Christian Hamel

2.5k total citations
39 papers, 1.5k citations indexed

About

Christian Hamel is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Christian Hamel has authored 39 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 12 papers in Ophthalmology and 7 papers in Genetics. Recurrent topics in Christian Hamel's work include Retinal Development and Disorders (16 papers), Mitochondrial Function and Pathology (9 papers) and Retinal Diseases and Treatments (7 papers). Christian Hamel is often cited by papers focused on Retinal Development and Disorders (16 papers), Mitochondrial Function and Pathology (9 papers) and Retinal Diseases and Treatments (7 papers). Christian Hamel collaborates with scholars based in France, Switzerland and Italy. Christian Hamel's co-authors include Cécile Delettre, Guy Lenaers, Dominique Bonneau, Pascal Reynier, Pascale Belenguer, Aurélien Olichon, Patrizia Amati‐Bonneau, Laurent J. Emorine, Valérie Mils and Laetitia Pelloquin and has published in prestigious journals such as PLoS ONE, Annals of Neurology and Scientific Reports.

In The Last Decade

Christian Hamel

39 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christian Hamel France 20 1.2k 323 265 203 158 39 1.5k
Christian P. Hamel France 26 2.0k 1.6× 933 2.9× 273 1.0× 216 1.1× 366 2.3× 71 2.4k
Alejandro Garanto Netherlands 24 1.5k 1.2× 453 1.4× 241 0.9× 178 0.9× 214 1.4× 62 1.7k
Vanita Berry United Kingdom 19 1.6k 1.3× 480 1.5× 716 2.7× 112 0.6× 58 0.4× 38 1.7k
Brian P. Brooks United States 22 884 0.7× 253 0.8× 360 1.4× 390 1.9× 148 0.9× 73 1.4k
Donna S. Mackay United Kingdom 31 2.4k 1.9× 917 2.8× 897 3.4× 207 1.0× 241 1.5× 48 2.6k
Matthew A. Lines Canada 19 634 0.5× 92 0.3× 283 1.1× 73 0.4× 48 0.3× 35 919
Alexey Obolensky Israel 21 1.3k 1.0× 511 1.6× 248 0.9× 117 0.6× 318 2.0× 54 1.6k
Lixing W. Reneker United States 23 934 0.7× 215 0.7× 153 0.6× 220 1.1× 66 0.4× 46 1.3k
Ralph J. Florijn Netherlands 21 1.0k 0.8× 470 1.5× 309 1.2× 213 1.0× 208 1.3× 46 1.3k
Rafal Farjo United States 17 932 0.7× 329 1.0× 117 0.4× 114 0.6× 201 1.3× 35 1.2k

Countries citing papers authored by Christian Hamel

Since Specialization
Citations

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

Fields of papers citing papers by Christian Hamel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christian Hamel

