Citation Impact
Citing Papers
A Genome-Wide Association Study Identifies Novel Loci for Paclitaxel-Induced Sensory Peripheral Neuropathy in CALGB 40101
2012
Lamin A/C–mediated neuromuscular junction defects in Emery-Dreifuss muscular dystrophy
2009
Nuclear Lamin-A Scales with Tissue Stiffness and Enhances Matrix-Directed Differentiation
2013 StandoutScience
Induced Pluripotent Stem Cells Generated from Patients with ALS Can Be Differentiated into Motor Neurons
2008 StandoutScience
Genetic Influences on Brain Gene Expression in Rats Selected for Tameness and Aggression
2014 StandoutNobel
Origins and Divergence of the Roma (Gypsies)
2001 Standout
Non-muscle myosin II takes centre stage in cell adhesion and migration
2009 Standout
Hereditary motor and sensory neuropathy‐russe: New autosomal recessive neuropathy in balkan gypsies
2001
Cell mechanics and the cytoskeleton
2010 StandoutNature
Gene activities that mediate increased life span of C. elegans insulin-like signaling mutants
2007 StandoutNobel
Abdominal obesity and metabolic syndrome
2006 StandoutNature
Nonalcoholic Fatty Liver Disease: From Steatosis to Cirrhosis
2006 Standout
Electroclinical characterization of epileptic seizures in leucine-rich, glioma-inactivated 1-deficient mice
2010
Life at the edge: the nuclear envelope and human disease
2002
Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome
2003 StandoutNature
Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features
2002
Pathological roles of MAPK signaling pathways in human diseases
2010 Standout
Structural basis for triplet repeat disorders: a computational analysis
1999 StandoutNobel
Glutamate uptake
2001 Standout
The genetics of ageing
2010 StandoutNature
Mammalian phosphoinositide kinases and phosphatases
2009 StandoutNobel
A truncated lamin A in the Lmna −/− mouse line
2012
Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005–2009
2010 Standout
Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy
1997 Nature
Design and validation of a histological scoring system for nonalcoholic fatty liver disease†
2005 Standout
The metabolic syndrome
2010 Standout
Hallmarks of aging: An expanding universe
2023 Standout
The functions of the nuclear envelope in mediating the molecular crosstalk between the nucleus and the cytoplasm
2011
Nuclear lamins and laminopathies
2011
Mtmr13/Sbf2-deficient mice: an animal model for CMT4B2
2007
Steatohepatitis in children
2002
Extreme variability of skeletal and cardiac muscle involvement in patients with mutations in exon 11 of the lamin A/C gene
2005
The human keratins: biology and pathology
2008 Standout
Amyotrophic lateral sclerosis
2011 Standout
Laminopathies: Multiple disorders arising from defects in nuclear architecture
2006
Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy
2002
Network medicine: a network-based approach to human disease
2010 Standout
Coordinated Transcription of Key Pathways in the Mouse by the Circadian Clock
2002 Standout
Lgi1 null mutant mice exhibit myoclonic seizures and CA1 neuronal hyperexcitability
2010
LGI1mutations in autosomal dominant and sporadic lateral temporal epilepsy
2009
Prevalence of Muscular Dystrophies: A Systematic Literature Review
2014 Standout
Incidence, prevalence, and predictors of chemotherapy-induced peripheral neuropathy: A systematic review and meta-analysis
2014 Standout
Autosomal dominant nocturnal frontal lobe epilepsy
2004
The metabolic syndrome
2005 Standout
Lipodystrophies: rare disorders causing metabolic syndrome
2004
Antibodies to Kv1 potassium channel-complex proteins leucine-rich, glioma inactivated 1 protein and contactin-associated protein-2 in limbic encephalitis, Morvan’s syndrome and acquired neuromyotonia
2010 Standout
Walking the Interactome for Prioritization of Candidate Disease Genes
2008
Investigation of LGI1 as the antigen in limbic encephalitis previously attributed to potassium channels: a case series
2010 Standout
Insulin and insulin resistance:
2004 Standout
Intermediate Filament Proteins and Their Associated Diseases
2004
LGI1 is mutated in familial temporal lobe epilepsy characterized by aphasic seizures
2002
A Novel Locus for Autosomal Recessive Peripheral Neuropathy in the EGR2 Region on 10q23
2000
Laminopathies and the long strange trip from basic cell biology to therapy
2009
Molecular mechanisms of muscular dystrophies: old and new players
2006
The epilepsy gene LGI1 encodes a secreted glycoprotein that binds to the cell surface
2006
Neuronal nicotinic receptors: from structure to pathology
2004
The Hallmarks of Aging
2013 Standout
CHRNB2 Is the Second Acetylcholine Receptor Subunit Associated with Autosomal Dominant Nocturnal Frontal Lobe Epilepsy*
2001
A Putative Src Homology 3 Domain Binding Motif but Not the C-terminal Dystrophin WW Domain Binding Motif Is Required for Dystroglycan Function in Cellular Polarity in Drosophila
2007 StandoutNobel
Molecular biology of amyotrophic lateral sclerosis: insights from genetics
2006
Nesprins: intracellular scaffolds that maintain cell architecture and coordinate cell function?
