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2. TP53 variants in p53 signatures and the clonality of STICs in RRSO samples

3. Germline Whole-Gene Deletion of FH Diagnosed from Tumor Profiling

4. Retrospective evaluation of risk-reducing salpingo-oophorectomy for BRCA1/2 pathogenic variant carriers among a cohort study in a single institution

6. Characterization of the STK11 splicing variant as a normal splicing isomer in a patient with Peutz–Jeghers syndrome harboring genomic deletion of the STK11 gene

7. The Use of Next-Generation Sequencing in Molecular Diagnosis of Neurofibromatosis Type 1: A Validation Study

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