Search Results - "Klint, Margaret"

Exome Sequencing Identifies Carriers of the Autosomal Dominant Cancer Predisposition Disorders Beyond Current Practice Guideline Recommendations by Samadder, N Jewel, Gay, Emily, Lindpere, Vanda, Bublitz, Michelle L, Bandel, Lorelei A, Armasu, Sebastian M, Vierkant, Robert A, Ferber, Matthew J, Klee, Eric W, Larson, Nicholas B, Kruisselbrink, Teresa M, Egan, Jan B, Kemppainen, Jennifer L, Bidwell, Jessa S, Anderson, Jennifer L, McAllister, Tammy M, Walker, T'Nita S, Kunze, Katie L, Golafshar, Michael A, Klint, Margaret A, Presutti, Richard J, Bobo, William V, Sekulic, Aleksander, Summer-Bolster, Jolene M, Willman, Cheryl L, Lazaridis, Konstantinos N

“…The autosomal dominant cancer predisposition disorders hereditary breast and ovarian cancer (HBOC) and Lynch syndrome (LS) are genetic conditions for which…”
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Comparison of Universal Genetic Testing vs Guideline-Directed Targeted Testing for Patients With Hereditary Cancer Syndrome by Samadder, N Jewel, Riegert-Johnson, Douglas, Boardman, Lisa, Rhodes, Deborah, Wick, Myra, Okuno, Scott, Kunze, Katie L, Golafshar, Michael, Uson, Jr, Pedro L S, Mountjoy, Luke, Ertz-Archambault, Natalie, Patel, Neej, Rodriguez, Eduardo A, Lizaola-Mayo, Blanca, Lehrer, Michael, Thorpe, Cameron S, Yu, Nathan Y, Esplin, Edward D, Nussbaum, Robert L, Sharp, Richard R, Azevedo, Cindy, Klint, Margaret, Hager, Megan, Macklin-Mantia, Sarah, Bryce, Alan H, Bekaii-Saab, Tanios S, Sekulic, Aleksandar, Stewart, A Keith

“…Hereditary factors play a key role in the risk of developing several cancers. Identification of a germline predisposition can have important implications for…”
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Germline Cancer Susceptibility Gene Testing in Unselected Patients With Colorectal Adenocarcinoma: A Multicenter Prospective Study by Uson, Pedro L.S., Riegert-Johnson, Douglas, Boardman, Lisa, Kisiel, John, Mountjoy, Luke, Patel, Neej, Lizaola-Mayo, Blanca, Borad, Mitesh J., Ahn, Daniel, Sonbol, Mohamad B., Jones, Jeremy, Leighton, Jonathan A., Gurudu, Suryakanth, Singh, Harminder, Klint, Margaret, Kunze, Katie L., Golafshar, Michael A., Esplin, Ed D., Nussbaum, Robert L., Stewart, A. Keith, Bekaii-Saab, Tanio S., Jewel Samadder, Niloy

“…Hereditary factors play a role in the development of colorectal cancer (CRC). Identification of germline predisposition can have implications on treatment and…”
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Universal genetic testing versus guideline-directed testing for hereditary cancer syndromes among traditionally underrepresented patients in a community oncology program by Jones, Jeremy Clifton, Coston, Tucker, Kunze, Katie, Golafshar, Michael A., Rao, Rohit, Wysokinska, Ewa Maria, Johnson, Elizabeth, Esplin, Edward D., Nussbaum, Robert Luke, Heald, Brandie, Klint, Margaret, Barrus, Kathleen, Bekaii-Saab, Tanios S., Dronca, Roxana Stefania, Samadder, Jewel

“…10588 Background: Detection of pathogenic germline variants (PGVs) has implications for cancer screening, prognostication, treatment selection, clinical trial…”
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Abstract P056: Germline cancer susceptibility gene testing in unselected patients with soft tissue sarcoma: a multi-center prospective study by Ailts, Isaak, Golafshar, Michael A., Kunze, Katie L., Klint, Margaret, Barrus, Kathleen, Nussbaum, Samuel, Esplin, Edward, Leach, Brandie, Young, Sarah, Samadder, Niloy Jewel, Seetharam, Mahesh

“…Abstract Sarcomas are rare heterogenous mesenchymal tumors with over 75 different subtypes, with varying biology and outcomes, with no clear inciting factor in…”
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Germline Genetic Testing in Unselected Squamous and Non-Squamous Head and Neck Cancers by Brake, Daniela A, Idler, Beau M, Kunze, Katie L, Golafshar, Michael A, Heald, Brandie, Young, Sarah, Klint, Margaret, Barrus, Kathleen, Esplin, Edward D, Nussbaum, Robert L, Samadder, N Jewel, Hinni, Michael L, Chang, Brent A

