Evidence map›Paper›PMID 29326753›Full record

ArticleFrontiers in genetics2017

A Novel Role for

Amina Kamar, Akl C Fahed, Kamel Shibbani, Nehme El-Hachem, Salim Bou-Slaiman, Mariam Arabi, Mazen Kurban, Jonathan G Seidman, Christine E Seidman, Rachid Haidar and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact, top 86% 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

4 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
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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 6 institutions in 3 countries.

Amina KamarDepartment of Biology, American University of Beirut, Beirut, Lebanon.
Akl C FahedDepartment of Genetics, Harvard Medical School, Boston, MA, United States.
Kamel ShibbaniDepartment of Biochemistry and Molecular Genetics, American University of Beirut, Beirut, Lebanon.
Nehme El-HachemFaculty of Medicine, McGill University, Montreal, QC, Canada.
Salim Bou-SlaimanDepartment of Biochemistry and Molecular Genetics, American University of Beirut, Beirut, Lebanon.
Mariam ArabiDepartment of Pediatrics and Adolescent Medicine, American University of Beirut, Beirut, Lebanon.
Mazen KurbanDepartment of Biochemistry and Molecular Genetics, American University of Beirut, Beirut, Lebanon.
Jonathan G SeidmanDepartment of Genetics, Harvard Medical School, Boston, MA, United States.
Christine E SeidmanDepartment of Genetics, Harvard Medical School, Boston, MA, United States.
Rachid HaidarDepartment of Surgery, American University of Beirut, Beirut, Lebanon.
Elias BaydounDepartment of Biology, American University of Beirut, Beirut, Lebanon.
Georges NemerDepartment of Medicine, Massachusetts General Hospital, Boston, MA, United States.
Fadi BitarDepartment of Pediatrics and Adolescent Medicine, American University of Beirut, Beirut, Lebanon.
American University of Beirut · LBHarvard University · USColumbia University · USHoward Hughes Medical Institute · USMassachusetts General Hospital · USMcGill University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite an obvious role for consanguinity in congenital heart disease (CHD), most studies fail to document a monogenic model of inheritance except for few cases. We hereby describe a first-degree cousins consanguineous Lebanese family with 7 conceived children: 2 died

Indexed as

congenital heart diseaseCSRP1polydactylyTRPS1

Identifiers

PMID29326753
PMCPMC5741687
OpenAlexW2772045358

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.