The Role of Risk-Reducing Surgery in Hereditary Breast and Ovarian Cancer von Hartmann, Lynn C, Lindor, Noralane M

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Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer von Win, Aung Ko, Jenkins, Mark A, Dowty, James G, Antoniou, Antonis C, Lee, Andrew, Giles, Graham G, Buchanan, Daniel D, Clendenning, Mark, Rosty, Christophe, Ahnen, Dennis J, Thibodeau, Stephen N, Casey, Graham, Gallinger, Steven, Le Marchand, Loïc, Haile, Robert W, Potter, John D, Zheng, Yingye, Lindor, Noralane M, Newcomb, Polly A, Hopper, John L, MacInnis, Robert J

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American Society of Clinical Oncology Policy Statement Update: Genetic and Genomic Testing for Cancer Susceptibility von Robson, Mark E, Bradbury, Angela R, Arun, Banu, Domchek, Susan M, Ford, James M, Hampel, Heather L, Lipkin, Stephen M, Syngal, Sapna, Wollins, Dana S, Lindor, Noralane M

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Molecular Biomarkers for the Evaluation of Colorectal Cancer: Guideline From the American Society for Clinical Pathology, College of American Pathologists, Association for Molecula... von Sepulveda, Antonia R, Hamilton, Stanley R, Allegra, Carmen J, Grody, Wayne, Cushman-Vokoun, Allison M, Funkhouser, William K, Kopetz, Scott E, Lieu, Christopher, Lindor, Noralane M, Minsky, Bruce D, Monzon, Federico A, Sargent, Daniel J, Singh, Veena M, Willis, Joseph, Clark, Jennifer, Colasacco, Carol, Rumble, R Bryan, Temple-Smolkin, Robyn, Ventura, Christina B, Nowak, Jan A

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Risk of breast cancer in Lynch syndrome: a systematic review von Win, Aung Ko, Lindor, Noralane M, Jenkins, Mark A

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American Society of Clinical Oncology Expert Statement: Collection and Use of a Cancer Family History for Oncology Providers von LU, Karen H, WOOD, Marie E, RUBINSTEIN, Wendy S, STOFFEL, Elena M, SNYDER, Carrie, SYNGAL, Sapna, MERRILL, Janette K, WOLLINS, Dana Swartzberg, HUGHES, Kevin S, DANIELS, Molly, BURKE, Cathy, FORD, James, KAUFF, Noah D, KOHLMANN, Wendy, LINDOR, Noralane M, MULVEY, Therese M, ROBINSON, Linda

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Comprehensive annotation of BRCA1 and BRCA2 missense variants by functionally validated sequence-based computational prediction models von Hart, Steven N., Hoskin, Tanya, Shimelis, Hermela, Moore, Raymond M., Feng, Bingjian, Thomas, Abigail, Lindor, Noralane M., Polley, Eric C., Goldgar, David E., Iversen, Edwin, Monteiro, Alvaro N.A., Suman, Vera J., Couch, Fergus J.

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Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches von Guidugli, Lucia, Shimelis, Hermela, Masica, David L., Pankratz, Vernon S., Lipton, Gary B., Singh, Namit, Hu, Chunling, Monteiro, Alvaro N.A., Lindor, Noralane M., Goldgar, David E., Karchin, Rachel, Iversen, Edwin S., Couch, Fergus J.

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Potential impact of family history–based screening guidelines on the detection of early‐onset colorectal cancer von Gupta, Samir, Bharti, Balambal, Ahnen, Dennis J., Buchanan, Daniel D., Cheng, Iona C., Cotterchio, Michelle, Figueiredo, Jane C., Gallinger, Steven J., Haile, Robert W., Jenkins, Mark A., Lindor, Noralane M., Macrae, Finlay A., Le Marchand, Loïc, Newcomb, Polly A., Thibodeau, Stephen N., Win, Aung Ko, Martinez, Maria Elena

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Whole-Genome Sequencing in Healthy People von Lindor, Noralane M., MD, Thibodeau, Stephen N., PhD, Burke, Wylie, MD, PhD

