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28 results for “Birth defects”

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ClinicalTrials.gov32/100

Effectiveness of Comprehensive Tertiary Interventions on Incidence and Clinical Outcomes of Birth Defects

ClinicalTrials.gov study NCT03725878. IPD Sharing: UNDECIDED. Countries: 1. Publications: 4.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov32/100

Genetic Study to Determine the Cause of Birth Defects in Newborns in Texas

ClinicalTrials.gov study NCT07102966. IPD Sharing: YES. Countries: 1. Publications: 1.

controlledIPD-YESFeb 2026View details →
ClinicalTrials.gov32/100

Genomic Sequencing and Personalized Treatment for Birth Defects in Neonatal Intensive Care Units

ClinicalTrials.gov study NCT02551081. IPD Sharing: Not stated. Countries: 1. Publications: 10.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov32/100

Phenotypic and Genetic Assessment of Tracheal and Esophageal Birth Defects in Patients

ClinicalTrials.gov study NCT03455881. IPD Sharing: Not stated. Countries: 1. Publications: 19.

restrictedIPD-UNDECIDEDFeb 2026View details →
geo24/100

Ash1l loss-of-function results in structural birth defects and altered cortical development [scRNA-seq]

GEO Series GSE252688. Mus musculus. 7 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenJan 2025View details →
geo24/100

Gastrulation-stage gene expression in Nipbl+/- mouse embryos foreshadows the development of syndromic birth defects

GEO Series GSE151589. Mus musculus. 31 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenMay 2023View details →
ClinicalTrials.gov24/100

Genetic and Nutritional Causes of Heart Birth Defects

ClinicalTrials.gov study NCT00368732. IPD Sharing: Not stated. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov24/100

Miscarriage Preventing Herbal Medicines and the Risk of Birth Defects: a Population-based Cohort Study

ClinicalTrials.gov study NCT06048276. IPD Sharing: YES. Countries: 1. Publications: 0.

controlledIPD-YESFeb 2026View details →
ClinicalTrials.gov24/100

The Pilot Study of High-throughput Sequencing in Neonatal Birth Defects

ClinicalTrials.gov study NCT03984266. IPD Sharing: YES. Countries: 1. Publications: 0.

controlledIPD-YESFeb 2026View details →
ClinicalTrials.gov24/100

Birth Defect Registry in South West Region of France

ClinicalTrials.gov study NCT05231447. IPD Sharing: Not stated. Countries: 1. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
geo20/100

Cystic Fibrosis Pigs Develop Lung Disease and Exhibit Defective Bacterial Eradication at Birth

GEO Series GSE21071. Sus scrofa. 40 samples. Type: Expression profiling by array.

openGEO-OpenSep 2010View details →
ClinicalTrials.gov20/100

Bupropion & Cardio Birth Defect (Slone)

ClinicalTrials.gov study NCT01597661. IPD Sharing: Not stated. Countries: 0. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov20/100

Birth Defects Associated With Exposure to Lamotrigine in Pregnancy (EUROCAT)

ClinicalTrials.gov study NCT01055327. IPD Sharing: Not stated. Countries: 0. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
geo20/100

Dll3 and Notch1 genetic interactions model axial segmental and craniofacial malformations of human birth defects

GEO Series GSE8027. Mus musculus. 9 samples. Type: Expression profiling by array.

openGEO-OpenJul 2007View details →
geo16/100

Investigating the mechanisms by which SMAD6 mutations cause tracheoesophageal birth defects

GEO Series GSE305960. Homo sapiens. 54 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenDec 2025View details →
CCDI Data Catalog16/100

Gabriella Miller Kids First Pediatric Research Program for Infantile Hemangiomas Associated with Multi-Organ Structural Birth Defects

Infantile hemangiomas are the most common benign vascular tumor in infants, affecting 4-5% of children. Thirty percent of segmental infantile hemangiomas on the face and scalp are associated with birth defects of multiple organs. This condition is known as PHACE, an acronym for posterior fossa brain malformations, segmental facial hemangiomas, arterial anomalies, cardiac defects, eye anomalies, and sternal clefting. Genomic analysis of PHACE will inform treatment and expand knowledge about the causes of birth defects affecting the brain, arteries, heart, eye, midline development and hearing. The knowledge gained in this study will be used to drive strategies for prevention and provide critical targets for treatments for a range of birth defects and infantile hemangiomas.

unknownView details →
geo12/100

Paternal exposure alone induces alcohol-related birth defects in a mouse model: Implications of paternal drinking in FAS birth defects.

GEO Series GSE218362. Mus musculus. 16 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenJun 2024View details →
CCDI Federation: Data Node12/100

Gabriella Miller Kids First Pediatric Research Program in Genetics at the Intersection of Childhood Cancer and Birth Defects

Birth defects and childhood cancer share biological pathways that are important for cell growth and division. We propose that sequencing pediatric patients suffering both conditions will allow us to discover the underlying genes and in turn advance our understanding of the causes of these devastating diseases.

unknownView details →
CCDI Hub12/100

Gabriella Miller Kids First Pediatric Research Program in Genetics at the Intersection of Childhood Cancer and Birth Defects

Open the record for dataset details and reuse information.

unknownView details →
C3DC4/100

Gabriella Miller Kids First Pediatric Research Program in Genetics at the Intersection of Childhood Cancer and Birth Defects

Open the record for dataset details and reuse information.

unknownView details →

ScienceDex guides

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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

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