Evidence map›Paper›PMID 36833187›Full record

ArticleGenes2023

Spectrum of Causative Mutations in Patients with Hemophilia A in Russia.

Olesya Pshenichnikova, Valentina Salomashkina, Julia Poznyakova, Daria Selivanova, Daria Chernetskaya, Elena Yakovleva, Oksana Dimitrieva, Elena Likhacheva, Farida Perina, Nadezhda Zozulya and 1 more

Open access · goldAbstract read
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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

11 authors at 2 institutions in 1 country.

Olesya PshenichnikovaLaboratory of Genetic Engineering of National Medical Research Center for Hematology, Novy Zykovski Lane 4a, 125167 Moscow, Russia.ORCID 0000-0001-5752-8146
Valentina SalomashkinaLaboratory of Genetic Engineering of National Medical Research Center for Hematology, Novy Zykovski Lane 4a, 125167 Moscow, Russia.
Julia PoznyakovaLaboratory of Genetic Engineering of National Medical Research Center for Hematology, Novy Zykovski Lane 4a, 125167 Moscow, Russia.
Daria SelivanovaLaboratory of Genetic Engineering of National Medical Research Center for Hematology, Novy Zykovski Lane 4a, 125167 Moscow, Russia.
Daria ChernetskayaLaboratory of Genetic Engineering of National Medical Research Center for Hematology, Novy Zykovski Lane 4a, 125167 Moscow, Russia.
Elena YakovlevaCoagulopathies Department of National Medical Research Center for Hematology, Novy Zykovski Lane 4a, 125167 Moscow, Russia.
Oksana DimitrievaCoagulopathies Department of National Medical Research Center for Hematology, Novy Zykovski Lane 4a, 125167 Moscow, Russia.
Elena LikhachevaCoagulopathies Department of National Medical Research Center for Hematology, Novy Zykovski Lane 4a, 125167 Moscow, Russia.
Farida PerinaCenter for Pediatric Oncology and Hematology of State Autonomous Healthcare Institution 'Sverdlovsk Regional Children's Clinical Hospital', Serafima Deryabina Street 32, 620149 Ekaterinburg, Russia.
Nadezhda ZozulyaCoagulopathies Department of National Medical Research Center for Hematology, Novy Zykovski Lane 4a, 125167 Moscow, Russia.
Vadim SurinLaboratory of Genetic Engineering of National Medical Research Center for Hematology, Novy Zykovski Lane 4a, 125167 Moscow, Russia.
National Medical Research Center for Hematology · RURegional Children's Clinical Hospital No. 1 · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hemophilia A (HA) is one of the most widespread, X-linked, inherited bleeding disorders, which results from defects in the

Indexed as

Hemophilia AChromosome InversionFactor VIIIHumansMutationNucleotidesRussiaFactor VIIINucleotidesF8 genegenetic diagnosticshemophilia Apathogenic variant

Identifiers

PMID36833187
PMCPMC9957479
OpenAlexW4317426363

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.