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A general framework for functionally informed set-based analysis: Application to a large-scale colorectal cancer study von Dong, Xinyuan, Su, Yu-Ru, Barfield, Richard, Bien, Stephanie A., He, Qianchuan, Harrison, Tabitha A., Huyghe, Jeroen R., Keku, Temitope O., Lindor, Noralane M., Schafmayer, Clemens, Chan, Andrew T., Gruber, Stephen B., Jenkins, Mark A., Kooperberg, Charles, Peters, Ulrike, Hsu, Li

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The Clinical Phenotype of Lynch Syndrome Due to Germ-Line PMS2 Mutations von Senter, Leigha, Clendenning, Mark, Sotamaa, Kaisa, Hampel, Heather, Green, Jane, Potter, John D, Lindblom, Annika, Lagerstedt, Kristina, Thibodeau, Stephen N, Lindor, Noralane M, Young, Joanne, Winship, Ingrid, Dowty, James G, White, Darren M, Hopper, John L, Baglietto, Laura, Jenkins, Mark A, de la Chapelle, Albert

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Identification and Management of Women With BRCA Mutations or Hereditary Predisposition for Breast and Ovarian Cancer von Pruthi, Sandhya, MD, Gostout, Bobbie S., MD, Lindor, Noralane M., MD

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A review of a multifactorial probability-based model for classification of BRCA1 and BRCA2 variants of uncertain significance (VUS) von Lindor, Noralane M., Guidugli, Lucia, Wang, Xianshu, Vallée, Maxime P., Monteiro, Alvaro N. A., Tavtigian, Sean, Goldgar, David E., Couch, Fergus J.

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Returning genomic results in a Federally Qualified Health Center: the intersection of precision medicine and social determinants of health von Shaibi, Gabriel Q., Kullo, Iftikhar J., Singh, Davinder P., Hernandez, Valentina, Sharp, Richard R., Cuellar, Idali, De Filippis, Eleanna, Levey, Sharon, Breitkopf, Carmen Radecki, Mandarino, Lawrence J., Yang, Ping, Thibodeau, Stephen N., Lindor, Noralane M.

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Penetrance and outcomes at 1-year following return of actionable variants identified by genome sequencing von Lee, Christopher, Elsekaily, Omar, Kochan, David C., Alhalabi, Lubna, Faizee, Faizan, Sharp, Richard, Lindor, Noralane M., Kullo, Iftikhar J.

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A New Comprehensive Colorectal Cancer Risk Prediction Model Incorporating Family History, Personal Characteristics, and Environmental Factors von Zheng, Yingye, Hua, Xinwei, Win, Aung K., MacInnis, Robert J., Gallinger, Steven, Le Marchand, Loic, Lindor, Noralane M., Baron, John A., Hopper, John L., Dowty, James G., Antoniou, Antonis C., Zheng, Jiayin, Jenkins, Mark A., Newcomb, Polly A.

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Increased Cancer Risks in Myotonic Dystrophy von Win, Aung Ko, MBBS, MPH, Perattur, Promilla G., MBBS, Pulido, Jose S., MD, MS, MPH, MBA, Pulido, Christine M, Lindor, Noralane M., MD

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The PREMM1,2,6 Model Predicts Risk of MLH1 , MSH2 , and MSH6 Germline Mutations Based on Cancer History von Kastrinos, Fay, Steyerberg, Ewout W, Mercado, Rowena, Balmaña, Judith, Holter, Spring, Gallinger, Steven, Siegmund, Kimberly D, Church, James M, Jenkins, Mark A, Lindor, Noralane M, Thibodeau, Stephen N, Burbidge, Lynn Anne, Wenstrup, Richard J, Syngal, Sapna

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RECQL4 is essential for the transport of p53 to mitochondria in normal human cells in the absence of exogenous stress von De, Siddharth, Kumari, Jyoti, Mudgal, Richa, Modi, Priyanka, Gupta, Shruti, Futami, Kazunobu, Goto, Hideyuki, Lindor, Noralane M, Furuichi, Yasuhiro, Mohanty, Debasisa, Sengupta, Sagar

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