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Charite N. Ricker, MS, CGC

Photo of Charite N. Ricker, MS, CGC
Title(s)Assistant Professor Of Clinical Medicine
SchoolKeck School of Medicine of Usc
Address2020 Zonal Ave. IRD#710
Health Sciences Campus
Los Angeles CA 90033
Phone+1 323 409 7710
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    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 leads the genetic counseling team at Los Angeles General 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.

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    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.
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    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. Provider perceptions and insights on polygenic risk scores for colorectal cancer: A qualitative study. J Genet Couns. 2025 Dec; 34(6):e70135. Esmundo S, Caceres N, Ricker C, Idos GE, Loroña NC, Castellon-Lopez Y, Schmit SL, Meade CD, Gwede CK, Nguyen NT, Figueiredo JC. PMID: 41217042; PMCID: PMC12604444.
      View in: PubMed   Mentions:
    2. Patient-centered integration of tumor and germline genetic results can improve cancer care. Nat Med. 2025 Oct; 31(10):3248-3251. Church AJ, Bhattacharyya O, Culver JO, Amzaleg Y, Linnenbringer E, Smart M, Ip-Toma C, Rivera AR, Davis B, Ricker C, Lenz HJ, Gray SW, Hampel H, Craig DW. PMID: 40425841.
      View in: PubMed   Mentions:    Fields:    
    3. Optimizing participant and community engagement in cancer genomic sequencing research. Genet Med. 2025 Sep; 27(9):101483. Crossnohere NL, Schuster ALR, Blair CK, Bland H, Carpten JD, Claus EB, Colditz GA, Diehl D, Ding L, Drake BF, Fields RC, George S, Janeway K, Kim H, Lenz HJ, Mack JW, Ricker C, Stern MC, Sussman A, Trent J, Van Allen E, Verhaak R, Willman C, Bridges JFP, Mishra SI, Kwan BM, PE-CGS Network. PMID: 40517303; PMCID: PMC12777742.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    4. The impact of language discordance on genetic counselors' ability to establish a working alliance with patients. J Genet Couns. 2025 Jun; 34(3):e70019. Burton A, Schlegel D, Ricker C, Yashar BM. PMID: 40305284; PMCID: PMC12043036.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    5. Interpreter use in telehealth genetic counseling sessions. J Genet Couns. 2025 Apr; 34(2):e2026. Padilla LK, Hodges PD, Ricker C, Geurts JL. PMID: 40176391.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    6. Assessment of MYC Gene and WNT Pathway Alterations in Early-Onset Colorectal Cancer Among Hispanic/Latino Patients Using Integrated Multi-Omics Approaches. medRxiv. 2025 Feb 22. Carranza FG, Waldrup B, Jin Y, Amzaleg Y, Postel M, Craig DW, Carpten JD, Salhia B, Hernandez D, Gutierrez N, Ricker CN, Culver JO, Chavez CE, Stern MC, Baezconde-Garbanati L, Lenz HJ, Velazquez-Villarreal E. PMID: 40034762; PMCID: PMC11875251.
      View in: PubMed   Mentions: 4  
    7. Exome sequencing identifies HELB as a novel susceptibility gene for non-mucinous, non-high-grade-serous epithelial ovarian cancer. Eur J Hum Genet. 2025 Mar; 33(3):297-303. Dicks EM, Tyrer JP, Ezquina S, Jones M, Baierl J, Peng PC, Diaz M, Goode E, Winham SJ, Dörk T, Gorp TV, Fazio A, Bowtell DDL, Garsed DW, Odunsi K, Moysich K, Pavanello M, Fostira F, Webb PM, Soukupová J, Cohen PA, Sieh W, Fortner RT, Ricker C, Karlan B, Campbell I, Brenton JD, Ramus SJ, Gayther SA, Pharoah PDP. PMID: 39939714; PMCID: PMC11894177.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    8. Breast Cancer MRI Screening of Patients After Multiplex Gene Panel Testing. JAMA Netw Open. 2025 01 02; 8(1):e2454447. Naghi LA, Culver JO, Ricker C, Sturgeon D, Kingham K, Hodan R, Chun NM, Kidd J, Bonner J, Hong C, Morales-Pichardo J, Mills M, Lindsey S, McDonnell K, Ladabaum U, Ford JM, Gruber SB, Kurian AW, Idos GE. PMID: 39804645; PMCID: PMC11731224.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    9. Integrative multi-omics profiling of colorectal cancer from a Hispanic/Latino cohort of patients. medRxiv. 2024 Nov 15. Waldrup B, Carranza F, Jin Y, Amzaleg Y, Postel M, Craig DW, Carpten JD, Salhia B, Ricker CN, Culver JO, Chavez CE, Stern MC, Baezconde-Garbanati L, Lenz HJ, Velazquez-Villarreal EI. PMID: 39606335; PMCID: PMC11601710.
