Mutation screening of RAD51C in high-risk breast and ovarian cancer families

Por Lu, Wenping, Wang, Xianshu, Lin, Hongsheng, Lindor, Noralane M., Couch, Fergus J.
Publicado em 2012

Microcephalin regulates BRCA2 and Rad51-associated DNA double strand break repair

Por Wu, Xianglin, Mondal, Gourish, Wang, Xianshu, Wu, Jianmin, Yang, Lin, Pankratz, Vernon S., Rowley, Matthew, Couch, Fergus J.
Publicado em 2009

Association of Mitotic Regulation Pathway Polymorphisms with Pancreatic Cancer Risk and Outcome

Por Couch, Fergus J., Wang, Xianshu, Bamlet, William R., de Andrade, Mariza, Petersen, Gloria M., McWilliams, Robert R.
Publicado em 2010

Association of Breast Cancer Susceptibility Variants with Risk of Pancreatic Cancer

Por Couch, Fergus J., Wang, Xianshu, McWilliams, Robert R., Bamlet, William R., de Andrade, Mariza, Petersen, Gloria M.
Publicado em 2009

Surgical Treatments for Infantile Purulent Meningitis Complicated by Subdural Effusion

Por Wang, Xianshu, Zhang, Xiaoru, Cao, Hongbin, Jing, Shiyuan, Yang, Zhiguo, Cheng, Zhenghai, Liu, Ye, Li, Xin, Gao, Feifei, Ji, Yuanqi
Publicado no Med Sci Monit (2015)

Evaluation of associations between common variation in mitotic regulatory pathways and risk of overall and high grade breast cancer

Por Stevens, Kristen N., Wang, Xianshu, Fredericksen, Zachary, Pankratz, V. Shane, Cerhan, James, Vachon, Celine M., Olson, Janet E., Couch, Fergus J.
Publicado em 2011

A review of a multifactorial probability based model for classification of BRCA1 and BRCA2 variants of uncertain significance (VUS)

Por Lindor, Noralane M., Guidugli, Lucia, Wang, Xianshu, Vallée, Maxime P., Monteiro, Alvaro N.A., Tavtigian, Sean, Goldgar, David E., Couch, Fergus J.
Publicado em 2011

Association of Genetic Variation in Mitotic Kinases with Breast Cancer Risk

Por Wang, Xianshu, Fredericksen, Zachary S., Vierkant, Robert A., Pankratz, V. Shane, Cerhan, James R., Justenhoven, Christina, Brauch, Hiltrud, Olson, Janet E., Couch, Fergus J.
Publicado em 2009

Frequent Truncating Mutation of TFAM Induces Mitochondrial DNA Depletion and Apoptotic Resistance in Microsatellite-Unstable Colorectal Cancer

Por Guo, Jianhui, Zheng, Li, Liu, Wenyong, Wang, Xianshu, Wang, Zemin, Wang, Zehua, French, Amy J., Kang, Dongchon, Chen, Lin, Thibodeau, Stephen N., Liu, Wanguo
Publicado em 2011

Association of Genetic Variation in Genes Implicated in the β–Catenin Destruction Complex with Risk of Breast Cancer

Por Wang, Xianshu, Goode, Ellen L., Fredericksen, Zachary S., Vierkant, Robert A., Pankratz, V. Shane, Rider, David N., Vachon, Celine M., Cerhan, James R., Olson, Janet E., Couch, Fergus J.
Publicado em 2008

Genetic variation in the chromosome 17q23 amplicon and breast cancer risk

Por Kelemen, Linda E, Wang, Xianshu, Fredericksen, Zachary S, Pankratz, V Shane, Pharoah, Paul DP, Ahmed, Shahana, Dunning, Alison M, Easton, Douglas F, Vierkant, Robert A, Cerhan, James R, Goode, Ellen L, Olson, Janet E, Couch, Fergus J
Publicado em 2009

Genetic variation in stromal proteins decorin and lumican with breast cancer: investigations in two case-control studies

