Courtney Berrios

1.0k total citations
18 papers, 444 citations indexed

About

Courtney Berrios is a scholar working on Genetics, Molecular Biology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Courtney Berrios has authored 18 papers receiving a total of 444 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 7 papers in Molecular Biology and 7 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Courtney Berrios's work include Ethics in Clinical Research (7 papers), Genomics and Rare Diseases (7 papers) and Congenital gastrointestinal and neural anomalies (6 papers). Courtney Berrios is often cited by papers focused on Ethics in Clinical Research (7 papers), Genomics and Rare Diseases (7 papers) and Congenital gastrointestinal and neural anomalies (6 papers). Courtney Berrios collaborates with scholars based in United States, United Kingdom and Canada. Courtney Berrios's co-authors include Aravinda Chakravarti, Ashish Kapoor, Sumantra Chatterjee, Stacey Gabriel, Qian Jiang, Maria X. Sosa, Dallas R. Auer, Hao Li, Jennifer A. Akiyama and Sarah Soden and has published in prestigious journals such as New England Journal of Medicine, Cell and PLoS ONE.

In The Last Decade

Courtney Berrios

17 papers receiving 440 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Courtney Berrios United States 9 240 180 132 39 37 18 444
Yuzuo Bai China 13 344 1.4× 29 0.2× 130 1.0× 42 1.1× 31 0.8× 42 511
Joachim Wölfle Germany 10 85 0.4× 155 0.9× 116 0.9× 4 0.1× 68 1.8× 24 335
Xiangqing Sun United States 9 41 0.2× 106 0.6× 85 0.6× 21 0.5× 5 0.1× 23 256
Noël P. Burtt United States 3 127 0.5× 233 1.3× 177 1.3× 12 0.3× 15 0.4× 3 354
N. E. Skakkeb�k Denmark 11 108 0.5× 115 0.6× 166 1.3× 19 0.5× 34 0.9× 13 404
Asterios Kukuvitis Canada 10 64 0.3× 145 0.8× 126 1.0× 13 0.3× 35 0.9× 17 402
Sarah Bocchini Italy 9 115 0.5× 243 1.4× 129 1.0× 16 0.4× 58 1.6× 25 385
Everlayny F. Costalonga Brazil 13 49 0.2× 200 1.1× 165 1.3× 21 0.5× 48 1.3× 22 421
Marlène Huyvaert France 7 235 1.0× 246 1.4× 159 1.2× 13 0.3× 17 0.5× 7 401
Siri Fredheim Denmark 13 268 1.1× 312 1.7× 55 0.4× 60 1.5× 9 0.2× 18 460

Countries citing papers authored by Courtney Berrios

Since Specialization
Citations

This map shows the geographic impact of Courtney Berrios's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Courtney Berrios with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Courtney Berrios more than expected).

Fields of papers citing papers by Courtney Berrios

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Courtney Berrios. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Courtney Berrios. The network helps show where Courtney Berrios may publish in the future.

