Citation Impact
Citing Papers
Actin retrograde flow actively aligns and orients ligand-engaged integrins in focal adhesions
2017 StandoutNobel
Prevalence of the Congenital Long-QT Syndrome
2009
Simultaneous prediction of protein folding and docking at high resolution
2009 StandoutNobel
The effect of COVID certificates on vaccine uptake, health outcomes, and the economy
2022 StandoutNobel
Mechanisms of SARS-CoV-2 entry into cells
2021 Standout
Cardiomyocytes derived from human embryonic stem cells in pro-survival factors enhance function of infarcted rat hearts
2007 Standout
Nrf2-Keap1 signaling in oxidative and reductive stress
2018 Standout
Severe progressive form of congenital muscular dystrophy with calf pseudohypertrophy, macroglossia and respiratory insufficiency
2002
Cellular senescence in aging and age-related disease: from mechanisms to therapy
2015 Standout
The muscular dystrophies
2002 Standout
Structural Insight into KCNQ (Kv7) Channel Assembly and Channelopathy
2007
Genetic Analyses of Integrin Signaling
2010
Attitudes, acceptance and hesitancy among the general population worldwide to receive the COVID-19 vaccines and their contributing factors: A systematic review
2021
A Structural Requirement for Processing the Cardiac K+ Channel KCNQ1
2004
The genetic basis of long QT and short QT syndromes: A mutation update
2009
The very small-conductance K+ channel KVLQT1 and epithelial function
2000
Prevalence of Muscular Dystrophies: A Systematic Literature Review
2014 Standout
Coiled Coils Direct Assembly of a Cold-Activated TRP Channel
2006 StandoutNobel
Mild muscular dystrophy due to a nonsense mutation in the LAMA2 gene resulting in exon skipping
2001
Fibrosis development in early-onset muscular dystrophies: Mechanisms and translational implications
2016
Ubiquitin-dependent regulation of COPII coat size and function
2012 StandoutNatureNobel
Human Splicing Finder: an online bioinformatics tool to predict splicing signals
2009 Standout
Structure–function relations of the giant elastic protein titin in striated and smooth muscle cells
2007
Systems approaches to preventing transplanted cell death in cardiac repair
2008
Prospects forde novophasing withde novoprotein models
2009 StandoutNobel
Designing hydrogels for controlled drug delivery
2016 Standout
Non-invasive testing of acquired long QT syndrome Evidence for multiple arrhythmogenic substrates
2001
Hepatitis C virus: How genetic variability affects pathobiology of disease
2011
85th ENMC International Workshop on Congenital Muscular Dystrophy 6th International CMD Workshop 1st Workshop of the Myo-Cluster Project ‘GENRE’27–28th October 2000, Naarden, The Netherlands
2002
Integrins: Redundant or Important Players in Skeletal Muscle?
2003
The opposing roles of laminin-binding integrins in cancer
2016
Sirt1 plays an important role in mediating greater functionality of human ES/iPS-derived vascular endothelial cells
2010 StandoutNobel
The expanding phenotype of laminin α2 chain (merosin) abnormalities: case series and review
2001
Wavelet transforms and the ECG: a review
2005 Standout
The long QT syndromes: genetic basis and clinical implications
2000
A recessive C-terminal Jervell and Lange-Nielsen mutation of the KCNQ1 channel impairs subunit assembly
2000
The effects of cardioactive drugs on cardiomyocytes derived from human induced pluripotent stem cells
2009 StandoutNobel
Congenital Muscular Dystrophy in Arab Children
2006
Antitumor Antibiotics: Bleomycin, Enediynes, and Mitomycin
2005 Standout
Enhanced Expression of the α7β1 Integrin Reduces Muscular Dystrophy and Restores Viability in Dystrophic Mice
2001
Cell-Based Therapy for Myocardial Ischemia and Infarction: Pathophysiological Mechanisms
2007
2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death
2015 Standout
Recent Stem Cell Advances: Induced Pluripotent Stem Cells for Disease Modeling and Stem Cell–Based Regeneration
2010 StandoutNobel
Model for long QT syndrome type 2 using human iPS cells demonstrates arrhythmogenic characteristics in cell culture
2011 StandoutNobel
Fiber Types in Mammalian Skeletal Muscles
2011 Standout
IGF-IR signaling attenuates the age-related decline of diastolic cardiac function
2012
Spectrum of Mutations in Long-QT Syndrome Genes
2000
Response of Hepatitis C Virus to Long-Term Passage in the Presence of Alpha Interferon: Multiple Mutations and a Common Phenotype
2013 StandoutNobel
cAMP-mediated regulation of murine intestinal/pancreatic Na+/HCO 3 − cotransporter subtype pNBC1
2003 StandoutNobel
Satellite Cells and the Muscle Stem Cell Niche
2013 Standout
Role of Extracellular Matrix in Adaptation of Tendon and Skeletal Muscle to Mechanical Loading
2004 Standout
Works of Nicolas Vignier being referenced
Increased myofilament Ca2+ sensitivity and diastolic dysfunction as early consequences of Mybpc3 mutation in heterozygous knock-in mice
2012
Structure, Genetic Localization, and Identification of the Cardiac and Skeletal Muscle Transcripts of the Human Integrin α7 Gene (ITGA7)
1999
Merosin-deficient congenital muscular dystrophy with severe mental retardation and normal cranial MRI: a report of two siblings
1998
Response to pegylated interferon alfa‐2a and ribavirin in chronic hepatitis C genotype 4
2009
Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts unlinked to the LAMA2, FCMD and MEB loci
2000
Striated muscle laminopathies
2014
Spontaneous muscular dystrophy caused by a retrotransposal insertion in the mouse laminin α2 chain gene
2003
Can Cold or Heat Shock Improve Skeletal Myoblast Engraftment in Infarcted Myocardium?
2005
Length and protein kinase A modulations of myocytes in cardiac myosin binding protein C-deficient mice
2005
Genomic Organization of the KCNQ1 K + Channel Gene and Identification of C-Terminal Mutations in the Long-QT Syndrome
1999
Attitudes towards the COVID-19 Vaccine and Willingness to Get Vaccinated among Healthcare Workers in French Guiana: The Influence of Geographical Origin
2021
Partial laminin ?2 chain deficiency in a patient with myopathy resembling inclusion body myositis
2000
Breakthrough Infections of SARS-CoV-2 Gamma Variant in Fully Vaccinated Gold Miners, French Guiana, 2021
2021
Congenital muscular dystrophy with primary partial laminin α2 chain deficiency: Molecular study
2001