Simon Topp
12PUBLICATIONS
163CO-AUTHORS
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Publications (12)
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|Mar 31, 2026
Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis.Paul J Hop, Maarten Kooyman, Brendan J Kenna
|Jul 02, 2024
Author Correction: The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration.Sarah Opie-Martin, Alfredo Iacoangeli, Simon D Topp
|Sep 28, 2023
SLCO5A1 and synaptic assembly genes contribute to impulsivity in juvenile myoclonic epilepsy.Delnaz Roshandel, Eric J Sanders, Amy Shakeshaft
|Nov 13, 2022
The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration.Sarah Opie-Martin, Alfredo Iacoangeli, Simon D Topp
|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
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Frequent Collaborators
7 joint publications
Ammar Al-Chalabi
7 joint publications
Kelly L Williams
6 joint publications
John E Landers
6 joint publications
Nicola Ticozzi
5 joint publications
Jonathan D Glass
5 joint publications
Jan H Veldink
5 joint publications
Ahmad Al-Khleifat
5 joint publications
Philip Van Damme
5 joint publications
Russell McLaughlin
4 joint publications
Vincenzo Silani
