Pascal Reynier - Concepedia

Author

Pascal Reynier

Also Known As

Anne-Déborah Bouhnik, Brigitte Sokolo, Cecile Thiery, Dominique Bonneau, P REYNIER, P Reynier, P. Reynier, Pascal Reynier, Patrick Reynier, Pauline M. Reynier

448

Publications

17.2K

Citations

H-Index

228

Concepts

All Affiliations

Inserm Université d'Angers Centre Hospitalier Universitaire d'Angers Centre National de la Recherche Scientifique Singapore Eye Research Institute

About

Pascal Reynier is an author at Inserm specializing in medicine, mitochondrial function, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	40	87	4.6K
2	Natural Sciences	12	12	737
3	Health Sciences	10	10	291
4	Engineering	4	4	229
5	Arts	1	1	95

Pascal Reynier

187

Publications

11.2K

Citations

H-Index

Page 1

	Year	Citations
Mitochondrial DNA content affects the fertilizability of human oocytes Pascal Reynier, Pascale May‐Panloup, M.-F. Chrétien, Molecular Human Reproduction	2001	513
OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes Patrizia Amati‐Bonneau, Maria Lucia Valentino, Pascal Reynier, Brain Opa1 GeneGenome InstabilityMitochondrial BiogenesisOphthalmologyMitochondrial Function	2007	510
Multi-system neurological disease is common in patients with OPA1 mutations Patrick Yu‐Wai‐Man, Philip G. Griffiths, Gráinne S. Gorman, Brain	2010	437
Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance Gavin Hudson, Patrizia Amati‐Bonneau, Emma L. Blakely, Brain	2007	416
Low oocyte mitochondrial DNA content in ovarian insufficiency Pascale May‐Panloup, M.-F. Chrétien, Caroline Jacques, Human Reproduction	2004	292
OPA1 links human mitochondrial genome maintenance to mtDNA replication and distribution Ghizlane Elachouri, Sara Vidoni, Claudia Zanna, Genome Research	2010	229
Prevalence of rare mitochondrial DNA mutations in mitochondrial disorders Sylvie Bannwarth, Vincent Procaccio, Anne Sophie Lebre, Journal of Medical Genetics	2013	189
Relationship between diminished ovarian reserve and mitochondrial biogenesis in cumulus cells Lisa Boucret, Juan Manuel Chao de la Barca, Catherine Morinière, Human Reproduction	2015	186
Increase of mitochondrial DNA content and transcripts in early bovine embryogenesis associated with upregulation of mtTFA and NRF1 transcription factors Pascale May‐Panloup, Xavier Vignon, Marie-Françoise Chrétien, Reproductive Biology and Endocrinology	2005	169
OPA1 R445H mutation in optic atrophy associated with sensorineural deafness Patrizia Amati‐Bonneau, Agnès Guichet, Aurélien Olichon, Annals of Neurology	2005	167

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