Skip to Content


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 
Whole exome sequencing confirms the clinical diagnosis of Marfan syndrome combined with X-linked hypophosphatemia., Sheng, Xunlun, Chen Xue, Lei Bo, Chen Rui, Wang Hui, Zhang Fangxia, Rong Weining, Ha Ruoshui, Liu Yani, Zhao Feng, et al. , Journal of translational medicine, 2015, Volume 13, p.179, (2015) Abstract
Whole Exome Sequencing and Analysis Of Mutations In Sézary Syndrome, Xi, Lui, Ni Xiao, Koshelev Misha, Drummond Jennifer, Muzny Donna M., Zhang Xiang, and Duvic Madeleine , Blood, Volume 122, Number 21, p.2558–2558, (2013)
Whole exome capture in solution with 3 Gbp of data., Bainbridge, Matthew N., Wang Min, Burgess Daniel L., Kovar Christie, Rodesch Matthew J., D'Ascenzo Mark, Kitzman Jacob, Wu Yuan-Qing, Newsham Irene, Richmond Todd A., et al. , Genome biology, 2010, Volume 11, Issue 6, p.R62, (2010) Abstract
When is ancient polymorphism a potential problem for molecular phylogenetics?, Rogers, J., and Comuzzie A. G. , American journal of physical anthropology, 1995 Oct, Volume 98, Issue 2, p.216-8; discussion 224-8, (1995)
What everybody should know about the rat genome and its online resources., Twigger, Simon N., Pruitt Kim D., Fernández-Suárez Xosé M., Karolchik Donna, Worley Kim C., Maglott Donna R., Brown Garth, Weinstock George, Gibbs Richard A., Kent Jim, et al. , Nature genetics, 2008 May, Volume 40, Issue 5, p.523-7, (2008) Abstract
A weighted false discovery rate control procedure reveals alleles at FOXA2 that influence fasting glucose levels., Xing, Chao, Cohen Jonathan C., and Boerwinkle Eric , American journal of human genetics, 2010 Mar 12, Volume 86, Issue 3, p.440-6, (2010) Abstract
The weed paves the way., Gibbs, R. A. , Nature genetics, 1999 Jul, Volume 22, Issue 3, p.219-20, (1999)
WebWise: guide to the Baylor College of Medicine Human Genome Sequencing Center's web site., Pruitt, K. D. , Genome research, 1998 Mar, Volume 8, Issue 3, p.170-4, (1998)
WDR62 missense mutation in a consanguineous family with primary microcephaly., Bacino, Carlos A., Arriola Luis A., Wiszniewska Joanna, and Bonnen Penelope E. , American journal of medical genetics. Part A, 2012 Mar, Volume 158A, Issue 3, p.622-5, (2012) Abstract
WDR35 mutation in siblings with Sensenbrenner syndrome: a ciliopathy with variable phenotype., Bacino, Carlos A., Dhar Shweta U., Brunetti-Pierri Nicola, Lee Brendan, and Bonnen Penelope E. , American journal of medical genetics. Part A, 2012 Nov, Volume 158A, Issue 11, p.2917-24, (2012) Abstract
VitisExpDB: a database resource for grape functional genomics., Doddapaneni, Harshavardhan, Lin Hong, Walker Andrew M., Yao Jiqiang, and Civerolo Edwin L. , BMC plant biology, 2008, Volume 8, p.23, (2008) Abstract
Virulence effect of Enterococcus faecalis protease genes and the quorum-sensing locus fsr in Caenorhabditis elegans and mice., Sifri, Costi D., Mylonakis Eleftherios, Singh Kavindra V., Qin Xiang, Garsin Danielle A., Murray Barbara E., Ausubel Frederick M., and Calderwood Stephen B. , Infection and immunity, 2002 Oct, Volume 70, Issue 10, p.5647-50, (2002) Abstract
Variation in GRM3 affects cognition, prefrontal glutamate, and risk for schizophrenia., Egan, Michael F., Straub Richard E., Goldberg Terry E., Yakub Imtiaz, Callicott Joseph H., Hariri Ahmad R., Mattay Venkata S., Bertolino Alessandro, Hyde Thomas M., Shannon-Weickert Cynthia, et al. , Proceedings of the National Academy of Sciences of the United States of America, 2004 Aug 24, Volume 101, Issue 34, p.12604-9, (2004) Abstract
