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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:

Detailed Phenotyping and Therapeutic Strategies for Intronic ABCA4 Variants in Stargardt Disease
Mubeen Khan, Gavin Arno, Ana Fakin, et al.
Molecular Therapy — Nucleic Acids (2020) Vol. 21, pp. 412-427
Open Access | Times Cited: 67

Showing 1-25 of 67 citing articles:

Multimodal spatiotemporal phenotyping of human retinal organoid development
Philipp Wahle, Giovanna Brancati, Christoph Harmel, et al.
Nature Biotechnology (2023) Vol. 41, Iss. 12, pp. 1765-1775
Open Access | Times Cited: 74
A look into retinal organoids: methods, analytical techniques, and applications
Tess A. V. Afanasyeva, Julio C. Corral-Serrano, Alejandro Garanto, et al.
Cellular and Molecular Life Sciences (2021) Vol. 78, Iss. 19-20, pp. 6505-6532
Open Access | Times Cited: 73
Pluripotent stem cell-derived models of retinal disease: Elucidating pathogenesis, evaluating novel treatments, and estimating toxicity
Marzena Kurzawa‐Akanbi, Nikolaos Tzoumas, Julio C. Corral-Serrano, et al.
Progress in Retinal and Eye Research (2024) Vol. 100, pp. 101248-101248
Open Access | Times Cited: 12
Phototoxicity avoidance is a potential therapeutic approach for retinal dystrophy caused by EYS dysfunction
Yuki Otsuka, Keiko Imamura, Akio Oishi, et al.
JCI Insight (2024) Vol. 9, Iss. 8
Open Access | Times Cited: 10
Whole genome sequencing and in vitro splice assays reveal genetic causes for inherited retinal diseases
Zeinab Fadaie, Laura Whelan, Tamar Ben‐Yosef, et al.
npj Genomic Medicine (2021) Vol. 6, Iss. 1
Open Access | Times Cited: 47
Consensus Guidelines for the Design and In Vitro Preclinical Efficacy Testing N-of-1 Exon Skipping Antisense Oligonucleotides
Annemieke Aartsma‐Rus, Alejandro Garanto, Willeke M. C. van Roon‐Mom, et al.
Nucleic Acid Therapeutics (2022) Vol. 33, Iss. 1, pp. 17-25
Open Access | Times Cited: 33
Antisense oligonucleotide therapy corrects splicing in the common Stargardt disease type 1-causing variant ABCA4 c.5461-10T>C
Melita Kaltak, Petra de Bruijn, Davide Piccolo, et al.
Molecular Therapy — Nucleic Acids (2023) Vol. 31, pp. 674-688
Open Access | Times Cited: 23
An Overview of the Genetics of ABCA4 Retinopathies, an Evolving Story
Saoud Al‐Khuzaei, Suzanne Broadgate, Charlotte R. Foster, et al.
Genes (2021) Vol. 12, Iss. 8, pp. 1241-1241
Open Access | Times Cited: 40
Therapy Approaches for Stargardt Disease
Elena Piotter, Michelle E. McClements, Robert E. MacLaren
Biomolecules (2021) Vol. 11, Iss. 8, pp. 1179-1179
Open Access | Times Cited: 36
Analysis of Pathogenic Pseudoexons Reveals Novel Mechanisms Driving Cryptic Splicing
Niall P. Keegan, Steve D. Wilton, Sue Fletcher
Frontiers in Genetics (2022) Vol. 12
Open Access | Times Cited: 28
Biallelic CLCN2 mutations cause retinal degeneration by impairing retinal pigment epithelium phagocytosis and chloride channel function
Ping Xu, Zhuolin Chen, Jianchi Ma, et al.
Human Genetics (2023) Vol. 142, Iss. 4, pp. 577-593
Closed Access | Times Cited: 14
The Role of Small Molecules and Their Effect on the Molecular Mechanisms of Early Retinal Organoid Development
Ellie L. Wagstaff, Andrea Heredero Berzal, Camiel J. F. Boon, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 13, pp. 7081-7081
