Associated Papers
Recurrent oligodendroglioma with changed 1p/19q status.
Barresi V et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology, 2022
35144313 (PubMed )
Supplement: NEUP-42-160-s001.xlsx › Foglio1
Genomic Signature of Oral Squamous Cell Carcinomas from Non-Smoking Non-Drinking Patients.
Koo K et al.
Cancers, 2021
33804510 (PubMed )
Supplement: cancers-13-01029-s001.zip › Supplementary_Data.xlsx › Somatic_mutations
Tumor sequencing is useful to refine the analysis of germline variants in unexplained high-risk breast cancer families.
Van Marcke C et al.
Breast Cancer Research : Bcr, 2020
32295625 (PubMed )
Supplement: 13058_2020_1273_MOESM1_ESM.xlsx › Table_S2
Germline mutations in candidate predisposition genes in individuals with cutaneous melanoma and at least two independent additional primary cancers.
Pritchard AL et al.
Plos One, 2018
29641532 (PubMed )
Supplement: pone.0194098.s003.xlsx › UK10K_AD
Diagnostics of Primary Immunodeficiencies through Next-Generation Sequencing.
Gallo V et al.
Frontiers in Immunology, 2016
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