Zobrazeno 1 - 10
of 64
pro vyhledávání: '"June A. Peters"'
Autor:
Mark H. Greene, Allison Werner-Lin, Kevin Roy, Mae Carlson, Ashley Pantaleao, Maria Isabel Achatz, Sharon A. Savage, Jennifer L. Young, Payal P. Khincha, June A. Peters, Renee C. Bremer, Norman B. Epstein
Publikováno v:
Fam Process
Li-Fraumeni Syndrome (LFS) is a hereditary disorder that confers an approximately 90% lifetime risk of cancer and requires comprehensive lifetime cancer screening. We explored healthcare roles for managing LFS-related cancer risks and treatments that
Autor:
Hormuzd A. Katki, June A. Peters, Megan N. Frone, Margaret A. Tucker, Ana F. Best, Mark H. Greene
Publikováno v:
Cancer Epidemiology, Biomarkers & Prevention. 28:293-302
Background: Eligibility guidelines for genetic testing may be revisited, given technological advances, plummeting costs, and proposals for population mutation screening. A key property of eligibility criteria is the tradeoff between the number of mut
Autor:
Renee C. Bremer, Jennifer T. Loud, Payal P. Khincha, Ashley Pantaleao, Mark H. Greene, Allison Werner-Lin, Sharon A. Savage, Maria Isabel Achatz, Jennifer L. Young, Jessica Bayer, Lori Zaspel, June A. Peters
Publikováno v:
Journal of Psychosocial Oncology. 37:178-193
PURPOSE: Li-Fraumeni Syndrome (LFS) is an inherited tumor predisposition syndrome with lifetime cancer risks approaching 100% and evolving risk-management strategies. This study evaluated couples’ coping with LFS-related burdens. RESEARCH APPROACH:
Autor:
Mark H. Greene, Jennifer T. Loud, Lindsey M. Hoskins, Jennifer L. Young, Allison Werner-Lin, Anne L. Ersig, June A. Peters
Publikováno v:
Journal of Family Nursing. 25:28-53
In families with hereditary breast/ovarian cancer, complex disease histories challenge established patterns of family communication and influence decision-making for clinical surveillance, genetic testing, and risk management. An interdisciplinary te
Autor:
June A. Peters, Luba Djurdjinovic
Publikováno v:
Journal of Genetic Counseling. 26:195-198
Autor:
Sharon A. Savage, Douglas R. Stewart, Neelam Giri, Mark H. Greene, Phuong L. Mai, Blanche P. Alter, Renee C. Bremer, Jennifer T. Loud, June A. Peters
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics
To define the frequency with which adult research participants consent to be offered clinically validated research genetic test results (RR) and incidental findings (IF). Consents were obtained from 506 adults enrolled in one of three studies within
Autor:
Sharon A. Savage, Renee C. Bremer, Philip S. Rosenberg, June A. Peters, Ana F. Best, Phuong L. Mai, Jennifer T. Loud, Payal P. Khincha, Rosamma DeCastro
Publikováno v:
Cancer. 122:3673-3681
BACKGROUND Li-Fraumeni syndrome (LFS) is an autosomal dominant cancer predisposition syndrome characterized by a very high lifetime cancer risk and an early age at diagnosis of a wide cancer spectrum. Precise estimates for the risk of first and subse
Autor:
Shannon Givens, Phuong L. Mai, Renee C. Bremer, Regina Kenen, Sharon A. Savage, June A. Peters
Publikováno v:
Journal of Genetic Counseling. 25:529-542
This study presents findings of a mixed-method descriptive exploration of the role of friends and spirituality/religiosity in easing the burden of families with the rare inherited disorder, Li-Fraumeni Syndrome (LFS). LFS is caused by germline mutati
Autor:
Ana F, Best, Margaret A, Tucker, Megan N, Frone, Mark H, Greene, June A, Peters, Hormuzd A, Katki
Publikováno v:
Cancer Epidemiol Biomarkers Prev
BACKGROUND: Eligibility guidelines for genetic testing may be revisited, given technological advances, plummeting costs, and proposals for population mutation-screening. A key property of eligibility criteria is the tradeoff between the number of mut
Autor:
Sadie P. Hutson, June A. Peters, Blanche P. Alter, Paul K. J. Han, Ann G. Carr, Jada G. Hamilton, Amy E. Frohnmayer
Publikováno v:
Journal of Genetic Counseling. 24:760-770
Inherited bone marrow failure syndromes (IBMFS) including Fanconi anemia, dyskeratosis congenita, Diamond-Blackfan anemia, and Shwachman-Diamond syndrome are rare genetic disorders characterized by hematologic complications and increased risk of canc