      View in: PubMed   Mentions: 7  
    10. Spanish language opportunities in genetic counseling training programs in the United States. J Genet Couns. 2025 Apr; 34(2):e1958. Vine MK, Kellom E, Kuhl A, Simone L, Ricker CN, Birkeland L. PMID: 39192515; PMCID: PMC11953460.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    11. Family communication of cancer genetic test results in an ethnically diverse population: a qualitative exploration of more than 200 patients. J Community Genet. 2024 Aug; 15(4):363-374. Hodan R, Picus M, Stanclift C, Ormond KE, Pichardo JM, Kurian AW, Ricker C, Idos GE. PMID: 38814439; PMCID: PMC11410745.
      View in: PubMed   Mentions: 2  
    12. Selection of Germline Genetic Testing Panels in Patients With Cancer: ASCO Guideline. J Clin Oncol. 2024 Jul 20; 42(21):2599-2615. Tung N, Ricker C, Messersmith H, Balmaña J, Domchek S, Stoffel EM, Almhanna K, Arun B, Chavarri-Guerra Y, Cohen SA, Cragun D, Crew KD, Hall MJ, Idos G, Lopez G, Pal T, Pirzadeh-Miller S, Pritchard C, Rana HQ, Swami U, Vidal GA. PMID: 38759122.
      View in: PubMed   Mentions: 30     Fields:    Translation:Humans
    13. Selection of Germline Genetic Testing Panels in Patients With Cancer: ASCO Guideline Clinical Insights. JCO Oncol Pract. 2024 Oct; 20(10):1308-1313. Ricker C, Arun B, Pirzadeh-Miller S, Stoffel EM, Messersmith H, Tung N. PMID: 38759126.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    14. Breast and colorectal cancer risks among over 6,000 CHEK2 pathogenic variant carriers: A comparison of missense versus truncating variants. Cancer Genet. 2023 11; 278-279:84-90. Mundt E, Mabey B, Rainville I, Ricker C, Singh N, Gardiner A, Manley S, Slavin T. PMID: 37839337.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    15. Current chemoprevention approaches in Lynch syndrome and Familial adenomatous polyposis: a global clinical practice survey. Front Oncol. 2023; 13:1141810. Mraz KA, Hodan R, Rodgers-Fouche L, Arora S, Balaguer F, Guillem JG, Jeter JM, Kanth P, Li D, Liska D, Melson J, Perez K, Ricker C, Shirts BH, Vilar E, Katona BW, Dominguez-Valentin M. PMID: 37293588; PMCID: PMC10247284.
      View in: PubMed   Mentions: 7  
    16. Development and pilot testing of a training for bilingual community education professionals about hereditary breast and ovarian cancer among Latinas: ÁRBOLES Familiares. Transl Behav Med. 2022 01 18; 12(1). Vadaparampil ST, Moreno Botero L, Fuzzell L, Garcia J, Jandorf L, Hurtado-de-Mendoza A, Campos-Galvan C, Peshkin BN, Schwartz MD, Lopez K, Ricker C, Fiallos K, Quinn GP, Graves KD. PMID: 34255089; PMCID: PMC8827003.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    17. Increased burden of familial-associated early-onset cancer risk among minority Americans compared to non-Latino Whites. Elife. 2021 06 22; 10. Feng Q, Nickels E, Muskens IS, de Smith AJ, Gauderman WJ, Yee AC, Ricker C, Mack T, Leavitt AD, Godley LA, Wiemels JL, Wiemels JL. PMID: 34155975; PMCID: PMC8219377.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    18. A Case Series of Multiple Primary Malignancies Among Patients With Advanced Melanoma. Cureus. 2021 Jun; 13(6):e15480. Ebia MI, Capone S, Ricker C, Thomas JS, Tulpule V, Kang I, D'Souza A, Freyer DR, Miller K, In GK. PMID: 34262818; PMCID: PMC8260217.
