Evidence mapPaperPMID 37601975Full record

ArticleCell genomics2023

Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent

Eduardo A Maury, Maxwell A Sherman, Giulio Genovese, Thomas G Gilgenast, Tushar Kamath, S J Burris, Prashanth Rajarajan, Erin Flaherty, Schahram Akbarian, Andrew Chess and 13 more

Open access · goldAbstract read
In one paragraph

Article in Cell genomics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
12.2field-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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Disease insights from brain somatic mosaicism.Experimental & molecular medicine · 2026
    Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Functional comparison of control and 3' deletion humanbioRxiv : the preprint server for biology · 2025
    Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Genome-wide association testing beyond SNPs.Nature reviews. Genetics · 2025
    Review
  20. 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

23 authors at 7 institutions in 2 countries.

Eduardo A MauryDivision of Genetics and Genomics, Manton Center for Orphan Disease, Boston Children's Hospital, Boston, MA, USA.
Maxwell A ShermanBrigham and Women's Hospital, Division of Genetics & Center for Data Sciences, Boston, MA, USA.
Giulio GenoveseProgram in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Thomas G GilgenastDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA, USA.
Tushar KamathStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
S J BurrisStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Prashanth RajarajanNash Family Department of Neuroscience, Friedman Brain Institute, Department of Genetics & Genomics, Icahn Institute of Genomics and Multiscale Biology, Department of Psychiatry, Pamela Sklar Division of Psychiatric Genomics, Icahn School of Medicine of Mount Sinai, New York, NY, USA.
Erin FlahertyNash Family Department of Neuroscience, Friedman Brain Institute, Department of Genetics & Genomics, Icahn Institute of Genomics and Multiscale Biology, Department of Psychiatry, Pamela Sklar Division of Psychiatric Genomics, Icahn School of Medicine of Mount Sinai, New York, NY, USA.
Schahram AkbarianNash Family Department of Neuroscience, Friedman Brain Institute, Department of Genetics & Genomics, Icahn Institute of Genomics and Multiscale Biology, Department of Psychiatry, Pamela Sklar Division of Psychiatric Genomics, Icahn School of Medicine of Mount Sinai, New York, NY, USA.
Andrew ChessNash Family Department of Neuroscience, Friedman Brain Institute, Department of Genetics & Genomics, Icahn Institute of Genomics and Multiscale Biology, Department of Psychiatry, Pamela Sklar Division of Psychiatric Genomics, Icahn School of Medicine of Mount Sinai, New York, NY, USA.
Steven A McCarrollProgram in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Po-Ru LohProgram in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Jennifer E Phillips-CreminsDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA, USA.
Kristen J BrennandNash Family Department of Neuroscience, Friedman Brain Institute, Department of Genetics & Genomics, Icahn Institute of Genomics and Multiscale Biology, Department of Psychiatry, Pamela Sklar Division of Psychiatric Genomics, Icahn School of Medicine of Mount Sinai, New York, NY, USA.
Evan Z MacoskoStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
James T R WaltersMRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychiatry and Clinical Neurosciences, Cardiff University, Cardiff, Wales.
Michael O'DonovanMRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychiatry and Clinical Neurosciences, Cardiff University, Cardiff, Wales.
Patrick SullivanDepartment of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Psychiatric Genomic Consortium Schizophrenia and CNV workgroup
Brain Somatic Mosaicism Network
Jonathan SebatUniversity of California San Diego, Department of Psychiatry, Department of Cellular & Molecular Medicine, Beyster Center of Psychiatric Genomics, San Diego, CA, USA.
Eunjung A LeeDivision of Genetics and Genomics, Manton Center for Orphan Disease, Boston Children's Hospital, Boston, MA, USA.
Christopher A WalshDivision of Genetics and Genomics, Manton Center for Orphan Disease, Boston Children's Hospital, Boston, MA, USA.
Broad Institute · USCardiff University · GBUniversity of Pennsylvania · USAllen Institute for Brain Science · USUniversity of North Carolina at Chapel Hill · USBrigham and Women's Hospital · USUniversity of San Diego · US

