Adegbola AA et al., 2015. Monoallelic expression of the human FOXP2 speech gene. Proc Natl Acad Sci U S A. 112(22):6848-54. doi: 10.1073/pnas.1411270111.

Alarcon M et al. 2008. Linkage, association and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. Am J Hum Genet. 82: 150-159. 10.1016/j.ajhg.2007.09.005.

Arking DE et al., 2008. A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. Am J Hum Genet. 82: 160-164. 10.1016/j.ajhg.2007.09.015.

Asperger H. 1944. ‘Autistic psychopathy’ in childhood. In Frith U. Autism and Asperger syndrome. Cambridge University Press. pp. 37–92.

Bakkaloglu B et al., 2008. Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders. Am J Hum Genet. 82: 165-173. 10.1016/j.ajhg.2007.09.017.

Bishop SL et al., 2013. Subcategories of restricted and repetitive behaviors in children with autism spectrum disorders. J Autism Dev Disord. 43(6):1287-97. doi: 10.1007/s10803-012-1671-0.

Casanova MF et al., 2002. Minicolumnar pathology in autism. Neurology. 58(3):428-32.

Eapen V 2013. Exploring links between genotypes, phenotypes and clinical predictors of response to early intensive behavioral intervention in autism spectrum disorder. Front Hum Neurosci. 7:567. doi: 10.3389/fnhum.2013.00567.

Fan LW et al., 2015. Exposure to serotonin adversely affects oligodendrocyte development and myelination in vitro. J Neurochem. 133(4):532-43. doi: 10.1111/jnc.12988.

Francis SM et al. 2016. Variants in adjacent oxytocin/vasopressin gene region and ssociations with ASD diagnosis and other autism related endophenotypes. Front Neurosci. 10:195. doi: 10.3389/fnins.2016.00195.

Freitag CM et al., 2008. Perception of biological motion in autism spectrum disorders. Neuropsychologia. 46(5):1480-94. doi: 10.1016/j.neuropsychologia.2007.12.025.

Gialluisi et al., 2016. Investigating the effects of copy number variants on reading and language performance. J Neurodev Disord. 2016 May 15;8:17. doi: 10.1186/s11689-016-9147-8. eCollection 2016.

Goin-Kochel RP et al., 2008. Level of functioning in autism spectrum disorders: phenotypic congruence among affected siblings. J Autism Dev Disord. 38(6):1019-27.

Jeste SS and DH Geschwind. 2014. Disentangling the heterogeneity of autism spectrum disorder through genetic findings. Nat Rev Neurol. 10(2):74-81. doi: 10.1038/nrneurol.2013.278.

Klin A. 1991. Young autistic children’s listening preferences in regard to speech: a possible characterization of the symptom of social withdrawal. J. Autism Dev. Disord. 21, 29–42. doi:10.1007/BF02206995.

Lai CS et al., 2001. A forkhead-domain gene is mutated in a severe speech and language disorder. Nature. 2001, 413: 519-523. 10.1038/35097076.

Losh M et al., 2012. Pragmatic Language in autism and fragile X syndrome: Genetic and clinical applications. Perspect Lang Learn Educ. 19:48-55

Malishkevich A et al., 2015. Activity-dependent neuroprotective protein (ADNP) exhibits striking sexual dichotomy impacting on autistic and Alzheimer’s pathologies. Transl Psychiatry. 5:e501. doi: 10.1038/tp.2014.138.

Matsunami N et al., 2013. Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population. PLoS One. 2013;8(1):e52239. doi: 10.1371/journal.pone.0052239.

Mikhail FM et al., 2011. Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation and/or autism spectrum disorders. Am J Med Genet A. 155A: 2386-2396.

Newbury DF, Monaco AP 2010. Genetic advances in the study of speech and language disorders. Neuron. 2010, 68: 309-320. 10.1016/j.neuron.2010.10.001.

Notwell JH et al., 2016. TBR1 regulates autism risk genes in the developing neocortex. Genome Res. 26(8):1013-22. doi: 10.1101/gr.203612.115.

Poot M. 2015. Connecting the CNTNAP2 networks with neurodevelopmental disorders. Mol Syndromol. 6(1):7-22. doi: 10.1159/000371594.

Rendall AR et al., 2016. Learning delays in a mouse model of Autism Spectrum Disorder. Behav Brain Res. 303:201-7. doi: 10.1016/j.bbr.2016.02.006.

Rutherford M et al., 2002. Reading the mind in the voice: a study with normal adults and adults with Asperger syndrome and high functioning autism. J. Autism Dev. Disord. 32:189–194. doi:10.1023/A:101 5497629971.

Schmidt GL et al., 2008. Impairments in phonological processing and nonverbal intellectual function in parents of children with autism. J Clin Exp Neuropsychol. 2008 Jul;30(5):557-67. doi: 10.1080/13803390701551225.

SIDER, 2015. SIDER 4.1: Side Effect Resources http://sideeffects.embl.de

Sucksmith, E.; Roth, I. and Hoekstra, R. A. 2011. Autistic traits below the clinical threshold: reexamining the broader autism phenotype in the 21st century. Neuropsychology Review, 21(4) pp. 360–389.

Theiss C et al., 2002. Aluminum impairs gap junctional intercellular communication between astroglial cells in vitro. Cell Tissue Res. 310(2):143-54.

Torrico B et al., 2016. Lack of replication of previous autism spectrum disorder GWAS hits in European populations. Autism Res. doi: 10.1002/aur.1662.

Valencia AV et al., 2012. Evidence for association and epistasis between the genetic markers SLC6A4 and HTR2A in autism etiology. Biomedica. 32(4):585-601. doi: 10.1590/S0120-41572012000400014.

Wierenga CJ et al., 2008. GABAergic synapses are formed without the involvement of dendritic protrusions. Nat Neurosci. 11(9):1044-52.

Uzunova G et al., 2015. Excitatory/inhibitory imbalance in autism spectrum disorders: Implications for interventions and therapeutics. World J Biol Psychiatry. 1-13.

Zurek AA, 2016. a5GABAA receptor deficiency causes autism-like behaviors. Ann Clin Transl Neurol. 3(5): 392–398. doi: 10.1002/acn3.303

 

• Uncategorized