Associated Papers
Functional Enrichment Analysis of Rare Mutations in Patients with Brain Arteriovenous Malformations.
Zholdybayeva E et al.
Biomedicines, 2025
Indicators of HSV1 Infection, ECM-Receptor Interaction, and Chromatin Modulation in a Nuclear Family with Schizophrenia.
Huang YC et al.
Journal of Personalized Medicine, 2023
37763159 (PubMed )
Supplement: jpm-13-01392-s001.zip › Supplementary_Table_S3.xlsx › Variants
Molecular characterization of sub-frontal recurrent medulloblastomas reveals potential clinical relevance.
Chen Z et al.
Frontiers in Neurology, 2023
37181548 (PubMed )
Supplement: Data_Sheet_2.xlsx › Germline_mutation-case_2
Identification of recurrent variants implicated in disease in bicuspid aortic valve patients through whole-exome sequencing.
Chen S et al.
Human Genomics, 2022
Identification of pathways and genes associated with cerebral palsy.
Zhu Q et al.
Genes & Genomics, 2018
A population-specific uncommon variant in GRIN3A associated with schizophrenia.
Takata A et al.
Biological Psychiatry, 2013
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