Loading...

Charite N. Ricker, MS, CGC

Title(s)Instructor of Clinical Medicine
Address2020 Zonal Ave. IRD#710
Health Sciences Campus
Los Angeles CA 90033
Phone+1 323 409 7710
vCardDownload vCard

    Collapse Overview 
    Collapse Overview
    Charité Ricker, MS is a genetic counselor with the USC Norris Comprehensive Cancer Center and Clinical Instructor of Medicine in the USC Keck School of Medicine. She provides cancer genetic counseling at LAC+USC Medical Center for individuals and family at risk of having inherited cancer syndromes.

    Ms. Ricker has extensive experience as a cancer genetic counselor and the majority of her clinical work has been in the underserved patient setting. Her particular research interest is focused on the provision of genetic services to ethnically diverse patient populations and its impact and the outcomes.

    Collapse Bibliographic 
    Collapse Publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
    Newest   |   Oldest   |   Most Cited   |   Most Discussed   |   Timeline   |   Field Summary   |   Plain Text
    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Two synchronous malignancies: nodular melanoma and renal cell carcinoma in a patient with an underlying germline BRCA2 mutation. BMJ Case Rep. 2019 Jun 20; 12(6). Snow A, Ricker C, In GK. PMID: 31227566.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    2. Secondary Germline Finding in Liquid Biopsy of a Deceased Patient; Case Report and Review of the Literature. Front Oncol. 2018; 8:259. Veyseh M, Ricker C, Espenschied C, Raymond V, D'Souza A, Barzi A. PMID: 30050867.
      View in: PubMed   Mentions:
    3. Haplotype analyses of the c.1027C>T and c.2167_2168delAT recurrent truncating mutations in the breast cancer-predisposing gene PALB2. Breast Cancer Res Treat. 2016 11; 160(1):121-129. Catucci I, Casadei S, Ding YC, Volorio S, Ficarazzi F, Falanga A, Marchetti M, Tondini C, Franchi M, Adamson A, Mandell J, Walsh T, Olopade OI, Manoukian S, Radice P, Ricker C, Weitzel J, King MC, Peterlongo P, Neuhausen SL. PMID: 27624329.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    4. Increased yield of actionable mutations using multi-gene panels to assess hereditary cancer susceptibility in an ethnically diverse clinical cohort. Cancer Genet. 2016 Apr; 209(4):130-7. Ricker C, Culver JO, Lowstuter K, Sturgeon D, Sturgeon JD, Chanock CR, Gauderman WJ, McDonnell KJ, Idos GE, Gruber SB. PMID: 26908360.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    5. 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 Research Network. J Clin Oncol. 2013 Jan 10; 31(2):210-6. Weitzel JN, Clague J, Martir-Negron A, Ogaz R, Herzog J, Ricker C, Jungbluth C, Cina C, Duncan P, Unzeitig G, Saldivar JS, Beattie M, Feldman N, Sand S, Port D, Barragan DI, John EM, Neuhausen SL, Larson GP. PMID: 23233716.
      View in: PubMed   Mentions: 54     Fields:    Translation:Humans
    6. Closing the loop: an interactive action-research conference format for delivering updated medical information while eliciting Latina patient/family experiences and psychosocial needs post-genetic cancer risk assessment. Fam Cancer. 2012 Sep; 11(3):449-58. Macdonald DJ, Deri J, Ricker C, Perez MA, Ogaz R, Feldman N, Viveros LA, Paz B, Weitzel JN, Blazer KR. PMID: 22678665.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    7. Pathological characteristics of BRCA-associated breast cancers in Hispanics. Breast Cancer Res Treat. 2011 Nov; 130(1):281-9. Lagos-Jaramillo VI, Press MF, Ricker CN, Dubeau L, Mai PL, Weitzel JN. PMID: 21604016.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    8. Social-cognitive aspects of underserved Latinas preparing to undergo genetic cancer risk assessment for hereditary breast and ovarian cancer. Psychooncology. 2008 Aug; 17(8):774-82. Lagos VI, Perez MA, Ricker CN, Blazer KR, Santiago NM, Feldman N, Viveros L, Weitzel JN. PMID: 18646245.
      View in: PubMed   Mentions: 25     Fields:    Translation:Humans
    9. Evidence for common ancestral origin of a recurring BRCA1 genomic rearrangement identified in high-risk Hispanic families. Cancer Epidemiol Biomarkers Prev. 2007 Aug; 16(8):1615-20. Weitzel JN, Lagos VI, Herzog JS, Judkins T, Hendrickson B, Ho JS, Ricker CN, Lowstuter KJ, Blazer KR, Tomlinson G, Scholl T. PMID: 17646271.
      View in: PubMed   Mentions: 38     Fields:    Translation:HumansCells
    10. If we build it ... will they come?--establishing a cancer genetics services clinic for an underserved predominantly Latina cohort. J Genet Couns. 2006 Dec; 15(6):505-14. Ricker C, Lagos V, Feldman N, Hiyama S, Fuentes S, Kumar V, Gonzalez K, Palomares M, Blazer K, Lowstuter K, MacDonald D, Weitzel J. PMID: 17106633.
      View in: PubMed   Mentions: 29     Fields:    Translation:Humans
    11. Beliefs and interest in cancer risk in an underserved Latino cohort. Prev Med. 2007 Mar; 44(3):241-5. Ricker CN, Hiyama S, Fuentes S, Feldman N, Kumar V, Uman GC, Nedelcu R, Blazer KR, MacDonald DJ, Weitzel JN. PMID: 17027932.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansPHPublic Health
    12. Prevalence of BRCA mutations and founder effect in high-risk Hispanic families. Cancer Epidemiol Biomarkers Prev. 2005 Jul; 14(7):1666-71. Weitzel JN, Lagos V, Blazer KR, Nelson R, Ricker C, Herzog J, McGuire C, Neuhausen S. PMID: 16030099.
      View in: PubMed   Mentions: 76     Fields:    Translation:Humans
    13. Outcomes from intensive training in genetic cancer risk counseling for clinicians. Genet Med. 2005 Jan; 7(1):40-7. Blazer KR, MacDonald DJ, Ricker C, Sand S, Uman GC, Weitzel JN. PMID: 15654227.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    Charite's Networks
    Concepts (95)
    Derived automatically from this person's publications.
    _
    Co-Authors (5)
    People in Profiles who have published with this person.
    _
    Similar People (60)
    People who share similar concepts with this person.
    _
    Same Department
    Search Department
    _