Associated Papers
The genomic and evolutionary landscapes of anaplastic thyroid carcinoma.
Zeng PYF et al.
Cell Reports, 2024
Oncogenic Mutations in PI3K/AKT/mTOR Pathway Effectors Associate with Worse Prognosis in BRAFV600E -Driven Papillary Thyroid Cancer Patients.
Pappa T et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2021
A Novel Inherited Mutation of SCN8A in a Korean Family with Benign Familial Infantile Epilepsy Using Diagnostic Exome Sequencing.
Han JY et al.
Annals of Clinical and Laboratory Science, 2017
Diagnostic exome sequencing identifies a heterozygous MBD5 frameshift mutation in a family with intellectual disability and epilepsy.
Han JY et al.
European Journal of Medical Genetics, 2017
Germline Variants of Prostate Cancer in Japanese Families.
Hayano T et al.
Plos One, 2016
27701467 (PubMed )
Supplement: pone.0164233.s005.xlsx › Table_S5
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