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
Evolutionary history of adenomas to colorectal cancer in FAP families.
Yang C et al.
Frontiers in Genetics, 2024
39021676 (PubMed )
Supplement: DataSheet1.ZIP › Somatic › 18R12365.xls › SNVIndel
Massively Parallel Sequencing of Genes Implicated in Heritable Cardiac Disorders: A Strategy for a Small Diagnostic Laboratory.
Leong IUS et al.
Medical Sciences (basel, Switzerland), 2017
29099038 (PubMed )
Supplement: medsci-05-00022-s001.zip › Supplementary_data_1.pdf
Evaluation of Bioinformatic Programmes for the Analysis of Variants within Splice Site Consensus Regions.
Tang R et al.
Advances in Bioinformatics, 2016
27313609 (PubMed )
Supplement: 5614058.f1.pdf
Denaturing HPLC-based approach for detecting RYR2 mutations involved in malignant arrhythmias.
Bagattin A et al.
Clinical Chemistry, 2004
Gene symbol: RYR2. Disease: Effort-induced polymorphic ventricular arrhythmias.
Veronese C et al.
Human Genetics, 2004
Gene symbol: RYR2. Disease: Effort-induced polymorphic ventricular arrhythmias.
Veronese C et al.
Human Genetics, 2004
Gene symbol: RYR2. Disease: Effort-induced polymorphic ventricular arrhythmias.
Bagattin A et al.
Human Genetics, 2004
Gene symbol: RYR2. Disease: Effort-induced polymorphic ventricular arrhythmias.
Bagattin A et al.
Human Genetics, 2004
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