Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Genes in non-syndromic congenital heart disease-CIDR

ABSTRACT: Genes in non-syndromic congenital heart disease-CIDR

PROVIDER: PRJNA644673 | ENA |

REPOSITORIES: ENA

ACCESS DATA

Json Xml

Similar Datasets

Genes in non-syndromic congenital heart disease-CIDR

Project description:Genes in non-syndromic congenital heart disease-CIDR

| PRJNA644674 | ENA

Array CGH in congenital heart disease

Project description:Congenital heart disease (CHD) is the most frequent birth defect and affects nearly 1% of newborns. The etiology of CHD is largely unknown and only a small percentage can be assigned to environmental risk factors such as maternal diseases or exposure to mutagenic agents during pregnancy. Chromosomal imbalances have been identified in many forms of syndromic CHD, but next to nothing is known about the impact of DNA copy number changes in non-syndromic CHD. Here we present a sub-megabase resolution array CGH screen of a cohort with CHD as the sole abnormality at the time of diagnosis. Keywords: array CGH In this BAC array CGH study 104 patients with congenital heart disease and some of their parents were screened for DNA copy number changes at submegabase resolution. No dye swap was performed.

2008-05-11 | E-GEOD-7527 | biostudies-arrayexpress

Array CGH in congenital heart disease

2008-05-12 | GSE7527 | GEO

Loss of ADAMTS19 causes progressive non-syndromic heart valve disease

Project description:Loss of ADAMTS19 causes progressive non-syndromic heart valve disease

| PRJNA430237 | ENA

Array-CGH in Chinese children with congenital heart disease

Project description:We used Affymetrix CytoScan750K array to detect the pathogenic copy number variations in 7 Chinese children with congenital heart disease

2021-10-01 | E-MTAB-8315 | biostudies-arrayexpress

Integrated multiomic characterization of congenital heart disease

Project description:Integrated multiomic characterization of congenital heart disease

| PRJNA839343 | ENA

PCGC: Congenital Heart Disease Genetic Network Study

Project description:PCGC: Congenital Heart Disease Genetic Network Study

| PRJNA183421 | ENA

Developmental Mechanisms of Human Congenital Heart Disease

Project description:Developmental Mechanisms of Human Congenital Heart Disease

| PRJNA380445 | ENA

Congenital Heart Disease Pilot

Project description:This pilot study aims to generate pilot data to inform future study designs by resequencing the whole exomes of 10 unrelated individuals diagnosed with Congenital Heart Disease (CHD).

| EGAS00001000425 | EGA

Congenital heart disease in Csx/ Nkx2.5 mutant embryos

Project description:We have developed gene-targeted mice with deletion of Nkx2.5. Embryos were isolated at embryonic day 9.5 and the middle third containing the heart was run on Affymetrix Mu11kA and Mu11kB arrays. For more information about this model see http://cardiogenomics.med.harvard.edu/groups/proj1/pages/csx_home.html Keywords = Congenital heart disease Keywords: other

2002-08-02 | GSE78 | GEO

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data