References
1 American Psychiatric Association: Diagnostic and Statistical Manual of Mental Disorders, ed 4. Washington, APA, 1994.
2 Baron-Cohen S, Scott FJ, Allison C, Williams J, Bolton P, Matthews FE, Brayne C: Prevalence of autism-spectrum conditions: UK school-based population study. Br J Psychiatry 2009;194:500–509.
3 Bailey A, Le Couteur A, Gottesman I, Bolton P, Simonoff E, Yuzda E, Rutter M: Autism as a strongly genetic disorder: evidence from a British twin study. Psychol Med 1995;25:63–77.
4 Baron-Cohen S, Lombardo MV, Auyeung B, Ashwin E, Chakrabarti B, Knickmeyer R: Why are autism spectrum conditions more prevalent in males? PLoS Biol 2011;9:e1001081.
5 Frith U: Autism and Asperger’s Syndrome. Cambridge, Cambridge University Press, 1991.
6 Jolliffe T, Baron-Cohen S: Are people with autism or Asperger’s syndrome faster than normal on the Embedded Figures Task? J Child Psychol Psychiatry 1997;38:527–534.
7 Lawson J, Baron-Cohen S, Wheelwright S: Empathising and systemising in adults with and without Asperger syndrome. J Autism Dev Disord 2004;34:301–310.
8 O’Riordan M, Plaisted K, Driver J, Baron-Cohen S: Superior visual search in autism. J Exp Psychol Hum Percept Perform 2001;27:719–730.
9 Knickmeyer RC, Wheelwright S, Fane BA, Hines M, Baron-Cohen S: Autistic traits in people with congenital adrenal hyperplasia: a test of the fetal testosterone theory of autism. Horm Behav 2006;50:148–153.
10 Manning JT, Baron-Cohen S, Wheelwright S, Sanders G: The 2nd to 4th digit ratio and autism. Dev Med Child Neurol 2001;43:160–164.
11 Ingudomnukul E, Wheelwright S, Baron-Cohen S, Knickmeyer R: Elevated rates of testosterone-related disorders in women with autism spectrum conditions. Horm Behav 2007;51:597–604.
12 Knickmeyer RC, Hoekstra R, Wheelwright S, Baron-Cohen S: Age of menarche in females with autism spectrum conditions. Dev Med Child Neurol 2006;48:1007–1008.
13 Ruta L, Ingudomnukul E, Taylor K, Chakrabarti B, Baron-Cohen S: Increased serum androstenedione in adults with autism spectrum conditions. Psychoneuroendocrinology 2011;36:1154–1163.
14 Henningsson S, Jonsson L, Ljunggren E, Westberg L, Gillberg C, Rastam M, Anckarsater H, Nygren G, Landen M, Thuresson K, Betancur C, Leboyer M, Gillberg C, Eriksson E, Melke J: Possible association between the androgen receptor gene and autism spectrum disorder. Psychoneuroendocrinology 2009;34:752–761.
15 Schmidtova E, Kelemenova S, Celec P, Ficek A, Ostatnikova D: Polymorphisms in genes involved in testosterone metabolism in Slovak autistic boys. Endocrinologist 2010;20:245–249.
16 Chakrabarti B, Dudbridge F, Kent L, Wheelwright S, Hill-Cawthorne G, Allison C, Banerjee-Basu S, Baron-Cohen S: Genes related to sex steroids, neural growth, and social-emotional behavior are associated with autistic traits, empathy, and Asperger syndrome. Autism Res 2009;2:157–177.
17 Sarachana T, Xu M, Wu R, Hu V: Sex hormones in autism: androgens and estrogens differentially and reciprocally regulate RORA, a novel candidate gene for autism. PLoS One 2011;6:e17116.
18 Kallai J, Csatho A, Kover F, Makany T, Nemes J, Horvath K, Kovacs N, Manning JT, Nadel L, Nagy F: MRI-assessed volume of left and right hippocampi in females correlates with the relative length of the second and fourth fingers (the 2D: 4D ratio). Psychiatry Res 2005;140:199–210.
19 Chura LR, Lombardo MV, Ashwin E, Auyeung B, Chakrabarti B, Bullmore ET, Baron-Cohen S: Organizational effects of fetal testosterone on human corpus callosum size and asymmetry. Psychoneuroendocrinology 2010;35:122–132.
20 Lombardo MV, Ashwin E, Auyeung B, Chakrabarti B, Taylor K, Hackett G, Bullmore ET, Baron-Cohen S: Fetal testosterone influences sexually dimorphic gray matter in the human brain. J Neurosci 2012;32:674–680.
21 Pfaff D, Rapin I, Goldman S: Male predominance in autism: neuroendocrine influences on arousal and social anxiety. Autism Res 2011;4:163–176.
22 Yan J, Oliveira G, Coutinho A, Yang C, Feng J, Katz C, Sram J, Bockholt A, Jones IR, Craddock N, Cook EH, Vicente A, Sommer SS: Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients. Mol Psychiatry 2005;10:329–332.
23 Carney RM, Wolpert CM, Ravan SA, Shahbazian M, Ashley-Koch A, Cuccaro ML, Vance JM, Pericak-Vance MA: Identification of MeCP2 mutations in a series of females with autistic disorder. Pediatr Neurol 2003;28:205–211.
24 Filges I, Rothlisberger B, Blattner A, Boesch N, Demougin P, Wenzel F, Huber AR, Heinimann K, Weber P, Miny P: Deletion in Xp22.11: PTCHD1 is a candidate gene for X-linked intellectual disability with or without autism. Clin Genet 2011;79:79–85.
25 Gong XH, Bacchelli E, Blasi F, Toma C, Betancur C, Chaste P, Delorme R, Durand CM, Fauchereau F, Botros HG, Leboyer M, Mouren-Simeoni MC, Nygren G, Anckarsater H, Rastam M, Gillberg