Antibody to Capsular Polysaccharides of Streptococcus pneumoniae: Prevalence, Persistence, and Response to Revaccination von Musher, Daniel M., Groover, Jean E., Rowland, Jack M., Watson, David A., Struewing, Jeffery B., Baughn, Robert E., Mufson, Maurice A.

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The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies von McCarty, Catherine A, Chisholm, Rex L, Chute, Christopher G, Kullo, Iftikhar J, Jarvik, Gail P, Larson, Eric B, Li, Rongling, Masys, Daniel R, Ritchie, Marylyn D, Roden, Dan M, Struewing, Jeffery P, Wolf, Wendy A

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SJS/TEN 2017: Building Multidisciplinary Networks to Drive Science and Translation von White, Katie D., Abe, Riichiro, Ardern-Jones, Michael, Beachkofsky, Thomas, Bouchard, Charles, Carleton, Bruce, Chodosh, James, Cibotti, Ricardo, Davis, Robert, Denny, Joshua C., Dodiuk-Gad, Roni P., Ergen, Elizabeth N., Goldman, Jennifer L., Holmes, James H., Hung, Shuen-Iu, Lacouture, Mario E., Lehloenya, Rannakoe J., Mallal, Simon, Manolio, Teri A., Micheletti, Robert G., Mitchell, Caroline M., Mockenhaupt, Maja, Ostrov, David A., Pavlos, Rebecca, Pirmohamed, Munir, Pope, Elena, Redwood, Alec, Rosenbach, Misha, Rosenblum, Michael D., Roujeau, Jean-Claude, Saavedra, Arturo P., Saeed, Hajirah N., Struewing, Jeffery P., Sueki, Hirohiko, Sukasem, Chonlaphat, Sung, Cynthia, Trubiano, Jason A., Weintraub, Jessica, Wheatley, Lisa M., Williams, Kristina B., Worley, Brandon, Chung, Wen-Hung, Shear, Neil H., Phillips, Elizabeth J.

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Parity, Oral Contraceptives, and the Risk of Ovarian Cancer among Carriers and Noncarriers of a BRCA1 or BRCA2 Mutation von Modan, Baruch, Hartge, Patricia, Hirsh-Yechezkel, Galit, Chetrit, Angela, Lubin, Flora, Beller, Uzi, Ben-Baruch, Gilad, Fishman, Amiram, Menczer, Joseph, Struewing, Jeffery P, Tucker, Margaret A, Ebbers, Sara M, Friedman, Eitan, Piura, Benjamin, Wacholder, Sholom

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Enhancing GTEx by bridging the gaps between genotype, gene expression, and disease von Stranger, Barbara E, Brigham, Lori E, Hasz, Richard, Hunter, Marcus, Johns, Christopher, Johnson, Mark, Kopen, Gene, Leinweber, William F, Lonsdale, John T, McDonald, Alisa, Mestichelli, Bernadette, Myer, Kevin, Roe, Brian, Salvatore, Michael, Shad, Saboor, Thomas, Jeffrey A, Walters, Gary, Washington, Michael, Wheeler, Joseph, Bridge, Jason, Foster, Barbara A, Gillard, Bryan M, Karasik, Ellen, Kumar, Rachna, Miklos, Mark, Moser, Michael T, Jewell, Scott D, Montroy, Robert G, Rohrer, Daniel C, Valley, Dana R, Davis, David A, Mash, Deborah C, Gould, Sarah E, Guan, Ping, Koester, Susan, Little, A Roger, Martin, Casey, Moore, Helen M, Rao, Abhi, Struewing, Jeffery P, Volpi, Simona, Hansen, Kasper D, Hickey, Peter F, Rizzardi, Lindsay F, Hou, Lei, Liu, Yaping, Molinie, Benoit, Park, Yongjin, Rinaldi, Nicola, Wang, Li, Van Wittenberghe, Nicholas, Claussnitzer, Melina, Gelfand, Ellen T, Li, Qin, Linder, Sandra, Zhang, Rui, Smith, Kevin S, Tsang, Emily K, Chen, Lin S, Demanelis, Kathryn, Doherty, Jennifer A, Jasmine, Farzana, Kibriya, Muhammad G, Jiang, Lihua, Lin, Shin, Wang, Meng, Jian, Ruiqi, Li, Xiao, Chan, Joanne, Bates, Daniel, Diegel, Morgan, Halow, Jessica, Haugen, Eric, Johnson, Audra, Kaul, Rajinder, Lee, Kristen, Maurano, Matthew T, Nelson, Jemma, Neri, Fidencio J, Sandstrom, Richard, Fernando, Marian S, Linke, Caroline, Oliva, Meritxell, Skol, Andrew, Wu, Fan, Akey, Joshua M, Feinberg, Andrew P, Li, Jin Billy, Pierce, Brandon L, Stamatoyannopoulos, John A, Tang, Hua, Ardlie, Kristin G, Kellis, Manolis, Snyder, Michael P, Montgomery, Stephen B

