Diagnostic Yield and Genotype-Phenotype Overlap in Pediatric Autism Spectrum Disorder Patients Using Whole-Exome Sequencing and Phenotype-Driven Variant Interpretation: A Single-Center Cohort Study.

Andreya Yaneva, Mariya Levkova, Milena Stoyanova, Mari Hachmeriyan, Lyudmila Angelova, Rouzha Pancheva

Abstract read

In one paragraph

Article in Children (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it

0cells of the map it votes in

1citing 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

1 citing paper in PubMed.

AI-Guided Systems Neurogenomics in Neurodevelopmental Disorders.Genes · 2026
Review

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.

Andreya YanevaDepartment of Medical Genetics, Medical University Varna, Marin Drinov Str. 55, 9000 Varna, Bulgaria.

Mariya LevkovaDepartment of Medical Genetics, Medical University Varna, Marin Drinov Str. 55, 9000 Varna, Bulgaria.ORCID 0000-0002-9358-7263

Milena StoyanovaDepartment of Medical Genetics, Medical University Varna, Marin Drinov Str. 55, 9000 Varna, Bulgaria.

Mari HachmeriyanDepartment of Medical Genetics, Medical University Varna, Marin Drinov Str. 55, 9000 Varna, Bulgaria.ORCID 0000-0002-8847-4651

Lyudmila AngelovaDepartment of Medical Genetics, Medical University Varna, Marin Drinov Str. 55, 9000 Varna, Bulgaria.

Rouzha PanchevaDepartment of Hygiene and Epidemiology, Faculty of Public Health, Medical University Varna, 9002 Varna, Bulgaria.

Funding

European Union - NextGenerationEU BG-RRP-2.004-0009-C02

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

autismphenotype-genotype correlationvariant interpretationwhole-exome sequencing

Identifiers

PMID42073023

DOI10.3390/children13040444

PMCPMC13114441

What Socratic 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 Socratic graph.