Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Carrie L. Blout"'
Autor:
Anna C. F. Lewis, Emma F. Perez, Anya E. R. Prince, Hana R. Flaxman, Lizbeth Gomez, Deanna G. Brockman, Paulette D. Chandler, Benjamin J. Kerman, Matthew S. Lebo, Jordan W. Smoller, Scott T. Weiss, Carrie L. Blout Zawatksy, James B. Meigs, Robert C. Green, Jason L. Vassy, Elizabeth W. Karlson
Publikováno v:
Genome Medicine, Vol 14, Iss 1, Pp 1-16 (2022)
Abstract Background Polygenic risk scores (PRS), which offer information about genomic risk for common diseases, have been proposed for clinical implementation. The ways in which PRS information may influence a patient’s health trajectory depend on
Externí odkaz:
https://doaj.org/article/b19f80c5d7664fe791e51eb803730865
Autor:
Kurt D. Christensen, Mengran Zhang, Lauren N. Galbraith, Einat Granot-Hershkovitz, Sarah C. Nelson, Sara Gonzalez, Maria Argos, Krista M. Perreira, Martha L. Daviglus, Carmen R. Isasi, Jianwen Cai, Gregory A. Talavera, Carrie L. Blout Zawatsky, Robert C. Green, Rosario Isasi, Robert Kaplan, Tamar Sofer
Publikováno v:
HGG Advances, Vol 4, Iss 1, Pp 100160- (2023)
Summary: We investigated the awareness, perceived usefulness, and use of genetic testing among Hispanic and Latino individuals. Annual follow-up surveys for the Hispanic Community Health Study/Study of Latinos (HCHS/SOL) from 2019 to April 2020 asses
Externí odkaz:
https://doaj.org/article/8ff2e6c54d70411d90040259888b69d3
Autor:
Brittan Armstrong, Kurt D. Christensen, Casie A. Genetti, Richard B. Parad, Jill Oliver Robinson, Carrie L. Blout Zawatsky, Bethany Zettler, Alan H. Beggs, Ingrid A. Holm, Robert C. Green, Amy L. McGuire, Hadley Stevens Smith, Stacey Pereira, The BabySeq Project Team
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Introduction: With increasing utility and decreasing cost of genomic sequencing, augmentation of standard newborn screening (NBS) programs with newborn genomic sequencing (nGS) has been proposed. Before nGS can be integrated into newborn screening, p
Externí odkaz:
https://doaj.org/article/a5e73206e51142deb82cd9b8ec557eff
Autor:
Carrie L. Blout Zawatsky, Jennifer R. Leonhard, Megan Bell, Michelle M. Moore, Natasha J. Petry, Dylan M. Platt, Robert C. Green, Catherine Hajek, Kurt D. Christensen
Publikováno v:
Journal of Personalized Medicine, Vol 12, Iss 11, p 1929 (2022)
This paper describes one healthcare system’s approach to strategically deploying genetic specialists and pharmacists to support the implementation of a precision medicine program. In 2013, Sanford Health initiated the development of a healthcare sy
Externí odkaz:
https://doaj.org/article/9eb8a21672434a41bb0f39857a8feec3
Autor:
Georgia L. Wiesner, Alanna Kulchak Rahm, Paul Appelbaum, Sharon Aufox, Sarah T. Bland, Carrie L. Blout, Kurt D. Christensen, Wendy K. Chung, Ellen Wright Clayton, Robert C. Green, Margaret H. Harr, Nora Henrikson, Christin Hoell, Ingrid A. Holm, Gail P. Jarvik, Iftikhar J. Kullo, Philip E. Lammers, Eric B. Larson, Noralane M. Lindor, Maddalena Marasa, Melanie F. Myers, Josh F. Peterson, Cynthia A. Prows, James D. Ralston, Hila Milo Rasouly, Richard R. Sharp, Maureen E. Smith, Sara L. Van Driest, Janet L. Williams, Marc S. Williams, Julia Wynn, Kathleen A. Leppig
Publikováno v:
Journal of Personalized Medicine, Vol 10, Iss 2, p 30 (2020)
A goal of the 3rd phase of the Electronic Medical Records and Genomics (eMERGE3) Network was to examine the return of results (RoR) of actionable variants in more than 100 genes to consenting participants and their healthcare providers. Each of the 1
Externí odkaz:
https://doaj.org/article/9adbd2515be142cca8ebd1ce1b4cda9d
Akademický článek
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Autor:
Carrie L. Blout Zawatsky, David Bick, Louise Bier, Birgit Funke, Matthew Lebo, Katie L. Lewis, Ekaterina Orlova, Emily Qian, Lauren Ryan, Marci L. B. Schwartz, Emily R. Soper
Publikováno v:
Journal of Genetic Counseling. 32:281-299
Genetic counseling for patients who are pursuing genetic testing in the absence of a medical indication, referred to as elective genomic testing (EGT), is becoming more common. This type of testing has the potential to detect genetic conditions befor
Akademický článek
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Akademický článek
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Publikováno v:
Journal of Genetic Counseling.