Publications by authors named "Heidi Anthoni"

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The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language.
Heidi Anthoni, Lara E Sucheston, Barbara A Lewis, Isabel Tapia-Páez, Xiaotang Fan

Behav Genet· July 2012

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SNP variations in the 7q33 region containing DGKI are associated with dyslexia in the Finnish and German populations.
Hans Matsson, Kristiina Tammimies, Marco Zucchelli, Heidi Anthoni, Päivi Onkamo

Behav Genet· January 2011

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Brain-derived neurotrophic factor controls activity-dependent maturation of CA1 synapses by downregulating tonic activation of presynaptic kainate receptors.
Marko Sallert, Tomi Rantamäki, Aino Vesikansa, Heidi Anthoni, Kirsi Harju

J Neurosci· September 2009

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Further evidence for DYX1C1 as a susceptibility factor for dyslexia.
Faten Dahdouh, Heidi Anthoni, Isabel Tapia-Páez, Myriam Peyrard-Janvid, Gerd Schulte-Körne

Psychiatr Genet· April 2009

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Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample.
Kerstin U Ludwig, Johannes Schumacher, Gerd Schulte-Körne, Inke R König, Andreas Warnke, Heidi Anthoni

Psychiatr Genet· December 2008

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A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia.
Heidi Anthoni, Marco Zucchelli, Hans Matsson, Bertram Müller-Myhsok, Ingegerd Fransson

Hum Mol Genet· March 2007

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Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.
Johannes Schumacher, Heidi Anthoni, Faten Dahdouh, Inke R König, Axel M Hillmer

Am J Hum Genet· January 2006

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Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene.
Myriam Peyrard-Janvid, Heidi Anthoni, Päivi Onkamo, Päivi Lahermo, Marco Zucchelli

Hum Genet· April 2004

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