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Andreja Avbersek

Researcher at UCL Institute of Neurology

Publications -  29
Citations -  2473

Andreja Avbersek is an academic researcher from UCL Institute of Neurology. The author has contributed to research in topics: Epilepsy & Medicine. The author has an hindex of 11, co-authored 21 publications receiving 1880 citations. Previous affiliations of Andreja Avbersek include Epilepsy Society & UCB.

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Journal ArticleDOI

Analysis of shared heritability in common disorders of the brain

Verneri Anttila, +720 more
- 22 Jun 2018 - 
TL;DR: It is demonstrated that, in the general population, the personality trait neuroticism is significantly correlated with almost every psychiatric disorder and migraine, and it is shown that both psychiatric and neurological disorders have robust correlations with cognitive and personality measures.
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Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies

Bassel Abou-Khalil, +158 more
TL;DR: The authors perform genome-wide association studies for 3 broad and 7 subtypes of epilepsy and identify 16 loci - 11 novel - that are further annotated by eQTL and partitioned heritability analyses that provide leads for epilepsy therapies based on underlying pathophysiology.
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Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies

Richard Anney, +111 more
- 30 Jul 2014 - 
TL;DR: This meta-analysis describes a new locus not previously implicated in epilepsy and provides further evidence about the genetic architecture of these disorders, with the ultimate aim of assisting in disease classification and prognosis.
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Does the Primary Literature Provide Support for Clinical Signs Used to Distinguish Psychogenic Nonepileptic Seizures From Epileptic Seizures

TL;DR: Postictal stertorous breathing proved to distinguish convulsive PNES from generalised tonic clonic seizures (GTCS) and should be added to the list of useful clinical signs.
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Clinical and dopamine transporter imaging characteristics of non-manifest LRRK2 and GBA mutation carriers in the Parkinson's Progression Markers Initiative (PPMI): a cross-sectional study

Tanya Simuni, +132 more
- 01 Jan 2020 - 
TL;DR: The authors' data show evidence of subtle motor and non-motor signs of Parkinson's disease in non-manifesting carriers compared with healthy controls that can precede DAT deficit.