Evidence map›Paper›PMID 39408661›Full record

ArticleInternational journal of molecular sciences2024

The Aggravation of Neuropsychiatric Symptoms in the Offspring of a Korean Family with Intellectual Disability and Developmental Delay Caused by a Novel

Ji Yoon Han, Tae Yun Kim, Jin Gwack, Joonhong Park

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in International journal of molecular sciences, 2024. 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.

  1. Cellular Functional Analyses ofHuman mutation · 2026
    Article
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

4 authors.

Ji Yoon HanDepartment of Pediatrics, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea.ORCID 0000-0002-4174-5266
Tae Yun KimDepartment of Thoracic and Cardiovascular Surgery, Jeonbuk National University Medical School and Hospital, Jeonju 54907, Republic of Korea.ORCID 0000-0002-0534-9119
Jin GwackDepartment of Preventive Medicine, Jeonbuk National University Medical School, Jeonju 54907, Republic of Korea.ORCID 0000-0003-0932-9542
Joonhong ParkResearch Institute of Clinical Medicine of Jeonbuk National University-Biomedical Research Institute of Jeonbuk National University Hospital, Jeonju 54907, Republic of Korea.ORCID 0000-0001-7354-4234

Funding

Jeonbuk National University Medical School and Hospital 0
6 · The paper itself

Abstract

The

Indexed as

Developmental DisabilitiesHomeodomain ProteinsIntellectual DisabilityPedigreeTranscription FactorsAdultChildChild, PreschoolExome SequencingFemaleHumansMaleMutationPhenotypeRepublic of KoreaSpasms, InfantileARX protein, humanHomeodomain ProteinsTranscription Factorsagenesis of the corpus callosumAristaless-related homeobox, X linkedARXclinical exome sequencingdevelopmental epileptic encephalopathyintellectual developmental disorder, X linked 29

Identifiers

PMID39408661
PMCPMC11476583

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.