Page 162 - Read Online

Guerra et al. J Transl Genet Genom 2019;3:9. I https://doi.org/10.20517/jtgg.2018.03 Page 29 of 31

trait locus influencing dyslexia. Nat Genet 2002;30:86-91.
142. Tzenova J, Kaplan BJ, Petryshen TL, Field LL. Confirmation of a dyslexia susceptibility locus on chromosome 1p34-p36 in a set of 100
Canadian families. Am J Med Genet B Neuropsychiatr Genet 2004;127B:117-24.
143. De Kovel CG, Hol FA, Heister JG, Willemen JJ, Sandkuijl LA, et al. Genomewide scan identifies susceptibility locus for dyslexia on Xq27
in an extended Dutch family. J Med Genet 2004;41:652-7.
144. Taipale M, Kaminen N, Nopola-Hemmi J, Haltia T, Myllyluoma B, et al. A candidate gene for developmental dyslexia encodes a nuclear
tetratricopeptide repeat domain protein dynamically regulated in brain. Proc Natl Acad Sci USA 2003;100:11553-8.
145. Lim CK, Ho CS, Chou CH, Wayne MM. Association of the rs3743205 variant of DYX1C1 with dyslexia in Chinese children. Behav Brain
Funct 2011;7:16.
146. Massinen S, Tammimies K, Tapia-Paez I, Matsson H, Hokkanen ME, et al. Functional interaction of DYX1C1 with estrogen receptors
suggests involvement of hormonal pathways in dyslexia. Hum Mol Genet 2009;18: 2802-12.
147. Moffat JJ, Ka M, Jung EM, Kim WY. Genes and brain malformations associated with abnormal neuron positioning. Mol Brain 2015;8:72.
148. Raskind W, Peter B, Richards T, Eckert MM, Berninger VW. The genetics of reading disabilities: from phenotypes to candidate genes. Front
Psychol 2013;3:601.
149. Meng H, Smith SD, Hager K, Held M, Liu J, et al. DCDC2 is associated with reading disability and modulates neuronal development in the
brain. Proc Natl Acad Sci USA 2005;102:17053-8.
150. Scerri TS, Macpherson E, Martinelli A, Wa WC, Monaco AP, et al. The DCDC2 deletion is not a risk factor for dyslexia. Transl Psychiatry
2017;25:7:e1182.
151. Chen Y, Zhao H, Zhang YX, Zuo PX. DCDC2 gene polymorphisms are associated with developmental dyslexia in Chinese Uyghur
children. Neural Regen Res 2017;12:259-266.
152. Francks C, Paracchini S, Smith SD, Richardson AJ, Scerri TS, et al. A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia
in families from the United Kingdom and from the United States. Am J Hum Genet 2004;75:1046-58.
153. Harold D, Paracchini S, Scerri T, Dennis M, Cope N, et al. Further evidence that the KIAA0319 gene confers susceptibility to developmental
dyslexia. Mol Psychiatry 2006;11:1085-91, 1061.
154. Scerri TS, Morris AP, Buckingham LL, Newbury DF, Miller LL, et al. DCDC2, KIAA0319 and CMIP are associated with reading-related
traits. Biol Psychiatry 2011;70:237-45.
155. Pinel P, Fauchereau F, Moreno A, Barbot A, Lathrop M, et al. Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are
associated with altered brain activation in distinct language-related regions. J Neurosci 2012;32:817-25.
156. Sundaresan V, Mambetisaeva E, Andrews W, Annan A, Knöll B, et al. Dynamic expression patterns of Robo (Robo1 and Robo2) in the
developing murine central nervous system. J Comp Neurol 2003;468:467-81.
157. Hannula-Jouppi K, Kaminen-Ahola N, Taipale M, Eklund R, Nopola-Hemmi J, et al. The axon guidance receptor gene ROBO1 is a
candidate gene for developmental dyslexia. PLoS Genet 2005;1:e50.
158. Anthoni H, Zucchelli M, Matsson H, Muller-Myhsok B, Fransson I, et al. A locus on 2p12 containing the co-regulated MRPL19 and
C2ORF3 genes is associated to dyslexia. Hum Mol Genet 2007;16:667-77.
159. Kim M, Roesener A, Mendonca P, Mastik GS. Robo1 and Robo2 have distinct roles in pioneer longitudinal axon guidance. Dev Biol
2011;358:181-8.
160. Landi N, Frost S, Mencl W, Preston JL, Jacobsen LK, et al. The COMT Val/Met polymorphism is associated with reading-related skills and
consistent patterns of functional neural activation. Dev Sci 2012;16:13-23.
161. Scerri TS, Paracchini S, Morris A, MacPhie IL, Talcott J, et al. Identification of candidate genes for dyslexia susceptibility on chromosome
18. PLoS One 2010;5:e13712.
162. Eicher J, Powers N, Cho K, Miller LL, Mueller KL, et al. Associations of prenatal nicotine exposure and the dopamine related genes
ANKK1 and DRD2 to verbal language. PLoS One 2013;8:e63762.
163. Stein C, Truitt B, Deng F, Ciesla AA, Qiu F, et al. Association between AVPR1A, DRD2, and ASPM and endophenotypes of communication
disorders. Psychiatr Genet 2014;24:191-200.
164. Chen H, Wang G, Xia J, Zhou Y, Gao Y, et al. Stuttering candidate genes DRD2 but not SLC6A3 is associated with developmental dyslexia
in Chinese population. Behav Brain Funct 2014;10:29.
165. Veerappa A, Padakannaya P, Ramachandra N. Copy number variation-based polymorphism in a new pseudoautosomal region 3 (PAR3) of a
human X-chromosome-transposed region (XTR) in the Y chromosome. Funct Integr Genomics 2013;13:285-93.
166. Veerappa A, Saldanha M, Padakannaya P, Ramachandra NB. Family based genome-wide copy number scan identifies complex
rearrangements at 17q21.31 in dyslexics. Am J Med Genet B Neuropsychiatr Genet 2014;165:572-80.
167. Gialluisi A, Visconti A, Willcutt E, Smith SD, Pennington BF, et al. Investigating the effects of copy number variants on reading and
language performance. J Neurodevelop Disord 2016;8:17.
168. Craig F, Lamanna AL, Margari F, Matera E, Simone M, et al. Overlap between autism spectrum disorders and attention deficit hyperactivity
disorder: searching for distinctive/common clinical features. Autism Res 2015;8:328-37.
169. Tarazi FI, Sahli ZT, Pleskow J, Mousa SA. Asperger’s syndrome: diagnosis, comorbidity and therapy. Expert Rev Neurother 2015;15:281-
93.
170. Mody M, Belliveau J. Speech and language impairments in autism: insights from behavior and neuroimaging. N Am J Med Sci 2012;5:157.
171. Gernsbacher M, Morson E, Grace E. Language and speech in autism. Annu Rev Linguist 2014;2:413-25.
172. Roll P, Vernes SC, Bruneau N, Cillario J, Ponsole-Lenfant M, et al. Molecular networks implicated in speech-related disorders: FOXP2
regulates the SRPX2/uPAR complex. Hum Mol Genet 2010;19:4848-60.