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C. Ricker · SciRah

Researcher profile · Semantic Scholar

C. Ricker

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C. Ricker — researcher profile on SciRah

h-index: 23
Works: 121
Citations: 1,920

Most-cited papers

Management of Male Breast Cancer: ASCO Guideline.
M. Hassett, M. Somerfield, E. R. Baker, F. Cardoso +10 more
2020Journal of Clinical Oncology214 citations
Semantic Scholar
Delivery Of Cascade Screening For Hereditary Conditions: A Scoping Review Of The Literature
Megan C. Roberts, W. Dotson, Christopher S. DeVore, E. Bednar +12 more
2018Health Affairs163 citations Open access
Semantic Scholar
Selection of Germline Genetic Testing Panels in Patients With Cancer: ASCO Guideline
N. Tung, C. Ricker, H. Messersmith, J. Balmaña +17 more
2024Journal of Clinical Oncology90 citations
Semantic Scholar
Increased Yield of Actionable Mutations Using Multi-Gene Panels to Assess Hereditary Cancer Susceptibility in an Ethnically Diverse Clinical Cohort
C. Ricker, Julie O. Culver, K. Lowstuter, D. Sturgeon +6 more
2016Cancer Genetics81 citations Open access
Semantic Scholar
Pathogenic and likely pathogenic variants in PALB2, CHEK2 and other known breast cancer susceptibility genes among 1054 BRCA-negative Hispanics with breast cancer
J. Weitzel, S. Neuhausen, Aaron W Adamson, Shu Tao +15 more
2019Cancer62 citations Open access
Semantic Scholar
Genomic Disparities in Breast Cancer Among Latinas
Filipa Lynce, K. Graves, L. Jandorf, C. Ricker +5 more
2016Cancer Control: Journal of the Moffitt Cancer Cente53 citations Open access
Semantic Scholar
Unexpected CDH1 Mutations Identified on Multigene Panels Pose Clinical Management Challenges.
K. Lowstuter, C. Espenschied, D. Sturgeon, C. Ricker +13 more
2017JCO Precision Oncology50 citations
Semantic Scholar
Multicenter Prospective Cohort Study of the Diagnostic Yield and Patient Experience of Multiplex Gene Panel Testing For Hereditary Cancer Risk
G. Idos, A. Kurian, C. Ricker, D. Sturgeon +25 more
2019JCO Precision Oncology47 citations Open access
Semantic Scholar
Risk assessment and genetic counseling for hereditary breast and ovarian cancer syndromes—Practice resource of the National Society of Genetic Counselors
J. Berliner, S. Cummings, Brittany Boldt Burnett, C. Ricker
2021Journal of Genetic Counseling44 citations Open access
Semantic Scholar
Patient communication of cancer genetic test results in a diverse population.
C. Ricker, Rachel Koff, C. Qu, Julie O. Culver +20 more
2018Translational Behavioral Medicine42 citations Open access
Semantic Scholar
Psychosocial outcomes following germline multi-gene panel testing in an ethnically and economically diverse cohort of patients
Julie O. Culver, C. Ricker, J. Bonner, J. Kidd +21 more
2020Cancer37 citations Open access
Semantic Scholar
PD-1 inhibition therapy for advanced cutaneous squamous cell carcinoma: a retrospective analysis from the University of Southern California
G. In, Poorva Vaidya, A. Filkins, D. Hermel +16 more
2020Journal of Cancer Research and Clinical Oncology31 citations Open access
Semantic Scholar
DNA mismatch repair deficiency and hereditary syndromes in Latinos with colorectal cancer
C. Ricker, D. Hanna, Cheng Peng, Nathalie T Nguyen +11 more
2017Cancer27 citations Open access
Semantic Scholar
Integration of Universal Germline Genetic Testing for All New Breast Cancer Patients
Julie O. Culver, Yael Freiberg, C. Ricker, Jacob G. Comeaux +18 more
2022Annals of Surgical Oncology25 citations Open access
Semantic Scholar
A Pilot Randomized Trial of an Educational Intervention to Increase Genetic Counseling and Genetic Testing among Latina Breast Cancer Survivors
Claire C. Conley, Eida M. Castro-Figueroa, L. Moreno, J. Dutil +9 more
2020Journal of Genetic Counseling24 citations Open access
Semantic Scholar
Nivolumab use for BRCA gene mutation carriers with recurrent epithelial ovarian cancer: A case series
K. Matsuo, S. Spragg, M. Ciccone, E. Blake +3 more
2018Gynecologic Oncology Reports23 citations Open access
Semantic Scholar
Barriers and Facilitators to Genetic Education, Risk Assessment, and Testing: Considerations on Advancing Equitable Genetics Care
