Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Pauleen Sanchez"'
Autor:
Danielle B. McKenna, Pauleen Sanchez, Jacquelyn Powers, Jamie Brower, Louise Wang, Rebecca Mueller, Heather Symecko, Jada G. Hamilton, Temima Wildman, Susan M. Domchek, Fergus J. Couch, Judy E. Garber, Kenneth Offit, Mark E. Robson, Bryson W. Katona
Publikováno v:
Journal of Genetic Counseling. 32:342-350
Germline genetic testing for inherited cancer risk is increasingly being performed with multigene panel testing with MUTYH often included on colorectal cancer- and polyposis-focused panels, as well as on broader pan-cancer panels. With up to 1%-2% of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be66c081cf121151f6cf16038f6be542
https://doi.org/10.1002/jgc4.1641
https://doi.org/10.1002/jgc4.1641
PURPOSE: This paper describes the acceptability and generalizability of an evidenced-based peer-led asthma self-management program. DESIGN AND METHODS: Adolescents with persistent asthma (n=259, ages 12–17 years) from three urban cities participate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::baf2ddd0eb10a4fe2823e15e5a20f3a1
https://europepmc.org/articles/PMC6501823/
https://europepmc.org/articles/PMC6501823/
Autor:
James Ding, JoEllen Weaver, Anh D. Le, Daniel J. Rader, Abigail Doucette, Susan M. Domchek, Rachel L. Kember, Peter Gabriel, Michael V. McLaughlin, Jacquelyn Powers, Daniel J. Lee, Renae Judy, Vivek Narayan, Lauren E. Schwartz, Kara N. Maxwell, Emily Feld, Scott M. Damrauer, Pauleen Sanchez
Publikováno v:
Journal of Clinical Oncology. 38:1576-1576
1576 Background: Approximately 5% of localized PCa and 12% of metastatic PCa are associated with germline mutations in DNA repair genes. The National Comprehensive Cancer Network (NCCN) issued genetic testing guidelines to identify PCa patients (pts)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b073de88a7e93d6f6c0e5aa507b57ce7
https://doi.org/10.1200/jco.2020.38.15_suppl.1576
https://doi.org/10.1200/jco.2020.38.15_suppl.1576
Autor:
Dana Farengo Clark, Judy Garber, Jada G. Hamilton, Sarah R. Kane, Fergus J. Couch, Temima Wildman, Susan M. Domchek, Kenneth Offit, Margaret S. Merrill, Jamie Brower, Jessica Ebrahimzadeh, Mark E. Robson, Pauleen Sanchez
Publikováno v:
Journal of Clinical Oncology. 38:e13680-e13680
e13680 Background: Multiplex genetic testing (MGT) simultaneously analyzes multiple cancer susceptibility genes and can reveal genetic variants of uncertain significance (VUS) that have unclear associations with cancer risks. Little is known about ho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46bff16cc4c6ed0a64d40245355d40b9
https://doi.org/10.1200/jco.2020.38.15_suppl.e13680
https://doi.org/10.1200/jco.2020.38.15_suppl.e13680