Associated Papers
Human iPSC-based breast cancer model identifies S100P-dependent cancer stemness induced by BRCA1 mutation.
Liu J et al.
Science Advances, 2025
40712032 (PubMed )
Supplement: sciadv.adi2370_tables_s8_and_s9.zip › adi2370_table_s9.xlsx › Mutant_corrected_iPSC-MCs_D20
Translational and clinical comparison of whole genome and transcriptome to panel sequencing in precision oncology.
Kerle IA et al.
Npj Precision Oncology, 2025
39794422 (PubMed )
Supplement: 41698_2024_788_MOESM6_ESM.xlsx › patient_10_MASTER_1_indels_
Evolutionary history of adenomas to colorectal cancer in FAP families.
Yang C et al.
Frontiers in Genetics, 2024
39021676 (PubMed )
Supplement: DataSheet1.ZIP › Somatic › 18R10494.xls › SNVIndel
Whole-exome sequencing of epithelial ovarian carcinomas differing in resistance to platinum therapy.
Hlaváč V et al.
Life Science Alliance, 2022
36229065 (PubMed )
Supplement: LSA-2022-01551_TableS16.xlsx › Table_S16
Multi-omics characterization reveals the pathogenesis of liver focal nodular hyperplasia.
Liu Y et al.
Iscience, 2022
36060063 (PubMed )
Supplement: mmc3.xlsx › Sheet1
Patient-derived models recapitulate heterogeneity of molecular signatures and drug response in pediatric high-grade glioma.
He C et al.
Nature Communications, 2021
34215733 (PubMed )
Supplement: 41467_2021_24168_MOESM5_ESM.xlsx › SD2c
Hints from a Female Patient with Breast Cancer Who Later Presented with Cowden Syndrome.
Wang WC et al.
Journal of Breast Cancer, 2020
32908792 (PubMed )
Supplement: jbc-23-430-s002.pdf
Clinicopathological features of pseudomyogenic hemangioendothelioma and precision therapy based on whole exome sequencing.
Wei J et al.
Cancer Communications (london, England), 2020
32227592 (PubMed )
Supplement: CAC2-40-197-s002.pdf
ALPK1 hotspot mutation as a driver of human spiradenoma and spiradenocarcinoma.
Rashid M et al.
Nature Communications, 2019
31101826 (PubMed )
Supplement: 41467_2019_9979_MOESM5_ESM.xlsx › Supp_table_2b
Genetic and epigenetic stability of oligodendrogliomas at recurrence.
Aihara K et al.
Acta Neuropathologica Communications, 2017
28270234 (PubMed )
Supplement: 40478_2017_422_MOESM1_ESM.xlsx › 3_Mutations
Genomic complexity and dynamics of clonal evolution in childhood acute myeloid leukemia studied with whole-exome sequencing.
Masetti R et al.
Oncotarget, 2016
27462774 (PubMed )
Supplement: oncotarget-07-56746-s001.pdf
Recurrent PTPRB and PLCG1 mutations in angiosarcoma.
Behjati S et al.
Nature Genetics, 2014
24633157 (PubMed )
Supplement: NIHMS57096-supplement-3.xlsx › SuppTable2
Select a paper to view details