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From human genome to cancer genome: the first decade., Wheeler, David A., and Wang Linghua , Genome research, 2013 Jul, Volume 23, Issue 7, p.1054-62, (2013) Abstract
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility., Wessel, Jennifer, Chu Audrey Y., Willems Sara M., Wang Shuai, Yaghootkar Hanieh, Brody Jennifer A., Dauriz Marco, Hivert Marie-France, Raghavan Sridharan, Lipovich Leonard, et al. , Nature communications, 2015, Volume 6, p.5897, (2015) 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
A genetic association study of activated partial thromboplastin time in European Americans and African Americans: the ARIC Study., Weng, Lu-Chen, Cushman Mary, Pankow James S., Basu Saonli, Boerwinkle Eric, Folsom Aaron R., and Tang Weihong , Human molecular genetics, 2015 Apr 15, Volume 24, Issue 8, p.2401-8, (2015) Abstract
Characterizing the cancer genome in lung adenocarcinoma., Weir, Barbara A., Woo Michele S., Getz Gad, Perner Sven, Ding Li, Beroukhim Rameen, Lin William M., Province Michael A., Kraja Aldi, Johnson Laura A., et al. , Nature, 2007 Dec 6, Volume 450, Issue 7171, p.893-8, (2007) Abstract
ENCODE: more genomic empowerment., Weinstock, George M. , Genome research, 2007 Jun, Volume 17, Issue 6, p.667-8, (2007)
The Cancer Genome Atlas Pan-Cancer analysis project., Weinstein, John N., Collisson Eric A., Mills Gordon B., Shaw Kenna Mills R., Ozenberger Brad A., Ellrott Kyle, Shmulevich Ilya, Sander Chris, and Stuart Joshua M. , Nature genetics, 2013 Oct, Volume 45, Issue 10, p.1113-20, (2013) Abstract
Efficient isolation of targeted Caenorhabditis elegans deletion strains using highly thermostable restriction endonucleases and PCR., Wei, Aguan, Yuan Alex, Fawcett Gloria, Butler Alice, Davis Theodore, Xu Shuang-yong, and Salkoff Lawrence , Nucleic acids research, 2002 Oct 15, Volume 30, Issue 20, p.e110, (2002) Abstract
Sequence variation in the soluble epoxide hydrolase gene and subclinical coronary atherosclerosis: interaction with cigarette smoking., Wei, Qi, Doris Peter A., Pollizotto Martin V., Boerwinkle Eric, Jacobs David R., Siscovick David S., and Fornage Myriam , Atherosclerosis, 2007 Jan, Volume 190, Issue 1, p.26-34, (2007) Abstract
COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritis., Watkin, Levi B., Jessen Birthe, Wiszniewski Wojciech, Vece Timothy J., Jan Max, Sha Youbao, Thamsen Maike, Santos-Cortez Regie L. P., Lee Kwanghyuk, Gambin Tomasz, et al. , Nature genetics, 2015 Apr 20, (2015) Abstract
The human genome: genes, pseudogenes, and variation on chromosome 7., Waterston, R. H., Hillier L. W., Fulton L. A., Fulton R. S., Graves T. A., Pepin K. H., Bork P., Suyama M., Torrents D., Chinwalla A. T., et al. , Cold Spring Harbor symposia on quantitative biology, 2003, Volume 68, p.13-22, (2003)
Heterozygous De Novo and Inherited Mutations in the Smooth Muscle Actin (ACTG2) Gene Underlie Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome., Wangler, Michael F., Gonzaga-Jauregui Claudia, Gambin Tomasz, Penney Samantha, Moss Timothy, Chopra Atul, Probst Frank J., Xia Fan, Yang Yaping, Werlin Steven, et al. , PLoS genetics, 2014 Mar, Volume 10, Issue 3, p.e1004258, (2014) Abstract
Heterozygous De Novo and Inherited Mutations in the Smooth Muscle Actin (ACTG2) Gene Underlie Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome, Wangler, Michael F., Gonzaga-Jauregui Claudia, Gambin Tomasz, Penney Samantha, Moss Timothy, Chopra Atul, Probst Frank J., Xia Fan, Yang Yaping, Werlin Steven, et al. , PLoS Genetics, 3/2014, Volume 10, Issue 3, p.e1004258, (2014)