Funding

MEDICAL SCIENTIST TRAININGT32GM007753 · HARVARD UNIVERSITY (MEDICAL SCHOOL) · 1985 to 2005
$11.4M
RESEARCH TRAINING-MEDICAL INFORMATICS 90T15LM007092 · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · 1992 to 2025
$10.8M
Medical Scientist Training ProgramT32GM144273 · NIGMS · HARVARD MEDICAL SCHOOL · 2022 to 2025
$5.6M
A cellular atlas of the primate and human basal gangliaU01MH124602 · NIMH · BROAD INSTITUTE, INC. · PI Fei Chen, GORDON J FISHELL · 2022 to 2023
$3.8M
MOLECULAR BIOPHYSICS TRAINING GRANTT32GM008313 · HARVARD UNIVERSITY (MEDICAL SCHOOL) · 1989 to 2005
$3.1M
PREDOCTORAL TRAINING IN GENETICST32GM007544 · UNIVERSITY OF MICHIGAN AT ANN ARBOR · 1985 to 2005
$2.9M
Cellular Imaging Core (CIC)P50HD105351 · BOSTON CHILDREN'S HOSPITAL · 2025 to 2025
$1.4M
Systematic Functional Interpretation of Regulatory Variants in Neuropsychiatric DisordersR01MH106575 · NIMH · ENDEAVOR HEALTH CLINICAL OPERATIONS · 2023 to 2025
$1.4M
Clinical Translational Research Center for Neurodevelopmental DisordersP50HD103573 · UNIV OF NORTH CAROLINA CHAPEL HILL · 2025 to 2025
$1.2M
From 3D genomes to neural connectomes: Higher-order chromatin mechanisms encoding long-term memoryDP1MH129957 · WASHINGTON UNIVERSITY · 2025 to 2025
$1.1M
Elucidating the 3-D epigenetic determinants of activity-dependent gene expression in mammalian neuronsR01NS114226 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI Jennifer Elizabeth Phillips-Cremins, Jason D Shepherd · 2022 to 2023
$968k
Rates and mechanisms of age-related somatic mutation in normal and Alzheimer brainR01AG070921 · BOSTON CHILDREN'S HOSPITAL · 2025 to 2025
$810k
NHGRI NIH HHS R01 HG006855NIA NIH HHS DP2 AG058488NIA NIH HHS DP2 AG072437NIA NIH HHS F30 AG069446NIA NIH HHS K01 AG051791NIA NIH HHS R01 AG070921NICHD NIH HHS P50 HD103573NICHD NIH HHS P50 HD105351NIDDK NIH HHS U01 DK127405NIEHS NIH HHS DP2 ES030554NIGMS NIH HHS T32 GM007544NIGMS NIH HHS T32 GM007753NIGMS NIH HHS T32 GM008313NIGMS NIH HHS T32 GM144273NIH HHS S10 OD026880NIH HHS S10 OD030463NIMH NIH HHS DP1 MH129957NIMH NIH HHS F31 MH124292NIMH NIH HHS F31 MH124393NIMH NIH HHS R01 MH104964NIMH NIH HHS R01 MH106056NIMH NIH HHS R01 MH106575NIMH NIH HHS R01 MH113715NIMH NIH HHS R37 MH120269NIMH NIH HHS U01 MH106883NIMH NIH HHS U01 MH109501NIMH NIH HHS U01 MH119746NIMH NIH HHS U01 MH124602NINDS NIH HHS R01 NS114226NLM NIH HHS T15 LM007092
6 · The paper itself

Abstract

While germline copy-number variants (CNVs) contribute to schizophrenia (SCZ) risk, the contribution of somatic CNVs (sCNVs)-present in some but not all cells-remains unknown. We identified sCNVs using blood-derived genotype arrays from 12,834 SCZ cases and 11,648 controls, filtering sCNVs at loci recurrently mutated in clonal blood disorders. Likely early-developmental sCNVs were more common in cases (0.91%) than controls (0.51%, p = 2.68e-4), with recurrent somatic deletions of exons 1-5 of the

Indexed as

ABCB11genomicsmosaicismNRXN1schizophreniasomaticstructural variantstreatment resistance

Identifiers

PMID37601975
PMCPMC10435376
OpenAlexW4383341307

What Socratic 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 Socratic graph.