Associated Papers
Deep exome sequencing identifies enrichment of deleterious mosaic variants in neurodevelopmental disorder genes and mitochondrial tRNA regions in bipolar disorder.
Nishioka M et al.
Molecular Psychiatry, 2023
Heterozygosity for neuronal ceroid lipofuscinosis predisposes to bipolar disorder.
Privitera F et al.
Revista Brasileira De Psiquiatria (sao Paulo, Brazil : 1999), 2023
35881528 (PubMed )
Supplement: 1516-4446-rbp-1516444620222650-suppl1.pdf
Systematic analysis of exonic germline and postzygotic de novo mutations in bipolar disorder.
Nishioka M et al.
Nature Communications, 2021
34145229 (PubMed )
Supplement: 41467_2021_23453_MOESM9_ESM.xlsx › Supplementary_Data_6
Novel HIVEP2 Variants in Patients with Intellectual Disability.
Park J et al.
Molecular Syndromology, 2019
Exome sequencing for bipolar disorder points to roles of de novo loss-of-function and protein-altering mutations.
Kataoka M et al.
Molecular Psychiatry, 2016
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