Gijs P. Tazelaar
Utrecht, UT, Netherlands
Last Updated: 09/26/2026
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Found 9 publications
Whole genome sequencing analysis reveals post-zygotic mutation variability in monozygotic twins discordant for amyotrophic lateral sclerosis.
Journal: Neurobiology of aging
Published: May 11, 2022
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS.
Journal: Science translational medicine
Published: February 23, 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.
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.
Journal: Nature genetics
Published: March 12, 2021
Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosis.
Journal: Scientific reports
Published: August 28, 2018
Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohort.
Journal: Neurobiology of aging
Published: May 11, 2018
Detection of long repeat expansions from PCR-free whole-genome sequence data.
Journal: Genome research
Published: June 01, 2017
Showing 1-9 of 9
Last Updated: 09/26/2026