Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Alicia Latham"'
Autor:
Ozge Ceyhan-Birsoy, Elise Fiala, Satshil Rana, Margaret Sheehan, Jennifer Kennedy, Zarina Yelskaya, Vikas Rai, Yirong Li, Ciyu Yang, Donna Wong, Ivelise Rijo, Jacklyn Casanova, Joshua Somar, Nikita Mehta, Hyeonjin Park, Silvana Ostafi, Kanika Arora, Angelika Padunan, Mark D. Ewalt, Umut Aypar, Panieh Terraf, Maksym Misyura, Sofia Haque, Gerald G. Behr, Tamanna Haque, Maria Sulis, Mark B. Geyer, Christopher Forlenza, Meghan C. Thompson, Maria Carlo, Alicia Latham, Ying Liu, Ahmet Zehir, Rose Brannon, Michael Berger, Luis A Diaz Jr, Ahmet Dogan, Marc Ladanyi, Kseniya Petrova-Drus, Khedoudja Nafa, Kenneth Offit, Maria Arcila, Zsofia K. Stadler, Michael F. Walsh, Diana Mandelker
Publikováno v:
Haematologica, Vol 999, Iss 1 (2024)
Not available.
Externí odkaz:
https://doaj.org/article/f666218e110145a987b006840114e720
Autor:
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
Publikováno v:
npj Precision Oncology, Vol 7, Iss 1, Pp 1-6 (2023)
Abstract Traditional genetic testing for patients with gastrointestinal stromal tumors (GISTs) focus on those with syndromic features. To assess whether expanded genetic testing of GIST patients could identify hereditary cancer predisposition, we ana
Externí odkaz:
https://doaj.org/article/8ed49bc9d2174d23ac73af0621960d66
Autor:
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
Publikováno v:
Genome Medicine, Vol 14, Iss 1, Pp 1-13 (2022)
Abstract Background Genetic testing (GT) for hereditary cancer predisposition is traditionally performed on selected genes based on established guidelines for each cancer type. Recently, expanded GT (eGT) using large hereditary cancer gene panels unc
Externí odkaz:
https://doaj.org/article/b27ebc51933945dda60cc3917da9b260
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 2, Pp n/a-n/a (2023)
Abstract Background Germline variants in the DNA mismatch repair (MMR) genes (MLH1, MSH2, MSH6, and PMS2) cause Lynch syndrome, an autosomal dominant hereditary cancer susceptibility syndrome. The risk for endometrial cancer is significantly higher i
Externí odkaz:
https://doaj.org/article/5f5b5db9029c43c68562281eb0dd665e
Autor:
Austin Y Shull, Alicia Latham-Schwark, Poornema Ramasamy, Kristin Leskoske, Dora Oroian, Marc R Birtwistle, Phillip J Buckhaults
Publikováno v:
PLoS ONE, Vol 7, Iss 8, p e43369 (2012)
BRAF(V600) inhibitors have offered a new gateway for better treatment of metastatic melanoma. However, the overall efficacy of BRAF(V600) inhibitors has been lower than expected in clinical trials, and many patients have shown resistance to the drug'
Externí odkaz:
https://doaj.org/article/7e04eaeb9f614ae28897f74bd0951a90
Autor:
Tiffany Y. Sia, Sushmita B. Gordhandas, Ozge Birsoy, Yelena Kemel, Anna Maio, Erin Salo-Mullen, Margaret Sheehan, Martee L. Hensley, Maria Rubinstein, Vicky Makker, Rachel N. Grisham, Roisin E. O’Cearbhaill, Kara Long Roche, Jennifer J. Mueller, Mario M. Leitao, Yukio Sonoda, Dennis S. Chi, Nadeem R. Abu-Rustum, Michael F. Berger, Lora H. Ellenson, Alicia Latham, Zsofia Stadler, Kenneth Offit, Carol Aghajanian, Britta Weigelt, Diana Mandelker, Ying L. Liu
Publikováno v:
Gynecologic Oncology. 174:34-41
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
Publikováno v:
American Society of Clinical Oncology Educational Book.
Cancers in young adults (commonly described as early-onset [EO] cancer) represent a group of malignancies that have unique and challenging biology and genetic, treatment, social, and psychological implications. Even more concerning is a rising trend
Autor:
Zsofia K. Stadler, Martin R. Weiser, Leonard B. Saltz, Julio Garcia-Aguilar, Andrea Cercek, Michael F. Berger, Kenneth Offit, Diana Mandelker, Arnold J. Markowitz, Rania Sheikh, Kaitlin A. Tkachuk, Ahmet Zehir, Philip B. Paty, Garrett M. Nash, Jaclyn F. Hechtman, David P. Kelsen, Nancy E. Kemeny, Louise Connell, Karuna Ganesh, Rona Yaeger, Neil H. Segal, Diane L. Reidy-Lagunes, Zalak Patel, Jinru Shia, Alicia Latham
Purpose:The prevalence and clinical characteristics of small bowel adenocarcinomas (SBA) in the setting of Lynch syndrome have not been well studied. We characterized SBA according to DNA mismatch repair and/or microsatellite instability (MMR/MSI) an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cab98c3a8f4ddac68d1594e5299a69a
https://doi.org/10.1158/1078-0432.c.6529974.v1
https://doi.org/10.1158/1078-0432.c.6529974.v1
Autor:
Zsofia K. Stadler, Martin R. Weiser, Leonard B. Saltz, Julio Garcia-Aguilar, Andrea Cercek, Michael F. Berger, Kenneth Offit, Diana Mandelker, Arnold J. Markowitz, Rania Sheikh, Kaitlin A. Tkachuk, Ahmet Zehir, Philip B. Paty, Garrett M. Nash, Jaclyn F. Hechtman, David P. Kelsen, Nancy E. Kemeny, Louise Connell, Karuna Ganesh, Rona Yaeger, Neil H. Segal, Diane L. Reidy-Lagunes, Zalak Patel, Jinru Shia, Alicia Latham
Supplemental Table 1: Clinical Characteristics, Treatment, and Recurrence Rates of of Patients with Stage II SBA Supplemental Table 2. Germline variants among SBA patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8e27efb7cf22b254979ce15e851ec79
https://doi.org/10.1158/1078-0432.22478535.v1
https://doi.org/10.1158/1078-0432.22478535.v1