Evidence map›Paper›PMID 30740155›Full record

ArticleOpen access Macedonian journal of medical sciences2019

The Role of Polymorphism Gen

Cut Aria Arina, Darwin Amir, Yahwardiah Siregar, Rosita J Sembiring

Open access · diamondAbstract read
In one paragraph

Article in Open access Macedonian journal of medical sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 8% 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, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Association BetweenFrontiers in genetics · 2021
    Review
  6. Hyperhomocysteinemia: Clinical Insights.Journal of central nervous system disease · 2020
    Review
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 at 2 institutions in 1 country.

Cut Aria ArinaMedical Faculty, Universitas Sumatera Utara, North Sumatera, Medan, Indonesia.
Darwin AmirMedical Faculty, Universitas Andalas, West Sumatera, Padang, Indonesia.
Yahwardiah SiregarMedical Faculty, Universitas Sumatera Utara, North Sumatera, Medan, Indonesia.
Rosita J SembiringMedical Faculty, Universitas Sumatera Utara, North Sumatera, Medan, Indonesia.
Universitas Sumatera Utara · IDAndalas University · ID

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStroke is a leading cause of disability and remains the second leading cause of death in the world. Some of the pathogenesis of stroke are interactions between genetic and acquired risk factors, the interaction is related with the atherosclerotic which is the main pathogenesis of ischaemic stroke. Previous studies demonstrated an association between methylene tetra hydro folate reductase (MTHFR) genotype and ischaemic stroke; the

aimThis study aims to know about the role of polymorphism gen

methodsThis study is a cross-sectional study, the sample was taken consecutively, after approval by the Medical Faculty Science's Ethics Committee at University Sumatera Utara. All sample matched with inclusion and exclusion criteria, demography data and blood sample were taken. Demography data were analysed using descriptive statistic.

resultsOf the 106 ischaemic stroke patients were divided into two groups, the first group is patients with hypertension (53 patients), and the second group is without hypertension (53 patients). We have done the PCR- RFLP to all the patients, we got 78 patients with

conclusionWe concluded that polymorphism

Indexed as

HypertensionIschaemic strokePolymorphism gen MTHFR C677T

Identifiers

PMID30740155
PMCPMC6352466
OpenAlexW2907909798

What OpenQuestion holds

Textmetadata
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.