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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.

Requested Article:

“I am not a number!” Opinions and preferences of people with intellectual disability about genetic healthcare
Iva Strnadová, Julie Loblinzk, Jackie Leach Scully, et al.
European Journal of Human Genetics (2023) Vol. 31, Iss. 9, pp. 1057-1065
Open Access | Times Cited: 15

Showing 15 citing articles:

2023 in the European Journal of Human Genetics
Alisdair McNeill
European Journal of Human Genetics (2024) Vol. 32, Iss. 2, pp. 135-137
Open Access | Times Cited: 180
Equitable and accessible informed healthcare consent process for people with intellectual disability: a systematic literature review
Manjekah Dunn, Iva Strnadová, Jackie Leach Scully, et al.
BMJ Quality & Safety (2023), pp. bmjqs-016113
Open Access | Times Cited: 15
“It was up to me to be curious”: Perceptions and Experiences of Students with Intellectual Disability on Genetics and Health Education
Iva Strnadová, Jennifer Hansen, Joanne Danker, et al.
Research Square (Research Square) (2025)
Closed Access
Collaborative contributions to genetics: Systemic and narrative approaches
Mariangels Ferrer‐Duch
Journal of Family Therapy (2025) Vol. 47, Iss. 2
Open Access
Genetic testing in cerebral palsy with clinical and neuroimaging variables
Esther Tantsis, Shekeeb S. Mohammad, Simon Paget, et al.
Developmental Medicine & Child Neurology (2025)
Open Access
Ethical challenges in autism genomics: Recommendations for researchers
Heini M. Natri, Carolyn Riley Chapman, Síofra Heraty, et al.
European Journal of Medical Genetics (2023) Vol. 66, Iss. 9, pp. 104810-104810
Open Access | Times Cited: 11
Access to healthcare for people with intellectual disability: a scoping review
Maryann Barrington, Karen Fisher, Ben Harris‐Roxas, et al.
Scandinavian Journal of Public Health (2025)
Closed Access
The need for co-educators to drive a new model of inclusive, person-centred and respectful co-healthcare with people with intellectual disability
Chloe Molnar, Iva Strnadová, Manjekah Dunn, et al.
Frontiers in Psychiatry (2024) Vol. 15
Open Access | Times Cited: 2
International Undiagnosed Diseases Programs (UDPs): components and outcomes
Ela Curic, Lisa Ewans, Ryan Pysar, et al.
Orphanet Journal of Rare Diseases (2023) Vol. 18, Iss. 1
Open Access | Times Cited: 6
Social and Behavioral Genomics: What Does It Mean for Pediatrics?
Daphne Oluwaseun Martschenko, Lucas J. Matthews, Maya Sabatello
The Journal of Pediatrics (2023) Vol. 264, pp. 113735-113735
Open Access | Times Cited: 4
Exploring the Barriers and Enablers for the Equitable and Accessible Informed Healthcare Consent Process for People with Intellectual Disability: A Systematic Literature Review
Manjekah Dunn, Iva Strnadová, Jackie Leach Scully, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 3
Attitude of Healthcare Providers Towards Care of People with Disabilities, in Hail Region, Saudi Arabia
Khalil Saleh, Gamil Ghaleb Alrubaiee, Talal Ali Hussein Al-Qalah, et al.
International Journal of General Medicine (2024) Vol. Volume 17, pp. 5181-5190
Open Access
Why don’t we all use genomic testing?
Alisdair McNeill
European Journal of Human Genetics (2023) Vol. 31, Iss. 9, pp. 971-972
Open Access | Times Cited: 1
Australasian genetic counselors' attitudes toward disability and prenatal testing: Findings from a cross‐sectional survey
Tatiane Yanes, Vaishnavi Nathan, Courtney K. Wallingford, et al.
Journal of Genetic Counseling (2023) Vol. 33, Iss. 4, pp. 822-833
Open Access
Short Communication: Lived experience perspectives on genetic testing for a rare eye disease
Mallorie T. Tam, Alonso Daboub, Hayami Lou, et al.
Journal of Community Genetics (2023) Vol. 15, Iss. 1, pp. 97-101
Open Access
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