Evidence map›Paper›PMID 28611551›Full record

ArticleMolecular syndromology2017

First Two Cases of Bloom Syndrome in Russia: Lack of Skin Manifestations in a

Evgeny N Suspitsin, Farida I Sibgatullina, Lydia V Lyazina, Evgeny N Imyanitov

Open access · bronzeAbstract read
In one paragraph

Article in Molecular syndromology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Pathogenic Germline DNA Repair Gene andJCO precision oncology · 2020
    Article
  5. Inherited Variants inCancers · 2019
    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

4 authors at 3 institutions in 1 country.

Evgeny N SuspitsinSt. Petersburg State Pediatric Medical University, Kazan, Russia.
Farida I SibgatullinaChildren Clinical Hospital of the Republic of Tatarstan, Kazan, Russia.
Lydia V LyazinaSt. Petersburg Center of Medical Genetics, Kazan, Russia.
Evgeny N ImyanitovSt. Petersburg State Pediatric Medical University, Kazan, Russia.
Institute of Oncology NN Petrov · RURepublican Clinical Hospital of the Ministry of Health of the Republic of Tatarstan · RUSaint Petersburg State Pediatric Medical University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bloom syndrome (BS) is an exceptionally rare hereditary disease. Typical manifestations of BS usually include growth deficiency, a characteristic facial appearance, skin hypersensitivity to ultraviolet irradiation, and a strong predisposition to early-onset cancers. We have previously described a recurrent

Indexed as

Bloom syndromeImmune deficiencyPhotosensitivityRecurrent mutationsShort stature

Identifiers

PMID28611551
PMCPMC5465803
OpenAlexW2578626215

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.