Hasil Pencarian - Kenneth Offit

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  1. 1
    Heterozygous mutations in DNA repair genes and hereditary breast cancer: a question of power.

    Heterozygous mutations in DNA repair genes and hereditary breast cancer: a question of power. oleh Nathan A Ellis, Kenneth Offit

    Diterbitkan 2012-09-01
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  2. 2
    Tissue-Specific Enrichment of Lymphoma Risk Loci in Regulatory Elements.

    Tissue-Specific Enrichment of Lymphoma Risk Loci in Regulatory Elements. oleh James E Hayes, Gosia Trynka, Joseph Vijai, Kenneth Offit, Soumya Raychaudhuri, Robert J Klein

    Diterbitkan 2015-01-01
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  3. 3
    Genetics healthcare providers' experiences counseling patients with results from consumer genomic testing

    Genetics healthcare providers' experiences counseling patients with results from consumer genomic testing oleh Magan Trottier, Dina Green, Hannah Ovadia, Amanda Catchings, Julia Gruberg, Victoria Groner, Catherine Fanjoy, Sita Dandiker, Kathleen Blazer, Jada G. Hamilton, Kenneth Offit

    Diterbitkan 2024-08-01
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  4. 4
    Development of a novel measure of advanced cancer patients’ perceived utility of secondary germline findings from tumor genomic profiling

    Development of a novel measure of advanced cancer patients’ perceived utility of secondary germline findings from tumor genomic profiling oleh Jada G. Hamilton, Ibrahim H. Shah, Caroline Salafia, Elizabeth Schofield, Margaux Genoff Garzon, Kechna Cadet, Zsofia K. Stadler, Jennifer L. Hay, Kenneth Offit, Mark E. Robson

    Diterbitkan 2023-12-01
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  5. 5
    Genetic analysis of the early natural history of epithelial ovarian carcinoma.

    Genetic analysis of the early natural history of epithelial ovarian carcinoma. oleh Bhavana Pothuri, Mario M Leitao, Douglas A Levine, Agnès Viale, Adam B Olshen, Crispinita Arroyo, Faina Bogomolniy, Narciso Olvera, Oscar Lin, Robert A Soslow, Mark E Robson, Kenneth Offit, Richard R Barakat, Jeff Boyd

    Diterbitkan 2010-04-01
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  6. 6
    Assessment of SLX4 Mutations in Hereditary Breast Cancers.

    Assessment of SLX4 Mutations in Hereditary Breast Cancers. oleh Sohela Shah, Yonghwan Kim, Irina Ostrovnaya, Rajmohan Murali, Kasmintan A Schrader, Francis P Lach, Kara Sarrel, Rohini Rau-Murthy, Nichole Hansen, Liyng Zhang, Tomas Kirchhoff, Zsofia Stadler, Mark Robson, Joseph Vijai, Kenneth Offit, Agata Smogorzewska

    Diterbitkan 2013-01-01
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  7. 7
    Comprehensive detection of germline variants by MSK-IMPACT, a clinical diagnostic platform for solid tumor molecular oncology and concurrent cancer predisposition testing

    Comprehensive detection of germline variants by MSK-IMPACT, a clinical diagnostic platform for solid tumor molecular oncology and concurrent cancer predisposition testing oleh Donavan T. Cheng, Meera Prasad, Yvonne Chekaluk, Ryma Benayed, Justyna Sadowska, Ahmet Zehir, Aijazuddin Syed, Yan Elsa Wang, Joshua Somar, Yirong Li, Zarina Yelskaya, Donna Wong, Mark E. Robson, Kenneth Offit, Michael F. Berger, Khedoudja Nafa, Marc Ladanyi, Liying Zhang

    Diterbitkan 2017-05-01
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  8. 8
    Expanded genetic testing of GIST patients identifies high proportion of non-syndromic patients with germline alterations

    Expanded genetic testing of GIST patients identifies high proportion of non-syndromic patients with germline alterations oleh Diana Mandelker, Antonio Marra, Nikita Mehta, Pier Selenica, Zarina Yelskaya, Ciyu Yang, Joshua Somar, Miika Mehine, Maksym Misyura, Olca Basturk, Alicia Latham, Maria Carlo, Michael Walsh, Zsofia K. Stadler, Kenneth Offit, Chaitanya Bandlamudi, Meera Hameed, Ping Chi, Jorge S. Reis-Filho, Ozge Ceyhan-Birsoy

    Diterbitkan 2023-01-01
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  9. 9
    Reversion mutations in germline BRCA1/2-mutant tumors reveal a BRCA-mediated phenotype in non-canonical histologies