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Polymorphisms in DNA double-strand break repair genes and risk of breast cancer : two population-based studies in USA and Poland, and meta-analyses von GARCIA-CLOSAS, Montserrat, EGAN, Kathleen M, ZATONSKI, Witold, BARDIN-MIKOLAJCZAK, Alicja, STRUEWING, Jeffery P, NEWCOMB, Polly A, BRINTON, Louise A, TITUS-ERNSTOFF, Linda, CHANOCK, Stephen, WELCH, Robert, LISSOWSKA, Jolanta, PEPLONSKA, Beata, SZESZENIA-DABROWSKA, Neonila

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Kin-cohort estimates for familial breast cancer risk in relation to variants in DNA base excision repair, BRCA1 interacting and growth factor genes von Sigurdson, Alice J, Hauptmann, Michael, Chatterjee, Nilanjan, Alexander, Bruce H, Doody, Michele Morin, Rutter, Joni L, Struewing, Jeffery P

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The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1 von Oddoux, Carole, Struewing, Jeffery P, Clayton, C. Mark, Neuhausen, Susan, Brody, Lawrence C, Kaback, Michael, Haas, Bruce, Norton, Larry, Borgen, Patrick, Jhanwar, Suresh, Goldgar, David, Ostrer, Harry, Offit, Kenneth

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FGFR2 variants and breast cancer risk: fine-scale mapping using African American studies and analysis of chromatin conformation von Udler, Miriam S., Meyer, Kerstin B., Pooley, Karen A., Karlins, Eric, Struewing, Jeffery P., Zhang, Jinghui, Doody, David R., MacArthur, Stewart, Tyrer, Jonathan, Pharoah, Paul D., Luben, Robert, Bernstein, Leslie, Kolonel, Laurence N., Henderson, Brian E., Le Marchand, Loic, Ursin, Giske, Press, Michael F., Brennan, Paul, Sangrajrang, Suleeporn, Gaborieau, Valerie, Odefrey, Fabrice, Shen, Chen-Yang, Wu, Pei-Ei, Wang, Hui-Chun, Kang, Daehee, Yoo, Keun-Young, Noh, Dong-Young, Ahn, Sei-Hyun, Ponder, Bruce A.J., Haiman, Christopher A., Malone, Kathleen E., Dunning, Alison M., Ostrander, Elaine A., Easton, Douglas F.

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A Single Nucleotide Polymorphism in the 5′ Untranslated Region of RAD51 and Risk of Cancer among BRCA1/2 Mutation Carriers von WANG, Wendy W, SPURDLE, Amanda B, TARONE, Robert E, DALY, Mary, LEVAVI, Hanoch, PIERCE, Heather, CHETRIT, Angela, YECHEZKEL, Galit Hirsh, CHENEVIX-TRENCH, Georgia, OFFIT, Kenneth, GODWIN, Andrew K, STRUEWING, Jeffery P, KOLACHANA, Prema, BOVE, Betsy, MODAN, Baruch, EBBERS, Sarah M, SUTHERS, Graeme, TUCKER, Margaret A, KAUFMAN, David J, DOODY, Michele M

