Associated Papers
DNA methylation analysis of NOTCH1 variants reveals the first episignature for non-syndromic congenital heart defects.
Dombrowsky G et al.
Genome Medicine, 2026
41501857 (PubMed )
Supplement: 13073_2025_1587_MOESM1_ESM.xlsx › Table_S5
Somatic mutation and selection at population scale.
Lawson ARJ et al.
Nature, 2025
41062696 (PubMed )
Supplement: 41586_2025_9584_MOESM6_ESM.xlsx › sitednds_oral
Identification of rare variants in novel candidate genes in pulmonary atresia patients by next generation sequencing.
Shi X et al.
Computational and Structural Biotechnology Journal, 2020
32128068 (PubMed )
Supplement: mmc2.xlsx › Table_S3
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