Citation Impact
Citing Papers
2017 Standout
Interleukin-1 in the pathogenesis and treatment of inflammatory diseases
2011 Standout
Exonic mutations in SCN9A (Na V 1.7) are found in a minority of patients with erythromelalgia
2014
Intracellular Nucleic Acid Sensors and Autoimmunity
2011 StandoutNobel
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis
2013 Standout
Arg-78 of Nprl2 catalyzes GATOR1-stimulated GTP hydrolysis by the Rag GTPases
2019
Benchmarking the stability of human detergent-solubilised voltage-gated sodium channels for structural studies using eel as a reference
2015 StandoutNobel
Somatic Mutations Activating the mTOR Pathway in Dorsal Telencephalic Progenitors Cause a Continuum of Cortical Dysplasias
2017
Ion channels: Function unravelled by dysfunction
2004
Na+ Channel ? Subunits: Overachievers of the Ion Channel Family
2011
Hydrophobic mismatch drives self-organization of designer proteins into synthetic membranes
2024 StandoutNobel
NaV1.1 channels and epilepsy
2010
Selective spider toxins reveal a role for the Nav1.1 channel in mechanical pain
2016 StandoutNatureNobel
Neurexins Physically and Functionally Interact with GABAA Receptors
2010 StandoutNobel
The Human Brainnetome Atlas: A New Brain Atlas Based on Connectional Architecture
2016 Standout
Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005–2009
2010 Standout
Guillain-Barré syndrome
2016 Standout
Formation and plasticity of GABAergic synapses: physiological mechanisms and pathophysiological implications
2003
The genetic landscape of the epileptic encephalopathies of infancy and childhood
2015
The Role of Ionotropic Glutamate Receptors in Childhood Neurodevelopmental Disorders: Autism Spectrum Disorders and Fragile X Syndrome
2014
22q11.21 Deletion Syndromes: A Review of Proximal, Central, and Distal Deletions and Their Associated Features
2015 Standout
Age-associated cognitive decline
2009 Standout
Disruption of an Evolutionarily Novel Synaptic Expression Pattern in Autism
2016 StandoutNobel
Modeling the human Na<sub>v</sub>1.5 sodium channel: structural and mechanistic insights of ion permeation and drug blockade
2017 StandoutNobel
The emerging role of synaptic cell-adhesion pathways in the pathogenesis of autism spectrum disorders
2009
mTOR at the nexus of nutrition, growth, ageing and disease
2020 Standout
Biological roles of glycans
2016 Standout
Clinical effects of insular damage in humans
2010
Autosomal dominant nocturnal frontal lobe epilepsy
2004
A mouse model of DEPDC5-related epilepsy: Neuronal loss of Depdc5 causes dysplastic and ectopic neurons, increased mTOR signaling, and seizure susceptibility
2017
Variations on an inhibitory theme: phasic and tonic activation of GABAA receptors
2005 Standout
Conservation and Diversification of Dileucine Signal Recognition by Adaptor Protein (AP) Complex Variants
2010
Pharmacological therapies for Angelman syndrome
2016
Wilson's disease and other neurological copper disorders
2014
Identification of Copy Number Variants on Human Chromosome 22 in Patients with a Variety of Clinical Findings
2011
mTOR Signaling in Epilepsy: Insights from Malformations of Cortical Development
2015
Autism
2013 Standout
Autoimmune antigenic targets at the node of Ranvier in demyelinating disorders
2015
The conundrums of understanding genetic risks for autism spectrum disorders
2011
A Central Nervous System-Restricted Isoform of the Interleukin-1 Receptor Accessory Protein Modulates Neuronal Responses to Interleukin-1
2009
Differential Regulation of Lipoprotein and Hepatitis C Virus Secretion by Rab1b
2017 StandoutNobel
Chloride channels as drug targets
2008
The body in the brain revisited
2009
Saliency, switching, attention and control: a network model of insula function
2010 Standout
CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics
2012
Structural Bases of Desensitization in AMPA Receptor-Auxiliary Subunit Complexes
2017 StandoutNobel
The human insula: Architectonic organization and postmortem MRI registration
2013
Large-scale brain networks and psychopathology: a unifying triple network model
2011 Standout
Sodium channelSCN1Aand epilepsy: Mutations and mechanisms
2010
Protein Sequence Editing of SKN-1A/Nrf1 by Peptide:N-Glycanase Controls Proteasome Gene Expression
2019 StandoutNobel
Endoplasmic Reticulum Retention and Associated Degradation of a GABAA Receptor Epilepsy Mutation That Inserts an Aspartate in the M3 Transmembrane Segment of the α1 Subunit
