References 4985 Wilson JG (1973). Environment and Birth Defects. Academic Press, New York.
86 Castillo‐Fernandez JE, Spector TD, Bell JT (2014). Epigenetics of discordant
monozygotic twins: implications for disease. Genome Med., 6 (7):60.
87 Berg J, Geschwind D (2012). Autism genetics: searching for specificity and
convergence. Genome Biol., 13 :1–16.
88 Griswold AJ, Dueker ND, Van Booven D, et al. (2015). Targeted massively
parallel sequencing of autism spectrum disorder‐associated genes in
a case control cohort reveals rare loss‐of‐function risk variants. Mol.
Autism, 6 :43.
89 O’Roak BJ, Deriziotis P, Lee C, et al. (2011). Exome sequencing in sporadic
autism spectrum disorders identifies severe de novo mutations. Nat Genet.,
43 (6):585–9.
90 Liu Z, Li Z, Zhi X, et al. (2017). Identification of de novo DNMT3A
mutations that cause West syndrome by using whole‐exome sequencing.
Mol. Neurobiol. DOI: 10.1007/s12035‐017‐0483‐9.
91 Li J, Cai T, Jiang Y, et al. (2016). Genes with de novo mutations are shared
by four neuropsychiatric disorders discovered from NPdenovo database.
Mol. Psychiatry, 21 (2):290–7.
92 Rees E, Kirov G, Walters JT, et al. (2015). Analysis of exome sequence in 604
trios for recessive genotypes in schizophrenia. Transl. Psychiatry, 5 :e607.
93 Bourgeron T (2016). Current knowledge on the genetics of autism and
propositions for future research. C. R. Biol., 339 (7–8):300–7.
94 Yoo H (2015). Genetics of autism spectrum disorder: Current status and
possible clinical applications. Exp. Neurobiol., 24 (4):257–72.
95 Kirov G (2015). CNVs in neuropsychiatric disorders. Human Mol. Genet.,
24 (R1):R45–9.
96 Hua R, Wei M, Zhang C (2015). The complex genetics in autism spectrum
disorders. Sci. China Life Sci., 58 (10):933–45.
97 De Rubeis S, Buxbaum JD (2015). Recent advances in the genetics of autism
spectrum disorder. Curr. Neurol. Neurosci. Rep., 15 (6):36.
98 Brandler WM, Sebat J (2015). From de novo mutations to personalized
therapeutic interventions in autism. Annu. Rev. Med., 66 :487–507.
99 Talkowski ME, Minikel EV, Gusella JF (2014). Autism spectrum disorder
genetics: diverse genes with diverse clinical outcomes. Harv. Rev. Psychiatry,
22 (2):65–75.
100 Krumm N, O’Roak BJ, Shendure J, Eichler EE (2014). A de novo convergence
of autism genetics and molecular neuroscience. Trends Neurosci.,
37 (2):95–105.
101 Marshall CR, Scherer SW (2012). Detection and characterization of copy
number variation in autism spectrum disorder. Methods Mol. Biol.,
838 :115–35.
102 Eapen V (2011). Genetic basis of autism: is there a way forward? Curr. Opin.
Psychiatry, 24 (3):226–36.