Xu, B, Roos, JL, Levy, S, van Rensburg, EJ, Gogos, JA, Karayiorgou, M.
Strong association of de novo copy number mutations with sporadic schizophrenia. Nat Genet
2008; 40: 880–5.
Geschwind, DH, Konopka, G.
Neuroscience in the era of functional genomics and systems biology. Nature
2009; 461: 908–15.
Crespi, B, Stead, P, Elliot, M.
Comparative genomics of autism and schizophrenia. Proc Natl Acad Sci USA
2010; 107 (suppl 1): 1736–41.
Guilmatre, A, Dubourg, C, Mosca, A–L, Legallic, S, Goldenberg, A, Drouin-Garraud, V, et al.
Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation. Arch Gen Psychiatry
2009; 66: 947–56.
Walsh, T, McClellan, JM, McCarthy, SE, Addington, AM, Pierce, SB, Cooper, GM, et al.
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia. Science
2008; 320: 539–43.
Dementia Praecox and Paraphrenia. R. E. Krieger Publishers, 1919.
A Clinical and Genetic Study of 1280 Cases of Mental Defect. Medical Research Council: Special Report Number 229. HMSO, 1938.
Schizophrenia spectrum disorders in people with intellectual disabilities. Curr Opin Psychiatry
2006; 19: 470–4.
Morgan, VA, Leonard, H, Bourke, J, Jablensky, AV.
Intellectual disability co-occurring with schizophrenia and other psychiatric illness: population-based study. Br J Psychiatry
2008; 193: 364–72.
Intellectual Disability. Understanding its Development, Causes, Classification, Evaluation, and Treatment. Oxford University Press, 2006.
The epidemiological horizon. In Schizophrenia (2nd edn) (eds Hirsch, SR, Weinberger, DR): 203–31. Blackwell, 2003.
Jablensky, A, Morgan, VA, Zubrick, S, Bower, C, Yellachich, L.
Pregnancy, delivery, and neonatal complications in a population cohort of women with schizophrenia and major affective disorders. Am J Psychiatry
2005; 162: 79–91.
Morgan, VA, Valuri, GM, Croft, ML, Griffith, JA, Shah, S, Young, DJ, et al.
Cohort profile: pathways of risk from conception to disease: the Western Australian schizophrenia high-risk e-Cohort. Int J Epidemiol
2010; November 19: Epub ahead of print.
Glasson, EJ, de Klerk, NH, Bass, AJ, Rosman, DL, Palmer, LJ, Holman, CDJ.
Cohort profile: The Western Australian Family Connections Genealogical Project. Int J Epidemiol
2008; 37: 30–5.
Croft, ML, Read, AW, de Klerk, N, Hansen, J, Kurinczuk, JJ.
Population based ascertainment of twins and their siblings, born in Western Australia 1980 to 1992, through the construction and validation of a maternally linked database of siblings. Twin Res
2002; 5: 317–23.
World Health Organization. International Statistical Classification of Diseases and Related Health Problems, Ninth Revision (ICD–9). WHO, 1977.
Castle, D, Jablensky, A, McGrath, J, Carr, V, Morgan, V, Waterreus, A, et al.
The Diagnostic Interview for Psychoses (DIP): development, reliability and applications. Psychol Med
2006; 36: 69–80.
A manual on terminology and classification in mental retardation. Am J Ment Defic
1959; 64 (suppl): 1–111.
Yeargin-Allsopp, M, Murphy, C, Cordero, J, Decouflé, P, Hollowell, J.
Reported biomedical causes and associated medical conditions for mental retardation among 10-year-old children, metropolitan Atlanta, 1985 to 1987. Dev Med Child Neurol
1997; 39: 142–9.
Badawi, N, Kurinczuk, JJ, Keogh, JM, Alessandri, LM, O'Sullivan, F, Burton, PR, et al.
Antepartum risk factors for newborn encephalopathy: the Western Australian case-control study. BMJ
1998; 317: 1549–53.
McNeil, TF, Sjöström, K.
McNeil–Sjöström Scale for Obstetric Complications.
Lund University, 1995.
World Health Organization. The ICD–10 Classification of Mental and Behavioural Disorders: Clinical Descriptions and Diagnostic Guidelines. WHO, 1992
Malaspina, D, Harlap, S, Fennig, S, Heiman, D, Nahon, D, Feldman, D, et al.
Advancing paternal age and the risk of schizophrenia. Arch Gen Psychiatry
2001; 58: 361–7.
Reichenberg, A, Gross, R, Weiser, M, Bresnahan, M, Silverman, J, Harlap, S, et al.
Advancing paternal age and autism. Arch Gen Psychiatry
2006; 63: 1026–32.
