In one paragraphReview in Genes, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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 registryThe 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 literatureWho cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
4 · The recordCorrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
5 · Who and what moneyAuthors and funding
10 authors.
Sopio GverdtsiteliDepartment of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, DK-2100 Copenhagen, Denmark.ORCID 0000-0002-7404-3631 Trine Bjørg HammerDepartment of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, DK-2100 Copenhagen, Denmark.
Xenia HermannResource Center for Rare Oral Diseases, Copenhagen University Hospital, Rigshospitalet, DK-2100 Copenhagen, Denmark.
Noemi Becser AndersenThe Epilepsy Clinic, Department of Neurology, Copenhagen University Hospital, Rigshospitalet, DK-2100 Copenhagen, Denmark.
David Ros-PardoMolecular Modeling Group, Centro de Biologia Molecular Severo Ochoa (CBM, CSIC-UAM), E-28049 Madrid, Spain.ORCID 0000-0002-8934-8585 Iñigo Marcos-AlcaldeMolecular Modeling Group, Centro de Biologia Molecular Severo Ochoa (CBM, CSIC-UAM), E-28049 Madrid, Spain.ORCID 0000-0002-0674-6423 Paulino Gómez-PuertasMolecular Modeling Group, Centro de Biologia Molecular Severo Ochoa (CBM, CSIC-UAM), E-28049 Madrid, Spain.ORCID 0000-0003-3131-729X Asli SilahtarogluDepartment of Cellular and Molecular Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3, DK-2200 Copenhagen, Denmark.ORCID 0000-0001-6181-2705 Zeynep TümerDepartment of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, DK-2100 Copenhagen, Denmark.ORCID 0000-0002-4777-5802 Funding
ERN-ITHACA N°101156387Spanish government grant MCIN/AEI/10.13039/501100011033/FEDER,EU.2022
6 · The paper itselfAbstract
PubMed holds no abstract for this paper.
Indexed as
Mutation, MissenseNeurodevelopmental DisordersTooth AbnormalitiesHumansPhenotypeamelocerebrohypohidrotic syndromeamelogenesis imperfectacomplex interactive developmental networksKohlschütter–Tönz syndromeROGDIROGDI-related neurodevelopmental and dental disorder
Identifiers
PMID41153423
PMCPMC12563357
What OpenQuestion holds
Textmetadata
LicenceCC BY
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