      View in: PubMed   Mentions: 3  
    19. Risk assessment and genetic counseling for hereditary breast and ovarian cancer syndromes-Practice resource of the National Society of Genetic Counselors. J Genet Couns. 2021 04; 30(2):342-360. Berliner JL, Cummings SA, Boldt Burnett B, Ricker CN. PMID: 33410258.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    20. Psychosocial outcomes following germline multigene panel testing in an ethnically and economically diverse cohort of patients. Cancer. 2021 04 15; 127(8):1275-1285. Culver JO, Ricker CN, Bonner J, Kidd J, Sturgeon D, Hodan R, Kingham K, Lowstuter K, Chun NM, Lebensohn AP, Rowe-Teeter C, Levonian P, Partynski K, Lara-Otero K, Hong C, Morales Pichardo J, Mills MA, Brown K, Lerman C, Ladabaum U, McDonnell KJ, Ford JM, Gruber SB, Kurian AW, Idos GE. PMID: 33320347; PMCID: PMC8058169.
      View in: PubMed   Mentions: 17     Fields:    Translation:HumansCells
    21. PD-1 inhibition therapy for advanced cutaneous squamous cell carcinoma: a retrospective analysis from the University of Southern California. J Cancer Res Clin Oncol. 2021 Jun; 147(6):1803-1811. In GK, Vaidya P, Filkins A, Hermel DJ, King KG, Ragab O, Tseng WW, Swanson M, Kokot N, Lang JE, Menendez L, DeClerck B, Kim G, Hu JC, Terando A, Jadvar H, Ricker C, Miller KA, Peng DH, Wysong A. PMID: 33210210; PMCID: PMC11801844.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    22. Inhibition of poly(ADP-ribose) polymerase induces synthetic lethality in BRIP1 deficient ovarian epithelial cells. Gynecol Oncol. 2020 12; 159(3):869-876. Ciccone MA, Adams CL, Bowen C, Thakur T, Ricker C, Culver JO, Maoz A, Melas M, Idos GE, Jeyasekharan AD, Matsuo K, Roman LD, Gruber SB, McDonnell KJ. PMID: 33032822; PMCID: PMC9893519.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansAnimalsCells
    23. BRCA1/2 mutations and risk-reducing bilateral salpingo-oophorectomy among Latinas: The UPTAKE study. J Genet Couns. 2021 04; 30(2):383-393. Lynce F, Schlam I, Geng X, Peshkin BN, Friedman S, Dutil J, Nahleh Z, Campos C, Ricker C, Rodriguez P, Denduluri N, Ahn J, Isaacs C, Graves KD. PMID: 33010199; PMCID: PMC10064975.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    24. A pilot randomized trial of an educational intervention to increase genetic counseling and genetic testing among Latina breast cancer survivors. J Genet Couns. 2021 04; 30(2):394-405. Conley CC, Castro-Figueroa EM, Moreno L, Dutil J, García JD, Burgos C, Ricker C, Kim J, Graves KD, Ashing KT, Quinn GP, Soliman H, Vadaparampil ST. PMID: 32936981; PMCID: PMC7960565.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    25. Management of Male Breast Cancer: ASCO Guideline. J Clin Oncol. 2020 06 01; 38(16):1849-1863. Hassett MJ, Somerfield MR, Baker ER, Cardoso F, Kansal KJ, Kwait DC, Plichta JK, Ricker C, Roshal A, Ruddy KJ, Safer JD, Van Poznak C, Yung RL, Giordano SH. PMID: 32058842.
      View in: PubMed   Mentions: 109     Fields:    Translation:Humans
    26. 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; PMCID: PMC6605957.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    27. Pathogenic and likely pathogenic variants in PALB2, CHEK2, and other known breast cancer susceptibility genes among 1054 BRCA-negative Hispanics with breast cancer. Cancer. 2019 08 15; 125(16):2829-2836. Weitzel JN, Neuhausen SL, Adamson A, Tao S, Ricker C, Maoz A, Rosenblatt M, Nehoray B, Sand S, Steele L, Unzeitig G, Feldman N, Blanco AM, Hu D, Huntsman S, Castillo D, Haiman C, Slavin T, Ziv E. PMID: 31206626; PMCID: PMC7376605.
      View in: PubMed   Mentions: 30     Fields:    Translation:Humans
    28. Multicenter Prospective Cohort Study of the Diagnostic Yield and Patient Experience of Multiplex Gene Panel Testing For Hereditary Cancer Risk. JCO Precis Oncol. 2019 Mar; 3. Idos GE, Kurian AW, Ricker C, Sturgeon D, Culver JO, Kingham KE, Koff R, Chun NM, Rowe-Teeter C, Lebensohn AP, Levonian P, Lowstuter K, Partynski K, Hong C, Mills MA, Petrovchich I, Ma CS, Hartman AR, Allen B, Wenstrup RJ, Lancaster JM, Brown K, Kidd J, Evans B, Mukherjee B, McDonnell KJ, Ladabaum U, Ford JM, Gruber SB. PMID: 34322651; PMCID: PMC8260917.