“…This study describes the prevalence of pathogenic germline variants (PGVs) in head and neck cancer patients, the incremental yield compared to a…”
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Effect of access to germline genetic testing on pancreatic cancer precision treatment across disease stage and ethnicity by Esplin, Edward D., Truty, Rebecca, Yang, Shan, Nielsen, Sarah M., Klint, Margaret, Lincoln, Stephen E, Ngo, Nhu, Das, Kingshuk, Samadder, Jewel, Nussbaum, Robert Luke

“…Abstract only e16783 Background: PARP inhibitor (PARPi) treatment was recently approved for pancreatic cancer (PaCa) patients with germline mutations in 2 DNA…”
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Abstract PD10-05: Universal genetic testing in breast cancer patients: A multi-center prospective study by Ernst, Brenda, Ertz-Archambault, Natalie, Rhodes, Deborah J, Northfelt, Donald W, Wick, Myra, Riegert-Johnson, Douglas L, Okuno, Scott, Kunze, Katie, Golafshar, Michael, Azevedo, Cindy M, Junior, PLS Uson, Esplin, ED, Nussbaum, Robert, Klint, Margaret, Mantia, Sarah, Hager, Megan, Stewart, Keith, Samadder, Niloy Jewel

“…Abstract Background: Hereditary factors play a key role in the risk of developing breast cancers. Identification of a germline predisposition can have…”
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Clinical Impact of Pathogenic Germline Variants in Pancreatic Cancer: Results From a Multicenter, Prospective, Universal Genetic Testing Study by Uson, Pedro L. S., Samadder, N. Jewel, Riegert-Johnson, Douglas, Boardman, Lisa, Borad, Mitesh J., Ahn, Daniel, Sonbol, Mohamad B., Faigel, Douglas O., Fukami, Norio, Pannala, Rahul, Kunze, Katie, Golafshar, Michael, Klint, Margaret, Esplin, Edward D., Nussbaum, Robert L., Stewart, A. Keith, Bekaii-Saab, Tanios

“…To report the prevalence and outcomes of unselected pancreatic cancer (PC) patients with pathogenic/likely pathogenic germline variants (PGVs) detected using a…”
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Universal Genetic Testing vs. Guideline-Directed Testing for Hereditary Cancer Syndromes Among Traditionally Underrepresented Patients in a Community Oncology Program by Jones, Jeremy C, Golafshar, Michael A, Coston, Tucker W, Rao, Rohit, Wysokinska, Ewa, Johnson, Elizabeth, Esplin, Edward D, Nussbaum, Robert L, Heald, Brandie, Klint, Margaret, Barrus, Kathleen, Uson, Jr, Pedro L, Nguyen, Cuong C, Colon-Otero, Gerald, Bekaii-Saab, Tanios S, Dronca, Roxana, Kunze, Katie L, Samadder, N Jewel

“…Background Detection of pathogenic germline variants (PGVs) has implications for cancer screening, prognosis, treatment selection, clinical trial enrollment,…”
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Abstract 1921: Universal genetic testing for hereditary cancer syndromes in an under-represented minority population by Khadarian, Kevork A., Pisipati, Sailaja, Jones, Jeremy C., Colon-Otero, Gerardo, Northfelt, Donald W., Gary, Lindsey, Ekpoh, Idara U., Moreno, Giovanna G., Esplin, Edward D., Nussbaum, Robert, Heald, Brandie, Klint, Margaret A., Barrus, Kathleen A., Bekaii-Saab, Tanios S., Sekulic, Aleksandar, Golafshar, Michael A., Kunze, Katie L., Willman, Cheryl L., Lazaridis, Konstantinos N., Samadder, Niloy Jewel

“…Abstract Hereditary factors play a role in the development of several cancers. Identification of germline predisposition can have implications for treatment…”
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Abstract 5768: Genetic screening in a tertiary medical center identifies carriers of cancer predisposition diseases that would be missed by clinical guidelines by Gay, Emily, Samadder, Niloy Jewel, Bublitz, Michelle L., Peterson, Melanie M., Wilson, Tammy A., Bandel, Lorelei A., Armasu, Sebastian M., Vierkant, Robert A., Ferber, Matthew J., Klee, Eric W., Larson, Nicholas B., Kruisselbrink, Teresa M., Curry, Timothy B., Egan, Jan B., Kemppainen, Jennifer L., Bidwell, Jessa S., Anderson, Jennifer L., McAllister, Tammy M., Walker, T'Nita S., Kunze, Katie L., Lindpere, Vanda, Golafshar, Michael A., Klint, Margaret, Presutti, Richard J., Bobo, William V., Sekulic, Aleksander, Bolster, Jolene M. Summer, Willman, Cheryl L., Lazaridis, Konstantinos N.

“…Abstract Two inherited autosomal dominant cancer predisposition conditions - BRCA related hereditary breast and ovarian cancer (HBOC) and Lynch syndrome (LS) -…”
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