Associated Papers
Chromatin Meets Condensates: Emerging Interplays Linking Nuclear Paraspeckles to Gene Activation.
Tu CH et al.
Epigenetics Reports, 2026
Case Report: A female case of X-linked intellectual disability syndrome type 34 caused by a NONO frameshift variant and literature review.
Zhang Y et al.
Frontiers in Pediatrics, 2026
Are NONO variants linked to congenital heart disease? Patient reports and review.
He P et al.
European Journal of Medical Genetics, 2025
Stress-Induced Membraneless Organelles in Neurons: Bridging Liquid-Liquid Phase Separation and Neurodevelopmental Dysfunction.
Bencsik N et al.
International Journal of Molecular Sciences, 2025
Functional assays in Drosophila facilitate classification of variants of uncertain significance associated with rare diseases.
Mok JW et al.
Genome Research, 2025
40467338 (PubMed )
Supplement: Supplemental_Table_S1.xlsx › Supplemental_Table1
NONO-related X-linked intellectual disability syndrome: Further clinical and molecular delineation.
Planté-Bordeneuve P et al.
European Journal of Medical Genetics, 2025
X-linked intellectual developmental disorder with onset of neonatal heart failure: A case report and literature review.
Xi H et al.
Molecular Genetics and Metabolism Reports, 2024
A novel NONO variant that causes developmental delay and cardiac phenotypes.
Itai T et al.
Scientific Reports, 2023
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