Authors' reply [2]

British Journal of Psychiatry

Volumn 191, Issue AUG., 2007, Pages 180-181

  McClellan, Jon ^a   Susser, Ezra ^b   King, Mary Claire ^a  

^a UNIVERSITY OF WASHINGTON   (United States)

^b Department of Medicine   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; AUTISM; BRAIN DEVELOPMENT; DIZYGOTIC TWINS; DNA POLYMORPHISM; EPIGENETICS; GENE CONTROL; GENE EXPRESSION; GENE IDENTIFICATION; GENE MUTATION; GENETIC ASSOCIATION; HUMAN; LETTER; MONOZYGOTIC TWINS; SCHIZOPHRENIA; SEX DIFFERENCE;

EID: 34547638434     PISSN: 00071250     EISSN: None     Source Type: Journal    
DOI: 10.1192/bjp.191.2.180a     Document Type: Letter

References (4)

1. Craddock, N., O'Donovan, M. C. & Owen, M. J. (2007) Phenotypic and genetic complexity of psychosis. Invited commentary on . . . Schizophrenia: a common disease caused by multiple rare alleles. British Journal of Psychiatry, 190, 200-203.
2. King, M. C. & Wilson, A. C. (1975) Evolution at two levels in humans and chimpanzees. Science, 188, 107-116.
3. King, M. C., Ahsan, H. & Susser, E. (2006) Designs for the genomic era. In Psychiatric Epidemiology: Searching for the Causes of Mental Disorders (eds E. Susser, S. Schwartz, A. Morebia, et al), pp. 401-412. Oxford University Press.
4. Sebat, J., Lakshmi, B., Malhotra, D., et al (2007) Strong association of de novo copy number mutations with autism. Science, 316, 445-449.