    Reversion mutations in germline BRCA1/2-mutant tumors reveal a BRCA-mediated phenotype in non-canonical histologies oleh Yonina R. Murciano-Goroff, Alison M. Schram, Ezra Y. Rosen, Helen Won, Yixiao Gong, Anne Marie Noronha, Yelena Y. Janjigian, Zsofia K. Stadler, Jason C. Chang, Soo-Ryum Yang, Diana Mandelker, Kenneth Offit, Michael F. Berger, Mark T. A. Donoghue, Chaitanya Bandlamudi, Alexander Drilon

    Diterbitkan 2022-11-01
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  10. 10
    Comparison of up-front cash cards and checks as incentives for participation in a clinician survey: a study within a trial

    Comparison of up-front cash cards and checks as incentives for participation in a clinician survey: a study within a trial oleh Lydia E. Pace, Yeonsoo S. Lee, Nadine Tung, Jada G. Hamilton, Camila Gabriel, Sahitya C. Raja, Colby Jenkins, Anthony Braswell, Susan M. Domchek, Heather Symecko, Kelsey Spielman, Beth Y. Karlan, Jenny Lester, Daniella Kamara, Jeffrey Levin, Kelly Morgan, Kenneth Offit, Judy Garber, Nancy L. Keating

    Diterbitkan 2020-08-01
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  11. 11
    Germline RAD51B variants confer susceptibility to breast and ovarian cancers deficient in homologous recombination

    Germline RAD51B variants confer susceptibility to breast and ovarian cancers deficient in homologous recombination oleh Jeremy Setton, Pier Selenica, Semanti Mukherjee, Rachna Shah, Isabella Pecorari, Biko McMillan, Isaac X. Pei, Yelena Kemel, Ozge Ceyhan-Birsoy, Margaret Sheehan, Kaitlyn Tkachuk, David N. Brown, Liying Zhang, Karen Cadoo, Simon Powell, Britta Weigelt, Mark Robson, Nadeem Riaz, Kenneth Offit, Jorge S. Reis-Filho, Diana Mandelker

    Diterbitkan 2021-10-01
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  12. 12
    P063: Prospective longitudinal validation of a breast cancer risk prediction model in a cohort of 130,058 individuals*

    P063: Prospective longitudinal validation of a breast cancer risk prediction model in a cohort of 130,058 individuals* oleh Brent Mabey, Elisha Hughes, Braden Probst, Holly Pederson, Timothy Simmons, Brian Morris, Brooke Hullinger, Susan Domchek, Charis Eng, Monique Gary, Jennifer Klemp, Semanti Mukherjee, Joseph Vijai, Kenneth Offit, Olufunmilayo Olopade, Sandhya Pruthi, Allison Kurian, Mark Robson, Pat Whitworth, Susanne Wagner, Jerry Lanchbury, Thomas Slavin, Alexander Gutin

    Diterbitkan 2023-01-01
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  13. 13
    Nucleotide excision repair deficiency is a targetable therapeutic vulnerability in clear cell renal cell carcinoma

    Nucleotide excision repair deficiency is a targetable therapeutic vulnerability in clear cell renal cell carcinoma oleh Aurel Prosz, Haohui Duan, Viktoria Tisza, Pranshu Sahgal, Sabine Topka, Gregory T. Klus, Judit Börcsök, Zsofia Sztupinszki, Timothy Hanlon, Miklos Diossy, Laura Vizkeleti, Dag Rune Stormoen, Istvan Csabai, Helle Pappot, Joseph Vijai, Kenneth Offit, Thomas Ried, Nilay Sethi, Kent W. Mouw, Sandor Spisak, Shailja Pathania, Zoltan Szallasi

    Diterbitkan 2023-11-01
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  14. 14
    Genetic variation in DNA repair pathways and risk of non-Hodgkin's lymphoma.

    Genetic variation in DNA repair pathways and risk of non-Hodgkin's lymphoma. oleh Justin Rendleman, Yevgeniy Antipin, Boris Reva, Christina Adaniel, Jennifer A Przybylo, Ana Dutra-Clarke, Nichole Hansen, Adriana Heguy, Kety Huberman, Laetitia Borsu, Ora Paltiel, Dina Ben-Yehuda, Jennifer R Brown, Arnold S Freedman, Chris Sander, Andrew Zelenetz, Robert J Klein, Yongzhao Shao, Mortimer Lacher, Joseph Vijai, Kenneth Offit, Tomas Kirchhoff

    Diterbitkan 2014-01-01
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  15. 15
    A Germline Variant on Chromosome 4q31.1 Associates with Susceptibility to Developing Colon Cancer Metastasis.

