Evidence map›Paper›PMID 38016473›Full record

ReviewNeuron2024

An evolutionary perspective on complex neuropsychiatric disease.

Jon M McClellan, Anthony W Zoghbi, Joseph D Buxbaum, Carolina Cappi, James J Crowley, Jonathan Flint, Dorothy E Grice, Suleyman Gulsuner, Conrad Iyegbe, Sanjeev Jain and 10 more

Abstract readReview
In one paragraph

Review in Neuron, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

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

  1. Pooled it
  2. Big data and psychiatry: advances, constraints and future directions.World psychiatry : official journal of the World Psychiatric Association (WPA) · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Loss of function of the chromatin remodeling geneProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  9. Binocular Circuitry as a Model for Understanding Experience-Dependent Circuit Development across the Mammalian Cortex.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Review
  10. Article
  11. Article
  12. A cross ancestry genetic study of psychiatric disorders from India.medRxiv : the preprint server for health sciences · 2024
    Article
  13. 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

20 authors.

Jon M McClellanDepartment of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA 98195, USA.
Anthony W ZoghbiMenninger Department of Psychiatry and Behavioral Sciences, Baylor College of Medicine, Houston, TX 77030, USA.
Joseph D BuxbaumDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Carolina CappiDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
James J CrowleyDepartment of Genetics, University of North Carolina, Chapel Hill, NC 27599, USA.
Jonathan FlintSemel Institute for Neuroscience and Human Behavior, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Dorothy E GriceDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Suleyman GulsunerDepartment of Medicine and Department of Genome Sciences, University of Washington, Seattle, WA 98195, USA.
Conrad IyegbeDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Sanjeev JainDepartment of Psychiatry, National Institute of Mental Health and Neurosciences, Bengaluru 560029, India.
Po-Hsiu KuoInstitute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University, Taipei 100, Taiwan.
Maria Claudia LattigFaculty of Sciences, University of the Andes, Bogotá, Colombia.
Maria Rita Passos-BuenoDepartment of Genetics and Evolutionary Biology, University of São Paulo, São Paulo, Brazil.
Meera PurushottamDepartment of Psychiatry, National Institute of Mental Health and Neurosciences, Bengaluru 560029, India.
Dan J SteinSAMRC Unit on Risk and Resilience in Mental Disorders, Department of Psychiatry, University of Cape Town, Cape Town, South Africa.
Anna B SunshineDepartment of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA 98195, USA; Department of Medicine and Department of Genome Sciences, University of Washington, Seattle, WA 98195, USA.
Ezra S SusserDepartment of Epidemiology, Mailman School of Public Health, and New York State Psychiatric Institute, Columbia University, New York, NY 10032, USA.
Christopher A WalshBroad Institute of MIT and Harvard, Cambridge, MA 02142, USA; Division of Genetics and Genomics and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA 02115, USA; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, MA 02115, USA.
Olivia WoottonSAMRC Unit on Risk and Resilience in Mental Disorders, Department of Psychiatry, University of Cape Town, Cape Town, South Africa.
Mary-Claire KingDepartment of Medicine and Department of Genome Sciences, University of Washington, Seattle, WA 98195, USA. Electronic address: mcking@uw.edu.

Funding

1/3 Genomics of Schizophrenia in the South African XhosaU01MH125054 · NIMH · UNIVERSITY OF WASHINGTON · PI GULSUNER, SULEYMAN, KING, MARY-CLAIRE · 2021 to 2025
$9.5M
Genetic Analysis and Manipulation Core (GAEC)P50HD105351 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI Hisashi Umemori · 2021 to 2026
$9.4M
1/4 Asian Bipolar Genetics Network (A-BIG-NET)R01MH130675 · NIMH · BROAD INSTITUTE, INC. · PI Hailiang Huang · 2022 to 2026
$9.0M
Identifying the genetic causes of depression in a deeply phenotyped population from South KoreaU01MH126798 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI AHN, YONG MIN, FLINT, JONATHAN · 2021 to 2025
$8.9M
Latino Ancestry Genomic Psychiatry CohortR01MH123451 · NIMH · SUNY DOWNSTATE MEDICAL CENTER · PI BIGDELI, TIM BERNARD, FANOUS, AYMAN H · 2020 to 2025
$7.1M
Genomics of Autism in Latinx AncestriesR01MH128813 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Joseph D. Buxbaum · 2022 to 2026
$3.7M
3/3 Genomics of Schizophrenia in the South African XhosaU01MH125053 · NIMH · UNIVERSITY OF CAPE TOWN · PI STEIN, DAN JOSEPH · 2021 to 2025
$3.5M
1/2 Rare Genetic Variation and Risk for Obsessive Compulsive DisorderR01MH124679 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI GRICE, DOROTHY E · 2021 to 2025
$3.0M
Genetic Architecture of Early-Onset Psychosis in MexicansU01MH124962 · NIMH · BOSTON CHILDREN'S HOSPITAL · PI ALMASY, LAURA A., GLAHN, DAVID C · 2021 to 2021
$2.9M
Utilizing Community-Based Participatory Action Research Approaches to Inform Equitable OCD Genetics Research in Diverse PopulationsU01MH125062 · NIMH · BAYLOR COLLEGE OF MEDICINE · PI STORCH, ERIC A. · 2021 to 2025
$2.6M
The Ancestral Populations Network Phenotypic Harmonization Working Group Administrative Supplement: 2/3 Genomics of Schizophrenia in the South African XhosaU01MH125058 · NIMH · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI WALL, MELANIE M · 2021 to 2025
$2.5M
Administrative Supplement: 1/2 Trans-ancestry genomic analysis of obsessive-compulsive disorderU01MH125050 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CROWLEY, JAMES JOSEPH, PATO, MICHELE T · 2021 to 2025
$1.8M
NICHD NIH HHS P50 HD105351NIMH NIH HHS K99 MH128540NIMH NIH HHS R00 MH128540NIMH NIH HHS R01 MH123451NIMH NIH HHS R01 MH124679NIMH NIH HHS R01 MH128813NIMH NIH HHS R01 MH130674NIMH NIH HHS R01 MH130675NIMH NIH HHS U01 MH124962NIMH NIH HHS U01 MH125050NIMH NIH HHS U01 MH125053NIMH NIH HHS U01 MH125054NIMH NIH HHS U01 MH125058NIMH NIH HHS U01 MH125062NIMH NIH HHS U01 MH126798
6 · The paper itself

Abstract

The forces of evolution-mutation, selection, migration, and genetic drift-shape the genetic architecture of human traits, including the genetic architecture of complex neuropsychiatric illnesses. Studying these illnesses in populations that are diverse in genetic ancestry, historical demography, and cultural history can reveal how evolutionary forces have guided adaptation over time and place. A fundamental truth of shared human biology is that an allele responsible for a disease in anyone, anywhere, reveals a gene critical to the normal biology underlying that condition in everyone, everywhere. Understanding the genetic causes of neuropsychiatric disease in the widest possible range of human populations thus yields the greatest possible range of insight into genes critical to human brain development. In this perspective, we explore some of the relationships between genes, adaptation, and history that can be illuminated by an evolutionary perspective on studies of complex neuropsychiatric disease in diverse populations.

Indexed as

Mental DisordersMutationHumans22q11 deletionassortative matingautismbipolar disordercausalityclinical heterogeneitycomplex neuropsychiatric diseaseconsanguinityde novo mutationevolutiongenetic driftgeneticsgenomicsmigrationOCDpolygenic inheritancerare allelesschizophreniaselectionsomatic mutation

Identifiers

PMID38016473
PMCPMC10842497

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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.