Tissue-Specific Enrichment of Lymphoma Risk Loci in Regulatory Elements

por Hayes, James E., Trynka, Gosia, Vijai, Joseph, Offit, Kenneth, Raychaudhuri, Soumya, Klein, Robert J.
Publicado 2015

Assessment of SLX4 Mutations in Hereditary Breast Cancers

por Shah, Sohela, Kim, Yonghwan, Ostrovnaya, Irina, Murali, Rajmohan, Schrader, Kasmintan A., Lach, Francis P., Sarrel, Kara, Rau-Murthy, Rohini, Hansen, Nichole, Zhang, Liyng, Kirchhoff, Tomas, Stadler, Zsofia, Robson, Mark, Vijai, Joseph, Offit, Kenneth, Smogorzewska, Agata
Publicado 2013

Cascading After Peridiagnostic Cancer Genetic Testing: An Alternative to Population-Based Screening

por Offit, Kenneth, Tkachuk, Kaitlyn A., Stadler, Zsofia K., Walsh, Michael F., Diaz-Zabala, Hector, Levin, Jeffrey D., Steinsnyder, Zoe, Ravichandran, Vignesh, Sharaf, Ravi N., Frey, Melissa K., Lipkin, Steven M., Robson, Mark E., Hamilton, Jada G., Vijai, Joseph, Mukherjee, Semanti
Publicado 2020

Sequencing at lymphoid neoplasm susceptibility loci maps six myeloma risk genes

por Waller, Rosalie Griffin, Klein, Robert J, Vijai, Joseph, McKay, James D, Clay-Gilmour, Alyssa, Wei, Xiaomu, Madsen, Michael J, Sborov, Douglas W, Curtin, Karen, Slager, Susan L, Offit, Kenneth, Vachon, Celine M, Lipkin, Steven M, Dumontet, Charles, Camp, Nicola J
Publicado 2021

Clonal Hematopoiesis and COVID-19 Severity in Cancer Patients

por Bolton, Kelly L., Foote, Michael, Jee, Justin, Safonov, Anton, Ptashkin, Ryan, Devlin, Sean, Gedvilaite, Erika, Gao, Teng, Papaemmanuil, Elli, Pessin, Melissa S., Kamboj, Mini, Vijai, Joseph, Offit, Kenneth, Awadalla, Phillip, Nataranjan, Pradeep, Berger, Michael F., Norton, Larry, Levine, Ross L., Zehir, Ahmet
Publicado 2020

Nucleotide excision repair deficiency is a targetable therapeutic vulnerability in clear cell renal cell carcinoma

por Prosz, Aurel, Duan, Haohui, Tisza, Viktoria, Sahgal, Pranshu, Topka, Sabine, Klus, Gregory T., Börcsök, Judit, Sztupinszki, Zsofia, Hanlon, Timothy, Diossy, Miklos, Vizkeleti, Laura, Stormoen, Dag Rune, Csabai, Istvan, Pappot, Helle, Vijai, Joseph, Offit, Kenneth, Ried, Thomas, Sethi, Nilay, Mouw, Kent W., Spisak, Sandor, Pathania, Shailja, Szallasi, Zoltan
Publicado 2023

Nucleotide excision repair deficiency is a targetable therapeutic vulnerability in clear cell renal cell carcinoma

por Prosz, Aurel, Duan, Haohui, Tisza, Viktoria, Sahgal, Pranshu, Topka, Sabine, Klus, Gregory T, Börcsök, Judit, Sztupinszki, Zsofia, Hanlon, Timothy, Diossy, Miklos, Vizkeleti, Laura, Stormoen, Dag Rune, Csabai, Istvan, Pappot, Helle, Vijai, Joseph, Offit, Kenneth, Ried, Thomas, Sethi, Nilay, Mouw, Kent W., Spisak, Sandor, Pathania, Shailja, Szallasi, Zoltan
Publicado 2023

Genetic Variation in DNA Repair Pathways and Risk of Non-Hodgkin's Lymphoma

por Rendleman, Justin, Antipin, Yevgeniy, Reva, Boris, Adaniel, Christina, Przybylo, Jennifer A., Dutra-Clarke, Ana, Hansen, Nichole, Heguy, Adriana, Huberman, Kety, Borsu, Laetitia, Paltiel, Ora, Ben-Yehuda, Dina, Brown, Jennifer R., Freedman, Arnold S., Sander, Chris, Zelenetz, Andrew, Klein, Robert J., Shao, Yongzhao, Lacher, Mortimer, Vijai, Joseph, Offit, Kenneth, Kirchhoff, Tomas
Publicado 2014

