Florence Coulet - Concepedia

Author

Florence Coulet

Also Known As

Capucine Delnatte, Carla Olivieri, Coulet Florence, Coulet, F., Coulet, Florence, F Coulet, F P Coulet, F. Coulet, Fabienne Lesueur, Florence Cou-Let

250

Publications

7.4K

Citations

H-Index

115

Concepts

All Affiliations

Sorbonne Université Assistance Publique – Hôpitaux de Paris Inserm Pitié-Salpêtrière Hospital Université Paris Cité

About

Florence Coulet is an author at Sorbonne Université specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	28	39	3.6K
2	Public Health	11	11	1.4K
3	Health Sciences	3	3	152
4	Engineering	1	1	18
5	Natural Sciences	1	1	17

Florence Coulet

Publications

6.5K

Citations

H-Index

Page 1

	Year	Citations
Mechanisms and therapeutic implications of hypermutation in gliomas Mehdi Touat, Yvonne Y. Li, Adam N. Boynton, Nature Neuro-oncologyMedicineTherapeutic ImplicationsHigh-grade GliomasCell Biology	2020	661
EIF2AK4 mutations cause pulmonary veno-occlusive disease, a recessive form of pulmonary hypertension Mélanie Eyries, David Montani, Barbara Girerd, Nature Genetics Pulmonary Arterial HypertensionPulmonary CirculationGeneticsPathologyEif2ak4 Mutations	2013	445
Mutations of the TGF-β type II receptorBMPR2 in pulmonary arterial hypertension Rajiv D. Machado, Micheala A. Aldred, Victoria James, Human Mutation HypertensionGeneticsPathologyPulmonary HypertensionClinical Genetics	2006	398
Clinical Outcomes of Pulmonary Arterial Hypertension in Carriers of <i>BMPR2</i> Mutation Benjamin Sztrymf, Florence Coulet, Barbara Girerd, American Journal of Respiratory and Critical Care Medicine	2008	295
Clinical Outcomes of Pulmonary Arterial Hypertension in Patients Carrying an <i>ACVRL1</i> ( <i>ALK1</i> ) Mutation Barbara Girerd, David Montani, Florence Coulet, American Journal of Respiratory and Critical Care Medicine	2010	288
Guidelines for splicing analysis in molecular diagnosis derived from a set of 327 combined in silico/in vitro studies on BRCA1 and BRCA2 variants Claude Houdayer, Virginie Caux‐Moncoutier, Sophie Krieger, Human Mutation	2012	238
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
Role of truncating mutations in MME gene in fetomaternal alloimmunisation and antenatal glomerulopathies Hanna Dêbiec, Jeroen Nauta, Florence Coulet, The Lancet Fetomaternal AlloimmunisationGlomerulonephritisGeneticsRenal PathologyMme Gene	2004	212
Identification of Hypoxia-response Element in the Human Endothelial Nitric-oxide Synthase Gene Promoter Florence Coulet, Sophie Nadaud, Monique Agrapart, Journal of Biological Chemistry	2003	199
Molecular genetic characterization of SMAD signaling molecules in pulmonary arterial hypertension Talat Nasim, Takeshi Ogo, Mohammad Ejaz Ahmed, Human Mutation GeneticsPulmonary HypertensionMolecular GeneticsDisease Gene IdentificationGenomics	2011	185

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