Power Analysis for PITX2c expression.

NIAID Data Ecosystem2026-03-08 收录

基因表达功效分析

心血管遗传学

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https://figshare.com/articles/dataset/_Power_Analysis_for_PITX2c_expression_/908006 数据链接链接失效反馈

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*Covariates were age, sex, donor status, and SNP yielding 3 degrees of freedom. #Covariates were age, sex, donor status, 3 AF history/rhythm at surgery groups, and SNP yielding 6 degrees of freedom.

创建时间：

2014-01-22

Table S1 - Identification of Critical Regions and Candidate Genes for Cardiovascular Malformations and Cardiomyopathy Associated with Deletions of Chromosome 1p36

心血管遗传学

染色体缺失分析

Exon-containing deletions in 1p36 cardiac-related genes found in various control and population-based cohorts catalogued in the Database of Genomic Variants. (DOC)

NIAID Data Ecosystem60

A Resource of Gene Expression Data from a Multiethnic Population Cohort of Induced Pluripotent Cell–Derived Cardiomyocytes. A Resource of Gene Expression Data from a Multiethnic Population Cohort of Induced Pluripotent Cell–Derived Cardiomyocytes

心血管遗传学

iPSC心肌细胞模型

Induced pluripotent stem cells (iPSCs), upon differentiation into somatic cell types, offer the ability to model the genetic states of tissues in the individuals from whom the iPSCs were derived. A re

NIAID Data Ecosystem60

Genome-wide association study identifies 18 novel loci associated with left atrial volume and function

全基因组关联分析

心血管遗传学

README Publication: Genome-wide association study identifies 18 novel loci associated with left atrial volume and function Ahlberg and Andreasen et al. Published: 29 July 2021, doi: h

Zenodo2021-08-02 更新20

A novel PRRX1 loss-of-function variation contributing to familial atrial fibrillation and congenital patent ductus arteriosus

心血管遗传学

基因变异

Abstract Atrial fibrillation (AF) represents the most common type of sustained cardiac arrhythmia in humans and confers a significantly increased risk for thromboembolic stroke, congestive heart failu

DataCite Commons2024-02-08 更新60

Genetic variants associated with coronary artery disease in Indians

心血管遗传学

动脉粥样硬化关联分析

Genetic variations were successfully associated among patients with coronary artery disease using Illumina Cardiometabochip containing 1,96,725 SNPs Illumina Cardio-metabochip is a custom designed SNP

NIAID Data Ecosystem40

Power Analysis for PITX2c expression.

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