Heinrichs, RW, Zakzanis, KK.
Neurocognitive deficit in schizophrenia: a quantitative review of the evidence. Neuropsychology
1998; 12: 426–45.
Hallmayer, JF, Kalaydjieva, L, Badcock, J, Dragovic, M, Howell, S, Michie, PT, et al.
Genetic evidence for a distinct subtype of schizophrenia characterized by pervasive cognitive deficit. Am J Hum Genet
2005; 77: 468–76.
Larsson, HJ, Eaton, WW, Madsen, KM, Vestergaard, M, Olesen, AV, Agerbo, E, et al.
Risk factors for autism: perinatal factors, parental psychiatric history, and socioeconomic status. Am J Epidemiol
2005; 161: 916–25.
Cascella, N, Schretlen, D, Sawa, A.
Schizophrenia and epilepsy: is there a shared susceptibility? Neurosci Res
2009; 63: 227–35.
Mula, M, Marotta, A, Monaco, F.
Epilepsy and bipolar disorders. Expert Rev Neurother
2010; 10: 13–23.
Perucca, E, Tomson, T.
Prenatal exposure to antiepileptic drugs. Lancet
2006; 367: 1467–9.
Bassett, A, Chow, E, AbdelMalik, P, Gheorghiu, M, Husted, J, Weksberg, R.
The schizophrenia phenotype in 22q11 Deletion Syndrome. Am J Psychiatry
2003; 160: 1580–6.
Ismail, B, Cantor-Graae, E, McNeil, T.
Minor physical anomalies in schizophrenia patients and their siblings. Am J Psychiatry
1998; 155: 1695–702.
Rzhetsky, A, Wajngurt, D, Park, N, Zheng, T.
Probing genetic overlap among complex human phenotypes. PNAS
2007; 104: 11694–9.
Grozeva, D, Kirov, G, Ivanov, D, Jones, IR, Jones, L, Green, EK, et al.
Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia. Arch Gen Psychiatry
2010; 67: 318–27.
Stefansson, H, Rujescu, D, Cichon, S, Pietiläinen, OP, Ingason, A, Steinberg, S, et al.
Large recurrent microdeletions associated with schizophrenia. Nature
2008; 455: 232–6.
Rosannoff, A, Handy, L, Rosanoff, I, Brush, S.
The etiology of so-called schizophrenic psychoses: with special reference to their occurrence in twins. Am J Psychiatry
1934; Sept: 247–86.
Cannon, M, Jones, PB, Murray, RM.
Obstetric complications and schizophrenia: historical and meta-analytic review. Am J Psychiatry
2002; 159: 1080–92.
Leonard, H, Wen, X.
The epidemiology of mental retardation: challenges and opportunities in the new millennium. Ment Retard Dev Disabil Res Rev
2002; 8: 117–34.
Hultman, CM, Sparen, P, Cnattingius, S.
Perinatal risk factors for infantile autism. Epidemiology
2002; 13: 417–23.
Prenatal contributions to epilepsy: lessons from the bedside. Epileptic Disord
2003; 5: 77–91.
Tsukimori, K, Nakano, H, Wake, N.
Difference in neutrophil superoxide generation during pregnancy between preeclampsia and essential hypertension. Hypertens Res
2007; 49: 1436–41.
Prenatal infection as a risk factor for schizophrenia. Schizophr Bull
2006; 32: 200–2.
Goodyer, IM, Park, RJ, Netherton, CM, Herbert, J.
Possible role of cortisol and dehydroepiandrosterone in human development and psychopathology. Br J Psychiatry
2001; 179: 243–9.
Nicodemus, KK, Marenco, S, Batten, AJ, Vakkalanka, R, Egan, MF, Straub, RE, et al.
Serious obstetric complications interact with hypoxia-regulated/vascular-expression genes to influence schizophrenia risk. Mol Psychiatry
2008; 13: 873–7.
Meyer, U, Yee, BK, Feldon, J.
The neurodevelopmental impact of prenatal infections at different times of pregnancy: the earlier the worse? Neuroscientist
2007; 13: 241–56.
Morgan, VA, Castle, D, Page, A, Fazio, S, Gurrin, L, Burton, P, et al.
Influenza epidemics and the incidence of schizophrenia, affective disorders and mental retardation in Western Australia: no evidence of a major effect. Schizophr Res
1997; 26: 25–39.
Psychosis during pregnancy: treatment considerations. Ann Clin Psychiatry
1995; 9: 175–9.
Bellis, MA, Hughes, K, Hughes, S, Ashton, JR.
Measuring paternal discrepancy and its public health consequences. J Epidemiol Community Health
2005; 59: 749–54.