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Page 1
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: quente e. 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.
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: quente e. Psychiatr Genet. 2012 Dec;22(6):307-8. doi: 10.1097/YPG.0b013e328353aeae. Psychiatr Genet. 2012. PMID: 22547140 No abstract available.
Cellular adhesion gene SELP is associated with rheumatoid arthritis and displays differential allelic expression.
Burkhardt J, Blume M, Petit-Teixeira E, Hugo Teixeira V, Steiner A, Quente E, Wolfram G, Scholz M, Pierlot C, Migliorini P, Bombardieri S, Balsa A, Westhovens R, Barrera P, Radstake TR, Alves H, Bardin T, Prum B, Emmrich F, Cornelis F, Ahnert P, Kirsten H. Burkhardt J, et al. Among authors: quente e. PLoS One. 2014 Aug 22;9(8):e103872. doi: 10.1371/journal.pone.0103872. eCollection 2014. PLoS One. 2014. PMID: 25147926 Free PMC article.
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: quente e. 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.