Evidence map›Paper›PMID 40231492›Full record

ArticleTurkish journal of haematology : official journal of Turkish Society of Haematology2025

Optical Genome Mapping as a New Approach to Detecting Cytogenetic Abnormalities: Why Is It Difficult in Multiple Myeloma?

Ayşe Gül Bayrak Tokaç, Mehmet Burak Mutlu, Simge Erdem, Aynur Aday

Abstract read
In one paragraph

Article in Turkish journal of haematology : official journal of Turkish Society of Haematology, 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
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

4 authors.

Ayşe Gül Bayrak Tokaçİstanbul University, İstanbul Faculty of Medicine, Department of Internal Medicine, Division of Medical Genetics, İstanbul, TürkiyeORCID 0000-0003-2228-0632
Mehmet Burak MutluDetagen Genetic Diseases Evaluation Center, Kayseri, TürkiyeORCID 0000-0001-7745-8165
Simge Erdemİstanbul University, İstanbul Faculty of Medicine, Department of Internal Medicine, Division of Hematology, İstanbul, TürkiyeORCID 0000-0001-8095-5445
Aynur Adayİstanbul University, İstanbul Faculty of Medicine, Department of Internal Medicine, Division of Medical Genetics, İstanbul, TürkiyeORCID 0000-0001-8072-0646

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Chromosome mappingGenomic structural variationMultiple myeloma

Identifiers

PMID40231492
PMCPMC12099464

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.