Evidence map›Paper›PMID 28289584›Full record

ArticleBalkan journal of medical genetics : BJMG2016

Mutation analysis of the

H Onay, D Kacamak, A N Kavasoglu, B Akgun, M Yalcinli, S Kose, B Ozbaran

Open access · goldAbstract read
In one paragraph

Article in Balkan journal of medical genetics : BJMG, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

18 citing papers in PubMed, 30 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

H OnayDepartment of Medical Genetics, Ege University School of Medicine, Izmir, Turkey.
D KacamakDepartment of Child and Adolescent Psychiatry, Ege University School of Medicine, Izmir, Turkey.
A N KavasogluDepartment of Medical Genetics, Ege University School of Medicine, Izmir, Turkey.
B AkgunDepartment of Medical Genetics, Ege University School of Medicine, Izmir, Turkey.
M YalcinliDepartment of Medical Genetics, Ege University School of Medicine, Izmir, Turkey.
S KoseDepartment of Medical Genetics, Ege University School of Medicine, Izmir, Turkey.
B OzbaranDepartment of Medical Genetics, Ege University School of Medicine, Izmir, Turkey.
Ege University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to identify the sequence mutations in the

Indexed as

Autism spectrum disorder (ASD)MutationNeurexin 1 (NRXN1) geneSanger sequencing

Identifiers

PMID28289584
PMCPMC5343326
OpenAlexW2592297462

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.