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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.

This is not a judgment on the citing paper.

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)

Schema constants (for re-runners): correction · crossref

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.