Clinical laboratories collaborate to resolve differences in variant interpretations submitted to ClinVar von Harrison, Steven M., Dolinsky, Jill S., Knight Johnson, Amy E., Pesaran, Tina, Azzariti, Danielle R., Bale, Sherri, Chao, Elizabeth C., Das, Soma, Vincent, Lisa, Rehm, Heidi L.

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Frequency of mutations in a large series of clinically ascertained ovarian cancer cases tested on multi-gene panels compared to reference controls von Lilyquist, Jenna, LaDuca, Holly, Polley, Eric, Davis, Brigette Tippin, Shimelis, Hermela, Hu, Chunling, Hart, Steven N., Dolinsky, Jill S., Couch, Fergus J., Goldgar, David E.

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The Contribution of Germline Predisposition Gene Mutations to Clinical Subtypes of Invasive Breast Cancer From a Clinical Genetic Testing Cohort von Hu, Chunling, Polley, Eric C, Yadav, Siddhartha, Lilyquist, Jenna, Shimelis, Hermela, Na, Jie, Hart, Steven N, Goldgar, David E, Shah, Swati, Pesaran, Tina, Dolinsky, Jill S, LaDuca, Holly, Couch, Fergus J

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Male breast cancer in a multi-gene panel testing cohort: insights and unexpected results von Pritzlaff, Mary, Summerour, Pia, McFarland, Rachel, Li, Shuwei, Reineke, Patrick, Dolinsky, Jill S., Goldgar, David E., Shimelis, Hermela, Couch, Fergus J., Chao, Elizabeth C., LaDuca, Holly

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Differences in TP53 Mutation Carrier Phenotypes Emerge From Panel-Based Testing von Rana, Huma Q, Gelman, Rebecca, LaDuca, Holly, McFarland, Rachel, Dalton, Emily, Thompson, Jennifer, Speare, Virginia, Dolinsky, Jill S, Chao, Elizabeth C, Garber, Judy E

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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... von LaDuca, Holly, Polley, Eric C., Yussuf, Amal, Hoang, Lily, Gutierrez, Stephanie, Hart, Steven N., Yadav, Siddhartha, Hu, Chunling, Na, Jie, Goldgar, David E., Fulk, Kelly, Smith, Laura Panos, Horton, Carolyn, Profato, Jessica, Pesaran, Tina, Gau, Chia-Ling, Pronold, Melissa, Davis, Brigette Tippin, Chao, Elizabeth C., Couch, Fergus J., Dolinsky, Jill S.

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Somatic TP53 variants frequently confound germ-line testing results von Weitzel, Jeffrey N, Chao, Elizabeth C, Nehoray, Bita, Van Tongeren, Lily R, LaDuca, Holly, Blazer, Kathleen R, Slavin, Thomas, FACMG, D A B M D, Pesaran, Tina, Rybak, Christina, Solomon, Ilana, Niell-Swiller, Mariana, Dolinsky, Jill S, Castillo, Danielle, Elliott, Aaron, Gau, Chia-Ling, Speare, Virginia, Jasperson, Kory

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Hereditary predisposition to ovarian cancer, looking beyond BRCA1 / BRCA2 von Minion, Lindsey E, Dolinsky, Jill S, Chase, Dana M, Dunlop, Charles L, Chao, Elizabeth C, Monk, Bradley J

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Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients von LaDuca, Holly, Stuenkel, A J, Dolinsky, Jill S., Keiles, Steven, Tandy, Stephany, Pesaran, Tina, Chen, Elaine, Gau, Chia-Ling, Palmaer, Erika, Shoaepour, Kamelia, Shah, Divya, Speare, Virginia, Gandomi, Stephanie, Chao, Elizabeth

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Triple-Negative Breast Cancer Risk Genes Identified by Multigene Hereditary Cancer Panel Testing von Shimelis, Hermela, LaDuca, Holly, Hu, Chunling, Hart, Steven N, Na, Jie, Thomas, Abigail, Akinhanmi, Margaret, Moore, Raymond M, Brauch, Hiltrud, Cox, Angela, Eccles, Diana M, Ewart-Toland, Amanda, Fasching, Peter A, Fostira, Florentia, Garber, Judy, Godwin, Andrew K, Konstantopoulou, Irene, Nevanlinna, Heli, Sharma, Priyanka, Yannoukakos, Drakoulis, Yao, Song, Feng, Bing-Jian, Tippin Davis, Brigette, Lilyquist, Jenna, Pesaran, Tina, Goldgar, David E, Polley, Eric C, Dolinsky, Jill S, Couch, Fergus J

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Diagnosing hereditary cancer predisposition in men with prostate cancer von Pritzlaff, Mary, Tian, Yuan, Reineke, Patrick, Stuenkel, A. J., Allen, Kyle, Gutierrez, Stephanie, Jackson, Michelle, Dolinsky, Jill S., LaDuca, Holly, Xu, Jianfeng, Black, Mary Helen, Helfand, Brian T.

