Absence of loss of heterozygosity of BRCA1 in a renal tumor from a BRCA1 germline mutation carrier

Por Alanee, Shaheen, Shah, Sohela, Murali, Rajmohan, Rau-Murthy, Rohini, Schrader, Kasmintan A., Offit, Kenneth
Publicado no Fam Cancer (2013)

Outcome of Genetic Evaluation of Kidney Cancer Patients Referred for Suspected Hereditary Cancer Syndromes

Por Stratton, Kelly L., Alanee, Shaheen, Glogowski, Emily A., Schrader, Kasmintan A., Rau-Murthy, Rohini, Klein, Robert, Russo, Paul, Coleman, Jonathan, Offit, Kenneth
Publicado no Urol Oncol (2015)

Hereditary diffuse gastric cancer: association with lobular breast cancer

Por Schrader, Kasmintan A., Masciari, Serena, Boyd, Niki, Wiyrick, Sara, Kaurah, Pardeep, Senz, Janine, Burke, Wylie, Lynch, Henry T., Garber, Judy E., Huntsman, David G.
Publicado em 2007

Description and Pilot Results from a Novel Method for Evaluating Return of Incidental Findings from Next Generation Sequencing Technologies

Por Goddard, Katrina A.B., Whitlock, Evelyn P., Berg, Jonathan S., Williams, Marc S., Webber, Elizabeth M., Webster, Jennifer A., Lin, Jennifer S., Schrader, Kasmintan A., Campos-Outcalt, Doug, Offit, Kenneth, Feigelson, Heather Spencer, Hollombe, Celine
Publicado em 2013

The Specificity of the FOXL2 c.402C>G Somatic Mutation: A Survey of Solid Tumors

Por Schrader, Kasmintan A., Gorbatcheva, Bella, Senz, Janine, Heravi-Moussavi, Alireza, Melnyk, Nataliya, Salamanca, Clara, Maines-Bandiera, Sarah, Cooke, Susanna L., Leung, Peter, Brenton, James D., Gilks, C. Blake, Monahan, John, Huntsman, David G.
Publicado em 2009

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 em 2013

Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast Cancer

Por Maxwell, Kara N., Hart, Steven N., Vijai, Joseph, Schrader, Kasmintan A., Slavin, Thomas P., Thomas, Tinu, Wubbenhorst, Bradley, Ravichandran, Vignesh, Moore, Raymond M., Hu, Chunling, Guidugli, Lucia, Wenz, Brandon, Domchek, Susan M., Robson, Mark E., Szabo, Csilla, Neuhausen, Susan L., Weitzel, Jeffrey N., Offit, Kenneth, Couch, Fergus J., Nathanson, Katherine L.
Publicado no Am J Hum Genet (2016)

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 em 2013

A Recessive Founder Mutation in Regulator of Telomere Elongation Helicase 1, RTEL1, Underlies Severe Immunodeficiency and Features of Hoyeraal Hreidarsson Syndrome

Por Ballew, Bari J., Joseph, Vijai, De, Saurav, Sarek, Grzegorz, Vannier, Jean-Baptiste, Stracker, Travis, Schrader, Kasmintan A., Small, Trudy N., O'Reilly, Richard, Manschreck, Chris, Harlan Fleischut, Megan M., Zhang, Liying, Sullivan, John, Stratton, Kelly, Yeager, Meredith, Jacobs, Kevin, Giri, Neelam, Alter, Blanche P., Boland, Joseph, Burdett, Laurie, Offit, Kenneth, Boulton, Simon J., Savage, Sharon A., Petrini, John H. J.
Publicado em 2013

Identification of a recurrent germline PAX5 mutation and susceptibility to pre-B cell acute lymphoblastic leukemia

Por Shah, Sohela, Schrader, Kasmintan A., Waanders, Esmé, Timms, Andrew E., Vijai, Joseph, Miething, Cornelius, Wechsler, Jeremy, Yang, Jun, Hayes, James, Klein, Robert J., Zhang, Jinghui, Wei, Lei, Wu, Gang, Rusch, Michael, Nagahawatte, Panduka, Ma, Jing, Chen, Shann-Ching, Song, Guangchun, Cheng, Jinjun, Meyers, Paul, Bhojwani, Deepa, Jhanwar, Suresh, Maslak, Peter, Fleisher, Martin, Littman, Jason, Offit, Lily, Rau-Murthy, Rohini, Fleischut, Megan Harlan, Corines, Marina, Murali, Rajmohan, Gao, Xiaoni, Manschreck, Christopher, Kitzing, Thomas, Murty, Vundavalli V., Raimondi, Susana, Kuiper, Roland P., Simons, Annet, Schiffman, Joshua D., Onel, Kenan, Plon, Sharon E., Wheeler, David, Ritter, Deborah, Ziegler, David S., Tucker, Kathy, Sutton, Rosemary, Chenevix-Trench, Georgia, Li, Jun, Huntsman, David G., Hansford, Samantha, Senz, Janine, Walsh, Thomas, Lee, Ming, Hahn, Christopher N., Roberts, Kathryn, King, Mary-Claire, Lo, Sarah M., Levine, Ross L., Viale, Agnes, Socci, Nicholas D., Nathanson, Katherine L., Scott, Hamish S., Daly, Mark, Lipkin, Steven M., Lowe, Scott W., Downing, James R., Altshuler, David, Sandlund, John T., Horwitz, Marshall S., Mullighan, Charles G., Offit, Kenneth
Publicado em 2013

Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant

Por Li, Jun, Woods, Susan L., Healey, Sue, Beesley, Jonathan, Chen, Xiaoqing, Lee, Jason S., Sivakumaran, Haran, Wayte, Nicci, Nones, Katia, Waterfall, Joshua J., Pearson, John, Patch, Anne-Marie, Senz, Janine, Ferreira, Manuel A., Kaurah, Pardeep, Mackenzie, Robertson, Heravi-Moussavi, Alireza, Hansford, Samantha, Lannagan, Tamsin R.M., Spurdle, Amanda B., Simpson, Peter T., da Silva, Leonard, Lakhani, Sunil R., Clouston, Andrew D., Bettington, Mark, Grimpen, Florian, Busuttil, Rita A., Di Costanzo, Natasha, Boussioutas, Alex, Jeanjean, Marie, Chong, George, Fabre, Aurélie, Olschwang, Sylviane, Faulkner, Geoffrey J., Bellos, Evangelos, Coin, Lachlan, Rioux, Kevin, Bathe, Oliver F., Wen, Xiaogang, Martin, Hilary C., Neklason, Deborah W., Davis, Sean R., Walker, Robert L., Calzone, Kathleen A., Avital, Itzhak, Heller, Theo, Koh, Christopher, Pineda, Marbin, Rudloff, Udo, Quezado, Martha, Pichurin, Pavel N., Hulick, Peter J., Weissman, Scott M., Newlin, Anna, Rubinstein, Wendy S., Sampson, Jone E., Hamman, Kelly, Goldgar, David, Poplawski, Nicola, Phillips, Kerry, Schofield, Lyn, Armstrong, Jacqueline, Kiraly-Borri, Cathy, Suthers, Graeme K., Huntsman, David G., Foulkes, William D., Carneiro, Fatima, Lindor, Noralane M., Edwards, Stacey L., French, Juliet D., Waddell, Nicola, Meltzer, Paul S., Worthley, Daniel L., Schrader, Kasmintan A., Chenevix-Trench, Georgia
Publicado no Am J Hum Genet (2016)