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Journal Article
The DNA sequence of the human X chromosome., Ross, Mark T., Grafham Darren V., Coffey Alison J., Scherer Steven, McLay Kirsten, Muzny Donna, Platzer Matthias, Howell Gareth R., Burrows Christine, Bird Christine P., et al. , Nature, 2005 Mar 17, Volume 434, Issue 7031, p.325-37, (2005) Abstract
The DNA sequence, annotation and analysis of human chromosome 3., Muzny, Donna M., Scherer Steven E., Kaul Rajinder, Wang Jing, Yu Jun, Sudbrak Ralf, Buhay Christian J., Chen Rui, Cree Andrew, Ding Yan, et al. , Nature, 2006 Apr 27, Volume 440, Issue 7088, p.1194-8, (2006) Abstract
Draft genome sequences and description of Lactobacillus rhamnosus strains L31, L34, and L35, Boonma, Prapaporn, Spinler Jennifer K., Qin Xiang, Jittaprasatsin Chutima, Muzny Donna M., Doddapaneni Harsha, Gibbs Richard, Petrosino Joe, Tumwasorn Somying, and Versalovic James , Standards in Genomic Sciences, 02/2014, Volume 9, Issue 3, p.744 - 754, (2014)
A Drosophila genetic resource of mutants to study mechanisms underlying human genetic diseases., Yamamoto, Shinya, Jaiswal Manish, Charng Wu-Lin, Gambin Tomasz, Karaca Ender, Mirzaa Ghayda, Wiszniewski Wojciech, Sandoval Hector, Haelterman Nele A., Xiong Bo, et al. , Cell, 2014 Sep 25, Volume 159, Issue 1, p.200-14, (2014) Abstract
DVL1 Frameshift Mutations Clustering in the Penultimate Exon Cause Autosomal-Dominant Robinow Syndrome., White, Janson, Mazzeu Juliana F., Hoischen Alexander, Jhangiani Shalini N., Gambin Tomasz, Alcino Michele Calijorne, Penney Samantha, Saraiva Jorge M., Hove Hanne, Skovby Flemming, et al. , American journal of human genetics, 2015 Mar 25, (2015) Abstract
EGFR-T790M is a rare lung cancer susceptibility allele with enhanced kinase activity., Vikis, Haris, Sato Mitsuo, James Michael, Wang Daolong, Wang Yian, Wang Min, Jia Dongmei, Liu Yan, Bailey-Wilson Joan E., Amos Christopher I., et al. , Cancer research, 2007 May 15, Volume 67, Issue 10, p.4665-70, (2007) Abstract
Electron cryomicroscopy and computer image processing techniques : use in structure-function studies of rotavirus., Venkataram Prasad, B. V., and Estes M. K. , Methods in molecular medicine, 2000, Volume 34, p.9-31, (2000) Abstract
Evidence for replicative mechanism in a CHD7 rearrangement in a patient with CHARGE syndrome., Vatta, Matteo, Niu Zhiyv, Lupski James R., Putnam Philip, Spoonamore Katherine G., Fang Ping, Eng Christine M., and Willis Alecia S. , American journal of medical genetics. Part A, 2013 Dec, Volume 161A, Issue 12, p.3182-6, (2013) Abstract
Evidence that multiple genetic variants of MC4R play a functional role in the regulation of energy expenditure and appetite in Hispanic children., Cole, Shelley A., Butte Nancy F., Voruganti Saroja V., Cai Guowen, Haack Karin, Kent Jack W., Blangero John, Comuzzie Anthony G., McPherson John D., and Gibbs Richard A. , The American journal of clinical nutrition, 2010 Jan, Volume 91, Issue 1, p.191-9, (2010) 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
Evolutionary genetics and implications of small size and twinning in callitrichine primates., Harris, Alan R., Tardif Suzette D., Vinar Tomas, Wildman Derek E., Rutherford Julienne N., Rogers Jeffrey, Worley Kim C., and Aagaard Kjersti M. , Proceedings of the National Academy of Sciences of the United States of America, 2014 Jan 28, Volume 111, Issue 4, p.1467-72, (2014) Abstract
Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling., Chaki, Moumita, Airik Rannar, Ghosh Amiya K., Giles Rachel H., Chen Rui, Slaats Gisela G., Wang Hui, Hurd Toby W., Zhou Weibin, Cluckey Andrew, et al. , Cell, 2012 Aug 3, Volume 150, Issue 3, p.533-48, (2012) Abstract
Exome sequencing of head and neck squamous cell carcinoma reveals inactivating mutations in NOTCH1., Agrawal, Nishant, Frederick Mitchell J., Pickering Curtis R., Bettegowda Chetan, Chang Kyle, Li Ryan J., Fakhry Carole, Xie Tong-Xin, Zhang Jiexin, Wang Jing, et al. , Science (New York, N.Y.), 2011 Aug 26, Volume 333, Issue 6046, p.1154-7, (2011) Abstract
