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Author Details

Michael R Johnson
Imperial College London
1995
79
32
PMIDPaper TitleJournal TitlePublished Year
37582616LGI1 Encephalitis and IgG4-Related Disease: Rare Conditions Collide.Neurol Neuroimmunol Neuroinflamm2023
37554649Translocator protein PET imaging in temporal lobe epilepsy: A reliable test-retest study using asymmetry index.Front Neuroimaging2023
35093191Epigenomic priming of immune genes implicates oligodendroglia in multiple sclerosis susceptibility.Neuron2022
33665823Cardiac glycosides cause cytotoxicity in human macrophages and ameliorate white adipose tissue homeostasis.Br J Pharmacol2022
34309761Cross-platform transcriptional profiling identifies common and distinct molecular pathologies in Lewy body diseases.Acta Neuropathol2021
34401672Signatures of TSPAN8 variants associated with human metabolic regulation and diseases.iScience2021
34018700Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsy.Ann Clin Transl Neurol2021
34177598Role of Common Genetic Variants for Drug-Resistance to Specific Anti-Seizure Medications.Front Pharmacol2021
32141622Testing association of rare genetic variants with resistance to three common antiseizure medications.Epilepsia2020
33758823Implication of sestrin3 in epilepsy and its comorbidities.Brain Commun2020
31785261A systems-level framework for anti-epilepsy drug discovery.Neuropharmacology2020
31956041Re: Time to move beyond genetics towards biomedical data-driven translational genomic research in severe paediatric epilepsies.Eur J Paediatr Neurol2020
31976861Human hippocampal CA3 damage disrupts both recent and remote episodic memories.Elife2020
31678583Proof-of-concept that network pharmacology is effective to modify development of acquired temporal lobe epilepsy.Neurobiol Dis2020
32308125Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study.Pharmacogenomics2020
32301721Epigenetics explained: a topic "primer" for the epilepsy community by the ILAE Genetics/Epigenetics Task Force.Epileptic Disord2020
30868120A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine.Epilepsia Open2019
31819912Genomic and clinical predictors of lacosamide response in refractory epilepsies.Epilepsia Open2019
31440723Comparative effectiveness of antiepileptic drugs in juvenile myoclonic epilepsy.Epilepsia Open2019
31420939Integrated systems-genetic analyses reveal a network target for delaying glioma progression.Ann Clin Transl Neurol2019
29288229Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients.Neurology2018
30177815A systems-level framework for drug discovery identifies Csf1R as an anti-epileptic drug target.Nat Commun2018
30033060Rare coding variants in genes encoding GABA<sub>A</sub> receptors in genetic generalised epilepsies: an exome-based case-control study.Lancet Neurol2018
27884611Microglial positron emission tomography (PET) imaging in epilepsy: Applications, opportunities and pitfalls.Seizure2017
28250018Genome-wide analysis of differential RNA editing in epilepsy.Genome Res2017
28212175Advances in epilepsy gene discovery and implications for epilepsy diagnosis and treatment.Curr Opin Neurol2017
28369215Focal CA3 hippocampal subfield atrophy following LGI1 VGKC-complex antibody limbic encephalitis.Brain2017
28960286Standardization procedure for plasma biomarker analysis in rat models of epileptogenesis: Focus on circulating microRNAs.Epilepsia2017
29291240Meta-Analysis of MicroRNAs Dysregulated in the Hippocampal Dentate Gyrus of Animal Models of Epilepsy.eNeuro2017
28530675Reevaluation of SNP heritability in complex human traits.Nat Genet2017
26691832Systems genetics identifies a convergent gene network for cognition and neurodevelopmental disease.Nat Neurosci2016
27955713Rare and common epilepsies converge on a shared gene regulatory network providing opportunities for novel antiepileptic drug discovery.Genome Biol2016
26708060NRSF and BDNF polymorphisms as biomarkers of cognitive dysfunction in adults with newly diagnosed epilepsy.Epilepsy Behav2016
25550428EvoTol: a protein-sequence based evolutionary intolerance framework for disease-gene prioritization.Nucleic Acids Res2015