Susceptibility Loci Associated with Specific and Shared Subtypes of Lymphoid Malignancies

por Vijai, Joseph, Kirchhoff, Tomas, Schrader, Kasmintan A., Brown, Jennifer, Dutra-Clarke, Ana Virginia, Manschreck, Christopher, Hansen, Nichole, Rau-Murthy, Rohini, Sarrel, Kara, Przybylo, Jennifer, Shah, Sohela, Cheguri, Srujana, Stadler, Zsofia, Zhang, Liying, Paltiel, Ora, Ben-Yehuda, Dina, Viale, Agnes, Portlock, Carol, Straus, David, Lipkin, Steven M., Lacher, Mortimer, Robson, Mark, Klein, Robert J., Zelenetz, Andrew, Offit, Kenneth
Publicado 2013

Development and Validation of a Breast Cancer Polygenic Risk Score on the Basis of Genetic Ancestry Composition

por Hughes, Elisha, Wagner, Susanne, Pruss, Dmitry, Bernhisel, Ryan, Probst, Braden, Abkevich, Victor, Simmons, Timothy, Hullinger, Brooke, Judkins, Thaddeus, Rosenthal, Eric, Roa, Benjamin, Domchek, Susan M., Eng, Charis, Garber, Judy, Gary, Monique, Klemp, Jennifer, Mukherjee, Semanti, Offit, Kenneth, Olopade, Olufunmilayo I., Vijai, Joseph, Weitzel, Jeffrey N., Whitworth, Pat, Yehia, Lamis, Gordon, Ora, Pederson, Holly, Kurian, Allison, Slavin, Thomas P., Gutin, Alexander, Lanchbury, Jerry S.
Publicado 2022

NBN Pathogenic Germline Variants are Associated with Pan-Cancer Susceptibility and In Vitro DNA Damage Response Defects

por Belhadj, Sami, Khurram, Aliya, Bandlamudi, Chaitanya, Palou-Márquez, Guillermo, Ravichandran, Vignesh, Steinsnyder, Zoe, Wildman, Temima, Catchings, Amanda, Kemel, Yelena, Mukherjee, Semanti, Fesko, Benjamin, Arora, Kanika, Mehine, Miika, Dandiker, Sita, Izhar, Aalin, Petrini, John, Domchek, Susan, Nathanson, Katherine L., Brower, Jamie, Couch, Fergus, Stadler, Zsofia, Robson, Mark, Walsh, Michael, Vijai, Joseph, Berger, Michael, Supek, Fran, Karam, Rachid, Topka, Sabine, Offit, Kenneth
Publicado 2023

The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk

por Slavin, Thomas P., Maxwell, Kara N., Lilyquist, Jenna, Vijai, Joseph, Neuhausen, Susan L., Hart, Steven N., Ravichandran, Vignesh, Thomas, Tinu, Maria, Ann, Villano, Danylo, Schrader, Kasmintan A., Moore, Raymond, Hu, Chunling, Wubbenhorst, Bradley, Wenz, Brandon M., D’Andrea, Kurt, Robson, Mark E., Peterlongo, Paolo, Bonanni, Bernardo, Ford, James M., Garber, Judy E., Domchek, Susan M., Szabo, Csilla, Offit, Kenneth, Nathanson, Katherine L., Weitzel, Jeffrey N., Couch, Fergus J.
Publicado 2017

Author Correction: The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk

por Slavin, Thomas P., Maxwell, Kara N., Lilyquist, Jenna, Vijai, Joseph, Neuhausen, Susan L., Hart, Steve N., Ravichandran, Vignesh, Thomas, Tinu, Maria, Ann, Villano, Danylo, Schrader, Kasmintan A., Moore, Raymond, Hu, Chunling, Wubbenhorst, Bradley, Wenz, Brandon M., D’Andrea, Kurt, Robson, Mark E., Peterlongo, Paolo, Bonanni, Bernardo, Ford, James M., Garber, Judy E., Domchek, Susan M., Szabo, Csilla, Offit, Kenneth, Nathanson, Katherine L., Weitzel, Jeffrey N., Couch, Fergus J.
Publicado 2017

Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins

por Carmi, Shai, Hui, Ken Y., Kochav, Ethan, Liu, Xinmin, Xue, James, Grady, Fillan, Guha, Saurav, Upadhyay, Kinnari, Ben-Avraham, Dan, Mukherjee, Semanti, Bowen, B. Monica, Thomas, Tinu, Vijai, Joseph, Cruts, Marc, Froyen, Guy, Lambrechts, Diether, Plaisance, Stéphane, Van Broeckhoven, Christine, Van Damme, Philip, Van Marck, Herwig, Barzilai, Nir, Darvasi, Ariel, Offit, Kenneth, Bressman, Susan, Ozelius, Laurie J., Peter, Inga, Cho, Judy H., Ostrer, Harry, Atzmon, Gil, Clark, Lorraine N., Lencz, Todd, Pe’er, Itsik
Publicado 2014

Germline ETV6 Mutations Confer Susceptibility to Acute Lymphoblastic Leukemia and Thrombocytopenia

por Topka, Sabine, Vijai, Joseph, Walsh, Michael F., Jacobs, Lauren, Maria, Ann, Villano, Danylo, Gaddam, Pragna, Wu, Gang, McGee, Rose B., Quinn, Emily, Inaba, Hiroto, Hartford, Christine, Pui, Ching-hon, Pappo, Alberto, Edmonson, Michael, Zhang, Michael Y., Stepensky, Polina, Steinherz, Peter, Schrader, Kasmintan, Lincoln, Anne, Bussel, James, Lipkin, Steve M., Goldgur, Yehuda, Harit, Mira, Stadler, Zsofia K., Mullighan, Charles, Weintraub, Michael, Shimamura, Akiko, Zhang, Jinghui, Downing, James R., Nichols, Kim E., Offit, Kenneth
Publicado 2015

Integrative Clinical Genomics of Metastatic Cancer

por Robinson, Dan R., Wu, Yi-Mi, Lonigro, Robert J., Vats, Pankaj, Cobain, Erin, Everett, Jessica, Cao, Xuhong, Rabban, Erica, Kumar-Sinha, Chandan, Raymond, Victoria, Schuetze, Scott, Alva, Ajjai, Siddiqui, Javed, Chugh, Rashmi, Worden, Francis, Zalupski, Mark M., Innis, Jeffrey, Mody, Rajen J., Tomlins, Scott A., Lucas, David, Baker, Laurence H., Ramnath, Nithya, Schott, Ann F., Hayes, Daniel F., Vijai, Joseph, Offit, Kenneth, Stoffel, Elena M., Roberts, J. Scott, Smith, David C., Kunju, Lakshmi P., Talpaz, Moshe, Cieslik, Marcin, Chinnaiyan, Arul M.
Publicado 2017

Germline SDHA mutations in children and adults with cancer

por Dubard Gault, Marianne, Mandelker, Diana, DeLair, Deborah, Stewart, Carolyn R., Kemel, Yelena, Sheehan, Margaret R., Siegel, Beth, Kennedy, Jennifer, Marcell, Vanessa, Arnold, Angela, Al-Ahmadie, Hikmat, Modak, Shakeel, Robson, Mark, Shukla, Neerav, Roberts, Stephen, Vijai, Joseph, Topka, Sabine, Kentsis, Alex, Cadoo, Karen, Carlo, Maria, Latham Schwark, Alicia, Reznik, Ed, Dinatale, Renzo, Hechtman, Jaclyn, Borras Flores, Ester, Jairam, Sowmaya, Yang, Ciyu, Li, Yirong, Bayraktar, Erol Can, Ceyhan-Birsoy, Ozge, Zhang, Liying, Kohlman, Wendy, Schiffman, Joshua, Stadler, Zsofia, Birsoy, Kivanc, Kung, Andrew, Offit, Kenneth, Walsh, Michael F.
Publicado 2018

The context-specific role of germline pathogenicity in tumorigenesis

por Srinivasan, Preethi, Bandlamudi, Chaitanya, Jonsson, Philip, Kemel, Yelena, Chavan, Shweta S., Richards, Allison L., Penson, Alexander V., Bielski, Craig M., Fong, Christopher, Syed, Aijazuddin, Jayakumaran, Gowtham, Prasad, Meera, Hwee, Jason, Sumer, Selcuk Onur, de Bruijn, Ino, Li, Xiang, Gao, JianJiong, Schultz, Nikolaus, Cambria, Roy, Galle, Jesse, Mukherjee, Semanti, Vijai, Joseph, Cadoo, Karen A., Carlo, Maria I., Walsh, Michael F., Mandelker, Diana, Ceyhan-Birsoy, Ozge, Shia, Jinru, Zehir, Ahmet, Ladanyi, Marc, Hyman, David M., Zhang, Liying, Offit, Kenneth, Robson, Mark E., Solit, David B., Stadler, Zsofia K., Berger, Michael F., Taylor, Barry S.
Publicado 2021

