Ohcanbohtosat - Hana Zouk
- Čájehuvvo 1 - 7 / 7
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1
Determining the characteristics of genetic disorders that predict inclusion in newborn genomic sequencing programs Dahkki Thomas Minten, Nina B. Gold, Sarah K. Bick, Sophia Adelson, Nils Gehlenborg, Laura M. Amendola, François Boemer, Alison J. Coffey, Nicolas Encina, Alessandra Ferlini, Janbernd Kirschner, Bianca Russell, Laurent Servais, Kristen L. Sund, Ryan J. Taft, Petros Tsipouras, Hana Zouk, David Bick, Robert C. Green
Almmustuhtton 2024Pré-impressão -
2
Returning actionable genomic results in a research biobank: Analytic validity, clinical implementation, and resource utilization Dahkki Carrie L. Blout Zawatsky, Nidhi Shah, Kalotina Machini, Emma Perez, Kurt D. Christensen, Hana Zouk, Marcie Steeves, Christopher Koch, Melissa Kurtz Uveges, Janelle Shea, Nina B. Gold, Joel B. Krier, Natalie Boutin, Lisa Mahanta, Heidi L. Rehm, Scott T. Weiss, Elizabeth W. Karlson, Jordan W. Smoller, Matthew S. Lebo, Robert C. Green
Almmustuhtton 2021Artigo -
3
Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies Dahkki Laura M. Amendola, Kathleen Muenzen, Leslie G. Biesecker, Kevin M. Bowling, Gregory M. Cooper, Michael O. Dorschner, Catherine C. Driscoll, Ann Katherine M. Foreman, Katie Golden‐Grant, John M. Greally, Lucia A. Hindorff, Dona Kanavy, Vaidehi Jobanputra, Jennifer J. Johnston, Eimear E. Kenny, Shannon McNulty, Priyanka Murali, Jeffrey Ou, Bradford C. Powell, Heidi L. Rehm, Bradley A. Rolf, Tamara S. Roman, Jessica Van Ziffle, Saurav Guha, Avinash Abhyankar, David R. Crosslin, Eric Venner, Bo Yuan, Hana Zouk, Gail P. Jarvik
Almmustuhtton 2020Artigo -
4
Association of Pathogenic Variants in Hereditary Cancer Genes With Multiple Diseases Dahkki Chenjie Zeng, Lisa A. Bastarache, Ran Tao, Eric Venner, Scott J. Hebbring, Justin Andujar, Harris T. Bland, David R. Crosslin, Siddharth Pratap, Ayorinde Cooley, Jennifer A. Pacheco, Kurt D. Christensen, Emma Perez, Carrie L. Blout Zawatsky, Leora Witkowski, Hana Zouk, Chunhua Weng, Kathleen A. Leppig, Patrick Sleiman, Hákon Hákonarson, Marc S. Williams, Yuan Luo, Gail P. Jarvik, Robert C. Green, Wendy K. Chung, Ali G. Gharavi, Niall J. Lennon, Heidi L. Rehm, Richard A. Gibbs, Josh F. Peterson, Dan M. Roden, Georgia L. Wiesner, Joshua C. Denny
Almmustuhtton 2022Artigo -
5
Frequency of genomic secondary findings among 21,915 eMERGE network participants Dahkki Allan Gordon, Hana Zouk, Eric Venner, Christine M. Eng, Birgit Funke, Laura M. Amendola, David Carrell, Rex L. Chisholm, Wendy K. Chung, Joshua C. Denny, Alexander Fedotov, Hákon Hákonarson, Iftikhar J. Kullo, Eric B. Larson, Magalie S. Leduc, Kathleen A. Leppig, Niall J. Lennon, Jodell E. Linder, Donna M. Muzny, Cynthia A. Prows, Laura J. Rasmussen‐Torvik, Hila Milo Rasouly, Dan M. Roden, Elisabeth A. Rosenthal, Maureen E. Smith, Ian B. Stanaway, Sara L. Van Driest, Kimberly Walker, Georgia L. Wiesner, Marc S. Williams, Leora Witkowski, David R. Crosslin, Richard A. Gibbs, Heidi L. Rehm, Gail P. Jarvik
Almmustuhtton 2020Artigo -
6
The landscape of reported VUS in multi-gene panel and genomic testing: Time for a change Dahkki Heidi L. Rehm, Joseph T. Alaimo, Swaroop Aradhya, Pınar Bayrak‐Toydemir, Hunter Best, Rhonda Brandon, Jillian G. Buchan, Elizabeth Chao, Elaine Chen, Jacob Clifford, Ana S.A. Cohen, Laura K. Conlin, Soma Das, Kyle Davis, Daniela del Gaudio, Florencia Del Viso, Christina DiVincenzo, Marcia Eisenberg, Lucia Guidugli, Monia Hammer, Steven M. Harrison, Kathryn E. Hatchell, Lindsay Havens Dyer, Lily Hoang, James Holt, Vaidehi Jobanputra, Izabela Karbassi, Hutton M. Kearney, Melissa Kelly, Jacob M. Kelly, Michelle L. Kluge, Timothy Komala, Paul Kruszka, Lynette Lau, Matthew S. Lebo, Christian R. Marshall, Dianalee McKnight, Kirsty McWalter, Yan Meng, Narasimhan Nagan, Christian S. Neckelmann, Nir Neerman, Zhiyv Niu, Vitoria Paolillo, Sarah A Paolucci, Denise Perry, Tina Pesaran, Kelly Radtke, Kristen Rasmussen, Kyle Retterer, Carol Saunders, Elizabeth Spiteri, Christine M. Stanley, Anna Szuto, Ryan J. Taft, Isabelle Thiffault, Brittany C. Thomas, Amanda Thomas‐Wilson, Erin Thorpe, Timothy Tidwell, Meghan C. Towne, Hana Zouk, Christian Marshall, Linyan Meng, Vaidehi Jobanputra, Ryan J. Taft, Euan A. Ashley, Ghunwa Nakouzi, Wei Shen, Stephen F. Kingsmore, Heidi L. Rehm
Almmustuhtton 2023Artigo -
7
Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network Dahkki 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
Almmustuhtton 2019Artigo
Ohcanreaiddut:
Laktáseaddji fáttát
Biology
Medicine
Gene
Genetics
Bioinformatics
Computational biology
Internal medicine
Biobank
Genetic testing
Genome
Alternative medicine
Cohort
Computer science
Exome
Exome sequencing
Genotype
Mutation
Pathology
Cancer
Cohort study
Concordance
DNA sequencing
Data collection
Data science
Data sharing
Disease
Genome-wide association study
Genomic sequencing
Genomics
Genotyping