Associated Papers
Genome-wide analysis of somatic noncoding mutation patterns and mitochondrial heteroplasmic shift in type B1 and B2 thymomas.
Fujikura K et al.
The Journal of Pathology, 2026
41344988 (PubMed )
Supplement: PATH-268-135-s001.xlsx › Table_S3
Shared and divergent contribution of vitamin A and oxytocin to the aetiology of autism spectrum disorder.
Wang T et al.
Computational and Structural Biotechnology Journal, 2023
38213898 (PubMed )
Supplement: mmc2.xlsx › RIVs_in_VARGs
New dead/H-box helicase gene (ddx41) mutation in an Italian family with recurrent leukemia.
Fazio F et al.
Leukemia & Lymphoma, 2021
Ferroportin disease: pathogenesis, diagnosis and treatment.
Pietrangelo A
Haematologica, 2017
The global prevalence of HFE and non-HFE hemochromatosis estimated from analysis of next-generation sequencing data.
Wallace DF et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2016
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