Evidence map›Paper›PMID 32699506›Full record

ReviewDialogues in clinical neuroscience2020

Neurodevelopmental disorders-the history and future of a diagnostic concept
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Deborah J Morris-Rosendahl, Marc-Antoine Crocq

Open access · diamondAbstract readHistorical ArticleReview
In one paragraph

Review in Dialogues in clinical neuroscience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 234 papers, 11 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
234citing papers in PubMed, 11 pooled it
20.7field-weighted citation impact, top 1% 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

234 citing papers in PubMed, 11 syntheses or guidelines pooled it, 463 citations in OpenAlex.

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  10. An updated catalog ofFrontiers in molecular neuroscience · 2023
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174 more citing papers are in PubMed but not listed here.

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

2 authors at 2 institutions in 2 countries.

Deborah J Morris-RosendahlClinical Genetics and Genomics, Royal Brompton and Harefield NHS Foundation Trust, London, UK; NHLI, Imperial College London, UK.
Marc-Antoine CrocqCentre Hospitalier, Rouffach, France; CAMUHA, Université de Haute-Alsace, Mulhouse, France.
Imperial College London · GBUniversité de Haute-Alsace · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This article describes the history of the diagnostic class of neurodevelopmental disorders (NDDs) up to DSM-5. We further analyze how the development of genetics will transform the classification and diagnosis of NDDs. In DSM-5, NDDs include intellectual disability (ID), autism spectrum disorder (ASD), and attention-deficit/hyperactivity disorder (ADHD). Physicians in German-, French- and English-speaking countries (eg, Weikard, Georget, Esquirol, Down, Asperger, and Kanner) contributed to the phenomenological definitions of these disorders throughout the 18th and 20th centuries. These diagnostic categories show considerable comorbidity and phenotypic overlap. NDDs are one of the chapters of psychiatric nosology most likely to benefit from the approach advocated by the National Institute of Mental Health's Research Domain Criteria project. Genetic research supports the hypothesis that ID, ASD, ADHD, schizophrenia, and bipolar disorder lie on a neurodevelopmental continuum. The identification of recurrently observed copy number variants and disruptive gene variants in ASD (eg, CDH8, 16p11.2, SCN2A) led to the adoption of the genotype-first approach to characterize individuals at the etiological level.
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Indexed as

Diagnostic and Statistical Manual of Mental DisordersForecastingHistory, 18th CenturyHistory, 19th CenturyHistory, 20th CenturyHistory, 21st CenturyHumansNeurodevelopmental DisordersADHDautism(CNV)copy number variantgeneticsgenome-wide association study (GWAS)intellectual disabilityneurodevelopmental disorderRDoC

Identifiers

PMID32699506
PMCPMC7365295
OpenAlexW3045023537

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.