Evidence map›Paper›PMID 31183366›Full record

ArticleBioMed research international2019

Whole-Exome Sequencing Identified a Novel Compound Heterozygous Genotype in

Mei Zhao, Lingling Hou, Huajing Teng, Jinchen Li, Jiesi Wang, Kunlin Zhang, Lin Yang

Open access · hybridAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in BioMed research international, 2019. 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
0.2field-weighted citation impact, top 49% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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 3 institutions in 1 country.

Mei ZhaoKey Lab of Mental Health, Institute of Psychology, Chinese Academy of Sciences, 4A Datun Rd., Beijing 100101, China.ORCID 0000-0003-3390-0198
Lingling HouBeijing Institutes of Life Science, Chinese Academy of Sciences, Beijing 100101, China.
Huajing TengBeijing Institutes of Life Science, Chinese Academy of Sciences, Beijing 100101, China.
Jinchen LiBeijing Institutes of Life Science, Chinese Academy of Sciences, Beijing 100101, China.
Jiesi WangKey Lab of Mental Health, Institute of Psychology, Chinese Academy of Sciences, 4A Datun Rd., Beijing 100101, China.
Kunlin ZhangKey Lab of Mental Health, Institute of Psychology, Chinese Academy of Sciences, 4A Datun Rd., Beijing 100101, China.
Lin YangDepartment of Pediatrics, Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi Province, China.ORCID 0000-0003-3629-3899
Chinese Academy of Sciences · CNInstitute of Psychology, Chinese Academy of Sciences · CNSecond Affiliated Hospital of Xi'an Jiaotong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pathogenic variants in the argininosuccinate lyase (

Indexed as

Argininosuccinate LyaseArgininosuccinic AciduriaExome SequencingHeterozygoteMutation, MissenseAmino Acid SubstitutionCitrullineHEK293 CellsHumansInfantMaleArgininosuccinate LyaseCitrulline

Identifiers

PMID31183366
PMCPMC6515145
OpenAlexW2943600862

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.