      View in: PubMed   Mentions: 28     Fields:    
    29. Clinical findings and outcomes of MRI staging of breast cancer in a diverse population. Breast Cancer Res Treat. 2019 Apr; 174(2):315-324. Raghavendra A, Wecsler J, Ji L, Sheth P, Ricker C, Church T, Sposto R, Lang J, Sener S, Larsen L, Tripathy D. PMID: 30542816; PMCID: PMC7494176.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    30. 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; PMCID: PMC6052887.
      View in: PubMed   Mentions: 2  
    31. Nivolumab use for BRCA gene mutation carriers with recurrent epithelial ovarian cancer: A case series. Gynecol Oncol Rep. 2018 Aug; 25:98-101. Matsuo K, Spragg SE, Ciccone MA, Blake EA, Ricker C, Pham HQ, Roman LD. PMID: 29998185; PMCID: PMC6038829.
      View in: PubMed   Mentions: 17  
    32. Delivery Of Cascade Screening For Hereditary Conditions: A Scoping Review Of The Literature. Health Aff (Millwood). 2018 05; 37(5):801-808. Roberts MC, Dotson WD, DeVore CS, Bednar EM, Bowen DJ, Ganiats TG, Green RF, Hurst GM, Philp AR, Ricker CN, Sturm AC, Trepanier AM, Williams JL, Zierhut HA, Wilemon KA, Hampel H. PMID: 29733730; PMCID: PMC11022644.
      View in: PubMed   Mentions: 90     Fields:    Translation:HumansPHPublic Health
    33. Patient communication of cancer genetic test results in a diverse population. Transl Behav Med. 2018 01 29; 8(1):85-94. Ricker CN, Koff RB, Qu C, Culver J, Sturgeon D, Kingham KE, Lowstuter K, Chun NM, Rowe-Teeter C, Lebensohn A, Levonian P, Partynski K, Lara-Otero K, Hong C, Petrovchich IM, Mills MA, Hartman AR, Allen B, Ladabaum U, McDonnell K, Ford JM, Gruber SB, Kurian AW, Idos GE. PMID: 29385580; PMCID: PMC6065549.
      View in: PubMed   Mentions: 26     Fields:    Translation:Humans
    34. DNA mismatch repair deficiency and hereditary syndromes in Latino patients with colorectal cancer. Cancer. 2017 Oct 01; 123(19):3732-3743. Ricker CN, Hanna DL, Peng C, Nguyen NT, Stern MC, Schmit SL, Idos GE, Patel R, Tsai S, Ramirez V, Lin S, Shamasunadara V, Barzi A, Lenz HJ, Figueiredo JC. PMID: 28640387; PMCID: PMC5610604.
      View in: PubMed   Mentions: 14     Fields:    Translation:HumansCells
    35. Spectrum of mismatch repair gene mutations and clinical presentation of Hispanic individuals with Lynch syndrome. Cancer Genet. 2017 04; 212-213:1-7. Sunga AY, Ricker C, Espenschied CR, Castillo D, Melas M, Herzog J, Bannon S, Cruz-Correa M, Lynch P, Solomon I, Gruber SB, Weitzel JN. PMID: 28449805; PMCID: PMC8800930.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    36. Genomic Disparities in Breast Cancer Among Latinas. Cancer Control. 2016 Oct; 23(4):359-372. Lynce F, Graves KD, Jandorf L, Ricker C, Castro E, Moreno L, Augusto B, Fejerman L, Vadaparampil ST. PMID: 27842325; PMCID: PMC5160045.
      View in: PubMed   Mentions: 35     Fields:    Translation:Humans
    37. 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; PMCID: PMC5551669.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    38. 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; PMCID: PMC4835267.
      View in: PubMed   Mentions: 47     Fields:    Translation:Humans
    39. 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; PMCID: PMC3532393.
      View in: PubMed   Mentions: 94     Fields:    Translation:Humans
    40. 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; PMCID: PMC3620038.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    41. 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; PMCID: PMC3526343.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    42. 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: 30     Fields:    Translation:Humans
    43. 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: 51     Fields:    Translation:HumansCells
    44. 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: 47     Fields:    Translation:Humans
    45. 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: 19     Fields:    Translation:HumansPHPublic Health
    46. 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: 91     Fields:    Translation:Humans
    47. 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: 17     Fields:    Translation:Humans
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