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Conference Paper
Genome-wide analysis of stepwise hepatocarcinogenesis using next generation sequencer, Midorikawa, Yutaka, Yamamoto Shogo, Ueda Hiroki, Sonoda Kotaro, Tsuji Shingo, Tatsuno Kenji, Shibata Tatsuhiro, Covington Kyle, Wheeler David A., Takayama Tadatoshi, et al. , HEPATOLOGY, Volume 58, p.396A–396A, (2013)
Journal Article
Analyses of deep mammalian sequence alignments and constraint predictions for 1% of the human genome., Margulies, Elliott H., Cooper Gregory M., Asimenos George, Thomas Daryl J., Dewey Colin N., Siepel Adam, Birney Ewan, Keefe Damian, Schwartz Ariel S., Hou Minmei, et al. , Genome research, 2007 Jun, Volume 17, Issue 6, p.760-74, (2007) Abstract
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks., Peloso, Gina M., Auer Paul L., Bis Joshua C., Voorman Arend, Morrison Alanna C., Stitziel Nathan O., Brody Jennifer A., Khetarpal Sumeet A., Crosby Jacy R., Fornage Myriam, et al. , American journal of human genetics, 2014 Feb 6, Volume 94, Issue 2, p.223-32, (2014) Abstract
Association of Rare Loss-Of-Function Alleles in HAL, Serum Histidine Levels and Incident Coronary Heart Disease., Yu, Bing, Li Alexander H., Muzny Donna, Veeraraghavan Narayanan, de Vries Paul S., Bis Joshua C., Musani Solomon K., Alexander Danny, Morrison Alanna C., Franco Oscar H., et al. , Circulation. Cardiovascular genetics, 2015 Jan 8, (2015) Abstract
Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease., Ueda, Hironori, Howson Joanna M. M., Esposito Laura, Heward Joanne, Snook Hywel, Chamberlain Giselle, Rainbow Daniel B., Hunter Kara M. D., Smith Annabel N., Di Genova Gianfranco, et al. , Nature, 2003 May 29, Volume 423, Issue 6939, p.506-11, (2003) Abstract
Autosomal-Dominant Multiple Pterygium Syndrome Is Caused by Mutations in MYH3., Chong, Jessica X., Burrage Lindsay C., Beck Anita E., Marvin Colby T., McMillin Margaret J., Shively Kathryn M., Harrell Tanya M., Buckingham Kati J., Bacino Carlos A., Jain Mahim, et al. , American journal of human genetics, 2015 May 7, Volume 96, Issue 5, p.841-9, (2015) Abstract
Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium., Grove, Megan L., Yu Bing, Cochran Barbara J., Haritunians Talin, Bis Joshua C., Taylor Kent D., Hansen Mark, Borecki Ingrid B., Cupples Adrienne L., Fornage Myriam, et al. , PloS one, 2013, Volume 8, Issue 7, p.e68095, (2013) Abstract
The Cancer Genome Atlas Pan-Cancer analysis project., Chang, Kyle, Creighton Chad J., Davis Caleb F., Donehower Lawrence, Drummond Jennifer, Wheeler David, Ally Adrian, Balasundaram Miruna, Birol Inanc, Butterfield Yaron S. N., et al. , Nature genetics, 2013 Sep 26, Volume 45, Issue 10, p.1113-20, (2013)
Chromosome rearrangement and diversification of Francisella tularensis revealed by the type B (OSU18) genome sequence., Petrosino, Joseph F., Xiang Qin, Karpathy Sandor E., Jiang Huaiyang, Yerrapragada Shailaja, Liu Yamei, Gioia Jason, Hemphill Lisa, Gonzalez Arely, Raghavan T. M., et al. , Journal of bacteriology, 2006 Oct, Volume 188, Issue 19, p.6977-85, (2006) Abstract
Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium: Design of prospective meta-analyses of genome-wide association studies from 5 cohorts., Psaty, Bruce M., O'Donnell Christopher J., Gudnason Vilmundur, Lunetta Kathryn L., Folsom Aaron R., Rotter Jerome I., Uitterlinden André G., Harris Tamara B., Witteman Jacqueline C. M., and Boerwinkle Eric , Circulation. Cardiovascular genetics, 2009 Feb, Volume 2, Issue 1, p.73-80, (2009) Abstract
Comparative and demographic analysis of orang-utan genomes., Locke, Devin P., Hillier Ladeana W., Warren Wesley C., Worley Kim C., Nazareth Lynne V., Muzny Donna M., Yang Shiaw-Pyng, Wang Zhengyuan, Chinwalla Asif T., Minx Pat, et al. , Nature, 2011 Jan 27, Volume 469, Issue 7331, p.529-33, (2011) Abstract
Differentially expressed nucleolar TGF-beta1 target (DENTT) in mouse development., Ozbun, Laurent L., Martínez Alfredo, Angdisen Jerry, Umphress Sarah, Kang Yang, Wang Min, You Ming, and Jakowlew Sonia B. , Developmental dynamics : an official publication of the American Association of Anatomists, 2003 Mar, Volume 226, Issue 3, p.491-511, (2003) Abstract
