Traditional Roles in a Non-Traditional Setting: Genetic Counseling in Precision Oncology

Por Everett, Jessica N., Gustafson, Shanna L., Raymond, Victoria M.
Publicado em 2014

First Description of Parathyroid Disease in Multiple Endocrine Neoplasia 2A Syndrome

Por Sisson, James C., Giordano, Thomas J., Raymond, Victoria M., Doherty, Gerard M., Gruber, Stephen B.
Publicado em 2008

Estimating probability of germline mismatch repair mutations in colorectal cancer patients with microsatellite stable tumors

Por Everett, Jessica N, Raymond, Victoria M, Gornick, Michele, Mangrulkar, Rajesh S, Blanco, Ignacio, Gruber, Stephen B
Publicado em 2011

Prevalence of Germline TP53 Mutations in a Prospective Series of Unselected Patients with Adrenocortical Carcinoma

Por Raymond, Victoria M., Else, Tobias, Everett, Jessica N., Long, Jessica M., Gruber, Stephen B., Hammer, Gary D.
Publicado em 2013

A review of statistical methods for testing genetic anticipation: looking for an answer in Lynch syndrome

Por Boonstra, Philip S., Gruber, Stephen B., Raymond, Victoria M., Huang, Shu-chen, Timshel, Susanne, Nilbert, Mef, Mukherjee, Bhramar
Publicado em 2010

Germline Findings in Tumor-Only Sequencing: Points to Consider for Clinicians and Laboratories

Por Raymond, Victoria M., Gray, Stacy W., Roychowdhury, Sameek, Joffe, Steve, Chinnaiyan, Arul M., Parsons, D. Williams, Plon, Sharon E.
Publicado no J Natl Cancer Inst (2015)

Calculation of Risk of Colorectal and Endometrial Cancer Among Patients with Lynch Syndrome

Por Stoffel, Elena, Mukherjee, Bhramar, Raymond, Victoria M., Tayob, Nabihah, Kastrinos, Fay, Sparr, Jennifer, Wang, Fei, Bandipalliam, Prathap, Syngal, Sapna, Gruber, Stephen B.
Publicado em 2009

Hereditary Prostate Cancer as a Feature of Lynch Syndrome

Por Bauer, Christina M., Ray, Anna M., Halstead-Nussloch, Bronwen A., Dekker, Robert G., Raymond, Victoria M., Gruber, Stephen B., Cooney, Kathleen A.
Publicado em 2011

ALLELE-SPECIFIC EXPRESSION OF APC IN ADENOMATOUS POLYPOSIS FAMILIES

Por Castellsagué, Ester, González, Sara, Guinó, Elisabet, Stevens, Kristen N., Borràs, Ester, Raymond, Victoria M., Lázaro, Conxi, Blanco, Ignacio, Gruber, Stephen B., Capellá, Gabriel
Publicado em 2010

Elevated Risk of Prostate Cancer Among Men With Lynch Syndrome

Por Raymond, Victoria M., Mukherjee, Bhramar, Wang, Fei, Huang, Shu-Chen, Stoffel, Elena M., Kastrinos, Fay, Syngal, Sapna, Cooney, Kathleen A., Gruber, Stephen B.
Publicado em 2013

The Risk of Pancreatic Cancer in Families with Lynch Syndrome

Por Kastrinos, Fay, Mukherjee, Bhramar, Tayob, Nabihah, Wang, Fei, Sparr, Jennifer, Raymond, Victoria M., Bandipalliam, Prathap, Stoffel, Elena M., Gruber, Stephen B., Syngal, Sapna
Publicado em 2009

The Clinical Phenotype of SDHC-Associated Hereditary Paraganglioma Syndrome (PGL3)

Por Else, Tobias, Marvin, Monica L., Everett, Jessica N., Gruber, Stephen B., Arts, H. Alexander, Stoffel, Elena M., Auchus, Richard J., Raymond, Victoria M.
Publicado em 2014

