Evidence map›Paper›PMID 41635665›Full record

ArticleActa clinica Croatica2025

THROMBOTIC RISK EVALUATION OF TWO METHYLENETETRAHYDROFOLATE REDUCTASE MUTATIONS C677t AND A1298c IN VENOUS THROMBOEMBOLISM.

Renata Kundid, Monika Kolundžić, Ivana Babić, Tatjana Kereš, Tomo Svaguša, Jasna Bingulac-Popović, Ana Hećimović, Irena Jukić

Abstract read
In one paragraph

Article in Acta clinica Croatica, 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

8 authors.

Renata Kundid
Monika Kolundžić
Ivana Babić
Tatjana Kereš
Tomo Svaguša
Jasna Bingulac-Popović
Ana Hećimović
Irena Jukić

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The MTHFR mutations C677T and A1298C combined with folate and vitamin B12 deficiency lead to hypercoagulability. We evaluated thrombotic risk due to MTHFR mutations, individually and in combination, in patients with venous thromboembolism (VTE). The case-control study included groups of 262 VTE patients and 101 healthy controls. Allelic distribution of MTHFR C677T/A1298C mutations was determined by real-time polymerase chain reaction and results were statistically analyzed using χ

Indexed as

AllelesGenotypeMTHFR (methylenetetrahydrofolate reductase)Venous thromboembolism

Identifiers

PMID41635665
PMCPMC12863379

What OpenQuestion holds

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Registered trials

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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.