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1,336
datasets available to search
ShareScore release 0.9.0
Dataset results
1,336 results for “congenital”
Epigenome wide Association and Stochastic Epigenetic Mutation analysis on 23 twin pairs heterogeneously affected by Congenital Hypothyroidism (CH).
GEO Series GSE161041. Homo sapiens. 46 samples. Type: Methylation profiling by array.
MicroRNA expression profiling of urine exosomes in children with congenital cytomegalovirus infection
GEO Series GSE252811. Homo sapiens. 30 samples. Type: Non-coding RNA profiling by array.
Genomic and transcriptomic data analyses highlight KPNB1 and MYL4 as novel risk genes for congenital heart disease
GEO Series GSE194103. Homo sapiens. 2 samples. Type: Expression profiling by high throughput sequencing.
Integrated analysis of copy number variation-associated lncRNAs identifies candidates contributing to the etiologies of congenital kidney anomalies.
GEO Series GSE223312. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
A multi-omics approach using a mouse model of cardiac malformations for prioritization of human congenital heart disease contributing genes [scRNA-seq]
GEO Series GSE171238. Mus musculus. 1 samples. Type: Expression profiling by high throughput sequencing.
Loss of ER and nuclear envelope-associated neutral sphingomyelinase SMPD4 causes a severe neurodevelopmental disorder with microcephaly and congenital arthrogryposis
GEO Series GSE133264. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
Analysis of copy number variants on chromosome 21 in Down syndrome-associated congenital heart defects
GEO Series GSE93004. Homo sapiens. 526 samples. Type: Genome variation profiling by array.
Human Otic progenitor cell models of congenital hearing loss applied to to Zika virus and cytomegalovirus infections
GEO Series GSE234062. Homo sapiens. 36 samples. Type: Expression profiling by high throughput sequencing.
Gene therapy of dominant CRX-Leber congenital amaurosis using patient retinal organoids I
GEO Series GSE152939. Homo sapiens. 38 samples. Type: Expression profiling by high throughput sequencing.
Congenital iRHOM2 deficiency causes ADAM17 dysfunction and environmentally directed immunodysregulatory disease [T cells]
GEO Series GSE184875. Homo sapiens. 37 samples. Type: Expression profiling by high throughput sequencing.
Community-Based Remote Cardiac Rehabilitation Program for Pediatric Patients With Complex Congenital Heart Disease
ClinicalTrials.gov study NCT06912412. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Molecular Basis of Congenital Heart Defects
ClinicalTrials.gov study NCT00579358. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Fertility and Pregnancy in Patients With Classic Congenital Adrenal Hyperplasia
ClinicalTrials.gov study NCT06153043. IPD Sharing: NO. Countries: 1. Publications: 0.
Study of Congenital Orofacial Clefts by Implementing Optical Genome Mapping
ClinicalTrials.gov study NCT06880094. IPD Sharing: NO. Countries: 1. Publications: 0.
Gene Mutations and Rescue in Human Congenital Diaphragmatic Hernia
ClinicalTrials.gov study NCT01098929. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Scientific Substantiation and Assessment of the Effectiveness of Pathogenetic Methods of Therapy for Congenital Ichthyosis in Children
ClinicalTrials.gov study NCT04996485. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Bosentan In Exercise Induced Pulmonary Arterial Hypertension in CongenitaL Heart diseasE
ClinicalTrials.gov study NCT01827059. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Visceral Adiposity Index and Triglyceride/High-density Lipoprotein Cholesterol Ratio in the Congenital Hypogonadotropic Hypogonadism and Effect of Testosteron Treatment
ClinicalTrials.gov study NCT02111434. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Repeated Treatments of QLT091001 in Subjects With Leber Congenital Amaurosis or Retinitis Pigmentosa (Extension of Study RET IRD 01)
ClinicalTrials.gov study NCT01521793. IPD Sharing: Not stated. Countries: 5. Publications: 0.
The Effect of High-Calorie Formula on Nutritional and Clinical Outcomes Among Infants After Congenital Heart Surgery
ClinicalTrials.gov study NCT05945459. IPD Sharing: NO. Countries: 1. Publications: 0.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.