Evidence map›Paper›PMID 37577800›Full record

ArticleCirculation. Genomic and precision medicine2023

Phenotype of ASDs Associated With 4p16 Risk Locus and Novel Genome-Wide Associations of ASD Patients in the Finnish Population.

Valtteri Muroke, Mikko Jalanko, Sanni Ruotsalainen, Markus Perola, Emmi Helle, Juha Sinisalo

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Circulation. Genomic and precision medicine, 2023. 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

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.

Valtteri MurokeDepartment of Cardiology, Helsinki University Hospital (V.M., M.J., J.S.), University of Helsinki, Finland.ORCID 0000-0003-0972-3873
Mikko JalankoDepartment of Cardiology, Helsinki University Hospital (V.M., M.J., J.S.), University of Helsinki, Finland.ORCID 0000-0001-5409-3300
Sanni RuotsalainenInstitute for Molecular Medicine Finland (FIMM), HiLIFE (S.R.), University of Helsinki, Finland.
Markus PerolaFinnish Institute for Health and Welfare, Helsinki, Finland (M.P.).ORCID 0000-0003-4842-1667
Emmi HelleStem Cells and Metabolism Research Program, Faculty of Medicine (E.H.), University of Helsinki, Finland.
Juha SinisaloDepartment of Cardiology, Helsinki University Hospital (V.M., M.J., J.S.), University of Helsinki, Finland.ORCID 0000-0002-0169-5137

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Autism Spectrum DisorderHeart Septal Defects, AtrialFinlandGenome-Wide Association StudyHumansPhenotypegenetic locigenomeheart defects, congenitalheart septal defect, atrialmutation

Identifiers

PMID37577800
PMCPMC10581411

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.