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Journal Article
A proposal to sequence the amphioxus genome submitted to the Joint Genome Institute of the US Department of Energy., Gibson-Brown, Jeremy J., Osoegawa Kazutoyo, McPherson John D., Waterston Robert H., de Jong Pieter J., Rokhsar Daniel S., and Holland Linda Z. , Journal of experimental zoology. Part B, Molecular and developmental evolution, 2003 Dec 15, Volume 300, Issue 1, p.5-22, (2003)
A proposed architecture for ambulatory systems development., Buffone, G. J., Petermann C. A., Bobroff R. B., Moore D. M., Dargahi R., Moreau D. R., Gilson H. S., Li Y., Fowler J., and Beck J. R. , Medinfo. MEDINFO, 1995, Volume 8 Pt 1, p.363-6, (1995) Abstract
Prospective associations of coronary heart disease loci in African Americans using the MetaboChip: the PAGE study., Franceschini, Nora, Hu Yijuan, Reiner Alex P., Buyske Steven, Nalls Mike, Yanek Lisa R., Li Yun, Hindorff Lucia A., Cole Shelley A., Howard Barbara V., et al. , PloS one, 2014, Volume 9, Issue 12, p.e113203, (2014) Abstract
PTPN11 mutations in Noonan syndrome type I: detection of recurrent mutations in exons 3 and 13., Maheshwari, M., Belmont J., Fernbach S., Ho T., Molinari L., Yakub I., Yu F., Combes A., Towbin J., Craigen W. J., et al. , Human mutation, 2002 Oct, Volume 20, Issue 4, p.298-304, (2002) Abstract
Pulmonary alveolar proteinosis caused by deletion of the GM-CSFRalpha gene in the X chromosome pseudoautosomal region 1., Martinez-Moczygemba, Margarita, Doan Minh L., Elidemir Okan, Fan Leland L., Cheung Sau Wai, Lei Jonathan T., Moore James P., Tavana Ghamartaj, Lewis Lora R., Zhu Yiming, et al. , The Journal of experimental medicine, 2008 Nov 24, Volume 205, Issue 12, p.2711-6, (2008) Abstract
Punctuated duplication seeding events during the evolution of human chromosome 2p11., Horvath, Julie E., Gulden Cassandra L., Vallente Rhea U., Eichler Marla Y., Ventura Mario, McPherson John D., Graves Tina A., Wilson Richard K., Schwartz Stuart, Rocchi Mariano, et al. , Genome research, 2005 Jul, Volume 15, Issue 7, p.914-27, (2005) Abstract
Quantitation of mixed-base populations of HIV-1 variants by automated DNA sequencing with BODIPY dye-labeled primers., Metzker, M. L., Ansari-Lari M. A., Liu X. M., Holder D. J., and Gibbs R. A. , BioTechniques, 1998 Sep, Volume 25, Issue 3, p.446-7, 450-2, 454, passim, (1998) Abstract
Quantitative Genetics of Response to Novelty and Other Stimuli by Infant Rhesus Macaques (Macaca mulatta) Across Three Behavioral Assessments., Fawcett, G. L., Dettmer A. M., Kay D., Raveendran M., Higley J. D., Ryan N. D., Cameron J. L., and Rogers J. , International journal of primatology, 2014 Feb 1, Volume 35, Issue 1, p.325-339, (2014) Abstract
Quantitative loci regulating plasma levels of gamma glutamyl transferase and albumin and their genetic correlations with cardiovascular risk factors., Bose, Tanushree, Voruganti Saroja V., Tejero Elizabeth M., Proffitt Michael J., Cox Laura A., VandeBerg John L., Mahaney Michael C., Rogers Jeffrey, Freeland-Graves Jeanne H., Cole Shelley A., et al. , Experimental biology and medicine (Maywood, N.J.), 2009 Dec, Volume 234, Issue 12,, 1519-24, (2009) Abstract
Quantitative monitoring of adenocarcinoma development in rodents by magnetic resonance imaging., Garbow, Joel R., Wang Min, Wang Yian, Lubet Ronald A., and You Ming , Clinical cancer research : an official journal of the American Association for Cancer Research, 2008 Mar 1, Volume 14, Issue 5, p.1363-7, (2008) Abstract
Quantitative trait loci affecting liver fat content in mice., Minkina, Olga, Cheverud James M., Fawcett Gloria, Semenkovich Clay F., and Kenney-Hunt Jane P. , G3 (Bethesda, Md.), 2012 Sep, Volume 2, Issue 9, p.1019-25, (2012) Abstract
Quantitative trait loci for peripheral blood cell counts: a study in baboons., Bertin, Angéline, Mahaney Michael C., Cox Laura A., Rogers Jeffrey, VandeBerg John L., Brugnara Carlo, and Platt Orah S. , Mammalian genome : official journal of the International Mammalian Genome Society, 2007 May, Volume 18, Issue 5, p.361-72, (2007) Abstract
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
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
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
Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF., Huffman, Jennifer E., de Vries Paul S., Morrison Alanna C., Sabater-Lleal Maria, Kacprowski Tim, Auer Paul L., Brody Jennifer A., Chasman Daniel I., Chen Ming-Huei, Guo Xiuqing, et al. , Blood, 2015 Sep 10, Volume 126, Issue 11, p.e19-29, (2015) 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
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
Rare variants in the notch signaling pathway describe a novel type of autosomal recessive Klippel-Feil syndrome., Karaca, Ender, Yuregir Ozge O., Bozdogan Sevcan T., Aslan Huseyin, Pehlivan Davut, Jhangiani Shalini N., Akdemir Zeynep C., Gambin Tomasz, Bayram Yavuz, Atik Mehmed M., et al. , American journal of medical genetics. Part A, 2015 Aug 4, (2015) 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
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
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
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
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

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