Bernard Arnaud

2.9k total citations · 1 hit paper
23 papers, 1.8k citations indexed

About

Bernard Arnaud is a scholar working on Molecular Biology, Ophthalmology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Bernard Arnaud has authored 23 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 11 papers in Ophthalmology and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Bernard Arnaud's work include Retinal Development and Disorders (10 papers), Retinal Diseases and Treatments (7 papers) and Photoreceptor and optogenetics research (4 papers). Bernard Arnaud is often cited by papers focused on Retinal Development and Disorders (10 papers), Retinal Diseases and Treatments (7 papers) and Photoreceptor and optogenetics research (4 papers). Bernard Arnaud collaborates with scholars based in France, United States and Switzerland. Bernard Arnaud's co-authors include Jean‐Michel Griffoin, Cécile Delettre, Guy Lenaers, Christian Hamel, Claude Turc‐Carel, Eric Perret, Nadine Gigarel, Corinne Lorenzo, Josseline Kaplan and Josiane Grosgeorge and has published in prestigious journals such as Nature Genetics, Biochemical and Biophysical Research Communications and European Journal of Biochemistry.

In The Last Decade

Bernard Arnaud

23 papers receiving 1.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy

2000 1.1k citations Cécile Delettre, Guy Lenaers et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Bernard Arnaud France	14	1.5k	390	370	293	211	23	1.8k
Yun-Zheng Le United States	21	1.3k 0.9×	888 2.3×	104 0.3×	232 0.8×	300 1.4×	53	1.9k
Sébastien Augustin France	21	778 0.5×	307 0.8×	184 0.5×	110 0.4×	116 0.5×	33	1.1k
Jean‐Michel Griffoin France	6	1.4k 1.0×	143 0.4×	444 1.2×	183 0.6×	30 0.1×	7	1.5k
Marcel V. Alavi Germany	16	995 0.7×	143 0.4×	167 0.5×	163 0.6×	38 0.2×	25	1.2k
Vesna Ponjavic Sweden	22	875 0.6×	666 1.7×	65 0.2×	212 0.7×	253 1.2×	55	1.3k
Shoji Notomi Japan	23	1.1k 0.7×	1.1k 2.7×	57 0.2×	179 0.6×	483 2.3×	62	1.8k
Ronald E. Hurd United States	7	892 0.6×	254 0.7×	41 0.1×	288 1.0×	80 0.4×	8	1.1k
Amr Al‐Saif United States	12	520 0.3×	193 0.5×	47 0.1×	164 0.6×	286 1.4×	14	1.0k
Stacey Hose United States	19	631 0.4×	456 1.2×	68 0.2×	62 0.2×	115 0.5×	44	993
Yasunari Munemasa Japan	22	718 0.5×	655 1.7×	31 0.1×	209 0.7×	237 1.1×	47	1.3k

Countries citing papers authored by Bernard Arnaud

Since Specialization

Citations

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

Fields of papers citing papers by Bernard Arnaud

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bernard Arnaud

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

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

Sénéćhal, Audrey, et al.. (2007). RRH, Encoding the RPE-Expressed Opsin-Like Peropsin, Is Not Mutated in Retinitis Pigmentosa and Allied Diseases. Ophthalmic Genetics. 28(1). 31–37. 2 indexed citations

Sénéćhal, Audrey, Bernard Arnaud, Carl Arndt, et al.. (2006). Screening Genes of the Retinoid Metabolism: Novel LRAT Mutation in Leber Congenital Amaurosis. American Journal of Ophthalmology. 142(4). 702–704. 36 indexed citations

Delettre, Cécile, et al.. (2006). Homozygous Deletion Related to Alu Repeats inRLBP1Causes Retinitis Punctata Albescens. Investigative Ophthalmology & Visual Science. 47(11). 4719–4719. 32 indexed citations

Maubaret, C., Jean‐Michel Griffoin, Bernard Arnaud, & Christian P. Hamel. (2005). Novel Mutations inMYO7AandUSH2Ain Usher Syndrome. Ophthalmic Genetics. 26(1). 25–29. 12 indexed citations

