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Author Details

Sanjay M Sisodiya
UCL Institute of Neurology
1986
416
82
Andrej Sali (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
37949657Hot brain: practical climate change advice for neurologists.Pract Neurol2024
38088023Dissecting genetics of spectrum of epilepsies with eyelid myoclonia by exome sequencing.Epilepsia2024
36941776Climate change and the brain.Brain2023
37755653Steps to Improve Precision Medicine in Epilepsy.Mol Diagn Ther2023
37961570Patterns of subregional cerebellar atrophy across epilepsy syndromes: An ENIGMA-Epilepsy study.bioRxiv2023
37479371Climate change and neurology: time to talk and to act.Lancet Neurol2023
37501353Epilepsy is an important feature of KBG syndrome associated with poorer developmental outcome.Epilepsia Open2023
37639957Erratum to ' Taking action on climate change: Testimonials and position statement from the International League Against Epilepsy Climate Change Commission' [Seizure Volume 106, March 2023, Pages 68-75].Seizure2023
37021337Sex-based electroclinical differences and prognostic factors in epilepsy with eyelid myoclonia.Epilepsia2023
37006128Widespread genomic influences on phenotype in Dravet syndrome, a 'monogenic' condition.Brain2023
37403762Missense variants in RPH3A cause defects in excitatory synaptic function and are associated with a clinically variable neurodevelopmental disorder.Genet Med2023
37364985Risk-conferring <i>HLA</i> variants in an epilepsy cohort: benefits of multifaceted use of whole genome sequencing in clinical practice.J Neurol Neurosurg Psychiatry2023
36549242Shaping the future of European epilepsy research: Final meeting report from EPICLUSTER.Epilepsy Res2023
36852571Multimodal mapping of regional brain vulnerability to focal cortical dysplasia.Brain2023
36715146SCN1A: bioinformatically informed revised boundaries for promoter and enhancer regions.Hum Mol Genet2023
36398398Short- and long-interval intracortical inhibition in EPM1 is related to genotype.Epilepsia2023
36774776Taking action on climate change: Testimonials and position statement from the International League Against Epilepsy Climate Change Commission.Seizure2023
36799507Distinct genetic basis of common epilepsies and structural magnetic resonance imaging measures.Epilepsia2023
34388852A systems-level analysis highlights microglial activation as a modifying factor in common epilepsies.Neuropathol Appl Neurobiol2022
35679801The role of common genetic variation in presumed monogenic epilepsies.EBioMedicine2022
35551471SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibility.Acta Neuropathol2022
35800886The impact of Transcranial Magnetic Stimulation (TMS) on seizure course in people with and without epilepsy.Clin Neurophysiol Pract2022
35764379Uncovering the burden of hidden ciliopathies in the 100 000 Genomes Project: a reverse phenotyping approach.J Med Genet2022
35395505National compliance with UK wide guidelines for usage of valproate in women of childbearing potential.Seizure2022
36178910Alternating hemiplegia of childhood: An electroclinical study of sleep and hemiplegia.PLoS One2022
35907043Risk factors and outcome of hyperammonaemia in people with epilepsy.J Neurol2022
36176564Case report: Dravet syndrome, feeding difficulties and gastrostomy.Front Neurol2022
36307934The spectrum of epilepsy with eyelid myoclonia: delineation of disease subtypes from a large multicenter study.Epilepsia2022
35866186Physiological symmetry of transcranial magnetic stimulation-evoked EEG spectral features.Hum Brain Mapp2022
35896547Structural network alterations in focal and generalized epilepsy assessed in a worldwide ENIGMA study follow axes of epilepsy risk gene expression.Nat Commun2022
36192182The Phenotypic Continuum of <i>ATP1A3</i>-Related Disorders.Neurology2022
36288729A founder event causing a dominant childhood epilepsy survives 800 years through weak selective pressure.Am J Hum Genet2022
35948562Local molecular and global connectomic contributions to cross-disorder cortical abnormalities.Nat Commun2022
35333312Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy.Brain2022
35298028A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetam.Epilepsia2022
35292555Electroclinical Features and Long-term Seizure Outcome in Patients With Eyelid Myoclonia With Absences.Neurology2022
34820881Non-coding regulatory elements: Potential roles in disease and the case of epilepsy.Neuropathol Appl Neurobiol2022
34693554Cardiac Investigations in Sudden Unexpected Death in DEPDC5-Related Epilepsy.Ann Neurol2022
32559314MRI and pathology correlations in the medulla in sudden unexpected death in epilepsy (SUDEP): a postmortem study.Neuropathol Appl Neurobiol2021
33570168The impact of COVID-19 in Dravet syndrome: A UK survey.Acta Neurol Scand2021
33903184Real-life survey of pitfalls and successes of precision medicine in genetic epilepsies.J Neurol Neurosurg Psychiatry2021
33504645<i>RHOBTB2</i> Mutations Expand the Phenotypic Spectrum of Alternating Hemiplegia of Childhood.Neurology2021
34859220Whole-genome sequencing: identification of additional pathogenic variation across the genome.Brain Commun2021
35141355Non-Stationary Outcome of Alternating Hemiplegia of Childhood into Adulthood.Mov Disord Clin Pract2021
34817708Rare and Complex Epilepsies from Childhood to Adulthood: Requirements for Separate Management or Scope for a Lifespan Holistic Approach?Curr Neurol Neurosci Rep2021
34814066Meeting report: EpiXchange II brings together European epilepsy research projects to discuss latest advances.Epilepsy Res2021
34729477K.Vita: a feasibility study of a blend of medium chain triglycerides to manage drug-resistant epilepsy.Brain Commun2021
34462915Carbon emission savings and short-term health care impacts from telemedicine: An evaluation in epilepsy.Epilepsia2021
34753039Late-life terminal seizure freedom in drug-resistant epilepsy: "Burned-out epilepsy".J Neurol Sci2021
345168224-Aminopyridine is a promising treatment option for patients with gain-of-function <i>KCNA2</i>-encephalopathy.Sci Transl Med2021
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