Concepedia

Author

Emmanuelle Cochet

Hôpital Armand-Trousseau

Also Known As

André Mégarbané, E Cochet, E. Cochet, Emmanuelle Cochet

19

Publications

1.3K

Citations

9

H-Index

6

Concepts

All Affiliations

Hôpital Armand-TrousseauSorbonne UniversitéInsermAssistance Publique – Hôpitaux de ParisMaladies génétiques d’expression pédiatrique
EC

About

Emmanuelle Cochet is an author at Hôpital Armand-Trousseau specializing in neurology, neuropathology, and neurogenetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

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Medicine

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Neurology

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Neuroscience

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Genetics

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Neuropathology

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Emmanuelle Cochet

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9

Publications

1.2K

Citations

9

H-Index

YearCitations

Mutations in <i>NALP12</i> cause hereditary periodic fever syndromes

Isabelle Jéru, Philippe Duquesnoy, Teresa Fernandes‐Alnemri,

Proceedings of the National Academy of Sciences

2008

365

Familial autoinflammation with neutrophilic dermatosis reveals a regulatory mechanism of pyrin activation

Seth L. Masters, Vasiliki Lagou, Isabelle Jéru,

Science Translational Medicine

2016

306

Mutations in the autoinflammatory cryopyrin-associated periodic syndrome gene: epidemiological study and lessons from eight years of genetic analysis in France

Laurence Cuisset, Isabelle Jéru, Bruno Dumont,

Annals of the Rheumatic Diseases

2010

175

Identification and functional consequences of a recurrent <i>NLRP12</i> missense mutation in periodic fever syndromes

Isabelle Jéru, Gaëlle Le Borgne, Emmanuelle Cochet,

Arthritis & Rheumatism

2011

101

Role of interleukin-1β in NLRP12-associated autoinflammatory disorders and resistance to anti-interleukin-1 therapy

Isabelle Jéru, Véronique Hentgen, Sylvain Normand,

Arthritis & Rheumatism

2011

100

The Risk of Familial Mediterranean Fever in MEFV Heterozygotes: A Statistical Approach

Isabelle Jéru, Véronique Hentgen, Emmanuelle Cochet,

PLoS ONE

2013

67

Exome sequencing in congenital ataxia identifies two new candidate genes and highlights a pathophysiological link between some congenital ataxias and early infantile epileptic encephalopathies

Stéphanie Valence, Emmanuelle Cochet, Christelle Rougeot,

Genetics in Medicine

2018

54

Brief Report: Involvement of <i>TNFRSF11A</i> Molecular Defects in Autoinflammatory Disorders

Isabelle Jéru, Emmanuelle Cochet, Philippe Duquesnoy,

Arthritis & Rheumatology

2014

32

Functional consequences of a germline mutation in the leucine‐rich repeat domain of NLRP3 identified in an atypical autoinflammatory disorder

Isabelle Jéru, Sandrine Marlin, Gaëlle Le Borgne,

Arthritis & Rheumatism

2010

32

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