Evidence map›Paper›PMID 24968245›Full record

ArticlePloS one2014

Corpus callosum size is highly heritable in humans, and may reflect distinct genetic influences on ventral and rostral regions.

Girma Woldehawariat, Pedro E Martinez, Peter Hauser, David M Hoover, Wayne W C Drevets, Francis J McMahon

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 39% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Inner Hemispheric and Interhemispheric Connectivity Balance in the Human Brain.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  7. Article
  8. Article
  9. Review
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

6 authors at 4 institutions in 1 country.

Girma WoldehawariatGenetic Basis of Mood & Anxiety Disorders Section, Human Genetics Branch, National Institute of Mental Health, NIH, DHHS, Bethesda, Maryland, United States of America.
Pedro E MartinezSection on Behavioral Endocrinology, National Institute of Mental Health, NIH, DHHS, Bethesda, Maryland, Unites States of America.
Peter HauserVISN 22 Network Office, Long Beach, California, United States of America.
David M HooverCenter for Information Technology, National Institutes of Health, Bethesda, Maryland, United States of America.
Wayne W C DrevetsLaureate Institute for Brain Research and the University of Oklahoma College of Medicine, Tulsa, Oklahoma, United States of America.
Francis J McMahonGenetic Basis of Mood & Anxiety Disorders Section, Human Genetics Branch, National Institute of Mental Health, NIH, DHHS, Bethesda, Maryland, United States of America.
United States Department of Health and Human Services · USCenter for Information Technology · USLaureate Institute for Brain Research · USVA Desert Pacific Healthcare Network · US

Funding

Mapping genes that contribute to bipolar disorderZIAMH002810 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI MCMAHON, FRANCIS J · 2009 to 2025
$31.2M
6 · The paper itself

Abstract

Anatomical differences in the corpus callosum have been found in various psychiatric disorders, but data on the genetic contributions to these differences have been limited. The current study used morphometric MRI data to assess the heritability of corpus callosum size and the genetic correlations among anatomical sub-regions of the corpus callosum among individuals with and without mood disorders. The corpus callosum (CC) was manually segmented at the mid-sagittal plane in 42 women (healthy, n = 14; major depressive disorder, n = 15; bipolar disorder, n = 13) and their 86 child or adolescent offspring. Four anatomical sub-regions (CC-genu, CC2, CC3 and CC-splenium) and total CC were measured and analyzed. Heritability and genetic correlations were estimated using a variance components method, with adjustment for age, sex, diagnosis, and diagnosis x age, where appropriate. Significant heritability was found for several CC sub-regions (P<0.01), with estimated values ranging from 48% (splenium) to 67% (total CC). There were strong and significant genetic correlations among most sub regions. Correlations between the genu and mid-body, between the genu and total corpus callosum, and between anterior and mid body were all >90%, but no significant genetic correlations were detected between ventral and rostral regions in this sample. Genetic factors play an important role in corpus callosum size among individuals. Distinct genetic factors seem to be involved in caudal and rostral regions, consistent with the divergent functional specialization of these brain areas.

Indexed as

AdolescentAdultBipolar DisorderCase-Control StudiesChildCorpus CallosumDepressive DisorderFemaleHumansMaleMiddle AgedOrgan SizePedigreeQuantitative Trait, Heritable

Identifiers

PMID24968245
PMCPMC4072678
OpenAlexW1981594798

What OpenQuestion holds

Textmetadata
LicenceCC0
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.