Por Kelemen, Linda E, Couch, Fergus J, Ahmed, Shahana, Dunning, Alison M, Pharoah, Paul DP, Easton, Douglas F, Fredericksen, Zachary S, Vierkant, Robert A, Pankratz, V Shane, Goode, Ellen L, Scott, Christopher G, Rider, David N, Wang, Xianshu, Cerhan, James R, Vachon, Celine M
Publicado em 2008

No evidence for association of inherited variation in genes involved in mitosis and percent mammographic density

Por Vachon, Celine M, Li, Jingmei, Scott, Christopher G, Hall, Per, Czene, Kamila, Wang, Xianshu, Liu, Jianjun, Fredericksen, Zachary S, Rider, David N, Wu, Fang-Fang, Olson, Janet E, Cunningham, Julie M, Stevens, Kristen N, Sellers, Thomas A, Pankratz, Shane V, Couch, Fergus J
Publicado em 2012

Common variation in Nemo-like kinase (NLK) is associated with risk of ovarian cancer

Por Stevens, Kristen N., Kelemen, Linda E., Wang, Xianshu, Fridley, Brooke L., Vierkant, Robert A., Fredericksen, Zachary, Armasu, Sebastian M., Tsai, Ya-Yu, Berchuck, Andrew, Narod, Steven A., Phelan, Catherine M., Sutphen, Rebecca, Birrer, Michael J., Schildkraut, Joellen M., Sellers, Thomas A., Goode, Ellen L., Couch, Fergus J.
Publicado em 2012

Mutations in CHEK2 Associated with Prostate Cancer Risk

Por Dong, Xiangyang, Wang, Liang, Taniguchi, Ken, Wang, Xianshu, Cunningham, Julie M., McDonnell, Shannon K., Qian, Chiping, Marks, Angela F., Slager, Susan L., Peterson, Brett J., Smith, David I., Cheville, John C., Blute, Michael L., Jacobsen, Steve J., Schaid, Daniel J., Tindall, Donald J., Thibodeau, Stephen N., Liu, Wanguo
Publicado em 2003

A genome-wide association study to identify genetic susceptibility loci that modify ductal and lobular postmenopausal breast cancer risk associated with menopausal hormone therapy...

Por Hein, Rebecca, Flesch-Janys, Dieter, Dahmen, Norbert, Beckmann, Lars, Lindström, Sara, Schoof, Nils, Czene, Kamila, Mittelstraß, Kirstin, Illig, Thomas, Seibold, Petra, Behrens, Sabine, Humphreys, Keith, Li, Jingmei, Liu, Jianjun, Olson, Janet E., Wang, Xianshu, Hankinson, Susan E., Truong, Thérèse, Menegaux, Florence, dos Santos Silva, Isabel, Johnson, Nichola, Chen, Shou-Tung, Yu, Jyh-Cherng, Ziogas, Argyrios, Kataja, Vesa, Kosma, Veli-Matti, Mannermaa, Arto, Anton-Culver, Hoda, Shen, Chen-Yang, Brauch, Hiltrud, Peto, Julian, Guénel, Pascal, Kraft, Peter, Couch, Fergus J., Easton, Douglas F., Hall, Per, Chang-Claude, Jenny
Publicado em 2013

Evaluation of chromosome 6p22 as a breast cancer risk modifier locus in a follow-up study of BRCA2 mutation carriers

Por Stevens, Kristen N., Wang, Xianshu, Fredericksen, Zachary, Pankratz, Vernon S., Greene, Mark H., Andrulis, Irene L., Thomassen, Mads, Caligo, Maria, Nathanson, Katherine L., Jakubowska, Anna, Osorio, Ana, Hamann, Ute, Godwin, Andrew K., Stoppa-Lyonnet, Dominique, Southey, Melissa, Buys, Saundra S., Singer, Christian F., Hansen, Thomas V.O., Arason, Adalgeir, Offit, Kenneth, Piedmonte, Marion, Montagna, Marco, Imyanitov, Evgeny, Tihomirova, Laima, Sucheston, Lara, Beattie, Mary, Neuhausen, Susan L., Szabo, Csilla I., Simard, Jacques, Spurdle, Amanda B., Healey, Sue, Chen, Xiaoqing, Rebbeck, Timothy R., Easton, Douglas F., Chenevix-Trench, Georgia, Antoniou, Antonis C, Couch, Fergus J.
Publicado em 2012