2005
STRING 8--a global view on proteins and their functional interactions in 630 organisms
2008 Standout
Drug resistant ADLTE and recurrent partial status epilepticus with dysphasic features in a family with a novel LGI1mutation: electroclinical, genetic, and EEG/fMRI findings
2009
Faciobrachial dystonic seizures precede Lgi1 antibody limbic encephalitis
2010 Standout
Clinical experience and laboratory investigations in patients with anti-NMDAR encephalitis
2010 Standout
Update on the pathophysiology of the epilepsies
2000
ToppGene Suite for gene list enrichment analysis and candidate gene prioritization
2009 Standout
Ligand-Gated Ion Channels: New Insights into Neurological Disorders and Ligand Recognition
2012
Diagnosis and Management of the Metabolic Syndrome
2005 Standout
Nuclear Membrane Proteins with Potential Disease Links Found by Subtractive Proteomics
2003 Science
The Posttranslational Processing of Prelamin A and Disease
2009
Molecular Pathology of Laminopathies
2021
TELOMERES AND THEIR CONTROL
2000 StandoutNobel
Rasmussen??s Syndrome
2000
A Novel Mechanism of Rapid Nuclear Neutrophil Extracellular Trap Formation in Response to Staphylococcus aureus
2010 Standout
A promiscuous biotin ligase fusion protein identifies proximal and interacting proteins in mammalian cells
2012 Standout
2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death
2015 Standout
Prevention and Management of Chemotherapy-Induced Peripheral Neuropathy in Survivors of Adult Cancers: American Society of Clinical Oncology Clinical Practice Guideline
2014 Standout
Altered language processing in autosomal dominant partial epilepsy with auditory features
2008
LGI Proteins in the Nervous System
2013
Reversible Photocontrol of Biological Systems by the Incorporation of Molecular Photoswitches
2013 StandoutNobel
A Model for Random Sampling and Estimation of Relative Protein Abundance in Shotgun Proteomics
2004 Standout
Multiple Pathways of Recombination Induced by Double-Strand Breaks in Saccharomyces cerevisiae
1999 Standout
The Nuclear Envelope and Human Disease
2004
Emerging Targets in Photopharmacology
2016 StandoutNobel
Loss of the inactive myotubularin-related phosphatase Mtmr13 leads to a Charcot–Marie–Tooth 4B2-like peripheral neuropathy in mice
2008
Computational design of a red fluorophore ligase for site-specific protein labeling in living cells
2014 StandoutNobel
Clinical Relevance of Atrial Fibrillation/Flutter, Stroke, Pacemaker Implant, and Heart Failure in Emery-Dreifuss Muscular Dystrophy
2003
Works of Djamel Grid being referenced
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy in a Spanish Family With a Ser252Phe Mutation in the CHRNA4 Gene
1999
A PCR Amplification Method Reveals Instability of the Dodecamer Repeat in Progressive Myoclonus Epilepsy (EPM1) and No Correlation between the Size of the Repeat and Age at Onset
1998
Autosomal dominant lateral temporal epilepsy: Clinical and genetic study of a large basque pedigree linked to chromosome 10q
1999
Mutations in FGD4 Encoding the Rho GDP/GTP Exchange Factor FRABIN Cause Autosomal Recessive Charcot-Marie-Tooth Type 4H
2007
Homozygous Defects in LMNA, Encoding Lamin A/C Nuclear-Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy in Human (Charcot-Marie-Tooth Disorder Type 2) and Mouse
2002
Allelic heterogeneity of mediterranean myoclonus and the cystatin B gene
1997
A clinical, electrophysiologic, neuropathologic, and genetic study of two large Algerian families with an autosomal recessive demyelinating form of Charcot‐Marie‐Tooth disease
1997