Evidence map›Paper›PMID 30121816›Full record

ArticleJournal of molecular neuroscience : MN2018

Genetic Risk Factors for Intracranial Aneurysm in the Kazakh Population.

Elena V Zholdybayeva, Yerkin Z Medetov, Akbota M Aitkulova, Yerbol T Makhambetov, Serik K Akshulakov, Assylbek B Kaliyev, Yerkebulan A Talzhanov, Gulmira N Kulmambetova, Aisha N Iskakova, Yerlan M Ramankulov

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of molecular neuroscience : MN, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

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  9. Aggrecan in Cardiovascular Development and Disease.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2020
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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

10 authors at 2 institutions in 1 country.

Elena V ZholdybayevaNational Center for Biotechnology, 13/5, Korgalzhinskoe Highway, Astana, Kazakhstan. lenazhol@gmail.com.ORCID http://orcid.org/0000-0002-9677-008X
Yerkin Z MedetovJSC "National Center of Neurosurgery", 34/1, Turan Avenue, Astana, Kazakhstan.
Akbota M AitkulovaNational Center for Biotechnology, 13/5, Korgalzhinskoe Highway, Astana, Kazakhstan.
Yerbol T MakhambetovJSC "National Center of Neurosurgery", 34/1, Turan Avenue, Astana, Kazakhstan.
Serik K AkshulakovJSC "National Center of Neurosurgery", 34/1, Turan Avenue, Astana, Kazakhstan.
Assylbek B KaliyevJSC "National Center of Neurosurgery", 34/1, Turan Avenue, Astana, Kazakhstan.
Yerkebulan A TalzhanovNational Center for Biotechnology, 13/5, Korgalzhinskoe Highway, Astana, Kazakhstan.
Gulmira N KulmambetovaNational Center for Biotechnology, 13/5, Korgalzhinskoe Highway, Astana, Kazakhstan.
Aisha N IskakovaNational Center for Biotechnology, 13/5, Korgalzhinskoe Highway, Astana, Kazakhstan.
Yerlan M RamankulovNational Center for Biotechnology, 13/5, Korgalzhinskoe Highway, Astana, Kazakhstan.
National Center for Biotechnology · KZAl-Farabi Kazakh National University · KZ

Funding

Ministry of Education and Science of the Republic of Kazakhstan № 0115РК00539
6 · The paper itself

Abstract

An intracranial aneurysm (IA) is a weak or thin area on a blood vessel in the brain that balloons as it fills with blood. Genetic factors can influence the risk of developing an aneurism. The purpose of this study was to explore the relationship between single nucleotide polymorphisms (SNPs) and IA in Kazakh population. The patients were genotyped for 60 single nucleotide polymorphisms. Genotyping was performed on the QuantStudio 12K Flex (Life Technologies). A linear regression analysis found 13 SNPs' significant association with development and rupture of IA: the rs1800956 polymorphism of the ENG gene, rs1756 46 polymorphism of the JDP2 gene, variant rs1800255 of the COL3A1, rs4667622 of the UBR3, rs2374513 of the c12orf75, rs3742321 polymorphism of the StAR, the rs3782356 polymorphism of MLL2 gene, rs3932338 to 214 kilobases downstream of PRDM9, rs7550260 polymorphism of the ARHGEF, rs1504749 polymorphism of the SOX17, the rs173686 polymorphism of CSPG2 gene, rs6460071 located on LIMK1 gene, and the rs4934 polymorphism of SERPINA3. A total of 13 SNPs were identified as potential genetic markers for the development and risk of rupture of aneurysms in the Kazakh population. Similar results were obtained after adjusting for the confounding factors of arterial hypertension and age.

Indexed as

Polymorphism, Single NucleotideAdultAgedCase-Control StudiesCollagen Type IIIDNA-Binding ProteinsEndoglinFemaleHistone-Lysine N-MethyltransferaseHumansIntracranial AneurysmKazakhstanLim KinasesMaleMiddle AgedNeoplasm ProteinsARHGEF1 protein, humanCOL3A1 protein, humanCollagen Type IIIDNA-Binding ProteinsEndoglinENG protein, humanHistone-Lysine N-MethyltransferaseJDP2 protein, humanKMT2D protein, humanLIMK1 protein, humanLim KinasesNeoplasm ProteinsPRDM9 protein, humanRepressor ProteinsRho Guanine Nucleotide Exchange FactorsSERPINA3 protein, humanSerpinsSOX17 protein, humanSOXF Transcription FactorsUbiquitin-Protein LigasesVCAN protein, humanVersicansGenotypingIntracranial aneurysmRisk factorsRuptured and unruptured aneurysmsSNP

Identifiers

PMID30121816
OpenAlexW2886251368

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.