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Medical imaging (X-ray, CT, MRI), electronic health records, clinical trials, ECG/EEG, pathology
14,877 datasets
England's maternal healthcare data measures the percentage of women who had an assessment with a midwife or maternity professional by 12 weeks of pregnancy. The dataset was published by the Department of Health and Social Care via DCLG Floor Targets Interactive. It covers the time period from 2009 to 2010.
2001 data from the Health Poverty Index's Income domain, part of the Root Causes analysis. The dataset was published by the Health Poverty Index using administrative data from the UK Department of Health and Office of the Deputy Prime Minister. It provides geographic coverage for Local Authority Districts and national-level data across England.
UK Veterinary Laboratories Agency annual publications detailing available disease surveillance and diagnostic tests. The data includes two separate price lists for disease surveillance/export tests and commercial diagnostics. The dataset is licensed under OGL-UK-3.0 and was last updated in July 2026.
Charlotte Van Isterdael's study analyzes challenges in the clinical translation of Advanced Therapy Medicinal Products (ATMPs) for academic and SME developers in the EU. The analysis is based on a scoping literature review of peer-reviewed publications from PubMed, Embase, and Scopus covering the last decade. The findings, published on figshare in 2026, identify key challenges in preclinical evidence, manufacturing, clinical trials, and the regulatory landscape.
Resat Misirlioglu's retrospective cohort study comprises 350 singleton pregnancies with a prenatal diagnosis of aberrant right subclavian artery (ARSA) from a tertiary perinatology center between January 2020 and April 2025. Cases are classified as isolated ARSA (n=200), ARSA with soft markers (n=80), or non-isolated ARSA (n=70). The dataset reports primary outcomes of chromosomal abnormalities and live-birth rates across these phenotypic groups.
22 unsolved patients with suspected inborn errors of immunity were reanalyzed using a structured RNA-guided approach. The study, authored by Willem T. K. Maassen and last updated in May 2026, identified conclusive diagnoses for 2 out of the 22 patients. This demonstrates how RNA-sequencing can improve diagnostic yield for complex genetic disorders.
A research article describes a multidisciplinary RNA-guided approach to reanalyze unsolved patients with inborn errors of immunity. The study by Willem T. K. Maassen, posted on figshare in May 2026, analyzed a cohort of 22 patients where standard genetic testing was inconclusive. The approach led to a conclusive diagnosis for 2 out of 22 patients.
A 2026 study by Willem T. K. Maassen presents a structured RNA-guided reanalysis of 22 patients with suspected inborn errors of immunity. The multidisciplinary approach used RNA-sequencing to detect aberrant expression, splicing, and mono-allelic expression to identify causative variants. The analysis provided conclusive diagnoses for 2 out of the 22 patients.
A structured RNA-guided approach for reanalyzing unsolved patients with inborn errors of immunity. The method was applied to a cohort of 22 patients where standard genetic testing was inconclusive. The work was authored by Willem T. K. Maassen and last updated in May 2026.
A research document detailing a structured RNA-guided approach to reanalyze 22 patients with suspected inborn errors of immunity (IEI) for whom standard genetic testing was inconclusive. The study, authored by Willem T. K. Maassen and posted on figshare in May 2026, describes the methodology and results of a multidisciplinary analysis. It reports a conclusive diagnosis for 2 out of 22 patients, demonstrating how RNA-sequencing can improve diagnostic yield.
A 27.7 KB document authored by Willem T. K. Maassen and last updated on 2026-05-27. It describes a multidisciplinary study applying RNA-guided analysis to a cohort of 22 patients with suspected inborn errors of immunity where standard genetic testing was inconclusive.
Willem T. K. Maassen's dataset from a 2026 figshare publication details a multidisciplinary RNA-guided reanalysis of 22 patients with suspected inborn errors of immunity (IEI) for whom standard genetic testing was inconclusive. The data likely contains results from evaluating aberrant expression, splicing, and mono-allelic expression to identify causative genetic variants. The study concluded with a diagnosis for 2 out of the 22 patients in the cohort.
Training dataset for the Carotid Vessel Wall Segmentation and Atherosclerosis Diagnosis Challenge at MICCAI 2022. The dataset was created by researchers at Tsinghua University and is hosted on the challenge website.
Bahia state's public health expenditures across municipalities, regions, and macro-regions from 2009 to 2012. The data, analyzed using the National Health Accounts model, shows a 28% increase in municipal spending over the four-year period. Author Andrei Souza Teles found spending was concentrated in macro-regions with higher installed capacity but remained insufficient relative to population needs.
A prospective observational study of 231 carotid atherosclerosis patients and 231 healthy controls from July 2018 to December 2019. The dataset, described in an Open Access paper by Xincheng Huang, includes serum PM20D1 levels, demographic characteristics, and various inflammatory and lipid biomarkers. It was analyzed to investigate PM20D1's role as a potential biomarker for disease severity and plaque stability.
BreCaHAD is a dataset for breast cancer histopathological annotation and diagnosis. It contains original images and JSON files providing ground-truth annotations for six cell and tissue classes, including mitosis, apoptosis, tumor nuclei, and tubules. The dataset was created by Alper Aksaç.
An electronic protocol database for chronic venous insufficiency (CVI) containing 2,877 specific data items. It was developed from a master protocol of 6,145 items covering vascular diseases through a bibliographic review and computerized using the SINPE© system. The protocol's functionality was validated in a pilot project analyzing data from medical records.
84 patients with obstructive sleep apnea were evaluated to correlate cephalometric measurements with apnea severity. The study, authored by Michele Tepedino, collected lateral cephalograms and polysomnography data, finding a statistical correlation between mandibular length and the apnea-hypopnea index. Patients with severe apnea showed reduced sagittal growth of the mandible and cranial base.
Manual annotations of invasive tumor tissue on diagnostic whole slide images from The Cancer Genome Atlas. Annotations were created by trained observers using QuPath software to enrich regions for molecular prediction studies, excluding non-tumor areas. The project merges COAD and READ tumor types into a single CRC category.
Histological images of colorectal cancer tumor tissue, manually outlined and cut into 512 px tiles at an effective magnification of 0.5 µm/px. All tiles were color-normalized using the Macenko method and labeled with the parent patient's MSI status, with patients split into a 2:1 training-test ratio and training tiles undersampled for class balance. The dataset was derived from the TCGA database by Jakob Nikolas Kather of RWTH Aachen University.