Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Karen A, Cadoo"'
Autor:
Robert F. Power, Damien E. Doherty, Roberta Horgan, Pat Fahey, David J. Gallagher, Maeve A. Lowery, Karen A. Cadoo
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 22, Iss 1, Pp 1-10 (2024)
Abstract Background Lynch syndrome is the most common cause of hereditary colorectal and endometrial cancer. Lifestyle modification may provide an opportunity for adjunctive cancer prevention. In this study, we aimed to characterise modifiable risk f
Externí odkaz:
https://doaj.org/article/d66eaffb320143358fda5da9460382f0
Autor:
Fionnuala Crowley, Karen A. Cadoo, Sarah Chiang, Diana L. Mandelker, Raazi Bajwa, Alexia Iasonos, Qin C. Zhou, Kathryn M. Miller, Martee L. Hensley, Roisin E. O'Cearbhaill
Publikováno v:
Gynecologic Oncology Reports, Vol 40, Iss , Pp 100980- (2022)
Objectives: Endometrial stromal sarcomas (ESS) are rare, accounting for
Externí odkaz:
https://doaj.org/article/1a67004b452b44ee8d5f7f3200f45c2c
Autor:
Harini Veeraraghavan, Claire F. Friedman, Deborah F. DeLair, Josip Ninčević, Yuki Himoto, Silvio G. Bruni, Giovanni Cappello, Iva Petkovska, Stephanie Nougaret, Ines Nikolovski, Ahmet Zehir, Nadeem R. Abu-Rustum, Carol Aghajanian, Dmitriy Zamarin, Karen A. Cadoo, Luis A. Diaz, Mario M. Leitao, Vicky Makker, Robert A. Soslow, Jennifer J. Mueller, Britta Weigelt, Yulia Lakhman
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-10 (2020)
Abstract To evaluate whether radiomic features from contrast-enhanced computed tomography (CE-CT) can identify DNA mismatch repair deficient (MMR-D) and/or tumor mutational burden-high (TMB-H) endometrial cancers (ECs). Patients who underwent targete
Externí odkaz:
https://doaj.org/article/039f6ea3eee241349cd91ff919a41db5
Autor:
Anastasia, Navitski, Duaa H, Al-Rawi, Vicky, Makker, Britta, Weigelt, Dmitriy, Zamarin, Ying, Liu, Angela G, Arnold, M Herman, Chui, Diana L, Mandelker, Michael, Walsh, Deborah F, DeLair, Karen A, Cadoo, Roisin E, O'Cearbhaill
Publikováno v:
JCO precision oncology. 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4167503b09e576bedb813726f11ddab8
https://pubmed.ncbi.nlm.nih.gov/36265117
https://pubmed.ncbi.nlm.nih.gov/36265117
Autor:
Sushmita Gordhandas, Eric Rios-Doria, Karen A Cadoo, Amanda Catchings, Anna Maio, Yelena Kemel, Margaret Sheehan, Megha Ranganathan, Dina Green, Anjali Aryamvally, Angela G Arnold, Erin Salo-Mullen, Beryl Manning-Geist, Tiffany Sia, Pier Selenica, Arnaud Da Cruz Paula, Chad Vanderbilt, Maksym Misyura, Mario M Leitao, Jennifer J Mueller, Vicky Makker, Maria Rubinstein, Claire F Friedman, Qin Zhou, Alexia Iasonos, Alicia Latham, Maria I Carlo, Yonina R Murciano-Goroff, Marie Will, Michael F Walsh, Shirin Issa Bhaloo, Lora H Ellenson, Ozge Ceyhan-Birsoy, Michael F Berger, Mark E Robson, Nadeem Abu-Rustum, Carol Aghajanian, Kenneth Offit, Zsofia Stadler, Britta Weigelt, Diana L Mandelker, Ying L Liu
Publikováno v:
JNCI: Journal of the National Cancer Institute. 115:560-569
Background We sought to determine the prevalence of germline pathogenic variants (gPVs) in unselected patients with endometrial cancer (EC), define biallelic gPVs within tumors, and describe their associations with clinicopathologic features. Methods
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec9f316b2b3f5be8abdd95005032897d
https://doi.org/10.1093/jnci/djad016
https://doi.org/10.1093/jnci/djad016
Autor:
Paulina Cybulska, Marina Stasenko, Raanan Alter, Vicky Makker, Karen A. Cadoo, Yukio Sonoda, Nadeem R. Abu-Rustum, Jennifer J. Mueller, Mario M. Leitao, Jr.
