Xavier Zanlonghi

1.8k total citations
44 papers, 523 citations indexed

About

Xavier Zanlonghi is a scholar working on Molecular Biology, Ophthalmology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Xavier Zanlonghi has authored 44 papers receiving a total of 523 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 23 papers in Ophthalmology and 6 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Xavier Zanlonghi's work include Retinal Development and Disorders (21 papers), Retinal Diseases and Treatments (15 papers) and Glaucoma and retinal disorders (6 papers). Xavier Zanlonghi is often cited by papers focused on Retinal Development and Disorders (21 papers), Retinal Diseases and Treatments (15 papers) and Glaucoma and retinal disorders (6 papers). Xavier Zanlonghi collaborates with scholars based in France, United States and United Kingdom. Xavier Zanlonghi's co-authors include Isabelle Meunier, Christian P. Hamel, Isabelle Audo, Béatrice Bocquet, Carl Arndt, Christina Zeitz, Gaël Manès, José‐Alain Sahel, Bernard Puech and Sabine Defoort‐Dhellemmes and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Xavier Zanlonghi

40 papers receiving 503 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Xavier Zanlonghi France	13	348	274	109	74	67	44	523
Ana Fakin Slovenia	12	428 1.2×	298 1.1×	106 1.0×	30 0.4×	54 0.8×	44	543
Marijke N. Zonneveld-Vrieling Netherlands	9	354 1.0×	259 0.9×	62 0.6×	89 1.2×	53 0.8×	9	432
Mor Hanany Israel	8	381 1.1×	185 0.7×	55 0.5×	36 0.5×	123 1.8×	12	448
Tamaki Gekka Japan	16	362 1.0×	400 1.5×	136 1.2×	49 0.7×	57 0.9×	38	560
Neringa Jurkutė United Kingdom	11	362 1.0×	159 0.6×	43 0.4×	34 0.5×	57 0.9×	23	400
Cristina Martínez-Fernández de la Cámara United Kingdom	16	500 1.4×	265 1.0×	78 0.7×	23 0.3×	106 1.6×	25	582
Yusuf K. Durlu Türkiye	11	255 0.7×	138 0.5×	49 0.4×	106 1.4×	29 0.4×	17	403
Kelly Wentz‐Hunter United States	13	446 1.3×	344 1.3×	105 1.0×	166 2.2×	28 0.4×	18	684
Aurore Germain France	5	317 0.9×	193 0.7×	56 0.5×	42 0.6×	68 1.0×	5	372
Jan Willem R. Pott Netherlands	11	351 1.0×	164 0.6×	35 0.3×	45 0.6×	35 0.5×	25	460

Countries citing papers authored by Xavier Zanlonghi

Since Specialization

Citations

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

Fields of papers citing papers by Xavier Zanlonghi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xavier Zanlonghi

This figure shows the co-authorship network connecting the top 25 collaborators of Xavier Zanlonghi. A scholar is included among the top collaborators of Xavier Zanlonghi 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 Xavier Zanlonghi. Xavier Zanlonghi 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

Dhaenens, Claire‐Marie, Isabelle Audo, A. Lecleire–Collet, et al.. (2024). The phenotypic spectrum of CEP250 gene variants. Ophthalmic Genetics. 46(4). 354–361. 1 indexed citations

Zanlonghi, Xavier, et al.. (2024). Variable expressivity of the autosomal dominant vitreoretinochoroidopathy (ADVIRC) phenotype associated with a novel variant in BEST1. Ophthalmic Genetics. 45(5). 470–475. 1 indexed citations

Uguen, Kévin, Sylvia Redon, Karen Rouault, et al.. (2024). An unusual diagnosis of alpha‐mannosidosis with ocular anomalies: Behind the scenes of a hidden copy number variation. American Journal of Medical Genetics Part A. 194(5). e63532–e63532.

