Brigitte Gilbert‐Dussardier

Author

Also Known As

B Gilbert-Dussardier, B Gilbert‐Dussardier, B. Gilbert-Dussardier, B. Gilbert‐Dussardier, BRIGITTE GILBERT‐DUSSARDIER, Bertrand Isidor, Brigitte Gilbert Dussardier, Brigitte Gilbert-Du-ssardier, Brigitte Gilbert-Dussardier, Brigitte Gilbert‐Dussardier

158

Publications

8.5K

Citations

H-Index

119

Concepts

All Affiliations

Inserm Centre Hospitalier Universitaire de Poitiers Assistance Publique – Hôpitaux de Paris Centre Hospitalier Universitaire de Tours Université de Poitiers

About

Brigitte Gilbert‐Dussardier is an author at Inserm specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	26	40	4.5K
2	Social Sciences	5	5	222
3	Public Health	3	3	180
4	Natural Sciences	2	2	2.3K
5	Health Sciences	1	1	51

Brigitte Gilbert‐Dussardier

Publications

7.6K

Citations

H-Index

Page 1

	Year	Citations
Disruptions of Topological Chromatin Domains Cause Pathogenic Rewiring of Gene-Enhancer Interactions Darío G. Lupiáñez, Katerina Kraft, Verena Heinrich, Cell ChromatinChromatin StructureChromatin RemodelingNatural SciencesEpigenetic Change	2015	2.2K
Bevacizumab in Patients With Hereditary Hemorrhagic Telangiectasia and Severe Hepatic Vascular Malformations and High Cardiac Output Sophie Dupuis‐Girod, Isabelle Ginon, Jean‐Christophe Saurin, JAMA	2012	378
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
Genotype-phenotype correlations in hereditary hemorrhagic telangiectasia: Data from the French-Italian HHT network Gaëtan Lesca, Carla Olivieri, Nelly Burnichon, Genetics in Medicine Genotype-phenotype CorrelationsHereditary Hemorrhagic TelangiectasiaGenetic DisorderGeneticsGenetic Epidemiology	2007	224
CHARGE and Kabuki Syndromes: Gene-Specific DNA Methylation Signatures Identify Epigenetic Mechanisms Linking These Clinically Overlapping Conditions Darci T. Butcher, Cheryl Cytrynbaum, Andrei L. Turinsky, The American Journal of Human Genetics	2017	202
De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability Sébastien Küry, Geeske M. van Woerden, Thomas Besnard, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsMolecular GeneticsDisease Gene Identification	2017	193
Comprehensive In Vivo Interrogation Reveals Phenotypic Impact of Human Enhancer Variants Evgeny Z. Kvon, Yiwen Zhu, Guy Kelman, Cell Human Enhancer VariantsGeneticsHuman PolymorphismGene CharacterizationSystems Biology	2020	182
Mutations in INF2 Are a Major Cause of Autosomal Dominant Focal Segmental Glomerulosclerosis Olivia Boyer, Geneviève Benoît, Olivier Gribouval, Journal of the American Society of Nephrology Glomerular DiseasePathologyCytoskeletonDisease Gene IdentificationGlomerulonephritis	2011	161
Delineation of 15q13.3 microdeletions Alice Masurel‐Paulet, Joris Andrieux, Patrick Callier, Clinical Genetics PsychiatryScientific Data ManagementCosmologyGeneticsSyndromic Autism	2010	150
Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factor Asif Ali, P. T. Christie, I. V. Grigorieva, Human Molecular Genetics Developmental BiologyDna BindingGata3 MutationsSplice Site MutationMedicine	2006	149

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