Variants for HDL-C, LDL-C, and triglycerides identified from admixture mapping and fine-mapping analysis in African American families., Shetty, Priya B., Tang Hua, Feng Tao, Tayo Bamidele, Morrison Alanna C., Kardia Sharon L. R., Hanis Craig L., Arnett Donna K., Hunt Steven C., Boerwinkle Eric, et al. , Circulation. Cardiovascular genetics, 2015 Feb, Volume 8, Issue 1, p.106-13, (2015) Abstract
Variability of dopamine D4 receptor (DRD4) gene sequence within and among nonhuman primate species., Livak, K. J., Rogers J., and Lichter J. B. , Proceedings of the National Academy of Sciences of the United States of America, 1995 Jan 17, Volume 92, Issue 2, p.427-31, (1995) Abstract
Using whole-genome sequence data to predict quantitative trait phenotypes in Drosophila melanogaster., Ober, Ulrike, Ayroles Julien F., Stone Eric A., Richards Stephen, Zhu Dianhui, Gibbs Richard A., Stricker Christian, Gianola Daniel, Schlather Martin, Mackay Trudy F. C., et al. , PLoS genetics, 2012, Volume 8, Issue 5, p.e1002685, (2012) Abstract
Using BODIPY dye-primer chemistry in large-scale sequencing., Muzny, D. M., Metzker M. L., Bouck J., Gorrell J. H., Ding Y., Maxim E., and Gibbs R. A. , IEEE engineering in medicine and biology magazine : the quarterly magazine of the Engineering in Medicine & Biology Society, 1998 Nov-Dec, Volume 17, Issue 6, p.88-93, (1998)
Using a pericentromeric interspersed repeat to recapitulate the phylogeny and expansion of human centromeric segmental duplications., Horvath, J. E., Gulden C. L., Bailey J. A., Yohn C., McPherson J. D., Prescott A., Roe B. A., de Jong P. J., Ventura M., Misceo D., et al. , Molecular biology and evolution, 2003 Sep, Volume 20, Issue 9, p.1463-79, (2003) Abstract
Use of wrapper algorithms coupled with a random forests classifier for variable selection in large-scale genomic association studies., Rodin, Andrei S., Litvinenko Anatoliy, Klos Kathy, Morrison Alanna C., Woodage Trevor, Coresh Josef, and Boerwinkle Eric , Journal of computational biology : a journal of computational molecular cell biology, 2009 Dec, Volume 16, Issue 12, p.1705-18, (2009) Abstract
The use of primers from highly conserved pol regions to identify uncharacterized retroviruses by the polymerase chain reaction., Donehower, L. A., Bohannon R. C., Ford R. J., and Gibbs R. A. , Journal of virological methods, 1990 Apr, Volume 28, Issue 1, p.33-46, (1990) Abstract
Use of fusions to green fluorescent protein in the detection of apoptosis., Shinbrot, Eve, Spencer Collin, Natale Valerie, and Kain Steven R. , Methods in enzymology, Volume 327, p.513, (2000)
Untangling the influences of unmodeled evolutionary processes on phylogenetic signal in a forensically important HIV-1 transmission cluster., Doyle, Vinson P., Andersen John J., Nelson Bradley J., Metzker Michael L., and Brown Jeremy M. , Molecular phylogenetics and evolution, 2014 Feb 28, Volume 75C, p.126-137, (2014) Abstract
Unlocking the bovine genome., Tellam, Ross L., Lemay Danielle G., Van Tassell Curtis P., Lewin Harris A., Worley Kim C., and Elsik Christine G. , BMC genomics, 2009, Volume 10, p.193, (2009) Abstract
Union makes strength: a worldwide collaborative genetic and clinical study to provide a comprehensive survey of RD3 mutations and delineate the associated phenotype., Perrault, Isabelle, Estrada-Cuzcano Alejandro, Lopez Irma, Kohl Susanne, Li Shiqiang, Testa Francesco, Zekveld-Vroon Renate, Wang Xia, Pomares Esther, Andorf Jean, et al. , PloS one, 2013, Volume 8, Issue 1, p.e51622, (2013) Abstract
Understanding the development of human bladder cancer by using a whole-organ genomic mapping strategy., Majewski, Tadeusz, Lee Sangkyou, Jeong Joon, Yoon Dong-Sup, Kram Andrzej, Kim Mi-Sook, Tuziak Tomasz, Bondaruk Jolanta, Lee Sooyong, Park Weon-Seo, et al. , Laboratory investigation; a journal of technical methods and pathology, 2008 Jul, Volume 88, Issue 7, p.694-721, (2008) Abstract

about seo