Resultats de la cerca - Struewing, Jeffery P. 

HapScope: a software system for automated and visual analysis of functionally annotated haplotypes per Zhang, Jinghui, Rowe, William L., Struewing, Jeffery P., Buetow, Kenneth H.

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Similar prevalence of founder BRCA1 and BRCA2 mutations among Ashkenazi and Non-Ashkenazi men with breast cancer: Evidence from 261 cases in Israel, 1976-1999 per Chodick, Gabriel, Struewing, Jeffery P., Ron, Elaine, Rutter, Joni L., Iscovich, Jose

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Potential Excess Mortality in BRCA1/2 Mutation Carriers beyond Breast, Ovarian, Prostate, and Pancreatic Cancers, and Melanoma per Mai, Phuong L., Chatterjee, Nilanjan, Hartge, Patricia, Tucker, Margaret, Brody, Lawrence, Struewing, Jeffery P., Wacholder, Sholom

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No evidence of excess breast cancer risk among mutation-negative women from BRCA mutation-positive families per Korde, Larissa A., Mueller, Christine M., Loud, Jennifer T., Struewing, Jeffery P., Nichols, Kathy, Greene, Mark H., Mai, Phuong L.

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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 per Sigurdson, Alice J, Hauptmann, Michael, Chatterjee, Nilanjan, Alexander, Bruce H, Doody, Michele Morin, Rutter, Joni L, Struewing, Jeffery P

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Systematic analysis of genetic alterations in tumors using Cancer Genome WorkBench (CGWB) per Zhang, Jinghui, Finney, Richard P., Rowe, William, Edmonson, Michael, Yang, Sei Hoon, Dracheva, Tatiana, Jen, Jin, Struewing, Jeffery P., Buetow, Kenneth H.

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Founder BRCA1/2 Mutations among Male Patients with Breast Cancer in Israel per 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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A Single Genetic Origin for the G101W CDKN2A Mutation in 20 Melanoma-Prone Families per 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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The BRCA1 Ashkenazi founder mutations occur on common haplotypes and are not highly correlated with anonymous single nucleotide polymorphisms likely to be used in genome-wide case-... per Pereira, Lutécia H Mateus, Pineda, Marbin A, Rowe, William H, Fonseca, Libia R, Greene, Mark H, Offit, Kenneth, Ellis, Nathan A, Zhang, Jinghui, Collins, Andrew, Struewing, Jeffery P

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Thyroid nodules, polymorphic variants in DNA repair and RET-related genes, and interaction with ionizing radiation exposure from nuclear tests in Kazakhstan per Sigurdson, Alice J., Land, Charles E., Bhatti, Parveen, Pineda, Marbin, Brenner, Alina, Carr, Zhanat, Gusev, Boris I., Zhumadilov, Zhaxibay, Simon, Steven L., Bouville, Andre, Rutter, Joni L., Ron, Elaine, Struewing, Jeffery P.

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The ATM missense mutation Ser49Cys and risk of breast cancer per Stredrick, Denise L., Garcia-Closas, Montserrat, Pineda, Marbin A., Bhatti, Parveen, Alexander, Bruce H., Doody, Michele M., Lissowska, Jolanta, Peplonska, Beata, Brinton, Louise A., Chanock, Stephen J., Struewing, Jeffery P., Sigurdson, Alice J.

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Breast cancer risk polymorphisms and interaction with ionizing radiation among U.S. Radiologic Technologists per Bhatti, Parveen, Doody, Michele M., Alexander, Bruce H., Yuenger, Jeff, Simon, Steven L., Weinstock, Robert M., Rosenstein, Marvin, Stovall, Marilyn, Abend, Michael, Preston, Dale L., Pharoah, Paul, Struewing, Jeffery P., Sigurdson, Alice J.

