Fanny Depasse

418 total citations
8 papers, 282 citations indexed

About

Fanny Depasse is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Fanny Depasse has authored 8 papers receiving a total of 282 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 4 papers in Ophthalmology and 3 papers in Genetics. Recurrent topics in Fanny Depasse's work include Retinal Development and Disorders (6 papers), Retinal Diseases and Treatments (3 papers) and Cell Adhesion Molecules Research (2 papers). Fanny Depasse is often cited by papers focused on Retinal Development and Disorders (6 papers), Retinal Diseases and Treatments (3 papers) and Cell Adhesion Molecules Research (2 papers). Fanny Depasse collaborates with scholars based in Belgium, United States and Germany. Fanny Depasse's co-authors include Françoise Meire, Elfride De Baere, Bart P. Leroy, Marc Abramowicz, Marc Schrooyen, Julie Désir, Yves Sznajer, Thomy de Ravel, Frauke Coppieters and Julie De Zaeytijd and has published in prestigious journals such as PLoS ONE, Scientific Reports and Human Mutation.

In The Last Decade

Fanny Depasse

8 papers receiving 276 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Fanny Depasse Belgium	8	199	119	104	35	34	8	282
Yue Xie China	11	255 1.3×	115 1.0×	48 0.5×	41 1.2×	33 1.0×	35	339
Delphine Blain United States	10	275 1.4×	119 1.0×	189 1.8×	59 1.7×	90 2.6×	24	432
Weining Rong China	10	246 1.2×	133 1.1×	56 0.5×	31 0.9×	69 2.0×	26	348
Ana Arteche‐López Spain	9	172 0.9×	58 0.5×	95 0.9×	22 0.6×	20 0.6×	23	262
Åsa Blixt Sweden	7	372 1.9×	95 0.8×	164 1.6×	42 1.2×	101 3.0×	9	463
Gaoen Ma China	9	275 1.4×	135 1.1×	61 0.6×	13 0.4×	79 2.3×	19	357
Meghan J. Marino United States	11	223 1.1×	203 1.7×	25 0.2×	28 0.8×	47 1.4×	18	341
Lori Fotheringham United States	3	320 1.6×	49 0.4×	80 0.8×	24 0.7×	45 1.3×	4	370
Lama AlAbdi Saudi Arabia	12	203 1.0×	61 0.5×	64 0.6×	32 0.9×	45 1.3×	26	318
Brian W. Rigatti United States	10	290 1.5×	127 1.1×	82 0.8×	173 4.9×	26 0.8×	13	401

Countries citing papers authored by Fanny Depasse

Since Specialization

Citations

This map shows the geographic impact of Fanny Depasse'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 Fanny Depasse with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fanny Depasse more than expected).

Fields of papers citing papers by Fanny Depasse

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fanny Depasse. 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 Fanny Depasse. The network helps show where Fanny Depasse may publish in the future.

Co-authorship network of co-authors of Fanny Depasse

This figure shows the co-authorship network connecting the top 25 collaborators of Fanny Depasse. A scholar is included among the top collaborators of Fanny Depasse 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 Fanny Depasse. Fanny Depasse is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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8 of 8 papers shown

Balikova, Irina, Fanny Depasse, Guillaume Smits, et al.. (2020). Three cases of molecularly confirmed Knobloch syndrome. Ophthalmic Genetics. 41(1). 83–87. 12 indexed citations

Cauwenbergh, Caroline Van, Frauke Coppieters, Sarah De Jaegere, et al.. (2017). Mutations in Splicing Factor Genes Are a Major Cause of Autosomal Dominant Retinitis Pigmentosa in Belgian Families. PLoS ONE. 12(1). e0170038–e0170038. 42 indexed citations

Schil, Kristof Van, Marcus Karlstetter, Alexander Aslanidis, et al.. (2016). Autosomal recessive retinitis pigmentosa with homozygous rhodopsin mutation E150K and non-coding cis-regulatory variants in CRX-binding regions of SAMD7. Scientific Reports. 6(1). 21307–21307. 19 indexed citations

Delbeke, Patricia, Patrick Van Bogaert, Georges Rodesch, et al.. (2014). Congenital Fixed Dilated Pupils Due to ACTA2– Multisystemic Smooth Muscle Dysfunction Syndrome. Journal of Neuro-Ophthalmology. 34(2). 137–143. 17 indexed citations

Coppieters, Frauke, Kristof Van Schil, Miriam Bauwens, et al.. (2014). Identity-by-descent–guided mutation analysis and exome sequencing in consanguineous families reveals unusual clinical and molecular findings in retinal dystrophy. Genetics in Medicine. 16(9). 671–680. 47 indexed citations

Bauwens, Miriam, Julie De Zaeytijd, Nicole Weisschuh, et al.. (2014). An AugmentedABCA4Screen Targeting Noncoding Regions Reveals a Deep Intronic Founder Variant in Belgian Stargardt Patients. Human Mutation. 36(1). 39–42. 55 indexed citations

Meire, Françoise, Isabelle Delpierre, Cécile Brachet, et al.. (2011). Nonsyndromic bilateral and unilateral optic nerve aplasia: first familial occurrence and potential implication of CYP26A1 and CYP26C1 genes.. PubMed. 17. 2072–9. 15 indexed citations

Désir, Julie, Yves Sznajer, Fanny Depasse, et al.. (2010). LTBP2 null mutations in an autosomal recessive ocular syndrome with megalocornea, spherophakia, and secondary glaucoma. European Journal of Human Genetics. 18(7). 761–767. 75 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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