Evidence map›Paper›PMID 29435918›Full record

ArticleMolecular neurobiology2018

PLP1 Gene Variation Modulates Leftward and Rightward Functional Hemispheric Asymmetries.

Sebastian Ocklenburg, Wanda M Gerding, Maximilian Raane, Larissa Arning, Erhan Genç, Jörg T Epplen, Onur Güntürkün, Christian Beste

Abstract read
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In one paragraph

Article in Molecular neurobiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

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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

8 authors at 4 institutions in 3 countries.

Sebastian OcklenburgInstitute of Cognitive Neuroscience, Biopsychology, Department of Psychology, Ruhr-University Bochum, Bochum, Germany. sebastian.ocklenburg@rub.de.ORCID http://orcid.org/0000-0001-5882-3200
Wanda M GerdingDepartment of Human Genetics, Ruhr-University Bochum, Bochum, Germany.
Maximilian RaaneFaculty of Health, ZBAF, University of Witten/Herdecke, Witten, Germany.
Larissa ArningDepartment of Human Genetics, Ruhr-University Bochum, Bochum, Germany.
Erhan GençInstitute of Cognitive Neuroscience, Biopsychology, Department of Psychology, Ruhr-University Bochum, Bochum, Germany.
Jörg T EpplenDepartment of Human Genetics, Ruhr-University Bochum, Bochum, Germany.
Onur GüntürkünInstitute of Cognitive Neuroscience, Biopsychology, Department of Psychology, Ruhr-University Bochum, Bochum, Germany.
Christian BesteCognitive Neurophysiology, Department of Child and Adolescent Psychiatry, Faculty of Medicine, TU Dresden, Dresden, Germany.
Ruhr University Bochum · DEWitten/Herdecke University · DENational Institute of Mental Health · JPUniversity Hospitals of the Ruhr-University of Bochum · DE

Funding

Deutsche Forschungsgemeinschaft BE4045/26-1Deutsche Forschungsgemeinschaft Gu227/16-1
6 · The paper itself

Abstract

Molecular neurobiological factors determining corpus callosum physiology and anatomy have been suggested to be one of the major factors determining functional hemispheric asymmetries. Recently, it was shown that allelic variations in two myelin-related genes, the proteolipid protein 1 gene PLP1 and the contactin 1 gene CNTN1, are associated with differences in interhemispheric integration. Here, we investigated whether three single nucleotide polymorphisms that were associated with interhemispheric integration via the corpus callosum in a previous study also are relevant for functional hemispheric asymmetries. To this end, we tested more than 900 healthy adults with the forced attention dichotic listening task, a paradigm to assess language lateralization and its modulation by cognitive control processes. Moreover, we used the line bisection task, a paradigm to assess functional hemispheric asymmetries in spatial attention. We found that a polymorphism in PLP1, but not CNTN1, was associated with performance differences in both tasks. Both functional hemispheric asymmetries and their modulation by cognitive control processes were affected. These findings suggest that both left and right hemisphere dominant cognitive functions can be modulated by allelic variation in genes affecting corpus callosum structure. Moreover, higher order cognitive processes may be relevant parameters when investigating the molecular basis of hemispheric asymmetries.

Indexed as

Acoustic StimulationAdolescentAdultAgedAttentionCerebrumDichotic Listening TestsFemaleFunctional LateralityGenotypeHumansMaleMiddle AgedMyelin Proteolipid ProteinPolymorphism, Single NucleotideYoung AdultMyelin Proteolipid ProteinPLP1 protein, humanCorpus callosumDichotic listeningFunctional hemispheric asymmetriesLine bisectionMolecular geneticsMyelin

Identifiers

PMID29435918
OpenAlexW2792606762

What OpenQuestion holds

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Registered trials

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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.