Acquired uniparental disomy of chromosome 9p in hematological malignancies., Wang, Linghua, Wheeler David A., and Prchal Josef T. , Experimental hematology, 2015 Nov 29, (2015) Abstract
FlyVar: a database for genetic variation in Drosophila melanogaster., Wang, Fei, Jiang Lichun, Chen Yong, Haelterman Nele A., Bellen Hugo J., and Chen Rui , Database : the journal of biological databases and curation, 2015, Volume 2015, (2015) Abstract
Identification of differentially expressed miRNAs in chicken lung and trachea with avian influenza virus infection by a deep sequencing approach., Wang, Ying, Brahmakshatriya Vinayak, Zhu Huifeng, Lupiani Blanca, Reddy Sanjay M., Yoon Byung-Jun, Gunaratne Preethi H., Kim Jonghwan, Chen Rui, Wang Junjun, et al. , BMC genomics, 2009, Volume 10, p.512, (2009) Abstract
The relationship of JAK2(V617F) and acquired UPD at chromosome 9p in polycythemia vera., Wang, L., Swierczek S. I., Lanikova L., Kim Sj, Hickman K., Walker K., Wang K., Drummond J., Doddapaneni H., Reid J. G., et al. , Leukemia, 2014 Apr, Volume 28, Issue 4, p.938-41, (2014)
Pol iota is a candidate for the mouse pulmonary adenoma resistance 2 locus, a major modifier of chemically induced lung neoplasia., Wang, Min, Devereux Theodora R., Vikis Haris G., McCulloch Scott D., Holliday Wanda, Anna Colleen, Wang Yian, Bebenek Katarzyna, Kunkel Thomas A., Guan Kunliang, et al. , Cancer research, 2004 Mar 15, Volume 64, Issue 6, p.1924-31, (2004) Abstract
New technique for lacrimal system intubation., Wang, Linghua, Chen Dong, and Wang Zhichong , American journal of ophthalmology, 2006 Aug, Volume 142, Issue 2, p.252-8, (2006) Abstract
Analysis of the Par2 modifier of pulmonary adenoma formation in mice., Wang, Min, Wang Yian, You Ming, and Devereux Theodora R. , Experimental lung research, 2005 Mar, Volume 31, Issue 2, p.193-204, (2005) Abstract
Exome capture sequencing identifies a novel mutation in BBS4., Wang, Hui, Chen Xianfeng, Dudinsky Lynn, Patenia Claire, Chen Yiyun, Li Yumei, Wei Yue, Abboud Emad B., Al-Rajhi Ali A., Lewis Richard Alan, et al. , Molecular vision, 2011, Volume 17, p.3529-40, (2011) Abstract
Novel somatic and germline mutations in intracranial germ cell tumours., Wang, Linghua, Yamaguchi Shigeru, Burstein Matthew D., Terashima Keita, Chang Kyle, Ng Ho-Keung, Nakamura Hideo, He Zongxiao, Doddapaneni Harshavardhan, Lewis Lora, et al. , Nature, 2014 Jun 4, (2014) Abstract
Comprehensive Molecular Diagnosis of a Large Chinese Leber Congenital Amaurosis Cohort., Wang, Hui, Wang Xia, Zou Xuan, Xu Shan, Li Hui, Soens Zachry Tore, Wang Keqing, Li Yumei, Dong Fangtian, Chen Rui, et al. , Investigative ophthalmology & visual science, 2015 Jun, Volume 56, Issue 6, p.3642-55, (2015) Abstract
Genomic sequencing of key genes in mouse pancreatic cancer cells., Wang, Y., Zhang Y., Yang J., Ni X., Liu S., Li Z., Hodges S. E., Fisher W. E., Brunicardi F. C., Gibbs R. A., et al. , Current molecular medicine, 2012 Mar, Volume 12, Issue 3, p.331-41, (2012) Abstract
An integrative variant analysis pipeline for accurate genotype/haplotype inference in population NGS data., Wang, Yi, Lu James, Yu Jin, Gibbs Richard A., and Yu Fuli , Genome research, 2013 May, Volume 23, Issue 5, p.833-42, (2013) Abstract

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