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The INSIG2 rs7566605 genetic variant does not play a major role in obesity in a sample of 24,722 individuals from four cohorts., Bressler, Jan, Fornage Myriam, Hanis Craig L., Kao Wen Hong Linda, Lewis Cora E., McPherson Ruth, Dent Robert, Mosley Thomas H., Pennacchio Len A., and Boerwinkle Eric , BMC medical genetics, 2009, Volume 10, p.56, (2009) Abstract
Initial testing (stage 1) of the PARP inhibitor BMN 673 by the pediatric preclinical testing program: PALB2 mutation predicts exceptional in vivo response to BMN 673., Smith, Malcolm A., Hampton Oliver A., Reynolds Patrick C., Kang Min H., Maris John M., Gorlick Richard, Kolb Anders E., Lock Richard, Carol Hernan, Keir Stephen T., et al. , Pediatric blood & cancer, 2015 Jan, Volume 62, Issue 1, p.91-8, (2015) Abstract
Initial sequencing and comparative analysis of the mouse genome., Waterston, Robert H., Lindblad-Toh Kerstin, Birney Ewan, Rogers Jane, Abril Josep F., Agarwal Pankaj, Agarwala Richa, Ainscough Rachel, Alexandersson Marina, An Peter, et al. , Nature, 2002 Dec 5, Volume 420, Issue 6915, p.520-62, (2002) Abstract
Initial sequencing and analysis of the human genome., Lander, E. S., Linton L. M., Birren B., Nusbaum C., Zody M. C., Baldwin J., Devon K., Dewar K., Doyle M., FitzHugh W., et al. , Nature, 2001 Feb 15, Volume 409, Issue 6822, p.860-921, (2001) Abstract
Inferring population mutation rate and sequencing error rate using the SNP frequency spectrum in a sample of DNA sequences., Liu, Xiaoming, Maxwell Taylor J., Boerwinkle Eric, and Fu Yun-Xin , Molecular biology and evolution, 2009 Jul, Volume 26, Issue 7, p.1479-90, (2009) Abstract
Infection of a yellow baboon with simian immunodeficiency virus from African green monkeys: evidence for cross-species transmission in the wild., Jin, M. J., Rogers J., Phillips-Conroy J. E., Allan J. S., Desrosiers R. C., Shaw G. M., Sharp P. M., and Hahn B. H. , Journal of virology, 1994 Dec, Volume 68, Issue 12, p.8454-60, (1994) Abstract
Increasing the number of URMS in genomic science; (1854F)., Murray, D., Whittington D., and Gibbs R. , 62nd Annual Meeting of The American Society of Human Genetics, San Francisco, California, (2012)
Incidental copy-number variants identified by routine genome testing in a clinical population., Boone, Philip M., Soens Zachry T., Campbell Ian M., Stankiewicz Pawel, Cheung Sau Wai, Patel Ankita, Beaudet Arthur L., Plon Sharon E., Shaw Chad A., McGuire Amy L., et al. , Genetics in medicine : official journal of the American College of Medical Genetics, 2013 Jan, Volume 15, Issue 1, p.45-54, (2013) Abstract
Inactivating Mutations in NPC1L1 and Protection from Coronary Heart Disease, , New England Journal of Medicine, 11/2014, p.141112140016008, (2014)
In transition: primate genomics at a time of rapid change., Rogers, Jeffrey , ILAR journal / National Research Council, Institute of Laboratory Animal Resources, 2013, Volume 54, Issue 2, p.224-33, (2013) Abstract
In silico genetics: identification of a functional element regulating H2-Ealpha gene expression., Liao, Guochun, Wang Jianmei, Guo Jingshu, Allard John, Cheng Janet, Ng Anh, Shafer Steve, Puech Anne, McPherson John D., Foernzler Dorothee, et al. , Science (New York, N.Y.), 2004 Oct 22, Volume 306, Issue 5696, p.690-5, (2004) Abstract
Imputing gene-treatment interactions when the genotype distribution is unknown using case-only and putative placebo analyses--a new method for the Genetics of Hypertension Associated Treatment (GenHAT) study., Davis, Barry R., Ford Charles E., Boerwinkle Eric, Arnett Donna, Eckfeldt John, and Black Henry , Statistics in medicine, 2004 Aug 15, Volume 23, Issue 15, p.2413-27, (2004) Abstract
