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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:

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

Showing 1-25 of 45 citing articles:

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
Structure and function of ABCA4 and its role in the visual cycle and Stargardt macular degeneration
Robert S. Molday, Fabian A. Garces, Jéssica Fernandes Scortecci, et al.
Progress in Retinal and Eye Research (2021) Vol. 89, pp. 101036-101036
Closed Access | Times Cited: 61
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
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
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
A genotype-phenotype correlation matrix for ABCA4 disease based on long-term prognostic outcomes
Winston Lee, Jana Zernant, Pei-Yin Su, et al.
JCI Insight (2021) Vol. 7, Iss. 2
Open Access | Times Cited: 32
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
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
Functional analysis and classification of homozygous and hypomorphic ABCA4 variants associated with Stargardt macular degeneration
Susan B. Curtis, Laurie L. Molday, Fabian A. Garces, et al.
Human Mutation (2020) Vol. 41, Iss. 11, pp. 1944-1956
Open Access | Times Cited: 31
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
Inherited retinal degeneration in Malay and Indian populations of Singapore and Malaysia: a prospective multicentre study
Shaobing Su, Choi Mun Chan, Yasmin Bylstra, et al.
Ophthalmic Genetics (2025), pp. 1-12
Closed 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
Parafoveal Photoreceptor Abnormalities in Asymptomatic Patients With RP1L1 Mutations in Families With Occult Macular Dystrophy
Yu Kato, Gen Hanazono, Kaoru Fujinami, et al.
Investigative Ophthalmology & Visual Science (2017) Vol. 58, Iss. 14, pp. 6020-6020
Open Access | Times Cited: 25
Stargardt disease: monitoring incidence and diagnostic trends in the Netherlands using a nationwide disease registry
Esmee H. Runhart, Patty P.A. Dhooge, Magda A. Meester‐Smoor, et al.
Acta Ophthalmologica (2021) Vol. 100, Iss. 4, pp. 395-402
Open Access | Times Cited: 20
Functional Characterization of ABCA4 Missense Variants Linked to Stargardt Macular Degeneration
Fabian A. Garces, Jéssica Fernandes Scortecci, Robert S. Molday
International Journal of Molecular Sciences (2020) Vol. 22, Iss. 1, pp. 185-185
Open Access | Times Cited: 19
Atrophy Expansion Rates in Stargardt Disease Using Ultra-Widefield Fundus Autofluorescence
Rachael C. Heath Jeffery, Jennifer A. Thompson, Johnny Lo, et al.
Ophthalmology Science (2021) Vol. 1, Iss. 1, pp. 100005-100005
Open Access | Times Cited: 17
Phenotypical Characteristics ofPOC1B-Associated Retinopathy in Japanese Cohort: Cone Dystrophy With Normal Funduscopic Appearance
Shuhei Kameya, Kaoru Fujinami, Shinji Ueno, et al.
Investigative Ophthalmology & Visual Science (2019) Vol. 60, Iss. 10, pp. 3432-3432
Open 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
Natural History of Visual Dysfunction in ABCA4 Retinopathy and Its Genetic Correlates
Maximilian Pfau, Laryssa A. Huryn, Marisa Boyle, et al.
American Journal of Ophthalmology (2023) Vol. 253, pp. 224-232
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
The Clinical Spectrum and Disease Course of DRAM2 Retinopathy
Tjaša Krašovec, Marija Volk, Maja Šuštar Habjan, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 13, pp. 7398-7398
Open Access | Times Cited: 7
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