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31 results
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Meiotic breakpoint mapping of a proposed X linked visual loss susceptibility locus in Leber's hereditary optic neuropathy.
Handoko HY, Wirapati PJ, Sudoyo HA, Sitepu M, Marzuki S. Handoko HY, et al. J Med Genet. 1998 Aug;35(8):668-71. doi: 10.1136/jmg.35.8.668. J Med Genet. 1998. PMID: 9719375 Free PMC article.
Genome-wide scan in 124 Indonesian sib-pair families with schizophrenia reveals genome-wide significant linkage to a locus on chromosome 3p26-21.
Irmansyah, Schwab SG; Heriani, Handoko HY, Kusumawardhani A, Widyawati I, Amir N, Nasrun MW, Holmans P, Knapp M, Wildenauer DB. Irmansyah, et al. Among authors: handoko hy. Am J Med Genet B Neuropsychiatr Genet. 2008 Oct 5;147B(7):1245-52. doi: 10.1002/ajmg.b.30763. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18449910
Length variations in the COII-tRNA(Lys) intergenic region of mitochondrial DNA in Indonesian populations.
Handoko HY, Lum JK, Gustiani, Rismalia, Kartapradja H, Sofro AS, Marzuki S. Handoko HY, et al. Hum Biol. 2001 Apr;73(2):205-23. doi: 10.1353/hub.2001.0018. Hum Biol. 2001. PMID: 11446425
Tumor necrosis factor haplotype analysis amongst schizophrenia probands from four distinct populations in the Asia-Pacific region.
Handoko HY, Nancarrow DJ, Hayward NK, Ohaeri JU, Aghanwa H, McGrath JJ, Levinson DF, Johns C, Walters MK, Nertney DA, Srinivasan TN, Thara R, Mowry BJ. Handoko HY, et al. Am J Med Genet B Neuropsychiatr Genet. 2003 Aug 15;121B(1):1-6. doi: 10.1002/ajmg.b.20059. Am J Med Genet B Neuropsychiatr Genet. 2003. PMID: 12898567
Association study of the dystrobrevin-binding gene with schizophrenia in Australian and Indian samples.
Holliday EG, Handoko HY, James MR, McGrath JJ, Nertney DA, Tirupati S, Thara R, Levinson DF, Hayward NK, Mowry BJ, Nyholt DR. Holliday EG, et al. Among authors: handoko hy. Twin Res Hum Genet. 2006 Aug;9(4):531-9. doi: 10.1375/183242706778025035. Twin Res Hum Genet. 2006. PMID: 16899160
Association study of candidate variants of COMT with neuroticism, anxiety and depression.
Wray NR, James MR, Dumenil T, Handoko HY, Lind PA, Montgomery GW, Martin NG. Wray NR, et al. Among authors: handoko hy. Am J Med Genet B Neuropsychiatr Genet. 2008 Oct 5;147B(7):1314-8. doi: 10.1002/ajmg.b.30744. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18384078
Identification of the semaphorin receptor PLXNA2 as a candidate for susceptibility to schizophrenia.
Mah S, Nelson MR, Delisi LE, Reneland RH, Markward N, James MR, Nyholt DR, Hayward N, Handoko H, Mowry B, Kammerer S, Braun A. Mah S, et al. Mol Psychiatry. 2006 May;11(5):471-8. doi: 10.1038/sj.mp.4001785. Mol Psychiatry. 2006. PMID: 16402134
Association study of candidate variants from brain-derived neurotrophic factor and dystrobrevin-binding protein 1 with neuroticism, anxiety, and depression.
Wray NR, James MR, Handoko HY, Dumenil T, Lind PA, Montgomery GW, Martin NG. Wray NR, et al. Among authors: handoko hy. Psychiatr Genet. 2008 Oct;18(5):219-25. doi: 10.1097/YPG.0b013e3283050aee. Psychiatr Genet. 2008. PMID: 18797396
Separate and interacting effects within the catechol-O-methyltransferase (COMT) are associated with schizophrenia.
Handoko HY, Nyholt DR, Hayward NK, Nertney DA, Hannah DE, Windus LC, McCormack CM, Smith HJ, Filippich C, James MR, Mowry BJ. Handoko HY, et al. Mol Psychiatry. 2005 Jun;10(6):589-97. doi: 10.1038/sj.mp.4001606. Mol Psychiatry. 2005. PMID: 15505638 Clinical Trial.
Association of PIP5K2A with schizophrenia: a study in an indonesian family sample.
Saggers-Gray L, Heriani H, Handoko HY, Irmansyah I, Kusumawardhani AA, Widyawati I, Amir N, Nasrun MW, Schwab SG, Wildenauer DB. Saggers-Gray L, et al. Among authors: handoko hy. Am J Med Genet B Neuropsychiatr Genet. 2008 Oct 5;147B(7):1310-3. doi: 10.1002/ajmg.b.30736. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18314871
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