Adrenocortical Carcinoma

Por Else, Tobias, Kim, Alex C., Sabolch, Aaron, Raymond, Victoria M., Kandathil, Asha, Caoili, Elaine M., Jolly, Shruti, Miller, Barbra S., Giordano, Thomas J., Hammer, Gary D.
Publicado em 2014

An Oncocytic Adrenal Tumor in a Patient with Birt-Hogg-Dubé Syndrome

Por Raymond, Victoria M., Long, Jessica M., Everett, Jessica N., Caoili, Elaine M., Gruber, Stephen B., Stoffel, Elena M., Giordano, Thomas J., Hammer, Gary D., Else, Tobias
Publicado em 2013

Illustrative case studies in the return of exome and genome sequencing results

Por Amendola, Laura M, Lautenbach, Denise, Scollon, Sarah, Bernhardt, Barbara, Biswas, Sawona, East, Kelly, Everett, Jessica, Gilmore, Marian J, Himes, Patricia, Raymond, Victoria M, Wynn, Julia, Hart, Ragan, Jarvik, Gail P
Publicado no Per Med (2015)

Adrenocortical Carcinoma Is a Lynch Syndrome–Associated Cancer

Por Raymond, Victoria M., Everett, Jessica N., Furtado, Larissa V., Gustafson, Shanna L., Jungbluth, Chelsy R., Gruber, Stephen B., Hammer, Gary D., Stoffel, Elena M., Greenson, Joel K., Giordano, Thomas J., Else, Tobias
Publicado em 2013

An American Founder Mutation in MLH1

Por Tomsic, Jerneja, Liyanarachchi, Sandya, Hampel, Heather, Morak, Monika, Thomas, Brittany C., Raymond, Victoria M., Chittenden, Anu, Schackert, Hans K., Gruber, Stephen B., Syngal, Sapna, Viel, Alessandra, Holinski-Feder, Elke, Thibodeau, Stephen N., de la Chapelle, Albert
Publicado em 2011

Mutation spectrum and risk of colorectal cancer in African American families with Lynch Syndrome

Por Guindalini, Rodrigo Santa Cruz, Win, Aung Ko, Gulden, Cassandra, Lindor, Noralane M., Newcomb, Polly A., Haile, Robert W., Raymond, Victoria, Stoffel, Elena, Hall, Michael, Llor, Xavier, Ukaegbu, Chinedu I., Solomon, Ilana, Weitzel, Jeffrey, Kalady, Matthew, Blanco, Amie, Terdiman, Jonathan, Shuttlesworth, Gladis A., Lynch, Patrick M., Hampel, Heather, Lynch, Henry T., Jenkins, Mark A., Olopade, Olufunmilayo I., Kupfer, Sonia S.
Publicado no Gastroenterology (2015)

Integrative clinical sequencing in the management of children and young adults with refractory or relapsed cancer

Por Mody, Rajen J., Wu, Yi-Mi, Lonigro, Robert J., Cao, Xuhong, Roychowdhury, Sameek, Vats, Pankaj, Frank, Kevin M., Prensner, John R., Asangani, Irfan, Palanisamy, Nallasivam, Dillman, Jonathan R., Rabah, Raja M., Kunju, Laxmi Priya, Everett, Jessica, Raymond, Victoria M., Ning, Yu, Su, Fengyun, Wang, Rui, Stoffel, Elena M., Innis, Jeffrey W., Roberts, J. Scott, Robertson, Patricia L., Yanik, Gregory, Chamdin, Aghiad, Connelly, James A., Choi, Sung, Harris, Andrew C., Kitko, Carrie, Rao, Rama Jasty, Levine, John E., Castle, Valerie P., Hutchinson, Raymond J., Talpaz, Moshe, Robinson, Dan R., Chinnaiyan, Arul M.
Publicado no JAMA (2015)