Evidence map›Paper›PMID 30950222›Full record

ArticleGenes, brain, and behavior2019

Genome sequencing for rightward hemispheric language dominance.

Amaia Carrion-Castillo, Lise Van der Haegen, Nathalie Tzourio-Mazoyer, Tulya Kavaklioglu, Solveig Badillo, Marie Chavent, Jérôme Saracco, Marc Brysbaert, Simon E Fisher, Bernard Mazoyer and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Genes, brain, and behavior, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

10 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. The molecular and cellular underpinnings of human brain lateralization.bioRxiv : the preprint server for biology · 2025
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  7. Large-Scale Phenomic and Genomic Analysis of Brain Asymmetrical Skew.Cerebral cortex (New York, N.Y. : 1991) · 2021
    Article
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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 6 institutions in 3 countries.

Amaia Carrion-CastilloLanguage and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands.
Lise Van der HaegenDepartment of Experimental Psychology, Ghent Institute for Functional and Metabolic Imaging, Ghent University, Ghent, Belgium.
Nathalie Tzourio-MazoyerGroupe d'Imagerie Neurofonctionnelle, Institut des Maladies Neurodégénératives, Centre National de la Recherche Scientifique, Commissariat à l'Energie Atomique, et Université de Bordeaux, Bordeaux, France.
Tulya KavakliogluLanguage and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands.
Solveig BadilloGroupe d'Imagerie Neurofonctionnelle, Institut des Maladies Neurodégénératives, Centre National de la Recherche Scientifique, Commissariat à l'Energie Atomique, et Université de Bordeaux, Bordeaux, France.
Marie ChaventInstitut de Mathématiques de Bordeaux, Centre National de la Recherche Scientifique, Institut National de la Recherche en Informatique et Automatique, et Université de Bordeaux, Bordeaux, France.
Jérôme SaraccoInstitut de Mathématiques de Bordeaux, Centre National de la Recherche Scientifique, Institut National de la Recherche en Informatique et Automatique, et Université de Bordeaux, Bordeaux, France.
Marc BrysbaertDepartment of Experimental Psychology, Ghent Institute for Functional and Metabolic Imaging, Ghent University, Ghent, Belgium.
Simon E FisherLanguage and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands.
Bernard MazoyerGroupe d'Imagerie Neurofonctionnelle, Institut des Maladies Neurodégénératives, Centre National de la Recherche Scientifique, Commissariat à l'Energie Atomique, et Université de Bordeaux, Bordeaux, France.
Clyde FrancksLanguage and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands.
Max Planck Institute for Psycholinguistics · NLGhent University · BEInstitut de Mathématiques de Bordeaux · FRUniversité de Bordeaux · FRInstitut des Maladies Neurodégénératives · FRRadboud University Nijmegen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Most people have left-hemisphere dominance for various aspects of language processing, but only roughly 1% of the adult population has atypically reversed, rightward hemispheric language dominance (RHLD). The genetic-developmental program that underlies leftward language laterality is unknown, as are the causes of atypical variation. We performed an exploratory whole-genome-sequencing study, with the hypothesis that strongly penetrant, rare genetic mutations might sometimes be involved in RHLD. This was by analogy with situs inversus of the visceral organs (left-right mirror reversal of the heart, lungs and so on), which is sometimes due to monogenic mutations. The genomes of 33 subjects with RHLD were sequenced and analyzed with reference to large population-genetic data sets, as well as 34 subjects (14 left-handed) with typical language laterality. The sample was powered to detect rare, highly penetrant, monogenic effects if they would be present in at least 10 of the 33 RHLD cases and no controls, but no individual genes had mutations in more than five RHLD cases while being un-mutated in controls. A hypothesis derived from invertebrate mechanisms of left-right axis formation led to the detection of an increased mutation load, in RHLD subjects, within genes involved with the actin cytoskeleton. The latter finding offers a first, tentative insight into molecular genetic influences on hemispheric language dominance.

Indexed as

Genome, HumanLanguageAdultFemaleFunctional LateralityGenotypeHumansMalePolymorphism, Geneticbrain asymmetryDNAdominancefunctional MRIgeneticshemispheric lateralizationlanguagelateralitynext generation sequencingwhole genome sequencing

Identifiers

PMID30950222
PMCPMC6850193
OpenAlexW2928786712

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.