Sadaf Ghorbani
Bergen, Norway
Last Updated: 09/26/2026
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Found 13 publications
Cell-type-resolved NRXN1 isoforms across human brain tissues and hiPSC organoids.
Journal: bioRxiv : the preprint server for biology
Published: November 26, 2025
Dynamic convergence of neurodevelopmental disorder risk genes across neurodevelopment.
Journal: bioRxiv : the preprint server for biology
Published: September 04, 2024
Transcriptomic and phenotypic convergence of neurodevelopmental disorder risk genes in vitro and in vivo.
Journal: Nature neuroscience
Published: August 23, 2024
3D genetic architecture of schizophrenia risk across three neuronal subtypes.
Journal: Molecular psychiatry
Published: June 17, 2024
Phenotypic complexities of rare heterozygous neurexin-1 deletions.
Journal: Nature
Published: December 12, 2023
Phenotypic complexities of rare heterozygous neurexin-1 deletions.
Journal: bioRxiv : the preprint server for biology
Published: November 14, 2023
Schizophrenia Risk Mapping and Functional Engineering of the 3D Genome in Three Neuronal Subtypes.
Journal: bioRxiv : the preprint server for biology
Published: July 28, 2023
Involvement of the 14-3-3 Gene Family in Autism Spectrum Disorder and Schizophrenia: Genetics, Transcriptomics and Functional Analyses.
Journal: Journal of clinical medicine
Published: April 30, 2020
Serine 19 phosphorylation and 14-3-3 binding regulate phosphorylation and dephosphorylation of tyrosine hydroxylase on serine 31 and serine 40.
Journal: Journal of neurochemistry
Published: June 28, 2019
Tyrosinemia Type 1 and symptoms of ADHD: Biochemical mechanisms and implications for treatment and prognosis.
Journal: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
Published: April 30, 2019
Phosphorylation dependence and stoichiometry of the complex formed by tyrosine hydroxylase and 14-3-3γ.
Journal: Molecular & cellular proteomics : MCP
Published: June 21, 2014
Last Updated: 09/26/2026