Antonella Consiglio

Bellvitge University Hospital — Spain

Biochemistry, Genetics and Molecular Biology · Life Sciences

36h-index14.0kcitations78works4.52yr avg
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Research Topics

Pluripotent Stem Cells Research(21), CRISPR and Genetic Engineering(21), Parkinson's Disease Mechanisms and Treatments(18), Neurogenesis and neuroplasticity mechanisms(12), Nuclear Receptors and Signaling(10)

Publications77 total

Low-frequency genetic variants in GAK enhance Golgi function and protect against Parkinson’s disease
2025Open Access
LRRK2-mutant microglia and neuromelanin synergize to drive dopaminergic neurodegeneration in an iPSC-based Parkinson’s disease model
Communications Biology·2025· 4 citedOpen Access
Astrocytic Ceruloplasmin Deficiency Triggers Iron Toxicity and Neurodegeneration in a LRRK2 Parkinson’s Tri-Culture Model
2025Open Access
Preparation of α-synuclein pre-formed fibrils (PFF) v2
2025Open Access
Preparation of α-synuclein pre-formed fibrils (PFF) v1
2025Open Access
α-Synuclein aggregates induce mitochondrial damage and trigger innate immunity to drive neuron–microglia communication
2025Open Access
Synaptosome extraction v1
2025Open Access
Western Blot v1
2025Open Access
Astrocytic Ceruloplasmin Deficiency Triggers Iron Toxicity and Neurodegeneration in a LRRK2 Parkinson's Tri-Culture Model
SSRN Electronic Journal·2025Open Access
LRRK2-mutant microglia and neuromelanin synergize to drive dopaminergic neurodegeneration in an iPSC-based Parkinson’s disease model
2024· 3 citedOpen Access
Identification of differential biological activity and synergy between the PARP inhibitor rucaparib and its major metabolite
Cell chemical biology·2024· 3 citedOpen Access
Blocking IL-6 signaling prevents astrocyte-induced neurodegeneration in an iPSC-based model of Parkinson’s disease
JCI Insight·2024· 41 citedOpen Access
Tetrahydrobiopterin (<scp>BH<sub>4</sub></scp>) treatment stabilizes tyrosine hydroxylase: Rescue of tyrosine hydroxylase deficiency phenotypes in human neurons and in a knock‐in mouse model
Journal of Inherited Metabolic Disease·2024· 7 citedOpen Access
Implantation of CPT1AM-expressing adipocytes reduces obesity and glucose intolerance in mice
Metabolic Engineering·2023· 19 citedOpen Access
<scp>iPSC</scp> ‐based modeling of <scp>THD</scp> recapitulates disease phenotypes and reveals neuronal malformation
EMBO Molecular Medicine·2023· 11 citedOpen Access
Immunosuppressive tocilizumab prevents astrocyte induced neurotoxicity in hiPSC-LRRK2 Parkinson’s disease by targeting receptor interleukin-6
2022· 2 citedOpen Access
iPSC-based modeling of THD recapitulates disease phenotypes and reveals neuronal malformation
2022· 1 citedOpen Access
Cationic Carbosilane Dendrimers Prevent Abnormal α-Synuclein Accumulation in Parkinson’s Disease Patient-Specific Dopamine Neurons
Biomacromolecules·2021· 20 citedOpen Access
Parkinson’s disease patient-specific neuronal networks carrying the LRRK2 G2019S mutation unveil early functional alterations that predate neurodegeneration
npj Parkinson s Disease·2021· 31 citedOpen Access
Neural Stem Cells in the Adult Olfactory Bulb Core Generate Mature Neurons in Vivo
Stem Cells·2021· 30 citedOpen Access
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Frequent Co-authors

Ángel Raya(28), Irene Fernández‐Carasa(10), Fred H. Gage(8), Carles Calatayud(8), Yvonne Richaud‐Patín(7), Michael J. Edel(6), Juan Carlos Izpisúa Belmonte(6), Maurizio Memo(6), Meritxell Pons‐Espinal(6), Adriana Sánchez‐Danés(5), Mario Ezquerra(5), Jordi Soriano(5), Patrizia Dell’Era(5), Helena Mira(4), Sebastian Jessberger(4), Ana María Cuervo(4), Miquel Vila(4), Giulia Carola(4), Eduardo Tolosa(4), Claudio Bordignon(4)