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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

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Showing 24 citing articles:

Association of Social Determinants of Health With Genetic Test Request and Completion Rates in Children With Neurologic Disorders
Jordan J. Cole, Jonathan Williams, Angela D. Sellitto, et al.
Neurology (2025) Vol. 104, Iss. 5
Closed Access | Times Cited: 2
Disparities in Genetic Testing for Neurologic Disorders
Aaron Baldwin, J. Nathan Copeland, Meron Azage, et al.
Neurology (2024) Vol. 102, Iss. 6
Closed Access | Times Cited: 8
Atypical Diabetes: What Have We Learned and What Does the Future Hold?
Stephen Stone, Ashok Balasubramanyam, Jennifer E. Posey
Diabetes Care (2024) Vol. 47, Iss. 5, pp. 770-781
Open Access | Times Cited: 6
Overcoming Barriers to Genomic Medicine Implementation
Heidi L. Rehm
Clinical Chemistry (2025) Vol. 71, Iss. 1, pp. 4-9
Closed Access
Striving Towards Equity in Cardiovascular Genomics Research
Javier Jurado Vélez, Nekayla Anderson, Ivree Datcher, et al.
Current Atherosclerosis Reports (2025) Vol. 27, Iss. 1
Open Access
A new approach for the detection of genetic alterations utilizing modified loop-mediated isothermal amplification reaction (LAMP)
Aneta Cierzniak, Małgorzata Małodobra-Mazur, Miron Tokarski
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access
Diencephalic-mesencephalic junction dysplasia: case report and literature review
Tenoch Herrada-Pineda, Ana Karen Pérez-Vázquez, Salvador Manrique-Guzmán, et al.
Child s Nervous System (2025) Vol. 41, Iss. 1
Closed Access
Attitudes regarding polygenic risk testing for lung cancer: a mixed-methods study
Hoda Badr, Jinyoung Byun, Melinda C. Aldrich, et al.
Annals of Behavioral Medicine (2025) Vol. 59, Iss. 1
Closed Access
Advancing fetal diagnosis and prognostication using comprehensive prenatal phenotyping and genetic testing
Olivier Fortin, Sarah B. Mulkey, Jamie L. Fraser
Pediatric Research (2024)
Closed Access | Times Cited: 3
Analysis of financial barriers experienced by prospective genetic counseling students
Dexter Lee, Julia Platt, Pamela Flodman, et al.
Genetics in Medicine (2024) Vol. 26, Iss. 11, pp. 101175-101175
Open Access | Times Cited: 2
Defining and Reducing Variant Classification Disparities
Moez Dawood, Shawn Fayer, Sriram Pendyala, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
Leveraging the Academic Artificial Intelligence Silecosystem to Advance the Community Oncology Enterprise
Kevin Mcdonnell
Journal of Clinical Medicine (2023) Vol. 12, Iss. 14, pp. 4830-4830
Open Access | Times Cited: 4
Interest in and Experience with Genetic Testing for Late-Onset Medical Conditions: Results from the National Poll on Healthy Aging
Samantha J. Feldman, D Blasco, M Mones, et al.
The Journal of Prevention of Alzheimer s Disease (2024)
Closed Access | Times Cited: 1
Policy and laboratory practice: How quality control procedures for genetic testing perpetuate biological essentialism and discrimination against transgender, gender diverse, and intersex people
Emerson J. Dusic, Lex N. Powers, Sarah V. Clowes Candadai, et al.
Journal of Genetic Counseling (2024)
Closed Access | Times Cited: 1
Survey of the Landscape of Society Practice Guidelines for Genetic Testing of Neurodevelopmental Disorders
Siddharth Srivastava, Jordan J. Cole, Julie S. Cohen, et al.
Annals of Neurology (2024) Vol. 96, Iss. 5, pp. 900-913
Open Access | Times Cited: 1
Using multiplexed functional data to reduce variant classification inequities in underrepresented populations
Moez Dawood, Shawn Fayer, Sriram Pendyala, et al.
Genome Medicine (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 1
Racial Disparities in Accessing Care along the Continuum of Cancer Genetic Service Delivery
I. Wagner, Ziming Xuan, Haibo Lu, et al.
Cancer Epidemiology Biomarkers & Prevention (2023) Vol. 33, Iss. 1, pp. 55-62
Closed Access | Times Cited: 2
Navigating Neurogenetics for Child and Adolescent Psychiatry Practice
Aaron J. Hauptman, Jay A. Salpekar, Julie S. Cohen, et al.
Journal of the American Academy of Child & Adolescent Psychiatry (2024) Vol. 63, Iss. 7, pp. 666-669
Closed Access
Reconciling diversity in health and genomic data collection with the regulation of AI in clinical genomics
Kyle McKibbin, Alice B. Popejoy, Mahsa Shabani
Genetics in Medicine (2024) Vol. 26, Iss. 7, pp. 101127-101127
Closed Access
Genomic testing in neonates
Jessica Salkind, Alison Mintoft, Giles S Kendall, et al.
Archives of Disease in Childhood Education & Practice (2024) Vol. 109, Iss. 6, pp. 292-296
Closed Access
Applying an ELSI lens to real-world data and novel genomic insights for personalized mental healthcare
Rachele Hendricks‐Sturrup, Sandra E. Yankah, Christine Y. Lu
Frontiers in Genetics (2024) Vol. 15
Open Access
Autism Spectrum Disorder and Clinical Genetic Testing
Fatma Doagu, Kristiina Tammimies
Springer eBooks (2024), pp. 1-22
Closed Access
Medicaid Coverage of NCCN- and ASCO/SSO-Guideline-Concordant BRCA Germline Testing for Patients with Breast Cancer: Opportunity to Embrace Rapid Advancements in Precision Medicine
Hattie H Huston-Paterson, Vanessa Mora, Beth Y. Karlan, et al.
Annals of Surgical Oncology (2024)
Closed Access
ACMG Seeks to Advance Equitable Access to Clinical Genetics/Genomics Testing

American Journal of Medical Genetics Part A (2023) Vol. 191, Iss. 10, pp. 2463-2464
Closed Access
ProxyTyper: Generation of Proxy Panels for Privacy-aware Outsourcing of Genotype Imputation
Degui Zhi, Xiaoqian Jiang, Arif Harmanci
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
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