Association of G72/G30 with schizophrenia in the Chinese population

Biochemical and Biophysical Research Communications

Volumn 319, Issue 4, 2004, Pages 1281-1286

  Wang, Xiaoyan ^a,b   He, Guang ^b   Gu, Niufan ^c   Yang, Jiandong ^a,b   Tang, Junxia ^a,b   Chen, Qi ^b   Liu, Xinmin ^b   Shen, Yifeng ^c   Qian, Xueqing ^a,b   Lin, Wei ^b   Duan, Yun ^a,b   Feng, Guoyin ^c   He, Lin ^a,b  

^a Shanghai Jiao Tong University Affiliated Sixth People s Hospital   (China)

^b SHANGHAI JIAO TONG UNIVERSITY   (China)

^c SHANGHAI MENTAL HEALTH CENTER   (China)

Author keywords

Association; Genetics; Haplotype; Schizophrenia

Indexed keywords

COMPLEMENTARY DNA;

ADULT; ALLELE; ARTICLE; CHINESE; CONTROLLED STUDY; DISEASE ASSOCIATION; DNA SEQUENCE; FEMALE; G30 GENE; G72 GENE; GENE; GENE LOCUS; GENETIC ASSOCIATION; GENETIC MARKER; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; POPULATION; POPULATION RESEARCH; PRIORITY JOURNAL; SCHIZOPHRENIA; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL SIGNIFICANCE;

ADULT; ALLELES; CARRIER PROTEINS; CHINA; FEMALE; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HAPLOTYPES; HUMANS; MALE; MIDDLE AGED; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEINS; SCHIZOPHRENIA;

EID: 2942521644     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbrc.2004.05.119     Document Type: Article

References (25)

