Evidence map›Paper›PMID 37354284›Full record

ArticleJournal of autism and developmental disorders2024

Visual-Motor Integration Deficits in 3q29 Deletion Syndrome.

Rebecca M Pollak, T Lindsey Burrell, Joseph F Cubells, Cheryl Klaiman, Melissa M Murphy, Celine A Saulnier, Elaine F Walker, Stormi Pulver White, Jennifer G Mulle

Open access · hybridAbstract read
In one paragraph

Article in Journal of autism and developmental disorders, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

7 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Adaptive behaviour deficits in individuals with 3q29 deletion syndrome.Journal of intellectual disability research : JIDR · 2024
    Article
  7. Adaptive behavior deficits in individuals with 3q29 deletion syndrome.medRxiv : the preprint server for health sciences · 2023
    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

9 authors at 4 institutions in 1 country.

Rebecca M PollakCenter for Advanced Biotechnology and Medicine and Department of Psychiatry, Robert Wood Johnson Medical School, Rutgers University, 679 Hoes Lane West, Piscataway, NJ, 08854, USA.
T Lindsey BurrellDepartment of Pediatrics, School of Medicine, Emory University, Atlanta, USA.
Joseph F CubellsDepartment of Human Genetics, School of Medicine, Emory University, Atlanta, USA.
Cheryl KlaimanDepartment of Pediatrics, School of Medicine, Emory University, Atlanta, USA.
Melissa M MurphyDepartment of Pediatrics, School of Medicine, Emory University, Atlanta, USA.
Celine A SaulnierDepartment of Pediatrics, School of Medicine, Emory University, Atlanta, USA.
Elaine F WalkerDepartment of Psychology, Emory University, Atlanta, USA.
Stormi Pulver WhiteDepartment of Pediatrics, School of Medicine, Emory University, Atlanta, USA.
Jennifer G MulleCenter for Advanced Biotechnology and Medicine and Department of Psychiatry, Robert Wood Johnson Medical School, Rutgers University, 679 Hoes Lane West, Piscataway, NJ, 08854, USA. jennifer.mulle@rutgers.edu.
Emory University · USChildren's Healthcare of Atlanta · USJohnson University · USRutgers, The State University of New Jersey · US

Funding

Modeling the Human Neuronal Phenotype of the Schizophrenia-Associated 3q29 deletionR01MH110701 · NIMH · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI BASSELL, GARY J, MULLE, JENNIFER GLADYS · 2017 to 2021
$3.2M
NIMH NIH HHS R01 MH110701
6 · The paper itself

Abstract

3q29 deletion syndrome (3q29del) is associated with neuropsychiatric and neurodevelopmental phenotypes. We previously reported that graphomotor weakness is present in up to 78% of individuals with 3q29del. We have now explored nuances of the graphomotor phenotype and its association with other comorbidities in this population. Participants were recruited from the online 3q29 registry (3q29deletion.org) for two days of deep phenotyping. 32 individuals with 3q29del (62.5% male) were evaluated with the Beery-Buktenica Developmental Test of Visual-Motor Integration (VMI) to assess visual-motor integration. Participants were also evaluated with measures of cognitive ability, executive function, adaptive behavior, and school function. Males with 3q29del performed significantly worse than females on the VMI and Motor Coordination subtest. VMI performance was significantly associated with ADHD diagnosis and cognitive ability. Compared to published data from individuals with 22q11.2 deletion syndrome, individuals with 3q29del showed significantly more impairment. The 3q29 deletion is associated with substantial deficits in visual-motor integration, Visual Perception, and Motor Coordination. Our data suggests that 3q29del may qualify as a nonverbal learning disability. Future studies should assess whether individuals with 3q29del would benefit from early interventions, including occupational therapy.

Indexed as

Chromosome DeletionChromosomes, Human, Pair 3Psychomotor PerformanceAdolescentAdultChildChromosome DisordersDevelopmental DisabilitiesExecutive FunctionFemaleHumansIntellectual DisabilityMalePhenotypeVisual PerceptionYoung Adult3q29 DeletionBeery-Buktenica Developmental Test of Visual-Motor IntegrationBeery VMICopy number variantsGraphomotor weaknessVMI

Identifiers

PMID37354284
PMCPMC11300491
OpenAlexW4381855695

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.