Associated Papers
Sex differences in the developing human cortex intersect with genetic risk of neurodevelopmental disorders.
Hennick K et al.
Biorxiv : the Preprint Server for Biology, 2025
40950053 (PubMed )
Supplement: media-31.xlsx › sex-gene-DNMs
Longitudinal multimodal profiling of IDH-wildtype glioblastoma reveals the molecular evolution and cellular phenotypes underlying prognostically different treatment responses.
Lucas CG et al.
Neuro-oncology, 2025
39560080 (PubMed )
Supplement: noae214_suppl_supplementary_tables.xlsx › Table_S6
ARID2, a rare cause of Coffin-Siris syndrome: A novel microdeletion at 12q12q13.11 causing severe short stature and literature review.
Xia D et al.
American Journal of Medical Genetics. Part A, 2023
ARID2, a Rare Cause of Coffin-Siris Syndrome: A Clinical Description of Two Cases.
Wang X et al.
Frontiers in Pediatrics, 2022
Association between ARID2 and RAS-MAPK pathway in intellectual disability and short stature.
Kang E et al.
Journal of Medical Genetics, 2021
Mutations in ARID2 are associated with intellectual disabilities.
Shang L et al.
Neurogenetics, 2015
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