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Volumn 18, Issue 1, 2005, Pages 31-35

Searching for a schizophrenia susceptibility gene in the 22q11 region

Author keywords

22q11; ARVCF; Schizophrenia; Single nucleotide polymorphisms (SNPs)

Indexed keywords

ADENINE NUCLEOTIDE; BASE; PYRIMIDINE NUCLEOTIDE;

EID: 17144406393     PISSN: 08953988     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (8)

References (18)
  • 1
    • 0033599714 scopus 로고    scopus 로고
    • Schizophrenia
    • Schultz, S. K. and Andreasen, N. C. (1999). Schizophrenia. Lancet 353, 1425-1430.
    • (1999) Lancet , vol.353 , pp. 1425-1430
    • Schultz, S.K.1    Andreasen, N.C.2
  • 4
    • 0028786445 scopus 로고
    • Potential linkage disequilibrium between schizophrenia and locus D22S278 on the long arm of chromosome 22
    • Moises, H. W., Yang, L., Li, T., Havsteen, B., Fimmers, R., Baur, M. P., Liu, X., and Gottesman, II. (1995). Potential linkage disequilibrium between schizophrenia and locus D22S278 on the long arm of chromosome 22. Am. J. Med. Genet. 60, 465-467.
    • (1995) Am. J. Med. Genet. , vol.60 , pp. 465-467
    • Moises, H.W.1    Yang, L.2    Li, T.3    Havsteen, B.4    Fimmers, R.5    Baur, M.P.6    Liu, X.7    Gottesman, I.I.8
  • 5
    • 0037006412 scopus 로고    scopus 로고
    • Schizophrenia and velo-cardio-facial syndrome
    • Murphy, K. C. (2002). Schizophrenia and velo-cardio-facial syndrome. Lancet 359, 426-430.
    • (2002) Lancet , vol.359 , pp. 426-430
    • Murphy, K.C.1
  • 6
    • 0032882849 scopus 로고    scopus 로고
    • High rates of schizophrenia in adults with velo-cardio-facial syndrome
    • Murphy, K. C., Jones, L. A., and Owen, M. J. (1999). High rates of schizophrenia in adults with velo-cardio-facial syndrome. Arch. Gen. Psychiatry 56, 940-945.
    • (1999) Arch. Gen. Psychiatry , vol.56 , pp. 940-945
    • Murphy, K.C.1    Jones, L.A.2    Owen, M.J.3
  • 8
    • 0033399702 scopus 로고    scopus 로고
    • Lack of evidence for association between the COMT locus and schizophrenia
    • Wei, J. and Hemmings, G. P. (1999). Lack of evidence for association between the COMT locus and schizophrenia. Psychiatr. Genet. 9, 183-186.
    • (1999) Psychiatr. Genet. , vol.9 , pp. 183-186
    • Wei, J.1    Hemmings, G.P.2
  • 9
    • 0023235253 scopus 로고
    • Haplotype relative risks: An easy reliable way to construct a proper control sample for risk calculations
    • Falk, C. T. and Rubinstein, P. (1987). Haplotype relative risks: an easy reliable way to construct a proper control sample for risk calculations. Ann. Hum. Genet. 51, 227-233.
    • (1987) Ann. Hum. Genet. , vol.51 , pp. 227-233
    • Falk, C.T.1    Rubinstein, P.2
  • 10
    • 0029858544 scopus 로고    scopus 로고
    • The TDT and other family-based test for linkage disequilibrium and association
    • Spielman, R. S. and Ewens, W. J. (1996). The TDT and other family-based test for linkage disequilibrium and association. Am. J. Hum. Genet. 59, 983-989.
    • (1996) Am. J. Hum. Genet. , vol.59 , pp. 983-989
    • Spielman, R.S.1    Ewens, W.J.2
  • 11
    • 0027377799 scopus 로고
    • Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM)
    • Spielman, R. S., McGinnis, R. E., and Ewens, W. J. (1993). Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM). Am. J. Hum. Genet. 52, 506-516.
    • (1993) Am. J. Hum. Genet. , vol.52 , pp. 506-516
    • Spielman, R.S.1    McGinnis, R.E.2    Ewens, W.J.3
  • 13
    • 0033966919 scopus 로고    scopus 로고
    • Family-based linkage disequilibrium mapping using SNP marker haplotypes: Application to a potential locus for schizophrenia at chromosome 22q11
    • Li, T., Ball, D., Zhao, J., Murray, R. M., Liu, X., Sham, P. C., and Collier, D. A. (2000). Family-based linkage disequilibrium mapping using SNP marker haplotypes: application to a potential locus for schizophrenia at chromosome 22q11. Mol. Psychiatry 5, 452.
    • (2000) Mol. Psychiatry , vol.5 , pp. 452
    • Li, T.1    Ball, D.2    Zhao, J.3    Murray, R.M.4    Liu, X.5    Sham, P.C.6    Collier, D.A.7
  • 14
    • 0035514706 scopus 로고    scopus 로고
    • Chromosomal microdeletions: Dissecting del22q11 syndrome
    • Lindsay, E. A. (2001). Chromosomal microdeletions: dissecting del22q11 syndrome. Nat. Rev. Genet. 2, 858-868.
    • (2001) Nat. Rev. Genet. , vol.2 , pp. 858-868
    • Lindsay, E.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.