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Journal of Neurogenetics|May 10, 2021
Compound heterozygous KCTD7 variants in progressive myoclonus epilepsyElizabeth A Burke, Morgan Sturgeon, Diane B Zastrow, et al.Journal of Neurogenetics|May 17, 2021
A cGMP-dependent protein kinase, encoded by the Drosophila foraging gene, regulates neurotransmission through changes in synaptic structure and functionJeffrey S Dason, Marla B SokolowskiJournal of Neurogenetics|May 20, 2021
Dysregulation of Myt1 expression acts as a potential peripheral biomarker for major depressive disorder and bipolar disorderMaryam Ghanbarirad, Mehrdad Hashemi, Seyed Mehdi Saberi, et al.Journal of Neurogenetics|February 25, 2025
Drosophila WDFY3/Bchs overexpression impairs neural functionMarek B Körner, Akhil Velluva, Linnaeus Bundalian, et al.Journal of Neurogenetics|March 11, 2024
The DST gene in neurobiologyRobert Lalonde, Catherine StrazielleJournal of Neurogenetics|May 20, 2024
Meta-analysis of the association between C9orf72 repeats and neurodegeneration diseasesPingfei Jin, Yong Li, Yao LiJournal of Neurogenetics|February 26, 2026
Neurocardiogenetics: Exploring the association of rare RYR2 variants with neuropsychiatric disorders in general and disease populationsSaif F Dababneh, Jason D Roberts, Sixuan Tan, et al.Journal of Neurogenetics|November 12, 2024
Targeted deletion of olfactory receptors in D. melanogaster via CRISPR/Cas9-mediated LexA knock-inRunqi Zhang, Renny Ng, Shiuan-Tze Wu, et al.Journal of Neurogenetics|May 18, 2026
Genetic architecture of hereditary spastic paraplegia: from monogenic to oligogenic modelsGiuseppe Pedullà, Maurizio Morelli, Monica Gagliardi, et al.Journal of Neurogenetics|April 10, 2026
A zinc finger MYM-type containing 3 (ZMYM3) allele is associated with autism spectrum disorder in Iranian peopleMaryam Razavi, Mobina Tabibian, Zahra Lakpour, et al.Pageof 79