Genetically Determined Height and Risk of Non-hodgkin Lymphoma

por Moore, Amy, Kane, Eleanor, Wang, Zhaoming, Panagiotou, Orestis A., Teras, Lauren R., Monnereau, Alain, Wong Doo, Nicole, Machiela, Mitchell J., Skibola, Christine F., Slager, Susan L., Salles, Gilles, Camp, Nicola J., Bracci, Paige M., Nieters, Alexandra, Vermeulen, Roel C. H., Vijai, Joseph, Smedby, Karin E., Zhang, Yawei, Vajdic, Claire M., Cozen, Wendy, Spinelli, John J., Hjalgrim, Henrik, Giles, Graham G., Link, Brian K., Clavel, Jacqueline, Arslan, Alan A., Purdue, Mark P., Tinker, Lesley F., Albanes, Demetrius, Ferri, Giovanni M., Habermann, Thomas M., Adami, Hans-Olov, Becker, Nikolaus, Benavente, Yolanda, Bisanzi, Simonetta, Boffetta, Paolo, Brennan, Paul, Brooks-Wilson, Angela R., Canzian, Federico, Conde, Lucia, Cox, David G., Curtin, Karen, Foretova, Lenka, Gapstur, Susan M., Ghesquières, Hervé, Glenn, Martha, Glimelius, Bengt, Jackson, Rebecca D., Lan, Qing, Liebow, Mark, Maynadie, Marc, McKay, James, Melbye, Mads, Miligi, Lucia, Milne, Roger L., Molina, Thierry J., Morton, Lindsay M., North, Kari E., Offit, Kenneth, Padoan, Marina, Patel, Alpa V., Piro, Sara, Ravichandran, Vignesh, Riboli, Elio, de Sanjose, Silvia, Severson, Richard K., Southey, Melissa C., Staines, Anthony, Stewart, Carolyn, Travis, Ruth C., Weiderpass, Elisabete, Weinstein, Stephanie, Zheng, Tongzhang, Chanock, Stephen J., Chatterjee, Nilanjan, Rothman, Nathaniel, Birmann, Brenda M., Cerhan, James R., Berndt, Sonja I.
Publicado 2020

Two high-risk susceptibility loci at 6p25.3 and 14q32.13 for Waldenström macroglobulinemia

por McMaster, Mary L., Berndt, Sonja I., Zhang, Jianqing, Slager, Susan L., Li, Shengchao Alfred, Vajdic, Claire M., Smedby, Karin E., Yan, Huihuang, Birmann, Brenda M., Brown, Elizabeth E., Smith, Alex, Kleinstern, Geffen, Fansler, Mervin M., Mayr, Christine, Zhu, Bin, Chung, Charles C., Park, Ju-Hyun, Burdette, Laurie, Hicks, Belynda D., Hutchinson, Amy, Teras, Lauren R., Adami, Hans-Olov, Bracci, Paige M., McKay, James, Monnereau, Alain, Link, Brian K., Vermeulen, Roel C. H., Ansell, Stephen M., Maria, Ann, Diver, W. Ryan, Melbye, Mads, Ojesina, Akinyemi I., Kraft, Peter, Boffetta, Paolo, Clavel, Jacqueline, Giovannucci, Edward, Besson, Caroline M., Canzian, Federico, Travis, Ruth C., Vineis, Paolo, Weiderpass, Elisabete, Montalvan, Rebecca, Wang, Zhaoming, Yeager, Meredith, Becker, Nikolaus, Benavente, Yolanda, Brennan, Paul, Foretova, Lenka, Maynadie, Marc, Nieters, Alexandra, de Sanjose, Silvia, Staines, Anthony, Conde, Lucia, Riby, Jacques, Glimelius, Bengt, Hjalgrim, Henrik, Pradhan, Nisha, Feldman, Andrew L., Novak, Anne J., Lawrence, Charles, Bassig, Bryan A., Lan, Qing, Zheng, Tongzhang, North, Kari E., Tinker, Lesley F., Cozen, Wendy, Severson, Richard K., Hofmann, Jonathan N., Zhang, Yawei, Jackson, Rebecca D., Morton, Lindsay M., Purdue, Mark P., Chatterjee, Nilanjan, Offit, Kenneth, Cerhan, James R., Chanock, Stephen J., Rothman, Nathaniel, Vijai, Joseph, Goldin, Lynn R., Skibola, Christine F., Caporaso, Neil E.
Publicado 2018