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RAD51 135G→C Modifies Breast Cancer Risk among BRCA2 Mutation Carriers: Results from a Combined Analysis of 19 Studies von Antoniou, Antonis C., Sinilnikova, Olga M., Simard, Jacques, Léoné, Mélanie, Dumont, Martine, Neuhausen, Susan L., Struewing, Jeffery P., Stoppa-Lyonnet, Dominique, Barjhoux, Laure, Hughes, David J., Coupier, Isabelle, Belotti, Muriel, Lasset, Christine, Bonadona, Valérie, Bignon, Yves-Jean, Rebbeck, Timothy R., Wagner, Theresa, Lynch, Henry T., Domchek, Susan M., Nathanson, Katherine L., Garber, Judy E., Weitzel, Jeffrey, Narod, Steven A., Tomlinson, Gail, Olopade, Olufunmilayo I., Godwin, Andrew, Isaacs, Claudine, Jakubowska, Anna, Lubinski, Jan, Gronwald, Jacek, Górski, Bohdan, Byrski, Tomasz, Huzarski, Tomasz, Peock, Susan, Cook, Margaret, Baynes, Caroline, Murray, Alexandra, Rogers, Mark, Daly, Peter A., Dorkins, Huw, Schmutzler, Rita K., Versmold, Beatrix, Engel, Christoph, Meindl, Alfons, Arnold, Norbert, Niederacher, Dieter, Deissler, Helmut, Spurdle, Amanda B., Chen, Xiaoqing, Waddell, Nicola, Cloonan, Nicole, Kirchhoff, Tomas, Offit, Kenneth, Friedman, Eitan, Kaufmann, Bella, Laitman, Yael, Galore, Gilli, Rennert, Gad, Lejbkowicz, Flavio, Raskin, Leon, Andrulis, Irene L., Ilyushik, Eduard, Ozcelik, Hilmi, Devilee, Peter, Vreeswijk, Maaike P.G., Greene, Mark H., Prindiville, Sheila A., Osorio, Ana, Benítez, Javier, Zikan, Michal, Szabo, Csilla I., Kilpivaara, Outi, Nevanlinna, Heli, Hamann, Ute, Durocher, Francine, Arason, Adalgeir, Couch, Fergus J., Easton, Douglas F., Chenevix-Trench, Georgia

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DNA damage among thyroid cancer and multiple cancer cases, controls, and long-lived individuals von Sigurdson, Alice J., Hauptmann, Michael, Alexander, Bruce H., Doody, Michele Morin, Thomas, Cynthia B., Struewing, Jeffery P., Jones, Irene M.

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Papillary thyroid cancer and polymorphic variants in TSHR-and RET-related genes : a nested case-control study within a cohort of U.S. radiologic technologists von LÖNN, Stefan, BHATTI, Parveen, ALEXANDER, Bruce H, PINEDA, Marbin A, DOODY, Michele M, STRUEWING, Jeffery P, SIGURDSON, Alice J

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BRCA1/2 testing in hereditary breast and ovarian cancer families: Effectiveness of problem-solving training as a counseling intervention von McInerney-Leo, Aideen, Biesecker, Barbara Bowles, Hadley, Donald W., Kase, Ronald G., Giambarresi, Therese R., Johnson, Elizabeth, Lerman, Caryn, Struewing, Jeffery P.

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BRCA1/2 testing in hereditary breast and ovarian cancer families II: Impact on relationships von McInerney-Leo, Aideen, Biesecker, Barbara Bowles, Hadley, Donald W., Kase, Ronald G., Giambarresi, Therese R., Johnson, Elizabeth, Lerman, Caryn, Struewing, Jeffery P.

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A Single Genetic Origin for the G101W CDKN2A Mutation in 20 Melanoma-Prone Families von Ciotti, Paola, Struewing, Jeffery P., Mantelli, Michela, Chompret, Agnès, Avril, Marie-Françoise, Santi, Pier Luigi, Tucker, Margaret A., Bianchi-Scarrà, Giovanna, Bressac-de Paillerets, Brigitte, Goldstein, Alisa M.

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Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families : Results of an international study von NEUHAUSEN, S. L, MAZOYER, S, SOLOMON, E, WEBER, B, COUCH, F, STRUEWING, J, TONIN, P, DUROCHER, F, NAROD, S, SKOLNICK, M. H, LENOIR, G, SEROVA, O, FRIEDMAN, L, PONDER, B, STOPPA-LYONNET, D, EASTON, D, KING, M.-C, GOLDGAR, D. E, STRATTON, M, OFFIT, K, CALIGO, A, TOMLINSON, G, CANNON-ALBRIGHT, L, BISHOP, T, KELSELL, D

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CHEK2:1100delC and female breast cancer in the United States von Mateus Pereira, Lutécia H., Sigurdson, Alice J., Doody, Michele M., Pineda, Marbin A., Alexander, Bruce H., Greene, Mark H., Struewing, Jeffery P.

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Founder BRCA1/2 Mutations among Male Patients with Breast Cancer in Israel von Struewing, Jeffery P., Coriaty, Zakia M., Ron, Elaine, Livoff, Alejandro, Konichezky, Mirian, Cohen, Pat, Resnick, Murray B., Lifzchiz-Mercerl, Beatriz, Lew, Sylvia, Iscovich, Jose

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Patients with Double Primary Tumors in the Breast and Ovary— Clinical Characteristics and BRCA1–2 Mutations Status von Fishman, Ami, Dekel, Eyal, Chetrit, Angela, Lerner-Geva, Liat, Bar-Am, Amiram, Beck, Dan, Beller, Uziel, Ben-Baruch, Gilad, Piura, Benjamin, Friedman, Eitan, Struewing, Jeffery P., Modan, Baruch

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