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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:

Computational Genomics in the Era of Precision Medicine: Applications to Variant Analysis and Gene Therapy
Yung-Chun Wang, Yuchang Wu, Julie Choi, et al.
Journal of Personalized Medicine (2022) Vol. 12, Iss. 2, pp. 175-175
Open Access | Times Cited: 16

Showing 16 citing articles:

PTEN mutations impair CSF dynamics and cortical networks by dysregulating periventricular neural progenitors
Tyrone DeSpenza, Emre Kiziltug, Garrett Allington, et al.
Nature Neuroscience (2025)
Closed Access | Times Cited: 2
TRIM71 mutations cause a neurodevelopmental syndrome featuring ventriculomegaly and hydrocephalus
Phan Q. Duy, Bettina Jux, Shujuan Zhao, et al.
Brain (2024) Vol. 147, Iss. 12, pp. 4292-4305
Closed Access | Times Cited: 5
Identification of hub biomarkers and exploring the roles of immunity, M6A, ferroptosis, or cuproptosis in rats with diabetic erectile dysfunction
Yi Wang, Xinyu Zhang, Yinhao Chen, et al.
Andrology (2022) Vol. 11, Iss. 2, pp. 316-331
Closed Access | Times Cited: 19
Healthcare applications of computational genomics
Joel J. P. C. Rodrigues, Abdul Razak Mohamed Sikkander, Suman Lata Tripathi, et al.
Elsevier eBooks (2025), pp. 259-278
Closed Access
Data-driven decision-making for precision diagnosis of digestive diseases
Song Jiang, Ting Wang, Kun-He Zhang
BioMedical Engineering OnLine (2023) Vol. 22, Iss. 1
Open Access | Times Cited: 10
Pathogenic variants in autism gene KATNAL2 cause hydrocephalus and disrupt neuronal connectivity by impairing ciliary microtubule dynamics
Tyrone DeSpenza, Amrita Singh, Garrett Allington, et al.
Proceedings of the National Academy of Sciences (2024) Vol. 121, Iss. 27
Closed Access | Times Cited: 3
Familial and syndromic forms of arachnoid cyst implicate genetic factors in disease pathogenesis
Hanya M Qureshi, Kedous Y. Mekbib, Garrett Allington, et al.
Cerebral Cortex (2022) Vol. 33, Iss. 6, pp. 3012-3025
Open Access | Times Cited: 11
A novel SMARCC1 BAFopathy implicates neural progenitor epigenetic dysregulation in human hydrocephalus
Amrita Singh, Garrett Allington, Stephen Viviano, et al.
Brain (2023) Vol. 147, Iss. 4, pp. 1553-1570
Closed Access | Times Cited: 6
Personalized medicine
Kholoud Bastaki, Umm-Kulthum Ismail Umlai, Puthen V. Jithesh
Elsevier eBooks (2023), pp. 1-32
Closed Access | Times Cited: 2
Prediction of Deleterious Single Amino Acid Polymorphisms with a Consensus Holdout Sampler
Óscar Álvarez-Machancoses, Eshel Faraggi, Enrique J. deAndrés‐Galiana, et al.
Current Genomics (2024) Vol. 25, Iss. 3, pp. 171-184
Open Access
Next-Gen Pharma
Rati Kailash Prasad Tripathi
Advances in healthcare information systems and administration book series (2024), pp. 28-53
Closed Access
De novo Variants Disrupt an LDB1-Regulated Transcriptional Network in Congenital Ventriculomegaly
Garrett Allington, Neel Mehta, Evan Dennis, et al.
(2024)
Closed Access
Zebrafish navigating the metabolic maze: insights into human disease – assets, challenges and future implications
Chandrashekar Yashaswini, Neelakanta Sarvashiva Kiran, Ankita Chatterjee
Journal of Diabetes & Metabolic Disorders (2024) Vol. 24, Iss. 1
Closed Access
Unveiling Key Biomarkers and Mechanisms in Septic Cardiomyopathy: A Comprehensive Transcriptome Analysis
Dandan Zhao, Jinqiang Zhuang, Liping Wang, et al.
Journal of Inflammation Research (2024) Vol. Volume 17, pp. 11451-11467
Open Access
Dual impact of PTEN mutation on CSF dynamics and cortical networks via the dysregulation of neural precursors and their interneuron descendants
Tyrone DeSpenza, Emre Kiziltug, Garrett Allington, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
A novelSMARCC1-mutant BAFopathy implicates epigenetic dysregulation of neural progenitors in hydrocephalus
Amrita Singh, Stephen Viviano, Garrett Allington, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access
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