Evidence map›Paper›PMID 28314818›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2017

Allometric Analysis Detects Brain Size-Independent Effects of Sex and Sex Chromosome Complement on Human Cerebellar Organization.

Catherine Mankiw, Min Tae M Park, P K Reardon, Ari M Fish, Liv S Clasen, Deanna Greenstein, Jay N Giedd, Jonathan D Blumenthal, Jason P Lerch, M Mallar Chakravarty and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
14.6field-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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 81 citations in OpenAlex.

  1. Pooled it
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  11. A Cross-Species Neuroimaging Study of Sex Chromosome Dosage Effects on Human and Mouse Brain Anatomy.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  12. Article
  13. Article
  14. A Comprehensive Analysis of Cerebellar Volumes in the 22q11.2 Deletion Syndrome.Biological psychiatry. Cognitive neuroscience and neuroimaging · 2023
    Article
  15. Triple X syndrome: Psychiatric disorders and impaired social functioning as a risk factor.European psychiatry : the journal of the Association of European Psychiatrists · 2022
    Article
  16. Article
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  18. Review
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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

11 authors at 5 institutions in 2 countries.

Catherine MankiwDevelopmental Neurogenomics Unit, Child Psychiatry Branch, National Institute of Mental Health, Bethesda, Maryland 20892.
Min Tae M ParkCerebral Imaging Center, Douglas Mental Health University Institute, Montreal, Quebec H4H 1R3, Canada.
P K ReardonDevelopmental Neurogenomics Unit, Child Psychiatry Branch, National Institute of Mental Health, Bethesda, Maryland 20892.
Ari M FishDevelopmental Neurogenomics Unit, Child Psychiatry Branch, National Institute of Mental Health, Bethesda, Maryland 20892.
Liv S ClasenDevelopmental Neurogenomics Unit, Child Psychiatry Branch, National Institute of Mental Health, Bethesda, Maryland 20892.
Deanna GreensteinDevelopmental Neurogenomics Unit, Child Psychiatry Branch, National Institute of Mental Health, Bethesda, Maryland 20892.
Jay N GieddDepartment of Psychiatry, University of California San Diego, La Jolla, California 92093.ORCID 0000-0003-2002-8978
Jonathan D BlumenthalDevelopmental Neurogenomics Unit, Child Psychiatry Branch, National Institute of Mental Health, Bethesda, Maryland 20892.
Jason P LerchDepartment of Medical Biophysics, University of Toronto, Toronto, Ontario M5G 1L7, Canada, and.
M Mallar ChakravartyCerebral Imaging Center, Douglas Mental Health University Institute, Montreal, Quebec H4H 1R3, Canada.
Armin RaznahanDevelopmental Neurogenomics Unit, Child Psychiatry Branch, National Institute of Mental Health, Bethesda, Maryland 20892, raznahana@mail.nih.gov.ORCID 0000-0002-5622-1190
National Institute of Mental Health · USDouglas Mental Health University Institute · CAUniversity of California San Diego · USUniversity of Toronto · CAWestern University · CA

Funding

Section on Developmental NeurogenomicsZIAMH002949 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI RAZNAHAN, ARMIN · 2016 to 2025
$30.0M
6 · The paper itself

Abstract

The cerebellum is a large hindbrain structure that is increasingly recognized for its contribution to diverse domains of cognitive and affective processing in human health and disease. Although several of these domains are sex biased, our fundamental understanding of cerebellar sex differences-including their spatial distribution, potential biological determinants, and independence from brain volume variation-lags far behind that for the cerebrum. Here, we harness automated neuroimaging methods for cerebellar morphometrics in 417 individuals to (1) localize normative male-female differences in raw cerebellar volume, (2) compare these to sex chromosome effects estimated across five rare sex (X/Y) chromosome aneuploidy (SCA) syndromes, and (3) clarify brain size-independent effects of sex and SCA on cerebellar anatomy using a generalizable allometric approach that considers scaling relationships between regional cerebellar volume and brain volume in health. The integration of these approaches shows that (1) sex and SCA effects on raw cerebellar volume are large and distributed, but regionally heterogeneous, (2) human cerebellar volume scales with brain volume in a highly nonlinear and regionally heterogeneous fashion that departs from documented patterns of cerebellar scaling in phylogeny, and (3) cerebellar organization is modified in a brain size-independent manner by sex (relative expansion of total cerebellum, flocculus, and Crus II-lobule VIIIB volumes in males) and SCA (contraction of total cerebellar, lobule IV, and Crus I volumes with additional X- or Y-chromosomes; X-specific contraction of Crus II-lobule VIIIB). Our methods and results clarify the shifts in human cerebellar organization that accompany interwoven variations in sex, sex chromosome complement, and brain size.

Indexed as

Abnormal KaryotypeAdolescentAdultAneuploidyCerebellumChildChromosomes, Human, XChromosomes, Human, YFemaleHumansMagnetic Resonance ImagingMaleOrgan Sizecerebellumdevelopmentgeneticsneuroimaging

Identifiers

PMID28314818
PMCPMC5456105
OpenAlexW2595560054

What OpenQuestion holds

Textmetadata
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.