Результати пошуку - Joon‐Ho Yu
- Показ 1 - 13 результатів із 13
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Attitudes of African Americans Toward Return of Results From Exome and Whole Genome Sequencing за авторством Joon‐Ho Yu, Julia M. Crouch, Seema M. Jamal, Holly K. Tabor, Michael J. Bamshad
Опубліковано 2013Artigo -
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Anthropologists' views on race, ancestry, and genetics за авторством Jennifer K. Wagner, Joon‐Ho Yu, Jayne O. Ifekwunigwe, Tanya M. Harrell, Michael J. Bamshad, Charmaine Royal
Опубліковано 2016Artigo -
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Practices and Policies of Clinical Exome Sequencing Providers: Analysis and Implications за авторством Seema M. Jamal, Joon‐Ho Yu, Jessica X. Chong, Karin M. Dent, Jessie H. Conta, Holly K. Tabor, Michael J. Bamshad
Опубліковано 2013Artigo -
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Informed consent for whole genome sequencing: A qualitative analysis of participant expectations and perceptions of risks, benefits, and harms за авторством Holly K. Tabor, Jacquie Stock, Tracy Brazg, Margaret J. McMillin, Karin M. Dent, Joon‐Ho Yu, Jay Shendure, Michael J. Bamshad
Опубліковано 2012Artigo -
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The Challenge of Informed Consent and Return of Results in Translational Genomics: Empirical Analysis and Recommendations за авторством Gail E. Henderson, Susan M. Wolf, Kristine J. Kuczynski, Steven Joffe, Richard R. Sharp, D. Williams Parsons, Bartha Maria Knoppers, Joon‐Ho Yu, Paul S. Appelbaum
Опубліковано 2014Artigo -
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Gene discovery for Mendelian conditions via social networking: de novo variants in KDM1A cause developmental delay and distinctive facial features за авторством Jessica X. Chong, Joon‐Ho Yu, Peter Lorentzen, Karen M. Park, Seema M. Jamal, Holly K. Tabor, Anita Rauch, Margarita Sáenz, Eugen Boltshauser, Karynne Patterson, Deborah A. Nickerson, Michael J. Bamshad
Опубліковано 2015Artigo -
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Pathogenic Variants for Mendelian and Complex Traits in Exomes of 6,517 European and African Americans: Implications for the Return of Incidental Results за авторством Holly K. Tabor, Paul L. Auer, Seema M. Jamal, Jessica X. Chong, Joon‐Ho Yu, Allan Gordon, Timothy A. Graubert, Christopher J. O’Donnell, Stephen S. Rich, Deborah A. Nickerson, Michael J. Bamshad
Опубліковано 2014Artigo -
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Addressing underrepresentation in genomics research through community engagement за авторством Amy A. Lemke, Edward D. Esplin, Aaron J. Goldenberg, Claudia Gonzaga‐Jauregui, Neil A. Hanchard, Julie Harris-Wai, Justin E. Ideozu, Rosario Isasi, Andrew P. Landstrom, Anya E. R. Prince, Erin Turbitt, Maya Sabatello, Samantha A. Schrier Vergano, Matthew R.G. Taylor, Joon‐Ho Yu, Kyle B. Brothers, Nanibaa’ A. Garrison
Опубліковано 2022Revisão -
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SeqFirst: Building equity access to a precise genetic diagnosis in critically ill newborns за авторством Tara Wenger, Abbey Scott, Lukas Kruidenier, Megan Sikes, Alexandra Keefe, Kati J. Buckingham, Colby T. Marvin, Kathryn M. Shively, Tamara Bacus, Olivia Sommerland, Kailyn Anderson, Heidi Gildersleeve, Chayna Davis, Jamie Love‐Nichols, Katherine E. MacDuffie, Danny E. Miller, Joon‐Ho Yu, Amy Snook, Britt Johnson, David L. Veenstra, Julia Parish-Morris, Kirsty McWalter, Kyle Retterer, Deborah Copenheaver, Bethany Friedman, Jane Juusola, Erin Ryan, Renee Varga, Dan Doherty, Katrina M. Dipple, Jessica X. Chong, Paul Kruszka, Michael J. Bamshad
Опубліковано 2025Artigo -
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Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine за авторством 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
Опубліковано 2016Artigo
Інструменти для пошуку:
Пов'язані теми
Biology
Gene
Exome sequencing
Genetics
Medicine
Exome
Genome
Mutation
Computer science
Law
Political science
Context (archaeology)
Genomics
Paleontology
Pathology
Psychology
Alternative medicine
Informed consent
Sociology
Whole genome sequencing
Biochemistry
Business
Computer security
Confidentiality
Data science
Data sharing
Health care
Marketing
Mendelian inheritance
Phenotype