Matthieu Moisse

11PUBLICATIONS
159CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)NeurogeneticsNeurology and neuromuscular diseasesInfant and child health
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Publications (11)

|Apr 01, 2022
Whole-genome sequencing reveals that variants in the Interleukin 18 Receptor Accessory Protein 3'UTR protect against ALS.

Chen Eitan, Aviad Siany, Elad Barkan

|Feb 23, 2022
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS.

Paul J Hop, Ramona A J Zwamborn, Eilis Hannon

|Jan 29, 2022
Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis.

Ahmad Al Khleifat, Alfredo Iacoangeli, Joke J F A van Vugt

|Apr 10, 2021
C9orf72-derived arginine-containing dipeptide repeats associate with axonal transport machinery and impede microtubule-based motility.

Laura Fumagalli, Florence L Young, Steven Boeynaems

|Mar 08, 2021
A Patient with neonatal cholestasis.

Kristl G Claeys, Luc Breysem, Eric Legius

|Jan 03, 2021
The Effect of SMN Gene Dosage on ALS Risk and Disease Severity.

Matthieu Moisse, Ramona A J Zwamborn, Joke van Vugt

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Frequent Collaborators

5 joint publications

Ammar Al-Chalabi

5 joint publications

Jan Veldink

5 joint publications

Philip Van Damme

3 joint publications

Jesús S Mora Pardina