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Exploring Myelination and Brain Development in Neurodevelopmental Disorders

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Selected Publications:

Shank3 mutation impairs glutamate signaling and myelination in ASD mouse model and human iPSC-derived OPCs |

Fischer I, Shohat S, Leichtmann-Bardoogo Y, Nayak R, Wiener G, Rosh I, Shemen A, Tripathi U, Rokach M, Bar E, Hussein Y, Carolin Castro A, Chen G, Soffer A, Schokoroy-Trangle S, Elad-Sfadia G, Assaf Y, Schroeder A, Monteiro P, Stern S, Maoz B and Barak B. 

2024

Science Advances logo_edited_edited.jpg

In individuals with Williams syndrome, dysregulation of methylation in non-coding regions of neuronal and oligodendrocyte DNA is associated with pathology and cortical development |

Schokoroy Trangle S, Rosenberg T, Parnas H, Levy G, Bar E, Marco A and Barak B. 

2022

Boaz Barak Neuroscience, Tel Aviv University

PubMed

Neuronal deletion of Gtf2i results in developmental microglial alterations in a mouse model related to Williams syndrome |

Bar E, Fischer I, Rokach M, Elad-Sfadia G, Shirenova S, Ophir O, Schokoroy-Trangle S,
Okun E and Barak B. 

2024

glia journal logo_edited.jpg

Selected News:

The Lab Team:

Boaz Barak lab team members
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