Amy L. McGuire

37.6k total citations · 3 hit papers
226 papers, 9.4k citations indexed

About

Amy L. McGuire is a scholar working on Genetics, Public Health, Environmental and Occupational Health and General Health Professions. According to data from OpenAlex, Amy L. McGuire has authored 226 papers receiving a total of 9.4k indexed citations (citations by other indexed papers that have themselves been cited), including 112 papers in Genetics, 99 papers in Public Health, Environmental and Occupational Health and 37 papers in General Health Professions. Recurrent topics in Amy L. McGuire's work include Ethics in Clinical Research (83 papers), Genomics and Rare Diseases (75 papers) and BRCA gene mutations in cancer (56 papers). Amy L. McGuire is often cited by papers focused on Ethics in Clinical Research (83 papers), Genomics and Rare Diseases (75 papers) and BRCA gene mutations in cancer (56 papers). Amy L. McGuire collaborates with scholars based in United States, United Kingdom and Canada. Amy L. McGuire's co-authors include Robert C. Green, Laurence B. McCullough, Simon N. Whitney, Heidi L. Rehm, David E. Golan, Yaniv Erlich, Eran Halperin, Melissa Gymrek, Timothy Caulfield and Wylie Burke and has published in prestigious journals such as Science, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

In The Last Decade

Amy L. McGuire

214 papers receiving 9.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

2013 1.6k citations Robert C. Green, Bruce R. Korf et al. Genetics in Medicine profile →
Identifying Personal Genomes by Surname Inference

2013 710 citations Melissa Gymrek, Amy L. McGuire et al. Science profile →
Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association

2018 370 citations Amy L. McGuire, Bruce D. Gelb et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Amy L. McGuire United States	46	4.7k	3.4k	1.6k	1.2k	1.2k	226	9.4k
Bartha Maria Knoppers Canada	44	2.8k 0.6×	3.6k 1.0×	1.2k 0.8×	1.7k 1.4×	801 0.7×	359	7.4k
Wylie Burke United States	57	6.6k 1.4×	3.2k 0.9×	1.5k 1.0×	1.2k 1.0×	1.9k 1.6×	250	13.5k
Muin J. Khoury United States	70	6.1k 1.3×	3.5k 1.0×	2.5k 1.6×	923 0.8×	967 0.8×	335	18.2k
Julian Little Canada	61	5.2k 1.1×	1.7k 0.5×	3.7k 2.3×	1.0k 0.8×	1.1k 0.9×	365	16.2k
Ellen Wright Clayton United States	38	2.1k 0.4×	2.0k 0.6×	750 0.5×	794 0.7×	372 0.3×	194	6.2k
Kelly E. Ormond United States	34	3.6k 0.8×	1.7k 0.5×	1.1k 0.7×	488 0.4×	776 0.6×	121	6.4k
Katrina Armstrong United States	58	2.5k 0.5×	1.7k 0.5×	584 0.4×	342 0.3×	757 0.6×	252	11.2k
Charles N. Rotimi United States	55	5.2k 1.1×	1.7k 0.5×	3.5k 2.2×	1.4k 1.1×	717 0.6×	240	13.3k
Pascal Borry Belgium	38	2.3k 0.5×	1.9k 0.6×	582 0.4×	737 0.6×	320 0.3×	251	5.2k
Timothy R. Rebbeck United States	56	5.6k 1.2×	1.2k 0.3×	3.0k 1.9×	350 0.3×	2.7k 2.2×	257	12.7k

Countries citing papers authored by Amy L. McGuire

Since Specialization

Citations

This map shows the geographic impact of Amy L. McGuire'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 Amy L. McGuire with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Amy L. McGuire more than expected).

Fields of papers citing papers by Amy L. McGuire

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Amy L. McGuire. 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 Amy L. McGuire. The network helps show where Amy L. McGuire may publish in the future.

Co-authorship network of co-authors of Amy L. McGuire

This figure shows the co-authorship network connecting the top 25 collaborators of Amy L. McGuire. A scholar is included among the top collaborators of Amy L. McGuire 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 Amy L. McGuire. Amy L. McGuire is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

McGuire, Amy L., et al.. (2025). Embracing Epistemic Humility: Rethinking Psychedelic Exceptionalism Through Diverse Perspectives. The American Journal of Bioethics. 25(1). 98–100.