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Racial and Ethnic Differences in Multigene Hereditary Cancer Panel Test Results for Women With Breast Cancer von Yadav, Siddhartha, LaDuca, Holly, Polley, Eric C, Hu, Chunling, Niguidula, Nancy, Shimelis, Hermela, Lilyquist, Jenna, Na, Jie, Lee, Kun Y, Gutierrez, Stephanie, Yussuf, Amal, Hart, Steven N, Davis, Brigette Tippin, Chao, Elizabeth C, Pesaran, Tina, Goldgar, David E, Dolinsky, Jill S, Couch, Fergus J

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Family communication and patient distress after germline genetic testing in individuals with pancreatic ductal adenocarcinoma von Peters, Mary Linton B., Stobie, Lindsey, Dudley, Beth, Karloski, Eve, Allen, Kyle, Speare, Virginia, Dolinsky, Jill S., Tian, Yuan, DeLeonardis, Kim, Krejdovsky, Jill, Button, Arlene, Lim, Cynthia, Borazanci, Erkut, Brand, Randall, Tung, Nadine

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Mutation prevalence tables for hereditary cancer derived from multigene panel testing von Hart, Steven N., Polley, Eric C., Yussuf, Amal, Yadav, Siddhartha, Goldgar, David E., Hu, Chunling, LaDuca, Holly, Smith, Laura P., Fujimoto, June, Li, Shuwei, Couch, Fergus J., Dolinsky, Jill S.

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Classification of variants of uncertain significance in BRCA1 and BRCA2 using personal and family history of cancer from individuals in a large hereditary cancer multigene panel te... von Li, Hongyan, LaDuca, Holly, Pesaran, Tina, Chao, Elizabeth C., Dolinsky, Jill S., Parsons, Michael, Spurdle, Amanda B., Polley, Eric C., Shimelis, Hermela, Hart, Steven N., Hu, Chunling, Couch, Fergus J., Goldgar, David E.

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Germline Pathogenic Variants in Cancer Predisposition Genes Among Women With Invasive Lobular Carcinoma of the Breast von Yadav, Siddhartha, Hu, Chunling, Nathanson, Katherine L., Weitzel, Jeffrey N., Goldgar, David E., Kraft, Peter, Gnanaolivu, Rohan D., Na, Jie, Huang, Hongyan, Boddicker, Nicholas J., Larson, Nicole, Gao, Chi, Yao, Song, Weinberg, Clarice, Vachon, Celine M., Trentham-Dietz, Amy, Taylor, Jack A., Sandler, Dale R., Patel, Alpa, Palmer, Julie R., Olson, Janet E., Neuhausen, Susan, Martinez, Elena, Lindstrom, Sara, Lacey, James V., Kurian, Allison W., John, Esther M., Haiman, Christopher, Bernstein, Leslie, Auer, Paul W., Anton-Culver, Hoda, Ambrosone, Christine B., Karam, Rachid, Chao, Elizabeth, Yussuf, Amal, Pesaran, Tina, Dolinsky, Jill S., Hart, Steven N., LaDuca, Holly, Polley, Eric C., Domchek, Susan M., Couch, Fergus J.

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A Rare TP53 Mutation Predominant in Ashkenazi Jews Confers Risk of Multiple Cancers von Powers, Jacquelyn, Pinto, Emilia M., Barnoud, Thibaut, Leung, Jessica C., Martynyuk, Tetyana, Kossenkov, Andrew, Philips, Aaron H., Desai, Heena, Hausler, Ryan, Kelly, Gregory, Le, Anh N., Li, Marilyn M., MacFarland, Suzanne P., Pyle, Louise C., Zelley, Kristin, Nathanson, Katherine L., Domchek, Susan M., Slavin, Thomas P., Weitzel, Jeffrey N., Stopfer, Jill E., Garber, Judy E., Joseph, Vijai, Offit, Kenneth, Dolinsky, Jill S., Gutierrez, Stephanie, McGoldrick, Kelly, Couch, Fergus J., Levin, Brooke, Edelman, Morris C., Levy, Carolyn Fein, Spunt, Sheri L., Kriwacki, Richard W., Zambetti, Gerard P., Ribeiro, Raul C., Murphy, Maureen E., Maxwell, Kara N.

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Genotype–phenotype associations among panel-based TP53+ subjects von Rana, Huma Q., Clifford, Jacob, Hoang, Lily, LaDuca, Holly, Black, Mary Helen, Li, Shuwei, McGoldrick, Kelly, Speare, Virginia, Dolinsky, Jill S., Gau, Chia-Ling, Garber, Judy E.

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DIAGNOSTIC EXOME SEQUENCING IN PEDIATRIC PATIENTS WITH CONGENITAL HEART DISEASE von Powis, Zoe, Thrush, Devon, Davis, Brigette Tippin, Dolinsky, Jill S

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Breast cancer risk is similar for CHEK2 founder and non-founder mutation carriers von Leedom, Tracey P, LaDuca, Holly, McFarland, Rachel, Li, Shuwei, Dolinsky, Jill S, Chao, Elizabeth C

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