Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Carrie L. Blout Zawatsky"'
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, 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
Publikováno v:
Journal of Genetic Counseling.
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. 4(1)
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 assessed parti
Autor:
Carrie L. Blout Zawatsky, Marc S. Williams, Grace O’Brien, Aeysha Chaudhry, Heidi L. Rehm, Jennifer M. Yeh, Pamela M. McMahon, Narmeen Rehman, Kurt D. Christensen, Ann Chen Wu, Christine Y. Lu, Robert C. Green, Natasha K. Stout, Michael Gooch, Lisa Diller
Publikováno v:
Genet Med
PURPOSE: Genetic testing for pediatric cancer predisposition syndromes (CPS) could augment newborn screening programs, but with uncertain benefits and costs. METHODS: We developed a simulation model to evaluate universal screening for a CPS panel. Co
Autor:
Stacey, Pereira, Amanda M, Gutierrez, Jill Oliver, Robinson, Kurt D, Christensen, Casie A, Genetti, Carrie L, Blout Zawatsky, Rebecca L, Hsu, Bethany, Zettler, Melissa Kurtz, Uveges, Richard B, Parad, Alan H, Beggs, Ingrid A, Holm, Robert C, Green, Amy L, McGuire
Publikováno v:
Genetics in Medicine. 25:100002
Most professional guidelines recommend against genetic screening for adult-onset only conditions until adulthood, yet others argue there may be benefit to disclosing such results. We explored parents' decision-making on this issue in the BabySeq Proj
Autor:
Chenjie Zeng, Lisa A. Bastarache, Ran Tao, Eric Venner, Scott Hebbring, Justin D. Andujar, Sarah 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 M. A. Sleiman, Hakon Hakonarson, 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
Publikováno v:
JAMA Oncol
IMPORTANCE: Knowledge about the spectrum of diseases associated with hereditary cancer syndromes may improve disease diagnosis and management for patients and help to identify high-risk individuals. OBJECTIVE: To identify phenotypes associated with h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::021e242fe873b19da40026843b3556ce
https://europepmc.org/articles/PMC9026237/
https://europepmc.org/articles/PMC9026237/
Autor:
Kathleen A. Leppig, Alanna Kulchak Rahm, Paul Appelbaum, Sharon Aufox, Sarah T. Bland, Adam Buchanan, Kurt D. Christensen, Wendy K. Chung, Ellen Wright Clayton, David Crosslin, Josh Denny, Shannon DeVange, Adam Gordon, Robert C. Green, Hakon Hakonarson, Margaret H. Harr, Nora Henrikson, Christin Hoell, Ingrid A. Holm, Iftikhar J. Kullo, Gail P. Jarvik, Philip E. Lammers, Eric B. Larson, Noralane M. Lindor, Maddalena Marasa, Melanie F. Myers, Emma Perez, Josh F. Peterson, Siddharth Pratap, Cynthia A. Prows, James D. Ralston, Hila Milo Rasouly, Dan M. Roden, Richard R. Sharp, Rajbir Singh, Gabriel Shaibi, Maureen E. Smith, Amy Sturm, Heidi A. Thiese, Sara L. Van Driest, Janet Williams, Marc S. Williams, Julia Wynn, Carrie L. Blout Zawatsky, Georgia L. Wiesner
Publikováno v:
Genet Med
PURPOSE: The goal of Electronic Medical Records and Genomics (eMERGE) Phase III Network was to return actionable sequence variants to 25,084 consenting participants from 10 different health care institutions across the United States. The purpose of t
Autor:
Heidi L. Rehm, Bethany Zettler, Amy L. McGuire, Sergei Roumiantsev, Dmitry Dukhovny, Kalotina Machini, Talia S. Schwartz, Ozge Ceyhan-Birsoy, Hadley Stevens Smith, Timothy W. Yu, Jill O. Robinson, Devan Petersen, Pankaj B. Agrawal, Chet Graham, Amy E. Roberts, Tiffany T. Nguyen Dolphyn, Tina K. Truong, Maegan Harden, Carrie L. Blout Zawatsky, Casie A. Genetti, Ingrid A. Holm, Shawn Fayer, Xingquan Lu, Harvey L. Levy, Vivek Ramanathan, Richard B. Parad, Leslie A. Frankel, Jaclyn B. Murry, Amanda M. Gutierrez, Wendi N. Betting, Kaitlyn B. Lee, Grace E. VanNoy, Susan E. Waisbren, Robert C. Green, Stacey Pereira, Alan H. Beggs, Matthew S. Lebo, Kurt D. Christensen, Medha Naik, Hayley A. Peoples, Rubaiya Islam, Uma Ramamurthy, Joel B. Krier
Publikováno v:
JAMA Pediatr
Importance Newborn genomic sequencing (nGS) may provide health benefits throughout the life span, but there are concerns that it could also have an unfavorable (ie, negative) psychosocial effect on families. Objective To assess the psychosocial effec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af8443c79829316490733916ea5ce473
https://europepmc.org/articles/PMC8383160/
https://europepmc.org/articles/PMC8383160/