The DNA sequence and analysis of human chromosome 14., Heilig, Roland, Eckenberg Ralph, Petit Jean-Louis, Fonknechten Núria, Da Silva Corinne, Cattolico Laurence, Levy Michaël, Barbe Valérie, de Berardinis Véronique, Ureta-Vidal Abel, et al. , Nature, 2003 Feb 6, Volume 421, Issue 6923, p.601-7, (2003) Abstract
Evolutionary and biomedical insights from the rhesus macaque genome., Gibbs, Richard A., Rogers Jeffrey, Katze Michael G., Bumgarner Roger, Weinstock George M., Mardis Elaine R., Remington Karin A., Strausberg Robert L., Venter Craig J., Wilson Richard K., et al. , Science (New York, N.Y.), 2007 Apr 13, Volume 316, Issue 5822, p.222-34, (2007) Abstract
Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex Neuropathy., Gonzaga-Jauregui, Claudia, Harel Tamar, Gambin Tomasz, Kousi Maria, Griffin Laurie B., Francescatto Ludmila, Ozes Burcak, Karaca Ender, Jhangiani Shalini N., Bainbridge Matthew N., et al. , Cell reports, 2015 Aug 18, Volume 12, Issue 7, p.1169-83, (2015) Abstract
Exome sequencing reveals homozygous TRIM2 mutation in a patient with early onset CMT and bilateral vocal cord paralysis., Pehlivan, Davut, Akdemir Zeynep Coban, Karaca Ender, Bayram Yavuz, Jhangiani Shalini, Yildiz Edibe Pembegul, Muzny Donna, Uluc Kayihan, Gibbs Richard A., Elcioglu Nursel, et al. , Human genetics, 2015 Apr 17, (2015) Abstract
The finished DNA sequence of human chromosome 12., Scherer, Steven E., Muzny Donna M., Buhay Christian J., Chen Rui, Cree Andrew, Ding Yan, Dugan-Rocha Shannon, Gill Rachel, Gunaratne Preethi, Harris Alan R., et al. , Nature, 2006 Mar 16, Volume 440, Issue 7082, p.346-51, (2006) Abstract
Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences., Strausberg, Robert L., Feingold Elise A., Grouse Lynette H., Derge Jeffery G., Klausner Richard D., Collins Francis S., Wagner Lukas, Shenmen Carolyn M., Schuler Gregory D., Altschul Stephen F., et al. , Proceedings of the National Academy of Sciences of the United States of America, 2002 Dec 24, Volume 99, Issue 26, p.16899-903, (2002) Abstract
Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease., Karaca, Ender, Harel Tamar, Pehlivan Davut, Jhangiani Shalini N., Gambin Tomasz, Akdemir Zeynep Coban, Gonzaga-Jauregui Claudia, Erdin Serkan, Bayram Yavuz, Campbell Ian M., et al. , Neuron, 2015 Nov 4, Volume 88, Issue 3, p.499-513, (2015) Abstract
Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949)., Davies, G., Armstrong N., Bis J. C., Bressler J., Chouraki V., Giddaluru S., Hofer E., Ibrahim-Verbaas C. A., Kirin M., Lahti J., et al. , Molecular psychiatry, 2015 Feb, Volume 20, Issue 2, p.183-92, (2015) Abstract
The genome of the social amoeba Dictyostelium discoideum., Eichinger, L., Pachebat J. A., Glöckner G., Rajandream M. - A., Sucgang R., Berriman M., Song J., Olsen R., Szafranski K., Xu Q., et al. , Nature, 2005 May 5, Volume 435, Issue 7038, p.43-57, (2005) Abstract
The genome sequence of taurine cattle: a window to ruminant biology and evolution., Elsik, Christine G., Tellam Ross L., Worley Kim C., Gibbs Richard A., Muzny Donna M., Weinstock George M., Adelson David L., Eichler Evan E., Elnitski Laura, Guigó Roderic, et al. , Science (New York, N.Y.), 2009 Apr 24, Volume 324, Issue 5926, p.522-8, (2009) Abstract
The genome sequence of taurine cattle: a window to ruminant biology and evolution., Elsik, Christine G., Tellam Ross L., Worley Kim C., Gibbs Richard A., Muzny Donna M., Weinstock George M., Adelson David L., Eichler Evan E., Elnitski Laura, Guigó Roderic, et al. , Science (New York, N.Y.), 2009 Apr 24, Volume 324, Issue 5926, p.522-8, (2009) Abstract
Genome sequence of the Brown Norway rat yields insights into mammalian evolution., Gibbs, Richard A., Weinstock George M., Metzker Michael L., Muzny Donna M., Sodergren Erica J., Scherer Steven, Scott Graham, Steffen David, Worley Kim C., Burch Paula E., et al. , Nature, 2004 Apr 1, Volume 428, Issue 6982, p.493-521, (2004) Abstract
Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium., Fornage, Myriam, Debette Stephanie, Bis Joshua C., Schmidt Helena, Ikram Arfan M., Dufouil Carole, Sigurdsson Sigurdur, Lumley Thomas, DeStefano Anita L., Fazekas Franz, et al. , Annals of neurology, 2011 Jun, Volume 69, Issue 6, p.928-39, (2011) Abstract

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