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2026-11-01 issue

Observed arrival · 2026-11-01

StudyTrace follows rare-disease research back to its sources

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Editorial interest 83/100 Selection signal · not a rating of the site

StudyTrace says it turns a rare-disease diagnosis into a plain-language report on research, treatments, and clinical trials.

Landing page captured for the 2026-11-01 issue.
For
People researching a rare-disease diagnosis
Worth noticing
It checks diagnoses against MONDO and says it can name researchers and centres across North America, Europe, and Australasia.

Field notes

The homepage offers Fabry disease, Marfan syndrome, and Huntington disease as example starting points. Its stated source set spans Europe PMC (including PubMed), ClinicalTrials.gov, and NIH RePORTER; the site says it checks diagnoses against the MONDO ontology. It also says reports can be saved as PDFs and names researchers and centres in North America, Europe, and Australasia. A disclaimer says the information is not medical advice.

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Landing page observed 2026-11-01. The live site may have changed.