1. Harrison P.J., Owen M.J. Genes for schizophrenia? Recent findings and their pathophysiological implications. Lancet. 361:2003;417-419
2. Lin M.W., Curtis D., Williams N., Arranz M., Nanko S., Collier D., McGuffin P., Murray R., Owen M., Gill M. Suggestive evidence for linkage of schizophrenia to markers on chromosome 13q14.1-q32. Psychiatr. Genet. 5:1995;117-126
3. Blouin J.L., Dombroski B.A., Nath S.K., Lasseter V.K., Wolyniec P.S., Nestadt G., Thornquist M., Ullrich G., McGrath J., Kasch L., Lamacz M., Thomas M.G., Gehrig C., Radhakrishna U., Snyder S.E., Balk K.G., Neufeld K., Swartz K.L., DeMarchi N., Papadimitriou G.N., Dikeos D.G., Stefanis C.N., Chakravarti A., Childs B., Pulver A.E. Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21. Nat. Genet. 20:1998;70-73
4. Shaw S.H., Kelly M., Smith A.B., Shields G., Hopkins P.J., Loftus J., Laval S.H., Vita A., De Hert M., Cardon L.R., Crow T.J., Sherrington R., DeLisi L.E. A genome-wide search for schizophrenia susceptibility genes. Am. J. Med. Genet. 81:1998;364-376
5. Brzustowicz L.M., Honer W.G., Chow E.W., Little D., Hogan J., Hodgkinson K., Bassett A.S. Linkage of familial schizophrenia to chromosome 13q32. Am. J. Hum. Genet. 65:1999;1096-1103
6. Levinson D.F., Holmans P., Straub R.E., Owen M.J., Wildenauer D.B., Gejman P.V., Pulver A.E., Laurent C., Kendler K.S., Walsh D., Norton N., Williams N.M., Schwab S.G., Lerer B., Mowry B.J., Sanders A.R., Antonarakis S.E., Blouin J.L., DeLeuze J.F., Mallet J. Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III. Am. J. Hum. Genet. 67:2000;652-663
7. Chumakov I., Blumenfeld M., Guerassimenko O., Cavarec L., Palicio M., Abderrahim H., Bougueleret L., Barry C., Tanaka H., La Rosa P., Puech A., Tahri N., Cohen-Akenine A., Delabrosse S., Lissarrague S., Picard F.P., Maurice K., Essioux L., Millasseau P., Grel P., Debailleul V., Simon A.M., Caterina D., Dufaure I., Malekzadeh K., Belova M., Luan J.J., Bouillot M., Sambucy J.L., Primas G., Saumier M., Boubkiri N., Martin-Saumier S., Nasroune M., Peixoto H., Delaye A., Pinchot V., Bastucci M., Guillou S., Chevillon M., Sainz-Fuertes R., Meguenni S., Aurich-Costa J., Cherif D., Gimalac A., Van Duijn C., Gauvreau D., Ouellette G., Fortier I., Raelson J., Sherbatich T., Riazanskaia N., Rogaev E., Raeymaekers P., Aerssens J., Konings F., Luyten W., Macciardi F., Sham P.C., Straub R.E., Weinberger D.R., Cohen N., Cohen D., Ouelette G., Realson J. Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia. Proc. Natl. Acad. Sci. USA. 99:2002;13675-13680
8. Tsai G., Coyle J.T. Glutamatergic mechanisms in schizophrenia. Annu. Rev.Pharmacol. Toxicol. 42:2002;165-179
9. Hattori E., Liu C., Badner J.A., Bonner T.I., Christian S.L., Maheshwari M., Detera-Wadleigh S.D., Gibbs R.A., Gershon E.S. Polymorphisms at the G72/G30 gene locus, on 13q33, are associated with bipolar disorder in two independent pedigree series. Am. J. Hum. Genet. 72:2003;1131-1140
10. American Psychiatric Association Diagnostic and statistical manual of mental disorders, DSM-III-R, third ed. rev., American Psychiatric Press, Washington, DC, 1987
11. Greenwood T.A., Alexander M., Keck P.E., McElroy S., Sadovnick A.D., Remick R.A., Kelsoe J.R. Evidence for linkage disequilibrium between the dopamine transporter and bipolar disorder. Am. J. Med. Genet. 105:2001;145-151
12. Ye S., Dhillon S., Ke X., Collins A.R., Day I.N. An efficient procedure for genotyping single nucleotide polymorphisms. Nucleic Acids Res. 29:2001;E88
13. Germer S., Holland M.J., Higuchi R. High-throughput SNP allele-frequency determination in pooled DNA samples by kinetic PCR. Genome Res. 10:2000;258-266
14. Tang J.X., Zhou J., Fan J.B., Li X.W., Shi Y.Y., Gu N.F., Feng G.Y., Xing Y.L., Shi J.G., He L. Family-based association study of DTNBP1 in 6p22.3 and schizophrenia. Mol. Psychiatry. 8:2003;717-718
15. Sham P.C., Curtis D. Monte Carlo tests for associations between disease and alleles at highly polymorphic loci. Ann. Hum. Genet. 59(Pt 1):1995;97-105
16. Zhao J.H., Sham P.C. Faster haplotype frequency estimation using unrelated subjects. Hum. Hered. 53:2002;36-41
17. Zhao J.H., Curtis D., Sham P.C. Model-free analysis and permutation tests for allelic associations. Hum. Hered. 50:2000;133-139
18. Stephens M., Smith N.J., Donnelly P. A new statistical method for haplotype reconstruction from population data. Am. J. Hum. Genet. 68:2001;978-989
19. Lewontin R.C. The interaction of selection and linkage. II. Optimum models. Genetics. 50:1964;757-782
20. ′ measure of overall gametic disequilibrium between multiallelic loci. Ann. Hum. Genet. 65:2001;395-406
21. Erdfelder E., Faul F., Buchner A. G*Power: a general power analysis program. Behav. Res. Methods. Instrum. Comput. 28:1996;1-11
22. Cohen J. Statistical power analysis for the behavioral sciences. second ed. 1988;Lawrence Erlbaum Association, Hillsdale, NJ
23. McPeek M.S., Strahs A. Assessment of linkage disequilibrium by the decay of haplotype sharing, with application to fine-scale genetics mapping. Am. J. Hum. Genet. 65:1999;858-875
24. ′ end of the Neuregulin 1 gene are genetically associated with schizophrenia in the Chinese population Mol. Psychiatry. 9:2004;11-12
25. Zhao X., Shi Y., Tang J., Tang R., Yu L., Gu N., Feng G., Zhu S., Liu H., Xing Y., Zhao S., Sang H., Guan Y., St Clair D., He L. A case control and family based association study of the neuregulin1 gene and schizophrenia. J. Med. Genet. 41:2004;31-34