Evidence map›Paper›PMID 30126146›Full record

ArticleGenes2018

Identification of Novel Candidate Markers of Type 2 Diabetes and Obesity in Russia by Exome Sequencing with a Limited Sample Size.

Yury A Barbitoff, Elena A Serebryakova, Yulia A Nasykhova, Alexander V Predeus, Dmitrii E Polev, Anna R Shuvalova, Evgenii V Vasiliev, Stanislav P Urazov, Andrey M Sarana, Sergey G Scherbak and 7 more

Open access · goldAbstract read
In one paragraph

Article in Genes, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

16 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Pharmacogenetics of Type 2 Diabetes-Progress and Prospects.International journal of molecular sciences · 2020
    Review
  13. Transcription Factor RREB1: from Target Genes towards Biological Functions.International journal of biological sciences · 2020
    Review
  14. Article
  15. Review
  16. Genetic Variation in ADAMTS13 is Related to VWF Levels, Atrial Fibrillation and Cerebral Ischemic Events.Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
    Article
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

17 authors at 4 institutions in 1 country.

Yury A BarbitoffBiobank of the Research Park, Saint Petersburg State University, 199034 Saint Petersburg, Russia. barbitoff@bioinf.me.ORCID 0000-0002-3222-440X
Elena A SerebryakovaBiobank of the Research Park, Saint Petersburg State University, 199034 Saint Petersburg, Russia. e.a.zhukova@spbu.ru.
Yulia A NasykhovaBiobank of the Research Park, Saint Petersburg State University, 199034 Saint Petersburg, Russia. yulnasa@gmail.com.
Alexander V PredeusBioinformatics Institute, 194100 Saint Petersburg, Russia. predeus@bioinf.me.ORCID 0000-0002-2750-1599
Dmitrii E PolevBiobank of the Research Park, Saint Petersburg State University, 199034 Saint Petersburg, Russia. dmitrii.polev@spbu.ru.
Anna R ShuvalovaBiobank of the Research Park, Saint Petersburg State University, 199034 Saint Petersburg, Russia. shuvalova_anna_radionovna@mail.ru.
Evgenii V VasilievCity Hospital No. 40, Sestroretsk, 197706 Saint Petersburg, Russia. Vasilievev@mail.ru.
Stanislav P UrazovCity Hospital No. 40, Sestroretsk, 197706 Saint Petersburg, Russia. urasta@list.ru.
Andrey M SaranaInstitute of Translation Biomedicine, Saint Petersburg State University, 199034 Saint Petersburg, Russia. asarana@mail.ru.
Sergey G ScherbakInstitute of Translation Biomedicine, Saint Petersburg State University, 199034 Saint Petersburg, Russia. sgsherbak@mail.ru.
Dmitrii V GladyshevCity Hospital No. 40, Sestroretsk, 197706 Saint Petersburg, Russia. gladyshev@gmail.com.
Maria S PokrovskayaFederal State Institution «National Medical Research Center for Preventive Medicine» of the Ministry of Healthcare of the Russian Federation, 101990 Moscow, Russia. mpokrovskaya@gnicpm.ru.
Oksana V SivakovaFederal State Institution «National Medical Research Center for Preventive Medicine» of the Ministry of Healthcare of the Russian Federation, 101990 Moscow, Russia. osivakova@gnicpm.ru.
Aleksey N MeshkovFederal State Institution «National Medical Research Center for Preventive Medicine» of the Ministry of Healthcare of the Russian Federation, 101990 Moscow, Russia. meshkov@lipidclinic.ru.ORCID 0000-0001-5989-6233
Oxana M DrapkinaFederal State Institution «National Medical Research Center for Preventive Medicine» of the Ministry of Healthcare of the Russian Federation, 101990 Moscow, Russia. odrapkina@gnicpm.ru.
Oleg S GlotovLaboratory of Prenatal Diagnostics of Hereditary Diseases, FSBSI «The Research Institute of Obstetrics, Gynaecology and Reproductology Named after D.O. Ott», 199034 Saint Petersburg, Russia. olglotov@mai.ru.
Andrey S GlotovBiobank of the Research Park, Saint Petersburg State University, 199034 Saint Petersburg, Russia. a.glotov@spbu.ru.
St Petersburg University · RUNational Research Center for Preventive Medicine · RUCity Hospital No. 40 · RUBioinformatics Institute · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type 2 diabetes (T2D) and obesity are common chronic disorders with multifactorial etiology. In our study, we performed an exome sequencing analysis of 110 patients of Russian ethnicity together with a multi-perspective approach based on biologically meaningful filtering criteria to detect novel candidate variants and loci for T2D and obesity. We have identified several known single nucleotide polymorphisms (SNPs) as markers for obesity (rs11960429), T2D (rs9379084, rs1126930), and body mass index (BMI) (rs11553746, rs1956549 and rs7195386) (

Indexed as

association studyexome sequencingnext-generation sequencingobesitysingle nucleotide polymorphismssusceptibility locustype 2 diabetes

Identifiers

PMID30126146
PMCPMC6115942
OpenAlexW2887293504

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.