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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:

Phenotype and Progression of Retinal Degeneration Associated With Nullizigosity of ABCA4
Ana Fakin, Anthony G. Robson, Kaoru Fujinami, et al.
Investigative Ophthalmology & Visual Science (2016) Vol. 57, Iss. 11, pp. 4668-4668
Open Access | Times Cited: 48

Showing 1-25 of 48 citing articles:

Deep-intronic ABCA4 variants explain missing heritability in Stargardt disease and allow correction of splice defects by antisense oligonucleotides
Riccardo Sangermano, Alejandro Garanto, Mubeen Khan, et al.
Genetics in Medicine (2019) Vol. 21, Iss. 8, pp. 1751-1760
Open Access | Times Cited: 178
Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromes
Michalis Georgiou, Anthony G. Robson, Kaoru Fujinami, et al.
Progress in Retinal and Eye Research (2024) Vol. 100, pp. 101244-101244
Closed Access | Times Cited: 53
The Role of Vitamin A in Retinal Diseases
Jana Sajovic, Andrej Meglič, Damjan Glavač, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 3, pp. 1014-1014
Open Access | Times Cited: 55
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
Detailed genetic characteristics of an international large cohort of patients with Stargardt disease: ProgStar study report 8
Kaoru Fujinami, Rupert W. Strauß, John Chiang, et al.
British Journal of Ophthalmology (2018) Vol. 103, Iss. 3, pp. 390-397
Open Access | Times Cited: 56
Prospective Cohort Study of Childhood-Onset Stargardt Disease: Fundus Autofluorescence Imaging, Progression, Comparison with Adult-Onset Disease, and Disease Symmetry
Michalis Georgiou, Thomas Kane, Preena Tanna, et al.
American Journal of Ophthalmology (2019) Vol. 211, pp. 159-175
Open Access | Times Cited: 49
Stargardt disease and progress in therapeutic strategies
Di Huang, Rachael C. Heath Jeffery, May T. Aung-Htut, et al.
Ophthalmic Genetics (2021) Vol. 43, Iss. 1, pp. 1-26
Open Access | Times Cited: 37
Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of More Than 3500 Inherited Retinal Disease Patients from the United Kingdom
William Woof, Thales A. C. de Guimarães, Saoud Al‐Khuzaei, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 5
The Effect on Retinal Structure and Function of 15 Specific ABCA4 Mutations: A Detailed Examination of 82 Hemizygous Patients
Ana Fakin, Anthony G. Robson, John Chiang, et al.
Investigative Ophthalmology & Visual Science (2016) Vol. 57, Iss. 14, pp. 5963-5963
Open Access | Times Cited: 45
Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of More Than 3500 Inherited Retinal Disease Patients from the United Kingdom
William Woof, Thales A. C. de Guimarães, Saoud Al‐Khuzaei, et al.
Ophthalmology Science (2024) Vol. 5, Iss. 2, pp. 100652-100652
Open Access | Times Cited: 4
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
Quantifying the Progression of Stargardt Disease in Double-Null ABCA4 Carriers Using Fundus Autofluorescence Imaging
Ivana Mihalek, Hanna De Bruyn, Tomislav Glavan, et al.
Translational Vision Science & Technology (2025) Vol. 14, Iss. 3, pp. 16-16
Open Access
Quantitative Fundus Autofluorescence in ABCA4-Related Retinopathy -Functional Relevance and Genotype-Phenotype Correlation
Philipp L. Müller, Martin Gliem, Myra McGuinnes, et al.
American Journal of Ophthalmology (2020) Vol. 222, pp. 340-350
Closed Access | Times Cited: 26
Phenotyping of ABCA4 Retinopathy by Machine Learning Analysis of Full-Field Electroretinography
Sophie Glinton, Antonio Calcagni, Watjana Lilaonitkul, et al.
Translational Vision Science & Technology (2022) Vol. 11, Iss. 9, pp. 34-34
Open Access | Times Cited: 16
Vitamin A, systemic T-cells, and the eye: Focus on degenerative retinal disease
Arun James Thirunavukarasu, A Catharine Ross, Rose Gilbert
Frontiers in Nutrition (2022) Vol. 9
Open Access | Times Cited: 15
Intrinsic differences in rod and cone membrane composition: implications for cone degeneration
Daniela M. Verra, Perrine Spinnhirny, Cristina Sandu, et al.
Graefe s Archive for Clinical and Experimental Ophthalmology (2022) Vol. 260, Iss. 10, pp. 3131-3148
Open Access | Times Cited: 13
ASSOCIATION BETWEEN GENOTYPE AND DISEASE PROGRESSION IN ITALIAN STARGARDT PATIENTS
Valentina Di Iorio, Ada Orrico, Gabriella Esposito, et al.
Retina (2018) Vol. 39, Iss. 7, pp. 1399-1409
Closed Access | Times Cited: 20
Variants in the ABCA4 gene in a Brazilian population with Stargardt disease.
Mariana Vallim Salles, Fabiana Louise Motta, Renan Paulo Martin, et al.
PubMed (2018) Vol. 24, pp. 546-559
Closed Access | Times Cited: 19
Stargardt macular dystrophy and therapeutic approaches
Kaoru Fujinami, Nadia K. Waheed, Yannik Laich, et al.
British Journal of Ophthalmology (2023), pp. bjo-323071
Open Access | Times Cited: 6
Genotype-phenotype severity correlation in a multicentric portuguese cohort of ABCA4-associated retinopathy
Catarina Ferreira, Sara Geada, Ana Marta, et al.
Deleted Journal (2024) Vol. 1, Iss. 2, pp. 100029-100029
Open Access | Times Cited: 2
Highly Variable Disease Courses in Siblings with Stargardt Disease
Dyon Valkenburg, Esmee H. Runhart, Nathalie M. Bax, et al.
Ophthalmology (2019) Vol. 126, Iss. 12, pp. 1712-1721
Open Access | Times Cited: 17
Different Phenotypes Represent Advancing Stages of ABCA4-Associated Retinopathy: A Longitudinal Study of 212 Chinese Families From a Tertiary Center
Yingwei Wang, Wenmin Sun, Jing Zhou, et al.
Investigative Ophthalmology & Visual Science (2022) Vol. 63, Iss. 5, pp. 28-28
Open Access | Times Cited: 10
Clinical features and molecular genetics of patients with ABCA4‐retinal dystrophies
Josephine Prener Holtan, Ingvild Aukrust, Ragnhild Wivestad Jansson, et al.
Acta Ophthalmologica (2020) Vol. 99, Iss. 5
Open Access | Times Cited: 14
CERKL-Associated Retinal Dystrophy
Malena Daich Varela, Emma Duignan, Samantha R. De Silva, et al.
Ophthalmology Retina (2023) Vol. 7, Iss. 10, pp. 918-931
Open Access | Times Cited: 5
Full-field ERG as a predictor of the natural course of ABCA4-associated retinal degenerations.
Marion Schroeder, Ulrika Kjellström
PubMed (2018) Vol. 24, pp. 1-16
Closed Access | Times Cited: 14
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