Major psychosis and chromosome 22: Genetics meets epigenetics

CNS Spectrums

Volumn 7, Issue 3, 2002, Pages 209-214

  Petronis, Arturas ^a   Popendikyte, Violeta ^a   Kan, Peixiang ^a   Sasaki, Tsukasa ^a  

^a CENTRE FOR ADDICTION AND MENTAL HEALTH   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMATIN STRUCTURE; CHROMOSOME 22; DNA METHYLATION; GENE EXPRESSION REGULATION; GENETIC SUSCEPTIBILITY; GENOME IMPRINTING; HUMAN; MANIC DEPRESSIVE PSYCHOSIS; MOLECULAR GENETICS; PRIORITY JOURNAL; REVIEW; SCHIZOPHRENIA;

EID: 0036236448     PISSN: 10928529     EISSN: None     Source Type: Journal    
DOI: 10.1017/S1092852900017570     Document Type: Review

References (72)

1. Genetics and psychiatry: An unheralded window on the environment
2. Exploring and explaining epigenetic effects
3. Variation in epigenetic inheritance
4. DNA methylation in eukaryotes: 20 Years on
5. The somatic replication of DNA methylation
6. Human morbid genetics revisited: Relevance of epigenetics
7. Schizophrenia: An epigenetic puzzle?
8. The genes for major psychosis: Aberrant sequence or regulation?
9. Chromosome 22 workshop report
10. Polymorphism in the cell division cycle 45 like gene and schizophrenia
11. Polymorphism in SNAP29 gene promoter region associated with schizophrenia
12. Systematic search for mutations in the human tissue inhibitor of metalloproteinases-3 (TIMP-3) gene on chromosome 22 and association study with schizophrenia
13. No evidence for a schizophrenia susceptibility gene in the vicinity of IL2RB on chromosome 22
14. Human adenosine A2a receptor (A2aAR) gene: Systematic mutation screening in patients with schizophrenia
15. Systematic search for mutations in the 14-3-3 eta chain gene on chromosome 22 in schizophrenics
16. 14-3-3 protein eta chain gene (YWHAH) polymorphism and its genetic association with schizophrenia
17. Analysis of GNAZ gene polymorphism in bipolar affective disorder
18. Mutational analysis of the synapsin III gene on chromosome 22q12-q13 in schizophrenia
19. Linkage and family-based association study of schizophrenia and the synapsin III locus that maps to chromosome 22q13
20. Global variation in the frequencies of functionally different catechol-O-methyltransferase alleles
21. Preferential transmission of the high activity allele of COMT in schizophrenia
22. Effect of COMT Va1108/158 Met genotype on frontal lobe function and risk for schizophrenia
23. Association study of a functional catechol-O-methyltransferase gene polymorphism in Japanese schizophrenics
24. Catechol-O-methyltransferase gene polymorphism in schizophrenia: Evidence for association between symptomatology and prognosis
25. Suicidal behavior in patients with schizophrenia is related to COMT polymorphism
26. Homicidal behavior in schizophrenia associated with a genetic polymorphism determining low catechol-O-methyltransferase (COMT) activity
27. Genotype determining low catechol-O-methyltransferase activity as a risk factor for obsessive-compulsive disorder
28. Family-based association studies support a sexually dimorphic effect of COMT and MAOA on genetic susceptibility to obsessive-compulsive disorder
29. Association between homozygosity at the COMT gene locus and obsessive compulsive disorder
30. Unstable genes-unstable mind?
31. Trinucleotide repeat expansion and neuropsychiatric disease
32. Association of CAG repeat loci on chromosome 22 with schizophrenia and bipolar disorder
33. Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11
34. Velocardio-facial syndrome: Implications of microdeletion 22q11 for schizophrenia and mood disorders
35. Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: Does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?
36. 22q11 deletion syndrome: A genetic subtype of schizophrenia
37. Velocardiofacial manifestations and microdeletions in schizophrenic inpatients
38. Velocardiofacial syndrome: Are structural changes in the temporal and mesial temporal regions related to schizophrenia?
39. Qualitative MRI findings in adults with 22q11 deletion syndrome and schizophrenia
40. Velo-cardio-facial syndrome and psychotic disorders: Implications for psychiatric genetics
41. Velocardiofacial syndrome in childhood-onset schizophrenia
42. Molecular analysis of velo-cardiofacial syndrome patients with psychiatric disorders
43. Propagating epigenetic states through meiosis: Where Mendel's gene is more than a DNA moiety
44. The Drosophila Fab-7 chromosomal element conveys epigenetic inheritance during mitosis and meiosis
45. Epigenetic control of transgene expression and imprinting by genotype-specific modifiers
46. Inheritance of allelic blueprints for methylation patterns
47. Epigenetic inheritance at the agouti locus in the mouse
48. Genetics of schizophrenia - New findings
49. A genome survey indicates a possible susceptibility locus for bipolar disorder on chromosome 22
50. A comprehensive genetic map of the human genome based on 5,264 microsatellites
51. A genome-wide scan in 301 families with sibling-pairs diagnosed with schizophrenia of schizoaffective disorder suggests linkage to chromosomes 2pcen and 10p14
52. Parental origin of the deletion 22q11.2 and brain development in velocardiofacial syndrome: A preliminary study
53. Epigenetics: Regulation through repression
54. The impact of genomic imprinting for neurobehavioral and developmental disorders
55. Imprinting and the epigenetic asymmetry between parental genomes
56. Sequence conservation and variability of imprinting in the beckwith-wiedemann syndrome gene cluster in human and mouse
57. DNA methylation at the putative promoter region of the human dopamine D2 receptor gene
58. Association study of a promoter polymorphism of UFDIL gene with schizophrenia
59. Possible association between schizophrenia and the 14-3-3 eta gene
60. Application of cDNA microarrays to examine gene expression differences in schizophrenia
61. Clinical and diagnostic aspects of fragile X syndrome
62. The DMPK gene of severely affected myotonic dystrophy patients is hypermethylated proximal to the largely expanded CTG repeat
63. CTCF-binding sites flank CTG/CAG repeats and form a methylation-sensitive insulator at the DM1 locus
64. Polyglutamine-containing proteins in schizophrenia: An effect of lymphoblastoid cells?
65. Mouse A9 cells containing single human chromosomes for analysis of genomic imprinting
66. Evidence for uniparental, paternal expression of the human GABAA receptor subunit genes, using microcell-mediated chromosome transfer
67. A model system to study genomic imprinting of human genes
68. Laser capture microdissection
69. A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands
70. Methylation-specific oligonucleotide microarray: A new potential for high throughput methylation analysis