Pelagia Deriziotis

Pelagia Deriziotis

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Pelagia Deriziotis

Pelagia Deriziotis

Publications by authors named "Pelagia Deriziotis"

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Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.

Nat Commun 2019 May 2;10(1):2079. Epub 2019 May 2.

CHU Sainte-Justine Research Center, Montreal, QC H3T 1C5, Canada.

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http://dx.doi.org/10.1038/s41467-019-10161-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497626PMC
May 2019

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.

Nat Commun 2019 02 15;10(1):883. Epub 2019 Feb 15.

CHU Sainte-Justine Research Center, Montreal, QC, H3T 1C5, Canada.

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http://dx.doi.org/10.1038/s41467-019-08800-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6377600PMC
February 2019

CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.

Nat Commun 2018 11 5;9(1):4619. Epub 2018 Nov 5.

CHU Sainte-Justine Research Center, Montreal, QC H3T 1C5, Canada.

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http://www.nature.com/articles/s41467-018-06014-6
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http://dx.doi.org/10.1038/s41467-018-06014-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6218476PMC
November 2018

Functional characterization of TBR1 variants in neurodevelopmental disorder.

Sci Rep 2018 09 24;8(1):14279. Epub 2018 Sep 24.

Language and Genetics Department, Max Planck Institute for Psycholinguistics, 6525 XD, Nijmegen, The Netherlands.

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http://dx.doi.org/10.1038/s41598-018-32053-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155134PMC
September 2018

Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders.

Hum Mol Genet 2018 Jun 26. Epub 2018 Jun 26.

Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen 6525 XD, The Netherlands.

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http://dx.doi.org/10.1093/hmg/ddy230DOI Listing
June 2018

Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders.

Hum Mol Genet 2018 04;27(7):1212-1227

Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen 6525 XD, The Netherlands.

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http://dx.doi.org/10.1093/hmg/ddy035DOI Listing
April 2018

Speech and Language: Translating the Genome.

Trends Genet 2017 09 3;33(9):642-656. Epub 2017 Aug 3.

Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands. Electronic address:

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http://dx.doi.org/10.1016/j.tig.2017.07.002DOI Listing
September 2017

Functional characterization of rare FOXP2 variants in neurodevelopmental disorder.

J Neurodev Disord 2016 28;8:44. Epub 2016 Nov 28.

Language and Genetics Department, Max Planck Institute for Psycholinguistics, Wundtlaan 1, 6525 XD Nijmegen, the Netherlands.

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http://dx.doi.org/10.1186/s11689-016-9177-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5126810PMC
November 2016

Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder.

Hum Mol Genet 2016 Feb 8;25(3):546-57. Epub 2015 Dec 8.

Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen 6525 XD, The Netherlands, Donders Institute for Brain, Cognition and Behaviour, Nijmegen 6525 EN, The Netherlands

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http://dx.doi.org/10.1093/hmg/ddv495DOI Listing
February 2016

The language-related transcription factor FOXP2 is post-translationally modified with small ubiquitin-like modifiers.

Sci Rep 2016 Feb 12;6:20911. Epub 2016 Feb 12.

Language and Genetics Department, Max Planck Institute for Psycholinguistics, Wundtlaan 1, 6525 XD, Nijmegen, The Netherlands.

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http://dx.doi.org/10.1038/srep20911DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4751435PMC
February 2016

A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairment.

Eur J Hum Genet 2015 Dec 8;23(12):1702-7. Epub 2015 Apr 8.

Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands.

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http://dx.doi.org/10.1038/ejhg.2015.66DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4795189PMC
December 2015

Insights into the genetic foundations of human communication.

Neuropsychol Rev 2015 Mar 18;25(1):3-26. Epub 2015 Jan 18.

Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, 6525XD, The Netherlands.

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http://dx.doi.org/10.1007/s11065-014-9277-2DOI Listing
March 2015

De novo TBR1 mutations in sporadic autism disrupt protein functions.

Nat Commun 2014 Sep 18;5:4954. Epub 2014 Sep 18.

1] Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen 6525XD, The Netherlands [2] Donders Institute for Brain, Cognition and Behaviour, Nijmegen 6525EN, The Netherlands.

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http://www.nature.com/articles/ncomms5954
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http://dx.doi.org/10.1038/ncomms5954DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4212638PMC
September 2014

Investigating protein-protein interactions in live cells using bioluminescence resonance energy transfer.

J Vis Exp 2014 May 26(87). Epub 2014 May 26.

Language and Genetics Department, Max Planck Institute for Psycholinguistics; Donders Institute for Brain, Cognition and Behaviour;

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http://dx.doi.org/10.3791/51438DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4207229PMC
May 2014

Prions and the proteasome.

Biochim Biophys Acta 2008 Dec 1;1782(12):713-22. Epub 2008 Jul 1.

Department of Neurodegenerative Disease, Institute of Neurology, University College London, London, WC1N 3BG, UK.

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http://dx.doi.org/10.1016/j.bbadis.2008.06.011DOI Listing
December 2008