Burton, Ben, Maurízio Battaglia Parodi, Ignasi Jürgens, et al.. (2023). LIGHTSITE II Randomized Multicenter Trial: Evaluation of Multiwavelength Photobiomodulation in Non-exudative Age-Related Macular Degeneration. Ophthalmology and Therapy. 12(2). 953–968. 28 indexed citations

Bocquet, Béatrice, Gilles Labesse, Carl Arndt, et al.. (2021). CRB1-Related Retinal Dystrophies in a Cohort of 50 Patients: A Reappraisal in the Light of Specific Müller Cell and Photoreceptor CRB1 Isoforms. International Journal of Molecular Sciences. 22(23). 12642–12642. 15 indexed citations

Muller, Jean, Christina Zeitz, Carolin D. Obermaier, et al.. (2021). Novel TTLL5 Variants Associated with Cone-Rod Dystrophy and Early-Onset Severe Retinal Dystrophy. International Journal of Molecular Sciences. 22(12). 6410–6410. 10 indexed citations

Bocquet, Béatrice, Anne‐Françoise Roux, Gilles Labesse, et al.. (2021). Retinitis Punctata Albescens and RLBP1-Allied Phenotypes. SHILAP Revista de lepidopterología. 1(3). 100052–100052. 6 indexed citations

Audo, Isabelle, Saddek Mohand‐Saïd, Élise Boulanger-Scemama, et al.. (2018). MERTK mutation update in inherited retinal diseases. Human Mutation. 39(7). 887–913. 44 indexed citations

Lasseaux, Eulalie, Christian Hamel, Sabine Defoort‐Dhellemmes, et al.. (2018). Mild form of oculocutaneous albinism type 1: phenotypic analysis of compound heterozygous patients with the R402Q variant of the TYR gene. British Journal of Ophthalmology. 103(9). 1239–1247. 26 indexed citations

10.

Ng, Bobby G., Hunter R. Underhill, Lars Palm, et al.. (2018). DPAGT1 Deficiency with Encephalopathy (DPAGT1-CDG): Clinical and Genetic Description of 11 New Patients. JIMD Reports. 44. 85–92. 15 indexed citations

11.

Leruez, Stéphanie, Christophe Verny, Dominique Bonneau, et al.. (2018). Cyclosporine A does not prevent second-eye involvement in Leber’s hereditary optic neuropathy. Orphanet Journal of Rare Diseases. 13(1). 33–33. 13 indexed citations

12.

Meunier, Isabelle, Gaël Manès, Béatrice Bocquet, et al.. (2014). Frequency and Clinical Pattern of Vitelliform Macular Dystrophy Caused by Mutations of Interphotoreceptor Matrix IMPG1 and IMPG2 Genes. Ophthalmology. 121(12). 2406–2414. 55 indexed citations

13.

Zeitz, Christina, Samuel G. Jacobson, Christian Hamel, et al.. (2013). Whole exome sequencing identifies mutations in LRIT3 as a cause for autosomal recessive complete congenital stationary night blindness. Investigative Ophthalmology & Visual Science. 54(15). 3350–3350. 2 indexed citations

14.

Audo, Isabelle, Gaël Manès, Saddek Mohand‐Saïd, et al.. (2010). Spectrum of Rhodopsin Mutations in French Autosomal Dominant Rod–Cone Dystrophy Patients. Investigative Ophthalmology & Visual Science. 51(7). 3687–3687. 42 indexed citations

15.

Hamel, Christian P., Isabelle Meunier, Carl Arndt, et al.. (2009). Extensive Macular Atrophy with Pseudodrusen-like Appearance: A New Clinical Entity. American Journal of Ophthalmology. 147(4). 609–620. 49 indexed citations

16.

Zanlonghi, Xavier, et al.. (2009). Evaluation of Macular Pigment Optical Density With a Color Perimetry Technique. Normal Values and Influence of Diet. 50(13). 2743–2743. 1 indexed citations

17.

Zanlonghi, Xavier, et al.. (2005). 473 Le glaucome : bases moléculaires et diagnostic génétique en France. Journal Français d Ophtalmologie. 28. 282–282. 2 indexed citations

18.

Becquet, F., et al.. (2003). [Efficiency of surgical treatment for chronic macular edema due to branch retinal vein occlusion].. PubMed. 26(6). 570–6. 11 indexed citations

19.

Becquet, F., et al.. (2003). [Radial optic neurotomy for severe central retinal vein occlusion: preliminary results].. PubMed. 26(6). 577–85. 6 indexed citations

20.

Zanlonghi, Xavier, Benoît Arnould, A Béchetoille, et al.. (2003). [Glaucoma and quality of life].. PubMed. 26 Spec No 2. S39–44. 11 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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