Zabetian CP - Search Results

1

Human genetics of plasma dopamine beta-hydroxylase activity: applications to research in psychiatry and neurology.

Cubells JF, Zabetian CP. Cubells JF, et al. Among authors: zabetian cp. Psychopharmacology (Berl). 2004 Aug;174(4):463-76. doi: 10.1007/s00213-004-1840-8. Epub 2004 Apr 16. Psychopharmacology (Berl). 2004. PMID: 15088079 Review.

2

Genotype-controlled analysis of plasma dopamine beta-hydroxylase activity in psychotic unipolar major depression.

Cubells JF, Price LH, Meyers BS, Anderson GM, Zabetian CP, Alexopoulos GS, Nelson JC, Sanacora G, Kirwin P, Carpenter L, Malison RT, Gelernter J. Cubells JF, et al. Among authors: zabetian cp. Biol Psychiatry. 2002 Mar 1;51(5):358-64. doi: 10.1016/s0006-3223(01)01349-x. Biol Psychiatry. 2002. PMID: 11904129

3

A genotype-controlled analysis of plasma dopamine beta-hydroxylase in healthy and alcoholic subjects: evidence for alcohol-related differences in noradrenergic function.

Köhnke MD, Zabetian CP, Anderson GM, Kolb W, Gaertner I, Buchkremer G, Vonthein R, Schick S, Lutz U, Köhnke AM, Cubells JF. Köhnke MD, et al. Among authors: zabetian cp. Biol Psychiatry. 2002 Dec 15;52(12):1151-8. doi: 10.1016/s0006-3223(02)01427-0. Biol Psychiatry. 2002. PMID: 12488060

4

The structure of linkage disequilibrium at the DBH locus strongly influences the magnitude of association between diallelic markers and plasma dopamine beta-hydroxylase activity.

Zabetian CP, Buxbaum SG, Elston RC, Köhnke MD, Anderson GM, Gelernter J, Cubells JF. Zabetian CP, et al. Am J Hum Genet. 2003 Jun;72(6):1389-400. doi: 10.1086/375499. Epub 2003 Apr 30. Am J Hum Genet. 2003. PMID: 12730829 Free PMC article.

5

Haplotype-controlled analysis of the association of a non-synonymous single nucleotide polymorphism at DBH (+ 1603C --> T) with plasma dopamine beta-hydroxylase activity.

Tang Y, Anderson GM, Zabetian CP, Köhnke MD, Cubells JF. Tang Y, et al. Among authors: zabetian cp. Am J Med Genet B Neuropsychiatr Genet. 2005 Nov 5;139B(1):88-90. doi: 10.1002/ajmg.b.30220. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 16152569

6

A single nucleotide polymorphism at DBH, possibly associated with attention-deficit/hyperactivity disorder, associates with lower plasma dopamine beta-hydroxylase activity and is in linkage disequilibrium with two putative functional single nucleotide polymorphisms.

Tang Y, Buxbaum SG, Waldman I, Anderson GM, Zabetian CP, Köhnke MD, Cubells JF. Tang Y, et al. Among authors: zabetian cp. Biol Psychiatry. 2006 Nov 15;60(10):1034-8. doi: 10.1016/j.biopsych.2006.02.017. Epub 2006 Apr 17. Biol Psychiatry. 2006. PMID: 16616730

7

Genotypic and haplotypic associations of the DBH gene with plasma dopamine beta-hydroxylase activity in African Americans.

Tang YL, Epstein MP, Anderson GM, Zabetian CP, Cubells JF. Tang YL, et al. Among authors: zabetian cp. Eur J Hum Genet. 2007 Aug;15(8):878-83. doi: 10.1038/sj.ejhg.5201838. Epub 2007 Apr 25. Eur J Hum Genet. 2007. PMID: 17457369

8

A quantitative-trait analysis of human plasma-dopamine beta-hydroxylase activity: evidence for a major functional polymorphism at the DBH locus.

Zabetian CP, Anderson GM, Buxbaum SG, Elston RC, Ichinose H, Nagatsu T, Kim KS, Kim CH, Malison RT, Gelernter J, Cubells JF. Zabetian CP, et al. Am J Hum Genet. 2001 Feb;68(2):515-22. doi: 10.1086/318198. Epub 2001 Jan 19. Am J Hum Genet. 2001. PMID: 11170900 Free PMC article.

9

Mutations in the dopamine beta-hydroxylase gene are associated with human norepinephrine deficiency.

Kim CH, Zabetian CP, Cubells JF, Cho S, Biaggioni I, Cohen BM, Robertson D, Kim KS. Kim CH, et al. Among authors: zabetian cp. Am J Med Genet. 2002 Mar 1;108(2):140-7. Am J Med Genet. 2002. PMID: 11857564

10

Variations in the dopamine beta-hydroxylase gene are not associated with the autonomic disorders, pure autonomic failure, or multiple system atrophy.

Cho S, Kim CH, Cubells JF, Zabetian CP, Hwang DY, Kim JW, Cohen BM, Biaggioni I, Robertson D, Kim KS. Cho S, et al. Among authors: zabetian cp. Am J Med Genet A. 2003 Jul 15;120A(2):234-6. doi: 10.1002/ajmg.a.20194. Am J Med Genet A. 2003. PMID: 12833405

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