Brendan J. Kenna
Utrecht, UT, Netherlands
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 10 publications
Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis.
Journal: Nature genetics
Published: August 15, 2025
Sex-specific DNA methylation differences in Amyotrophic lateral sclerosis.
Journal: bioRxiv : the preprint server for biology
Published: December 09, 2024
SpliPath enhances disease gene discovery in case-control analyses of rare splice-altering genetic variants.
Journal: Cell reports methods
Published: October 17, 2024
Telomere length analysis in amyotrophic lateral sclerosis using large-scale whole genome sequence data.
Journal: Frontiers in cellular neuroscience
Published: September 21, 2022
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.
Journal: Annals of neurology
Published: September 11, 2020
Genetic analysis of ALS cases in the isolated island population of Malta.
Journal: European journal of human genetics : EJHG
Published: May 06, 2020
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis.
Journal: Nature genetics
Published: February 25, 2016
Showing 1-10 of 10
Last Updated: 09/26/2026