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Simon Topp

12PUBLICATIONS

163CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)Cancer diagnosisEpigenetics (incl. genome methylation and epigenomics)Developmental genetics (incl. sex determination)Neurogenetics

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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

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

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