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

by Everett, Jessica N., Gustafson, Shanna L., Raymond, Victoria M.
Published 2014

Incorporating Genetic Counseling into Clinical Care for Children and Adolescents with Cancer

by Everett, Jessica N., Mody, Rajen J., Stoffel, Elena M., Chinnaiyan, Arul M.
Published in Future Oncol (2016)

Impact of changing guidelines on genetic testing and surveillance recommendations in a contemporary cohort of breast cancer survivors with family history of pancreatic cancer

by Wang, Annie, Everett, Jessica N., Chun, Jennifer, Cen, Cindy, Simeone, Diane M., Schnabel, Freya
Published in Sci Rep (2021)

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

by Everett, Jessica N, Raymond, Victoria M, Gornick, Michele, Mangrulkar, Rajesh S, Blanco, Ignacio, Gruber, Stephen B
Published 2011

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

by Raymond, Victoria M., Else, Tobias, Everett, Jessica N., Long, Jessica M., Gruber, Stephen B., Hammer, Gary D.
Published 2013

Returning Individual Research Results: Development of a Cancer Genetics Education and Risk Communication Protocol

by Roberts, J. Scott, Shalowitz, David I., Christensen, Kurt D., Everett, Jessica N., Kim, Scott Y. H., Raskin, Leon, Gruber, Stephen B.
Published 2010

Disclosing Individual CDKN2A Research Results to Melanoma Survivors: Interest, Impact, and Demands on Researchers

by Christensen, Kurt D., Roberts, J. Scott, Shalowitz, David I., Everett, Jessica N., Kim, Scott Y.H., Raskin, Leon, Gruber, Stephen B.
Published 2011

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

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

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

by 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
Published 2013

Physician Experiences and Understanding of Genomic Sequencing in Oncology

by Weipert, Caroline M., Ryan, Kerry A., Everett, Jessica N., Yashar, Beverly M., Chinnaiyan, Arul M., Roberts, J. Scott, De Vries, Raymond, Zikmund-Fisher, Brian J., Raymond, Victoria M.
Published in J Genet Couns (2017)

Adrenocortical Carcinoma Is a Lynch Syndrome–Associated Cancer

by 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
Published 2013

Screening for Germline Mismatch Repair Mutations Following Diagnosis of Sebaceous Neoplasm

by Everett, Jessica N., Raymond, Victoria M., Dandapani, Monica, Marvin, Monica, Kohlmann, Wendy, Chittenden, Anu, Koeppe, Erika, Gustafson, Shanna L., Else, Tobias, Fullen, Douglas R., Johnson, Timothy M., Syngal, Sapna, Gruber, Stephen B., Stoffel, Elena M.
Published in JAMA Dermatol (2014)

Comparing models of delivery for cancer genetics services among patients receiving primary care who meet criteria for genetic evaluation in two healthcare systems: BRIDGE randomize...

by Kaphingst, Kimberly A., Kohlmann, Wendy, Chambers, Rachelle Lorenz, Goodman, Melody S., Bradshaw, Richard, Chan, Priscilla A., Chavez-Yenter, Daniel, Colonna, Sarah V., Espinel, Whitney F., Everett, Jessica N., Gammon, Amanda, Goldberg, Eric R., Gonzalez, Javier, Hagerty, Kelsi J., Hess, Rachel, Kehoe, Kelsey, Kessler, Cecilia, Kimball, Kadyn E., Loomis, Shane, Martinez, Tiffany R., Monahan, Rachel, Schiffman, Joshua D., Temares, Dani, Tobik, Katie, Wetter, David W., Mann, Devin M., Kawamoto, Kensaku, Del Fiol, Guilherme, Buys, Saundra S., Ginsburg, Ophira
Published in BMC Health Serv Res (2021)

Secondary findings from clinical genomic sequencing: Prevalence, patient perspectives, family history assessment, and healthcare costs from a multi-site study

by Hart, M. Ragan, Biesecker, Barbara B., Blout, Carrie L., Christensen, Kurt D., Amendola, Laura M., Bergstrom, Katie L., Biswas, Sawona, Bowling, Kevin M., Brothers, Kyle B., Conlin, Laura K., Cooper, Greg M., Dulik, Matthew C., East, Kelly M., Everett, Jessica N., Finnila, Candice R., Ghazani, Arezou A., Gilmore, Marian J., Goddard, Katrina AB, Jarvik, Gail P., Johnston, Jennifer J., Kauffman, Tia L., Kelley, Whitley V., Krier, Joel B., Lewis, Katie L., McGuire, Amy L., Mullen, Carmit Mc, Ou, Jeffrey, Plon, Sharon E., Rehm, Heidi L., Richards, C. Sue, Romasko, Edward J., Sagardia, Ane Miren, Spinner, Nancy B., Thompson, Michelle L., Turbitt, Erin, Vassy, Jason L., Wilfond, Benjamin S., Veenstra, David L., Berg, Jonathan S., Green, Robert C., Biesecker, Leslie G., Hindorff, Lucia A.
Published in Genet Med (2018)