| Pathogenic Gαo Mutants Drive Dominant GPCR Coupling in GNAO1 Encephalopathies | The FASEB journal |  | | 2026 | 47 | 85 |
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| Loss of the conserved switch III region in a G protein leads to severe pediatric encephalopathy | Science signaling |  | | 2025 | 22 | 0 |
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| The role of acyl cycling in endogenous G protein localization | The Journal of biological chemistry | | | 2025 | 13 | 95 |
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| Clinical-molecular profiling of atypical GNAO1 patients : Novel pathogenic variants, unusual manifestations, and severe molecular dysfunction | Genes & diseases | | | 2025 | 41 | 30 |
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| Dominant Gα mutations in human disease : unifying mechanisms and treatment strategies | EMBO molecular medicine | | | 2025 | 42 | 258 |
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| Atypical GNAO1 variants in severe childhood speech disorders: clinical, genetic, and molecular insights | Molecular autism | | | 2025 | 17 | 26 |
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| Neomorphic Gαo mutations gain interaction with Ric8 proteins in GNAO1 encephalopathies | The Journal of clinical investigation | | | 2024 | 102 | 111 |
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| Response to Mortimer et al. “Clinical and molecular profiling in GNAO1 permits phenotype–genotype correlation” | Movement disorders | | | 2024 | 78 | 0 |
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| Clinical and Molecular Profiling in GNAO1 Permits Phenotype–Genotype Correlation | Movement disorders | | | 2024 | 103 | 221 |
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| GNAO1 Mutations Affecting the N‐Terminal α‐Helix of Gαo Lead to Parkinsonism | Movement disorders | | | 2024 | 119 | 265 |
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| Clinical Cases and the Molecular Profiling of a Novel Childhood Encephalopathy-Causing GNAO1 Mutation P170R | Cells | | | 2023 | 120 | 92 |
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| In-depth molecular profiling of an intronic GNAO1 mutant as the basis for personalized high-throughput drug screening | Med | | | 2023 | 139 | 1 |
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| Local and substrate-specific S-palmitoylation determines subcellular localization of Gαo | Nature communications | | | 2022 | 308 | 247 |
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| Gαi2-induced conductin/axin2 condensates inhibit Wnt/β-catenin signaling and suppress cancer growth | Nature communications | | | 2022 | 382 | 299 |
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| Restoration of the GTPase activity and cellular interactions of Gαo mutants by Zn2+ in GNAO1 encephalopathy models | Science advances | | | 2022 | 212 | 201 |
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| Pediatric encephalopathy: cinical, biochemical and cellular insights into the role of Gln52 of GNAO1 and GNAI1 for the dominant disease | Cells | | | 2021 | 409 | 243 |
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| Humanization of Drosophila Gαo to model GNAO1 paediatric encephalopathies | Biomedicines | | | 2020 | 320 | 165 |
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| HumanaFly: high-throughput transgenesis and expression of breast cancer transcripts in Drosophila eye discovers the RPS12-Wingless signaling axis | Scientific Reports | | | 2020 | 296 | 95 |
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| High capacity in G protein-coupled receptor signaling | Nature Communications | | | 2018 | 394 | 223 |
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| Gαo (GNAO1)encephalopathies: plasma membrane vs. Golgi functions | Oncotarget | | | 2018 | 266 | 157 |
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| Golgi-Resident Gαo Promotes Protrusive Membrane Dynamics | Cell | | | 2017 | 484 | 499 |
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| Reggie-1/Flotillin-2 regulates integrin trafficking and focal adhesion turnover via Rab11a | European Journal of Cell Biology | | | 2015 | 435 | 0 |
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