Evidence map›Paper›PMID 39571704›Full record

ArticleBone2025

A NOTCH2 pathogenic variant and HES1 regulate osteoclastogenesis in induced pluripotent stem cells.

Ernesto Canalis, Lauren Schilling, Emily Denker, Christopher Stoddard, Jungeun Yu

Abstract read
In one paragraph

Article in Bone, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Myeloid-Specific Deletion ofBiomedicines · 2026
    Article
  3. Review
  4. Article
  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Ernesto CanalisDepartment of Orthopaedic Surgery, UConn Health, Farmington, CT, USA; Department of Medicine, UConn Health, Farmington, CT, USA; UConn Musculoskeletal Institute, UConn Health, Farmington, CT, USA. Electronic address: canalis@uchc.edu.
Lauren SchillingUConn Musculoskeletal Institute, UConn Health, Farmington, CT, USA.
Emily DenkerUConn Musculoskeletal Institute, UConn Health, Farmington, CT, USA.
Christopher StoddardUConn Cell and Genome Engineering Core, UConn Health, Farmington, CT, USA.
Jungeun YuDepartment of Orthopaedic Surgery, UConn Health, Farmington, CT, USA; UConn Musculoskeletal Institute, UConn Health, Farmington, CT, USA.

Funding

Mechanisms and Treatment of Hajdu Cheney SyndromeR01AR078149 · NIAMS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI CANALIS, ERNESTO · 2021 to 2025
$1.8M
NIAMS NIH HHS R01 AR078149
6 · The paper itself

Abstract

Hajdu Cheney Syndrome (HCS), a monogenic disorder associated with NOTCH2 pathogenic variants, presents with neurological, craniofacial and skeletal abnormalities. Mouse models of the disease exhibit osteopenia. To determine the consequences of a HCS pathogenic variant in human cells, induced pluripotent NCRM1 and NCRM5 stem (iPS) cells harboring a NOTCH2

Indexed as

Cell DifferentiationInduced Pluripotent Stem CellsOsteoclastsOsteogenesisReceptor, Notch2Transcription Factor HES-1AnimalsBasic Helix-Loop-Helix ProteinsHajdu-Cheney SyndromeHumansMiceBasic Helix-Loop-Helix ProteinsHES1 protein, humanNOTCH2 protein, humanReceptor, Notch2Transcription Factor HES-1HES1NOTCHOsteoclastogenesisOsteogenesisStem cells

Identifiers

PMID39571704
PMCPMC11624087

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.