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Author

T. Courtin

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Sep 2026

Exploring the genetic spectrum of parkinsonism in Brazil.

WES proved valuable in detecting rare pathogenic variants in Brazilian patients, uncovering atypical phenotypes and expanding the spectrum of genetic findings, highlighting the need for broader genetic studies in admixed populations to refine diagnostics and better characterize such unique cohorts.

M. G. Ferreira, C. Tesson, T. Courtin et al. · 0 citations
Sep 2026

Monoallelic variants in BRSK1 are associated with a neurodevelopmental disorder with or without epilepsy.

The data support a model that heterozygous loss of BRSK1 leads to a neurodevelopmental syndrome with variable phenotypes and indicates that the three individual-derived alleles provide only a partial rescue and fail to normalize NMJ morphology and Futsch levels, suggesting that they are partial loss-of-function alleles...

Ming-Xi Deng, Meng-Qi Ma, Vanessa A. Gomez et al. · 0 citations
Jun 2026

RBMX functional retrocopy safeguards brain development in a species-dependent context.

It is demonstrated that RBMX and RBMXL1 share protein and RNA partners and act redundantly in brain development, with RBMXL1 buffering the impact of RBMX deficiency and establishing RBMXL1 as a functional paralog of RBMX that is likely buffering deleterious variation in a context- and dosage-dependent manner.

P. Tilliole, C. Mattausch, Peggy Tilly et al. · 0 citations

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