Associated Papers
Second report of TEDC1-related microcephaly caused by a novel biallelic mutation in an Iranian consanguineous family.
Sarli A et al.
Molecular Biology Reports, 2024
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
37248276 (PubMed )
Supplement: 41380_2023_2096_MOESM2_ESM.xlsx › TableS5
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_MOESM4_ESM.xlsx › Supplementary_Data_1
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
27217147 (PubMed )
Supplement: mp201669x3.xlsx › Table_S2
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