Common psychiatric diseases and human genetic variation

Community Genetics

Volumn 5, Issue 3, 2002, Pages 171-177

  Mukherjee, O ^a   Saleem, Q ^d,e   Purushottam, M ^a   Anand, A ^c   Brahmachari, S K ^b,e   Jain, Sanjeev ^a  

^a NATIONAL INSTITUTE OF MENTAL HEALTH AND NEUROSCIENCES   (India)

^b INDIAN INSTITUTE OF SCIENCE   (India)

^c JAWAHARLAL NEHRU CENTRE FOR ADVANCED SCIENTIFIC RESEARCH   (India)

^d TATA INSTITUTE OF FUNDAMENTAL RESEARCH   (India)

^e CSIR INSTITUTE OF GENOMICS AND INTEGRATIVE BIOLOGY   (India)

Author keywords

Bipolar disease; Genetic predisposition; India; Schizophrenia

Indexed keywords

ALCOHOL DEHYDROGENASE; DOPAMINE RECEPTOR; NEUROTRANSMITTER; SEROTONIN RECEPTOR; SEROTONIN TRANSPORTER;

ARTICLE; BRAIN; DEGENERATIVE DISEASE; ETHNIC GROUP; GENE EXPRESSION; GENE FREQUENCY; GENE LOCUS; GENETIC POLYMORPHISM; GENETIC VARIABILITY; HUMAN; HUNTINGTON CHOREA; INDIA; MACHADO JOSEPH DISEASE; MENTAL DISEASE; MICROSATELLITE INSTABILITY; POPULATION DISTRIBUTION; POPULATION GENETICS; PRIORITY JOURNAL; WESTERN EUROPE;

EID: 0036435635     PISSN: 14222795     EISSN: None     Source Type: Journal    
DOI: 10.1159/000066332     Document Type: Article

References (39)