2005
Human disorders of cortical development: from past to present
2006
A comprehensive review in current developments of benzothiazole-based molecules in medicinal chemistry
2014 Standout
MDGAs interact selectively with neuroligin-2 but not other neuroligins to regulate inhibitory synapse development
2012 StandoutNobel
Glycoproteomics
2022 StandoutNobel
Guidelines on the Use of Therapeutic Apheresis in Clinical Practice – Evidence‐Based Approach from the Writing Committee of the American Society for Apheresis: The Eighth Special Issue
2019 Standout
Ligand-Gated Ion Channels: New Insights into Neurological Disorders and Ligand Recognition
2012
Antibody-Mediated Encephalitis
2018 Standout
Elucidation of AMPA receptor–stargazin complexes by cryo–electron microscopy
2016 StandoutScienceNobel
Crystallographic insights into sodium-channel modulation by the β4 subunit
2013
Long Noncoding RNA and Cancer: A New Paradigm
2017 Standout
Selective lowering of synapsins induced by oligomeric α-synuclein exacerbates memory deficits
2017
Neue Ziele für die Photopharmakologie
2016 StandoutNobel
A neurologist’s guide to genome-wide association studies
2009
Neuropathic Pain: From Mechanisms to Treatment
2020 Standout
Involvement of GATOR complex genes in familial focal epilepsies and focal cortical dysplasia
2016
Autism-linked neuroligin-3 R451C mutation differentially alters hippocampal and cortical synaptic function
2011 StandoutNobel
Investigations in GABA A receptor antibody-associated encephalitis
2017
Congenital Disorders of Glycosylation from a Neurological Perspective
2021
Copper induces cell death by targeting lipoylated TCA cycle proteins
2022 StandoutScience
Artificial Molecular Machines
2015 Standout
Epilepsy: A Review of Selected Clinical Syndromes and Advances in Basic Science
2006
Protein Sorting at thetrans-Golgi Network
2014 Nobel
Religious Orders Study and Rush Memory and Aging Project
2018 Standout
Pharmacology of the Na v 1.1 domain IV voltage sensor reveals coupling between inactivation gating processes
2017 StandoutNobel
Candidate autism gene screen identifies critical role for cell-adhesion molecule CASPR2 in dendritic arborization and spine development
2012 StandoutNobel
The Proprioceptive Senses: Their Roles in Signaling Body Shape, Body Position and Movement, and Muscle Force
2012 Standout
Emerging Targets in Photopharmacology
2016 StandoutNobel
Neurological Aspects of Human Glycosylation Disorders
2015
Transcriptomes of germinal zones of human and mouse fetal neocortex suggest a role of extracellular matrix in progenitor self-renewal
2012 StandoutNobel
Chemistry and Biology Of Multicomponent Reactions
2012 Standout
Works of Patrick Cossette being referenced
A mutation in the GABAA receptor α1‐subunit is associated with absence epilepsy
2006
The genetic landscape of infantile spasms
2014
Disruption of AP1S1, Causing a Novel Neurocutaneous Syndrome, Perturbs Development of the Skin and Spinal Cord
2008
Sacred disease secrets revealed: the genetics of human epilepsy
2005
Molecular analysis of the A322D mutation in the GABAA receptor α1‐subunit causing juvenile myoclonic epilepsy
2005
Novel de novo SHANK3 mutation in autistic patients
2008
SYN2 is an autism predisposing gene: loss-of-function mutations alter synaptic vesicle cycling and axon outgrowth
2013
Lamotrigine Therapy of Epilepsy with Angelman's Syndrome
2007
Mutations in the calcium-related gene IL1RAPL1 are associated with autism
2008
Revisiting the role of the insula in refractory partial epilepsy
2008
Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy
2002
Functional characterization of the D188V mutation in neuronal voltage-gated sodium channel causing generalized epilepsy with febrile seizures plus (GEFS)
2003
Screening of GABRB3 in French‐Canadian families with idiopathic generalized epilepsy
2010
Voltage-Gated Na + Channel β1B: A Secreted Cell Adhesion Molecule Involved in Human Epilepsy
2011
A recurrent mutation in DEPDC5 predisposes to focal epilepsies in the French‐Canadian population
2013
Microsurgery of epileptic foci in the insular region
2009
Novel α1 and γ2 GABAA receptor subunit mutations in families with idiopathic generalized epilepsy
2011
Two definite cases of sudden unexpected death in epilepsy in a family with a DEPDC5 mutation
2015
Familial focal epilepsy with focal cortical dysplasia due to DEPDC 5 mutations
2015