Associated Papers
Computational analysis of congenital heart disease associated SNPs: unveiling their impact on the gene regulatory system.
Vashisht S et al.
Bmc Genomics, 2025
39838281 (PubMed )
Supplement: 12864_2025_11232_MOESM4_ESM.xlsx › ClinVar_CHD-SNPs_uniq
Classification of domains in predicted structures of the human proteome.
Schaeffer RD et al.
Proceedings of the National Academy of Sciences of the United States of America, 2023
36917664 (PubMed )
Supplement: pnas.2214069120.sd02.xlsx › Dataset_S2
Novel CRELD1 gene mutations in patients with atrioventricular septal defect.
Guo Y et al.
World Journal of Pediatrics : Wjp, 2010
Genetic factors in non-syndromic congenital heart malformations.
Wessels MW et al.
Clinical Genetics, 2010
CRELD1 mutations contribute to the occurrence of cardiac atrioventricular septal defects in Down syndrome.
Maslen CL et al.
American Journal of Medical Genetics. Part A, 2006
A maiden report on CRELD1 single-nucleotide polymorphism association in congenital heart disease patients of Mysore, South India.
Kusuma L et al.
Genetic Testing and Molecular Biomarkers, 0
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