Two synchronous malignancies: nodular melanoma and renal cell carcinoma in a patient with an underlying germline BRCA2 mutation

по Snow, Anson, Ricker, Charite, In, Gino K
Опубликовано в: BMJ Case Rep (2019)

Characteristics of Lynch syndrome in 13 Hispanic Families

по Ricker, Charite, Klipfel, Nancy, Ault, Glenn, Roman, Lynda, Spicer, Darcy, Lenz, Heinz-Josef
Опубликовано 2010

Secondary Germline Finding in Liquid Biopsy of a Deceased Patient; Case Report and Review of the Literature

по Veyseh, Maedah, Ricker, Charite, Espenschied, Carin, Raymond, Victoria, D’Souza, Anishka, Barzi, Afsaneh
Опубликовано в: Front Oncol (2018)

Familial Adenomatous Polyposis (FAP) in 9 Hispanic women

по Ricker, Charite, Ault, Glenn, El-Khoureiy, Anthony, Iqbal, Syma, Spicer, Darcy, Lenz, Heinz-Josef
Опубликовано 2010

Pathological characteristics of BRCA-associated breast cancers in Hispanics

по Lagos-Jaramillo, Veronica I., Press, Michael F., Ricker, Charité N., Dubeau, Louis, Mai, Phuong L., Weitzel, Jeffrey N.
Опубликовано 2011

Genomic Disparities in Breast Cancer Among Latinas

по Lynce, Filipa, Graves, Kristi D., Jandorf, Lina, Ricker, Charité, Castro, Eida, Moreno, Laura, Augusto, Bianca, Fejerman, Laura, Vadaparampil, Susan T.
Опубликовано в: Cancer Control (2016)

Nivolumab use for BRCA gene mutation carriers with recurrent epithelial ovarian cancer: A case series

по Matsuo, Koji, Spragg, Samantha E., Ciccone, Marcia A., Blake, Erin A., Ricker, Charité, Pham, Huyen Q., Roman, Lynda D.
Опубликовано в: Gynecol Oncol Rep (2018)

Clinical findings and outcomes of MRI staging of breast cancer in a diverse population

по Raghavendra, Akshara, Wecsler, Julie, Ji, Lingyun, Sheth, Pulin, Ricker, Charite, Church, Terry, Sposto, Richard, Lang, Julie, Sener, Stephen, Larsen, Linda, Tripathy, Debu
Опубликовано в: Breast Cancer Res Treat (2018)

A Case Series of Multiple Primary Malignancies Among Patients With Advanced Melanoma

по Ebia, Matthew I, Capone, Stephen, Ricker, Charité, Thomas, Jacob S, Tulpule, Varsha, Kang, Irene, D'Souza, Anishka, Freyer, David R, Miller, Kimberly, In, Gino K
Опубликовано в: Cureus (2021)

Closing the Loop: An interactive action-research conference format for delivering updated medical information while eliciting Latina patient/family experiences and psychosocial nee...

по MacDonald, Deborah J., Deri, Julia, Ricker, Charité, Perez, Martin A., Ogaz, Raquel, Feldman, Nancy, Viveros, Lori A., Paz, Benjamin, Weitzel, Jeffrey N., Blazer, Kathleen R.
Опубликовано 2012

Increased Yield of Actionable Mutations Using Multi-Gene Panels to Assess Hereditary Cancer Susceptibility in an Ethnically Diverse Clinical Cohort

по Ricker, Charité, Culver, Julie O., Lowstuter, Katrina, Sturgeon, Duveen, Sturgeon, Julia D., Chanock, Christopher R., Gauderman, William J., McDonnell, Kevin, Idos, Gregory, Gruber, Stephen B.
Опубликовано в: Cancer Genet (2016)

Increased burden of familial-associated early-onset cancer risk among minority Americans compared to non-Latino Whites

по Feng, Qianxi, Nickels, Eric, Muskens, Ivo S, de Smith, Adam J, Gauderman, W James, Yee, Amy C, Ricker, Charite, Mack, Thomas, Leavitt, Andrew D, Godley, Lucy A, Wiemels, Joseph L
Опубликовано в: eLife (2021)

A Pilot Randomized Trial of an Educational Intervention to Increase Genetic Counseling and Genetic Testing among Latina Breast Cancer Survivors

по Conley, Claire C., Castro-Figueroa, Eida M., Moreno, Laura, Dutil, Julie, García, Jennifer D., Burgos, Carolina, Ricker, Charité, Kim, Jongphil, Graves, Kristi D., Ashing, Kimlin Tam, Quinn, Gwendolyn P., Soliman, Hatem, Vadaparampil, Susan T.
Опубликовано в: J Genet Couns (2020)

DNA mismatch repair deficiency and hereditary syndromes in Latino patients with colorectal cancer

