Resultats de la cerca - Andrew Crenshaw
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1
Diversity in the Glucose Transporter-4 Gene (SLC2A4) in Humans Reflects the Action of Natural Selection along the Old-World Primates Evolution per Eduardo Tarazona‐Santos, Cristina Fabbri, Meredith Yeager, Wagner C. S. Magalhães, Laurie Burdett, Andrew Crenshaw, Davide Pettener, Stephen J. Chanock
Publicat 2010Artigo -
2
High-throughput single nucleotide polymorphism genotyping using nanofluidic Dynamic Arrays per Jun Wang, Min Lin, Andrew Crenshaw, Amy Hutchinson, Belynda Hicks, Meredith Yeager, Sonja I. Berndt, Wen‐Yi Huang, Richard B. Hayes, Stephen J. Chanock, Robert C. Jones, Ramesh Ramakrishnan
Publicat 2009Artigo -
3
Evolutionary Dynamics of the Human NADPH Oxidase Genes CYBB, CYBA, NCF2, and NCF4: Functional Implications per Eduardo Tarazona‐Santos, Moara Machado, Wagner C. S. Magalhães, Renee Chen, Fernanda Lyon, Laurie Burdett, Andrew Crenshaw, Cristina Fabbri, L.H. Pereira, Laélia Maria Pinto, Rodrigo A. F. Redondo, Ben Sestanovich, Meredith Yeager, Stephen J. Chanock
Publicat 2013Artigo -
4
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma in Caucasians from the USA per Janey L. Wiggs, Jae H. Kang, Brian L. Yaspan, Daniel B. Mirel, Cathy C. Laurie, Andrew Crenshaw, Wendy Brodeur, Stephanie M. Gogarten, Lana M. Olson, Wael Abdrabou, E. DelBono, Stephanie Loomis, Jonathan L. Haines, Louis R. Pasquale
Publicat 2011Artigo -
5
Prognostic Gene Expression Signature for Patients With Hepatitis C–Related Early-Stage Cirrhosis per Yujin Hoshida, Augusto Villanueva, Angelo Sangiovanni, Manel Solé, Chin Hur, Karin L. Andersson, Raymond T. Chung, Joshua Gould, Kensuke Kojima, Supriya Gupta, Bradley Taylor, Andrew Crenshaw, Stacey Gabriel, Beatriz Mínguez, Massimo Iavarone, Scott L. Friedman, Massimo Colombo, Josep M. Llovet, Todd R. Golub
Publicat 2013Artigo -
6
zCall: a rare variant caller for array-based genotyping per Jacqueline I. Goldstein, Andrew Crenshaw, Jason Carey, George Grant, Jared Maguire, Menachem Fromer, Colm O’Dushlaine, Jennifer L. Moran, Kimberly Chambert, Christine Stevens, Pamela Sklar, Christina M. Hultman, Shaun Purcell, Steven A. McCarroll, Patrick F. Sullivan, Mark J. Daly, Benjamin M. Neale
Publicat 2012Artigo -
7
Comprehensive resequence analysis of a 136 kb region of human chromosome 8q24 associated with prostate and colon cancers per Meredith Yeager, Nianqing Xiao, Richard B. Hayes, Pascal Bouffard, Brian Desany, Laura Burdett, Nick Orr, Casey Matthews, Liqun Qi, Andrew Crenshaw, Zdenek Markovic, Karin M. Fredrikson, Kevin B. Jacobs, Laufey T. Ámundadóttir, Thomas Jarvie, David J. Hunter, Robert N. Hoover, Gilles Thomas, Timothy T. Harkins, Stephen J. Chanock
Publicat 2008Artigo -
8
Limited Clinical Utility of a Genetic Risk Score for the Prediction of Fracture Risk in Elderly Subjects per Joel Eriksson, Daniel S. Evans, Carrie M. Nielson, Jian Shen, Priya Srikanth, Marc C. Hochberg, Shannon K. McWeeney, Peggy M. Cawthon, Beth Wilmot, Joseph M. Zmuda, Greg Tranah, Daniel B. Mirel, Sashi Challa, Michael A. Mooney, Andrew Crenshaw, Magnus K. Karlsson, Dan Mellström, Liesbeth Vandenput, Eric Orwoll, Claes Ohlsson
Publicat 2014Artigo -
9
Epidermal growth factor receptor inhibition attenuates liver fibrosis and development of hepatocellular carcinoma per Bryan C. Fuchs, Yujin Hoshida, Tsutomu Fujii, Lan Wei, Suguru Yamada, Gregory Y. Lauwers, Christopher M. McGinn, Danielle K. DePeralta, Xintong Chen, Toshihiko Kuroda, Michael Lanuti, Anthony D. Schmitt, Supriya Gupta, Andrew Crenshaw, Robert C. Onofrio, Bradley Taylor, Wendy Winckler, Nabeel Bardeesy, Peter Caravan, Todd R. Golub, Kenneth K. Tanabe
Publicat 2013Artigo -
10
