Sabine Fauré - Concepedia

Author

Sabine Fauré

Centre National de la Recherche Scientifique

Also Known As

Sabine Faure´, Sabine Fauré

Publications

5.6K

Citations

H-Index

Concepts

All Affiliations

Centre National de la Recherche Scientifique Genethon (France)Inserm Hôpital Saint-Vincent-de-Paul

About

Sabine Fauré is an author at Centre National de la Recherche Scientifique specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	4.9K
2	Molecular Biology	2	2	975
3	Molecular Genetics	2	2	290
4	Natural Sciences	1	1	3K
5	Clinical Genetics	1	1	199

Sabine Fauré

Publications

5.5K

Citations

H-Index

Page 1

	Year	Citations
A comprehensive genetic map of the human genome based on 5,264 microsatellites Colette Dib, Sabine Fauré, Cécile Fizames, Nature Genetic AnalysisHaplotype DeterminationMedicineGeneticsEvolutionary Biology	1996	3K
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome Nathalie Neyroud, Frédérique Tesson, Isabelle Denjoy, Nature Genetics Novel MutationChannelopathiesCardiomyopathyMolecular PhysiologyCardiac Muscle	1997	881
An STS-Based Map of the Human Genome Thomas J. Hudson, Lincoln Stein, Sebastian S. Gerety, Science Functional GenomicsGeneticsRadiation Hybrid MapGenome StructureMolecular Biology	1995	776
New susceptibility locus for rheumatoid arthritis suggested by a genome-wide linkage study François Cornélis, Sabine Fauré, María Martínez, Proceedings of the National Academy of Sciences	1998	470
Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping Dominique Hillaire, A. Leclerc, Sabine Fauré, Human Molecular Genetics Developmental BiologyMendelian DisorderGenetic DisorderMedicineGenetics	1994	199
Codon 102 of the Cardiac Troponin T Gene Is a Putative Hot Spot for Mutations in Familial Hypertrophic Cardiomyopathy Jean-Franc ̧ois Forissier, Lucie Carrier, Hend Farza, Circulation	1996	122
Localization of the Gene for Thiamine-Responsive Megaloblastic Anemia Syndrome, on the Long Arm of Chromosome 1, by Homozygosity Mapping Ellis J. Neufeld, Hanna Mandel, Tal Raz, The American Journal of Human Genetics ChromatinDevelopmental BiologyMendelian DisorderGenetic DisorderMedicine	1997	91
Genetic Exclusion of 14 Candidate Genes in Lipoatropic Diabetes Using Linkage Analysis in 10 Consanguineous Families<sup>1</sup> Corinne Vigouroux, Eliane Khallouf, Charlotte Bourut, The Journal of Clinical Endocrinology & Metabolism	1997	26
Aicardi–Goutières syndrome: monogenic recessive disease, genetically heterogeneous disease, or multifactorial disease? Sabine Fauré, Isabelle Bordelais, Catherine Marquette, Clinical Genetics	1999	15

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