Evidence map›Paper›PMID 27667698›Full record

ArticleBiological psychiatry2017

Data-Driven Phenotypic Categorization for Neurobiological Analyses: Beyond DSM-5 Labels.

Nicholas T Van Dam, David O'Connor, Enitan T Marcelle, Erica J Ho, R Cameron Craddock, Russell H Tobe, Vilma Gabbay, James J Hudziak, F Xavier Castellanos, Bennett L Leventhal and 1 more

Abstract read
In one paragraph

Article in Biological psychiatry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed, 3 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

48 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Review
  6. Article
  7. Longitudinal Clustering of Psychopathology Across Childhood and Adolescence: An Approach Toward Developmentally Based Classification.Clinical psychological science : a journal of the Association for Psychological Science · 2025
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  12. MULTIMODAL NEURAL CORRELATES OF CHILDHOOD PSYCHOPATHOLOGY.bioRxiv : the preprint server for biology · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Nicholas T Van DamCenter for the Developing Brain, Child Mind Institute; Departments of Psychiatry and Neuroscience, Icahn School of Medicine at Mount Sinai; Center for Biomedical Imaging and Neuromodulation, Nathan Kline Institute, Orangeburg, New York.
David O'ConnorCenter for the Developing Brain, Child Mind Institute; Center for Biomedical Imaging and Neuromodulation, Nathan Kline Institute, Orangeburg, New York.
Enitan T MarcelleCenter for the Developing Brain, Child Mind Institute; Department of Psychology, University of California, Berkeley, Berkeley.
Erica J HoCenter for the Developing Brain, Child Mind Institute.
R Cameron CraddockCenter for the Developing Brain, Child Mind Institute; Center for Biomedical Imaging and Neuromodulation, Nathan Kline Institute, Orangeburg, New York.
Russell H TobeCenter for Biomedical Imaging and Neuromodulation, Nathan Kline Institute, Orangeburg, New York.
Vilma GabbayDepartments of Psychiatry and Neuroscience, Icahn School of Medicine at Mount Sinai.
James J HudziakThe Child Study Center at NYU Langone Medical Center, New York.
F Xavier CastellanosThe Child Study Center at NYU Langone Medical Center, New York; Center for Biomedical Imaging and Neuromodulation, Nathan Kline Institute, Orangeburg, New York.
Bennett L LeventhalCenter for Biomedical Imaging and Neuromodulation, Nathan Kline Institute, Orangeburg, New York; Department of Psychiatry, University of California, San Francisco, San Francisco, California.
Michael P MilhamCenter for the Developing Brain, Child Mind Institute; Center for Biomedical Imaging and Neuromodulation, Nathan Kline Institute, Orangeburg, New York; Department of Psychiatry, University of Vermont, Burlington, Vermont. Electronic address: michael.milham@childmind.org.

Funding

The Neuroimmunology of AnhedoniaR01MH095807 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI GABBAY, VILMA · 2012 to 2016
$3.0M
Discovery Science of Human Brain Function Across the LifespanR01MH094639 · NIMH · NATHAN S. KLINE INSTITUTE FOR PSYCH RES · PI MILHAM, MICHAEL PETER · 2011 to 2014
$2.7M
Functional and Structural Connectivity in Adult Attention Deficit Hyperactivity DR01MH083246 · NIMH · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CASTELLANOS, FRANCISCO XAVIER · 2009 to 2011
$1.7M
Neural Substrates of Variability in Attention Deficit Hyperactivity Disorder (ADHR01MH081218 · NIMH · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CASTELLANOS, FRANCISCO XAVIER · 2008 to 2010
$1.7M
Connectivity of Anterior Cingulate Cortex Networks in AutismR21MH084126 · NIMH · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI DI MARTINO, ADRIANA · 2009 to 2010
$394k
NIMH NIH HHS R01 MH081218NIMH NIH HHS R01 MH083246NIMH NIH HHS R01 MH094639NIMH NIH HHS R01 MH095807NIMH NIH HHS R21 MH084126
6 · The paper itself

Abstract

backgroundData-driven approaches can capture behavioral and biological variation currently unaccounted for by contemporary diagnostic categories, thereby enhancing the ability of neurobiological studies to characterize brain-behavior relationships.

methodsA community-ascertained sample of individuals (N = 347, 18-59 years of age) completed a battery of behavioral measures, psychiatric assessment, and resting-state functional magnetic resonance imaging in a cross-sectional design. Bootstrap-based exploratory factor analysis was applied to 49 phenotypic subscales from 10 measures. Hybrid hierarchical clustering was applied to resultant factor scores to identify nested groups. Adjacent groups were compared via independent samples t tests and chi-square tests of factor scores, syndrome scores, and psychiatric prevalence. Multivariate distance matrix regression examined functional connectome differences between adjacent groups.

resultsReduction yielded six factors, which explained 77.8% and 65.4% of the variance in exploratory and constrained exploratory models, respectively. Hybrid hierarchical clustering of these six factors identified two, four, and eight nested groups (i.e., phenotypic communities). At the highest clustering level, the algorithm differentiated functionally adaptive and maladaptive groups. At the middle clustering level, groups were separated by problem type (maladaptive groups; internalizing vs. externalizing problems) and behavioral type (adaptive groups; sensation-seeking vs. extraverted/emotionally stable). Unique phenotypic profiles were also evident at the lowest clustering level. Group comparisons exhibited significant differences in intrinsic functional connectivity at the highest clustering level in somatomotor, thalamic, basal ganglia, and limbic networks.

conclusionsData-driven approaches for identifying homogenous subgroups, spanning typical function to dysfunction, not only yielded clinically meaningful groups, but also captured behavioral and neurobiological variation among healthy individuals.

Indexed as

ConnectomePhenotypeAdolescentAdultBrainCluster AnalysisCross-Sectional StudiesDiagnostic and Statistical Manual of Mental DisordersHumansMagnetic Resonance ImagingMental DisordersMiddle AgedMultivariate AnalysisNeuropsychological TestsYoung AdultHierarchical clusteringMultivariate distance matrix regressionPhenotypesPsychopathologyRDoCResting state fMRI

Identifiers

PMID27667698
PMCPMC5402759

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.