Expanded Gene Panel Use for Women With Breast Cancer: Identification and Intervention Beyond Breast Cancer Risk

por O’Leary, Erin, Iacoboni, Daniela, Holle, Jennifer, Michalski, Scott T., Esplin, Edward D., Yang, Shan, Ouyang, Karen
Publicado 2017

Underdiagnosis of Hereditary Colorectal Cancers Among Medicare Patients: Genetic Testing Criteria for Lynch Syndrome Miss the Mark

por Muller, Charles, Nielsen, Sarah M., Hatchell, Kathryn E., Yang, Shan, Michalski, Scott T., Hamlington, Barbara, Nussbaum, Robert L., Esplin, Edward D., Kupfer, Sonia S.
Publicado 2021

Yield and Utility of Germline Testing Following Tumor Sequencing in Patients With Cancer

por Lincoln, Stephen E., Nussbaum, Robert L., Kurian, Allison W., Nielsen, Sarah M., Das, Kingshuk, Michalski, Scott, Yang, Shan, Ngo, Nhu, Blanco, Amie, Esplin, Edward D.
Publicado 2020

Rate of Pathogenic Germline Variants in Patients With Lung Cancer

por Sorscher, Steven, LoPiccolo, Jaclyn, Heald, Brandie, Chen, Elaine, Bristow, Sara L., Michalski, Scott T., Nielsen, Sarah M., Lacoste, Alix, Keyder, Emil, Lee, Hayan, Nussbaum, Robert L., Martins, Renato, Esplin, Edward D.
Publicado 2023

Loss-of-function variants in CTNNA1 detected on multigene panel testing in individuals with gastric or breast cancer

por Clark, Dana Farengo, Michalski, Scott T., Tondon, Rashmi, Nehoray, Bita, Ebrahimzadeh, Jessica, Hughes, Sarah Kate, Soper, Emily R., Domchek, Susan M., Rustgi, Anil K., Pineda-Alvarez, Daniel, Anderson, Michael J., Katona, Bryson W.
Publicado 2020

Germline Pathogenic Variant Prevalence Among Latin American and US Hispanic Individuals Undergoing Testing for Hereditary Breast and Ovarian Cancer: A Cross-Sectional Study

por Ossa Gomez, Carlos Andrés, Achatz, Maria Isabel, Hurtado, Mabel, Sanabria-Salas, María Carolina, Sullcahuaman, Yasser, Chávarri-Guerra, Yanin, Dutil, Julie, Nielsen, Sarah M., Esplin, Edward D., Michalski, Scott T., Bristow, Sara L., Hatchell, Kathryn E., Nussbaum, Robert L., Pineda-Alvarez, Daniel E., Ashton-Prolla, Patricia
Publicado 2022

Germline hemizygous deletion of CDKN2A–CDKN2B locus in a patient presenting with Li–Fraumeni syndrome

por Chan, Sock Hoai, Lim, Weng Khong, Michalski, Scott T, Lim, Jing Quan, Ishak, Nur Diana Binte, Met-Domestici, Marie, Young, Cedric Ng Chuan, Vikstrom, Karen, Esplin, Edward D, Fulbright, Jennifer, Ang, Mei Kim, Wee, Joseph, Sittampalam, Kesavan, Farid, Mohamad, Lincoln, Stephen E, Itahana, Koji, Abdullah, Syafiq, Teh, Bin Tean, Ngeow, Joanne
Publicado 2016

Clinical Impact of Pathogenic Variants in DNA Damage Repair Genes beyond BRCA1 and BRCA2 in Breast and Ovarian Cancer Patients

por Espinel, Whitney, Champine, Marjan, Hampel, Heather, Jeter, Joanne, Sweet, Kevin, Pilarski, Robert, Pearlman, Rachel, Shane, Kate, Brock, Pamela, Westman, Judith A., Kipnis, Lindsay, Sotelo, Jilliane, Chittenden, Anu, Culver, Samantha, Stopfer, Jill E., Schneider, Katherine A., Sacca, Rosalba, Koeller, Diane R., Gaonkar, Shraddha, Vaccari, Erica, Kane, Sarah, Michalski, Scott T., Yang, Shan, Nielsen, Sarah M., Bristow, Sara L., Lincoln, Stephen E., Nussbaum, Robert L., Esplin, Edward D.
Publicado 2022