The molecular genetics of Schizophrenia : Molecular genetics of neurodegenerative diseases and psychosesCARDNO, A. G; MCGUFFIN, P.Neuropathology and applied neurobiology (Print). 1994, Vol 20, Num 4, pp 344-349, issn 0305-1846Article

Antidepressants for the treatment of depression in people with schizophrenia: a systematic reviewWHITEHEAD, C; MOSS, S; CARDNO, A et al.Psychological medicine (Print). 2003, Vol 33, Num 4, pp 589-599, issn 0033-2917, 11 p.Article

Autosome search for schizophrenia susceptibility genes in multiply affected familiesREES, M. I; FENTON, I; MANT, R et al.Molecular psychiatry. 1999, Vol 4, Num 4, pp 353-359, issn 1359-4184Article

A study of chromosome 4p markers and dopamine D5 receptor gene in schizophrenia and bipolar disorderASHERSON, P; MANT, R; MUIR, W et al.Molecular psychiatry. 1998, Vol 3, Num 4, pp 310-320, issn 1359-4184Article

Is disabling fatigue in childhood influenced by genes?FARMER, A; SCOURFIELD, J; MARTIN, N et al.Psychological medicine (Print). 1999, Vol 29, Num 2, pp 279-282, issn 0033-2917Article

A family based association study of T102C polymorphism in 5HT2A and schizophrenia plus identification of new polymorphisms in the promoterSPURLOCK, G; HEILS, A; LESCH, K. P et al.Molecular psychiatry. 1998, Vol 3, Num 1, pp 42-49, issn 1359-4184Article

The case for or against heterogeneity in the etiology of schizophrenia. The genetic evidenceCARDNO, A. G; FARMER, A. E.Schizophrenia research. 1995, Vol 17, Num 2, pp 153-159, issn 0920-9964Article

Electroconvulsive therapy in Paget's disease and hydrocephalusCARDNO, A. G; SIMPSON, C. J.Convulsive therapy. 1991, Vol 7, Num 1, pp 48-51, issn 0749-8055, 4 p.Article

Characterisation, mutation detection, and association analysis of alternative promoters and 5' UTRs of the human dopamine D3 receptor gene in schizophreniaANNEY, R. J; REES, M. I; JONES, G et al.Molecular psychiatry. 2002, Vol 7, Num 5, pp 493-502, issn 1359-4184Article

A meta-analysis and transmission disequilibrium study of association between the dopamine D3 receptor gene and schizophreniaWILLIAMS, J; SPURLOCK, G; MESZAROS, K et al.Molecular psychiatry. 1998, Vol 3, Num 2, pp 141-149, issn 1359-4184Article

Expansion of 50 CAG/CTG repeats excluded in schizophrenia by application of a highly efficient approach using repeat expansion detection and a PCR screening setBOWEN, T; GUY, C; SPEIGHT, G et al.American journal of human genetics. 1996, Vol 59, Num 4, pp 912-917, issn 0002-9297Article

Processing of words and faces by patients with left and right temporal lobe epilepsyELLIS, A. W; HILLAM, J. C; CARDNO, A et al.Behavioural neurology. 1991, Vol 4, Num 2, pp 121-128, issn 0953-4180Article

Psychiatric genetics : back to the futureOWEN, M. J; CARDNO, A. G; O'DONOVAN, M. C et al.Molecular psychiatry. 2000, Vol 5, Num 1, pp 22-31, issn 1359-4184Article

Sustained and selective attention as measures of genetic liability to schizophreniaJONES, L. A; CARDNO, A. G; SANDERS, R. D et al.Schizophrenia research. 2001, Vol 48, Num 2-3, pp 263-272, issn 0920-9964Article

Dimensions of psychosis in affected sibling pairsCARDNO, A. G; JONES, L. A; MURPHY, K. C et al.Schizophrenia bulletin. 1999, Vol 25, Num 4, pp 841-850, issn 0586-7614Article

Polydactyly and psychosis : Five cases of co-occurrenceCARDNO, A. G; MURPHY, K. C; JONES, L. A et al.British journal of psychiatry (Print). 1998, Vol 172, Num FEV, pp 184-185, issn 0007-1250Article

Factor-derived subsyndromes of schizophrenia and familial morbid risksCARDNO, A. G; HOLMANS, P. A; HARVEY, I et al.Schizophrenia research. 1997, Vol 23, Num 3, pp 231-238, issn 0920-9964Article

No evidence for allelic association between schizophrenia and a functional variant of the human dopamine β-hydroxylase gene (DBH)WILLIAMS, H. J; BRAY, N; MURPHY, K. C et al.American journal of medical genetics. 1999, Vol 88, Num 5, pp 557-559, issn 0148-7299Article

Sibling pairs with schizophrenia or schizoaffective disorder : associations of subtypes, symptoms and demographic variablesCARDNO, A. G; JONES, L. A; MURPHY, K. C et al.Psychological medicine (Print). 1998, Vol 28, Num 4, pp 815-823, issn 0033-2917Article

Linkage study of chromosome 6p in sib-pairs with schizophreniaDANIELS, J. K; SPURLOCK, G; OWEN, M. J et al.American journal of medical genetics. 1997, Vol 74, Num 3, pp 319-323, issn 0148-7299Article

Factor analysis of schizophrenic symptoms using the OPCRIT checklistCARDNO, A. G; JONES, L. A; MURPHY, K. C et al.Schizophrenia research. 1996, Vol 22, Num 3, pp 233-239, issn 0920-9964Article

Mutation screening and LD mapping in the VCFS deleted region of chromosome 22q11 in schizophrenia using a novel DNA pooling approachWILLIAMS, N. M; SPURLOCK, G; CARDNO, A. G et al.Molecular psychiatry. 2002, Vol 7, Num 10, pp 1092-1100, issn 1359-4184, 9 p.Article

The Kings Schizotypy Questionnaire as a quantitative measure of schizophrenia liabilityJONES, L. A; CARDNO, A. G; MURPHY, K. C et al.Schizophrenia research. 2000, Vol 45, Num 3, pp 213-221, issn 0920-9964Article

Sibling pairs with affective disorders: resemblance of demographic and clinical featuresO'MAHONY, E; CORVIN, A; GILL, M et al.Psychological medicine (Print). 2002, Vol 32, Num 1, pp 55-61, issn 0033-2917Article

No evidence for an allelic association between schizophrenia and markers D22S278 and D22S283WILLIAMS, N. M; JONES, L. A; MURPHY, K. C et al.American journal of medical genetics. 1997, Vol 74, Num 1, pp 37-39, issn 0148-7299Article