Resultats de la cerca - Samuel Aronson
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Building the foundation for genomics in precision medicine per Samuel Aronson, Heidi L. Rehm
Publicat 2015Revisão -
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The GeneInsight suite: a platform to support laboratory and provider use of DNA-based genetic testing per Samuel Aronson, Eugene Clark, Lawrence Babb, Samantha Baxter, Lisa Farwell, Birgit Funke, Amy Hernandez, Victoria A. Joshi, Elaine Lyon, Andrew R. Parthum, Franklin J. Russell, Matthew Varugheese, Thomas C. Venman, Heidi L. Rehm
Publicat 2011Artigo -
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A survey of informatics approaches to whole-exome and whole-genome clinical reporting in the electronic health record per Peter Tarczy‐Hornoch, Laura M. Amendola, Samuel Aronson, Levi A. Garraway, Stacy W. Gray, Robert W. Grundmeier, Lucia A. Hindorff, Gail P. Jarvik, Dean Karavite, Matthew S. Lebo, Sharon E. Plon, Eliezer M. Van Allen, Karen E. Weck, Peter S. White, Yaping Yang
Publicat 2013Artigo -
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Genomic Information for Clinicians in the Electronic Health Record: Lessons Learned From the Clinical Genome Resource Project and the Electronic Medical Records and Genomics Networ... per Marc S. Williams, Casey Overby Taylor, Nephi Walton, Scott Goehringer, Samuel Aronson, Robert R. Freimuth, Luke V. Rasmussen, Eric S. Hall, Cynthia A. Prows, Wendy K. Chung, Alexander Fedotov, Jordan G. Nestor, Chunhua Weng, Robb Rowley, Georgia L. Wiesner, Gail P. Jarvik, Guilherme Del Fiol
Publicat 2019Artigo -
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Results of a Remotely Delivered Hypertension and Lipid Program in More Than 10 000 Patients Across a Diverse Health Care Network per Alexander Blood, Christopher P. Cannon, William J. Gordon, Charlotte Mailly, Taylor E. MacLean, Samantha Subramaniam, Michela Tucci, J Crossen, Hunter Nichols, Kavishwar B. Wagholikar, David Zelle, Marian McPartlin, Lina Matta, Michael Oates, Samuel Aronson, Shawn N. Murphy, Adam Landman, Naomi D.L. Fisher, Thomas A. Gaziano, Jorge Plutzky, Benjamin M. Scirica
Publicat 2022Artigo -
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CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record per Brian H. Shirts, Joseph S Salama, Samuel Aronson, Wendy K. Chung, Stacy W. Gray, Lucia A. Hindorff, Gail P. Jarvik, Sharon E. Plon, Elena M. Stoffel, Peter Tarczy‐Hornoch, Eliezer M. Van Allen, Karen E. Weck, Christopher G. Chute, Robert R. Freimuth, Robert W. Grundmeier, Andrea L. Hartzler, Rongling Li, Peggy Peissig, Josh F. Peterson, Luke V. Rasmussen, Justin Starren, Marc S. Williams, Casey Lynnette Overby
Publicat 2015Artigo -
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Research Directions in the Clinical Implementation of Pharmacogenomics: An Overview of US Programs and Projects per Simona Volpi, Carol J. Bult, Rex L. Chisholm, Patricia A. Deverka, Geoffrey S. Ginsburg, Howard J. Jacob, Melpomeni Kasapi, Howard L. McLeod, Dan M. Roden, Marc S. Williams, Eric D. Green, Laura Lyman Rodriguez, Samuel Aronson, Larisa H. Cavallari, Joshua C. Denny, Lynn G. Dressler, Julie A. Johnson, Teri E. Klein, J. Steven Leeder, Micheline Piquette‐Miller, Minoli A. Perera, Laura J. Rasmussen‐Torvik, Heidi L. Rehm, Marylyn D. Ritchie, Todd C. Skaar, Nikhil Wagle, Richard M. Weinshilboum, Kristin Weitzel, Robert S. Wildin, John T. Wilson, Teri A. Manolio, Mary V. Relling
