Marie‐Claude Vinet

Author

Marie‐Claude Vinet

Inserm

Also Known As

Marie-Claude Vinet, MarieClaude Vinet, Marie‐Claude Vinet

Publications

1.3K

Citations

H-Index

Concepts

All Affiliations

Inserm Centre National de la Recherche Scientifique Institut Cochin Stanford University Collège de France

About

Marie‐Claude Vinet is an author at Inserm specializing in medicine, neuroscience, and molecular neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	1.1K
2	Social Sciences	3	3	1.1K
3	Cell Biology	3	3	1.1K
4	Cellular Physiology	3	3	1.1K
5	Molecular Biology	1	1	13

Marie‐Claude Vinet

Publications

1.3K

Citations

H-Index

Page 1

	Year	Citations
Doublecortin Is a Developmentally Regulated, Microtubule-Associated Protein Expressed in Migrating and Differentiating Neurons Fiona Francis, Annette Koulakoff, Dominique Boucher, Neuron Microtubule-associated ProteinNeuroregenerationDevelopmental BiologyMolecular NeuroscienceNeural Stem Cell	1999	997
Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12 Kemal Azlbi, L Bachner, J. Beckmann, Human Molecular Genetics	1993	101
Doublecortin Interacts with μ Subunits of Clathrin Adaptor Complexes in the Developing Nervous System Gaëlle Friocourt, Philippe Chafey, Pierre Billuart, Molecular and Cellular Neuroscience Synaptic TransmissionNeurotransmissionPeripheral NervesCellular NeurobiologySynaptic Signaling	2001	59
Doublecortin interacts with the ubiquitin protease DFFRX, which associates with microtubules in neuronal processes Gaëlle Friocourt, Caroline Kappeler, Yoann Saillour, Molecular and Cellular Neuroscience Ubiquitin Protease DffrxMolecular NeuroscienceNeurotransmitterCytoskeletonNeuronal Processes	2004	48
Linkage study of a large family with autosomal dominant polycystic kidney disease with reduced expression Lucien Bachner, Marie‐Claude Vinet, Roger Lacave, Human Genetics GlomerulonephritisUrologyMendelian DisorderReduced ExpressionKidney Research	1990	23
Determination of the gene structure of human oligophrenin-1 and identification of three novel polymorphisms by screening of DNA from 164 patients with non-specific X-linked mental retardation Pierre Billuart, Jamel Chelly, Alain Carrié, Annales de Génétique PsychiatryGenetic DisorderGeneticsPsychiatric GeneticsHuman Polymorphism	2000	13
Antenatal diagnosis in three pregnancies at risk for mannosidosis Livia Poënaru, Sylvte Girard, F. Thépot, Clinical Genetics	1979	11

Page 1