Skip to Content

Publications

Filters: First Letter Of Last Name is W  [Clear All Filters]
A B C D E F G H I J K L M N O P Q R S T U V [W] X Y Z   [Show ALL]
W
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
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
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
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)
Whole-exome sequencing of polycythemia vera revealed novel driver genes and somatic mutation shared by T cells and granulocytes., Wang, L., Swierczek S. I., Drummond J., Hickman K., Kim Sj, Walker K., Doddapaneni H., Muzny D. M., Gibbs R. A., Wheeler D. A., et al. , Leukemia, 2014 Apr, Volume 28, Issue 4, p.935-8, (2014)
Endometriosis is associated with progesterone resistance in the baboon (Papio anubis) oviduct: evidence based on the localization of oviductal glycoprotein 1 (OVGP1)., Wang, Chaohua, Mavrogianis Patricia A., and Fazleabas Asgerally T. , Biology of reproduction, 2009 Feb, Volume 80, Issue 2, p.272-8, (2009) Abstract
Rapid identification of heterozygous mutations in Drosophila melanogaster using genomic capture sequencing., Wang, Hui, Chattopadhyay Abanti, Li Zhe, Daines Bryce, Li Yumei, Gao Chunxu, Gibbs Richard, Zhang Kun, and Chen Rui , Genome research, 2010 Jul, Volume 20, Issue 7, p.981-8, (2010) Abstract
Intron-size constraint as a mutational mechanism in Rothmund-Thomson syndrome., Wang, Lisa L., Worley Kim, Gannavarapu Anu, Chintagumpala Murali M., Levy Moise L., and Plon Sharon E. , American journal of human genetics, 2002 Jul, Volume 71, Issue 1, p.165-7, (2002) Abstract
Comprehensive molecular diagnosis of 179 Leber congenital amaurosis and juvenile retinitis pigmentosa patients by targeted next generation sequencing., Wang, Xia, Wang Hui, Sun Vincent, Tuan Han-Fang, Keser Vafa, Wang Keqing, Ren Huanan, Lopez Irma, Zaneveld Jacques E., Siddiqui Sorath, et al. , Journal of medical genetics, 2013 Oct, Volume 50, Issue 10, p.674-88, (2013) Abstract
Whole-exome sequencing of human pancreatic cancers and characterization of genomic instability caused by MLH1 haploinsufficiency and complete deficiency., Wang, Linghua, Tsutsumi Shuichi, Kawaguchi Tokuichi, Nagasaki Koichi, Tatsuno Kenji, Yamamoto Shogo, Sang Fei, Sonoda Kohtaro, Sugawara Minoru, Saiura Akio, et al. , Genome research, 2012 Feb, Volume 22, Issue 2, p.208-19, (2012) Abstract
Pas1c1 is a candidate for the mouse pulmonary adenoma susceptibility 1 locus., Wang, Min, Futamura Manabu, Wang Yian, and You Ming , Oncogene, 2005 Mar 10, Volume 24, Issue 11, p.1958-63, (2005) Abstract
Genomic sequencing for cancer diagnosis and therapy., Wang, Linghua, and Wheeler David A. , Annual review of medicine, 2014, Volume 65, p.33-48, (2014) Abstract
A homozygous missense mutation in NEUROD1 is associated with non-syndromic autosomal recessive retinitis pigmentosa., Wang, Feng, Li Huajin, Xu Mingchu, Li Hui, Zhao Li, Yang Lizhu, Zaneveld Jacques E., Wang Keqing, Li Yumei, Sui Ruifang, et al. , Investigative ophthalmology & visual science, 2014 Dec 4, (2014) 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
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)
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
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
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


about seo