The Childhood Cancer Survivor Study: A National Cancer Institute–Supported Resource for Outcome and Intervention Research von ROBISON, Leslie L, ARMSTRONG, Gregory T, MULVIHILL, John J, NATHAN, Paul C, NEGLIA, Joseph P, PACKER, Roger J, RAJARAMAN, Preetha, SKLAR, Charles A, STOVALL, Marilyn, STRONG, Louise C, YASUI, Yutaka, ZELTZER, Lonnie K, BOICE, John D, CHOW, Eric J, DAVIES, Stella M, DONALDSON, Sarah S, GREEN, Daniel M, HAMMOND, Sue, MEADOWS, Anna T, MERTENS, Ann C

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Breast Cancer Risk in Childhood Cancer Survivors Without a History of Chest Radiotherapy: A Report From the Childhood Cancer Survivor Study von Henderson, Tara O, Moskowitz, Chaya S, Chou, Joanne F, Bradbury, Angela R, Neglia, Joseph Phillip, Dang, Chau T, Onel, Kenan, Novetsky Friedman, Danielle, Bhatia, Smita, Strong, Louise C, Stovall, Marilyn, Kenney, Lisa B, Barnea, Dana, Lorenzi, Elena, Hammond, Sue, Leisenring, Wendy M, Robison, Leslie L, Armstrong, Gregory T, Diller, Lisa R, Oeffinger, Kevin C

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A Single Nucleotide Polymorphism in the MDM2 Promoter Attenuates the p53 Tumor Suppressor Pathway and Accelerates Tumor Formation in Humans von Bond, Gareth L., Hu, Wenwei, Bond, Elisabeth E., Robins, Harlan, Lutzker, Stuart G., Arva, Nicoleta C., Bargonetti, Jill, Bartel, Frank, Taubert, Helge, Wuerl, Peter, Onel, Kenan, Yip, Linwah, Hwang, Shih-Jen, Strong, Louise C., Lozano, Guillermina, Levine, Arnold J.

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Gain of Function of a p53 Hot Spot Mutation in a Mouse Model of Li-Fraumeni Syndrome von Lang, Gene A., Iwakuma, Tomoo, Suh, Young-Ah, Liu, Geng, Rao, V.Ashutosh, Parant, John M., Valentin-Vega, Yasmine A., Terzian, Tamara, Caldwell, Lisa C., Strong, Louise C., El-Naggar, Adel K., Lozano, Guillermina

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Variants at 6q21 implicate PRDM1 in the etiology of therapy-induced second malignancies after Hodgkin's lymphoma von Best, Timothy, Li, Dalin, Skol, Andrew D, Kirchhoff, Tomas, Jackson, Sarah A, Yasui, Yutaka, Bhatia, Smita, Strong, Louise C, Domchek, Susan M, Nathanson, Katherine L, Olopade, Olufunmilayo I, Huang, R Stephanie, Mack, Thomas M, Conti, David V, Offit, Kenneth, Cozen, Wendy, Robison, Leslie L, Onel, Kenan

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The cancer predisposition revolution von Malkin, David, Garber, Judy E., Strong, Louise C., Friend, Stephen H.

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Characterization of BRCA1 and BRCA2 Mutations in a Large United States Sample von SINING CHEN, IVERSEN, Edwin S, CORIO, Camille, LEONDARIDIS, Leoni, TOMLINSON, Gail, DUTSON, Debra, KERBER, Rich, AMOS, Christopher I, STRONG, Louise C, BERRY, Donald A, EUHUS, David M, PARMIGIANI, Giovanni, FRIEBEL, Tara, FINKELSTEIN, Dianne, WEBER, Barbara L, EISEN, Andrea, PETERSON, Leif E, SCHILDKRAUT, Joellen M, ISAACS, Claudine, PESHKIN, Beth N

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Cancer Screening Recommendations for Individuals with Li-Fraumeni Syndrome von Kratz, Christian P, Achatz, Maria Isabel, Brugières, Laurence, Frebourg, Thierry, Garber, Judy E, Greer, Mary-Louise C, Hansford, Jordan R, Janeway, Katherine A, Kohlmann, Wendy K, McGee, Rose, Mullighan, Charles G, Onel, Kenan, Pajtler, Kristian W, Pfister, Stefan M, Savage, Sharon A, Schiffman, Joshua D, Schneider, Katherine A, Strong, Louise C, Evans, D Gareth R, Wasserman, Jonathan D, Villani, Anita, Malkin, David

