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Danai Dimitropoulou
Danai Dimitropoulou
Max Planck Society
Genetics
Biology
Autism
Missense mutation
Intellectual disability
5
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137
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Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder
2016
Human Molecular Genetics
Elliot Sollis
Sarah A. Graham
Arianna Vino
Henning Froehlich
Maaike Vreeburg
Danai Dimitropoulou
Christian Gilissen
Rolph Pfundt
Gudrun Rappold
Han G. Brunner
Pelagia Deriziotis
Simon E. Fisher
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Citations (52)
Identification and functional characterization of de novo FOXP1 variants in cases of autism, intellectual disability and language impairment.
2015
Elliot Sollis
Arianna Vino
Christian Gilissen
Henning Fröhlich
Sarah A. Graham
Rolph Pfundt
Danai Dimitropoulou
Han G. Brunner
Gudrun Rappold
Simon E. Fisher
Pelagia Derizioti
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Understanding the contribution of FOXP genes in language-related disorders
2015
Elliot Sollis
Arianna Vino
Christian Gilissen
H. Froehlich
Sarah A. Graham
Rolph Pfundt
Danai Dimitropoulou
H.G. Brunner
Gudrun Rappold
Simon E. Fisher
Pelagia Derizioti
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De novo TBR1 mutations in sporadic autism disrupt protein functions
2014
Nature Communications
Pelagia Deriziotis
Brian J. O'Roak
Sarah A. Graham
Sara Busquets Estruch
Danai Dimitropoulou
Raphael Bernier
Jennifer Gerdts
Jay Shendure
Evan E. Eichler
Simon E. Fisher
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Citations (85)
Functional characterisation of FOXP1 mutations found in patients with intellectual disability
2012
Pelagia Derizioti
H. Froehlich
Danai Dimitropoulou
Gudrun Rappold
Simon E. Fisher
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