Publikováno v:
Gynecologic Oncology Reports, Vol 26, Iss , Pp 87-90 (2018)
Objective: To report characteristics of patients with low-grade endometrioid endometrial carcinoma (EC) who develop brain metastases. Methods: We retrospectively identified all patients treated at our institution for FIGO grades 1/2 EC from 1/2000–
Externí odkaz:
https://doaj.org/article/e9a0fe5b72dd4783a0910a5ba87e6b45
Autor:
Bernard H. Bochner, Maria Carlo, Dean F. Bajorin, Michael F. Berger, Zsofia K. Stadler, Mark E. Robson, Kenneth Offit, Irina Ostrovnaya, David B. Solit, Gopakumar V. Iyer, Jonathan E. Rosenberg, Hikmat Al-Ahmadie, Jonathan A. Coleman, Karen A. Cadoo, Michael F. Walsh, Liying Zhang, Yelena Kemel, Diana Mandelker, Michal Wiseman, Manuel R. de Jesus Escano, Hong Truong, Nima Almassi, Timothy Clinton, Emily Bochner, Aleksandra Walasek, Vijai Joseph, Aliya Khurram, Chaitanya Bandlamudi, Preethi Srinivasan, Karissa Whiting, Eugene J. Pietzak
Supplementary Data from Inherited Germline Cancer Susceptibility Gene Variants in Individuals with Non–Muscle-Invasive Bladder Cancer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4064fd0e375df436c79f8f5c894e0e9
https://doi.org/10.1158/1078-0432.22488579.v1
https://doi.org/10.1158/1078-0432.22488579.v1
Autor:
Bernard H. Bochner, Maria Carlo, Dean F. Bajorin, Michael F. Berger, Zsofia K. Stadler, Mark E. Robson, Kenneth Offit, Irina Ostrovnaya, David B. Solit, Gopakumar V. Iyer, Jonathan E. Rosenberg, Hikmat Al-Ahmadie, Jonathan A. Coleman, Karen A. Cadoo, Michael F. Walsh, Liying Zhang, Yelena Kemel, Diana Mandelker, Michal Wiseman, Manuel R. de Jesus Escano, Hong Truong, Nima Almassi, Timothy Clinton, Emily Bochner, Aleksandra Walasek, Vijai Joseph, Aliya Khurram, Chaitanya Bandlamudi, Preethi Srinivasan, Karissa Whiting, Eugene J. Pietzak
Purpose:Identification of inherited germline variants can guide personalized cancer screening, prevention, and treatment. Pathogenic and likely pathogenic (P/LP) germline variants in cancer predisposition genes are frequent among patients with locall
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59ebbf4443292e7a701bab0be1872e8f
https://doi.org/10.1158/1078-0432.c.6532764
https://doi.org/10.1158/1078-0432.c.6532764
Autor:
Semanti Mukherjee, Chaitanya Bandlamudi, Matthew D. Hellmann, Yelena Kemel, Esther Drill, Hira Rizvi, Kaitlyn Tkachuk, Aliya Khurram, Michael F. Walsh, Marjorie G. Zauderer, Diana Mandelker, Sabine Topka, Ahmet Zehir, Preethi Srinivasan, Myvizhi Esai Selvan, Maria I. Carlo, Karen A. Cadoo, Alicia Latham, Jada G. Hamilton, Ying L. Liu, Steven M. Lipkin, Sami Belhadj, Gareth L. Bond, Zeynep H. Gümüş, Robert J. Klein, Marc Ladanyi, David B. Solit, Mark E. Robson, David R. Jones, Mark G. Kris, Joseph Vijai, Zsofia K. Stadler, Christopher I. Amos, Barry S. Taylor, Michael F. Berger, Charles M. Rudin, Kenneth Offit
Publikováno v:
Cancer Epidemiol Biomarkers Prev
Background: The genetic factors that modulate risk for developing lung cancer have not been fully defined. Here, we sought to determine the prevalence and clinical significance of germline pathogenic/likely pathogenic variants (PV) in patients with a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f14b3108bc280a9e40a27f4e7b70806
https://doi.org/10.1158/1055-9965.epi-21-1287
https://doi.org/10.1158/1055-9965.epi-21-1287
Autor:
David M. Hyman, Christopher M. Haqq, Willis H. Navarro, Drew W. Rasco, Joyce F. Liu, Karen A. Cadoo, Vicky Makker, Nicholas A. Cangemi, Jessica J. Tao
Supplementary Legend
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d6b016706b2cbd200409c2cca3ee589
https://doi.org/10.1158/1078-0432.22471076
https://doi.org/10.1158/1078-0432.22471076