Risultati della ricerca - Wendy Brodeur

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  1. 1
    Characterization and remediation of sample index swaps by non-redundant dual indexing on massively parallel sequencing platforms

    Characterization and remediation of sample index swaps by non-redundant dual indexing on massively parallel sequencing platforms di Maura Costello, Mark Fleharty, Justin Abreu, Yossi Farjoun, Steven Ferriera, Laurie Holmes, Brian Granger, Lisa Green, Tom Howd, Tamara Mason, Gina Vicente, Michael Dasilva, Wendy Brodeur, Timothy DeSmet, Sheila Dodge, Niall J. Lennon, Stacey Gabriel

    Pubblicazione 2018
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  2. 2
    Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma in Caucasians from the USA

    Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma in Caucasians from the USA di 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

    Pubblicazione 2011
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  3. 3
    Alzheimer's disease: early alterations in brain DNA methylation at ANK1, BIN1, RHBDF2 and other loci

    Alzheimer's disease: early alterations in brain DNA methylation at ANK1, BIN1, RHBDF2 and other loci di Philip L. De Jager, Gyan Srivastava, Katie Lunnon, Jeremy D. Burgess, Leonard C. Schalkwyk, Lei Yu, Matthew L. Eaton, Brendan T Keenan, Jason Ernst, Cristin McCabe, Anna Tang, Towfique Raj, Joseph M. Replogle, Wendy Brodeur, Stacey Gabriel, High Seng Chai, Curtis Younkin, Steven G. Younkin, Fanggeng Zou, Moshe Szyf, Charles B. Epstein, Julie A. Schneider, B Bernstein, Alex Meissner, Nilüfer Ertekin‐Taner, Lori B. Chibnik, Manolis Kellis, Jonathan Mill, David A. Bennett

    Pubblicazione 2014
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  4. 4
    Common Variants at 9p21 and 8q22 Are Associated with Increased Susceptibility to Optic Nerve Degeneration in Glaucoma

    Common Variants at 9p21 and 8q22 Are Associated with Increased Susceptibility to Optic Nerve Degeneration in Glaucoma di 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

    Pubblicazione 2012
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  5. 5
    Integrating common and rare genetic variation in diverse human populations

    Integrating common and rare genetic variation in diverse human populations di David Altshuler, Richard A Gibbs, Leena Peltonen, David Altshuler, Richard A Gibbs, Leena Peltonen, Emmanouil T. Dermitzakis, S. F. Schaffner, Fuli Yu, Leena Peltonen, Emmanouil T. Dermitzakis, Penelope E. Bonnen, David Altshuler, Richard A Gibbs, Paul I. W. de Bakker, Panos Deloukas, Stacey B. Gabriel, Rhian Gwilliam, Sarah Hunt, Michael Inouye, Xiaoming Jia, Aarno Palotie, Melissa Parkin, Pamela Whittaker, Fuli Yu, Kyle Chang, Alicia Hawes, Lora Lewis, Yanru Ren, David A. Wheeler, Richard A. Gibbs, Donna M. Muzny, C. Barnes, Katayoon Darvishi, Matthew E. Hurles, Joshua M. Korn, Kati Kristiansson, Charles Lee, Steven A. McCarrol, James Nemesh, Emmanouil T. Dermitzakis, Alon Keinan, Stephen B. Montgomery, Samuela Pollack, Alkes L. Price, Nicole Soranzo, Penelope E. Bonnen, Richard A Gibbs, Claudia Gonzaga‐Jauregui, Alon Keinan, Alkes L. Price, Fuli Yu, Verneri Anttila, Wendy Brodeur, Mark J. Daly, Stephen Leslie, Gil McVean, Loukas Moutsianas, Huy Nguyen, S. F. Schaffner, Qingrun Zhang, Mohammed J. R. Ghori, Ralph McGinnis, William McLaren, Samuela Pollack, Alkes L. Price, S. F. Schaffner, Fumihiko Takeuchi, Sharon R. Grossman, Ilya Shlyakhter, Elizabeth Hostetter, Pardis C. Sabeti, Clement Adebamowo, Morris W. Foster, Deborah R Gordon, Júlio Licinio, María Cristina Manca, Patricia A. Marshall, Ichiro Matsuda, Duncan Ngare, Vivian Ota Wang, Deepa Reddy, Charles N. Rotimi, Charmaine Royal, Richard R. Sharp, Changqing Zeng, Lisa Brooks, Jean E. McEwen

    Pubblicazione 2010
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  6. 6
    Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network

    Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network di Hana Zouk, Eric Venner, Niall J. Lennon, Donna M. Muzny, Debra Abrams, Samuel E. Adunyah, Ladia Albertson‐Junkans, Darren C. Ames, Paul S. Appelbaum, Samuel Aronson, Sharon Aufox, Lawrence Babb, Adithya Balasubramanian, Hana Bangash, Melissa Basford, Lisa Bastarache, Samantha Baxter, Meckenzie Behr, Barbara Benoit, Elizabeth Bhoj, Suzette J. Bielinski, Harris T. Bland, Carrie L. Blout Zawatsky, Kenneth M. Borthwick, Erwin P. Böttinger, Mark Bowser, Harrison Brand, Murray H. Brilliant, Wendy Brodeur, Pedro J. Caraballo, David Carrell, Andrew Carroll, Berta Almoguera, Lisa Castillo, Víctor M. Castro, Gauthami Chandanavelli, Theodore Chiang, Rex L. Chisholm, Kurt D. Christensen, Wendy K. Chung, Christopher G. Chute, Brittany City, Beth L. Cobb, John J. Connolly, Paul K. Crane, Katherine D. Crew, David R. Crosslin, Mariza de Andrade, Jessica De la Cruz, Shawn Denson, Joshua C. Denny, Tim DeSmet, Ozan Dikilitas, Christopher A. Friedrich, Stephanie M. Fullerton, Birgit Funke, Stacey Gabriel, Vivian S. Gainer, Ali G. Gharavi, Andrew M. Glazer, Joseph Glessner, Jessica Goehringer, Allan Gordon, Chet Graham, Robert C. Green, Justin H. Gundelach, Jyoti G. Dayal, Heather S. Hain, Hákon Hákonarson, Maegan Harden, John B. Harley, Margaret Harr, Andrea L. Hartzler, M. Geoffrey Hayes, Scott J. Hebbring, Nora B. Henrikson, Andrew D. Hershey, Christin Hoell, Ingrid A. Holm, Kayla M. Howell, George Hripcsak, Jianhong Hu, Gail P. Jarvik, Joy C. Jayaseelan, Yunyun Jiang, Yoonjung Yoonie Joo, Sheethal Jose, Navya Shilpa Josyula, Anne E. Justice, Sara E. Kalla, Divya Kalra, Elizabeth W. Karlson, Melissa Kelly, Brendan J. Keating, Eimear E. Kenny, Dustin Key, Krzysztof Kiryluk, Terrie Kitchner, Barbara J. Klanderman, Eric W. Klee

    Pubblicazione 2019
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  7. 7
    Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico

    Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico di A. L. Williams Amy, S. B R Jacobs Suzanne, Hortensia Moreno-Macías, Alicia Huerta-Chagoya, Claire Churchhouse, Carla Márquez‐Luna, María José Gómez-Vázquez, N. P. Burtt Noël, Carlos A. Aguilar‐Salinas, Clicerio González‐Villalpando, José C. Florez, Lorena Orozco, Teresa Tusié‐Luna, David Altshuler, Stephan Ripke, Alisa K. Manning, Humberto Garcia‐Ortíz, Benjamin M. Neale, David Reich, Daniel O. Stram, Juan Carlos Fernández-López, Sandra Romero‐Hidalgo, Nick Patterson, Christopher A Haiman, Irma Aguilar-Delfín, Angélica Martínez‐Hernández, Federico Centeno-Cruz, Elvia Mendoza‐Caamal, M. Revilla, Sergio Islas‐Andrade, Emilio J. Córdova, Martha Eunice Rodríguez-Arellano, Xavier Soberón, Jobinse Jose, M. A. González-Villalpando María Elena, Brian E. Henderson, Kristine R. Monroe, Lynne R. Wilkens, Laurence N. Kolonel, Loı̈c Le Marchand, Laura Riba, Ma Luisa, Rosario Rodríguez-Guillén, Ivette Cruz‐Bautista, M. Rodríguez‐Torres, Liliana Muñóz-Hernández, Tamara Sáenz, Donají Gómez, Ulices Alvirde, Robert C. Onofrio, Wendy Brodeur, Diane Gage, Jacquelyn Murphy, Jennifer Franklin, Scott Mahan, Kristin Ardlie, Andrew Crenshaw, Wendy Winckler, Kay Prüfer, M.V. Shunkov, Susanna Sawyer, Udo Stenzel, Janet Kelso, Monkol Lek, Sriram Sankararaman, Daniel G. MacArthur, А. П. Деревянко, Svante Pääbo, Suzanne B.R. Jacobs, Shuba Gopal, James A. Grammatikos, Ian C. P. Smith, Kevin Bullock, Amy Deik, Amanda L. Souza, Kerry A. Pierce, Clary B. Clish, Timothy R. Fennell, Yossi Farjoun, Stacey Gabriel, Myron D. Gross, Mark A. Pereira, Mark Seielstad, Woon‐Puay Koh, E. Shyong Tai, Jason Flannick, Pierre Fontanillas, Andrew P. Morris, Tanya M. Teslovich, Gil Atzmon, John Blangero, Donald W. Bowden, John C. Chambers, Yoon Shin Cho, Ravindranath Duggirala, Benjamin Gläser, Craig L. Hanis, Jaspal S. Kooner, Markku Laakso, Jong‐Young Lee

    Pubblicazione 2013
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