Alain Hovnanian - Concepedia

Author

Alain Hovnanian

Also Known As

A Hovnanian, A. HOVNANIAN, A. Hovnanian, Alain A. Hovnanian, Alain Hovnanian, Alain Hovnanian (798119), Andre Luiz Dresler Hovnanian, André Hovnanian, Hovnanian, A, Hovnanian, A.

386

Publications

22K

Citations

H-Index

165

Concepts

All Affiliations

Inserm Université Paris Cité Institut des Maladies Génétiques Imagine Hôpital Necker-Enfants Malades Centre for Human Genetics

About

Alain Hovnanian is an author at Inserm specializing in medicine, pathology, and dermatology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	52	97	12.1K
2	Natural Sciences	13	15	1.6K
3	Engineering	4	4	193
4	Health Sciences	2	2	119
5	Education	1	1	393

Alain Hovnanian

153

Publications

16.8K

Citations

H-Index

Page 1

	Year	Citations
TLR3 Deficiency in Patients with Herpes Simplex Encephalitis Shen‐Ying Zhang, Emmanuelle Jouanguy, Sophie Ugolini, Science Human Tlr3Innate Immune SystemImmunologyHerpes Simplex EncephalitisInnate Immunity	2007	1.1K
The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB Jo‐David Fine, Robin A.J. Eady, Eugene A. Bauer, Journal of the American Academy of Dermatology Inherited Epidermolysis BullosaDiagnosisPathologyClinical DermatologyDermatology	2008	921
Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome Stéphane Chavanas, Christine Bodemer, Ariane Rochat, Nature Genetics Mendelian DisorderGenetic DisorderGeneticsMolecular BiologySerine Protease Inhibitor	2000	838
Increased serine protease activity and cathelicidin promotes skin inflammation in rosacea Kenshi Yamasaki, Anna Di Nardo, Antonella Bardan, Nature Medicine InflammationMedicineCutaneous BiologySerine Protease ActivitySkin Pharmacology	2007	824
Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease Anavaj Sakuntabhai, Víctor L. Ruiz‐Pérez, Simon Carter, Nature Genetics Signal TransductionGenetic DisorderGeneticsCause Darier DiseaseMolecular Biology	1999	727
A European study of HLA-B in Stevens–Johnson syndrome and toxic epidermal necrolysis related to five high-risk drugs Christine Lonjou, Nicolas Borot, Peggy Sekula, Pharmacogenetics and Genomics	2008	614
Kallikrein 5 induces atopic dermatitis–like lesions through PAR2-mediated thymic stromal lymphopoietin expression in Netherton syndrome Anaïs Briot, Céline Deraison, Matthieu Lacroix, The Journal of Experimental Medicine	2009	482
Kallikrein‐mediated proteolysis regulates the antimicrobial effects of cathelicidins in skin Kenshi Yamasaki, Jürgen Schauber, Alvin B. Coda, The FASEB Journal Microbial PathogensAntimicrobial EffectsImmunologyAntimicrobial ChemotherapyDermatology	2006	456
Gene polymorphism in Netherton and common atopic disease Andrew J. Walley, Stéphane Chavanas, Miriam F. Moffatt, Nature Genetics Gene PolymorphismGeneticsHuman PolymorphismGenetic EpidemiologyGenetic Factor	2001	394
A marker for Stevens-Johnson syndrome …: ethnicity matters Christine Lonjou, Laure Thomas, Nicolas Borot, The Pharmacogenomics Journal EthnicityGenetic DisorderHistopathologyPathologyMedical History	2006	393

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