Fadi Nasser

771 total citations
20 papers, 292 citations indexed

About

Fadi Nasser is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Fadi Nasser has authored 20 papers receiving a total of 292 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 13 papers in Ophthalmology and 6 papers in Genetics. Recurrent topics in Fadi Nasser's work include Retinal Development and Disorders (15 papers), Retinal Diseases and Treatments (12 papers) and melanin and skin pigmentation (3 papers). Fadi Nasser is often cited by papers focused on Retinal Development and Disorders (15 papers), Retinal Diseases and Treatments (12 papers) and melanin and skin pigmentation (3 papers). Fadi Nasser collaborates with scholars based in Germany, Poland and United Kingdom. Fadi Nasser's co-authors include Eberhart Zrenner, Susanne Kohl, Nicole Weisschuh, Katarína Štingl, Laura Kuehlewein, Ditta Zobor, Saskia Biskup, Bernd Wissinger, Carolin D. Obermaier and Antje Bernd and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and American Journal of Ophthalmology.

In The Last Decade

Fadi Nasser

18 papers receiving 288 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Fadi Nasser Germany	10	235	155	81	51	26	20	292
Jennifer A. Halder United States	6	334 1.4×	103 0.7×	89 1.1×	48 0.9×	41 1.6×	6	415
Fernanda Belga Ottoni Porto Brazil	12	284 1.2×	157 1.0×	82 1.0×	43 0.8×	54 2.1×	19	351
Jan-Willem R. Pott Netherlands	8	293 1.2×	176 1.1×	71 0.9×	48 0.9×	38 1.5×	9	336
Bilge Esin Öztürk United States	8	201 0.9×	53 0.3×	68 0.8×	39 0.8×	41 1.6×	15	250
Amy Tillman United States	5	388 1.7×	218 1.4×	105 1.3×	87 1.7×	72 2.8×	8	435
Alexandra V. Garafalo United States	12	444 1.9×	303 2.0×	57 0.7×	101 2.0×	89 3.4×	26	497
Jean‐Paul Saraiva France	9	449 1.9×	266 1.7×	155 1.9×	59 1.2×	64 2.5×	12	531
Mor Hanany Israel	8	381 1.6×	185 1.2×	123 1.5×	55 1.1×	45 1.7×	12	448
Renate C. Zekveld-Vroon Netherlands	4	268 1.1×	170 1.1×	42 0.5×	51 1.0×	36 1.4×	5	297
Sarah De Jaegere Belgium	6	233 1.0×	121 0.8×	75 0.9×	23 0.5×	19 0.7×	7	252

Countries citing papers authored by Fadi Nasser

Since Specialization

Citations

This map shows the geographic impact of Fadi Nasser's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Fadi Nasser with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fadi Nasser more than expected).

Fields of papers citing papers by Fadi Nasser

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fadi Nasser. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Fadi Nasser. The network helps show where Fadi Nasser may publish in the future.

Co-authorship network of co-authors of Fadi Nasser

This figure shows the co-authorship network connecting the top 25 collaborators of Fadi Nasser. A scholar is included among the top collaborators of Fadi Nasser based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Fadi Nasser. Fadi Nasser is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Kempf, Melanie, et al.. (2024). Age-dependencies of the electroretinogram in healthy subjects. Documenta Ophthalmologica. 149(2). 99–113. 4 indexed citations

Kempf, Melanie, et al.. (2024). Adaptive optics retinal imaging in patients with usher syndrome. SHILAP Revista de lepidopterología. 4. 1349234–1349234. 1 indexed citations

Nowomiejska, Katarzyna, et al.. (2023). Elaborate Evaluation of Farnsworth Dichotomous D-15 Panel Test Can Help Differentiate between Best Vitelliform Macular Dystrophy and Autosomal Recessive Bestrophinopathy. Ophthalmic Research. 66(1). 481–488.

