Human Genome Epidemiology Literature Finder
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Records 1 - 3 (of 3 Records) |
| Query Trace: Dyslexia and FOXP2[original query] |
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| Imaging genetics of FOXP2 in dyslexia. European journal of human genetics : EJHG 2012 Feb 20 (2): 224-9. Wilcke Arndt, Ligges Carolin, Burkhardt Jana, Alexander Michael, Wolf Christiane, Quente Elfi, Ahnert Peter, Hoffmann Per, Becker Albert, Müller-Myhsok Bertram, Cichon Sven, Boltze Johannes, Kirsten Holg |
| Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample. Journal of neurodevelopmental disorders 2011 Mar 3 (1): 39-49. Peter Beate, Raskind Wendy H, Matsushita Mark, Lisowski Mark, Vu Tiffany, Berninger Virginia W, Wijsman Ellen M, Brkanac Zor |
| Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions. The Journal of neuroscience : the official journal of the Society for Neuroscience 2012 Jan 32 (3): 817-25. Pinel Philippe, Fauchereau Fabien, Moreno Antonio, Barbot Alexis, Lathrop Mark, Zelenika Diana, Le Bihan Denis, Poline Jean-Baptiste, Bourgeron Thomas, Dehaene Stanisl |
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