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1 . Academic Journal
Genetic Testing Uptake among Ovarian Cancer Survivors in the Genetic Risk Analysis in Ovarian Cancer (GRACE) Study
저자
by
Larissa L. White
;
Jennifer K. Sawyer
;
Jamilyn M. Zepp
;
Yolanda K. Prado
;
Ana A. Reyes
, et al.
소스
Cancers, Vol 16, Iss 14, p 2563 (2024)
Open Access (DOAJ)
Web of Science
Scopus
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7 . Academic Journal
Recommended care and care adherence following a diagnosis of Lynch syndrome: a mixed-methods study
저자
by
Kathleen F. Mittendorf
;
Jessica Ezzell Hunter
;
Jennifer L. Schneider
;
Elizabeth Shuster
;
Alan F. Rope
, et al.
소스
Hereditary Cancer in Clinical Practice, Vol 17, Iss 1, Pp 1-13 (2019)
Open Access (BioMed Central)
Open Access (DOAJ)
Web of Science
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7 . Academic Journal
Patient and provider perspectives on adherence to and care coordination of lynch syndrome surveillance recommendations: findings from qualitative interviews
저자
by
Jennifer L. Schneider
;
Katrina A. B. Goddard
;
Kristin R. Muessig
;
James V. Davis
;
Alan F. Rope
, et al.
소스
Hereditary Cancer in Clinical Practice, Vol 16, Iss 1, Pp 1-10 (2018)
Open Access (BioMed Central)
Open Access (DOAJ)
Web of Science
Scopus
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7 . Academic Journal
Feasibility of a Traceback Approach for Using Pathology Specimens to Facilitate Genetic Testing in the Genetic Risk Analysis in Ovarian Cancer (GRACE) Study Protocol
저자
by
Tia L. Kauffman
;
Yolanda K. Prado
;
Ana A. Reyes
;
Jamilyn M. Zepp
;
Jennifer Sawyer
, et al.
소스
Journal of Personalized Medicine, Vol 11, Iss 11, p 1194 (2021)
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7 .
Development and early implementation of an Accessible, Relational, Inclusive and Actionable approach to genetic counseling: The ARIA model
저자
by
Galen Joseph
;
Benjamin S. Wilfond
;
Laura M. Amendola
;
Claudia Guerra
;
Barbara B. Biesecker
, et al.
소스
Patient education and counseling, vol 104, iss 5
Patient Educ Couns
Full Text (Clinical Key)
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7 .
Recommended care and care adherence following a diagnosis of Lynch syndrome: a mixed-methods study
저자
by
Jamilyn M. Zepp
;
Kellene M. Bergen
;
Louise S. Acheson
;
Susan K. Peterson
;
Georgia L. Wiesner
, et al.
소스
Hereditary Cancer in Clinical Practice, Vol 17, Iss 1, Pp 1-13 (2019)
Hereditary Cancer in Clinical Practice
Open Access (BioMed Central)
Open Access (OpenAIRE)
Web of Science
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7 .
Missense variants in TAF1 and developmental phenotypes: Challenges of determining pathogenicity
저자
by
Emma Wakeling
;
Quan Li
;
Laurence E. Walsh
;
Maria J. Guillen Sacoto
;
Julie Vogt
, et al.
소스
Hum Mutat
Open Access (OpenAIRE)
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7 .
Laboratory-related outcomes from integrating an accessible delivery model for hereditary cancer risk assessment and genetic testing in populations with barriers to access
저자
by
Laura M. Amendola
;
Elizabeth Shuster
;
Michael C. Leo
;
Michael O. Dorschner
;
Bradley A. Rolf
, et al.
소스
Genetics in medicine : official journal of the American College of Medical Genetics
. 24(6)
Full Text (ScienceDirect)
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Scopus
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7 .
Feasibility of a Traceback Approach for Using Pathology Specimens to Facilitate Genetic Testing in the Genetic Risk Analysis in Ovarian Cancer (GRACE) Study Protocol
저자
by
Suzanne Bianca Salas
;
Sandra Soo-Jin Lee
;
Nora B. Henrikson
;
Ana Reyes
;
Jessica Martucci
, et al.
소스
Journal of Personalized Medicine
Volume 11
Issue 11
Journal of Personalized Medicine, Vol 11, Iss 1194, p 1194 (2021)
Open Access (OpenAIRE)
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7 .
Response to Hamosh et al
저자
by
John M. Graham
;
Joseph T. Shieh
;
Alan F. Rope
;
Philip F Giampietro
;
Lynne M. Bird
, et al.
소스
Am J Hum Genet
Full Text (ScienceDirect)
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