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:

Analysis of 14,392 whole genomes reveals 3.5% of Qataris carry medically actionable variants
Amal Elfatih, Chadi Saad, Said I. Ismail, et al.
European Journal of Human Genetics (2024) Vol. 32, Iss. 11, pp. 1465-1473
Open Access | Times Cited: 8

Showing 8 citing articles:

Genomic sequencing: the case for equity of care in the era of personalized medicine
Lina Ghaloul‐Gonzalez, Lisa S. Parker, Jonathan M. Davis, et al.
Pediatric Research (2025)
Closed Access | Times Cited: 1

Patterns of population structure and genetic variation within the Saudi Arabian population
D.K. Malomane, M. Williams, Christian D. Huber, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access

Genetics and Population Analysis
Prachi Balyan, Nismabi A Nisamudheen, Jan Zainab, et al.
Elsevier eBooks (2025)
Closed Access

Looking back at 2024 in the European Journal of Human Genetics
Alisdair McNeill
European Journal of Human Genetics (2025) Vol. 33, Iss. 2, pp. 141-143
Open Access

Opportunities and Challenges of Population Pharmacogenomics
Yitian Zhou, Yoomi Park, Mahamadou D. Camara, et al.
Annals of Human Genetics (2025)
Open Access

ACMG secondary findings in the Brazilian rare genomes project: insights from 5402 genome sequencing
Eduardo Perrone, Luiza do Amaral Virmond, Antônio Victor Campos Coelho, et al.
Journal of Human Genetics (2025)
Open Access

November in EJHG: looking at genetic counsellor training in Europe, novel clinical guidelines and ancestral impact on variant interpretation
Alisdair McNeill
European Journal of Human Genetics (2024) Vol. 32, Iss. 11, pp. 1343-1344
Closed Access

Study design and the sampling of deleterious rare variants in biobank-scale datasets
Margaret C. Steiner, Daniel P. Rice, Arjun Biddanda, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access

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