Nasser, Fadi, Susanne Kohl, Anne Kurtenbach, et al.. (2022). Ophthalmic and Genetic Features of Bardet Biedl Syndrome in a German Cohort. Genes. 13(7). 1218–1218. 8 indexed citations

Kuehlewein, Laura, Ditta Zobor, Katarína Štingl, et al.. (2021). Clinical Phenotype of PDE6B-Associated Retinitis Pigmentosa. International Journal of Molecular Sciences. 22(5). 2374–2374. 18 indexed citations

Stingl, Krunoslav, Melanie Kempf, Karl Ulrich Bartz‐Schmidt, et al.. (2021). Spatial and temporal resolution of the photoreceptors rescue dynamics after treatment with voretigene neparvovec. British Journal of Ophthalmology. 106(6). 831–838. 35 indexed citations

Nowomiejska, Katarzyna, Fadi Nasser, Katarína Štingl, et al.. (2021). Disease expression caused by different variants in the BEST1 gene: genotype and phenotype findings in bestrophinopathies. Acta Ophthalmologica. 100(3). e847–e858. 5 indexed citations

Nasser, Fadi, Melanie Kempf, Anne Kurtenbach, et al.. (2020). Correlating Adaptive Optics Images to Clinical Findings in Juvenile Macular Dystrophy with Hypotrichosis in Siblings with Homozygous <b><i>CDH3</i></b> Pathogenic Variation. Ophthalmic Research. 63(2). 141–151. 1 indexed citations

Weisschuh, Nicole, Carolin D. Obermaier, Florian Battke, et al.. (2020). Genetic architecture of inherited retinal degeneration in Germany: A large cohort study from a single diagnostic center over a 9‐year period. Human Mutation. 41(9). 1514–1527. 79 indexed citations

10.

Nasser, Fadi, Susanne Kohl, Laura Kuehlewein, et al.. (2019). A case of X-linked retinoschisis with atypical fundus appearance. Documenta Ophthalmologica. 139(1). 75–81.

11.

Nasser, Fadi, et al.. (2019). Hypotrichosis with cone-rod dystrophy in a patient with cadherin 3 (CDH3) mutation. Documenta Ophthalmologica. 138(2). 153–160. 4 indexed citations

12.

Straßer, Torsten, Fadi Nasser, H Langrová, et al.. (2019). Objective assessment of visual acuity: a refined model for analyzing the sweep VEP. Documenta Ophthalmologica. 138(2). 97–116. 13 indexed citations

13.

Nasser, Fadi, Anne Kurtenbach, Susanne Kohl, et al.. (2019). Retinal dystrophies with bull’s-eye maculopathy along with negative ERGs. Documenta Ophthalmologica. 139(1). 45–57. 11 indexed citations

14.

Weisschuh, Nicole, Fadi Nasser, Anneke I. den Hollander, et al.. (2019). CEP290 Mutation Spectrum and Delineation of the Associated Phenotype in a Large German Cohort: A Monocentric Study. American Journal of Ophthalmology. 211. 142–150. 28 indexed citations

15.

Nasser, Fadi, et al.. (2019). Ophthalmic features of retinitis pigmentosa in Cohen syndrome caused by pathogenic variants in the VPS13B gene. Acta Ophthalmologica. 98(3). e316–e321. 10 indexed citations

16.

Kohl, Susanne, et al.. (2018). Leber congenital amaurosis (LCA): Prevalence of mutations in a large German cohort and clinical characterization of the associated phenotype. Investigative Ophthalmology & Visual Science. 59(9). 1832–1832. 1 indexed citations

17.

Buena‐Atienza, Elena, Fadi Nasser, Susanne Kohl, & Bernd Wissinger. (2018). A 73,128 bp de novo deletion encompassing the OPN1LW/OPN1MW gene cluster in sporadic Blue Cone Monochromacy: a case report. BMC Medical Genetics. 19(1). 107–107. 2 indexed citations

18.

Nasser, Fadi, Nicole Weisschuh, Pietro Maffei, et al.. (2017). Ophthalmic features of cone‐rod dystrophy caused by pathogenic variants in the ALMS1 gene. Acta Ophthalmologica. 96(4). e445–e454. 25 indexed citations

19.

Schönbach, Etienne M., Mohamed Ibrahim, Rupert W. Strauß, et al.. (2016). Fixation Location and Stability Using the MP-1 Microperimeter in Stargardt Disease. Ophthalmology Retina. 1(1). 68–76. 37 indexed citations

20.

Kuehlewein, Laura, et al.. (2016). FUNDUS ALBIPUNCTATUS ASSOCIATED WITH CONE DYSFUNCTION. Retinal Cases & Brief Reports. 11(1). S73–S76. 10 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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