High-throughput identification of genotype-specific cancer vulnerabilities in mixtures of barcoded tumor cell lines per Channing Yu, Aristotle M. Mannan, Griselda M. Yvone, Kenneth N. Ross, Yan-Ling Zhang, Melissa A. Marton, Bradley R Taylor, Andrew Crenshaw, Joshua Gould, Pablo Tamayo, Barbara A. Weir, Aviad Tsherniak, Bang Wong, Levi A. Garraway, Alykhan F. Shamji, Michelle Palmer, Michael A. Foley, Wendy Winckler, Stuart L. Schreiber, Andrew L. Kung, Todd R. Golub
Publicat 2016Artigo -
11
Variants in interferon-alpha pathway genes and response to pegylated interferon-Alpha2a plus ribavirin for treatment of chronic hepatitis C virus infection in the hepatitis C antiv... per Tania M. Welzel, Timothy R. Morgan, Herbert L. Bonkovsky, Deepa Naishadham, Ruth M. Pfeiffer, Elizabeth C. Wright, Amy Hutchinson, Andrew Crenshaw, Arman Bashirova, Mary Carrington, Myhanh Dotrang, Richard K. Sterling, Karen L. Lindsay, Robert J. Fontana, William M. Lee, Adrian M. Di Bisceglie, Marc G. Ghany, David R. Gretch, Stephen J. Chanock, Raymond T. Chung, Thomas R. OʼBrien
Publicat 2009Artigo -
12
Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association per Karl C. Desch, Ayse Bilge Ozel, David Siemieniak, Yossi Kalish, Jordan A. Shavit, Courtney D. Thornburg, Anjali Sharathkumar, Caitlin McHugh, Cathy C. Laurie, Andrew Crenshaw, Daniel B. Mirel, Yoonhee Kim, Cheryl D. Cropp, Anne M. Molloy, Peadar N. Kirke, Joan E. Bailey‐Wilson, Alexander F. Wilson, James L. Mills, John M. Scott, Lawrence C. Brody, Jun Z. Li, David Ginsburg
Publicat 2012Revisão -
13
Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network per David R. Crosslin, Andrew McDavid, Noah Weston, Sarah C. Nelson, Xiuwen Zheng, Eugene Hart, Mariza de Andrade, Iftikhar J. Kullo, Catherine A. McCarty, Kimberly F. Doheny, Elizabeth Pugh, Abel Kho, M. Geoffrey Hayes, S. Pretel, Alexander Saip, Marylyn D. Ritchie, Dana C. Crawford, Paul K. Crane, Katherine M. Newton, Rongling Li, Daniel B. Mirel, Andrew Crenshaw, Eric B. Larson, Chris Carlson, Gail P. Jarvik
Publicat 2011Artigo -
14
Quality Control Procedures for Genome‐Wide Association Studies per Stephen Turner, Loren L. Armstrong, Yuki Bradford, Christopher S. Carlson, Dana C. Crawford, Andrew Crenshaw, Mariza de Andrade, Kimberly F. Doheny, Jonathan L. Haines, Geoffrey Hayes, Gail P. Jarvik, Lan Jiang, Iftikhar J. Kullo, Rongling Li, Hua Ling, Teri A. Manolio, Martha Matsumoto, Catherine A. McCarty, Andrew McDavid, Daniel B. Mirel, Justin Paschall, Elizabeth Pugh, Luke V. Rasmussen, Russell A. Wilke, Rebecca L. Zuvich, Marylyn D. Ritchie
Publicat 2011Artigo -
15
Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality per Rebecca L. Zuvich, Loren L. Armstrong, Suzette J. Bielinski, Yuki Bradford, Christopher S. Carlson, Dana C. Crawford, Andrew Crenshaw, Mariza de Andrade, Kimberly F. Doheny, Jonathan L. Haines, M. Geoffrey Hayes, Gail P. Jarvik, Lan Jiang, Iftikhar J. Kullo, Rongling Li, Hua Ling, Teri A. Manolio, Martha Matsumoto, Catherine A. McCarty, Andrew McDavid, Daniel B. Mirel, Lana M. Olson, Justin Paschall, Elizabeth Pugh, Luke V. Rasmussen, Laura J. Rasmussen‐Torvik, Stephen Turner, Russell A. Wilke, Marylyn D. Ritchie
Publicat 2011Artigo -
16
Evaluating Genetic Risk for Prostate Cancer among Japanese and Latinos per Iona Cheng, Gary K. Chen, Hidewaki Nakagawa, Jing He, Peggy Wan, Cathy C. Laurie, Jess Shen, Xin Sheng, Loreall Pooler, Andrew Crenshaw, Daniel B. Mirel, Atsushi Takahashi, Michiaki Kubo, Yusuke Nakamura, Ali Amin Al Olama, Sara Benlloch, Jenny Donovan, Michelle Guy, Freddie C. Hamdy, Zsofia Kote‐Jarai, David E. Neal, Lynne R. Wilkens, Kristine R. Monroe, Daniel O. Stram, Kenneth Muir, Rosalind A. Eeles, Douglas F. Easton, Laurence N. Kolonel, Brian E. Henderson, Loı̈c Le Marchand, Christopher A. Haiman