26382856MicroRNA profiles in hippocampal granule cells and plasma of rats with pilocarpine-induced epilepsy--comparison with human epileptic samples.Sci Rep2015
27066543Epileptic encephalopathy-causing mutations in DNM1 impair synaptic vesicle endocytosis.Neurol Genet2015
25615886Systems genetics identifies Sestrin 3 as a regulator of a proconvulsant gene network in human epileptic hippocampus.Nat Commun2015
23962720A genome-wide association study and biological pathway analysis of epilepsy prognosis in a prospective cohort of newly treated epilepsy.Hum Mol Genet2014
25282706Validation of a multigenic model to predict seizure control in newly treated epilepsy.Epilepsy Res2014
25063994Describing the genetic architecture of epilepsy through heritability analysis.Brain2014
24567120A comprehensive functional and clinical analysis of ABCC2 and its impact on treatment response to carbamazepine.Pharmacogenomics J2014
24323053The emerging agenda of stratified medicine in neurology.Nat Rev Neurol2014
24014519Faciobrachial dystonic seizures: the influence of immunotherapy on seizure control and prevention of cognitive impairment in a broadening phenotype.Brain2013
24314551Response to Lee et al.: SNP-based heritability analysis with dense data.Am J Hum Genet2013
23934111De novo mutations in epileptic encephalopathies.Nature2013
22976776Monozygotic twins with LRRK2 mutations: genetically identical but phenotypically discordant.Mov Disord2012
23259578cnvHiTSeq: integrative models for high-resolution copy number variation detection and genotyping using population sequencing data.Genome Biol2012
23217325Improved heritability estimation from genome-wide SNPs.Am J Hum Genet2012
21219308Comment on "Blinders, phenotype, and fashionable genetic analysis: a critical examination of the current state of epilepsy genetic studies".Epilepsia2011
21890419Heredity in epilepsy: neurodevelopment, comorbidity, and the neurological trait.Epilepsy Behav2011
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Collaborators

Josemir W Sander
West China Hospital of Sichuan University
Co-authored papers 14
Norman Delanty
FutureNeuro SFI Research Centre, The Royal College of Surgeons in Ireland
Co-authored papers 13
Sanjay M Sisodiya
UCL Institute of Neurology
Co-authored papers 13
Chantal Depondt
Hopital Universitaire de Bruxelles - Hopital Erasme
Co-authored papers 12
Gianpiero L Cavalleri
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Co-authored papers 12
Terence J O'Brien
Monash University
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Roland Krause
University of Luxembourg
Co-authored papers 9
David B Goldstein
Institute for Genomic Medicine, Columbia University Irving Medical Center
Co-authored papers 7
Alison J Coffey
Co-authored papers 7
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Illumina Cambridge Ltd.
Co-authored papers 6
Ingrid E Scheffer
Co-authored papers 5
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UK Dementia Research Institute Centre at Imperial College London
Co-authored papers 5
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University of North Carolina at Chapel Hill.
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Jane Rogers
The Wellcome Trust Sanger Institute
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Rachel A Gibson
Guy's Hospital
Co-authored papers 3
Owen J L Rackham
Duke-National University of Singapore
Co-authored papers 3
Nicole Walley
Duke University School of Medicine and Duke Health System
Co-authored papers 3
Matthias Schwab
and of Biochemistry and Pharmacy, University of Tuebingen
Co-authored papers 3
Massimo Pandolfo
Universite Libre de Bruxelles (ULB)
Co-authored papers 3
Dalia Kasperaviciute
Genomics England Ltd.
Co-authored papers 3
Aarno Palotie
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Colin P Doherty
St James's Hospital
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Kevin V Shianna
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John S Duncan
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Release 1.2