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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:

Pathogenic alleles in microtubule, secretory granule and extracellular matrix-related genes in familial keratoconus
Vishal Shinde, Nara Sobreira, Elizabeth Wohler, et al.
Human Molecular Genetics (2021) Vol. 30, Iss. 8, pp. 658-671
Open Access | Times Cited: 24

Showing 24 citing articles:

Molecular Subtype Identification and Potential Drug Prediction Based on Anoikis-Related Genes Expression in Keratoconus
Zhixin Jiang, Boyang Zhang, Shichong Jia, et al.
Investigative Ophthalmology & Visual Science (2025) Vol. 66, Iss. 2, pp. 3-3
Open Access | Times Cited: 1
Single cell RNA-seq of human cornea organoids identifies cell fates of a developing immature cornea
George Maiti, Maithê Rocha Monteiro de Barros, Nan Hu, et al.
PNAS Nexus (2022) Vol. 1, Iss. 5
Open Access | Times Cited: 20
Genetic Disorders of the Extracellular Matrix: From Cell and Gene Therapy to Future Applications in Regenerative Medicine
Shukti Chakravarti, Elena Enzo, Maithê Rocha Monteiro de Barros, et al.
Annual Review of Genomics and Human Genetics (2022) Vol. 23, Iss. 1, pp. 193-222
Open Access | Times Cited: 18
Pathogenesis of keratoconus: NRF2-antioxidant, extracellular matrix and cellular dysfunctions
Maithê Rocha Monteiro de Barros, Shukti Chakravarti
Experimental Eye Research (2022) Vol. 219, pp. 109062-109062
Open Access | Times Cited: 16
Single-nucleus RNA sequencing of midbrain blood-brain barrier cells in schizophrenia reveals subtle transcriptional changes with overall preservation of cellular proportions and phenotypes
Sofía Puvogel, Astrid M. Alsema, Laura Kracht, et al.
Molecular Psychiatry (2022) Vol. 27, Iss. 11, pp. 4731-4740
Open Access | Times Cited: 16
Whole-exome Sequencing Screening for Candidate Genes and Variants Associated with Primary Sporadic Keratoconus in Chinese Patients
Chunyuan Song, Ling Li, Chang Liu, et al.
Experimental Eye Research (2024) Vol. 245, pp. 109978-109978
Closed Access | Times Cited: 2
Disruption of the HIF-1 pathway in individuals with Ollier disease and Maffucci syndrome
Sarah R. Poll, Renan Paulo Martin, Elizabeth Wohler, et al.
PLoS Genetics (2022) Vol. 18, Iss. 12, pp. e1010504-e1010504
Open Access | Times Cited: 11
Complement-mediated inflammation and mitochondrial energy metabolism in the proteomic profile of myopic human corneas
Tianze Huang, Yuchen Wang, Zhonghai Wang, et al.
Journal of Proteomics (2023) Vol. 285, pp. 104949-104949
Closed Access | Times Cited: 6
Trio-based exome sequencing broaden the genetic spectrum in keratoconus
Li‐Yan Xu, Kaili Yang, Meng Zhu, et al.
Experimental Eye Research (2022) Vol. 226, pp. 109342-109342
Closed Access | Times Cited: 9
Sequence variants contributing to dysregulated inflammatory responses across keratoconic cone surface in adolescent patients with keratoconus
Katarzyna Jaśkiewicz, Magdalena Maleszka-Kurpiel, Michał Kabza, et al.
Frontiers in Immunology (2023) Vol. 14
Open Access | Times Cited: 5
Experimental Models for Keratoconus: Insights and challenges
Sujithra Shankar, Rashmi Deshmukh, Tejaswini Pingali, et al.
Experimental Eye Research (2024) Vol. 248, pp. 110122-110122
Closed Access | Times Cited: 1
Family-based exome sequencing identifies candidate genes related to keratoconus in Chinese families
Li–Yan Xu, Kaili Yang, Shanshan Yin, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 5
The ataxia-telangiectasia disease protein ATM controls vesicular protein secretion via CHGA and microtubule dynamics via CRMP5
Marina Reichlmeir, Ruth Pia Duecker, Hanna Röhrich, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Refractive errors in patients with Bardet Biedl syndrome
Leyla Yavuz Saricay, Grace Baldwin, Eric A. Moulton, et al.
Ophthalmic Genetics (2024) Vol. 45, Iss. 5, pp. 435-440
Closed Access
The ataxia-telangiectasia disease protein ATM controls vesicular protein secretion via CHGA and microtubule dynamics via CRMP5
Marina Reichlmeir, Ruth Pia Duecker, Hanna Röhrich, et al.
Neurobiology of Disease (2024) Vol. 203, pp. 106756-106756
Open Access
Whole-Exome Sequencing of 24 Spanish Families: Candidate Genes for Non-Syndromic Pediatric Keratoconus
Carmen González-Atienza, Eloísa Sánchez-Cazorla, Natalia Villoldo-Fernández, et al.
Genes (2023) Vol. 14, Iss. 10, pp. 1838-1838
Open Access | Times Cited: 1
Cornea and Sclera
Myron Yanoff, Joseph W. Sassani
Elsevier eBooks (2024), pp. 316-410.e21
Closed Access
Neuroimaging and epigenetic analysis reveal novel epigenetic loci in major depressive disorder
Hyun-Ho Yang, Kyu‐Man Han, Aram Kim, et al.
Psychological Medicine (2024) Vol. 54, Iss. 10, pp. 2585-2598
Closed Access
A genetic investigation in five Chinese families with keratoconus
Qinghong Lin, Xuejun Wang, Xiaoliao Peng, et al.
PeerJ (2024) Vol. 12, pp. e18037-e18037
Open Access
The Corneal Stroma
Shukti Chakravarti
Elsevier eBooks (2024)
Closed Access
Analysis of candidate variants in a Chinese family with monozygotic twins with keratoconus: a case report
Chunyuan Song, Kehua Wang, Ling Li, et al.
Ophthalmic Genetics (2024), pp. 1-9
Closed Access
Single cell RNA-seq identifies developing corneal cell fates in the human cornea organoid
George Maiti, Maithê Rocha Monteiro de Barros, Nan Hu, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 2
Progressive Keratoconus in a Patient With Severe Pectus Excavatum and a Cartilage Oligomeric Matrix Protein Gene Mutation: A Case Report
Nefeli Eleni Kounatidou, Georgios Kondylis, Olga Klavdianou, et al.
Eye & Contact Lens Science & Clinical Practice (2023)
Closed Access
Single-nucleus RNA sequencing of the midbrain blood-brain barrier cells in schizophrenia reveals subtle transcriptional changes with overall preservation of cellular proportions and phenotypes
Sofía Puvogel, Astrid M. Alsema, Laura Kracht, et al.
Research Square (Research Square) (2022)
Open Access
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