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:

Butterfly-Shaped Macular Dystrophy in Four Generations
Jay G. Prensky, George H. Bresnick
Archives of Ophthalmology (1983) Vol. 101, Iss. 8, pp. 1198-1203
Closed Access | Times Cited: 30

Showing 1-25 of 30 citing articles:

The spectrum of retinal dystrophies caused by mutations in the peripherin/RDS gene
Camiel J.F. Boon, Anneke I. den Hollander, Carel B. Hoyng, et al.
Progress in Retinal and Eye Research (2008) Vol. 27, Iss. 2, pp. 213-235
Closed Access | Times Cited: 215

Mutations in the peripherin/RDS gene are an important cause of multifocal pattern dystrophy simulating STGD1/fundus flavimaculatus
Camiel J.F. Boon, Mary J. van Schooneveld, A. I den Hollander, et al.
British Journal of Ophthalmology (2007) Vol. 91, Iss. 11, pp. 1504-1511
Open Access | Times Cited: 124

The Alabama Age-Related Macular Degeneration Grading System for donor eyes.
Christine A. Curcio, Nancy E. Medeiros, C. Leigh Millican
PubMed (1998) Vol. 39, Iss. 7, pp. 1085-96
Closed Access | Times Cited: 111

Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and perturbed retinal pigment epithelium integrity
Nicole T.M. Saksens, Mark P. Krebs, Frederieke E. Schoenmaker-Koller, et al.
Nature Genetics (2015) Vol. 48, Iss. 2, pp. 144-151
Open Access | Times Cited: 57

Butterfly-Shaped Pattern Dystrophy
Kang Zhang, Daniel C. Garibaldi, Yang Li, et al.
Archives of Ophthalmology (2002) Vol. 120, Iss. 4, pp. 485-485
Open Access | Times Cited: 86

Deletion in the Peripherin/RDS Gene in Two Unrelated Sardinian Families With Autosomal Dominant Butterfly-Shaped Macular Dystrophy
Maurizio Fossarello
Archives of Ophthalmology (1996) Vol. 114, Iss. 4, pp. 448-448
Closed Access | Times Cited: 56

Pattern Dystrophy of the Retinal Pigment Epithelium and Geographic Atrophy of the Macula
Michael F. Marmor, J. Arch McNamara
American Journal of Ophthalmology (1996) Vol. 122, Iss. 3, pp. 382-392
Open Access | Times Cited: 49

A novel mutation in the RDS/Peripherin gene causes adult-onset foveomacular dystrophy
Zhenglin Yang, Wei Lin, Darius M. Moshfeghi, et al.
American Journal of Ophthalmology (2003) Vol. 135, Iss. 2, pp. 213-218
Closed Access | Times Cited: 36

A novel RDS/peripherin gene mutation associated with diverse macular phenotypes
Zhenglin Yang, Yang Li, Li Jiang, et al.
Ophthalmic Genetics (2004) Vol. 25, Iss. 2, pp. 133-145
Closed Access | Times Cited: 30

Using Multimodal Imaging to Refine the Phenotype of PRPH2-associated Retinal Degeneration
Fritz Gerald P. Kalaw, Naomi E. Wagner, Thiago Barros de Oliveira, et al.
Ophthalmology Retina (2024)
Closed Access | Times Cited: 1

Genetic heterogeneity of butterfly-shaped pigment dystrophy of the fovea.
J.J. van Lith-Verhoeven, F.P.M. Cremers, L.J.M. van den Helm, et al.
Molecular vision (2003) Vol. 9, pp. 138-143
Closed Access | Times Cited: 23

Patterned dystrophies of the retinal pigment epithelium: A review
A. Pinckers
Ophthalmic Paediatrics and Genetics (1988) Vol. 9, Iss. 2, pp. 77-114
Closed Access | Times Cited: 21

Pattern dystrophy of the retinal pigment epithelium with vitelliform macular lesion: evolution in ten years
Felice Cardillo Piccolino, M. Zingírian
International Ophthalmology (1988) Vol. 11, Iss. 4, pp. 207-217
Closed Access | Times Cited: 16

Age-Dependent Phenotypic Expression of a Pattern Dystrophy of the Retina
U. Thomann, Ernst R. Büchi, Markus Suppiger, et al.
European Journal of Ophthalmology (1995) Vol. 5, Iss. 2, pp. 107-112
Closed Access | Times Cited: 6

Pattern dystrophies of the retinal pigment epithelium
H. P. Kempeneers, A. Dewachter, G. M. Kempeneers
Documenta Ophthalmologica (1991) Vol. 76, Iss. 3, pp. 261-272
Closed Access | Times Cited: 6

Pattern dystrophies of the retinal pigment epithelium
Peter G. Swann, H. Barry Collin, Aphrodite Livanes
Clinical and Experimental Optometry (2000) Vol. 83, Iss. 5, pp. 274-278
Closed Access | Times Cited: 4

Patterned dystrophy of the retinal pigment epithelium
A. Pinckers, J.R.M. Cruysberg
Ophthalmic Paediatrics and Genetics (1986) Vol. 7, Iss. 1, pp. 35-43
Closed Access | Times Cited: 4

Pathology of the hereditary macular dystrophies
Kenneth G. Noble
Seminars in Ophthalmology (1987) Vol. 2, Iss. 2, pp. 110-129
Closed Access | Times Cited: 4

Clinical aspects: outer retinal dystrophies
Alan C. Bird
Springer eBooks (1995), pp. 417-446
Closed Access | Times Cited: 3

Heritable Disorders of RPE, Bruch’s Membrane, and the Choriocapillaris
Arlene V. Drack
Springer eBooks (2006), pp. 96-134
Closed Access | Times Cited: 1

Spezielle Pathologie der Retina
Elmar P. Messmer, G. M. Ruggli, DJ Apple, et al.
Spezielle pathologische Anatomie (1997), pp. 995-1152
Closed Access | Times Cited: 2

The Pattern Dystrophies
Itay Chowers, Camiel J.F. Boon
Springer eBooks (2016), pp. 11-23
Closed Access

CTNNA1, a New HDGC Gene: Inactivating Mechanisms and Driven Phenotypes
Silvana Lobo, Paulo S. Pereira, Patrick R. Benusiglio, et al.
Springer eBooks (2023), pp. 55-78
Closed Access

Colour vision deficiencies in two unrelated Sardinian families with butterfly-shaped macular dystrophy
Maurizio Fossarello, Ignazio Alberto Zucca, Maria Silvana Galantuomo, et al.
Documenta ophthalmologica. Proceedings series (1997), pp. 169-178
Closed Access | Times Cited: 1

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