Gaël Manès - Concepedia

Author

Gaël Manès

Inserm ORCID

Also Known As

G MANES, G Manes, G. Manes, Gael A. Manes, Gael Manes, Gaël Manes, Gaël MANES, Gaël Manes, Gaël Manès, Manes, Gael

Publications

1.4K

Citations

H-Index

Concepts

All Affiliations

Inserm Université de Montpellier Institute for Neurosciences of Montpellier Centre National de la Recherche Scientifique Hôpital Gui de Chauliac

About

Gaël Manès is an author at Inserm specializing in medicine, genetics, and ophthalmology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	14	841
2	Natural Sciences	2	2	110
3	Cell Biology	2	2	65
4	Social Sciences	1	1	32
5	Biology	1	1	30

Gaël Manès

Publications

1.3K

Citations

H-Index

Page 1

	Year	Citations
Retinopathy and Vision Loss in Insulin-dependent Diabetes in Europe Anne Katrin Sjølie, Judith Stephenson, S J Aldington, Ophthalmology Diabetic RetinopathyOcular DiseaseOphthalmologyDiabetesEye Tracking	1997	216
Mutations in IMPG1 Cause Vitelliform Macular Dystrophies Gaël Manès, Isabelle Meunier, Almudena Ávila‐Fernández, The American Journal of Human Genetics Ocular DiseaseMendelian DisorderOphthalmologyGenetic DisorderGenetics	2013	79
Frequency and Clinical Pattern of Vitelliform Macular Dystrophy Caused by Mutations of Interphotoreceptor Matrix IMPG1 and IMPG2 Genes Isabelle Meunier, Gaël Manès, Béatrice Bocquet, Ophthalmology Ocular DiseaseOphthalmologyCorneal DystrophyMedicineGenetics	2014	75
Systematic Screening of BEST1 and PRPH2 in Juvenile and Adult Vitelliform Macular Dystrophies: A Rationale for Molecular Analysis Isabelle Meunier, Audrey Sénéćhal, Claire‐Marie Dhaenens, Ophthalmology Ocular DiseaseOphthalmologyExperimental OphthalmologyGeneticsSystematic Screening	2011	74
Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies Claire Angebault, Pierre‐Olivier Guichet, Yasmina Talmat-Amar, The American Journal of Human Genetics Rtn4ip1 Cause IsolatedMendelian DisorderGenetic DisorderGeneticsOptic Neuropathy	2015	72
Relative Frequencies of Inherited Retinal Dystrophies and Optic Neuropathies in Southern France: Assessment of 21-year Data Management Béatrice Bocquet, Annie Lacroux, Marie-Odile Surget, Ophthalmic Epidemiology	2013	68
Dominant mutations in mtDNA maintenance gene SSBP1 cause optic atrophy and foveopathy Camille Piro-Mégy, Emmanuelle Sarzi, Aleix Tarrés-Solé, Journal of Clinical Investigation GeneticsDominant Optic AtrophyMolecular BiologyMolecular GeneticsDisease Gene Identification	2019	64
Spectrum of Rhodopsin Mutations in French Autosomal Dominant Rod–Cone Dystrophy Patients Isabelle Audo, Gaël Manès, Saddek Mohand‐Saïd, Investigative Ophthalmology & Visual Science	2010	55
Homozygosity mapping in autosomal recessive retinitis pigmentosa families detects novel mutations. Béatrice Bocquet, Nour‐Al‐Dain Marzouka, Maxime Hebrard, PubMed Central	2013	50
Mutation in NDUFA13/GRIM19 leads to early onset hypotonia, dyskinesia and sensorial deficiencies, and mitochondrial complex I instability Claire Angebault, Majida Charif, Naïg Guegen, Human Molecular Genetics GeneticsMolecular BiologyMolecular GeneticsDisease Gene IdentificationMendelian Disorder	2015	49

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