Schizophrenia and velo-cardio-facial syndrome

Lancet

Volumn 359, Issue 9304, 2002, Pages 426-430

  Murphy, Kieran C ^a  

^a KING'S COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CELL VIABILITY; CHROMOSOME 22Q; CHROMOSOME DELETION; CHROMOSOME IDENTIFICATION; CHROMOSOME MAP; CONGENITAL MALFORMATION; DISEASE ASSOCIATION; DISEASE PREDISPOSITION; GENE IDENTIFICATION; GENE LOCUS; GENE SEQUENCE; GENETIC SUSCEPTIBILITY; HUMAN; MOLECULAR GENETICS; MONOZYGOTIC TWINS; MULTIPLE MALFORMATION SYNDROME; NEURAL CREST CELL; PHENOTYPE; PRIORITY JOURNAL; REVIEW; RISK FACTOR; SCHIZOPHRENIA; SEQUENCE ANALYSIS; VELOCARDIOFACIAL SYNDROME;

EID: 0037006412     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(02)07604-3     Document Type: Review

References (54)

1. A single dominant gene still cannot account for the transmission of schizophrenia
2. The genetic basis of schizophrenia
3. Molecular genetic studies of schizophrenia
4. Dissecting the genetic complexity of schizophrenia
5. Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: Does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?
6. Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome
7. Chromosome 22q11 deletions: An under-recognised cause of idiopathic learning disability
8. Schizophrenia, CATCH 22 and FISH
9. Velo-cardio-facial syndrome: Language and psychological profiles
10. Intelligence and psychological adjustment in velocardiofacial syndrome: A study of 37 children and adolescents with VCFS
11. Epidemiology of schizophrenia
12. Late-onset psychosis in the velo-cardio-facial syndrome
13. Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives
14. High rates of schizophrenia in adults with velo-cardio-facial syndrome
15. Psychiatric disorders in mental retardation
16. Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11
17. Velocardiofacial syndrome in childhood-onset schizophrenia
18. Velocardiofacial manifestations and microdeletions in schizophrenic inpatients
19. 22q11 deletion syndrome in adults with schizophrenia
20. Sequential strategy to identify a susceptibility gene for schizophrenia: Report of potential linkage on chromosome 22q12-q13.1
21. A combined analysis of D22S278 marker alleles in affected sib-pairs: Support for a susceptibility locus for schizophrenia at chromosome 22q12
22. Follow-up report of potential linkage for schizophrenia on chromosome 22q: Part 3
23. Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21
24. A genome-wide search for schizophrenia susceptibility genes
25. Linkage of a composite inhibitory phenotype to a chromosome 22q locus in eight Utah families
26. Implications of normal brain development for the pathogenesis of schizophrenia
27. Is schizophrenia a neurodevelopmental disorder?
28. Deletions of human chromosome 22 and associated birth defects
29. Information-processing and attention dysfunctions in schizophrenia
30. The gene encoding proline dehydrogenase modulates sensorimotor gating in mice
31. Clinical correlates of septum pellucidum cavities: An unusual association with psychosis
32. Cerebellum and schizophrenia: A selective review
33. Meta-analysis of brain and cranial size in schizophrenia
34. Brain anomalies in velo-cardio-facial syndrome
35. Cerebellar atrophy in a patient with velo-cardio-facial syndrome
36. Qualitative MRI findings in adults with 22q11 deletion syndrome and schizophrenia
37. Structural brain abnormalities associated with deletion of chromosome 22q11: A quantitative neuroimaging study of adults with velo-cardio-facial syndrome
38. Midline brain anomalies and schizophrenia in people with CATCH 22 syndrome
39. Velocardiofacial syndrome: Are structural changes in the temporal and mesial temporal regions related to schizophrenia?
40. Meta-analysis of regional brain volumes in schizophrenia
41. Reduction of the parahippocampal gyrus and the hippocampus in patients with chronic schizophrenia
42. Detection of a deletion within 22q11 which has no overlap with the DiGeorge syndrome critical region
43. Patient with a 22q11.2 deletion with no overlap of the minimal DiGeorge syndrome critical region (MDGCR)
44. A novel 22q11.2 microdeletion in DiGeorge syndrome
45. UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome
46. The DiGeorge syndrome minimal critical region contains a Goosecoid-like (GSCL) homeobox gene, which is expressed early in human development
47. Possible role for COMT in psychosis associated with velo-cardio-facial syndrome
48. Evidence for association between polymorphisms of the catechol-O-methyltransferase (COMT) and monoamine oxidase (MAO) genes and schizophrenia in adults with velo-cardio-facial syndrome?
49. Animal models with construct validity for schizophrenia
50. From neuropathology to neurodevelopment
51. Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice
52. TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome
53. DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1