N. Rodriguez, C. Ricker, E. Stoffel, S. Syngal
2023Gastroenterology21 citations Open access
Semantic Scholar
Breast and colorectal cancer risks among over 6,000 CHEK2 pathogenic variant carriers: A comparison of missense versus truncating variants.
Erin Mundt, B. Mabey, Irene Rainville, C. Ricker +4 more
2023Cancer Genetics21 citations Open access
Semantic Scholar
Development and pilot testing of a training for bilingual community education professionals about hereditary breast and ovarian cancer among Latinas: ÁRBOLES Familiares.
S. Vadaparampil, Laura Moreno Botero, L. Fuzzell, Jennifer D. Garcia +10 more
2021Translational Behavioral Medicine19 citations Open access
Semantic Scholar
Transcriptome analysis provides critical answers to the “variants of uncertain significance” conundrum
M. Postel, Julie O. Culver, C. Ricker, D. Craig
2022Human Mutation18 citations Open access
Semantic Scholar
Inhibition of poly(ADP-ribose) polymerase induces synthetic lethality in BRIP1 deficient ovarian epithelial cells
M. Ciccone, C. Adams, C. Bowen, Teena Thakur +10 more
2020Gynecologic Oncology15 citations Open access
Semantic Scholar
Barriers and Facilitators to Genetic Education, Risk Assessment, and Testing: Considerations on Advancing Equitable Genetics Care
N. Rodriguez, C. Ricker, E. Stoffel, S. Syngal
2023Clinical Gastroenterology and Hepatology14 citations Open access
Semantic Scholar
Risk‐reducing mastectomy decisions among women with mutations in high‐ and moderate‐ penetrance breast cancer susceptibility genes
Jacob G. Comeaux, Julie O. Culver, John E Lee, Danielle Dondanville +6 more
2022Molecular Genetics & Genomic Medicine13 citations Open access
Semantic Scholar
Haplotype analyses of the c.1027C>T and c.2167_2168delAT recurrent truncating mutations in the breast cancer predisposing gene PALB2
Irene Catucci, S. Casadei, Yuan C. Ding, S. Volorio +16 more
2016Breast Cancer Research and Treatment12 citations Open access
Semantic Scholar
Priorities to promote participant engagement in the Participant Engagement and Cancer Genome Sequencing (PE-CGS) Network
Anne L. R. Schuster, N. Crossnohere, Melinda Bachini, Cindy K. Blair +22 more
2023Cancer Epidemiology, Biomarkers and Prevention9 citations Open access
Semantic Scholar
Spectrum of Mismatch Repair Gene Mutations and Clinical Presentation of Hispanic Individuals with Lynch syndrome
Annette Y. Sunga, C. Ricker, C. Espenschied, D. Castillo +8 more
2017Cancer Genetics9 citations Open access
Semantic Scholar
Current chemoprevention approaches in Lynch syndrome and Familial adenomatous polyposis: a global clinical practice survey
Kathryn A. Mraz, Rachel Hodan, Linda H Rodgers-Fouche, S. Arora +13 more
2023Frontiers in Oncology8 citations Open access
Semantic Scholar
Increased burden of familial-associated early-onset cancer risk among minority Americans compared to non-Latino Whites
Qian-Xi Feng, Eric M. Nickels, I. Muskens, A. D. de Smith +7 more
2021eLife8 citations Open access
Semantic Scholar
Clinical implications of conflicting variant interpretations in the cancer genetics clinic
Elyssa Zukin, Julie O. Culver, Yuxi Liu, Yun-Qi Yang +16 more
2023Genetics in Medicine7 citations Open access
Semantic Scholar
Perspectives on Spanish language concordant cancer genetic counseling sessions from the Spanish‐speaking population
Sharisse Jimenez, A. Matthews, R. Darrah, A. Schreiber +2 more
2022Journal of Genetic Counseling7 citations
Semantic Scholar
BRCA1/2 mutations and risk-reducing bilateral salpingo-oophorectomy among Latinas: The UPTAKE study
F. Lynce, I. Schlam, Xue Geng, B. Peshkin +10 more
2020Journal of Genetic Counseling6 citations Open access
Semantic Scholar
Secondary Germline Finding in Liquid Biopsy of a Deceased Patient; Case Report and Review of the Literature
Maedah Veyseh, C. Ricker, C. Espenschied, V. Raymond +2 more
2018Frontiers in Oncology6 citations Open access
Semantic Scholar
Clinical findings and outcomes of MRI staging of breast cancer in a diverse population
A. Raghavendra, Julie Wecsler, Ling-Yun Ji, P. Sheth +7 more
2018Breast Cancer Research and Treatment5 citations Open access
