Associated Papers
Characterization of the genomic alterations in poorly differentiated thyroid cancer.
Lee Y et al.
Scientific Reports, 2023
37932340 (PubMed )
Supplement: 41598_2023_46466_MOESM2_ESM.xlsx › P02
Molecular networks of hepatoblastoma predisposition and oncogenesis in Beckwith-Wiedemann syndrome.
Sobel Naveh NS et al.
Hepatology Communications, 2022
35507738 (PubMed )
Supplement: HEP4-6-2132-s005.xlsx › Supplemental_Table_1.
A recurrent point mutation in PRKCA is a hallmark of chordoid gliomas.
Rosenberg S et al.
Nature Communications, 2018
29915258 (PubMed )
Supplement: 41467_2018_4622_MOESM6_ESM.xlsx › _S3
Case Report: Exome sequencing reveals recurrent RETSAT mutations and a loss-of-function POLDIP2 mutation in a rare undifferentiated tongue sarcoma.
Chan JYK et al.
F1000research, 2018
Prediction and prioritization of neoantigens: integration of RNA sequencing data with whole-exome sequencing.
Karasaki T et al.
Cancer Science, 2017
27960040 (PubMed )
Supplement: CAS-108-170-s006.xlsx › Suppl_Table_3
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