Evidence map›Paper›PMID 36833440›Full record

ArticleGenes2023

Association of Single-Nucleotide Polymorphisms Rs2779249 (chr17:26128581 C>A) and Rs rs2297518 (chr17: chr17:27769571 G>A) of the

Polina V Alyabyeva, Marina M Petrova, Diana V Dmitrenko, Natalia P Garganeeva, Galina A Chumakova, Mustafa Al-Zamil, Vera V Trefilova, Regina F Nasyrova, Natalia A Shnayder

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Genes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 42% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

9 authors at 5 institutions in 1 country.

Polina V AlyabyevaShared Core Facilities Molecular and Cell Technologies, V.F. Voino-Yasenetsky Krasnoyarsk State Medical University, 660022 Krasnoyarsk, Russia.ORCID 0000-0002-8833-1052
Marina M PetrovaShared Core Facilities Molecular and Cell Technologies, V.F. Voino-Yasenetsky Krasnoyarsk State Medical University, 660022 Krasnoyarsk, Russia.
Diana V DmitrenkoShared Core Facilities Molecular and Cell Technologies, V.F. Voino-Yasenetsky Krasnoyarsk State Medical University, 660022 Krasnoyarsk, Russia.ORCID 0000-0003-4639-6365
Natalia P GarganeevaDepartment of General Medical Practice and Outpatient Therapy, Siberian State Medical University, 634050 Tomsk, Russia.ORCID 0000-0002-7353-7154
Galina A ChumakovaDepartment of Therapy and General Medical Practice with a Course of Postgraduate Professional Education, Altai State Medical University, 656038 Barnaul, Russia.
Mustafa Al-ZamilDepartment of Physiotherapy, Faculty of Continuing Medical Education, Peoples' Friendship University of Russia, 117198 Moscow, Russia.ORCID 0000-0002-3643-982X
Vera V TrefilovaNeurological Department No. 16, Hospital for War Veterans, 193079 St. Petersburg, Russia.
Regina F NasyrovaInstitute of Personalized Psychiatry and Neurology, V.M. Bekhterev National Medical Research Center for Psychiatry and Neurology, 192019 St. Petersburg, Russia.ORCID 0000-0003-1874-9434
Natalia A ShnayderShared Core Facilities Molecular and Cell Technologies, V.F. Voino-Yasenetsky Krasnoyarsk State Medical University, 660022 Krasnoyarsk, Russia.ORCID 0000-0002-2840-837X
Krasnoyarsk State Medical University · RUSt.Petersburg V.M.Bekhterev Psychoneurological Research Institute · RUAltai State Medical University · RUPeoples' Friendship University of Russia · RUSiberian State Medical University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inducible nitric oxide (NO) synthase (iNOS), encoded by the

Indexed as

Autoimmune DiseasesHypertensionTension-Type HeadacheAdultGenetic Predisposition to DiseaseHumansNitric Oxide Synthase Type IIPilot ProjectsPolymorphism, Single NucleotideSiberiaNitric Oxide Synthase Type IINOS2 protein, humanbiomarkerhypertensioniNOSNOS2overlap syndromers2779249single-nucleotide polymorphismtension-type headache

Identifiers

PMID36833440
PMCPMC9957272
OpenAlexW4321373363

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.