Resultados de Búsqueda por Autor :: APM

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Universal Germline Panel Testing for Individuals With Pheochromocytoma and Paraganglioma Produces High Diagnostic Yield por Carolyn Horton, Holly LaDuca, Ashley Deckman, Kate Durda, Michelle Jackson, Marcy E. Richardson, Yuan Tian, Amal Yussuf, Kory Jasperson, Tobias Else

Publicado 2022

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Double <i>CHEK2</i> Pathogenic and Low-Risk Variants and Associated Cancer Phenotypes por Brittany Bychkovsky, Nihat Buğra Ağaoğlu, Carolyn Horton, Linda M. Polfus, Marcy E. Richardson, Colin C. Young, Rochelle Scheib, Judy E. Garber, Huma Rana

Publicado 2025

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3

Closing the gap: Systematic integration of multiplexed functional data resolves variants of uncertain significance in BRCA1, TP53, and PTEN por Shawn Fayer, Carolyn Horton, Jennifer N. Dines, Alan F. Rubin, Marcy E. Richardson, Kelly McGoldrick, Felicia Hernandez, Tina Pesaran, Rachid Karam, Brian H. Shirts, Douglas M. Fowler, Lea M. Starita

Publicado 2021

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Diagnostic Outcomes of Concurrent DNA and RNA Sequencing in Individuals Undergoing Hereditary Cancer Testing por Carolyn Horton, Lily Hoang, Heather Zimmermann, Colin C. Young, Jessica Grzybowski, Kate Durda, Huy Gia Vuong, David Burks, Ashley Cass, Holly LaDuca, Marcy E. Richardson, Steven M. Harrison, Elizabeth Chao, Rachid Karam

Publicado 2023

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5

Differences in Cancer Phenotypes Among Frequent <i>CHEK2</i> Variants and Implications for Clinical Care—Checking <i>CHEK2</i> por Brittany Bychkovsky, Nihat Buğra Ağaoğlu, Carolyn Horton, Jing Zhou, Amal Yussuf, Parichehr Hemyari, Marcy E. Richardson, Colin C. Young, Holly LaDuca, Deborah L. McGuinness, Rochelle Scheib, Judy E. Garber, Huma Q. Rana

Publicado 2022

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6

A clinical guide to hereditary cancer panel testing: evaluation of gene-specific cancer associations and sensitivity of genetic testing criteria in a cohort of 165,000 high-risk pa... por Holly LaDuca, Eric C. Polley, Amal Yussuf, Lily Hoang, Stephanie Gutierrez, Steven N. Hart, Siddhartha Yadav, Chunling Hu, Jie Na, David E. Goldgar, Kelly Fulk, Laura P. Smith, Carolyn Horton, Jessica Profato, Tina Pesaran, Chia-Ling Gau, Melissa Pronold, Brigette Tippin Davis, Elizabeth Chao, Fergus J. Couch, Jill S. Dolinsky

Publicado 2019

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Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 1.2014 por Mary B. Daly, Robert Pilarski, Jennifer E. Axilbund, Saundra S. Buys, James M. Ford, Susan Friedman, Judy E. Garber, Carolyn Horton, Virginia Kaklamani, Catherine Klein, Wendy Kohlmann, Allison W. Kurian, Jennifer K. Litton, Lisa Madlensky, P. Kelly Marcom, Sofía D. Merajver, Kenneth Offit, Tuya Pal, Boris Pasche, Gwen Reiser, Kristen M. Shannon, Elizabeth M. Swisher, Nicoleta Voian, Jeffrey N. Weitzel, Alison J. Whelan, Georgia L. Wiesner, Mary A. Dwyer, Rashmi Kumar

Publicado 2014

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8

Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium por Laura M. Amendola, Gail P. Jarvik, Michael C. Leo, Heather M. McLaughlin, Yassmine Akkari, Michelle D. Amaral, Jonathan S. Berg, Sawona Biswas, Kevin M. Bowling, Laura K. Conlin, Gregory M. Cooper, Michael O. Dorschner, Matthew C. Dulik, Arezou A. Ghazani, Rajarshi Ghosh, Robert C. Green, Ragan Hart, Carolyn Horton, Jennifer J. Johnston, Matthew S. Lebo, Aleksandar Milosavljevic, Jeffrey Ou, Christine M. Pak, Ronak Y. Patel, Sumit Punj, Carolyn Sue Richards, Joseph S Salama, Natasha T. Strande, Yaping Yang, Sharon E. Plon, Leslie G. Biesecker, Heidi L. Rehm

Publicado 2016

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9

Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium por Laura M. Amendola, Gail P. Jarvik, Michael C. Leo, Heather M. McLaughlin, Yassmine Akkari, Michelle D. Amaral, Jonathan S. Berg, Sawona Biswas, Kevin M. Bowling, Laura K. Conlin, Gregory M. Cooper, Michael O. Dorschner, Matthew C. Dulik, Arezou A. Ghazani, Rajarshi Ghosh, Robert C. Green, Ragan Hart, Carolyn Horton, Jennifer J. Johnston, Matthew S. Lebo, Aleksandar Milosavljević, Jeffrey Ou, Christine M. Pak, Ronak Y. Patel, Sumit Punj, Carolyn Sue Richards, Joseph S Salama, Natasha T. Strande, Yaping Yang, Sharon E. Plon, Leslie G. Biesecker, Heidi L. Rehm

Publicado 2016

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10

2022 CGA-IGC Annual Meeting: The collaborative group of the Americas on Inherited Gastrointestinal Cancer November 11–13, 2022 por Sarah Kane, Nikita Mehta, Yelena Kemel, Vignesh Ravichandran, Ryan Ptashkin, Anna Maio, Amanda Catchings, Dina Green, Megha Ranganathan, Erin Mullen, Diana Mandelker, Zsofia K. Stadler, Alicia Latham, J. N. Cooper, Sarah McGee, Lauren Bokovitz, Sudipto Mukherjee, David Liska, James S. Blachly, Hetty E. Carraway, Harry Lesmana, Brittany Griffin, Giulia Martina Cavestro, Marta Puzzono, Alessandro Mannucci, Simone Grannò, Laura Poliani, Luca Albarello, Silvana Lobo, Patrick R. Benusiglio, Florence Coulet, Lise Boussemart, Lisa Golmard, Isabel Spier, Robert Hu ̈neburg, Stefan Aretz, Liselotte van Hest, Judith Balmañ, Sigrid Tinschert, Bryson W. Katona, Melyssa Aronson, Augusto Antoniazzi, Carolyn Horton, Rachid Karam, Leticia Moreira, Jolanda van Dieren, Chrystelle Colas, Paulo S. Pereira, Carla Oliveíra

Publicado 2023

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