Lee, John H., Andrea Gilbert, Achint K. Singh, et al.. (2025). Anaplastic meningioma in a 6-year-old with somatic YAP1::MAML2 fusion and multiple endocrine neoplasia type 4 (MEN4) syndrome. Cancer Genetics. 292-293. 106–110. 1 indexed citations

Guerrini, Christi J., Jill O. Robinson, Mohamed I. Elsaid, et al.. (2025). FIGG at 5: An update on U.S. public perspectives on forensic investigative genetic genealogy five years after its introduction to criminal investigations. Forensic Science International. 367. 112372–112372. 1 indexed citations

Malek, Janet, Jill O. Robinson, Jamie Fong, et al.. (2025). Dilemmas in diagnosing Alzheimer's disease: The peril and promise of self-fulfilling prophecies. Journal of Alzheimer s Disease. 105(3). 736–739.

Majumder, Mary A., et al.. (2024). Large-scale genotype prediction from RNA sequence data necessitates a new ethical and policy framework. Nature Genetics. 56(8). 1537–1540. 1 indexed citations

McGuire, Amy L., et al.. (2024). Dangers of under‐treatment and over‐treatment with inhaled corticosteroids in children with asthma. Pediatric Pulmonology. 60(1). e27327–e27327.

Christensen, Kurt D., Hadley Stevens Smith, Stacey Pereira, et al.. (2024). P491: Enrollment of a diverse population into a trial of newborn genomic sequencing: Preliminary data from the BabySeq Project. SHILAP Revista de lepidopterología. 2. 101390–101390. 1 indexed citations

Uveges, Melissa Kurtz, Hadley Stevens Smith, Stacey Pereira, et al.. (2024). Family genetic risk communication and reverse cascade testing in the BabySeq project. Genetics in Medicine. 27(3). 101350–101350.

Gutierrez, Amanda M., Jill O. Robinson, Mary A. Majumder, et al.. (2023). Views of Adolescents and Young Adults with Cancer and Their Oncologists Toward Patients' Participation in Genomic Research. Journal of Adolescent and Young Adult Oncology. 12(5). 773–781. 2 indexed citations

10.

McGuire, Amy L., et al.. (2023). Solving Crimes While Protecting Genetic Privacy. 3(4). 109–111.

11.

Green, Robert C., Nidhi Shah, Casie A. Genetti, et al.. (2023). Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq Project. The American Journal of Human Genetics. 110(7). 1034–1045. 25 indexed citations

12.

Merner, Amanda R., Kristin M. Kostick, Michelle Pham, et al.. (2023). Participant perceptions of changes in psychosocial domains following participation in an adaptive deep brain stimulation trial. Brain stimulation. 16(4). 990–998. 8 indexed citations

13.

Guerrini, Christi J. & Amy L. McGuire. (2022). An Ethics Framework for Evaluating Ownership Practices in Biomedical Citizen Science. Citizen Science Theory and Practice. 7(1).

14.

Guerrini, Christi J., et al.. (2022). “Idealists and capitalists”: ownership attitudes and preferences in genomic citizen science. New Genetics and Society. 41(2). 74–95. 2 indexed citations

15.

Smith, Hadley Stevens, Emily Bonkowski, Amanda M. Gutierrez, et al.. (2022). Key drivers of family-level utility of pediatric genomic sequencing: a qualitative analysis to support preference research. European Journal of Human Genetics. 31(4). 445–452. 8 indexed citations

16.

Schwartz, Talia S., Kurt D. Christensen, Melissa Kurtz Uveges, et al.. (2021). Effects of participation in a U.S. trial of newborn genomic sequencing on parents at risk for depression. Journal of Genetic Counseling. 31(1). 218–229. 7 indexed citations

17.

Majumder, Mary A. & Amy L. McGuire. (2020). Data Sharing in the Context of Health-Related Citizen Science. The Journal of Law Medicine & Ethics. 48(S1). 167–177. 8 indexed citations

18.

Guerrini, Christi J., Amy L. McGuire, & Mary A. Majumder. (2017). Myriad Take Two: Can Genomic Databases Remain Secret?. SSRN Electronic Journal.

19.

Gymrek, Melissa, Amy L. McGuire, David E. Golan, Eran Halperin, & Yaniv Erlich. (2013). Identifying Personal Genomes by Surname Inference. Science. 339(6117). 321–324. 710 indexed citations breakdown →

20.

Bledsoe, Marianna J., Ellen Wright Clayton, Amy L. McGuire, et al.. (2012). Return of research results from genomic biobanks: cost matters. Genetics in Medicine. 15(2). 103–105. 45 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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