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Courtney Berrios, MSc

TitleSenior Genetics Counselor
InstitutionChildren's Mercy Kansas City
DepartmentGenomic Medicine Center
Address2401 Gillham Rd
Kansas City MO 64108
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    Other Positions
    TitleResearch Assistant Professor
    InstitutionUniversity of Missouri-Kansas City
    DepartmentPediatrics


    Collapse Biography 
    Collapse education and training
    Johns Hopkins University Bloomberg School of Public Health, Baltimore, MDScM2008Genetic Counseling
    Durham University, Durham, England, UKMSc2005Population Genetics

    Collapse Bibliography 
    Collapse selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    1. Chapman CR, Dwyer P, Owens K, Berrios C, Natri HM, L Caplan A, P Quinn G. Wanted, but Elusive: Clear Solutions for Addressing Potential Group Harm in Data-Centric Research. Am J Bioeth. 2025 Apr; 25(4):W13-W16. PMID: 40067136.
      View in: PubMed
    2. Berrios C, Basey T, Bradley-Ewing A, Daniels-Young S, Lewis D, Feldman K, Moffatt ME, Pastinen T, Grundberg E. Black community member perceptions and ethics recommendations on epigenomic research. Clin Epigenetics. 2025 Feb 22; 17(1):33. PMID: 39987106.
      View in: PubMed
    3. Cohen ASA, Berrios CD, Zion TN, Barrett CM, Moore R, Boillat E, Belden B, Farrow EG, Thiffault I, Zuccarelli BD, Pastinen T. Genomic Answers for Kids: Toward more equitable access to genomic testing for rare diseases in rural populations. Am J Hum Genet. 2024 05 02; 111(5):825-832. PMID: 38636509.
      View in: PubMed
    4. Barrett C, Berrios C. Downstream Exclusion in Rural Rare Disease Precision Medicine Research. Am J Bioeth. 2024 Mar; 24(3):106-108. PMID: 38394024.
      View in: PubMed
    5. Berrios C, McBeth M, Bradley-Ewing A, Schuetz N, Campbell A, Talebizadeh Z, Garrett JR, Falicov T, Martinez F, Hurley EA. Developing a community-led rare disease ELSI research agenda. Orphanet J Rare Dis. 2024 Jan 22; 19(1):23. PMID: 38254122.
      View in: PubMed
    6. Chapman CR, Quinn GP, Natri HM, Berrios C, Dwyer P, Owens K, Heraty S, Caplan AL. Consideration and Disclosure of Group Risks in Genomics and Other Data-Centric Research: Does the Common Rule Need Revision? Am J Bioeth. 2025 Feb; 25(2):47-60. PMID: 38010648.
      View in: PubMed
    7. Berrios C, Neal S, Zion T, Pastinen T. Comparing Attitudes About Genomic Privacy and Data Sharing in Adolescents and Parents of Children Enrolled in a Genomic Research Repository. AJOB Empir Bioeth. 2024; 15(1):33-40. PMID: 37487180.
      View in: PubMed
    8. Strenk ME, Berrios C, Garrett JR. Addressing the Burdens That Newborn Screening Imposes on Underserved Communities. Am J Bioeth. 2023 07; 23(7):79-82. PMID: 37339296.
      View in: PubMed
    9. Kane NJ, Cohen ASA, Berrios C, Jones B, Pastinen T, Hoffman MA. Committing to genomic answers for all kids: Evaluating inequity in genomic research enrollment. Genet Med. 2023 09; 25(9):100895. PMID: 37194653.
      View in: PubMed
    10. Zion TN, Berrios CD, Cohen ASA, Bartik L, Cross LA, Engleman KL, Fleming EA, Gadea RN, Hughes SS, Jenkins JL, Kussmann J, Lawson C, Schwager C, Strenk ME, Welsh H, Rush ET, Amudhavalli SM, Sullivan BR, Zhou D, Gannon JL, Heese BA, Moore R, Boillat E, Biswell RL, Louiselle DA, Puckett LMB, Beyer S, Neal SH, Sierant V, McBeth M, Belden B, Walter AM, Gibson M, Cheung WA, Johnston JJ, Thiffault I, Farrow EG, Grundberg E, Pastinen T. Insurance denials and diagnostic rates in a pediatric genomic research cohort. Genet Med. 2023 05; 25(5):100020. PMID: 36718845.
