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International Journal of Molecular Sciences|August 26, 2022
Vascular Smooth Muscle Cell Neutral Sphingomyelinase 2 in the Release of Exosomes and Vascular CalcificationAngelina Pavlic, Nasim Bahram Sangani, Johanna Kerins, et al.
Progress in Neurobiology|July 27, 2021
The role of Extracellular Vesicles during CNS developmentNasim Bahram Sangani, Ana Rita Gomes, Leopold M G Curfs, et al.
Acta Histochemica|September 19, 2018
A simple and efficient toolset for analysing mitochondrial trafficking in neuronal cellsVictor A Shahen, Laurence C Cantrill, Nasim Bahram Sangani, et al.
Cell Communication and Signaling : CCS|June 17, 2026
Neural peer pressure: intercellular dynamics and emergent phenotypes in the mosaic Rett syndrome brainJarno Koetsier, Chris P Reutelingsperger, Leopold M G Curfs, et al.
Communications Biology|June 11, 2025
Integrative analysis of 115 transcriptomic studies decodes the molecular landscape of neurodevelopmental disordersJarno Koetsier, Lars M T Eijssen, Leon J Schurgers, et al.
International Journal of Molecular Sciences|December 16, 2020
Extracellular Vesicles in CNS Developmental DisordersAna Rita Gomes, Nasim Bahram Sangani, Tiago G Fernandes, et al.
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry|March 26, 2019
Integrated analysis of human transcriptome data for Rett syndrome finds a network of involved genesFriederike Ehrhart, Susan L Coort, Lars Eijssen, et al.
Scientific Reports|June 25, 2024
A novel insight into neurological disorders through HDAC6 protein-protein interactionsNasim Bahram Sangani, Jarno Koetsier, Jonathan Mélius, et al.
Cellular and Molecular Life Sciences : CMLS|September 21, 2024
Involvement of extracellular vesicle microRNA clusters in developing healthy and Rett syndrome brain organoidsNasim Bahram Sangani, Jarno Koetsier, Ana Rita Gomes, et al.
Plos Genetics|March 12, 2016
Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative GeneKerstin U Ludwig, Syeda Tasnim Ahmed, Anne C Böhmer, et al.
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