Gonzalo P. Solis
Geneve, GE 1211, Switzerland
Last Updated: 09/26/2026
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Found 31 publications
Loss of the conserved switch III region in a G protein leads to severe pediatric encephalopathy.
Journal: Science signaling
Published: October 28, 2025
Atypical GNAO1 variants in severe childhood speech disorders: clinical, genetic, and molecular insights.
Journal: Molecular autism
Published: October 07, 2025
The role of acyl cycling in endogenous G protein localization.
Journal: The Journal of biological chemistry
Published: September 17, 2025
A Personalized 14-3-3 Disease-Targeting Workflow Yields Repositioning Drug Candidates.
Journal: Cells
Published: March 03, 2025
Dominant Gα mutations in human disease: unifying mechanisms and treatment strategies.
Journal: EMBO molecular medicine
Published: February 05, 2025
Response to Mortimer et al. "Clinical and molecular profiling in GNAO1 permits phenotype-genotype correlation".
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: August 29, 2024
Clinical-molecular profiling of atypical GNAO1 patients: Novel pathogenic variants, unusual manifestations, and severe molecular dysfunction.
Journal: Genes & diseases
Published: August 13, 2024
Clinical and Molecular Profiling in GNAO1 Permits Phenotype-Genotype Correlation.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: January 26, 2024
GNAO1 Mutations Affecting the N-Terminal α-Helix of Gαo Lead to Parkinsonism.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: September 25, 2023
Neomorphic Gαo mutations gain interaction with Ric8 proteins in GNAO1 encephalopathies.
Journal: The Journal of clinical investigation
Published: May 15, 2023
Last Updated: 09/26/2026