Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson’s disease
Paul J. Hop(Utrecht University), John E. Landers(University of Massachusetts Chan Medical School)
Cited by 70
Related Papers
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis
|Nature Genetics|2009|404
Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study
|The Lancet Neurology|2010|226
Reduced expression of the <i>Kinesin-Associated Protein 3</i> ( <i>KIFAP3</i> ) gene increases survival in sporadic amyotrophic lateral sclerosis
|Proceedings of the National Academy of Sciences|2009|185
Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder
|Nature Communications|2021|52