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List of works by Sanjay M Sisodiya

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Identification of common variants associated with human hippocampal and intracranial volumes

scientific article published on 15 April 2012
Common genetic variants influence human subcortical brain structures

scientific article
The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

scientific article
Analysis of shared heritability in common disorders of the brain

scientific article published on 21 June 2018
Novel genetic loci underlying human intracranial volume identified through genome-wide association

scientific article (publication date: 3 October 2016)
Novel genetic loci associated with hippocampal volume

scientific article published on 18 January 2017
ENIGMA and the individual: Predicting factors that affect the brain in 35 countries worldwide

scientific article published on 4 December 2015
Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery

scientific article published in October 2017
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.

scientific article published on 06 September 2013
De novo variants in neurodevelopmental disorders with epilepsy

scientific article published on 25 June 2018
SCN1A testing for epilepsy: application in clinical practice.

scientific article published on 15 April 2013
CHD2 variants are a risk factor for photosensitivity in epilepsy

scientific article published on 17 March 2015
The genetic architecture of the human cerebral cortex

scientific article
Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy

scientific article
Genetic architecture of subcortical brain structures in 38,851 individuals

scientific article published on 21 October 2019
Genome annotation for clinical genomic diagnostics: strengths and weaknesses

scientific article
Neurologic phenotypes associated with / mutations: Expanding the spectrum of disease

scientific article published on 09 November 2018
Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study

article
The landscape of epilepsy-related GATOR1 variants

scientific article published on 10 August 2018
Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2

scientific article published on 29 October 2019
Diagnostic implications of genetic copy number variation in epilepsy plus

scientific article published on 13 March 2019
Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition

scientific article published on 30 October 2019
The spectrum of intermediate SCN8A-related epilepsy

scientific article published on 10 April 2019
Correction to: The landscape of epilepsy-related GATOR1 variants

scientific article published on 01 July 2019
An assessment of the Irish population for large-scale genetic mapping studies involving epilepsy and other complex diseases

Re-annotation of 191 developmental and epileptic encephalopathy-associated genes unmasks de novo variants in SCN1A

scientific article published on 02 December 2019
Clinical spectrum of STX1B-related epileptic disorders.

scientific article published on 8 February 2019
Correction: The landscape of epilepsy-related GATOR1 variants

scientific article published on 01 August 2019
Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

scholarly article published 28 August 2017
Possible role of SCN4A skeletal muscle mutation in apnea during seizure

scientific article published on 01 July 2019
Genetics of epilepsy: epilepsy research foundation workshop report

scientific article published in June 2007
The genetic architecture of the human cerebral cortex

White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA-Epilepsy study

scientific article published on 20 August 2020
1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans

scientific article published on 22 March 2021
NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns

scientific article published on 04 November 2020
Comparative effectiveness of antiepileptic drugs in juvenile myoclonic epilepsy

scientific article published on 04 July 2019
Testing association of rare genetic variants with resistance to three common antiseizure medications

scientific article published on 06 March 2020
Advancing research toward faster diagnosis, better treatment, and end of stigma in epilepsy

scientific article published on 18 June 2019
Climate change and epilepsy: Time to take action

scientific article published on 20 September 2019
Climate change and the brain

scientific article published in 2023
Spectrum of epilepsy with eyelid myoclonia: Delineation of disease subtypes from a large multicenter study

Patterns of subregional cerebellar atrophy across epilepsy syndromes: An ENIGMA‐Epilepsy study

Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia

scientific article published on 01 March 2020
A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetam

scientific article published in April 2022
Associations between epilepsy-related polygenic risk and brain morphology in childhood

A worldwide ENIGMA study on epilepsy-related gray and white matter compromise across the adult lifespan

Neuropeptide depletion in the amygdala in sudden unexpected death in epilepsy: A postmortem study

scientific article published on 20 January 2020
Climate change and hyponatremia‐related hospital admissions in people with focal epilepsy exposed to carbamazepine or its derivatives

scientific article published on 2 August 2025
Patterns of subregional cerebellar atrophy across epilepsy syndromes: An ENIGMA-Epilepsy study

Genomic and clinical predictors of lacosamide response in refractory epilepsies

scientific article published on 25 September 2019

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