Ela Bar
Overview
Explore the profile of Ela Bar including associated specialties, affiliations and a list of published articles.
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Articles
8
Citations
68
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0
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Recent Articles
1.
Fischer I, Shohat S, Leichtmann-Bardoogo Y, Nayak R, Wiener G, Rosh I, et al.
Sci Adv
. 2024 Oct;
10(41):eadl4573.
PMID: 39392881
Autism spectrum disorder (ASD) is characterized by social and neurocognitive impairments, with mutations of the gene being prominent in patients with monogenic ASD. Using the InsG3680 mouse model with a...
2.
Bar E, Fischer I, Rokach M, Elad-Sfadia G, Shirenova S, Ophir O, et al.
Glia
. 2024 Mar;
72(6):1117-1135.
PMID: 38450767
Williams syndrome (WS) is a genetic neurodevelopmental disorder caused by a heterozygous microdeletion, characterized by hypersociability and unique neurocognitive abnormalities. Of the deleted genes, GTF2I has been linked to hypersociability...
3.
Sade A, Levy G, Trangle S, Elad Sfadia G, Bar E, Ophir O, et al.
Commun Biol
. 2023 Dec;
6(1):1269.
PMID: 38097729
Gtf2i encodes the general transcription factor II-I (TFII-I), with peak expression during pre-natal and early post-natal brain development stages. Because these stages are critical for proper brain development, we studied...
4.
Ophir O, Levy G, Bar E, Kimchi Feldhorn O, Rokach M, Elad Sfadia G, et al.
Biomedicines
. 2023 Aug;
11(8).
PMID: 37626769
Williams syndrome (WS) is a neurodevelopmental disorder characterized by distinctive cognitive and personality profiles which also impacts various physiological systems. The syndrome arises from the deletion of about 25 genes...
5.
Trangle S, Rosenberg T, Parnas H, Levy G, Bar E, Marco A, et al.
Mol Psychiatry
. 2022 Dec;
28(3):1112-1127.
PMID: 36577841
Williams syndrome (WS) is a neurodevelopmental disorder caused by a heterozygous micro-deletion in the WS critical region (WSCR) and is characterized by hyper-sociability and neurocognitive abnormalities. Nonetheless, whether and to...
6.
Fischer I, Shohat S, Levy G, Bar E, Trangle S, Efrati S, et al.
Int J Mol Sci
. 2022 Oct;
23(19).
PMID: 36232395
Autism spectrum disorder (ASD) is a multifactorial neurodevelopmental disorder (NDD) characterized by impaired social communication and repetitive behavior, among other symptoms. ASD is highly heritable, with being one of the...
7.
Levi H, Bar E, Cohen-Adiv S, Sweitat S, Kanner S, Galron R, et al.
Glia
. 2021 Dec;
70(3):536-557.
PMID: 34854502
Ataxia-telangiectasia (A-T) is a multisystem autosomal recessive disease caused by mutations in the ATM gene and characterized by cerebellar atrophy, progressive ataxia, immunodeficiency, male and female sterility, radiosensitivity, cancer predisposition,...
8.
Bar E, Barak B
Glia
. 2019 May;
67(11):2125-2141.
PMID: 31058364
Microglia are the immune cells of the brain, involved in synapse formation, circuit sculpting, myelination, plasticity, and cognition. Being active players during early development as well as in adulthood, microglia...