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Imaging genetics of FOXP2 in dyslexia.
Wilcke A, Ligges C, Burkhardt J, Alexander M, Wolf C, Quente E, Ahnert P, Hoffmann P, Becker A, Müller-Myhsok B, Cichon S, Boltze J, Kirsten H. Wilcke A, et al. Among authors: boltze j. Eur J Hum Genet. 2012 Feb;20(2):224-9. doi: 10.1038/ejhg.2011.160. Epub 2011 Sep 7. Eur J Hum Genet. 2012. PMID: 21897444 Free PMC article.
The role of gene DCDC2 in German dyslexics.
Wilcke A, Weissfuss J, Kirsten H, Wolfram G, Boltze J, Ahnert P. Wilcke A, et al. Among authors: boltze j. Ann Dyslexia. 2009 Jun;59(1):1-11. doi: 10.1007/s11881-008-0020-7. Epub 2009 Feb 24. Ann Dyslexia. 2009. PMID: 19238550
Association of rs2069459 in the CDK5 gene with dyslexia in a German cohort.
Burkhardt J, Kirsten H, Holland H, Krupp W, Ligges C, Quente E, Boltze J, Ahnert P, Wilcke A. Burkhardt J, et al. Among authors: boltze j. Psychiatr Genet. 2012 Dec;22(6):307-8. doi: 10.1097/YPG.0b013e328353aeae. Psychiatr Genet. 2012. PMID: 22547140 No abstract available.
Genetic risk variants for dyslexia on chromosome 18 in a German cohort.
Mueller B, Ahnert P, Burkhardt J, Brauer J, Czepezauer I, Quente E, Boltze J, Wilcke A, Kirsten H. Mueller B, et al. Among authors: boltze j. Genes Brain Behav. 2014 Mar;13(3):350-6. doi: 10.1111/gbb.12118. Epub 2014 Feb 3. Genes Brain Behav. 2014. PMID: 24373531 Free article.
194 results