Semantic Scholar
Safety of multiplex gene testing for inherited cancer risk: Interim analysis of a clinical trial.
A. Kurian, G. Idos, Julie O. Culver, C. Ricker +16 more
20165 citations
Semantic Scholar
Selection of Germline Genetic Testing Panels in Patients With Cancer: ASCO Guideline Clinical Insights.
C. Ricker, B. Arun, Sara M. Pirzadeh-Miller, E. Stoffel +2 more
2024JCO Oncology Practice4 citations
Semantic Scholar
Whole exome sequencing and replication for breast cancer among Hispanic/Latino women identifies FANCM as a susceptibility gene for estrogen-receptor-negative breast cancer
Jovia L. Nierenberg, Aaron W Adamson, D. Hu, S. Huntsman +15 more
2023medRxiv4 citations Open access
Semantic Scholar
Exploring Stakeholders' Perspectives on Implementing Universal Germline Testing for Colorectal Cancer: Findings From a Clinical Practice Survey
Linda H Rodgers-Fouche, S. Arora, C. Ricker, Dan Li +12 more
2023JCO Precision Oncology4 citations Open access
Semantic Scholar
Family communication of cancer genetic test results in an ethnically diverse population: a qualitative exploration of more than 200 patients
Rachel Hodan, M. Picus, C. Stanclift, K. Ormond +4 more
2024Journal of Community Genetics3 citations Open access
Semantic Scholar
Behavioral beliefs about genetic counseling among high‐risk Latina breast cancer survivors in Florida and Puerto Rico
Jessica N. Rivera Rivera, Claire C. Conley, Eida M. Castro-Figueroa, L. Moreno +6 more
2022Cancer Medicine3 citations Open access
Semantic Scholar
A Case Series of Multiple Primary Malignancies Among Patients With Advanced Melanoma
M. Ebia, Stephen Capone, C. Ricker, Jacob S. Thomas +6 more
2021Cureus3 citations Open access
Semantic Scholar
Yield of multiplex panel testing compared to expert opinion and validated prediction models.
G. Idos, A. Kurian, C. Ricker, D. Sturgeon +16 more
20163 citations
Semantic Scholar
Exome sequencing identifies HELB as a novel susceptibility gene for non-mucinous, non-high-grade-serous epithelial ovarian cancer
E. Dicks, J. Tyrer, Suzana Ezquina, Michelle R. Jones +26 more
2025European Journal of Human Genetics2 citations Open access
Semantic Scholar
Whole exome sequencing identifies FANCM as a susceptibility gene for estrogen-receptor-negative breast cancer in Hispanic/Latina women
Jovia L. Nierenberg, Aaron W Adamson, D. Hu, S. Huntsman +17 more
2025Nature Communications2 citations Open access
Semantic Scholar
Provider discussion of genetic counseling among high-risk Spanish-preferring Latina breast cancer survivors.
Claire C. Conley, Jessica N. Rivera Rivera, Eida M. Castro-Figueroa, L. Moreno +6 more
2022Translational Behavioral Medicine2 citations Open access
Semantic Scholar
Two synchronous malignancies: nodular melanoma and renal cell carcinoma in a patient with an underlying germline BRCA2 mutation
Anson Snow, C. Ricker, G. In
2019BMJ Case Reports2 citations Open access
Semantic Scholar
Promoting breast cancer screening after multiplex genetic panel testing (MGPT) and genetic counseling.
G. Idos, A. Kurian, C. Ricker, D. Sturgeon +15 more
20182 citations
Semantic Scholar
Value of germline multi-gene panel next generation sequencing (NGS) in identification of hereditary cancer syndromes (HCS) in colorectal cancer population (CRC).
Jing Gu, C. Ricker, A. Barzi
20182 citations
Semantic Scholar
Inactivation of the Tumor Suppressor BRCA1 Interacting Protein C-terminal Helicase 1 (BRIP1) Gene Confers Increased Susceptibility to Platinum Antineoplastic Agents and Augments the Synergistic Response to Poly (ADP-ribose) Polymerase (PARP) Inhibition in Ovarian Epithelial Cells
M. Ciccone, C. Ricker, Julie O. Culver, A. Maoz +4 more
20162 citations
Semantic Scholar
“The GI Gap” in Genetic Testing for Inherited Susceptibility to Cancer: 1402
G. Idos, A. Kurian, K. McDonnell, C. Ricker +16 more
20152 citations
Semantic Scholar
Abstract 1128: Comprehensive multi-omics analysis of colorectal cancer tumors in diverse populations
B. Waldrup, F. Carranza, Yu-Xin Jin, Y. Amzaleg +11 more
2025Cancer Research1 citations
Semantic Scholar

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