Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Angela Jacobson"'
Autor:
Brian H. Shirts, Peter G. Shields, Dan Jones, Lori Nelsen, Sameer Mahesh, Jo L. Freudenheim, Shyamal Bastola, Kisa Weeman, Yinong Liu, Electra D. Paskett, Esther H. Rehmus, Matthew F. Kalady, Wendy L. Frankel, Jeffrey Zangmeister, Paul J. Goodfellow, Brandie Heald, Christopher Bigley, Mitchell Haut, Shelly Cummings, Kristin Miller, Mark Arnold, Sharon Cole, Chaoyang Li, Albert de la Chapelle, Ian M. Paquette, Weiqiang Zhao, Rachel Pearlman, Ahmet Yilmaz, Filix Kencana, Heather Hampel, Peter P. Stanich, Albert Malcolm, Thomas W. Prior, Richard M. Goldberg, Joanna M. Brell, David J Draper, Aruna Gowda, Jason Bacher, Charles Bane, Ilene Lattimer, Angela Jacobson, Colin C. Pritchard, Benjamin Swanson
Publikováno v:
JCO Precis Oncol
PURPOSE Hereditary cancer syndromes infer high cancer risks and require intensive surveillance. Identification of high-risk individuals among patients with colorectal cancer (CRC) needs improvement. METHODS Three thousand three hundred ten unselected
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22454ae340b5efe29cea1172370f2579
https://doi.org/10.1200/po.20.00525
https://doi.org/10.1200/po.20.00525
Autor:
Dustin E, Bosch, Matthew M, Yeh, Stephen J, Salipante, Angela, Jacobson, Stacey A, Cohen, Eric Q, Konnick, Vera A, Paulson
Publikováno v:
JCO precision oncology. 6
Mismatch repair (MMR) immunohistochemistry (IHC) is frequently used to inform prognosis, select (immuno-)therapy, and identify patients for heritable cancer syndrome testing. However, false-negative and false-positive MMR IHC interpretations have bee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d8ceb5f07baffeba2799173956ef5968
https://pubmed.ncbi.nlm.nih.gov/36044719
https://pubmed.ncbi.nlm.nih.gov/36044719
Autor:
Dustin E. Bosch, Matthew M. Yeh, Stephen J. Salipante, Angela Jacobson, Stacey A. Cohen, Eric Q. Konnick, Vera A. Paulson
Publikováno v:
JCO Precision Oncology.
PURPOSE Mismatch repair (MMR) immunohistochemistry (IHC) is frequently used to inform prognosis, select (immuno-)therapy, and identify patients for heritable cancer syndrome testing. However, false-negative and false-positive MMR IHC interpretations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09df8e655a8dbd0666ad8ce511245f1c
https://doi.org/10.1200/po.22.00227
https://doi.org/10.1200/po.22.00227
Autor:
Heather Hampel, Brian H. Shirts, Lorraine V. Naylor, Margaret Miller, Colin C. Pritchard, Sarah A. Hall, Ming K. Lee, Kathleen A. Leppig, Robin L. Bennett, Robert J. Livingston, Jonathan F. Tait, Emily H. Turner, Cathleen Goetsch, Suleyman Gulsuner, Tom Walsh, Sheena M. Scroggins, Silvia Casadei, Mary Claire King, Stephen J. Salipante, Angela Jacobson, Fuki M. Hisama
Publikováno v:
Genetics in Medicine. 18:974-981
Screening multiple genes for inherited cancer predisposition expands opportunities for cancer prevention; however, reports of variants of uncertain significance (VUS) may limit clinical usefulness. We used an expert-driven approach, exploiting all av
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9df35b5c34df740e3761372e713fef2e
https://doi.org/10.1038/gim.2015.212
https://doi.org/10.1038/gim.2015.212
Autor:
Brian H. Shirts, Nathan Hickman, Lauren Thomas Garrett, Laura M. Amendola, Elisabeth A. Rosenthal, Angela Jacobson, Robin L. Bennett
Publikováno v:
Journal of Genetic Counseling
Multi-gene cancer panels often identify variants of uncertain clinical significance (VUS) that pose a challenge to health care providers in managing a patient's cancer risk. Family segregation analysis can yield powerful data to re-classify a VUS (as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6dbfbb491c21aa05f96642567bed1902
https://doi.org/10.1007/s10897-016-9993-2
https://doi.org/10.1007/s10897-016-9993-2
Autor:
Andrew S. McFaddin, Cigdem H. Ussakli, Anna Newlin, Christina M. Lockwood, Eric Q. Konnick, Peter P. Stanich, Brian H. Shirts, Stephanie More, Angela Jacobson, Colin C. Pritchard, Heather M. Byers, Jonathan F. Tait, Amanda Hamblett
Publikováno v:
JCO Precis Oncol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8372ae3e55c783c94559464d27a0da92
https://europepmc.org/articles/PMC7446443/
https://europepmc.org/articles/PMC7446443/
Autor:
Albert de la Chapelle, Ahmet Yilmaz, Brian H. Shirts, Colin C. Pritchard, Mallory Beightol, Jason Bacher, Heather Hampel, Rachel Pearlman, Wendy L. Frankel, Weiqiang Zhao, Angela Jacobson, Richard M. Goldberg, Electra D. Paskett, Dan Jones, Paul J. Goodfellow, Kristin Miller, Peter G. Shields
Publikováno v:
JAMA Oncol
Importance Universal tumor screening for Lynch syndrome (LS) in colorectal cancer (CRC) is recommended and involves up to 6 sequential tests. Somatic gene testing is performed on stage IV CRCs for treatment determination. The diagnostic workup for pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69acde0e05a6dfb351024a24d8783fdd
https://pubmed.ncbi.nlm.nih.gov/29801118
https://pubmed.ncbi.nlm.nih.gov/29801118
Autor:
Brian H. Shirts, Rachel Pearlman, Mary Claire King, Heather Hampel, John Michael O. Ranola, Colin C. Pritchard, Tom Walsh, Sarah Upham, Eric Q. Konnick, Angela Jacobson
Publikováno v:
American journal of human genetics. 103(1)
Present guidelines for classification of constitutional variants do not incorporate inferences from mutations seen in tumors, even when these are associated with a specific molecular phenotype. When somatic mutations and constitutional mutations lead
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::353e53d2b9f07bcf3fe8c8b1d99e607e
https://pubmed.ncbi.nlm.nih.gov/29887214
https://pubmed.ncbi.nlm.nih.gov/29887214
Autor:
William M. Grady, Robin L. Bennett, Melissa P. Upton, Angela Jacobson, Mercy Y. Laurino, Colin C. Pritchard, Gail P. Jarvik, Britta Sjoding, Deborah J. Bowen, Fuki M. Hisama, Lorraine V. Naylor, Wylie Burke, Stacey A. Cohen, Alessandro Fichera
Publikováno v:
Cancer. 122:393-401
BACKGROUND Lynch syndrome confers a hereditary predisposition to colorectal and other cancers. Universal tumor screening (UTS) for Lynch syndrome is recommended by several professional societies, but the implementation can be complex. This article de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::227c872a3fdb8bb23b91a3c37e35f523
https://doi.org/10.1002/cncr.29758
https://doi.org/10.1002/cncr.29758