Arndt, Carl, et al.. (2005). Retinal Electrophysiological Results in Patients Receiving Lamotrigine Monotherapy. Epilepsia. 46(7). 1055–1060. 9 indexed citations

Jacobi, Frank, Christian Hamel, Bernard Arnaud, et al.. (2003). A novel CACNA1F mutation in a french family with the incomplete type of X-linked congenital stationary night blindness. American Journal of Ophthalmology. 135(5). 733–736. 20 indexed citations

Chavanieu, Alain, Guy Subra, Bernard Arnaud, et al.. (2002). BIGH3 (TGFBI) Arg124 mutations influence the amyloid conversion of related peptides in vitro. European Journal of Biochemistry. 269(21). 5149–5156. 29 indexed citations

Arnaud, Bernard, et al.. (2002). Accuracy of IRAS GT interferometer and potential acuity meter prediction of visual acuity after phacoemulsification. Journal of Cataract & Refractive Surgery. 28(1). 131–138. 5 indexed citations

10.

Villain, Max, Georges‐Philippe Pageaux, M Veyrac, et al.. (2002). Effect of acetazolamide on ocular hemodynamics in pseudotumor cerebri associated with inflammatory bowel disease. American Journal of Ophthalmology. 134(5). 778–780. 6 indexed citations

11.

Bareil, Corinne, Christian Hamel, Valérie Delague, et al.. (2001). Segregation of a mutation in CNGB1 encoding the β-subunit of the rod cGMP-gated channel in a family with autosomal recessive retinitis pigmentosa. Human Genetics. 108(4). 328–334. 83 indexed citations

12.

Bareil, Corinne, Valérie Delague, Bernard Arnaud, et al.. (2000). W179R: A novel missense mutation in the peripherin/RDS gene in a family with autosomal dominant retinitis pigmentosa. Human Mutation. 15(6). 583–584. 6 indexed citations

13.

Blanc, Dominique, et al.. (2000). Keratographic analysis of a family with keratoconus in identical twins. Journal of Cataract & Refractive Surgery. 26(12). 1830–1832. 15 indexed citations

14.

Arnaud, Bernard, et al.. (2000). Keratectasia Induced by Laser in situ Keratomileusis in Keratoconus. Journal of Refractive Surgery. 16(3). 368–370. 82 indexed citations

15.

Chavanieu, Alain, Jean Derancourt, Bernard Arnaud, et al.. (2000). In Vitro Creation of Amyloid Fibrils from Native and Arg124Cys Mutated βIGH3(110–131) Peptides, and Its Relevance for Lattice Corneal Amyloid Dystrophy Type I. Biochemical and Biophysical Research Communications. 273(2). 649–653. 28 indexed citations

16.

Delettre, Cécile, Guy Lenaers, Jean‐Michel Griffoin, et al.. (2000). Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy. Nature Genetics. 26(2). 207–210. 1131 indexed citations breakdown →

17.

Bareil, Corinne, Christian Hamel, Nathalie Pallarès-Ruiz, et al.. (1999). Molecular analysis of the rhodopsin gene in southern France: identification of the first duplication responsible for retinitis pigmentosa, c.998^999ins4. Ophthalmic Genetics. 20(3). 173–182. 14 indexed citations

18.

Marlhens, F., Jean‐Michel Griffoin, Corinne Bareil, et al.. (1998). Autosomal recessive retinal dystrophy associated with two novel mutations in the RPE65 gene. European Journal of Human Genetics. 6(5). 527–531. 53 indexed citations

19.

Bareil, Corinne, Christian Hamel, Bernard Arnaud, Jacques Demaille, & Mireille Claustres. (1997). A complex allele (1064 del TC and IVS2 + 22 ins 7) in the peripherin/RDS gene in retinitis pigmentosa with macular dystrophy. Ophthalmic Genetics. 18(3). 129–138. 8 indexed citations

20.

Dryja, Thaddeus P., et al.. (1996). Missense mutation in the gene encoding the α subunit of rod transducin in the Nougaret form of congenital stationary night blindness. Nature Genetics. 13(3). 358–360. 132 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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