Evidence map›Paper›PMID 35571017›Full record

ArticleFrontiers in genetics2022

Genetic Landscape of Nephropathic Cystinosis in Russian Children.

K V Savostyanov, A A Pushkov, O A Shchagina, V V Maltseva, E A Suleymanov, I S Zhanin, N N Mazanova, A P Fisenko, P S Mishakova, A V Polyakov and 3 more

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

Article in Frontiers in genetics, 2022. 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
1.5field-weighted citation impact, top 19% 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, 10 citations in OpenAlex.

  1. Article
  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

13 authors at 3 institutions in 1 country.

K V SavostyanovNational Medical Research Center for Children's Health Federal State Autonomous Institution of the Ministry of Health of the Russian Federation, Moscow, Russia.
A A PushkovNational Medical Research Center for Children's Health Federal State Autonomous Institution of the Ministry of Health of the Russian Federation, Moscow, Russia.
O A ShchaginaResearch Centre for Medical Genetics, Moscow, Russia.
V V MaltsevaNational Medical Research Center for Children's Health Federal State Autonomous Institution of the Ministry of Health of the Russian Federation, Moscow, Russia.
E A SuleymanovMinistry of Public Health, Republic of Chechnya, Grozny, Russia.
I S ZhaninNational Medical Research Center for Children's Health Federal State Autonomous Institution of the Ministry of Health of the Russian Federation, Moscow, Russia.
N N MazanovaNational Medical Research Center for Children's Health Federal State Autonomous Institution of the Ministry of Health of the Russian Federation, Moscow, Russia.
A P FisenkoNational Medical Research Center for Children's Health Federal State Autonomous Institution of the Ministry of Health of the Russian Federation, Moscow, Russia.
P S MishakovaResearch Centre for Medical Genetics, Moscow, Russia.
A V PolyakovResearch Centre for Medical Genetics, Moscow, Russia.
E V BalanovskaResearch Centre for Medical Genetics, Moscow, Russia.
R A ZinchenkoResearch Centre for Medical Genetics, Moscow, Russia.
A N TsyginNational Medical Research Center for Children's Health Federal State Autonomous Institution of the Ministry of Health of the Russian Federation, Moscow, Russia.
Research Centre for Medical Genetics · RUScientific Center of Children's Health · RUMinistry of Health of the Russian Federation · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nephropathic cystinosis is a rare autosomal recessive disorder characterized by amino acid cystine accumulation and caused by biallelic mutations in the

Indexed as

childrencystinecystinosislysosomal storage diseasesnovel mutations in the CTNS geneselective screeningtherapy monitoring

Identifiers

PMID35571017
PMCPMC9096100
OpenAlexW4225014752

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.