      View in: PubMed
    11. Berrios C, Bollinger J, Yan J, Biesecker B, Chakravarti A. Identifying Needs, Challenges, and Benefits Among Adults and Parents of Children With Hirschsprung Disease. J Pediatr Gastroenterol Nutr. 2022 05 01; 74(5):e103-e108. PMID: 35149644.
      View in: PubMed
    12. Berrios C, Sadaro SK, Sandritter T, Wagner JA, Soden S, Black B, Abdel-Rahman S. Parental understanding and attitudes following pharmacogenomic testing for pediatric neuropsychiatric patients. Pharmacogenomics. 2022 04; 23(6):345-354. PMID: 35311353.
      View in: PubMed
    13. Cohen ASA, Farrow EG, Abdelmoity AT, Alaimo JT, Amudhavalli SM, Anderson JT, Bansal L, Bartik L, Baybayan P, Belden B, Berrios CD, Biswell RL, Buczkowicz P, Buske O, Chakraborty S, Cheung WA, Coffman KA, Cooper AM, Cross LA, Curran T, Dang TTT, Elfrink MM, Engleman KL, Fecske ED, Fieser C, Fitzgerald K, Fleming EA, Gadea RN, Gannon JL, Gelineau-Morel RN, Gibson M, Goldstein J, Grundberg E, Halpin K, Harvey BS, Heese BA, Hein W, Herd SM, Hughes SS, Ilyas M, Jacobson J, Jenkins JL, Jiang S, Johnston JJ, Keeler K, Korlach J, Kussmann J, Lambert C, Lawson C, Le Pichon JB, Leeder JS, Little VC, Louiselle DA, Lypka M, McDonald BD, Miller N, Modrcin A, Nair A, Neal SH, Oermann CM, Pacicca DM, Pawar K, Posey NL, Price N, Puckett LMB, Quezada JF, Raje N, Rowell WJ, Rush ET, Sampath V, Saunders CJ, Schwager C, Schwend RM, Shaffer E, Smail C, Soden S, Strenk ME, Sullivan BR, Sweeney BR, Tam-Williams JB, Walter AM, Welsh H, Wenger AM, Willig LK, Yan Y, Younger ST, Zhou D, Zion TN, Thiffault I, Pastinen T. Genomic answers for children: Dynamic analyses of >1000 pediatric rare disease genomes. Genet Med. 2022 06; 24(6):1336-1348. PMID: 35305867.
      View in: PubMed
    14. Berrios C, Hurley EA, Willig L, Thiffault I, Saunders C, Pastinen T, Goggin K, Farrow E. Challenges in genetic testing: clinician variant interpretation processes and the impact on clinical care. Genet Med. 2021 12; 23(12):2289-2299. PMID: 34257423.
      View in: PubMed
    15. Kapoor A, Nandakumar P, Auer DR, Sosa MX, Ross H, Bollinger J, Yan J, Berrios C, Chakravarti A. Multiple, independent, common variants at RET, SEMA3 and NRG1 gut enhancers specify Hirschsprung disease risk in European ancestry subjects. J Pediatr Surg. 2021 Dec; 56(12):2286-2294. PMID: 34006365.
      View in: PubMed
    16. Stancil SL, Berrios C, Abdel-Rahman S. Adolescent perceptions of pharmacogenetic testing. Pharmacogenomics. 2021 04; 22(6):335-343. PMID: 33849282.
      View in: PubMed
    17. Berrios CD, Chakravarti A, Biesecker BB. High Levels of Interest in Reproductive Genetic Information in Parents of Children and Adults With Hirschsprung Disease. J Pediatr Gastroenterol Nutr. 2019 09; 69(3):299-305. PMID: 31107799.