Publicat 2012Artigo -
17
Enhancing the Power of Genetic Association Studies through the Use of Silver Standard Cases Derived from Electronic Medical Records per Andrew McDavid, Paul K. Crane, Katherine M. Newton, David R. Crosslin, Wayne C. McCormick, Noah Weston, Kelly Ehrlich, Eugene Hart, Robert G. Harrison, Walter A. Kukull, Carla Rottscheit, Peggy Peissig, Elisha Stefanski, Catherine A. McCarty, Rebecca L. Zuvich, Marylyn D. Ritchie, Jonathan L. Haines, Joshua C. Denny, Gerard D. Schellenberg, Mariza de Andrade, Iftikhar J. Kullo, Rongling Li, Daniel B. Mirel, Andrew Crenshaw, James D. Bowen, Ge Li, Debby W. Tsuang, Susan M. McCurry, Linda Teri, Eric B. Larson, Gail P. Jarvik, Chris Carlson
Publicat 2013Artigo -
18
Candidate Gene Association Resource (CARe) per Yan V. Sun, Guillaume Lettre, Taylor Young, Deborah Farlow, James P. Pirruccello, Kenechi G. Ejebe, Brendan J. Keating, Qiong Yang, Ming‐Huei Chen, Nina Lapchyk, Andrew Crenshaw, Liuda Ziaugra, Anthony Rachupka, Emelia J. Benjamin, L. Adrienne Cupples, Myriam Fornage, Ervin R. Fox, Susan R. Heckbert, Joel N. Hirschhorn, Christopher Newton‐Cheh, Marcia M. Nizzari, Dina N. Paltoo, George Papanicolaou, Sanjay R. Patel, Bruce M. Psaty, Daniel J. Rader, Susan Redline, Stephen S. Rich, Jerome I. Rotter, Herman A. Taylor, Russell P. Tracy, Ramachandran S. Vasan, James G. Wilson, Sekar Kathiresan, Richard R. Fabsitz, Eric Boerwinkle, Stacey Gabriel
Publicat 2010Artigo -
19
Multiple loci identified in a genome-wide association study of prostate cancer per Gilles Thomas, Kevin B. Jacobs, Meredith Yeager, Peter Kraft, Sholom Wacholder, Nick Orr, Kai Yu, Nilanjan Chatterjee, Robert Welch, Amy Hutchinson, Andrew Crenshaw, Géraldine Cancel‐Tassin, Brian Staats, Zhaoming Wang, Jesús González Bosquet, Jun Fang, Xiang Deng, Sonja I. Berndt, Eugenia E. Calle, Heather Spencer Feigelson, Michael J. Thun, Carmen Rodríguez, Demetrius Albanes, Jarmo Virtamo, Stephanie J. Weinstein, Fredrick R. Schumacher, Edward L. Giovannucci, Walter C. Willett, Olivier Cussenot, Antoine Valéri, Gerald L. Andriole, E. David Crawford, Margaret A. Tucker, Daniela S. Gerhard, Joseph F. Fraumeni, Robert N. Hoover, Richard B. Hayes, David J. Hunter, Stephen J. Chanock
Publicat 2008Artigo -
20
Common Variants at 9p21 and 8q22 Are Associated with Increased Susceptibility to Optic Nerve Degeneration in Glaucoma per Janey L. Wiggs, Brian L. Yaspan, Michael A. Hauser, Jae H. Kang, R. Rand Allingham, Lana M. Olson, Wael Abdrabou, Bao Jian Fan, Dan Y. Wang, Wendy Brodeur, Donald L. Budenz, Joseph Caprioli, Andrew Crenshaw, Kristy Crooks, E. DelBono, Kimberly F. Doheny, David S. Friedman, Douglas Gaasterland, Terry Gaasterland, Cathy C. Laurie, Richard K. Lee, Paul R. Lichter, Stephanie Loomis, Yutao Liu, Felipe A. Medeiros, Cathy McCarty, Daniel B. Mirel, Sayoko E. Moroi, David C. Musch, Anthony Realini, Frank W. Rozsa, Joel S. Schuman, Kathleen M. Scott, Kuldev Singh, Joshua D. Stein, Edward H. Trager, Paul VanVeldhuisen, Douglas Vollrath, Gadi Wollstein, Sachiko Yoneyama, Kang Zhang, Robert N. Weinreb, Jason Ernst, Manolis Kellis, Tomohiro Masuda, Donald J. Zack, Julia E. Richards, Margaret A. Pericak‐Vance, Louis R. Pasquale, Jonathan L. Haines
Publicat 2012Revisão
Eines de cerca:
Matèries relacionades
Biology
Genetics
Gene
Genotype
Medicine
Single-nucleotide polymorphism
Genome-wide association study
Genetic association
Internal medicine
Population
Environmental health
Cancer
Computational biology
Allele
Computer science
Haplotype
Immunology
Endocrinology
Data mining
Diabetes mellitus
Genome
Locus (genetics)
Oncology
Type 2 diabetes
Cancer research
Evolutionary biology
Gene expression
Genotyping
Paleontology
Prostate cancer