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Adverse Drug Reaction Causality Assessment Tools for Drug-Induced Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis: Room for Improvement per Goldman, Jennifer L., Chung, Wen-Hung, Lee, Brian R., Chen, Chun-Bing, Lu, Chun-Wei, Hoetzenecker, Wolfram, Micheletti, Robert, Yasuda, Sally Usdin, Margolis, David J., Shear, Neil H., Struewing, Jeffery P, Pirmohamed, Munir

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POLYMORPHISMS IN ESTROGEN BIOSYNTHESIS AND METABOLISM-RELATED GENES, IONIZING RADIATION EXPOSURE, AND RISK OF BREAST CANCER AMONG U.S. RADIOLOGIC TECHNOLOGISTS per Sigurdson, Alice J., Bhatti, Parveen, Chang, Shih-chen, Rajaraman, Preetha, Doody, Michele M., Bowen, Laura, Simon, Steven L., Weinstock, Robert M., Linet, Martha S., Rosenstein, Marvin, Stovall, Marilyn, Alexander, Bruce H., Preston, Dale L., Struewing, Jeffery P.

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The eMERGE Network: A consortium of biorepositories linked to electronic medical records data for conducting genomic studies per 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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Analysis of genetic variation in Ashkenazi Jews by high density SNP genotyping per Olshen, Adam B, Gold, Bert, Lohmueller, Kirk E, Struewing, Jeffery P, Satagopan, Jaya, Stefanov, Stefan A, Eskin, Eleazar, Kirchhoff, Tomas, Lautenberger, James A, Klein, Robert J, Friedman, Eitan, Norton, Larry, Ellis, Nathan A, Viale, Agnes, Lee, Catherine S, Borgen, Patrick I, Clark, Andrew G, Offit, Kenneth, Boyd, Jeff

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FGFR2 variants and breast cancer risk: fine-scale mapping using African American studies and analysis of chromatin conformation per 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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SJS/TEN 2017: Building Multidisciplinary Networks to Drive Science and Translation() per 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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RAD51 135G→C Modifies Breast Cancer Risk among BRCA2 Mutation Carriers: Results from a Combined Analysis of 19 Studies per 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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AURKA F31I Polymorphism and Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers: A CIMBA study per Couch, Fergus J., Sinilnikova, Olga, Vierkant, Robert A, Pankratz, V. Shane, Fredericksen, Zachary S., Stoppa-Lyonnet, Dominique, Coupier, Isabelle, Hughes, David, Hardouin, Agnès, Berthet, Pascaline, Peock, Susan, Cook, Margaret, Baynes, Caroline, Hodgson, Shirley, Morrison, Patrick J., Porteous, Mary E., Jakubowska, Anna, Lubinski, Jan, Gronwald, Jacek, Spurdle, Amanda B., Schmutzler, Rita, Versmold, Beatrix, Engel, Christoph, Meindl, Alfons, Sutter, Christian, Horst, Jurgen, Schaefer, Dieter, Offit, Kenneth, Kirchhoff, Tomas, Andrulis, Irene L., Ilyushik, Eduard, Glendon, Gordon, Devilee, Peter, Vreeswijk, Maaike P.G., Vasen, Hans F.A., Borg, Ake, Backenhorn, Katja, Struewing, Jeffery P., Greene, Mark H., Neuhausen, Susan L., Rebbeck, Timothy R., Nathanson, Katherine, Domchek, Susan, Wagner, Theresa, Garber, Judy E., Szabo, Csilla, Zikan, Michal, Foretova, Lenka, Olson, Janet E., Sellers, Thomas A., Lindor, Noralane, Nevanlinna, Heli, Tommiska, Johanna, Aittomaki, Kristiina, Hamann, Ute, Rashid, Muhammad U., Torres, Diana, Simard, Jacques, Durocher, Francine, Guenard, Frederic, Lynch, Henry T., Isaacs, Claudine, Weitzel, Jeffrey, Olopade, Olufunmilayo I., Narod, Steven, Daly, Mary B., Godwin, Andrew K., Tomlinson, Gail, Easton, Douglas F., Chenevix-Trench, Georgia, Antoniouon, Antonis C.

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