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List of works by Serena Lattante

ATXN2 trinucleotide repeat length correlates with risk of ALS.

scientific article

Characterization of the p.L145F and p.S135N Mutations in SOD1: Impact on the Metabolism of Fibroblasts Derived from Amyotrophic Lateral Sclerosis Patients

scientific article published on 22 April 2022

Contribution of ATXN2 intermediary polyQ expansions in a spectrum of neurodegenerative disorders

scientific article

Defining the genetic connection linking amyotrophic lateral sclerosis (ALS) with frontotemporal dementia (FTD).

scientific article published on 10 April 2015

High-Throughput Genetic Testing in ALS: The Challenging Path of Variant Classification Considering the ACMG Guidelines

scientific article published on 24 September 2020

Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype ⬇️

scientific article published on April 29, 2012

Mutations in the PFN1 gene are not a common cause in patients with amyotrophic lateral sclerosis and frontotemporal lobar degeneration in France ⬇️

scientific article published on November 24, 2012

Screening UBQLN-2 in French frontotemporal lobar degeneration and frontotemporal lobar degeneration–amyotrophic lateral sclerosis patients ⬇️

scientific article published on April 10, 2013

TARDBP and FUS mutations associated with amyotrophic lateral sclerosis: summary and update

scientific article published on 29 April 2013

TREM2 mutations are rare in a French cohort of patients with frontotemporal dementia ⬇️

scientific article published on June 4, 2013

The S100A4 Transcriptional Inhibitor Niclosamide Reduces Pro-Inflammatory and Migratory Phenotypes of Microglia: Implications for Amyotrophic Lateral Sclerosis

scientific article published on 16 October 2019

Wolf-Hirschhorn syndrome due to pure and translocation forms of monosomy 4p16.1 → pter

scientific article published on 08 July 2011

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