1. Wright AF, Carothers AD, Pirastu M: Population choice in mapping genes for complex diseases. Nature Genet 1999;23:397-404.
2. McDowall TW: The insane Indians and their treatment. J Ment Sci 1897;53:683-702.
3. Leff J, Sartorius N, Jablensky A, Korten A, Ernberg G: The International Pilot Study of Schizophrenia: Five-year follow-up findings. Psychol Med 1992;22:131-145.
4. Jablensky A, Hugler H, Von Cranach M, Kalinov K: Kraepelin revisited: A reassessment and statistical analysis of dementia praecox and manic-depressive insanity in 1908. Psychol Med 1993;23:843-858.
5. Callan AF: Schizophrenia in Afro-Caribbean immigrants. J Roy Soc Med 1996;89;253-256.
6. Sharpley M, Hutchinson G, McKenzie K, Murray RM: Understanding the excess of psychosis among the African-Caribbean population in England. Review of current hypotheses. Br J Psychiatry Suppl 2001;40:s60-s68.
7. Tautz D, Schlotterer C: Simple sequences. Curr Opin Genet Dev 1994;4:832-837.
8. Brahmachari SK, Meera G, Sarkar PS, Balagu-rumoorthy P: Simple repetitive sequences in the genome: Structural and functional significance. Electrophoresis 1995;16:1705-1714.
9. Reddy PS, Housman DE: The complex pathology of trinucleotide repeats. Curr Opin Cell Biol 1997;9:364-372.
10. Rubinsztein DC, Amos W, Leggo J,Goodburn S, Jain S, Li SH, Margolis RL, Ross CA, Ferguson-Smith MA: Microsatellite evolution - Evidence for directionality and variation in rate between species. Nature Genet 1995;67:495-498.
11. Saleem Q, Anand A, Jain S, Brahmachari SK: The polyglutamine motif is highly conserved at the Clock locus in various organisms and is not polymorphic in humans. Hum Genet 2001; 109:136-142.
12. Mott FW: Hereditary aspects of nervous and mental diseases. BMJ 1910;2:1013-1020.
13. McInnis MG, McMahon FJ, Crow T, Ross CA, DeLisi LE: Anticipation in schizophrenia: A review and reconsideration. Am J Med Genet 1999;88:686-693.
14. Jain S, Jayne L, Delisi LE, Crow TJ, Margolis RL, Li Shi-Hua, Goodburn S, Walsh C, Paykel ES, Ferguson-Smith MA, Ross CA, Rubinsztein DC: Analysis of thirteen trinucleotide repeat loci as candidate genes for schizophrenia and bipolar disorder. Am J Med Genet 1996; 67:139-146.
15. Chandy KG, Fantino E, Wittekindt O, Kalman K, Tong LL, Ho TH, Gutman GA, Crocq MA, Ganguli R, Nimgaonkar V, Morsis-Rosendahl DJ, Gargus JJ: Isolation of vel potassium channel gene hSKCa3 containing a polymorphic CAG repeat: A candidate for schizophrenia and bipolar disorder? Mol Psychiatry 1998;3: 32-37.
16. Saleem Q, Vijayakumar M, Mutsuddi M, Chowdhary N, Jain S, Brahmachari SK: Variation at the MJD locus in major psychoses. Am J Med Genet 1998;81:440-442.
17. Saleem Q, Sreevidya VS, Sudhir J, Vijaya Sa-vithri, GowdaY, Rao CB, Benegal V, Majum-dar PP, Anand A, Brahmachari SK: Association analysis of CAG repeats at the KCNN3 locus in Indian patients with bipolar disorder and schizophrenia. Am J Med Genet 2000;96: 744-748.
18. Vincent JB, Paterson AD, Strong E, Petronis A, Kennedy JL: The unstable trinuceotide repeat story of major psychosis. Am J Med Genet 2000;97:77-97.
19. Chung M-Y, Ranum LPW, Duwick IA, Servadio A, Zoghbi HY, Orr HT: Evidence for a mechanism predisposing to intergenerational CAG repeat instability in Spinocerebellar ataxia type. Nature Genet 1993;5:254-258.
20. Geschwind DH, Perlman S, Figueroa CP, Treiman IJ, Pulst SM: The prevalence and wide clinical spectrum of spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia. Am J Hum Genet 1997;60:842-850.
21. Moseley ML, Benzow KA, Schut LJ, Bird TD, Gomez CM, Barkhaus PE, Blindauer KA, Labuda M, Pandolfo M, Koob MD, Ranum LP: Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families. Neurology 1998;51:1666-1671.
22. Filla A, De Michele G, Santoro L, Calabrese O, Castaldo I, Giuffrida S, Restivo D, Serlenga L, Condorelli DF, Bonuccelli U, Scala R, Coppola G, Caruso G, Cocozza S: Spinocerebellar ataxia type 2 in southern Italy: A clinical and molecular study of 30 families. J Neurol 1999; 246:467-471.
