Evidence map›Paper›PMID 38970057›Full record

ArticleJournal of neurodevelopmental disorders2024

An integrated clinical approach to children at genetic risk for neurodevelopmental and psychiatric conditions: interdisciplinary collaboration and research infrastructure.

Jane Summers, Danielle Baribeau, Polina Perlman, Ny Hoang, Sunny Cui, Aneta Krakowski, Patricia Ambrozewicz, Ariel Ho, Thanuja Selvanayagam, Kinga A Sándor-Bajusz and 7 more

Abstract read
In one paragraph

Article in Journal of neurodevelopmental disorders, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–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

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Systematic Review: The Psychosocial Impacts of Autism-Related Genetic Testing.Journal of the American Academy of Child and Adolescent Psychiatry · 2026
    Pooled it
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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

17 authors.

Jane SummersDepartment of Psychiatry, Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada.
Danielle BaribeauDepartment of Psychiatry, Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada.
Polina PerlmanDepartment of Psychiatry, Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada.
Ny HoangProgram in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
Sunny CuiProgram in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
Aneta KrakowskiDepartment of Psychiatry, Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada.
Patricia AmbrozewiczProgram in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
Ariel HoProgram in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
Thanuja SelvanayagamProgram in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
Kinga A Sándor-BajuszProgram in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
Katrina PaladProgram in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
Nishi PatelProgram in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
Sarah McGaugheyProgram in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
Louise GallagherDepartment of Psychiatry, Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada.
Stephen W SchererThe Centre for Applied Genomics, The Hospital for Sick Children, Toronto, ON, Canada.
Peter SzatmariDepartment of Psychiatry, The Hospital for Sick Children, Toronto, ON, Canada.
Jacob VorstmanDepartment of Psychiatry, Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada. jacob.vorstman@sickkids.ca.ORCID 0000-0002-1677-3126

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA sizeable proportion of pathogenic genetic variants identified in young children tested for congenital differences are associated with neurodevelopmental psychiatric disorders (NPD). In this growing group, a genetic diagnosis often precedes the emergence of diagnosable developmental concerns. Here, we describe DAGSY (Developmental Assessment of Genetically Susceptible Youth), a novel interdisciplinary 'genetic-diagnosis-first' clinic integrating psychiatric, psychological and genetic expertise, and report our first observations and feedback from families and referring clinicians.

methodsWe retrieved data on referral sources and indications, genetic and NPD diagnoses and recommendations for children seen at DAGSY between 2018 and 2022. Through a survey, we obtained feedback from twenty families and eleven referring clinicians.

results159 children (mean age 10.2 years, 57.2% males) completed an interdisciplinary (psychiatry, psychology, genetic counselling) DAGSY assessment during this period. Of these, 69.8% had a pathogenic microdeletion or microduplication, 21.5% a sequence-level variant, 4.4% a chromosomal disorder, and 4.4% a variant of unknown significance with emerging evidence of pathogenicity. One in four children did not have a prior NPD diagnosis, and referral to DAGSY was motivated by their genetic vulnerability alone. Following assessment, 76.7% received at least one new NPD diagnosis, most frequently intellectual disability (24.5%), anxiety (20.7%), autism spectrum (18.9%) and specific learning (16.4%) disorder. Both families and clinicians responding to our survey expressed satisfaction, but also highlighted some areas for potential improvement.

conclusionsDAGSY addresses an unmet clinical need for children identified with genetic variants that confer increased vulnerability for NPD and provides a crucial platform for research in this area. DAGSY can serve as a model for interdisciplinary clinics integrating child psychiatry, psychology and genetics, addressing both clinical and research needs for this emerging population.

Indexed as

Mental DisordersNeurodevelopmental DisordersAdolescentChildFemaleGenetic Predisposition to DiseaseHumansMaleGenetic disorderGeneticsInterdisciplinary clinicMental healthNeurodevelopmental disorderPsychiatryPsychologyResearch framework

Identifiers

PMID38970057
PMCPMC11229023

What OpenQuestion holds

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Registered trials

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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.