Open Access | Times Cited: 32
Retinal organoids as models for development and diseases
Xiao Zhang, Wen Wang, Zi‐Bing Jin
Cell Regeneration (2021) Vol. 10, Iss. 1
Open Access | Times Cited: 29
Photoreceptor degeneration in ABCA4-associated retinopathy and its genetic correlates
Maximilian Pfau, Catherine A. Cukras, Laryssa A. Huryn, et al.
JCI Insight (2022) Vol. 7, Iss. 2
Open Access | Times Cited: 21
Multidisciplinary team directed analysis of whole genome sequencing reveals pathogenic non-coding variants in molecularly undiagnosed inherited retinal dystrophies
Malena Daich Varela, James Bellingham, Fabiana Louise Motta, et al.
Human Molecular Genetics (2022) Vol. 32, Iss. 4, pp. 595-607
Open Access | Times Cited: 19
Rare missense mutations in ABCA7 might increase Alzheimer’s disease risk by plasma membrane exclusion
Liene Bossaerts, Elisabeth Hendrickx Van de Craen, Rita Cacace, et al.
Acta Neuropathologica Communications (2022) Vol. 10, Iss. 1
Open Access | Times Cited: 17
Identification of a Complex Allele in IMPG2 as a Cause of Adult-Onset Vitelliform Macular Dystrophy
Irene Vázquez-Domínguez, Catherina H. Z. Li, Zeinab Fadaie, et al.
Investigative Ophthalmology & Visual Science (2022) Vol. 63, Iss. 5, pp. 27-27
Open Access | Times Cited: 17
Retina-on-Chip: Engineering Functional in vitro Models of the Human Retina using Organ-on-Chip Technology
Tarek Gensheimer, Devin Veerman, Edwin van Oosten, et al.
Lab on a Chip (2025)
Open Access
Preclinical assessment of splicing modulation therapy for ABCA4 variant c.768G>T in Stargardt disease
Dyah W. Karjosukarso, Femke Bukkems, Lonneke Duijkers, et al.
Communications Medicine (2025) Vol. 5, Iss. 1
Open Access
ABCA4 Deep Intronic Variants Contributed to Nearly Half of Unsolved Stargardt Cases With a Milder Phenotype
Yingwei Wang, Pangfeng Wang, Yi Zhen, et al.
Investigative Ophthalmology & Visual Science (2025) Vol. 66, Iss. 1, pp. 65-65
Open Access
Progression of Atrophy as a Function of ABCA4 Variants and Age of Onset in Stargardt Disease
Jeroen A. A. H. Pas, Catherina H. Z. Li, Filip Van den Broeck, et al.
Investigative Ophthalmology & Visual Science (2025) Vol. 66, Iss. 4, pp. 76-76
Open Access
Retinal organoids in disease modeling and drug discovery: Opportunities and challenges
Koushik Chakrabarty, Divyani Nayak, Jayasree Debnath, et al.
Survey of Ophthalmology (2023) Vol. 69, Iss. 2, pp. 179-189
Closed Access | Times Cited: 9
Demonstration of the pathogenicity of a common non-exomic mutation in ABCA4 using iPSC-derived retinal organoids and retrospective clinical data
Erin R. Burnight, Beau J. Fenner, Ian C. Han, et al.
Human Molecular Genetics (2023) Vol. 33, Iss. 16, pp. 1379-1390
Closed Access | Times Cited: 9
Preclinical Development of Antisense Oligonucleotides to Rescue Aberrant Splicing Caused by an Ultrarare ABCA4 Variant in a Child with Early-Onset Stargardt Disease
Nuria Suárez-Herrera, Catherina H. Z. Li, Nico Leijsten, et al.
Cells (2024) Vol. 13, Iss. 7, pp. 601-601
Open Access | Times Cited: 3
The Rise of Retinal Organoids for Vision Research
Kritika Sharma, Tim U. Krohne, Volker Busskamp
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 22, pp. 8484-8484
Open Access | Times Cited: 22
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