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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:

AutoCaSc: Prioritizing candidate genes for neurodevelopmental disorders
Johann Lieberwirth, Benjamin Büttner, Chiara Klöckner, et al.
Human Mutation (2022) Vol. 43, Iss. 12, pp. 1795-1807
Open Access | Times Cited: 10

Showing 10 citing articles:

PubTator 3.0: an AI-powered literature resource for unlocking biomedical knowledge
Chih-Hsuan Wei, Alexis Allot, Po‐Ting Lai, et al.
Nucleic Acids Research (2024) Vol. 52, Iss. W1, pp. W540-W546
Open Access | Times Cited: 36
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings
Axel Schmidt, Magdalena Danyel, Kathrin Grundmann, et al.
Nature Genetics (2024) Vol. 56, Iss. 8, pp. 1644-1653
Open Access | Times Cited: 11
Re-evaluation and re-analysis of 152 research exomes five years after the initial report reveals clinically relevant changes in 18%
Tobias Bartolomaeus, Julia Hentschel, Rami Abou Jamra, et al.
European Journal of Human Genetics (2023) Vol. 31, Iss. 10, pp. 1154-1164
Open Access | Times Cited: 13
An integrative scoring approach for prioritization of rare autism spectrum disorder candidate variants from whole exome sequencing data
Apurba Shil, Noa Arava, Noam Levi, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access
Next-generation phenotyping integrated in a national framework for patients with ultra-rare disorders improves genetic diagnostics and yields new molecular findings
Axel Schmidt, Magdalena Danyel, Kathrin Grundmann, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 10
Case Report—An Inherited Loss-of-Function NRXN3 Variant Potentially Causes a Neurodevelopmental Disorder with Autism Consistent with Previously Described 14q24.3-31.1 Deletions
René G. Feichtinger, Martin Preisel, Karin Brugger, et al.
Genes (2023) Vol. 14, Iss. 6, pp. 1217-1217
Open Access | Times Cited: 4
De novo variants in the PABP domain of PABPC1 lead to developmental delay
Meret Wegler, Xiangbin Jia, Mariëlle Alders, et al.
Genetics in Medicine (2022) Vol. 24, Iss. 8, pp. 1761-1773
Open Access | Times Cited: 5
Unveiling the hidden: revisiting the potential of old genetic data for rare disease research
Allan Bayat
European Journal of Human Genetics (2023) Vol. 31, Iss. 10, pp. 1093-1094
Closed Access | Times Cited: 2
De novo variants in CNOT9 cause a neurodevelopmental disorder with or without epilepsy
Lydia von Wintzingerode, Bruria Ben‐Zeev, Claudia Cesario, et al.
Genetics in Medicine (2023) Vol. 25, Iss. 7, pp. 100859-100859
Closed Access | Times Cited: 1
Re-evaluation and Re-analysis of 152 research exomes five years after the initial report reveals clinically relevant changes in 20%
Tobias Bartolomaeus, Julia Hentschel, Rami Abou Jamra, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access
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