Evidence map›Paper›PMID 30425912›Full record

ArticleBalkan journal of medical genetics : BJMG2018

M Vukovic, N Radlovic, Z Lekovic, K Vucicevic, N Maric, N Kotur, V Gasic, M Ugrin, M Stojiljkovic, L Dokmanovic and 2 more

Open access · goldAbstract read
In one paragraph

Article in Balkan journal of medical genetics : BJMG, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 29% of its field
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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. UGT1A1 Fragment Analysis: Genotyping the (TA)Journal of clinical laboratory analysis · 2026
    Article
  2. Review
  3. Article
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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

12 authors at 3 institutions in 3 countries.

M VukovicDepartment for Medical Genetics, University Clinical Centre of the Republic of Srpska, Banja Luka, Bosnia and Hercegovina.
N RadlovicDepartment of Gastroenterology and Nutrition, University Children's Hospital, School of Medicine, University of Belgrade, Belgrade, Serbia.
Z LekovicDepartment of Gastroenterology and Nutrition, University Children's Hospital, School of Medicine, University of Belgrade, Belgrade, Serbia.
K VucicevicDepartment of Physiology, Faculty of Medical Sciences, University of Kragujevac, Kragujevac, Serbia.
N MaricClinic for Children Diseases, University Clinical Centre of the Republic of Srpska, Banja Luka, Bosnia and Hercegovina.
N KoturLaboratory for Molecular Biomedicine, Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Belgrade, Serbia.
V GasicLaboratory for Molecular Biomedicine, Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Belgrade, Serbia.
M UgrinLaboratory for Molecular Biomedicine, Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Belgrade, Serbia.
M StojiljkovicLaboratory for Molecular Biomedicine, Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Belgrade, Serbia.
L DokmanovicDepartment of Hematology and Oncology, University Children's Hospital, School of Medicine, University of Belgrade, Belgrade, Serbia.
B ZukicLaboratory for Molecular Biomedicine, Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Belgrade, Serbia.
S PavlovicLaboratory for Molecular Biomedicine, Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Belgrade, Serbia.
University of Belgrade · RSUniversity Clinical Centre · PLUniversity of Kragujevac · RS

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The UGT1A1 enzyme is involved in the metabolism of bilirubin and numerous medications. Unconjugated hyperbilirubinemia, commonly presented as Gilbert syndrome (GS), is a result of decreased activity of the UGT1A1 enzyme, variable number of TA repeats in the promoter of the

Indexed as

Gilbert syndrome (GS)Population pharmacogenetics, UGT1A1 (TA)n promoter variantsUnconjugated hyperbilirubinemia

Identifiers

PMID30425912
PMCPMC6231317
OpenAlexW2899449478

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.