Evidence map›Paper›PMID 42792940›Full record

ArticleGenes2026

Insight into Essential and Complex Autism Spectrum Disorders: Clinical Characteristics, Chromosomal Microarray Analysis, and Risk Factors.

Beyhan Tüysüz, Evrim Çifçi Sunamak, Gizem Durcan, Birol Öztürk, Dilek Uludağ Alkaya, Hazal Cansu Çulpan, Mehmet Barış Korkmaz, Burak Doğangün, Ertuğrul Kıykım

Abstract read
In one paragraph

Article in Genes, 2026. 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

9 authors.

Beyhan TüysüzDepartment of Pediatric Genetics, Cerrahpaşa Medical Faculty, Istanbul University-Cerrahpaşa, Istanbul 34098, Türkiye.
Evrim Çifçi SunamakDepartment of Pediatric Genetics, Cerrahpaşa Medical Faculty, Istanbul University-Cerrahpaşa, Istanbul 34098, Türkiye.ORCID 0000-0003-2952-3094
Gizem DurcanDepartment of Child and Adolescent Psychiatry, Cerrahpasa Medical Faculty, Istanbul University-Cerrahpasa, Istanbul 34098, Türkiye.ORCID 0000-0002-7863-4551
Birol ÖztürkDepartment of Pediatric Genetics, Cerrahpaşa Medical Faculty, Istanbul University-Cerrahpaşa, Istanbul 34098, Türkiye.
Dilek Uludağ AlkayaDepartment of Pediatric Genetics, Cerrahpaşa Medical Faculty, Istanbul University-Cerrahpaşa, Istanbul 34098, Türkiye.ORCID 0000-0002-0495-6152
Hazal Cansu ÇulpanDepartment of Public Health, Cerrahpasa Medical Faculty, Istanbul University-Cerrahpasa, Istanbul 34098, Türkiye.ORCID 0000-0001-9244-3818
Mehmet Barış KorkmazDepartment of Neurology, Cerrahpasa Medical Faculty, Istanbul University-Cerrahpasa, Istanbul 34098, Türkiye.
Burak DoğangünDepartment of Child and Adolescent Psychiatry, Cerrahpasa Medical Faculty, Istanbul University-Cerrahpasa, Istanbul 34098, Türkiye.
Ertuğrul KıykımDepartment of Pediatric Nutrition and Metabolism, Cerrahpasa Medical Faculty, Istanbul University-Cerrahpasa, Istanbul 34098, Türkiye.ORCID 0000-0001-5170-5594

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 DisorderDNA Copy Number VariationsChildChild, PreschoolFemaleGenetic Predisposition to DiseaseHumansMaleMicroarray AnalysisPhenotypeRisk FactorsTurkeyautism spectrum diseasecomplex phenotypecopy number variationsessential phenotypegenesrisk factors

Identifiers

PMID42792940
PMCPMC13606228

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.