    A Germline Variant on Chromosome 4q31.1 Associates with Susceptibility to Developing Colon Cancer Metastasis. oleh Sanford D Markowitz, Nora L Nock, Stephanie L Schmit, Zsofia K Stadler, Vijai Joseph, Lu Zhang, Joseph E Willis, Peter Scacheri, Martina Veigl, Mark D Adams, Leon Raskin, John F Sullivan, Kelly Stratton, Jinru Shia, Nathan Ellis, Hedy S Rennert, Christopher Manschreck, Li Li, Kenneth Offit, Robert C Elston, Gadi Rennert, Stephen B Gruber

    Diterbitkan 2016-01-01
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  16. 16
    Diagnostic yield and clinical relevance of expanded genetic testing for cancer patients

    Diagnostic yield and clinical relevance of expanded genetic testing for cancer patients oleh Ozge Ceyhan-Birsoy, Gowtham Jayakumaran, Yelena Kemel, Maksym Misyura, Umut Aypar, Sowmya Jairam, Ciyu Yang, Yirong Li, Nikita Mehta, Anna Maio, Angela Arnold, Erin Salo-Mullen, Margaret Sheehan, Aijazuddin Syed, Michael Walsh, Maria Carlo, Mark Robson, Kenneth Offit, Marc Ladanyi, Jorge S. Reis-Filho, Zsofia K. Stadler, Liying Zhang, Alicia Latham, Ahmet Zehir, Diana Mandelker

    Diterbitkan 2022-08-01
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  17. 17
    Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies.

    Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies. oleh Joseph Vijai, Tomas Kirchhoff, Kasmintan A Schrader, Jennifer Brown, Ana Virginia Dutra-Clarke, Christopher Manschreck, Nichole Hansen, Rohini Rau-Murthy, Kara Sarrel, Jennifer Przybylo, Sohela Shah, Srujana Cheguri, Zsofia Stadler, Liying Zhang, Ora Paltiel, Dina Ben-Yehuda, Agnes Viale, Carol Portlock, David Straus, Steven M Lipkin, Mortimer Lacher, Mark Robson, Robert J Klein, Andrew Zelenetz, Kenneth Offit

    Diterbitkan 2013-01-01
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  18. 18
    Novel pedigree analysis implicates DNA repair and chromatin remodeling in multiple myeloma risk.

    Novel pedigree analysis implicates DNA repair and chromatin remodeling in multiple myeloma risk. oleh Rosalie G Waller, Todd M Darlington, Xiaomu Wei, Michael J Madsen, Alun Thomas, Karen Curtin, Hilary Coon, Venkatesh Rajamanickam, Justin Musinsky, David Jayabalan, Djordje Atanackovic, S Vincent Rajkumar, Shaji Kumar, Susan Slager, Mridu Middha, Perrine Galia, Delphine Demangel, Mohamed Salama, Vijai Joseph, James McKay, Kenneth Offit, Robert J Klein, Steven M Lipkin, Charles Dumontet, Celine M Vachon, Nicola J Camp

    Diterbitkan 2018-02-01
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  19. 19
    A recessive founder mutation in regulator of telomere elongation helicase 1, RTEL1, underlies severe immunodeficiency and features of Hoyeraal Hreidarsson syndrome.

    A recessive founder mutation in regulator of telomere elongation helicase 1, RTEL1, underlies severe immunodeficiency and features of Hoyeraal Hreidarsson syndrome. oleh Bari J Ballew, Vijai Joseph, Saurav De, Grzegorz Sarek, Jean-Baptiste Vannier, Travis Stracker, Kasmintan A Schrader, Trudy N Small, Richard O'Reilly, Chris Manschreck, Megan M Harlan Fleischut, Liying Zhang, John Sullivan, Kelly Stratton, Meredith Yeager, Kevin Jacobs, Neelam Giri, Blanche P Alter, Joseph Boland, Laurie Burdett, Kenneth Offit, Simon J Boulton, Sharon A Savage, John H J Petrini

    Diterbitkan 2013-08-01
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  20. 20
    The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk

    The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk oleh Thomas P. Slavin, Kara N. Maxwell, Jenna Lilyquist, Joseph Vijai, Susan L. Neuhausen, Steven N. Hart, Vignesh Ravichandran, Tinu Thomas, Ann Maria, Danylo Villano, Kasmintan A. Schrader, Raymond Moore, Chunling Hu, Bradley Wubbenhorst, Brandon M. Wenz, Kurt D’Andrea, Mark E. Robson, Paolo Peterlongo, Bernardo Bonanni, James M. Ford, Judy E. Garber, Susan M. Domchek, Csilla Szabo, Kenneth Offit, Katherine L. Nathanson, Jeffrey N. Weitzel, Fergus J. Couch

    Diterbitkan 2017-06-01
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