Evidence map›Paper›PMID 29208651›Full record

ArticleG3 (Bethesda, Md.)2018

A 12.3-kb Duplication Within the

Stefanie Lehner, Mahnaz Ekhlasi-Hundrieser, Carsten Detering, Hanna Allerkamp, Christiane Pfarrer, Mario von Depka Prondzinski

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in G3 (Bethesda, Md.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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

6 authors.

Stefanie LehnerDepartment of Fundamental Research, Werlhof Institute GmbH, 30159 Hannover, Germany sle@werlhof-institut.de.ORCID 0000-0002-0683-8547
Mahnaz Ekhlasi-HundrieserDepartment of Fundamental Research, Werlhof Institute GmbH, 30159 Hannover, Germany.ORCID 0000-0001-8187-1147
Carsten DeteringDepartment of Fundamental Research, Werlhof Institute GmbH, 30159 Hannover, Germany.
Hanna AllerkampDepartment of Fundamental Research, Werlhof Institute GmbH, 30159 Hannover, Germany.
Christiane PfarrerInstitute for Anatomy, University of Veterinary Medicine Hannover Foundation, 30173 Hannover, Germany.
Mario von Depka ProndzinskiDepartment of Fundamental Research, Werlhof Institute GmbH, 30159 Hannover, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Von Willebrand Disease (VWD) type 3 is a serious and sometimes fatal hereditary bleeding disorder. In pigs, the disease has been known for decades, and affected animals are used as models for the human disease. Due to the recessive mode of inheritance of VWD type 3, severe bleeding is typically seen in homozygous individuals. We sequenced the complete porcine

Indexed as

Gene DuplicationAnimalsBase SequenceCodon, NonsenseExonsFrameshift MutationGenetic Predisposition to DiseaseGenotypeHigh-Throughput Nucleotide SequencingHumansSwineSwine Diseasesvon Willebrand Diseasesvon Willebrand FactorCodon, Nonsensevon Willebrand FactorBleeding disorderFrameshiftNonsense-mediated decaySus scrofaVon Willebrand factor

Identifiers

PMID29208651
PMCPMC5919753

What OpenQuestion holds

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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.