Bénédicte Mousson de Camaret

Author

Also Known As

Benedicte Mousson De Camaret, Benedicte Mousson de Camaret, Bénédicte Mousson de Camaret, Bénédicte MOUSSON de CAMARET, Bénédicte Mousson De Camaret, Bénédicte Mousson de Camaret, Bénédicte Mousson de camaret, Mousson De Camaret, Benedicte

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

Inserm Centre National de la Recherche Scientifique Hôpital Debrousse Centre Hospitalier Universitaire d'Angers Hôpital Edouard Herriot

About

Bénédicte Mousson de Camaret is an author at Inserm specializing in medicine, genetics, and mitochondrial function.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	282
2	Natural Sciences	1	1	51
3	Biochemistry	1	1	51
4	Cell Biology	1	1	21
5	Hepatology	1	1	27

Bénédicte Mousson de Camaret

Publications

968

Citations

H-Index

Page 1

	Year	Citations
Prevalence of rare mitochondrial DNA mutations in mitochondrial disorders Sylvie Bannwarth, Vincent Procaccio, Anne Sophie Lebre, Journal of Medical Genetics	2013	189
Structural organization of mitochondrial human complex I: role of the ND4 and ND5 mitochondria-encoded subunits and interaction with prohibitin Ingrid Bourges, Claire Ramus, Bénédicte Mousson de Camaret, Biochemical Journal	2004	133
Complete loss of expression of the <i>ANT1</i> gene causing cardiomyopathy and myopathy Andoni Echaniz‐Laguna, Maïté Chassagne, Jennifer Ceresuela, Journal of Medical Genetics	2011	72
SURF1 deficiency causes demyelinating Charcot-Marie-Tooth disease Andoni Echaniz‐Laguna, Daniele Ghezzi, Maïté Chassagne, Neurology	2013	64
Quantification of Mitochondrial DNA Deletion, Depletion, and Overreplication: Application to Diagnosis Béatrice Chabi, Bénédicte Mousson de Camaret, Hervé Duborjal, Clinical Chemistry	2003	63
Kinetic properties of mutant deoxyguanosine kinase in a case of reversible hepatic mtDNA depletion Bénédicte Mousson de Camaret, Jan‐Willem Taanman, Sylvie Padet, Biochemical Journal Kinetic PropertiesGeneticsMolecular BiologyMolecular GeneticsRedox Biology	2007	51
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
POLG1 Variations Presenting as Multiple Sclerosis Andoni Echaniz‐Laguna, Maïté Chassagne, J. de Sèze, Archives of Neurology	2010	39
Large Functional Range of Steady-State Levels of Nuclear and Mitochondrial Transcripts Coding for the Subunits of the Human Mitochondrial OXPHOS System Hervé Duborjal, Réjane Beugnot, Bénédicte Mousson de Camaret, Genome Research	2002	38
Alterations in voltage-sensing of the mitochondrial permeability transition pore in ANT1-deficient cells Judit Dóczi, Beáta Törőcsik, Andoni Echaniz‐Laguna, Scientific Reports	2016	36

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