Evidence map›Paper›PMID 41751632›Full record

SynthesisGenes2026

Genetic Mapping of the 22q11.2 Deletion Syndrome (DiGeorge Syndrome) Microdeletion Types Revealed Novel Candidate Breakpoints.

Louis Papageorgiou, Elena Nikolopoulou, Eleni Koniari, Kyriaki Hatziagapiou, Dimitrios Chaniotis, Apostolos Beloukas, George P Chrousos, Elias Eliopoulos, Trias Thireou

Abstract readSystematic Review
PubMed Full text at PMC Publisher
In one paragraph

Synthesis in Genes, 2026. 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
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Louis PapageorgiouDepartment of Biomedical Sciences, University of West Attica, Agioy Spyridonos 28, 12243 Egaleo, Greece.ORCID 0000-0001-9577-9923
Elena NikolopoulouLaboratory of Genetics, Department of Biotechnology, Agricultural University of Athens, 11855 Athens, Greece.
Eleni KoniariUniversity Research Institute of Maternal and Child Health and Precision Medicine, School of Medicine, National Kapodistrian University of Athens, 11527 Athens, Greece.ORCID 0009-0008-6294-1988
Kyriaki HatziagapiouUniversity Research Institute of Maternal and Child Health and Precision Medicine, School of Medicine, National Kapodistrian University of Athens, 11527 Athens, Greece.ORCID 0000-0002-1469-1928
Dimitrios ChaniotisDepartment of Biomedical Sciences, University of West Attica, Agioy Spyridonos 28, 12243 Egaleo, Greece.ORCID 0000-0003-2313-1305
Apostolos BeloukasDepartment of Biomedical Sciences, University of West Attica, Agioy Spyridonos 28, 12243 Egaleo, Greece.ORCID 0000-0001-5639-0528
George P ChrousosUniversity Research Institute of Maternal and Child Health and Precision Medicine, School of Medicine, National Kapodistrian University of Athens, 11527 Athens, Greece.ORCID 0000-0002-3098-5264
Elias EliopoulosLaboratory of Genetics, Department of Biotechnology, Agricultural University of Athens, 11855 Athens, Greece.ORCID 0000-0002-0919-0571
Trias ThireouLaboratory of Genetics, Department of Biotechnology, Agricultural University of Athens, 11855 Athens, Greece.ORCID 0000-0002-6894-0774

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Chromosome BreakpointsDiGeorge SyndromeChromosome DeletionChromosome MappingChromosomes, Human, Pair 22Humans22q11.2 deletion syndromebreak pointsclinical genomicsDiGeorge SyndromegeneticsgenomicsLCRspalindromic analysis

Identifiers

PMID41751632
PMCPMC12940653

What OpenQuestion holds

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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.