      View in: PubMed
    18. Berrios C, Koertje C, Noel-MacDonnell J, Soden S, Lantos J. Parents of newborns in the NICU enrolled in genome sequencing research: hopeful, but not na?ve. Genet Med. 2020 02; 22(2):416-422. PMID: 31467447.
      View in: PubMed
    19. Tilghman JM, Ling AY, Turner TN, Sosa MX, Krumm N, Chatterjee S, Kapoor A, Coe BP, Nguyen KH, Gupta N, Gabriel S, Eichler EE, Berrios C, Chakravarti A. Molecular Genetic Anatomy and Risk Profile of Hirschsprung's Disease. N Engl J Med. 2019 Apr 11; 380(15):1421-1432. PMID: 30970187.
      View in: PubMed
    20. Lewis KL, Facio FM, Berrios CD. Using the diffusion of innovations model to guide participant engagement in the genomics era. J Genet Couns. 2019 04; 28(2):419-427. PMID: 30653790.
      View in: PubMed
    21. Thiffault I, Farrow E, Zellmer L, Berrios C, Miller N, Gibson M, Caylor R, Jenkins J, Faller D, Soden S, Saunders C. Clinical genome sequencing in an unbiased pediatric cohort. Genet Med. 2019 02; 21(2):303-310. PMID: 30008475.
      View in: PubMed
    22. Berrios C, James CA, Raraigh K, Bollinger J, Murray B, Tichnell C, Applegate CD, Bergner AL. Enrolling Genomics Research Participants through a Clinical Setting: the Impact of Existing Clinical Relationships on Informed Consent and Expectations for Return of Research Results. J Genet Couns. 2018 02; 27(1):263-273. PMID: 28932961.
      View in: PubMed
    23. Gui H, Schriemer D, Cheng WW, Chauhan RK, Antinolo G, Berrios C, Bleda M, Brooks AS, Brouwer RW, Burns AJ, Cherny SS, Dopazo J, Eggen BJ, Griseri P, Jalloh B, Le TL, Lui VC, Luz?n-Toro B, Matera I, Ngan ES, Pelet A, Ruiz-Ferrer M, Sham PC, Shepherd IT, So MT, Sribudiani Y, Tang CS, van den Hout MC, van der Linde HC, van Ham TJ, van IJcken WF, Verheij JB, Amiel J, Borrego S, Ceccherini I, Chakravarti A, Lyonnet S, Tam PK, Garcia-Barcel? MM, Hofstra RM. Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes. Genome Biol. 2017 03 08; 18(1):48. PMID: 28274275.
      View in: PubMed
    24. Tang CS, Gui H, Kapoor A, Kim JH, Luz?n-Toro B, Pelet A, Burzynski G, Lantieri F, So MT, Berrios C, Shin HD, Fern?ndez RM, Le TL, Verheij JB, Matera I, Cherny SS, Nandakumar P, Cheong HS, Anti?olo G, Amiel J, Seo JM, Kim DY, Oh JT, Lyonnet S, Borrego S, Ceccherini I, Hofstra RM, Chakravarti A, Kim HY, Sham PC, Tam PK, Garcia-Barcel? MM. Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease. Hum Mol Genet. 2016 12 01; 25(23):5265-5275. PMID: 27702942.
      View in: PubMed
    25. Chatterjee S, Kapoor A, Akiyama JA, Auer DR, Lee D, Gabriel S, Berrios C, Pennacchio LA, Chakravarti A. Enhancer Variants Synergistically Drive Dysfunction of a Gene Regulatory Network In Hirschsprung Disease. Cell. 2016 Oct 06; 167(2):355-368.e10. PMID: 27693352.
      View in: PubMed
    26. Kapoor A, Jiang Q, Chatterjee S, Chakraborty P, Sosa MX, Berrios C, Chakravarti A. Population variation in total genetic risk of Hirschsprung disease from common RET, SEMA3 and NRG1 susceptibility polymorphisms. Hum Mol Genet. 2015 May 15; 24(10):2997-3003. PMID: 25666438.
      View in: PubMed
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