Evidence map›Paper›PMID 31216015›Full record

ArticleCerebral cortex (New York, N.Y. : 1991)2020

Altered Brain Structure in Infants with Turner Syndrome.

M L Davenport, E Cornea, K Xia, J J Crowley, M W Halvorsen, B D Goldman, D Reinhartsen, M DeRamus, R Pretzel, M Styner and 3 more

Open access · greenAbstract read
In one paragraph

Article in Cerebral cortex (New York, N.Y. : 1991), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
2.9field-weighted citation impact, top 9% 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, 2 syntheses or guidelines pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Guideline
  3. Article
  4. Using Organoids to Model Sex Differences in the Human Brain.Biological psychiatry global open science · 2024
    Review
  5. Review
  6. Review
  7. Review
  8. Observational
  9. Early Development of Infants with Turner Syndrome.Journal of developmental and behavioral pediatrics : JDBP · 2020
    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

13 authors at 1 institution in 1 country.

M L DavenportDepartment of Pediatrics, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
E CorneaDepartment of Psychiatry, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
K XiaDepartment of Psychiatry, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
J J CrowleyDepartment of Genetics, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
M W HalvorsenDepartment of Genetics, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
B D GoldmanFrank Porter Graham Child Development Institute, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
D ReinhartsenCarolina Institute for Developmental Disabilities, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
M DeRamusCarolina Institute for Developmental Disabilities, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
R PretzelCarolina Institute for Developmental Disabilities, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
M StynerDepartment of Psychiatry, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
J H GilmoreDepartment of Psychiatry, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
S R HooperDepartment of Psychiatry, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
R C KnickmeyerDepartment of Psychiatry, University of North Carolina at Chapel Hill, North Carolina, 27599, USA.
University of North Carolina at Chapel Hill · US

Funding

North Carolina Translational & Clinical Sciences Institute (NC TraCS)UL1TR001111 · NCATS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BUSE, JOHN BERNARD, CAREY, TIMOTHY S · 2013 to 2017
$43.9M
UNC Neuroscience Center Research Cores: MicroscopyP30NS045892 · NINDS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ZYLKA, MARK J. · 2003 to 2022
$11.5M
Preclinical CoreP50HD103573 · NICHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Mark D Shen · 2020 to 2026
$9.7M
Preclinical CoreU54HD079124 · NICHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MOY, SHERYL S · 2013 to 2019
$8.0M
Sex Differences in Early Brain Development; Brain Development in Turner SyndromeK01MH083045 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KNICKMEYER, REBECCA · 2008 to 2012
$764k
Emotion-Modulated Psychophysiology of Autism Spectrum DisordersR21MH085254 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BENNING, STEPHEN D, DICHTER, GABRIEL S · 2009 to 2010
$416k
NCATS NIH HHS UL1 TR001111NICHD NIH HHS P50 HD103573NICHD NIH HHS U54 HD079124NIMH NIH HHS K01 MH083045NIMH NIH HHS R21 MH085254NINDS NIH HHS P30 NS045892
6 · The paper itself

Abstract

Turner syndrome (TS) is a genetic disorder affecting approximately 1:2000 live-born females. It results from partial or complete X monosomy and is associated with a range of clinical issues including a unique cognitive profile and increased risk for certain behavioral problems. Structural neuroimaging studies in adolescents, adults, and older children with TS have revealed altered neuroanatomy but are unable to identify when in development differences arise. In addition, older children and adults have often been exposed to years of growth hormone and/or exogenous estrogen therapy with potential implications for neurodevelopment. The study presented here is the first to test whether brain structure is altered in infants with TS. Twenty-six infants with TS received high-resolution structural MRI scans of the brain at 1 year of age and were compared to 47 typically developing female and 39 typically developing male infants. Results indicate that the typical neuroanatomical profile seen in older individuals with TS, characterized by decreased gray matter volumes in premotor, somatosensory, and parietal-occipital cortex, is already present at 1 year of age, suggesting a stable phenotype with origins in the prenatal or early postnatal period.

Indexed as

BrainFemaleHumansInfantMagnetic Resonance ImagingOrgan SizeTurner SyndromeinfantMRIneuroimagingTurner syndrome

Identifiers

PMID31216015
PMCPMC7444739
OpenAlexW2981191325

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.