Marc Abitbol

4.5k total citations
107 papers, 3.4k citations indexed

About

Marc Abitbol is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Marc Abitbol has authored 107 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 71 papers in Molecular Biology, 19 papers in Ophthalmology and 17 papers in Genetics. Recurrent topics in Marc Abitbol's work include Retinal Development and Disorders (24 papers), Retinal Diseases and Treatments (12 papers) and Glaucoma and retinal disorders (9 papers). Marc Abitbol is often cited by papers focused on Retinal Development and Disorders (24 papers), Retinal Diseases and Treatments (12 papers) and Glaucoma and retinal disorders (9 papers). Marc Abitbol collaborates with scholars based in France, Switzerland and United States. Marc Abitbol's co-authors include Jacques Mallet, Dominique Marchant, M Ménasche, Anne‐Lise Delezoide, Michel Vekemans, Marie O. Péquignot, Christian Ménini, Alexandra Kobetz, Thomas Rhyner and C. Marsac and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Marc Abitbol

106 papers receiving 3.3k citations

Peers

Marc Abitbol

GENET

IMMUN

OPHTH

CMN

Michael R. Bösl Germany

Amir Rattner United States

Chyuan‐Sheng Lin United States

Françoise Meire Belgium

Martin Holzenberger France

Patrick Calvas France

K. Sue O’Shea United States

Tom Glaser United States

Stefan Isenmann Germany

José M. Millán Spain

Michael R. Bösl Germany

Marc Abitbol

1.5k ×0.7

463 ×0.7

GENET

558 ×1.3

IMMUN

158 ×0.4

OPHTH

694 ×1.7

CMN

Citations per year, relative to Marc Abitbol Marc Abitbol (= 1×) peers Michael R. Bösl

Countries citing papers authored by Marc Abitbol

Since Specialization

Citations

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

Fields of papers citing papers by Marc Abitbol

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marc Abitbol

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

Abitbol, Marc, Jacqueline Leroy, Laurent Jonet, et al.. (2018). Acetylcholinesterase and Butyrylcholinesterase anchoring in murine ocular compartments, role of Colq and PRiMA. Investigative Ophthalmology & Visual Science. 59(9). 3092–3092. 1 indexed citations

Dinet, Virginie, Giuseppe D. Ciccotosto, Kimberley Delaunay, et al.. (2016). Amyloid Precursor-Like Protein 2 deletion-induced retinal synaptopathy related to congenital stationary night blindness: structural, functional and molecular characteristics. Molecular Brain. 9(1). 64–64. 9 indexed citations

Lacassagne, Emmanuelle, Florence Rigaudière, Karine Bigot, et al.. (2011). Phenotypic variability in a French family with a novel mutation in the BEST1 gene causing multifocal best vitelliform macular dystrophy.. PubMed. 17. 309–22. 24 indexed citations

Boutboul, Sandrine, Elena Basli, T. Gaujoux, et al.. (2011). OCT and HRT Analysis Of The Cornea In Muckle-Wells Syndrome. Investigative Ophthalmology & Visual Science. 52(14). 1083–1083. 2 indexed citations

Bièche, Ivan, Olivier Roche, Ingrid Laurendeau, et al.. (2006). Identification of the first intragenic deletion of the PITX2 gene causing an Axenfeld-Rieger Syndrome: case report. BMC Medical Genetics. 7(1). 82–82. 14 indexed citations

Frau, E, Claire Magnon, Paule Opolon, et al.. (2006). A gene transfer comparative study of HSA-conjugated antiangiogenic factors in a transgenic mouse model of metastatic ocular cancer. Cancer Gene Therapy. 14(3). 251–261. 7 indexed citations

Bourcier, Tristan, Sandrine Boutboul, Marc Abitbol, et al.. (2004). Des opacités cornéennes. La Revue de Médecine Interne. 26(6). 518–519. 1 indexed citations

Provost, Alexandra, et al.. (2003). Expression of SR–BI receptor and StAR protein in rat ocular tissues. Comptes Rendus Biologies. 326(9). 841–851. 18 indexed citations

Miné, Manuèle, M. Brivet, Guy Touati, et al.. (2003). Splicing Error in E1α Pyruvate Dehydrogenase mRNA Caused by Novel Intronic Mutation Responsible for Lactic Acidosis and Mental Retardation. Journal of Biological Chemistry. 278(14). 11768–11772. 41 indexed citations

10.

Péquignot, Marie O., Alexandra Provost, Sophie La Salle, et al.. (2003). Major role of BAX in apoptosis during retinal development and in establishment of a functional postnatal retina. Developmental Dynamics. 228(2). 231–238. 110 indexed citations

11.

Camand, Olivier, Sophie Turban, Marc Abitbol, & Michèle Guerre-Millo. (2002). Embryonic expression of the leptin receptor gene in mesoderm-derived tissues. Comptes Rendus Biologies. 325(2). 77–87. 5 indexed citations

12.

Péquignot, Marie O., Isabelle Desguerre, Runu Dey, et al.. (2001). New Splicing-site Mutations in the SURF1Gene in Leigh Syndrome Patients. Journal of Biological Chemistry. 276(18). 15326–15329. 24 indexed citations

13.

Schorderet, Daniel F., M Ménasche, Sabine Morand, et al.. (2000). Genomic Characterization and Embryonic Expression of the Mouse Bigh3 (Tgfbi) Gene. Biochemical and Biophysical Research Communications. 274(2). 267–274. 51 indexed citations

14.

Agulhon, Cendra, Patricia Blanchet, Alexandra Kobetz, et al.. (1999). Expression of FMR1, FXR1, and FXR2 Genes in Human Prenatal Tissues. Journal of Neuropathology & Experimental Neurology. 58(8). 867–880. 41 indexed citations

15.

Rouillac, Christelle, Dominique Marchant, Lucien Bachner, et al.. (1998). Mapping of a Congenital Microcoria Locus to 13q31-q32. The American Journal of Human Genetics. 62(5). 1117–1122. 15 indexed citations

16.

Bondurand, Nadège, Alexandra Kobetz, Véronique Pingault, et al.. (1998). Expression of the SOX10 gene during human development. FEBS Letters. 432(3). 168–172. 94 indexed citations

17.

Khani, Shahrokh C., et al.. (1996). Characterization and Chromosomal Localization of the Gene for Human Rhodopsin Kinase. Genomics. 35(3). 571–576. 19 indexed citations

18.

Abitbol, Marc, Christian Ménini, Marion Gérard, et al.. (1995). The rat phospholipase Cβ 4 gene is expressed at high abundance in cerebellar Purkinje cells. Neuroreport. 6(14). 1837–1841. 38 indexed citations

19.

Waele, Catherine de, Marc Abitbol, Mireille Chat, et al.. (1994). Distribution of Glutamatergic Receptors and GAD mRNA‐Containing Neurons in the Vestibular Nuclei of Normal and Hemilabyrinthectomized Rats. European Journal of Neuroscience. 6(4). 565–576. 65 indexed citations

20.

Abitbol, Marc, Christian Ménini, Anne‐Lise Delezoide, et al.. (1993). Nucleus basalis magnocellularis and hippocampus are the major sites of FMR-1 expression in the human fetal brain. Nature Genetics. 4(2). 147–153. 227 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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