Inherited Mutations in 17 Breast Cancer Susceptibility Genes Among a Large Triple-Negative Breast Cancer Cohort Unselected for Family History of Breast Cancer

Por Couch, Fergus J., Hart, Steven N., Sharma, Priyanka, Toland, Amanda Ewart, Wang, Xianshu, Miron, Penelope, Olson, Janet E., Godwin, Andrew K., Pankratz, V. Shane, Olswold, Curtis, Slettedahl, Seth, Hallberg, Emily, Guidugli, Lucia, Davila, Jaime I., Beckmann, Matthias W., Janni, Wolfgang, Rack, Brigitte, Ekici, Arif B., Slamon, Dennis J., Konstantopoulou, Irene, Fostira, Florentia, Vratimos, Athanassios, Fountzilas, George, Pelttari, Liisa M., Tapper, William J., Durcan, Lorraine, Cross, Simon S., Pilarski, Robert, Shapiro, Charles L., Klemp, Jennifer, Yao, Song, Garber, Judy, Cox, Angela, Brauch, Hiltrud, Ambrosone, Christine, Nevanlinna, Heli, Yannoukakos, Drakoulis, Slager, Susan L., Vachon, Celine M., Eccles, Diana M., Fasching, Peter A.
Publicado no J Clin Oncol (2015)

Subtyping of Breast Cancer by Immunohistochemistry to Investigate a Relationship between Subtype and Short and Long Term Survival: A Collaborative Analysis of Data for 10,159 Cases...

Por Blows, Fiona M., Driver, Kristy E., Schmidt, Marjanka K., Broeks, Annegien, van Leeuwen, Flora E., Wesseling, Jelle, Cheang, Maggie C., Gelmon, Karen, Nielsen, Torsten O., Blomqvist, Carl, Heikkilä, Päivi, Heikkinen, Tuomas, Nevanlinna, Heli, Akslen, Lars A., Bégin, Louis R., Foulkes, William D., Couch, Fergus J., Wang, Xianshu, Cafourek, Vicky, Olson, Janet E., Baglietto, Laura, Giles, Graham G., Severi, Gianluca, McLean, Catriona A., Southey, Melissa C., Rakha, Emad, Green, Andrew R., Ellis, Ian O., Sherman, Mark E., Lissowska, Jolanta, Anderson, William F., Cox, Angela, Cross, Simon S., Reed, Malcolm W. R., Provenzano, Elena, Dawson, Sarah-Jane, Dunning, Alison M., Humphreys, Manjeet, Easton, Douglas F., García-Closas, Montserrat, Caldas, Carlos, Pharoah, Paul D., Huntsman, David
Publicado em 2010

Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers

Por Wang, Xianshu, Pankratz, V. Shane, Fredericksen, Zachary, Tarrell, Robert, Karaus, Mary, McGuffog, Lesley, Pharaoh, Paul D.P., Ponder, Bruce A.J., Dunning, Alison M., Peock, Susan, Cook, Margaret, Oliver, Clare, Frost, Debra, Sinilnikova, Olga M., Stoppa-Lyonnet, Dominique, Mazoyer, Sylvie, Houdayer, Claude, Hogervorst, Frans B.L., Hooning, Maartje J., Ligtenberg, Marjolijn J., Spurdle, Amanda, Chenevix-Trench, Georgia, Schmutzler, Rita K., Wappenschmidt, Barbara, Engel, Christoph, Meindl, Alfons, Domchek, Susan M., Nathanson, Katherine L., Rebbeck, Timothy R., Singer, Christian F., Gschwantler-Kaulich, Daphne, Dressler, Catherina, Fink, Anneliese, Szabo, Csilla I., Zikan, Michal, Foretova, Lenka, Claes, Kathleen, Thomas, Gilles, Hoover, Robert N., Hunter, David J., Chanock, Stephen J., Easton, Douglas F., Antoniou, Antonis C., Couch, Fergus J.
Publicado em 2010