Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jill, Krejdovsky"'
Autor:
Arlene Button, Cynthia Lim, Virginia Speare, Kyle Allen, Lindsey Stobie, Mary Linton B. Peters, Eve Karloski, Jill S. Dolinsky, Kim DeLeonardis, Beth Dudley, Jill Krejdovsky, Erkut Borazanci, Yuan Tian, Randall E. Brand, Nadine Tung
Publikováno v:
Cancer. 125:2488-2496
BACKGROUND Germline genetic testing currently is recommended for patients with pancreatic ductal adenocarcinoma (PDAC). In the current study, the authors assessed how often results are communicated to first-degree relatives within 3 months and the em
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76955e0459b1cd030684306f32a8b135
https://doi.org/10.1002/cncr.32077
https://doi.org/10.1002/cncr.32077
Uptake in genetic testing in patients with pancreatic cancer with oncologist-driven testing protocol
Autor:
Traci King, Page Widick, Rodrigo Paredes, Oliver Klein, Jill Krejdovsky, Nadine M. Tung, Mary Linton Bounetheau Peters
Publikováno v:
Journal of Clinical Oncology. 40:33-33
33 Background: The objective was to compare the uptake of genetic testing in patients with pancreatic adenocarcinoma (PDAC) seen at a single center (1) before the 2019 NCCN recommendation of universal screening for genetic mutations in all new PDAC d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6b37b9863c5ae35f49ff99e4c4dac07
https://doi.org/10.1200/jco.2022.40.28_suppl.033
https://doi.org/10.1200/jco.2022.40.28_suppl.033
Autor:
Jill Krejdovsky, Mary Helen Black, James Ohr, Holly LaDuca, Mary Linton B. Peters, A. James Moser, Arlene Colvin, Nadine Tung, Eve Karloski, Jill S. Dolinsky, Weijing Sun, Virginia Speare, John C. Rhee, Nathan Bahary, Kim DeLeonardis, Melissa E. Hogg, Amer H. Zureikat, Kenneth H. Lee, James Cheng Yen Lee, Randall E. Brand, Beth Dudley, Allan Tsung, Herbert J. Zeh, Lindsey Stobie, Erkut Borazanci, Cynthia Lim, Emily Dalton
Publikováno v:
Cancer. 124:3520-3527
BACKGROUND The objective of this study was to investigate the prevalence of pathogenic germline variants (PGVs) in 32 cancer susceptibility genes in individuals with newly diagnosed pancreatic ductal adenocarcinoma (PDAC). A key secondary objective w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::deea147ea8100e362dc752ee1007e461
https://doi.org/10.1002/cncr.31628
https://doi.org/10.1002/cncr.31628
Autor:
Randall, Brand, Erkut, Borazanci, Virginia, Speare, Beth, Dudley, Eve, Karloski, Mary Linton B, Peters, Lindsey, Stobie, Nathan, Bahary, Herbert, Zeh, Amer, Zureikat, Melissa, Hogg, Kenneth, Lee, Allan, Tsung, John, Rhee, James, Ohr, Weijing, Sun, James, Lee, A James, Moser, Kim, DeLeonardis, Jill, Krejdovsky, Emily, Dalton, Holly, LaDuca, Jill, Dolinsky, Arlene, Colvin, Cynthia, Lim, Mary Helen, Black, Nadine, Tung
Publikováno v:
Cancer. 124(17)
The objective of this study was to investigate the prevalence of pathogenic germline variants (PGVs) in 32 cancer susceptibility genes in individuals with newly diagnosed pancreatic ductal adenocarcinoma (PDAC). A key secondary objective was to evalu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::28e5bef24ab10c3d1d35713ee24fbc8b
https://pubmed.ncbi.nlm.nih.gov/30067863
https://pubmed.ncbi.nlm.nih.gov/30067863
Autor:
Kristin Sedgwick, Kirsten Timms, Benjamin B. Roa, Nadine Tung, Richard J. Wenstrup, Anne-Renee Hartman, Brian Allen, Judy Garber, Kathleen A. Soltis, Leif W. Ellisen, Jill Krejdovsky, Christina I. Herold, Chiara Battelli, Kim DeLeonardis, Satish Bhatnagar, Karla R. Bowles, Rajesh R. Kaldate
Publikováno v:
Cancer. 121:25-33
BACKGROUND Next-generation sequencing (NGS) allows for simultaneous sequencing of multiple cancer susceptibility genes and, for an individual, may be more efficient and less expensive than sequential testing. The authors assessed the frequency of del
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6467372be16c4bd5357faaffe1605274
https://doi.org/10.1002/cncr.29010
https://doi.org/10.1002/cncr.29010
Autor:
Nadine, Tung, Chiara, Battelli, Brian, Allen, Rajesh, Kaldate, Satish, Bhatnagar, Karla, Bowles, Kirsten, Timms, Judy E, Garber, Christina, Herold, Leif, Ellisen, Jill, Krejdovsky, Kim, DeLeonardis, Kristin, Sedgwick, Kathleen, Soltis, Benjamin, Roa, Richard J, Wenstrup, Anne-Renee, Hartman
Publikováno v:
Cancer. 121(1)
Next-generation sequencing (NGS) allows for simultaneous sequencing of multiple cancer susceptibility genes and, for an individual, may be more efficient and less expensive than sequential testing. The authors assessed the frequency of deleterious ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a7e69fa73e10243c274bc4937bcf3f28
https://pubmed.ncbi.nlm.nih.gov/25186627
https://pubmed.ncbi.nlm.nih.gov/25186627
Autor:
Kristin Sedgwick, Jill Krejdovsky, Lindsey Stobie, Phil Connors, Kim DeLeonardis, Nadine Tung, Katherine Clifton
Publikováno v:
Journal of Clinical Oncology. 34:e13107-e13107
e13107Background: The utility of genetic testing for germline mutations in high-penetrance cancer susceptibility genes is well established. However, the clinical utility of mutations in more moderate-penetrance genes is less clear. The aim of this st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8417950425ba29f2858cf67dea1af29
https://doi.org/10.1200/jco.2016.34.15_suppl.e13107
https://doi.org/10.1200/jco.2016.34.15_suppl.e13107