Výsledky vyhledávání - "Megan Ensinger"

Akademický článek

A multicenter study of clinical impact of variant of uncertain significance reclassification in breast, ovarian and colorectal cancer susceptibility genes

Autor: Sukh Makhnoon, Brooke Levin, Megan Ensinger, Kristin Mattie, Robert J. Volk, Zhongming Zhao, Tito Mendoza, Sanjay Shete, Laila Samiian, Generosa Grana, Andrew Grainger, Banu Arun, Brian H. Shirts, Susan K. Peterson

Publikováno v: Cancer Medicine, Vol 12, Iss 3, Pp 2875-2884 (2023)

Abstract Background Clinical interpretation of genetic test results is complicated by variants of uncertain significance (VUS) that have an unknown impact on health but can be clarified through reclassification. There is little empirical evidence reg

Externí odkaz: https://doaj.org/article/acfe02508a074b7284c546f73e104e7b

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Use of breast surveillance between women with pathogenic variants and variants of uncertain significance in breast cancer susceptibility genes

Autor: Sukh Makhnoon, Minxing Chen, Brooke Levin, Megan Ensinger, Kristin D. Mattie, Generosa Grana, Sanjay Shete, Banu K. Arun, Susan K. Peterson

Publikováno v: Cancer. 128:3709-3717

Use of surveillance mammography and magnetic resonance imaging (MRI) has been understudied among women with variant of uncertain significance (VUS) compared to pathogenic and likely pathogenic variants (P/LP).Using data from two cancer settings, we c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de7b35ba0a27859de8029dc6f8d115d8
https://doi.org/10.1002/cncr.34429

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A multicenter study of clinical impact of variant of uncertain significance reclassification in breast, ovarian and colorectal cancer susceptibility genes

Publikováno v: Cancer medicineREFERENCES.

10512 Background: Up to 10% of all cancers are attributable to germline mutations and identifying mutation carriers is critical for cancer prevention. Clinical interpretation of genetic test results is complicated by variants of uncertain significanc

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff5a731d2e3a106f0b19d23678c50aa4
https://pubmed.ncbi.nlm.nih.gov/36426404

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Abstract P6-02-04: Use of breast surveillance between women with pathogenic variants and variants of uncertain significance in breast cancer susceptibility genes

Autor: Sukh Makhnoon, Minxing Chen, Brooke Levin, Megan Ensinger, Kristin Mattie, Generosa Grana, Sanjay Shete, Banu K. Arun, Susan K. Peterson

Publikováno v: Cancer Research. 83:P6-02

Background: Surveillance is a fundamental tool in the early detection and secondary prevention of many cancers. For women at increased genetic risk of breast cancer, mammography and breast magnetic resonance imaging (MRI) serve as the standard screen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e434e3394f8f26698f8e556cafbf19d6
https://doi.org/10.1158/1538-7445.sabcs22-p6-02-04

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Development and Initial Assessment of a Patient Education Video about Pharmacogenetics

Autor: Megan Ensinger, Nancy P. Callanan, Susanne B. Haga, Rachel Mills

Publikováno v: Journal of Personalized Medicine, Vol 7, Iss 2, p 4 (2017)
Journal of Personalized Medicine; Volume 7; Issue 2; Pages: 4
Journal of Personalized Medicine

As few patient-friendly resources about pharmacogenetics are currently available, we aimed to create and assess a patient educational video on pharmacogenetic testing. A primary literature and resources review was conducted to inform the content and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2598ad654c46ae67eee34b701197744a
https://doi.org/10.3390/jpm7020004

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