Zobrazeno 1 - 10
of 516
pro vyhledávání: '"E. Salo"'
Akademický článek
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Autor:
Margaret Sheehan, Kelsey Breen, David Wylie, Zsofia K. Stadler, Erin E. Salo-Mullen, Malwina Tuman, Jada G. Hamilton, Megan Harlan Fleischut, Kenneth Offit, Corinna Bertelsen
Publikováno v:
JCO Oncol Pract
PURPOSE: With onset of the COVID-19 pandemic, telehealth became the primary modality for health care appointments. This study examined patient experiences with and preferences for telehealth at a cancer genetic counseling clinic throughout the first
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f62db5750403c88c754316f0ebb7f385
https://doi.org/10.1200/op.21.00301
https://doi.org/10.1200/op.21.00301
Autor:
Anna Arutyunova, Maria I. Carlo, Jada G. Hamilton, Rebecca Gebert, Mark E. Robson, Erin E. Salo-Mullen, Vivek Narayan, Melissa Batson, Heather Symecko, Kelsey Spielman, Amanda Catchings, Zsofia K. Stadler, Ibrahim H Shah, Stacy Pundock, Elizabeth Schofield, Susan M. Domchek, Kenneth Offit, Karen Cadoo, Rebecca Mueller, Kelsey Breen, Magan Trottier, Kim A. Reiss
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics
Purpose: To address demands for timely germline information to guide treatments, we evaluated experiences of patients with ovarian, pancreatic, and prostate cancer with a mainstreaming genetic testing model wherein multigene panel testing was ordered
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d65921dfb8882a8a828209c579ff688
https://doi.org/10.1038/s41436-021-01262-2
https://doi.org/10.1038/s41436-021-01262-2
Autor:
David B. Solit, Angela G. Arnold, Mark E. Robson, Diana Mandelker, Michael F. Berger, Shweta S. Chavan, Maksym Misyura, Michael Walsh, Anna Maio, Sarah R. Kane, Karen Cadoo, Yelena Kemel, Preethi Srinivasan, Ying Liu, Jinru Shia, Kenneth Offit, Kelsey Breen, Jennifer Kennedy, Margaret Sheehan, Semanti Mukherjee, Caitlin Bourque, Chaitanya Bandlamudi, Zalak Patel, Maria I. Carlo, Zsofia K. Stadler, Amanda Catchings, Erin E. Salo-Mullen, Arnold J. Markowitz, Barry S. Taylor, Prince Rainier Tejada, Rosalba Sacca, Vanessa Marcell, Alicia Latham, Ozge Ceyhan-Birsoy, Mark T.A. Donoghue, Kimberly Amoroso, Megha Ranganathan
Publikováno v:
JCO Precision Oncology. :455-465
PURPOSE NTHL1 and MSH3 have been implicated as autosomal recessive cancer predisposition genes. Although individuals with biallelic NTHL1 and MSH3 pathogenic variants (PVs) have increased cancer and polyposis risk, risks for monoallelic carriers are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ba859253338af25f8aa87589967d494
https://doi.org/10.1200/po.20.00443
https://doi.org/10.1200/po.20.00443
Autor:
M. Herman Chui, Ciyu Yang, Maksym Misyura, Zsofia K. Stadler, Jorge S. Reis-Filho, Gowtham Jayakumaran, Sowmya Jairam, Ryan Ptashkin, Nikita Mehta, Marc Ladanyi, Ozge Ceyhan-Birsoy, Kenneth Offit, Anna Maio, Yirong Li, Yelena Kemel, Mark E. Robson, Maria I. Carlo, Margaret Sheehan, Alicia Latham, Pier Selenica, Ahmet Zehir, Erin E. Salo-Mullen, Michael Walsh, Umut Aypar, Diana Mandelker
Publikováno v:
JNCI: Journal of the National Cancer Institute. 113:1751-1760
Background Genetic testing for Li-Fraumeni syndrome (LFS) is performed by using blood specimens from patients selected based on phenotype-dependent guidelines. This approach is problematic for understanding the LFS clinical spectrum because patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0bf2b3c7c4c2c021738ad09f79e233b0
https://doi.org/10.1093/jnci/djab117