по Ricker, Charité N., Hanna, Diana L., Peng, Cheng, Nguyen, Nathalie T., Stern, Mariana C., Schmit, Stephanie L., Idos, Greg E., Patel, Ravi, Tsai, Steven, Ramirez, Veronica, Lin, Sonia, Shamasunadara, Vinay, Barzi, Afsaneh, Lenz, Heinz‐Josef, Figueiredo, Jane C.
Опубликовано в: Cancer (2017)

Pathogenic and likely pathogenic variants in PALB2, CHEK2 and other known breast cancer susceptibility genes among 1054 BRCA-negative Hispanics with breast cancer

по Weitzel, Jeffrey, Neuhausen, Susan L., Adamson, Aaron, Tao, Shu, Ricker, Charité, Maoz, Asaf, Rosenblatt, Margalit, Nehoray, Bita, Sand, Sharon, Steele, Linda, Unzeitig, Gary, Feldman, Nancy, Blanco, Amie, Hu, Donglei, Huntsman, Scott, Castillo, Danielle, Haiman, Christopher, Slavin, Thomas, Ziv, Elad
Опубликовано в: Cancer (2019)

Prevalence and Type of BRCA Mutations in Hispanics Undergoing Genetic Cancer Risk Assessment in the Southwestern United States: A Report From the Clinical Cancer Genetics Community...

по Weitzel, Jeffrey N., Clague, Jessica, Martir-Negron, Arelis, Ogaz, Raquel, Herzog, Josef, Ricker, Charité, Jungbluth, Chelsy, Cina, Cheryl, Duncan, Paul, Unzeitig, Gary, Saldivar, J. Salvador, Beattie, Mary, Feldman, Nancy, Sand, Sharon, Port, Danielle, Barragan, Deborah I., John, Esther M., Neuhausen, Susan L., Larson, Garrett P.
Опубликовано 2013

Haplotype analyses of the c.1027C>T and c.2167_2168delAT recurrent truncating mutations in the breast cancer predisposing gene PALB2

по Catucci, Irene, Casadei, Silvia, Ding, Yuan Chun, Volorio, Sara, Ficarazzi, Filomena, Falanga, Anna, Marchetti, Marina, Tondini, Carlo, Franchi, Michela, Adamson, Aaron, Mandel, Jessica, Walsh, Tom, Olopade, Olufunmilayo I, Manoukian, Siranoush, Radice, Paolo, Ricker, Charite, Weitzel, Jeffrey, King, Mary-Claire, Peterlongo, Paolo, Neuhausen, Susan L.
Опубликовано в: Breast Cancer Res Treat (2016)

Patient communication of cancer genetic test results in a diverse population

по Ricker, Charité N, Koff, Rachel B, Qu, Chenxu, Culver, Julie, Sturgeon, Duveen, Kingham, Kerry E, Lowstuter, Katrina, Chun, Nicolette M, Rowe-Teeter, Courtney, Lebensohn, Alexandra, Levonian, Peter, Partynski, Katlyn, Lara-Otero, Karlena, Hong, Christine, Petrovchich, Iva M, Mills, Meredith A, Hartman, Anne-Renee, Allen, Brian, Ladabaum, Uri, McDonnell, Kevin, Ford, James M, Gruber, Stephen B, Kurian, Allison W, Idos, Gregory E
Опубликовано в: Transl Behav Med (2018)

Psychosocial outcomes following germline multigene panel testing in an ethnically and economically diverse cohort of patients

по Culver, Julie O., Ricker, Charité N., Bonner, Joseph, Kidd, John, Sturgeon, Duveen, Hodan, Rachel, Kingham, Kerry, Lowstuter, Katrina, Chun, Nicolette M., Lebensohn, Alexandra P., Rowe‐Teeter, Courtney, Levonian, Peter, Partynski, Katlyn, Lara‐Otero, Karlena, Hong, Christine, Morales Pichardo, Jennifer, Mills, Meredith A., Brown, Krystal, Lerman, Caryn, Ladabaum, Uri, McDonnell, Kevin J., Ford, James M., Gruber, Stephen B., Kurian, Allison W., Idos, Gregory E.
Опубликовано в: Cancer (2020)

Multicenter Prospective Cohort Study of the Diagnostic Yield and Patient Experience of Multiplex Gene Panel Testing For Hereditary Cancer Risk

по Idos, Gregory E., Kurian, Allison W., Ricker, Charité, Sturgeon, Duveen, Culver, Julie O., Kingham, Kerry E., Koff, Rachel, Chun, Nicolette M., Rowe-Teeter, Courtney, Lebensohn, Alexandra P., Levonian, Peter, Lowstuter, Katrina, Partynski, Katlyn, Hong, Christine, Mills, Meredith A., Petrovchich, Iva, Ma, Cindy S., Hartman, Anne-Renee, Allen, Brian, Wenstrup, Richard J., Lancaster, Johnathan M., Brown, Krystal, Kidd, John, Evans, Brent, Mukherjee, Bhramar, McDonnell, Kevin J., Ladabaum, Uri, Ford, James M., Gruber, Stephen B.
Опубликовано в: JCO Precis Oncol (2019)