Identification of common genetic markers of paroxysmal neurological disorders using a network analysis approach
Muhammad Ilyas(Islamia College University), Henry Houlden(University College London), Thomas Bourinaris(University College London), Maria Imdad(Hazara University), Habib Ahmad(Islamia College University), Vincenzo Salpietro(University College London), Akmal Ahmad(Hazara University), Ayesha Tariq(National Center for Nanoscience and Technology), Stéphanie Efthymiou(Queen Mary University of London)
Cited by 9
Related Papers
Genome-wide association study reveals genetic risk underlying Parkinson's disease
|Nature Genetics|2009|2k
A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1
|Nature Medicine|1998|349
Spinocerebellar ataxia: an update
|Journal of Neurology|2018|348
5′ Splice Site Mutations in tau Associated with the Inherited Dementia FTDP-17 Affect a Stem-Loop Structure That Regulates Alternative Splicing of Exon 10
|Journal of Biological Chemistry|1999|299
<i>SNCA</i> variants are associated with increased risk for multiple system atrophy
|Annals of Neurology|2009|283