Exome sequencing of ion channel genes reveals complex profiles confounding personal risk assessment in epilepsy., Klassen, Tara, Davis Caleb F., Goldman Alica, Burgess Dan, Chen Tim, Wheeler David, McPherson John, Bourquin Traci, Lewis Lora, Villasana Donna, et al. , Cell, 2011 Jun 24, Volume 145, Issue 7, p.1036-48, (2011) Abstract
Fine mapping and candidate gene analyses of pulmonary adenoma resistance 1, a major genetic determinant of mouse lung adenoma resistance., Wang, Min, Zhang Zhongqiu, Zhang Zhuo, Vikis Haris, Yan Ying, Wang Yian, and You Ming , Cancer research, 2007 Mar 15, Volume 67, Issue 6, p.2508-16, (2007) Abstract
Fine mapping of chromosome 6q23-25 region in familial lung cancer families reveals RGS17 as a likely candidate gene., You, Ming, Wang Daolong, Liu Pengyuan, Vikis Haris, James Michael, Lu Yan, Wang Yian, Wang Min, Chen Qiong, Jia Dongmei, et al. , Clinical cancer research : an official journal of the American Association for Cancer Research, 2009 Apr 15, Volume 15, Issue 8, p.2666-74, (2009) 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
Finishing a whole-genome shotgun: release 3 of the Drosophila melanogaster euchromatic genome sequence., Celniker, Susan E., Wheeler David A., Kronmiller Brent, Carlson Joseph W., Halpern Aaron, Patel Sandeep, Adams Mark, Champe Mark, Dugan Shannon P., Frise Erwin, et al. , Genome biology, 2002, Volume 3, Issue 12, p.RESEARCH0079, (2002) Abstract
The First Myriapod Genome Sequence Reveals Conservative Arthropod Gene Content and Genome Organisation in the Centipede Strigamia maritima., Chipman, Ariel D., Ferrier David E. K., Brena Carlo, Qu Jiaxin, Hughes Daniel S. T., Schröder Reinhard, Torres-Oliva Montserrat, Znassi Nadia, Jiang Huaiyang, Almeida Francisca C., et al. , PLoS biology, 2014 Nov, Volume 12, Issue 11, p.e1002005, (2014) Abstract
FOXO1 is Required for Binding of PR on IRF4, Novel Transcriptional Regulator of Endometrial Stromal Decidualization., Vasquez, Yasmin M., Mazur Erik C., Li Xilong, Kommagani Ramakrishna, Jiang Lichun, Chen Rui, Lanz Rainer B., Kovanci Ertug, Gibbons William E., and DeMayo Francesco J. , Molecular endocrinology (Baltimore, Md.), 2015 Mar, Volume 29, Issue 3, p.421-33, (2015) Abstract
From vulnerable plaque to vulnerable patient: a call for new definitions and risk assessment strategies: Part I., Naghavi, Morteza, Libby Peter, Falk Erling, Casscells Ward S., Litovsky Silvio, Rumberger John, Badimon Juan Jose, Stefanadis Christodoulos, Moreno Pedro, Pasterkamp Gerard, et al. , Circulation, 2003 Oct 7, Volume 108, Issue 14, p.1664-72, (2003) Abstract
From vulnerable plaque to vulnerable patient: a call for new definitions and risk assessment strategies: Part II., Naghavi, Morteza, Libby Peter, Falk Erling, Casscells Ward S., Litovsky Silvio, Rumberger John, Badimon Juan Jose, Stefanadis Christodoulos, Moreno Pedro, Pasterkamp Gerard, et al. , Circulation, 2003 Oct 14, Volume 108, Issue 15, p.1772-8, (2003) Abstract
Functional and evolutionary insights from the genomes of three parasitoid Nasonia species., Werren, John H., Richards Stephen, Desjardins Christopher A., Niehuis Oliver, Gadau Jürgen, Colbourne John K., Werren John H., Richards Stephen, Desjardins Christopher A., Niehuis Oliver, et al. , Science (New York, N.Y.), 2010 Jan 15, Volume 327, Issue 5963, p.343-8, (2010) Abstract
Fxr1 knockout mice show a striated muscle phenotype: implications for Fxr1p function in vivo., Mientjes, Edwin J., Willemsen Rob, Kirkpatrick Laura L., Nieuwenhuizen Ingeborg M., Hoogeveen-Westerveld Marianne, Verweij Marcel, Reis Surya, Bardoni Barbara, Hoogeveen Andre T., Oostra Ben A., et al. , Human molecular genetics, 2004 Jul 1, Volume 13, Issue 13, p.1291-302, (2004) Abstract
Gastrointestinal microbiome signatures of pediatric patients with irritable bowel syndrome., Saulnier, Delphine M., Riehle Kevin, Mistretta Toni-Ann, Diaz Maria-Alejandra, Mandal Debasmita, Raza Sabeen, Weidler Erica M., Qin Xiang, Coarfa Cristian, Milosavljevic Aleksandar, et al. , Gastroenterology, 2011 Nov, Volume 141, Issue 5, p.1782-91, (2011) Abstract


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