Microcephaly Gene Links Trithorax and REST/NRSF to Control Neural Stem Cell Proliferation and Differentiation

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CDK6 associates with the centrosome during mitosis and is mutated in a large Pakistani family with primary microcephaly

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Time is of the essence: the molecular mechanisms of primary microcephalyPreprint

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Mutations of KIF14 cause primary microcephaly by impairing cytokinesis

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What next-generation sequencing (NGS) technology has enabled us to learn about primary autosomal recessive microcephaly (MCPH)

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Dissecting the Genetic and Etiological Causes of Primary Microcephaly

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A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani family

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RRP7A links primary microcephaly to dysfunction of ribosome biogenesis, resorption of primary cilia, and neurogenesis

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Histone H3 lysine methylation in cognition and intellectual disability disordersPreprint

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CIT, a gene involved in neurogenic cytokinesis, is mutated in human primary microcephaly

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Autosomal Recessive Primary Microcephaly: Not Just a Small Brain

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RTTN Mutations Cause Primary Microcephaly and Primordial Dwarfism in Humans

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Epigenetic and Transcriptional Pre-patterning—An Emerging Theme in Cortical Neurogenesis

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Microcephaly Modeling of Kinetochore Mutation Reveals a Brain-Specific Phenotype

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Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndromePreprint

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Variants inCUL4Bare Associated with Cerebral Malformations

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Unexpected Transcriptional Programs Contribute to Hippocampal Memory Deficits and Neuronal Stunting after Early-Life Adversity

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The genetics of congenitally small brains

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The C2H2-ZF transcription factor Zfp335 recognizes two consensus motifs using separate zinc finger arraysPreprint

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The COMPASS Family Protein ASH2L Mediates Corticogenesis via Transcriptional Regulation of Wnt Signaling

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Trithorax maintains the functional heterogeneity of neural stem cells through the transcription factor Buttonhead

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ZNHIT3 is defective in PEHO syndrome, a severe encephalopathy with cerebellar granule neuron loss

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Multifaceted Microcephaly-Related Gene MCPH1

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Comparison of the Efficacy of Different Drugs on Non-Motor Symptoms of Parkinson’s Disease: a Network Meta-Analysis

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Zinc finger protein Zfp335 is required for the formation of the naïve T cell compartment

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The Mitotic Apparatus and Kinetochores in Microcephaly and Neurodevelopmental Diseases

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Posterior Neocortex-Specific Regulation of Neuronal Migration by CEP85L Identifies Maternal Centriole-Dependent Activation of CDK5

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Genetic Primary Microcephalies: When Centrosome Dysfunction Dictates Brain and Body Size

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Identification of candidate gene FAM183A and novel pathogenic variants in known genes: High genetic heterogeneity for autosomal recessive intellectual disability

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Molecular analysis of 23 Pakistani families with autosomal recessive primary microcephaly using targeted next-generation sequencing

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CITK Loss Inhibits Growth of Group 3 and Group 4 Medulloblastoma Cells and Sensitizes Them to DNA-Damaging Agents

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Refining the phenotype associated with CASC5 mutation

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Loss of Zfp335 triggers cGAS/STING-dependent apoptosis of post-β selection thymocytes

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Epigenetic Mechanisms Regulating Differentiation of Neural Stem/Precursor Cells

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A novel WDR62 mutation causes primary microcephaly in a large consanguineous Saudi family

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MEKK3 coordinates with FBW7 to regulate WDR62 stability and neurogenesis

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Phf21b imprints the spatiotemporal epigenetic switch essential for neural stem cell differentiationPreprint

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Molecular signatures from multi‐omics of autism spectrum disorders and schizophrenia

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Congenital Microcephaly: A Debate on Diagnostic Challenges and Etiological Paradigm of the Shift from Isolated/Non-Syndromic to Syndromic Microcephaly

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The Yin and Yang of Autosomal Recessive Primary Microcephaly Genes: Insights from Neurogenesis and Carcinogenesis

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NRSF/REST lies at the intersection between epigenetic regulation, miRNA-mediated gene control and neurodevelopmental pathways associated with Intellectual disability (ID) and Schizophrenia

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Quantitative Phosphoproteomic Study Reveals that Protein Kinase A Regulates Neural Stem Cell Differentiation Through Phosphorylation of Catenin Beta-1 and Glycogen Synthase Kinase 3β

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Association Between Invisible Basal Ganglia and ZNF335 Mutations: A Case Report

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Zfp335 establishes eTreg lineage and neonatal immune tolerance by targeting Hadha-mediated fatty acid oxidation

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