Evidence map›Paper›PMID 40565606›Full record

ArticleGenes2025

Results of Chromosomal Microarray Need to Always Be Checked by (Molecular) Cytogenetics-Even If They Seem to Be Simple Deletions.

Thomas Liehr, Sylke Singer, Ulrike Mau-Holzmann, Stefanie Kankel, Niklas Padutsch, Luisa Person, Eva Daumiller, Uwe Kornak

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Genes, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

8 authors.

Thomas LiehrJena University Hospital, Friedrich Schiller University, Institute of Human Genetics, Am Klinikum 1, 07747 Jena, Germany.ORCID 0000-0003-1672-3054
Sylke SingerInstitut für Medizinische Genetik und Angewandte Genomik, Calwerstr. 7, 72076 Tübingen, Germany.
Ulrike Mau-HolzmannInstitut für Medizinische Genetik und Angewandte Genomik, Calwerstr. 7, 72076 Tübingen, Germany.ORCID 0000-0002-4125-4643
Stefanie KankelJena University Hospital, Friedrich Schiller University, Institute of Human Genetics, Am Klinikum 1, 07747 Jena, Germany.
Niklas PadutschJena University Hospital, Friedrich Schiller University, Institute of Human Genetics, Am Klinikum 1, 07747 Jena, Germany.
Luisa PersonJena University Hospital, Friedrich Schiller University, Institute of Human Genetics, Am Klinikum 1, 07747 Jena, Germany.
Eva DaumillerGenetikum Stuttgart, Lautenschlagerstr. 23, 70173 Stuttgart, Germany.
Uwe KornakUniversitätsmedizin Göttingen, Institut für Humangenetik, Heinrich-Düker-Weg 12, 37073 Göttingen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Intellectual DisabilityAdolescentAdultChildChild, PreschoolChromosome DeletionCytogenetic AnalysisDNA Copy Number VariationsFemaleHumansIn Situ Hybridization, FluorescenceMaleOligonucleotide Array Sequence Analysischromosomal microarraycomplex rearrangementsfluorescence in situ hybridizationloss of copy numberssecond test

Identifiers

PMID40565606
PMCPMC12192749

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.