Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Hayley A Peoples"'
Autor:
Stacey Pereira, Jill Oliver Robinson, Hayley A Peoples, Amanda M Gutierrez, Mary A Majumder, Amy L McGuire, Mark A Rothstein
Publikováno v:
PLoS ONE, Vol 12, Iss 9, p e0184525 (2017)
The importance of health privacy protections in the era of the "Facebook Generation" has been called into question. The ease with which younger people share personal information about themselves has led to the assumption that they are less concerned
Externí odkaz:
https://doaj.org/article/9697ba5596694554a5eb769785d14117
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/
Autor:
Ozge Ceyhan-Birsoy, Jaclyn B. Murry, Kalotina Machini, Matthew S. Lebo, Timothy W. Yu, Shawn Fayer, Casie A. Genetti, Talia S. Schwartz, Pankaj B. Agrawal, Richard B. Parad, Ingrid A. Holm, Amy L. McGuire, Robert C. Green, Heidi L. Rehm, Alan H. Beggs, Wendi N. Betting, Kurt D. Christensen, Dmitry Dukhovny, Leslie A. Frankel, Chet Graham, Amanda M. Guiterrez, Maegan Harden, Joel B. Krier, Harvey L. Levy, Xingquan Lu, Medha Naik, Tiffany T. Nguyen, Hayley A. Peoples, Stacey Pereira, Devan Petersen, Uma Ramamurthy, Vivek Ramanathan, Amy Roberts, Jill O. Robinson, Serguei Roumiantsev, Tina K. Truong, Grace E. VanNoy, Susan E. Waisbren
Publikováno v:
The American Journal of Human Genetics. 104:76-93
Genomic sequencing provides many opportunities in newborn clinical care, but the challenges of interpreting and reporting newborn genomic sequencing (nGS) results need to be addressed for its broader and effective application. The BabySeq Project is
Autor:
Monica H. Wojcik, Tian Zhang, Ozge Ceyhan-Birsoy, Casie A. Genetti, Matthew S. Lebo, Timothy W. Yu, Richard B. Parad, Ingrid A. Holm, Heidi L. Rehm, Alan H. Beggs, Robert C. Green, Pankaj B. Agrawal, Wendi N. Betting, Kurt D. Christensen, Dmitry Dukhovny, Shawn Fayer, Leslie A. Frankel, Chet Graham, Amanda M. Guiterrez, Maegan Harden, Joel B. Krier, Harvey L. Levy, Xingquan Lu, Kalotina Machini, Amy L. McGuire, Jaclyn B. Murry, Medha Naik, Tiffany T. Nguyen, Hayley A. Peoples, Stacey Pereira, Devan Petersen, Uma Ramamurthy, Vivek Ramanathan, Amy Roberts, Jill O. Robinson, Serguei Roumiantsev, Talia S. Schwartz, Tina K. Truong, Grace E. VanNoy, Susan E. Waisbren
Publikováno v:
Genet Med
Purpose Newborn screening (NBS) is performed to identify neonates at risk for actionable, severe, early-onset disorders, many of which are genetic. The BabySeq Project randomized neonates to receive conventional NBS or NBS plus exome sequencing (ES)
Autor:
Casie A. Genetti, Talia S. Schwartz, Jill O. Robinson, Grace E. VanNoy, Devan Petersen, Stacey Pereira, Shawn Fayer, Hayley A. Peoples, Pankaj B. Agrawal, Wendi N. Betting, Ingrid A. Holm, Amy L. McGuire, Susan E. Waisbren, Timothy W. Yu, Robert C. Green, Alan H. Beggs, Richard B. Parad, Ozge Ceyhan-Birsoy, Kurt D. Christensen, Dmitry Dukhovny, Leslie A. Frankel, Chet Graham, Amanda M. Gutierrez, Maegan Harden, Joel B. Krier, Matthew S. Lebo, Harvey L. Levy, Xingquan Lu, Kalotina Machini, Jaclyn B. Murry, Medha Naik, Tiffany T. Nguyen, Uma Ramamurthy, Vivek Ramanathan, Heidi L. Rehm, Amy Roberts, Serguei Roumiantsev, Tina K. Truong
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics
Purpose: Newborn genomic sequencing (nGS) has great potential to improve pediatric care. Parental interest and concerns about genomics are relatively unexplored. Understanding why parents decline research consent for nGS may reveal implementation bar
Publikováno v:
Journal of palliative care. 35(1)
Objectives: Little is known about how clinicians perceive prognostic uncertainty. Our study objective was to identify factors that influence how prognostic uncertainty is viewed by physicians, as it relates to their communications with families. Desi
Autor:
Amanda M. Gutierrez, Mark A. Rothstein, Stacey Pereira, Jill O. Robinson, Hayley A. Peoples, Mary A. Majumder, Amy L. McGuire
Publikováno v:
PLoS ONE
PLoS ONE, Vol 12, Iss 9, p e0184525 (2017)
PLoS ONE, Vol 12, Iss 9, p e0184525 (2017)
Background The importance of health privacy protections in the era of the “Facebook Generation” has been called into question. The ease with which younger people share personal information about themselves has led to the assumption that they are
Publikováno v:
ACM Transactions on Computer-Human Interaction (TOCHI); Feb2023, Vol. 30 Issue 1, p1-48, 48p
Autor:
Pereira, Stacey1, Robinson, Jill Oliver1, Peoples, Hayley A.1, Gutierrez, Amanda M.1, Majumder, Mary A.1, Mcguire, Amy L.1, Rothstein, Mark A.2 mark.rothstein@lousiville.edu
Publikováno v:
PLoS ONE. 9/19/2017, Vol. 12 Issue 9, p1-11. 11p.
Autor:
Armstrong, Brittan, Christensen, Kurt D., Genetti, Casie A., Parad, Richard B., Robinson, Jill Oliver, Blout Zawatsky, Carrie L., Zettler, Bethany, Beggs, Alan H., Holm, Ingrid A., Green, Robert C., McGuire, Amy L., Smith, Hadley Stevens, Pereira, Stacey
Publikováno v:
Frontiers in Genetics; 4/27/2022, Vol. 13, p1-10, 10p