Additional file 7 of CVD-associated SNPs with regulatory potential reveal novel non-coding disease genes

NIAID Data Ecosystem2026-05-01 收录

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https://figshare.com/articles/dataset/Additional_file_7_of_CVD-associated_SNPs_with_regulatory_potential_reveal_novel_non-coding_disease_genes/23751800 数据链接链接失效反馈

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Additional file 7: Table S6. Result SNEEP Per GWAS.

创建时间：

2023-07-25

Deep learning enables genetic analysis of the human thoracic aorta. Deep learning enables genetic analysis of the human thoracic aorta

医学影像深度学习量化

心血管疾病遗传学

Enlargement or aneurysm of the aorta predisposes to dissection, an important cause of sudden death. We trained a deep learning model to evaluate the dimensions of the ascending and descending thoracic

NIAID Data Ecosystem50

Supplementary Material for: Single Nucleotide Polymorphisms Associated with Coronary Heart Disease Predict Incident Ischemic Stroke in the Atherosclerosis Risk in Communities Study

心血管疾病遗传学

缺血性卒中预测

Ischemic stroke and coronary heart disease (CHD) may share genetic factors contributing to a common etiology. This study investigates whether 51 single nucleotide polymorphisms (SNPs) associated with

NIAID Data Ecosystem20

Additional file 2 of A validated heart-specific model for splice-disrupting variants in childhood heart disease

心血管疾病遗传学

剪接变异分析

Additional file2: Table S2. CHD gene list. Genes were categorized into Tier 1 (moderate to strong association with CHD) or Tier 2 (limited association with CHD). Gene Median gene expression (Transcrip

Figshare2024-10-15 更新20

Table1_Evaluation of 71 Coronary Artery Disease Risk Variants in a Multiethnic Cohort.xlsx

心血管疾病遗传学

跨种族风险变异验证

BackgroundCoronary heart disease (CHD) is the most common cause of death worldwide. Previous studies have identified numerous common CHD susceptibility loci, with the vast majority identified in popul

NIAID Data Ecosystem30

Restrictive genetic instrument for height used in 2-sample MR analysis including independent (distance threshold = 10,000 kb, r 2 = 0.001), genome-wide significant ( p −8 ) variants, excluding those SNPs nominally ( p < 0.05) associated with coronary artery disease, HDL, LDL, total cholesterol, triglycerides, fasting glucose, fasting insulin, diabetes, BMI, waist-to-hip ratio, and systolic blood pressure in the MR-Base database.

孟德尔随机化

心血管疾病遗传学

(XLSX)

NIAID Data Ecosystem20