Nicolas Marotta

5PUBLICATIONS
27CO-AUTHORS
Neurology and neuromuscular diseasesGene mappingSensory systemsGene and molecular therapy
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Publications (5)

|Sep 07, 2026
Pathogenic KIF1A variants differentially disrupt axonal trafficking and impede synaptic development.

|Jul 14, 2026
Translatable electrophysiological and behavioral abnormalities in a humanized model of SYNGAP1-disorder.

|Nov 24, 2025
CRISPR-mediated transcriptional activation as a mutation-independent therapeutic strategy for SYNGAP1-related intellectual disability.

Laura Sichlinger, Molly B Reilly, Sakshi Arora

|Jan 02, 2021
Emerging and converging molecular mechanisms in dystonia.

Paulina Gonzalez-Latapi, Nicolas Marotta, Niccolò E Mencacci

|Nov 25, 2020
EIF2AK2 Missense Variants Associated with Early Onset Generalized Dystonia.

Demy J S Kuipers, Wim Mandemakers, Chin-Song Lu

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Frequent Collaborators

3 joint publications

Benjamin L Prosser

1 joint publications

Demy J S Kuipers

1 joint publications

Tu-Hsueh Yeh

1 joint publications

Katja Lohmann