Evidence map›Paper›PMID 25583500›Full record

Trial reportProceedings of the National Academy of Sciences of the United States of America2015

New human-specific brain landmark: the depth asymmetry of superior temporal sulcus.

François Leroy, Qing Cai, Stephanie L Bogart, Jessica Dubois, Olivier Coulon, Karla Monzalvo, Clara Fischer, Hervé Glasel, Lise Van der Haegen, Audrey Bénézit and 11 more

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed, 4 pooled it
9.7field-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

85 citing papers in PubMed, 4 syntheses or guidelines pooled it, 211 citations in OpenAlex.

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25 more citing papers are in PubMed but not listed here.

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

21 authors at 12 institutions in 7 countries.

François LeroyCognitive Neuroimaging Unit, U992, francois.leroy@cea.fr.
Qing CaiShanghai Key Laboratory of Brain Functional Genomics, East China Normal University, Shanghai 200241, China;
Stephanie L BogartDivision of Developmental and Cognitive Neuroscience, Yerkes National Primate Research Center, Atlanta, GA 30322;
Jessica DuboisCognitive Neuroimaging Unit, U992.
Olivier CoulonLaboratory for Systems and Information Science, UMR CNRS 7296, Aix-Marseille University, Marseille 13284, France;
Karla MonzalvoCognitive Neuroimaging Unit, U992.
Clara FischerAnalysis and Processing of Information Unit.
Hervé GlaselCognitive Neuroimaging Unit, U992.
Lise Van der HaegenDepartment of Experimental Psychology, Ghent University, Ghent B-9000, Belgium;
Audrey BénézitCognitive Neuroimaging Unit, U992.
Ching-Po LinInstitute of Neuroscience, National Yang-Ming University, Taipei City 112, Taiwan;
David N KennedyCenter for Morphometric Analysis, Neuroscience Center, Massachusetts General Hospital, Boston, MA 02114;
Aya S IharaCenter for Information and Neural Networks, National Institute of Information and Communications Technology, Osaka 565-0871 Japan;
Lucie Hertz-PannierClinical and Translational Applications Research Unit, U663, and.
Marie-Laure MoutardNeuropediatrics Department, Trousseau Hospital, Assistance Publique Hôpitaux de Paris, Paris 75012, France; and.
Cyril PouponNuclear Magnetic Resonance Imaging and Spectroscopy Unit, Office of Atomic Energy and Alternative Energies (CEA), INSERM, NeuroSpin, Gif-sur-Yvette 91191, France;
Marc BrysbaertAnalysis and Processing of Information Unit.
Neil RobertsClinical Research Imaging Centre, College of Medicine and Veterinary Medicine, University of Edinburgh, Edinburgh EH8 9YL, United Kingdom.
William D HopkinsDivision of Developmental and Cognitive Neuroscience, Yerkes National Primate Research Center, Atlanta, GA 30322;
Jean-François ManginAnalysis and Processing of Information Unit.
Ghislaine Dehaene-LambertzCognitive Neuroimaging Unit, U992.
Cognitive Neuroimaging Lab · FREmory National Primate Research CenterApplications Research (United States) · USAssistance Publique – Hôpitaux de Paris · FRCommissariat à l'Énergie Atomique et aux Énergies Alternatives · FREast China Normal University · CNGhent University · BELaboratoire d’Informatique et Systèmes · FRMassachusetts General Hospital · USNational Institute of Information and Communications Technology · JPNational Yang Ming Chiao Tung University · TWUniversity of Edinburgh · GB

Funding

Exposing the Deep Content of the Publication: Knowledge Extraction for Neuroimaging in Child PsychiatryR01MH083320 · NIMH · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI FRAZIER, JEAN A, KENNEDY, DAVID NELSON · 2009 to 2020
$6.3M
Hemispheric Specialization and CommunicationR01NS042867 · NINDS · GEORGIA STATE UNIVERSITY · PI HOPKINS, WILLIAM D · 2002 to 2015
$3.3M
NIMH NIH HHS R01 MH083320NINDS NIH HHS R01 NS042867
6 · The paper itself

Abstract

Identifying potentially unique features of the human cerebral cortex is a first step to understanding how evolution has shaped the brain in our species. By analyzing MR images obtained from 177 humans and 73 chimpanzees, we observed a human-specific asymmetry in the superior temporal sulcus at the heart of the communication regions and which we have named the "superior temporal asymmetrical pit" (STAP). This 45-mm-long segment ventral to Heschl's gyrus is deeper in the right hemisphere than in the left in 95% of typical human subjects, from infanthood till adulthood, and is present, irrespective of handedness, language lateralization, and sex although it is greater in males than in females. The STAP also is seen in several groups of atypical subjects including persons with situs inversus, autistic spectrum disorder, Turner syndrome, and corpus callosum agenesis. It is explained in part by the larger number of sulcal interruptions in the left than in the right hemisphere. Its early presence in the infants of this study as well as in fetuses and premature infants suggests a strong genetic influence. Because this asymmetry is barely visible in chimpanzees, we recommend the STAP region during midgestation as an important phenotype to investigate asymmetrical variations of gene expression among the primate lineage. This genetic target may provide important insights regarding the evolution of the crucial cognitive abilities sustained by this sulcus in our species, namely communication and social cognition.

Indexed as

Agenesis of Corpus CallosumChild Development Disorders, PervasiveCognitionSitus InversusTemporal LobeTurner SyndromeAdultAnimalsChildFemaleHumansInfantMaleMiddle AgedPan troglodytesRadiographyanatomyasymmetrybrainhuman-specificSTS

Identifiers

PMID25583500
PMCPMC4313811
OpenAlexW2060735786

What OpenQuestion holds

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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.