23. Basu P, Chattopadhyay B, Gangopadhaya PK, Mukherjee SC, Sinha KK, Das SK, Roychoudhury S, Majumder PP, Bhattacharyya NP: Analysis of CAG repeats in SCA1, SCA2, SCA3, SCA6, SCA7 and DRPLA loci in spinocerebellar ataxia patients and distribution of CAG repeats at the SCA1, SCA2 and SCA6 loci in nine ethnic populations of eastern India. Hum Genet 2000;106:597-604.
24. Leggo J, Dalton A, Morrison PJ, Dodge A, Connarty M, Kptze MJ, Rubinsztein DC: Analysis of Spinocerebellar ataxia types 1, 2, 3, and 6, dentatorubral-pallidoluysian atrophy and Friedreich's ataxia genes in Spinocerebellar ataxia patients in the UK. J Med Genet 1997;34:982-985.
25. Goldberg YP, Kremer B, Andrew SE, Theilmann J, Graham RK, Squitteri F, Telenius H, Adam S, Sajoo A, Starr E, et al: Molecular analysis of new mutations of Huntington's disease: Intermediate alleles and sex of origin effects. Nature Genet 1993;5:174-179.
26. n repeat in sporadic Huntington's disease. Nature Genet 1993;5: 168-173.
27. Squitieri F, Andrew SE, Goldberg YP, Kremer B, Spence N, Zeisler J, Nichol K, Theilmann J, Greenberg J, Goto J, et al: DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence. Hum Mol Genet 1994;3:2103-2114.
28. Takano H, Cancel G, Ikeuchi T, Lorenzetti D, Mawad R, Stevanin G, Didierjean O, Durr A, Oyake M, Shimohata T, Sasaki R, Koide R, Igarashi S, Hayashi S, Takiyama Y, Nishizawa M, Tanaka H, Zoghbi H, Brice A, Tsuji S: Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations. Am J Hum Genet 1998;63:1060-1066.
29. Saleem Q, Choudhry S, Mukerji M, Bashyam L, Padma MV, Chakravathy A, Maheshwari ML, Jain S, Brahmachari SK: Molecular analysis of autosomal dominant heredity ataxias in the Indian population: High frequency of SCA2 and evidence for a common founder mutation. Hum Genet 2000;106:179-187.
30. Holmes SE, O'Hearn EE, McInnis MG, Gorelick-Feldman DA, Kleiderlein JJ, Callahan C, Kwak NG, Ingersoll-Ashworth RG, Sherr M, Sumner AJ, Sharp AH, Ananth U, Seltzer WK, Boss MA, Vieria-Saecker AM, Epplen JT, Riess O, Ross CA, Margolis RL: Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA12. Nature Genet 1999;23:391-392.
31. Srivastava AK, Choudhry S, Gopinath MS, Roy S, Tripathi M, Brahmachari SK, Jain S: Molecular and clinical correlation in five Indian families with spinocerebellar ataxia 12. Ann Neurol 2001;50:796-800.
32. Harper PS: Epidemiology of Huntington's disease; in Harper PS (ed): Huntington's Disease, ed 2. London, Saunders, 1996, pp 201-239.
33. Saleem Q, Muthane U, Verma IC, Brahmachari SK, Jain S: Expanding colonies and expanding repeats. Lancet 2002;359:895-896.
34. Gelernter J, Kranzler H, Lacobelle J: Population studies of polymorphisms at loci of neu-ropsychiatry interest [tryptophan hydroxylase (TPH), dopamine transporter protein (SLC6A3), D3 dopamine receptor (DRD3), apolipoprotein E (APOE), μOpioid receptor (OPRM1), and ciliary neurotrophic factor (CNTF)]. Genomics 1998;52:289-297.
35. Arranz MJ, Munro J, Birkett J, Bolonna A, Mancamma D, Sodhi M, Lesch KP, Meyer JF, Sham P, Collier DA, Murray RM, Kerwin RW: Pharmacogenetic prediction of clozapine response. Lancet 2000;355:615-616.
36. Saleem Q, Ganesh S, Vijaykumar M, Reddy YC, Brahmachari SK, Jain S: Association analysis of 5HT transporter gene in bipolar disorder in the Indian population. Am J Med Genet 2000;96:170-172.
37. Shaikh KJ, Daniel N, Sherrin T, Murthy A, Thennarasu K, Anand A, Benegal V, Jain S: Polymorphisms at the DRD2 locus in early-onset alcohol dependence in the Indian population. Addict Biol 2001;6:331-335.
38. Emsley RA, Roberts MC, Rataemane S, Preto-rius J, Oosthuizen PP, Turner J, Niehaus DJ, Keyter N, Stein DJ: Ethnicity and treatment response in schizophrenia: A comparison of 3 ethnic groups. J Clin Psychiatry 2002;63:9-14.
39. Johnson GC, Esposito L, Barratt BJ, Smith AN, Heward J, Di Genova G, Ueda H, Cordell HJ, Eaves IA, Dudbridge F, Twells RC, Payne F, Hughes W, Nutland S, Stevens H, Carr P, Tuomilehto-Wolf E, Tuomilehto J, Gough SC, Clayton DG, Todd JA: Haplotype tagging for the identification of common disease genes. Nat Genet 2001;29:233-237.