Evidence map›Paper›PMID 37404458›Full record

ArticleMultidisciplinary respiratory medicine2023

Germline variant of CTC1 gene in a patient with pulmonary fibrosis and myelodysplastic syndrome.

Martina Doubková, Zuzana Vrzalová, Marianna Štefániková, Libor Červinek, Kateřina Staňo Kozubík, Ivona Blaháková, Šárka Pospíšilová, Michael Doubek

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

Article in Multidisciplinary respiratory medicine, 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
0.5field-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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

8 authors at 2 institutions in 1 country.

Martina DoubkováDepartment of Pulmonary Diseases and Tuberculosis, University Hospital and Faculty of Medicine, Brno.
Zuzana VrzalováCentral European Institute of Technology, Masaryk University, Brno.
Marianna ŠtefánikováDepartment of Pulmonary Diseases and Tuberculosis, University Hospital and Faculty of Medicine, Brno.
Libor ČervinekDepartment of Internal Medicine - Hematology and Oncology, University Hospital and Faculty of Medicine, Brno.
Kateřina Staňo KozubíkCentral European Institute of Technology, Masaryk University, Brno.
Ivona BlahákováCentral European Institute of Technology, Masaryk University, Brno.
Šárka PospíšilováCentral European Institute of Technology, Masaryk University, Brno.
Michael DoubekCentral European Institute of Technology, Masaryk University, Brno.
Central European Institute of Technology – Masaryk University · CZUniversity Hospital Brno · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Telomeropathies are associated with a wide range of diseases and less common combinations of various pulmonary and extrapulmonary disorders. Case presentation: In proband with high-risk myelodysplastic syndrome and interstitial pulmonary fibrosis, whole exome sequencing revealed a germline heterozygous variant of Conclusions: In our case report, we describe a rare case of coincidence of pulmonary fibrosis and hematological malignancy caused by a germline gene mutation in

Indexed as

CTC1 geneinterstitial pulmonary fibrosismyelodysplastic syndrome

Identifiers

PMID37404458
PMCPMC10316942
OpenAlexW4379471256

What OpenQuestion holds

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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.