Barcoding allows immediate downloading of PowerPoint presentations by smart phones

por Riegert-Johnson, Douglas, Roberts, Maegan
Publicado 2011

Gastric adenomas in familial adenomatous polyposis are common, but subtle, and have a benign course

por Ngamruengphong, Saowanee, Boardman, Lisa A, Heigh, Russell I, Krishna, Murli, Roberts, Maegan E, Riegert-Johnson, Douglas L
Publicado 2014

Cancer and Lhermitte-Duclos disease are common in Cowden syndrome patients

por Riegert-Johnson, Douglas L, Gleeson, Ferga C, Roberts, Maegan, Tholen, Krysta, Youngborg, Lauren, Bullock, Melvin, Boardman, Lisa A
Publicado 2010

Age-adjusted association of homologous recombination genes with ovarian cancer using clinical exomes as controls

por Arvai, Kevin J., Roberts, Maegan E., Torene, Rebecca I., Susswein, Lisa R., Marshall, Megan L., Zhang, Zhancheng, Carter, Natalie J., Yackowski, Lauren, Rinella, Erica S., Klein, Rachel T., Hruska, Kathleen S., Retterer, Kyle
Publicado 2019

Patterns of germline and somatic testing after universal tumor screening for Lynch syndrome: A clinical practice survey of active members of the Collaborative Group of the Americas...

por Hodan, Rachel, Rodgers‐Fouche, Linda, Arora, Sanjeevani, Dominguez‐Valentin, Mev, Kanth, Priyanka, Katona, Bryson W., Mraz, Kathryn A., Roberts, Maegan E., Vilar, Eduardo, Soto‐Azghani, Cynthia M., Brand, Randall E, Esplin, Edward D., Perez, Kimberly
Publicado 2022

MSH6 and PMS2 germ-line pathogenic variants implicated in Lynch syndrome are associated with breast cancer

por Roberts, Maegan E, Jackson, Sarah A, Susswein, Lisa R, Zeinomar, Nur, Ma, Xinran, Marshall, Megan L, Stettner, Amy R, Milewski, Becky, Xu, Zhixiong, Solomon, Benjamin D, Terry, Mary Beth, Hruska, Kathleen S, Klein, Rachel T, Chung, Wendy K
Publicado 2018

High-grade endometrial stromal sarcoma as the initial presentation of an adult patient with Peutz-Jeghers Syndrome: a case report

por Noriega-Iriondo, Maria Fernanda, Colon-Otero, Gerardo, Kipp, Benjamin R, Copland, John A, Ferber, Matthew J, Marlow, Laura A, Roberts, Maegan E, Robertson, Matthew W, Dinh, Tri A, Attia, Steven, Geiger, Xochiquetzal J, Riegert-Johnson, Douglas L
Publicado 2015

Determining the clinical validity of hereditary colorectal cancer and polyposis susceptibility genes using the Clinical Genome Resource Clinical Validity Framework

por Seifert, Bryce A., McGlaughon, Jennifer L., Jackson, Sarah A., Ritter, Deborah I, Roberts, Maegan E., Schmidt, Ryan J., Thompson, Bryony A., Jimenez, Sharisse, Trapp, Mackenzie, Lee, Kristy, Plon, Sharon E., Offit, Kenneth, Stadler, Zsofia K., Zhang, Liying, Greenblatt, Marc S., Ferber, Matthew J.
Publicado 2018

Classification of BRCA2 Variants of Uncertain Significance (VUS) Using an ACMG/AMP Model Incorporating a Homology-Directed Repair (HDR) Functional Assay

por Hu, Chunling, Susswein, Lisa R., Roberts, Maegan E., Yang, Hana, Marshall, Megan L., Hiraki, Susan, Berkofsky-Fessler, Windy, Gupta, Sounak, Shen, Wei, Dunn, Carolyn A., Huang, Huaizhi, Na, Jie, Domchek, Susan M., Yadav, Siddhartha, Monteiro, Alvaro N.A., Polley, Eric C., Hart, Steven N., Hruska, Kathleen S., Couch, Fergus J.
Publicado 2022

Functional and Clinical Characterization of Variants of Uncertain Significance Identifies a Hotspot for Inactivating Missense Variants in RAD51C

por Hu, Chunling, Nagaraj, Anil Belur, Shimelis, Hermela, Montalban, Gemma, Lee, Kun Y., Huang, Huaizhi, Lumby, Carolyn A., Na, Jie, Susswein, Lisa R., Roberts, Maegan E., Marshall, Megan L., Hiraki, Susan, LaDuca, Holly, Chao, Elizabeth, Yussuf, Amal, Pesaran, Tina, Neuhausen, Susan L., Haiman, Christopher A., Kraft, Peter, Lindstrom, Sara, Palmer, Julie R., Teras, Lauren R., Vachon, Celine M., Yao, Song, Ong, Irene, Nathanson, Katherine L., Weitzel, Jeffrey N., Boddicker, Nicholas, Gnanaolivu, Rohan, Polley, Eric C., Mer, Georges, Cui, Gaofeng, Karam, Rachid, Richardson, Marcy E., Domchek, Susan M., Yadav, Siddhartha, Hruska, Kathleen S., Dolinsky, Jill, Weroha, S. John, Hart, Steven N., Simard, Jacques, Masson, Jean Yves, Pang, Yuan-Ping, Couch, Fergus J.
Publicado 2023