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Journal Article
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project., Birney, Ewan, Stamatoyannopoulos John A., Dutta Anindya, Guigó Roderic, Gingeras Thomas R., Margulies Elliott H., Weng Zhiping, Snyder Michael, Dermitzakis Emmanouil T., Thurman Robert E., et al. , Nature, 2007 Jun 14, Volume 447, Issue 7146, p.799-816, (2007) Abstract
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project., Birney, Ewan, Stamatoyannopoulos John A., Dutta Anindya, Guigó Roderic, Gingeras Thomas R., Margulies Elliott H., Weng Zhiping, Snyder Michael, Dermitzakis Emmanouil T., Thurman Robert E., et al. , Nature, 2007 Jun 14, Volume 447, Issue 7146, p.799-816, (2007) Abstract
Identification and removal of colanic acid from plasmid DNA preparations: implications for gene therapy., Firozi, P., Zhang W., Chen L., Quiocho F. A., Worley K. C., and Templeton N. S. , Gene therapy, 2010 Dec, Volume 17, Issue 12, p.1484-99, (2010) Abstract
Identification of a novel tumor suppressor gene p34 on human chromosome 6q25.1., Wang, Min, Vikis Haris G., Wang Yian, Jia Dongmei, Wang Daolong, Bierut Laura J., Bailey-Wilson Joan E., Amos Christopher I., Pinney Susan M., Petersen Gloria M., et al. , Cancer research, 2007 Jan 1, Volume 67, Issue 1, p.93-9, (2007) Abstract
Identification of a QTL for adipocyte volume and of shared genetic effects with aspartate aminotransferase., Bose, Tanushree, Voruganti Saroja V., Tejero Elizabeth M., Proffit Michael J., Cox Laura A., VandeBerg John L., Mahaney Michael C., Rogers Jeffrey, Freeland-Graves Jeanne H., Cole Shelley A., et al. , Biochemical genetics, 2010 Jun, Volume 48, Issue 5-6, p.538-47, (2010) Abstract
Identification of genes subject to positive selection in uropathogenic strains of Escherichia coli: a comparative genomics approach., Chen, Swaine L., Hung Chia-Seui, Xu Jian, Reigstad Christopher S., Magrini Vincent, Sabo Aniko, Blasiar Darin, Bieri Tamberlyn, Meyer Rekha R., Ozersky Philip, et al. , Proceedings of the National Academy of Sciences of the United States of America, 2006 Apr 11, Volume 103, Issue 15, p.5977-82, (2006) Abstract
Identification of new markers in Xp21 between DXS28 (C7) and DMD., Worley, K. C., Towbin J. A., Zhu X. M., Barker D. F., Ballabio A., Chamberlain J., Biesecker L. G., Blethen S. L., Brosnan P., and Fox J. E. , Genomics, 1992 Aug, Volume 13, Issue 4, p.957-61, (1992) Abstract
Identification of quantitative trait loci affecting murine long bone length in a two-generation intercross of LG/J and SM/J Mice., Norgard, Elizabeth A., Roseman Charles C., Fawcett Gloria L., Pavlicev Mihaela, Morgan Clinton D., Pletscher Susan L., Wang Bing, and Cheverud James M. , Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2008 Jun, Volume 23, Issue 6, p.887-95, (2008) 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
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
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
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
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
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
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
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
Integrated and sequence-ordered BAC- and YAC-based physical maps for the rat genome., Krzywinski, Martin, Wallis John, Gösele Claudia, Bosdet Ian, Chiu Readman, Graves Tina, Hummel Oliver, Layman Dan, Mathewson Carrie, Wye Natasja, et al. , Genome research, 2004 Apr, Volume 14, Issue 4, p.766-79, (2004) Abstract
Integrating common and rare genetic variation in diverse human populations., Altshuler, David M., Gibbs Richard A., Peltonen Leena, Altshuler David M., Gibbs Richard A., Peltonen Leena, Dermitzakis Emmanouil, Schaffner Stephen F., Yu Fuli, Peltonen Leena, et al. , Nature, 2010 Sep 2, Volume 467, Issue 7311, p.52-8, (2010) Abstract
Integrating the UMLS into VNS Retriever., Barber, S., Fowler J., Long K. B., Dargahi R., and Meyer B. , Proceedings / the ... Annual Symposium on Computer Application [sic] in Medical Care. Symposium on Computer Applications in Medical Care, 1992, p.273-7, (1992) Abstract
Integrative genomic characterization of oral squamous cell carcinoma identifies frequent somatic drivers., Pickering, Curtis R., Zhang Jiexin, Yoo Suk Young, Bengtsson Linnea, Moorthy Shhyam, Neskey David M., Zhao Mei, Ortega Alves Marcus V., Chang Kyle, Drummond Jennifer, et al. , Cancer discovery, 2013 Jul, Volume 3, Issue 7, p.770-81, (2013) Abstract
Interactions of dietary whole-grain intake with fasting glucose- and insulin-related genetic loci in individuals of European descent: a meta-analysis of 14 cohort studies., Nettleton, Jennifer A., McKeown Nicola M., Kanoni Stavroula, Lemaitre Rozenn N., Hivert Marie-France, Ngwa Julius, van Rooij Frank J. A., Sonestedt Emily, Wojczynski Mary K., Ye Zheng, et al. , Diabetes care, 2010 Dec, Volume 33, Issue 12, p.2684-91, (2010) Abstract
Internet Contig Explorer (iCE)--a tool for visualizing clone fingerprint maps., Fjell, Christopher D., Bosdet Ian, Schein Jacqueline E., Jones Steven J. M., and Marra Marco A. , Genome research, 2003 Jun, Volume 13, Issue 6A, p.1244-9, (2003) Abstract
Investigating single nucleotide polymorphism (SNP) density in the human genome and its implications for molecular evolution., Zhao, Zhongming, Fu Yun-Xin, Hewett-Emmett David, and Boerwinkle Eric , Gene, 2003 Jul 17, Volume 312, p.207-13, (2003) Abstract
The KAT6B-related disorders genitopatellar syndrome and Ohdo/SBBYS syndrome have distinct clinical features reflecting distinct molecular mechanisms., Campeau, Philippe M., Lu James T., Dawson Brian C., Fokkema Ivo F. A. C., Robertson Stephen P., Gibbs Richard A., and Lee Brendan H. , Human mutation, 2012 Nov, Volume 33, Issue 11, p.1520-5, (2012) Abstract
l7Rn6 encodes a novel protein required for clara cell function in mouse lung development., Fernández-Valdivia, Rodrigo, Zhang Ying, Pai Sonia, Metzker Michael L., and Schumacher Armin , Genetics, 2006 Jan, Volume 172, Issue 1, p.389-99, (2006) Abstract

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