Open Access Helper

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:

A homozygous Y443C variant in the RNPC3 is associated with severe syndromic congenital hypopituitarism and diffuse brain atrophy
Diğdem Bezen, Orkide Kutlu, S. Mouilleron, et al.
American Journal of Medical Genetics Part A (2022) Vol. 188, Iss. 9, pp. 2701-2706
Closed Access | Times Cited: 4

Showing 4 citing articles:

Connecting genotype and phenotype in minor spliceosome diseases
Antto J. Norppa, Mariia Shcherbii, Mikko J. Frilander
RNA (2025) Vol. 31, Iss. 3, pp. 284-299
Open Access
Hypothyroidism is a causal determinant of age-related cataract risk in European population: a Mendelian randomization study
Shu Liu, Qi Sun, Qingwei Gu, et al.
Frontiers in Endocrinology (2024) Vol. 15
Open Access | Times Cited: 3
Congenital hydrocephalus: new Mendelian mutations and evidence for oligogenic inheritance
Valérie Jacquemin, Nassim Versbraegen, Sarah Duerinckx, et al.
Human Genomics (2023) Vol. 17, Iss. 1
Open Access | Times Cited: 6
A <i>Novel RNPC3</i> Gene Variant Expands the Phenotype in Patients with Congenital Hypopituitarism and Neuropathy
Zehra Yavaş Abalı, Ezgi Gökpınar İli, Firdevs Baş, et al.
Hormone Research in Paediatrics (2023) Vol. 97, Iss. 2, pp. 157-164
Open Access | Times Cited: 3
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