Evidence map›Paper›PMID 28148224›Full record

ArticleBMC genetics2017

Erratum to: Diagnosis implications of the whole genome sequencing in a large Lebanese family with hyaline fibromatosis syndrome.

Zahraa Haidar, Ramzi Temanni, Eliane Chouery, Puthen Jithesh, Wei Liu, Rashid Al-Ali, Ena Wang, Francesco M Marincola, Nadine Jalkh, Soha Haddad and 3 more

Abstract readPublished Erratum
In one paragraph

Article in BMC genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Zahraa HaidarUnité de Génétique Médicale, Faculté de Médecine, Université Saint-Joseph, Beirut, Lebanon.
Ramzi TemanniBioinformatics Division, Sidra Medical & Research Center, Doha, Qatar.
Eliane ChoueryUnité de Génétique Médicale, Faculté de Médecine, Université Saint-Joseph, Beirut, Lebanon.
Puthen JitheshBioinformatics Division, Sidra Medical & Research Center, Doha, Qatar.
Wei LiuGenomics Core Laboratory, Translational Medicine Division, Sidra Medical & Research Center, Doha, Qatar.
Rashid Al-AliBioinformatics Division, Sidra Medical & Research Center, Doha, Qatar.
Ena WangGenomics Core Laboratory, Translational Medicine Division, Sidra Medical & Research Center, Doha, Qatar.
Francesco M MarincolaResearch office, Sidra Medical & Research Center, Doha, Qatar.
Nadine JalkhUnité de Génétique Médicale, Faculté de Médecine, Université Saint-Joseph, Beirut, Lebanon.
Soha HaddadDepartment of Radiology, Hotel Dieu de France University hospital-Beirut, Beirut, Lebanon.
Wassim HaidarDepartment of General surgery, Dar Al Amal University Hospital-Baalbeck, Baalbeck, Lebanon.
Lotfi ChouchaneLaboratory of Genetic Medicine and Immunology, Weill Cornell Medicine-Qatar, Doha, Qatar.
André MégarbanéInstitut Jérôme Lejeune, 37, rue des Volontaires, Paris, 75015, France. andre.megarbane@yahoo.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID28148224
PMCPMC5286771

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.