Publicat 2018Revisão -
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Automated typing of red blood cell and platelet antigens: a whole-genome sequencing study per William J. Lane, Connie M. Westhoff, Nicholas Gleadall, Maria Aguad, Robin Smeland‐Wagman, Sunitha Vege, Daimon P. Simmons, Helen Mah, Matthew S. Lebo, Klaudia Walter, Nicole Soranzo, Emanuele Di Angelantonio, John Danesh, David J. Roberts, Nick Watkins, Willem H. Ouwehand, Adam S. Butterworth, Richard M. Kaufman, Heidi L. Rehm, Leslie E. Silberstein, Robert C. Green, David W. Bates, Carrie L. Blout Zawatsky, Kurt D. Christensen, Allison L. Cirino, Carolyn Y. Ho, Joel B. Krier, Lisa Soleymani Lehmann, Calum A. MacRae, Cynthia C. Morton, Denise Perry, Christine E. Seidman, Shamil Sunyaev, Jason L. Vassy, Erica F. Schonman, Tiffany Nguyen, Eleanor Steffens, Wendi N. Betting, Samuel Aronson, Ozge Ceyhan‐Birsoy, Kalotina Machini, Heather M. McLaughlin, Danielle R. Azzariti, Ellen Tsai, Jennifer Blumenthal‐Barby, Lindsay Z. Feuerman, Amy L. McGuire, Kaitlyn Lee, Jill O. Robinson, Melody J. Slashinski, Pamela M. Diamond, Kelly Cue Davis, Peter A. Ubel, Peter Kraft, J. Scott Roberts, Judy E. Garber, Tina Hambuch, Michael F. Murray, Isaac S. Kohane, Sek Won Kong
Publicat 2018Artigo -
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Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network per 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
Publicat 2019Artigo -
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Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine per Robert C. Green, Katrina A.B. Goddard, Gail P. Jarvik, Laura M. Amendola, Paul S. Appelbaum, Jonathan S. Berg, Barbara A. Bernhardt, Leslie G. Biesecker, Sawona Biswas, Carrie L. Blout Zawatsky, Kevin M. Bowling, Kyle B. Brothers, Wylie Burke, Charlisse Caga-Anan, Arul M. Chinnaiyan, Wendy K. Chung, Ellen Wright Clayton, Gregory M. Cooper, Kelly M. East, James P. Evans, Stephanie M. Fullerton, Levi A. Garraway, Jeremy R. Garrett, Stacy W. Gray, Gail E. Henderson, Lucia A. Hindorff, Ingrid A. Holm, Michelle Lewis, Carolyn M. Hutter, Pasi A. Jänne, Steven Joffe, David Kaufman, Bartha Maria Knoppers, Barbara A. Koenig, Ian D. Krantz, Teri A. Manolio, Laurence B. McCullough, Jean E. McEwen, Amy L. McGuire, Donna M. Muzny, R Myers, Deborah A. Nickerson, Jeffrey Ou, D. Williams Parsons, Gloria M. Petersen, Sharon E. Plon, Heidi L. Rehm, J. Scott Roberts, Dan R. Robinson, Joseph S Salama, Sarah Scollon, Richard R. Sharp, Brian H. Shirts, Nancy B. Spinner, Holly K. Tabor, Peter Tarczy‐Hornoch, David L. Veenstra, Nikhil Wagle, Karen E. Weck, Benjamin S. Wilfond, Kirk C. Wilhelmsen, Susan M. Wolf, Julia Wynn, Joon‐Ho Yu, Michelle D. Amaral, Laura M. Amendola, Paul S. Appelbaum, Samuel Aronson, Nonie S. Arora, Danielle R. Azzariti, Gregory S. Barsh, E. Martina Bebin, Barbara B. Biesecker, Leslie G. Biesecker, Sawona Biswas, Carrie L. Blout Zawatsky, Kevin M. Bowling, Kyle B. Brothers, Brian Brown, Amber Burt, Peter H. Byers, Charlisse Caga-Anan, Muge G. Calikoglu, Sara J. Carlson, Nizar Chahin, Arul M. Chinnaiyan, Kurt D. Christensen, Wendy K. Chung, Allison L. Cirino, Ellen Wright Clayton, Laura K. Conlin, Gregory M. Cooper, David R. Crosslin, James V. Davis, Kelly Cue Davis, Matthew A. Deardorff, Batsal Devkota, Raymond De Vries, Pamela M. Diamond, Michael O. Dorschner
Publicat 2016Artigo
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