Rick A. Van Der Spek

Utrecht, UT, Netherlands

Last Updated: 09/26/2026

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Found 22 publications

Lessons from a systematic review of family-based studies in ALS.

Lessons from a systematic review of family-based studies in ALS.

Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration

Published: August 12, 2026

Genetic variability in sporadic amyotrophic lateral sclerosis.

Genetic variability in sporadic amyotrophic lateral sclerosis.

Journal: Brain : a journal of neurology

Published: November 16, 2022

Telomere length analysis in amyotrophic lateral sclerosis using large-scale whole genome sequence data.

Telomere length analysis in amyotrophic lateral sclerosis using large-scale whole genome sequence data.

Journal: Frontiers in cellular neuroscience

Published: September 21, 2022

Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.

Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.

Journal: Nature genetics

Published: February 01, 2022

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.

Journal: Nature genetics

Published: March 12, 2021

Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors.

Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors.

Journal: Nature genetics

Published: December 23, 2020

Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis.

Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis.

Journal: NPJ genomic medicine

Published: December 15, 2020

The Effect of SMN Gene Dosage on ALS Risk and Disease Severity.

The Effect of SMN Gene Dosage on ALS Risk and Disease Severity.

Journal: Annals of neurology

Published: September 11, 2020

Whole-genome sequencing reveals that variants in the Interleukin 18 Receptor Accessory Protein 3'UTR protect against ALS.

Whole-genome sequencing reveals that variants in the Interleukin 18 Receptor Accessory Protein 3'UTR protect against ALS.

Journal: Nature neuroscience

Published: April 22, 2020

ATXN1 repeat expansions confer risk for amyotrophic lateral sclerosis and contribute to TDP-43 mislocalization.

ATXN1 repeat expansions confer risk for amyotrophic lateral sclerosis and contribute to TDP-43 mislocalization.

Journal: Brain communications

Published: March 24, 2020

Associations between lifestyle and amyotrophic lateral sclerosis stratified by C9orf72 genotype: a longitudinal, population-based, case-control study.

Associations between lifestyle and amyotrophic lateral sclerosis stratified by C9orf72 genotype: a longitudinal, population-based, case-control study.

Journal: The Lancet. Neurology

Published: March 24, 2020

Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors.

Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors.

Journal: Nature genetics

Published: February 24, 2020

Showing 1-12 of 22

Last Updated: 09/26/2026