Dominique Bonneau - Concepedia

Author

Dominique Bonneau

Also Known As

BONNEAU, Dominique, Bonneau, D., Bonneau, Dominique, Boris Keren, Christine Francannet, D BONNEAU, D Bonneau, D. BONNEAU, D. Bonneau, DOMINIQUE BONNEAU

652

Publications

23.4K

Citations

H-Index

328

Concepts

All Affiliations

Inserm Centre National de la Recherche Scientifique Centre Hospitalier Universitaire d'Angers Université d'Angers Assistance Publique – Hôpitaux de Paris

About

Dominique Bonneau is an author at Inserm specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	51	115	10.4K
2	Engineering	20	36	1.6K
3	Health Sciences	10	10	364
4	Natural Sciences	10	10	973
5	Management	1	1	13

Dominique Bonneau

263

Publications

18.7K

Citations

H-Index

Page 1

	Year	Citations
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome Laura Crisponi, Manila Deiana, Angela Loi, Nature Genetics Transcriptional RegulationDevelopmental BiologyGenetic DisorderGeneticsPathogenesis	2001	974
Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome Tetsuya Niihori, Yoko Aoki, Yoko Narumi, Nature Genetics Mendelian DisorderGenetic DisorderGermline KrasGeneticsDermatology	2006	593
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
Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly Karine Poirier, Nicolas Lebrun, Loïc Broix, Nature Genetics Developmental AnomalyDevelopmental BiologyBrain DevelopmentDevelopmental GeneticsGenetics	2013	488
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey, Nature Gene DosageGeneticsHuman PolymorphismMolecular GeneticsChromosome 16P11.2	2011	474
Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders Claire S. Leblond, Jutta Heinrich, Richard Delorme, PLoS Genetics	2012	437
Multi-system neurological disease is common in patients with OPA1 mutations Patrick Yu‐Wai‐Man, Philip G. Griffiths, Gráinne S. Gorman, Brain	2010	437
High cumulative risks of cancer in patients with <i>PTEN</i> hamartoma tumour syndrome Virginie Bubien, Françoise Bonnet, Véronique Brouste, Journal of Medical Genetics	2013	358
X–linked spastic paraplegia and Pelizaeus–Merzbacher disease are allelic disorders at the proteolipid protein locus Pascale Saugier-Véber, Arnold Münnich, Dominique Bonneau, Nature Genetics Allelic DisordersMedicineGeneticsSpastic ParaplegiaProteolipid Protein Locus	1994	352
Mutations of <i>ARX</i> are associated with striking pleiotropy and consistent genotype–phenotype correlation Mitsuhiro Kato, Soma Das, Kristin Petras, Human Mutation GeneticsPathologyMolecular GeneticsMendelian DisorderGenotype-phenotype Association	2004	327

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