Citation notice #9696 · 2026-08-11 12:17:58.608255+00:00
AI-Enhanced Sensemaking: Exploring the Design of a Generative AI-Based Assistant to Support Genetic Professionals
Correction
Crossref
Open
cites 10.1038/s41431-021-00852-7, which carries a correction notice dated 2021-08-15. One-hop deterministic notice: the citation edge exists in the Pith bibliography graph; no model judged whether the citation was load-bearing.
Citing paper Event page Original DOI Notice DOI File a formal challenge All reference changes
01Evidence
Raw extraction · bibliography line · bibliography index 57
Matalonga, L. et al. 2021. Solving patients with rare diseases through programmatic reanalysis of genome - phenome data. European journal of human genetics: EJHG . 29, 9 (Sep. 2021), 1337 –1347. DOI:https://doi.org/10.1038/s41431-021-00852-7
02Event
- Type
- Correction
- Source
- Crossref
- Original DOI
- 10.1038/s41431-021-00852-7
- Notice DOI
- 10.1038/s41431-021-00934-6
- Date
- 2021-08-15
- Title
- Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data
- Reasons
- ['Correction']
- Work
- - (2021)
03Dispute this notice
If this citation does not depend on the flagged claim, or the event is wrong, say so. Disputes are public. For a signed challenge against the paper itself, use the formal challenge form.