Germline multigene panel testing in acute and chronic pancreatitis von Ramsey, Mitchell L, Heald, Brandie, Gokun, Yevgeniya, Baker, Josie, Groce, J Royce, Han, Samuel, Hart, Phil A, Krishna, Somashekar G, Lara, Luis F, Lee, Peter J, Papachristou, Georgios I, Pearlman, Rachel, Poll, Sarah, Roberts, Maegan E, Stanich, Peter P

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

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Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline CDH1 sequence variants von Lee, Kristy, Krempely, Kate, Roberts, Maegan E., Anderson, Michael J., Carneiro, Fatima, Chao, Elizabeth, Dixon, Katherine, Figueiredo, Joana, Ghosh, Rajarshi, Huntsman, David, Kaurah, Pardeep, Kesserwan, Chimene, Landrith, Tyler, Li, Shuwei, Mensenkamp, Arjen R., Oliveira, Carla, Pardo, Carolina, Pesaran, Tina, Richardson, Matthew, Slavin, Thomas P., Spurdle, Amanda B., Trapp, Mackenzie, Witkowski, Leora, Yi, Charles S., Zhang, Liying, Plon, Sharon E., Schrader, Kasmintan A., Karam, Rachid

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

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Gastric adenomas in familial adenomatous polyposis are common, but subtle, and have a benign course von Ngamruengphong, Saowanee, Boardman, Lisa A, Heigh, Russell I, Krishna, Murli, Roberts, Maegan E, Riegert-Johnson, Douglas L

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

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A clinical scoring system to identify patients with sebaceous neoplasms at risk for the Muir–Torre variant of Lynch syndrome von Roberts, Maegan E., Riegert-Johnson, Douglas L., Thomas, Brittany C., Rumilla, Kandelaria M., Thomas, Colleen S., Heckman, Michael G., Purcell, Jennifer U., Hanson, Nancy B., Leppig, Kathleen A., Lim, Justin, Cappel, Mark A.

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Phenotypic continuum between POLE‐related recessive disorders: A case report and literature review von Roberts, Maegan E., Nimrichter, Sarah, Marshall, Megan L., Flynn, Elizabeth K., Person, Rick, Hruska, Kathleen S., Kruszka, Paul, Juusola, Jane

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Self Diagnosis of Lynch Syndrome Using Direct to Consumer Genetic Testing: A Case Study von Roberts, Maegan E., Riegert-Johnson, Douglas L., Thomas, Brittany C.

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Response to Evans et al von Roberts, Maegan E., Zeinomar, Nur, Solomon, Benjamin D., Terry, Mary Beth, Chung, Wendy K.

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

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Monoallelic MUTYH pathogenic variants ascertained via multi-gene hereditary cancer panels are not associated with colorectal, endometrial, or breast cancer von Thompson, Amanda Bartenbaker, Sutcliffe, Erin G., Arvai, Kevin, Roberts, Maegan E., Susswein, Lisa R., Marshall, Megan L., Torene, Rebecca, Postula, Kristen J. Vogel, Hruska, Kathleen S., Bai, Shaochun

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Response to Wang et al von Roberts, Maegan E., Zeinomar, Nur, Solomon, Benjamin D., Terry, Mary Beth, Chung, Wendy K.

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Response to ten Broeke et al von Roberts, Maegan E., Zeinomar, Nur, Solomon, Benjamin D., Terry, Mary Beth, Chung, Wendy K.

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

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Multi-gene panel testing confirms phenotypic variability in MUTYH-Associated Polyposis von Sutcliffe, Erin G., Bartenbaker Thompson, Amanda, Stettner, Amy R., Marshall, Megan L., Roberts, Maegan E., Susswein, Lisa R., Wang, Ying, Klein, Rachel T., Hruska, Kathleen S., Solomon, Benjamin D.

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Differences in cancer prevalence among CHEK2 carriers identified via multi-gene panel testing von Sutcliffe, Erin G., Stettner, Amy R., Miller, Stacey A., Solomon, Sheila R., Marshall, Megan L., Roberts, Maegan E., Susswein, Lisa R., Arvai, Kevin J., Klein, Rachel T., Murphy, Patricia D., Hruska, Kathleen S.

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Fibroblast testing can inform medical management in individuals with mosaic variants detected on hereditary cancer panels von Sutcliffe, Erin G., Mester, Jessica L., Susswein, Lisa R., Roberts, Maegan E., Marshall, Megan L., Hruska, Kathleen S.

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Ancestry‐specific hereditary cancer panel yields: Moving toward more personalized risk assessment von Roberts, Maegan E., Susswein, Lisa R., Janice Cheng, Wanchun, Carter, Natalie J., Carter, Amber C., Klein, Rachel T., Hruska, Kathleen S., Marshall, Megan L.

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Utility of Expedited Hereditary Cancer Testing in the Surgical Management of Patients with a New Breast Cancer Diagnosis von Theobald, Kristin A., Susswein, Lisa R., Marshall, Megan L., Roberts, Maegan E., Mester, Jessica L., Speyer, Darrow, Williams, Ravin N. W., Knapke, Sara C., Solomon, Sheila R., Murphy, Patricia D., Klein, Rachel T., Hruska, Kathleen S., Solomon, Benjamin D.

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