Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Rebecca Yee Bassett"'
Autor:
Windy Berkofsky-Fessler, Constance Murphy, Deborah Pencarinha, Jessica K. Booker, Rebecca Yee Bassett, Haiyan Wan, Mingjuan Liao, Melanie Hussong, Nina Sanapareddy, Elisabeth McKeen, Kathleen S. Hruska, Patricia D. Murphy, Rachel Nusbaum, Erica S. Rinella, Rachel T. Klein, Zhixiong Xu, Joaquin Villar, Lisa R. Susswein, Maria L Cremona
Publikováno v:
Cancer Research. 75:P4-12
Introduction: Expansion of genetic testing technologies has brought multi-gene panels for cancer susceptibility into the clinic; however, the clinical utility of these next-generation sequencing (NGS) panels is largely unknown. Hypothesis: We hypothe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e2b9d08ab3081576ea5b46673fb7fa3
https://doi.org/10.1158/1538-7445.sabcs14-p4-12-05
https://doi.org/10.1158/1538-7445.sabcs14-p4-12-05
Autor:
Leslie R. Boyd, Katherine J. Sapra, Rachelle Lorenz Chambers, Stephanie V. Blank, John P. Curtin, Bhavana Pothuri, Melissa K. Frey, Sarah H. Kim, Jessica Martineau, Rachel Sobolev, Gabriella Sandler, Rebecca Yee Bassett
Publikováno v:
Gynecologic oncology. 146(1)
Objective To evaluate the results of multigene panel testing among Ashkenazi Jewish compared with non-Ashkenazi Jewish patients. Methods We reviewed the medical records for all patients who underwent multigene panel testing and targeted BRCA1/2 testi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9925a94a0f7bffeea5e9218e47e7b989
https://pubmed.ncbi.nlm.nih.gov/28495237
https://pubmed.ncbi.nlm.nih.gov/28495237
Autor:
Stephanie V. Blank, Jessica Martineau, Melissa K. Frey, Sarah H. Kim, Rebecca Yee Bassett, Jing-Yi Chern, Emily Dalton
Publikováno v:
Gynecologic oncology. 139(2)
Objective The availability of next-generation sequencing and identification of multiple cancer-related genes has caused a shift away from single gene testing towards multi-gene panel testing for hereditary cancer syndromes. However, the utility of pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe5f0e698136096dc55a6866865a8088
https://pubmed.ncbi.nlm.nih.gov/26296696
https://pubmed.ncbi.nlm.nih.gov/26296696
Autor:
Jessica Martineau, Sarah H. Kim, Melissa K. Frey, Rachel Sobolev, Rachelle Lorenz Chambers, G. Sandler, Rebecca Yee Bassett, Stephanie V. Blank
Publikováno v:
Gynecologic Oncology. 141:10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2992d5dfe4140dff842ca0898100ece4
https://doi.org/10.1016/j.ygyno.2016.04.055
https://doi.org/10.1016/j.ygyno.2016.04.055
Autor:
Jing-Yi Chern, Sarah S. Lee, Melissa K. Frey, Rebecca Yee Bassett, Stephanie V. Blank, Jessica Martineau
Publikováno v:
Journal of Clinical Oncology. 33:1555-1555
1555 Background: Among patients undergoing genetic testing for BRCA1/2 mutations, 7% will harbor a variant of uncertain significance (VUS), a finding with more emotional than clinical weight. The o...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28cc55ddbc88d9fbb094262b5be67ead
https://doi.org/10.1200/jco.2015.33.15_suppl.1555
https://doi.org/10.1200/jco.2015.33.15_suppl.1555
Publikováno v:
Journal of Clinical Oncology. 33:1536-1536
1536 Background: The availability of next-generation sequencing coupled with the recent discovery of multiple cancer-related genes has caused a shift away from single gene testing towards multi-gene panel testing for familial cancer syndromes. Howeve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1922ebfc43cb5e3344bca803d784bafd
https://doi.org/10.1200/jco.2015.33.15_suppl.1536
https://doi.org/10.1200/jco.2015.33.15_suppl.1536