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Author Details
Full Name
Sanjay M Sisodiya
Affiliation
UCL Institute of Neurology
ORCID
Career Start Year
1986
Papers
416
H Index
82
Expertise
CM4AI Collaborator
Andrej Sali (CM4AI)
PMID
Paper Title
Journal Title
Published Year
37949657
Hot brain: practical climate change advice for neurologists.
Pract Neurol
2024
38088023
Dissecting genetics of spectrum of epilepsies with eyelid myoclonia by exome sequencing.
Epilepsia
2024
36941776
Climate change and the brain.
Brain
2023
37755653
Steps to Improve Precision Medicine in Epilepsy.
Mol Diagn Ther
2023
37961570
Patterns of subregional cerebellar atrophy across epilepsy syndromes: An ENIGMA-Epilepsy study.
bioRxiv
2023
37479371
Climate change and neurology: time to talk and to act.
Lancet Neurol
2023
37501353
Epilepsy is an important feature of KBG syndrome associated with poorer developmental outcome.
Epilepsia Open
2023
37639957
Erratum 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].
Seizure
2023
37021337
Sex-based electroclinical differences and prognostic factors in epilepsy with eyelid myoclonia.
Epilepsia
2023
37006128
Widespread genomic influences on phenotype in Dravet syndrome, a 'monogenic' condition.
Brain
2023
37403762
Missense variants in RPH3A cause defects in excitatory synaptic function and are associated with a clinically variable neurodevelopmental disorder.
Genet Med
2023
37364985
Risk-conferring <i>HLA</i> variants in an epilepsy cohort: benefits of multifaceted use of whole genome sequencing in clinical practice.
J Neurol Neurosurg Psychiatry
2023
36549242
Shaping the future of European epilepsy research: Final meeting report from EPICLUSTER.
Epilepsy Res
2023
36852571
Multimodal mapping of regional brain vulnerability to focal cortical dysplasia.
Brain
2023
36715146
SCN1A: bioinformatically informed revised boundaries for promoter and enhancer regions.
Hum Mol Genet
2023
36398398
Short- and long-interval intracortical inhibition in EPM1 is related to genotype.
Epilepsia
2023
36774776
Taking action on climate change: Testimonials and position statement from the International League Against Epilepsy Climate Change Commission.
Seizure
2023
36799507
Distinct genetic basis of common epilepsies and structural magnetic resonance imaging measures.
Epilepsia
2023
34388852
A systems-level analysis highlights microglial activation as a modifying factor in common epilepsies.
Neuropathol Appl Neurobiol
2022
35679801
The role of common genetic variation in presumed monogenic epilepsies.
EBioMedicine
2022
35551471
SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibility.
Acta Neuropathol
2022
35800886
The impact of Transcranial Magnetic Stimulation (TMS) on seizure course in people with and without epilepsy.
Clin Neurophysiol Pract
2022
35764379
Uncovering the burden of hidden ciliopathies in the 100 000 Genomes Project: a reverse phenotyping approach.
J Med Genet
2022
35395505
National compliance with UK wide guidelines for usage of valproate in women of childbearing potential.
Seizure
2022
36178910
Alternating hemiplegia of childhood: An electroclinical study of sleep and hemiplegia.
PLoS One
2022
35907043
Risk factors and outcome of hyperammonaemia in people with epilepsy.
J Neurol
2022
36176564
Case report: Dravet syndrome, feeding difficulties and gastrostomy.
Front Neurol
2022
36307934
The spectrum of epilepsy with eyelid myoclonia: delineation of disease subtypes from a large multicenter study.
Epilepsia
2022
35866186
Physiological symmetry of transcranial magnetic stimulation-evoked EEG spectral features.
Hum Brain Mapp
2022
35896547
Structural network alterations in focal and generalized epilepsy assessed in a worldwide ENIGMA study follow axes of epilepsy risk gene expression.
Nat Commun
2022
36192182
The Phenotypic Continuum of <i>ATP1A3</i>-Related Disorders.
Neurology
2022
36288729
A founder event causing a dominant childhood epilepsy survives 800 years through weak selective pressure.
Am J Hum Genet
2022
35948562
Local molecular and global connectomic contributions to cross-disorder cortical abnormalities.
Nat Commun
2022
35333312
Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy.
Brain
2022
35298028
A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetam.
Epilepsia
2022
35292555
Electroclinical Features and Long-term Seizure Outcome in Patients With Eyelid Myoclonia With Absences.
Neurology
2022
34820881
Non-coding regulatory elements: Potential roles in disease and the case of epilepsy.
Neuropathol Appl Neurobiol
2022
34693554
Cardiac Investigations in Sudden Unexpected Death in DEPDC5-Related Epilepsy.
Ann Neurol
2022
32559314
MRI and pathology correlations in the medulla in sudden unexpected death in epilepsy (SUDEP): a postmortem study.
Neuropathol Appl Neurobiol
2021
33570168
The impact of COVID-19 in Dravet syndrome: A UK survey.
Acta Neurol Scand
2021
33903184
Real-life survey of pitfalls and successes of precision medicine in genetic epilepsies.
J Neurol Neurosurg Psychiatry
2021
33504645
<i>RHOBTB2</i> Mutations Expand the Phenotypic Spectrum of Alternating Hemiplegia of Childhood.
Neurology
2021
34859220
Whole-genome sequencing: identification of additional pathogenic variation across the genome.
Brain Commun
2021
35141355
Non-Stationary Outcome of Alternating Hemiplegia of Childhood into Adulthood.
Mov Disord Clin Pract
2021
34817708
Rare and Complex Epilepsies from Childhood to Adulthood: Requirements for Separate Management or Scope for a Lifespan Holistic Approach?
Curr Neurol Neurosci Rep
2021
34814066
Meeting report: EpiXchange II brings together European epilepsy research projects to discuss latest advances.
Epilepsy Res
2021
34729477
K.Vita: a feasibility study of a blend of medium chain triglycerides to manage drug-resistant epilepsy.
Brain Commun
2021
34462915
Carbon emission savings and short-term health care impacts from telemedicine: An evaluation in epilepsy.
Epilepsia
2021
34753039
Late-life terminal seizure freedom in drug-resistant epilepsy: "Burned-out epilepsy".
J Neurol Sci
2021
34516822
4-Aminopyridine is a promising treatment option for patients with gain-of-function <i>KCNA2</i>-encephalopathy.
Sci Transl Med
2021
1 - 50 of 416
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