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Effects of MDM2, MDM4 and TP53 codon 72 polymorphisms on cancer risk in a cohort study of carriers of TP53 germline mutations von Fang, Shenying, Krahe, Ralf, Lozano, Guillermina, Han, Younghun, Chen, Wei, Post, Sean M, Zhang, Baili, Wilson, Charmaine D, Bachinski, Linda L, Strong, Louise C, Amos, Christopher I

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Clinically Relevant Changes in Family History of Cancer Over Time von Ziogas, Argyrios, Horick, Nora K, Kinney, Anita Y, Lowery, Jan T, Domchek, Susan M, Isaacs, Claudine, Griffin, Constance A, Moorman, Patricia G, Edwards, Karen L, Hill, Deirdre A, Berg, Jonathan S, Tomlinson, Gail E, Anton-Culver, Hoda, Strong, Louise C, Kasten, Carol H, Finkelstein, Dianne M, Plon, Sharon E

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Characterization of genomic alterations in radiation-associated breast cancer among childhood cancer survivors, using comparative genomic hybridization (CGH) arrays von Yang, Xiaohong R, Killian, J Keith, Hammond, Sue, Burke, Laura S, Bennett, Hunter, Wang, Yonghong, Davis, Sean R, Strong, Louise C, Neglia, Joseph, Stovall, Marilyn, Weathers, Rita E, Robison, Leslie L, Bhatia, Smita, Mabuchi, Kiyohiko, Inskip, Peter D, Meltzer, Paul

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Li–Fraumeni Syndrome Disease Model: A Platform to Develop Precision Cancer Therapy Targeting Oncogenic p53 von Zhou, Ruoji, Xu, An, Gingold, Julian, Strong, Louise C., Zhao, Ruiying, Lee, Dung-Fang

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Activating mutation in MET oncogene in familial colorectal cancer von Neklason, Deborah W, Done, Michelle W, Sargent, Nykole R, Schwartz, Ann G, Anton-Culver, Hoda, Griffin, Constance A, Ahnen, Dennis J, Schildkraut, Joellen M, Tomlinson, Gail E, Strong, Louise C, Miller, Alexander R, Stopfer, Jill E, Burt, Randall W

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Bayesian Semiparametric Estimation of Cancer-Specific Age-at-Onset Penetrance With Application to Li-Fraumeni Syndrome von Shin, Seung Jun, Yuan, Ying, Strong, Louise C., Bojadzieva, Jasmina, Wang, Wenyi

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Cancer mortality in relatives of desmoid sarcoma patients von Strong, Louise C., Schnitman, Anita

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Assessing BRCA Carrier Probabilities in Extended Families von Barcenas, Carlos H, Hosain, G M Monawar, Arun, Banu, Zong, Jihong, Zhou, Xiaojun, Chen, Jianfang, Cortada, Jill M, Mills, Gordon B, Tomlinson, Gail E, Miller, Alexander R, Strong, Louise C, Amos, Christopher I

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Recommendations for Surveillance for Children with Leukemia-Predisposing Conditions von Porter, Christopher C, Druley, Todd E, Erez, Ayelet, Kuiper, Roland P, Onel, Kenan, Schiffman, Joshua D, Wolfe Schneider, Kami, Scollon, Sarah R, Scott, Hamish S, Strong, Louise C, Walsh, Michael F, Nichols, Kim E

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Penetrance Estimates Over Time to First and Second Primary Cancer Diagnosis in Families with Li-Fraumeni Syndrome: A Single Institution Perspective von Shin, Seung Jun, Dodd-Eaton, Elissa B., Gao, Fan, Bojadzieva, Jasmina, Chen, Jingxiao, Kong, Xianhua, Amos, Christopher, Ning, Jing, Strong, Louise C., Wang, Wenyi

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Lung cancer risk in germline p53 mutation carriers: association between an inherited cancer predisposition, cigarette smoking, and cancer risk von HWANG, Shih-Jen, CHENG, Li Shu-Chung, LOZANO, Guillermina, AMOS, Christopher I, XIANGJUN GU, STRONG, Louise C

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Early onset HER2‐positive breast cancer is associated with germline TP53 mutations von Melhem‐Bertrandt, Amal, Bojadzieva, Jasmina, Ready, Kaylene J., Obeid, Elias, Liu, Diane D., Gutierrez‐Barrera, Angelica M., Litton, Jennifer K., Olopade, Olufunmilayo I., Hortobagyi, Gabriel N., Strong, Louise C., Arun, Banu K.

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