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

All Works

20 of 20 papers shown
1.
Kostic, Corinne, et al.. (2021). Quantification of the early pupillary dilation kinetic to assess rod and cone activity. Scientific Reports. 11(1). 9549–9549. 1 indexed citations
2.
Hamel, Christian, Laëtitia Lagoutte, Gaël Manès, et al.. (2019). Natural models for retinitis pigmentosa: progressive retinal atrophy in dog breeds. Human Genetics. 138(5). 441–453. 33 indexed citations
3.
Angebault, Claire, Jérémy Fauconnier, Simone Patergnani, et al.. (2018). ER-mitochondria cross-talk is regulated by the Ca 2+ sensor NCS1 and is impaired in Wolfram syndrome. Science Signaling. 11(553). 105 indexed citations
4.
Perrault, Isabelle, Nicolas Goudin, Marlène Rio, et al.. (2018). Basal exon skipping and nonsense-associated altered splicing allows bypassing complete CEP290 loss-of-function in individuals with unusually mild retinal disease. Human Molecular Genetics. 27(15). 2689–2702. 26 indexed citations
5.
Sarzi, Emmanuelle, Mélanie Cavalier, Marie Seveno, et al.. (2017). Optical Coherence Tomography: Imaging Mouse Retinal Ganglion Cells <em>In Vivo</em>. Journal of Visualized Experiments. 9 indexed citations
6.
Zobor, Ditta, Annette Werner, Franco Stanzial, et al.. (2017). The Clinical Phenotype of CNGA3 -Related Achromatopsia: Pretreatment Characterization in Preparation of a Gene Replacement Therapy Trial. Investigative Ophthalmology & Visual Science. 58(2). 821–821. 39 indexed citations
7.
Benaglio, Paola, Almudena Ávila‐Fernández, Shyana Harper, et al.. (2014). Mutational screening of splicing factor genes in cases with autosomal dominant retinitis pigmentosa. PubMed. 20. 843–51. 13 indexed citations
8.
Benkafadar, Nesrine, et al.. (2014). Impairment of Visual Function and Retinal ER Stress Activation in Wfs1-Deficient Mice. PLoS ONE. 9(5). e97222–e97222. 32 indexed citations
9.
Gueneau, Lucie, Laurence Duplomb, Pierre Sarda, et al.. (2013). Congenital neutropenia with retinopathy, a new phenotype without intellectual deficiency or obesity secondary to VPS13B mutations. American Journal of Medical Genetics Part A. 164(2). 522–527. 11 indexed citations
10.
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
11.
Audo, Isabelle, Saddek Mohand‐Saïd, Claire‐Marie Dhaenens, et al.. (2011). RP1 and autosomal dominant rod-cone dystrophy: Novel mutations, a review of published variants, and genotype-phenotype correlation. Human Mutation. 33(1). 73–80. 31 indexed citations
12.
Arndt, Carl, et al.. (2010). Electrophysiological Retinal Pigment Epithelium Changes Observed with Indocyanine Green, Trypan Blue and Triamcinolone. Ophthalmic Research. 44(1). 17–23. 7 indexed citations
13.
Polok, Bozena, Pascal Escher, Aude Ambresin, et al.. (2009). Mutations in CNNM4 Cause Recessive Cone-Rod Dystrophy with Amelogenesis Imperfecta. The American Journal of Human Genetics. 84(2). 259–265. 72 indexed citations
14.
Lenaers, Guy, Pascal Reynier, Ghizlane Elachouri, et al.. (2009). OPA1 functions in mitochondria and dysfunctions in optic nerve. The International Journal of Biochemistry & Cell Biology. 41(10). 1866–1874. 66 indexed citations
15.
Hamel, Christian & Guy Lenaers. (2007). Neuropathies optiques héréditaires. 4(3). 1–16. 2 indexed citations
16.
Rolling, Fabienne, Guylène Le Meur, Knut Stieger, et al.. (2006). Gene therapeutic prospects in early onset of severe retinal dystrophy: restoration of vision in RPE65 Briard dogs using an AAV serotype 4 vector that specifically targets the retinal pigmented epithelium.. PubMed. 161(10-12). 497–508; discussion 508. 18 indexed citations
17.
Cornille, Karen, Andreas Müller, Guy Lenaers, et al.. (2006). Modèle murin de neuropathie optique transitoire par inhibition in vivo de l'expression d'OPA1 (gène impliqué dans la maladie de Kjer). Journal Français d Ophtalmologie. 29(8). 875–880. 5 indexed citations
18.
Olichon, Aurélien, Emmanuelle Guillou, Cécile Delettre, et al.. (2006). Mitochondrial dynamics and disease, OPA1. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1763(5-6). 500–509. 176 indexed citations
19.
Perrault, Isabelle, Sylvain Hanein, S. Gerber, et al.. (2004). Retinal Dehydrogenase 12 (RDH12) Mutations in Leber Congenital Amaurosis. The American Journal of Human Genetics. 75(4). 639–646. 151 indexed citations
20.
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

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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Breakdown of academic impact, for papers by Christian P. Hamel Breakdown of academic impact, for papers by Alejandro Garanto Breakdown of academic impact, for papers by Vanita Berry Breakdown of academic impact, for papers by Brian P. Brooks Breakdown of academic impact, for papers by Donna S. Mackay Breakdown of academic impact, for papers by Matthew A. Lines Breakdown of academic impact, for papers by Alexey Obolensky Breakdown of academic impact, for papers by Lixing W. Reneker Breakdown of academic impact, for papers by Ralph J. Florijn Breakdown of academic impact, for papers by Rafal Farjo
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