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A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants

artículo científico publicado en 2012

Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders

Blood RNA biomarkers in prodromal PARK4 and rapid eye movement sleep behavior disorder show role of complexin 1 loss for risk of Parkinson's disease.

artículo científico publicado en 2017

Genomewide scan and fine-mapping linkage studies in four European samples with bipolar affective disorder suggest a new susceptibility locus on chromosome 1p35-p36 and provides further evidence of loci on chromosome 4q31 and 6q24.

artículo científico publicado en 2005

Large-scale replication and heterogeneity in Parkinson disease genetic loci

artículo científico publicado en 2012

Mutations in CIZ1 cause adult onset primary cervical dystonia

artículo científico publicado en 2012

Protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants

artículo científico publicado en 2013

Sensory neuropathy and nociception in rodent models of Parkinson's disease

artículo científico publicado en 2019

The first genomewide interaction and locus-heterogeneity linkage scan in bipolar affective disorder: strong evidence of epistatic effects between loci on chromosomes 2q and 6q.

artículo científico publicado en 2007

Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder families

scientific article published on 04 February 2020

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