Maarten Kooyman
5PUBLICATIONS
129CO-AUTHORS
Get your video featured.
Publish with JoVEGet your video featured.
Publish with JoVE
Publications (5)
Sort by Publication Date:
|Mar 31, 2026
Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis.Paul J Hop, Maarten Kooyman, Brendan J Kenna
|Oct 11, 2024
A Rare Noncoding Enhancer Variant in SCN5A Contributes to the High Prevalence of Brugada Syndrome in Thailand.Roddy Walsh, John Mauleekoonphairoj, Isabella Mengarelli
|Jun 10, 2024
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's disease.Paul J Hop, Dongbing Lai, Pamela J Keagle
|Feb 01, 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.Wouter van Rheenen, Rick A A van der Spek, Mark K Bakker
|Dec 07, 2021
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.Wouter van Rheenen, Rick A A van der Spek, Mark K Bakker
Pageof 1
Frequent Collaborators
4 joint publications
John E Landers
4 joint publications
Jan H Veldink
4 joint publications
Nicola Ticozzi
3 joint publications
Wouter van Rheenen
3 joint publications
Blaž Koritnik
3 joint publications
Vera Fominykh
3 joint publications
Simon Topp
3 joint publications
Boris Rogelj
3 joint publications
Marc Gotkine
3 joint publications
Ahmad Al Khleifat