Co-authorship network of co-authors of Courtney Berrios

This figure shows the co-authorship network connecting the top 25 collaborators of Courtney Berrios. A scholar is included among the top collaborators of Courtney Berrios based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Courtney Berrios. Courtney Berrios is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Berrios, Courtney, Andrea Bradley‐Ewing, Keith Feldman, et al.. (2025). Black community member perceptions and ethics recommendations on epigenomic research. Clinical Epigenetics. 17(1). 33–33.
2.
Cohen, Ana S.A., Courtney Berrios, Bradley Belden, et al.. (2024). Genomic Answers for Kids: Toward more equitable access to genomic testing for rare diseases in rural populations. The American Journal of Human Genetics. 111(5). 825–832. 5 indexed citations
3.
Quinn, Gwendolyn P., et al.. (2023). Consideration and Disclosure of Group Risks in Genomics and Other Data-Centric Research: Does the Common Rule Need Revision?. The American Journal of Bioethics. 25(2). 47–60. 6 indexed citations
4.
Cohen, Ana S.A., et al.. (2023). Committing to genomic answers for all kids: Evaluating inequity in genomic research enrollment. Genetics in Medicine. 25(9). 100895–100895. 8 indexed citations
5.
Berrios, Courtney, et al.. (2022). Parental Understanding and Attitudes Following Pharmacogenomic Testing for Pediatric Neuropsychiatric Patients. Pharmacogenomics. 23(6). 345–354. 1 indexed citations
6.
Saulnier, Katie M., Alison Berner, Brian D. Earp, et al.. (2022). Studying Vulnerable Populations Through an Epigenetics Lens: Proceed with Caution. Canadian Journal of Bioethics. 5(1). 68–68. 5 indexed citations
7.
Berrios, Courtney, Emily A. Hurley, Laurel K. Willig, et al.. (2021). Challenges in genetic testing: clinician variant interpretation processes and the impact on clinical care. Genetics in Medicine. 23(12). 2289–2299. 13 indexed citations
8.
Berrios, Courtney, et al.. (2021). Adolescent Perceptions of Pharmacogenetic Testing. Pharmacogenomics. 22(6). 335–343. 7 indexed citations
9.
Kapoor, Ashish, Priyanka Nandakumar, Dallas R. Auer, et al.. (2021). Multiple, independent, common variants at RET, SEMA3 and NRG1 gut enhancers specify Hirschsprung disease risk in European ancestry subjects. Journal of Pediatric Surgery. 56(12). 2286–2294. 4 indexed citations
10.
Berrios, Courtney, et al.. (2019). Parents of newborns in the NICU enrolled in genome sequencing research: hopeful, but not naïve. Genetics in Medicine. 22(2). 416–422. 33 indexed citations
11.
Lewis, Katie L., Flavia M. Facio, & Courtney Berrios. (2019). Using the diffusion of innovations model to guide participant engagement in the genomics era. Journal of Genetic Counseling. 28(2). 419–427. 1 indexed citations
12.
Berrios, Courtney, Aravinda Chakravarti, & Barbara B. Biesecker. (2019). High Levels of Interest in Reproductive Genetic Information in Parents of Children and Adults With Hirschsprung Disease. Journal of Pediatric Gastroenterology and Nutrition. 69(3). 299–305. 2 indexed citations
13.
Ling, Albee Y., Tychele N. Turner, Maria X. Sosa, et al.. (2019). Molecular Genetic Anatomy and Risk Profile of Hirschsprung’s Disease. New England Journal of Medicine. 380(15). 1421–1432. 113 indexed citations
14.
Thiffault, Isabelle, Emily Farrow, Lee Zellmer, et al.. (2018). Clinical genome sequencing in an unbiased pediatric cohort. Genetics in Medicine. 21(2). 303–310. 31 indexed citations
15.
Berrios, Courtney, Cynthia A. James, Karen S. Raraigh, et al.. (2017). Enrolling Genomics Research Participants through a Clinical Setting: the Impact of Existing Clinical Relationships on Informed Consent and Expectations for Return of Research Results. Journal of Genetic Counseling. 27(1). 263–273. 20 indexed citations
16.
Chatterjee, Sumantra, Ashish Kapoor, Jennifer A. Akiyama, et al.. (2016). Enhancer Variants Synergistically Drive Dysfunction of a Gene Regulatory Network In Hirschsprung Disease. Cell. 167(2). 355–368.e10. 94 indexed citations
17.
Kapoor, Ashish, Qian Jiang, Sumantra Chatterjee, et al.. (2015). Population variation in total genetic risk of Hirschsprung disease from common RET, SEMA3 and NRG1 susceptibility polymorphisms. Human Molecular Genetics. 24(10). 2997–3003. 52 indexed citations
18.
Jiang, Qian, Yen-Yi Ho, Hao Li, Courtney Berrios, & Aravinda Chakravarti. (2011). Copy Number Variants in Candidate Genes Are Genetic Modifiers of Hirschsprung Disease. PLoS ONE. 6(6). e21219–e21219. 49 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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