan, Buhay Christian J., Kremitzki Colin, et al. , Nature, 2012 Mar 1, Volume 483, Issue 7387, p.82-6, (2012) Abstract
Stress, genomes, and evolution., Mittelman, David, and Wilson John H. , Cell stress & chaperones, 2010 Sep, Volume 15, Issue 5, p.463-6, (2010) Abstract
Strategic transformation of population studies: recommendations of the working group on epidemiology and population sciences from the national heart, lung, and blood advisory council and board of external experts., 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.363-8, (2015) Abstract
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)., Gerhard, Daniela S., Wagner Lukas, Feingold Elise A., Shenmen Carolyn M., Grouse Lynette H., Schuler Greg, Klein Steven L., Old Susan, Rasooly Rebekah, Good Peter, et al. , Genome research, 2004 Oct, Volume 14, Issue 10B, p.2121-7, (2004) Abstract
Stargazin and other transmembrane AMPA receptor regulating proteins interact with synaptic scaffolding protein MAGI-2 in brain., Deng, Fang, Price Maureen G., Davis Caleb F., Mori Mayra, and Burgess Daniel L. , The Journal of neuroscience : the official journal of the Society for Neuroscience, 2006 Jul 26, Volume 26, Issue 30, p.7875-84, (2006) Abstract
SSTR5 P335L monoclonal antibody differentiates pancreatic neuroendocrine neuroplasms with different SSTR5 genotypes., Zhou, Guisheng, Gingras Marie-Claude, Liu Shi-He, Sanchez Robbi, Edwards Dean, Dawson David, Christensen Kurt, Paganelli Giovanni, Gibbs Richard, Fisher William, et al. , Surgery, 2011 Dec, Volume 150, Issue 6, p.1136-42, (2011) Abstract
Squamous Cell Carcinoma of the Oral Tongue in Young Non-Smokers Is Genomically Similar to Tumors in Older Smokers, Pickering, C. R., Zhang J., Neskey D. M., Zhao M., Jasser S. A., Wang J., Ward A., Tsai C. J., Ortega Alves M. V., Zhou J. H., et al. , Clinical Cancer Research, 07/2014, Volume 20, Issue 14, p.3842 - 3848, (2014)
Spontaneous mutagenesis is elevated in protease-defective cells., Al Mamun, Abu Amar M., and Humayun Zafri M. , Molecular microbiology, 2009 Feb, Volume 71, Issue 3, p.629-39, (2009) Abstract
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


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