Joël Lunardi - Concepedia

Author

Joël Lunardi

Also Known As

J LUNARDI, J Lunardi, J. LUNARDI, J. Lunardi, Joel Lunardi, Joël Lunardi, Joël L. Lunardi, Joël Lunardi, Jöel Lunardi, Lunardi, Joël

367

Publications

8.5K

Citations

H-Index

155

Concepts

All Affiliations

Inserm Centre Hospitalier Universitaire de Grenoble Université Joseph Fourier CEA Grenoble Commissariat à l'Énergie Atomique et aux Énergies Alternatives

About

Joël Lunardi is an author at Inserm specializing in medicine, molecular biology, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	33	56	3.7K
2	Natural Sciences	21	28	1.4K
3	Public Health	6	6	885
4	Engineering	4	4	111
5	Health Sciences	2	2	87

Joël Lunardi

107

Publications

7.9K

Citations

H-Index

Page 1

	Year	Citations
Incidence and Risk Factors of Arrhythmic Events in Catecholaminergic Polymorphic Ventricular Tachycardia Meiso Hayashi, Isabelle Denjoy, Fabrice Extramiana, Circulation	2009	551
Proteomics Analysis of Cellular Response to Oxidative Stress Thierry Rabilloud, Manfred Heller, Françoise Gasnier, Journal of Biological Chemistry	2002	389
A comparison between Sypro Ruby and ruthenium II tris (bathophenanthroline disulfonate) as fluorescent stains for protein detection in gels Thierry Rabilloud, Jean‐Marc Strub, Sylvie Luche, PROTEOMICS Molecular BiologyFluorescent StainsProtein DetectionBioanalysisAnalytical Chemistry	2001	306
Homozygous mutation of AURKC yields large-headed polyploid spermatozoa and causes male infertility Klaus Dieterich, Ricardo Soto‐Rifo, A.K. Faure, Nature Genetics SpermatogenesisInfertilityAndrologyDevelopmental BiologyFertility	2007	274
Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human Nathalie Roux-Buisson, Marine Cacheux, Anne Fourest‐Lieuvin, Human Molecular Genetics	2012	258
Development and implementation of standardized respiratory chain spectrophotometric assays for clinical diagnosis Fadia Medja, Stéphane Allouche, Paule Frachon, Mitochondrion AsthmaAdvanced Lung DiseaseMedicineBioanalysisDiagnosis	2009	204
Presence of Two Different Genetic Traits in Malignant Hyperthermia Families Nicole Monnier, R Krivosic-Horber, Jean‐François Payen, Anesthesiology	2002	200
A recessive form of central core disease, transiently presenting as multi‐minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene Ana Ferreiro, Nicole Monnier, Norma B. Romero, Annals of Neurology GeneticsGenetic EpidemiologyPathologyDisease Gene IdentificationGenetic Medicine	2002	200
A Recurrent Deletion of DPY19L2 Causes Infertility in Man by Blocking Sperm Head Elongation and Acrosome Formation Radu Harbuz, Raoudha Zouari, Virginie Pierre, The American Journal of Human Genetics SpermatogenesisAcrosome FormationInfertilityAndrologyDevelopmental Biology	2011	195
Two‐dimensional electrophoresis of human placental mitochondria and protein identification by mass spectrometry: Toward a human mitochondrial proteome Thierry Rabilloud, Sylvie Kieffer, Vincent Procaccio, Electrophoresis	1998	194

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