https://doi.org/10.1093/jnci/djab117
Autor:
Ying L. Liu, Anna Maio, Yelena Kemel, Erin E. Salo‐Mullen, Margaret Sheehan, Prince Ray Tejada, Magan Trottier, Angela G. Arnold, Megan Harlan Fleischut, Alicia Latham, Maria I. Carlo, Yonina R. Murciano‐Goroff, Michael F. Walsh, Diana Mandelker, Nikita Mehta, Chaitanya Bandlamudi, Kanika Arora, Ahmet Zehir, Michael F. Berger, David B. Solit, Carol Aghajanian, Luis A. Diaz, Mark E. Robson, Carol L. Brown, Kenneth Offit, Jada G. Hamilton, Zsofia K. Stadler
Publikováno v:
CancerREFERENCES. 128(21)
Germline risk assessment is increasing as part of cancer care; however, disparities in subsequent genetic counseling are unknown.Pan-cancer patients were prospectively consented to tumor-normal sequencing via custom next generation sequencing panel (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ffb1325acf2187b07cabf51a21770cb
https://pubmed.ncbi.nlm.nih.gov/36041233
https://pubmed.ncbi.nlm.nih.gov/36041233
Autor:
Ibrahim H. Shah, Erin E. Salo-Mullen, Kimberly A. Amoroso, David Kelsen, Zsofia K. Stadler, Jada G. Hamilton
Publikováno v:
Hereditary cancer in clinical practice. 20(1)
Background Hereditary Diffuse Gastric Cancer (HDGC) syndrome is an autosomal dominant hereditary cancer predisposition associated with germline pathogenic/likely pathogenic variants in the CDH1 gene. Identifying early stage HDGC is difficult, and pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ecfe6b2010a6fce6bd2c19e19317b0cc
https://pubmed.ncbi.nlm.nih.gov/36056367
https://pubmed.ncbi.nlm.nih.gov/36056367
Autor:
Felipe Quezada-Diaz, Martin R. Weiser, Julio Garcia-Aguilar, John D. Catalano, Erin E. Salo-Mullen, Irbaz Hameed, J. Joshua Smith, Jose G. Guillem, Alexa von Mueffling, Zsofia K. Stadler
Publikováno v:
J Am Coll Surg
Background Because of increased risk of metachronous colorectal cancer (CRC), all patients with Lynch syndrome (LS) are offered a total colectomy. However, because metachronous CRC rate by mismatch repair (MMR) gene is uncertain, and total colectomy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35e557bf5fce82eda3042e871d9a23e3
https://doi.org/10.1016/j.jamcollsurg.2020.01.005
https://doi.org/10.1016/j.jamcollsurg.2020.01.005
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
J. Joshua Smith, Erin E. Salo-Mullen, Henry Walch, Diana Mandelker, Asha Krishnan, Michael F. Berger, Felix Steinruecke, Neil H. Segal, Gustavo Dos Santos Fernandes, Diane Reidy-Lagunes, Garrett M. Nash, Kimeisha Belanfanti, Leonard B. Saltz, Andrea Cercek, Zsofia K. Stadler, Karuna Ganesh, Anna M. Varghese, Chaitanya Bandlamudi, Mark E. Robson, Melissa Lumish, Jinru Shia, Vijai Joseph, Julio Garcia Aguilar, Nikolaus Schultz, Walid K. Chatila, Robin B. Mendelsohn, P. Paty, Kenneth Offit, Nancy E. Kemeny, Arnold J. Markowitz, Liying Zhang, Louise Catherine Connell, Preethi Srinivasan, Yelena Kemel, Barry S. Taylor, Ozge Birsoy, Jose G. Guillem, David B. Solit, Jesse Galle, Rona Yaeger, Sebastian Mondaca, Efsevia Vakiani, Luis A. Diaz, Anna Maio, Lerie Palmaira, Prince Rainier Tejada, Martin R. Weiser
Publikováno v:
J Natl Cancer Inst
Background The causative factors for the recent increase in early-onset colorectal cancer (EO-CRC) incidence are unknown. We sought to determine if early-onset disease is clinically or genomically distinct from average-onset colorectal cancer (AO-CRC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3723ce25fffa6cdb6d9d05fbf0a82091
https://europepmc.org/articles/PMC8634406/
https://europepmc.org/articles/PMC8634406/