Improved ligation-anchored PCR strategy for identification of 5' ends of transcripts., Ansari-Lari, M. A., Jones S. N., Timms K. M., and Gibbs R. A. , BioTechniques, 1996 Jul, Volume 21, Issue 1, p.34-6, 38, (1996)
The importance of context to the genetic architecture of diabetes-related traits is revealed in a genome-wide scan of a LG/J × SM/J murine model., Lawson, Heather A., Lee Arthur, Fawcett Gloria L., Wang Bing, Pletscher Susan L., Maxwell Taylor J., Ehrich Thomas H., Kenney-Hunt Jane P., Wolf Jason B., Semenkovich Clay F., et al. , Mammalian genome : official journal of the International Mammalian Genome Society, 2011 Apr, Volume 22, Issue 3-4, p.197-208, (2011) Abstract
The importance of being cis: evolution of orthologous fish and mammalian enhancer activity., Ritter, Deborah I., Li Qiang, Kostka Dennis, Pollard Katherine S., Guo Su, and Chuang Jeffrey H. , Molecular biology and evolution, 2010 Oct, Volume 27, Issue 10, p.2322-32, (2010) Abstract
Immunoglobulin locus associates with serum IgG levels and albuminuria., Herring, Stacy M., Gokul Nisha, Monita Monique, Bell Rebecca, Boerwinkle Eric, Wenderfer Scott E., Braun Michael C., and Doris Peter A. , Journal of the American Society of Nephrology : JASN, 2011 May, Volume 22, Issue 5, p.881-9, (2011) Abstract
Identity and function of a large gene network underlying mutagenic repair of DNA breaks., Al Mamun, Abu Amar M., Lombardo Mary-Jane, Shee Chandan, Lisewski Andreas M., Gonzalez Caleb, Lin Dongxu, Nehring Ralf B., Saint-Ruf Claude, Gibson Janet L., Frisch Ryan L., et al. , Science (New York, N.Y.), 2012 Dec 7, Volume 338, Issue 6112, p.1344-8, (2012) Abstract
Identifying gene disruptions in novel balanced de novo constitutional translocations in childhood cancer patients by whole-genome sequencing., Ritter, Deborah I., Haines Katherine, Cheung Hannah, Davis Caleb F., Lau Ching C., Berg Jonathan S., Brown Chester W., Thompson Patrick A., Gibbs Richard, Wheeler David A., et al. , Genetics in medicine : official journal of the American College of Medical Genetics, 2015 Jan 8, (2015) Abstract
Identifying gene disruptions in novel balanced de novo constitutional translocations in childhood cancer patients by whole-genome sequencing., Ritter, Deborah I., Haines Katherine, Cheung Hannah, Davis Caleb F., Lau Ching C., Berg Jonathan S., Brown Chester W., Thompson Patrick A., Gibbs Richard, Wheeler David A., et al. , Genetics in medicine : official journal of the American College of Medical Genetics, 2015 Jan 8, (2015) Abstract
Identification of TP53 as an acute lymphocytic leukemia susceptibility gene through exome sequencing., Powell, Bradford C., Jiang Lichun, Muzny Donna M., Treviño Lisa R., Dreyer Zoann E., Strong Louise C., Wheeler David A., Gibbs Richard A., and Plon Sharon E. , Pediatric blood & cancer, 2012 Dec 19, (2012) Abstract
Identification of three novel Ca(2+) channel gamma subunit genes reveals molecular diversification by tandem and chromosome duplication., Burgess, D. L., Davis Caleb F., Gefrides L. A., and Noebels J. L. , Genome research, 1999 Dec, Volume 9, Issue 12, p.1204-13, (1999) Abstract
Identification of rat genes by TWINSCAN gene prediction, RT-PCR, and direct sequencing., Wu, Jiaqian, Shteynberg David, Arumugam Manimozhiyan, Gibbs Richard A., and Brent Michael R. , Genome research, 2004 Apr, Volume 14, Issue 4, p.665-71, (2004) Abstract
Identification of rat genes by TWINSCAN gene prediction, RT-PCR, and direct sequencing., Wu, Jiaqian, Shteynberg David, Arumugam Manimozhiyan, Gibbs Richard A., and Brent Michael R. , Genome research, 2004 Apr, Volume 14, Issue 4, p.665-71, (2004) Abstract


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