Manzoor A Bhat
13PUBLICATIONS
9CO-AUTHORS
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Publications (13)
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|Feb 09, 2026
Human CNTNAP1 Variants Associated With Severe Neurological Deficits: Additional Cases and Literature Review.Lacey B Sell, Derek Garcia, Alexandra Hollá
|Apr 23, 2025
A Novel Mutation in CNTNAP1 Gene Causes Disorganization of Axonal Domains, Hypomyelination and Severe Neurological Deficits.Lacey B Sell, Carson Zabel, Sabine Weller Grønborg
|Aug 09, 2022
Drosophila Homolog of the Human Carpenter Syndrome Linked Gene, MEGF8, Is Required for Synapse Development and Function.Shuting Chen, Anand Venkatesan, Yong Qi Lin
|Jun 07, 2022
Microglial mTOR Activation Upregulates Trem2 and Enhances β-Amyloid Plaque Clearance in the 5XFAD Alzheimer's Disease Model.Qian Shi, Cheng Chang, Afaf Saliba
|Nov 05, 2021
Tbx1, a gene encoded in 22q11.2 copy number variant, is a link between alterations in fimbria myelination and cognitive speed in mice.Takeshi Hiramoto, Akira Sumiyoshi, Takahira Yamauchi
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