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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An integrative model for the comprehensive classification of BRCA1 and BRCA2 variants of uncertain clinical significance von Iversen, Edwin S., Lipton, Gary, Hart, Steven N., Lee, Kun Y., Hu, Chunling, Polley, Eric C., Pesaran, Tina, Yussuf, Amal, LaDuca, Holly, Chao, Elizabeth, Karam, Rachid, Goldgar, David E., Couch, Fergus J., Monteiro, Alvaro N. A.

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Paired tumor sequencing and germline testing in breast cancer management: An experience of a single academic center von Elliott, Elizabeth, Speare, Virginia, Coggan, James, Espenschied, Carin, LaDuca, Holly, Yussuf, Amal F., Burgess, Kelly, Gray, Phillip, Cobleigh, Melody, Rao, Ruta, Patel, Jeremy, Kuzel, Timothy, Buckingham, Lela E., Usha, Lydia

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Characterization of POT1 tumor predisposition syndrome: Tumor prevalence in a clinically diverse hereditary cancer cohort von Herrera-Mullar, Jennifer, Fulk, Kelly, Brannan, Terra, Yussuf, Amal, Polfus, Linda, Richardson, Marcy E., Horton, Carolyn

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Germline Genetic Testing After Cancer Diagnosis von Kurian, Allison W, Abrahamse, Paul, Furgal, Allison, Ward, Kevin C, Hamilton, Ann S, Hodan, Rachel, Tocco, Rachel, Liu, Lihua, Berek, Jonathan S, Hoang, Lily, Yussuf, Amal, Susswein, Lisa, Esplin, Edward D, Slavin, Thomas P, Gomez, Scarlett L, Hofer, Timothy P, Katz, Steven J

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

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Correction to: Pathogenic variants among females with breast cancer and a nonâbreast cancer reveal opportunities for cancer interception von Bychkovsky, Brittany L, Lo, Min-Tzu, Yussuf, Amal, Horton, Carrie, Hemyari, Parichehr, LaDuca, Holly, Garber, Judy E

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Double jeopardy? A closer look at cancer histories of individuals with multiple germline pathogenic variants von Horton, Carolyn, Lo, Min-Tzu, Yussuf, Amal, Young, Colin, Carraway, Cassidy, Agaoglu, Nihat Bugra, Bychkovsky, Brittany L., Rana, Huma Q.

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Abstract P2-09-03: Pathogenic variants among female breast cancer patients with a subsequent cancer demonstrate preventable cancer burden von Bychkovsky, Brittany L., Lo, Min-Tzu, Yussuf, Amal, Horton, Carrie, Hemyari, Parichehr, LaDuca, Holly, Garber, Judy E., Rana, Huma Q.

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Majority of Epilepsy Mutations are in Genes with Therapeutic Associations (P2.281) von Weltmer, Elaine, Newman, Heather, Yussuf, Amal, Wang, Jing

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Development and Validation of the PREMMplus Model for Multigene Hereditary Cancer Risk Assessment von Yurgelun, Matthew B, Uno, Hajime, Furniss, C Sloane, Ukaegbu, Chinedu, Horiguchi, Miki, Yussuf, Amal, LaDuca, Holly, Chittenden, Anu, Garber, Judy E, Syngal, Sapna

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Prevalence and spectrum of pathogenic variants among patients with multiple primary cancers evaluated by clinical characteristics von Bychkovsky, Brittany L., Lo, Min‐Tzu, Yussuf, Amal, Horton, Carrie, Richardson, Marcy, LaDuca, Holly, Garber, Judy E., Rana, Huma Q.

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Many testing roads can lead to KCNQ2 diagnosis. (P1.234) von Yussuf, Amal, Powis, Zoe, Blanco, Kirsten, Wang, Jing

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Phenotype is not Always a Positive Predictor of Detection Rate in Epilepsy Panels (P1.231) von Newman, Heather, Powis, Zoe, Yussuf, Amal, Wang, Jing

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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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Pathogenic variants among females with breast cancer and a non-breast cancer reveal opportunities for cancer interception von Bychkovsky, Brittany L., Lo, Min-Tzu, Yussuf, Amal, Horton, Carrie, Hemyari, Parichehr, LaDuca, Holly, Garber, Judy E., Scheib, Rochelle, Rana, Huma Q.

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Prevalence and spectrum of pathogenic variants among patients with multiple primary cancers von Bychkovsky, Brittany L., Lo, Min-Tzu, Tian, Yuan, Yussuf, Amal, Horton, Carrie, Richardson, Marcy, LaDuca, Holly, Garber, Judy Ellen, Rana, Huma Q.

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Correction to: Pathogenic variants among females with breast cancer and a non‑breast cancer reveal opportunities for cancer interception von Bychkovsky, Brittany L., Lo, Min-Tzu, Yussuf, Amal, Horton, Carrie, Hemyari, Parichehr, LaDuca, Holly, Garber, Judy E., Scheib, Rochelle, Rana, Huma Q.

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An updated quantitative model to classify missense variants in the TP53 gene: A novel multifactorial strategy von Fortuno, Cristina, Pesaran, Tina, Dolinsky, Jill, Yussuf, Amal, McGoldrick, Kelly, Tavtigian, Sean V., Goldgar, David, Spurdle, Amanda B., James, Paul A.

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Clinical and molecular characteristics of NF1 mutations identified on hereditary cancer multi-gene panels von Safonov, Anton Mikhailovich, Speare, Virginia, Dolinsky, Jill S., Yussuf, Amal, Gau, Chia-Ling, Nathanson, Katherine

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