Evidence map›Paper›PMID 42450630›Full record

ArticleBiology2026

Atypical Phenotype of Myotonic Dystrophy Type 1 with Variant Repeats at the Age of Diagnosis.

Nemanja Radovanovic, Jovan Pesovic, Vanja Viric, Nikola Andrejic, Ivo Bozovic, Goran Brajuskovic, Dusanka Savic-Pavicevic, Stojan Peric

Abstract read
In one paragraph

Article in Biology, 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

8 authors.

Nemanja RadovanovicCentre for Human Molecular, Faculty of Biology, University of Belgrade, Studentski Trg 16, 11000 Belgrade, Serbia.ORCID 0000-0002-0592-8890
Jovan PesovicCentre for Human Molecular, Faculty of Biology, University of Belgrade, Studentski Trg 16, 11000 Belgrade, Serbia.ORCID 0000-0002-8304-2067
Vanja ViricNeurology Clinic, University Clinical Centre of Serbia, Dr Subotica Starijeg 6, 11000 Belgrade, Serbia.
Nikola AndrejicNeurology Clinic, University Clinical Centre of Serbia, Dr Subotica Starijeg 6, 11000 Belgrade, Serbia.ORCID 0009-0005-4175-4030
Ivo BozovicNeurology Clinic, University Clinical Centre of Serbia, Dr Subotica Starijeg 6, 11000 Belgrade, Serbia.ORCID 0000-0002-6623-0779
Goran BrajuskovicCentre for Human Molecular, Faculty of Biology, University of Belgrade, Studentski Trg 16, 11000 Belgrade, Serbia.ORCID 0000-0002-3935-6755
Dusanka Savic-PavicevicCentre for Human Molecular, Faculty of Biology, University of Belgrade, Studentski Trg 16, 11000 Belgrade, Serbia.ORCID 0000-0002-2079-4077
Stojan PericNeurology Clinic, University Clinical Centre of Serbia, Dr Subotica Starijeg 6, 11000 Belgrade, Serbia.ORCID 0000-0002-2979-556X

Funding

Ministry of Science, Technological Development, and Innovation 451-03-33/2026-03/200178Ministry of Science, Technological Development, and Innovation 451-03-475 34/2026-03/200178Science Fund of the Republic of Serbia 7754217
6 · The paper itself

Abstract

Myotonic dystrophy type 1 (DM1) is caused by an expansion of CTG repeats in the

Indexed as

age at diagnosisDMPKgenetic modifiermyotonic dystrophy type 1repeat expansionrepeat interruptionsvariant repeats

Identifiers

PMID42450630
PMCPMC13359955

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.