Associated Papers
Identification of Novel Mosaic Variants in Focal Epilepsy-Associated Patients' Brain Lesions.
Garcia CAB et al.
Genes, 2025
40282380 (PubMed )
Supplement: genes-16-00421-s001.zip › Table_S2_Candidate_Somatic_Variants.xlsx › Sheet1
Uncommon variants in FLG2 and TCHHL1 are associated with remission of atopic dermatitis in a large longitudinal US cohort.
Berna R et al.
Archives of Dermatological Research, 2022
Whole-exome sequencing in a patient with synchronous triple primary malignancies involving lung cancer: a case report.
Li D et al.
Precision Clinical Medicine, 2020
35692627 (PubMed )
Supplement: pbaa019_supplemental_file.zip › Supplementary_table_2.xlsx › Supplementary_table_1
Genomic characterization of Chinese ovarian clear cell carcinoma identifies driver genes by whole exome sequencing.
Yang Q et al.
Neoplasia (new York, N.y.), 2020
The genomic landscape of TERT promoter wildtype-IDH wildtype glioblastoma.
Diplas BH et al.
Nature Communications, 2018
29802247 (PubMed )
Supplement: 41467_2018_4448_MOESM11_ESM.xlsx › 8_SNV_WGS
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