Frank P. Diekstra
Utrecht, UT, Netherlands
Last Updated: 09/26/2026
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Found 19 publications
Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosis.
Journal: Scientific reports
Published: August 28, 2018
Whole blood transcriptome analysis in amyotrophic lateral sclerosis: A biomarker study.
Journal: PloS one
Published: February 12, 2018
Meta-analysis of pharmacogenetic interactions in amyotrophic lateral sclerosis clinical trials.
Journal: Neurology
Published: May 19, 2017
The role of de novo mutations in the development of amyotrophic lateral sclerosis.
Journal: Human mutation
Published: April 25, 2017
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis.
Journal: Nature genetics
Published: February 25, 2016
Susceptibility loci for sporadic brain arteriovenous malformation; a replication study and meta-analysis.
Journal: Journal of neurology, neurosurgery, and psychiatry
Published: December 08, 2014
Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?
Journal: Brain : a journal of neurology
Published: October 29, 2014
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS.
Journal: Neuron
Published: September 16, 2014
Clonality of anti-GM1 IgM antibodies in multifocal motor neuropathy and the Guillain-Barré syndrome.
Clonality of anti-GM1 IgM antibodies in multifocal motor neuropathy and the Guillain-Barré syndrome.
Journal: Journal of neurology, neurosurgery, and psychiatry
Published: March 18, 2014
C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysis.
Journal: Annals of neurology
Published: December 12, 2013
Last Updated: 09/26/2026