1. Comprehensive variant calling from whole‐genome sequencing identifies a complex inversion that disrupts ZFPM2 in familial congenital diaphragmatic hernia
   Thomas J. Nicholas et al, 2022, Molecular Genetics & Genomic Medicine CrossRef
2. In silico analysis of GATA4 variants demonstrates main contribution to congenital heart disease
   Shiva Abbasi et al, 2021, Journal of Cardiovascular and Thoracic Research CrossRef
3. First report of polymorphisms in MTRR, GATA4, VEGF, and ISL1 genes in Pakistani children with isolated ventricular septal defects (VSD)
   Sumbal Sarwar et al, 2021, Italian Journal of Pediatrics CrossRef