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Volumn 37, Issue 1, 2012, Pages 46-52

Parent-of-origin effects of FAS and PDLIM1 in attention-deficit/hyperactivity disorder

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; ATTENTION DEFICIT DISORDER; FAS GENE; FATHER; GENE; GENE FREQUENCY; GENE MAPPING; GENE MUTATION; GENE REPLICATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HUMAN; MOTHER; NUCLEOTIDE SEQUENCE; PDLIM1 GENE; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 84255168909     PISSN: 11804882     EISSN: 14882434     Source Type: Journal    
DOI: 10.1503/jpn.100173     Document Type: Article
Times cited : (18)

References (43)
  • 1
    • 0033038226 scopus 로고    scopus 로고
    • Genetic basis of attention deficit and hyperactivity
    • Thapar A, Holmes J, Poulton K, et al. Genetic basis of attention deficit and hyperactivity. Br J Psychiatry 1999;174:105-11.
    • (1999) Br J Psychiatry , vol.174 , pp. 105-111
    • Thapar, A.1    Holmes, J.2    Poulton, K.3
  • 2
    • 20444412281 scopus 로고    scopus 로고
    • Molecular genetics of attention-deficit/hyperactivity disorder
    • Faraone SV, Perlis RH, Doyle AE, et al. Molecular genetics of attention-deficit/hyperactivity disorder. Biol Psychiatry 2005;57: 1313-23.
    • (2005) Biol Psychiatry , vol.57 , pp. 1313-1323
    • Faraone, S.V.1    Perlis, R.H.2    Doyle, A.E.3
  • 3
    • 70350223638 scopus 로고    scopus 로고
    • Genetics of attention-deficit hyperactivity disorder (ADHD)
    • Sharp SI, McQuillin A, Gurling HM. Genetics of attention-deficit hyperactivity disorder (ADHD). Neuropharmacology 2009;57:590-600.
    • (2009) Neuropharmacology , vol.57 , pp. 590-600
    • Sharp, S.I.1    McQuillin, A.2    Gurling, H.M.3
  • 4
    • 70350140352 scopus 로고    scopus 로고
    • The genetics of attention-deficit/ hyperactivity disorder
    • Coghill D, Banaschewski T. The genetics of attention-deficit/ hyperactivity disorder. Expert Rev Neurother 2009;9:1547-65.
    • (2009) Expert Rev Neurother , vol.9 , pp. 1547-1565
    • Coghill, D.1    Banaschewski, T.2
  • 5
    • 77950859536 scopus 로고    scopus 로고
    • Molecular genetics of attention-deficit/hyperactivity disorder: An overview
    • Banaschewski T, Becker K, Scherag S, et al. Molecular genetics of attention-deficit/hyperactivity disorder: an overview. Eur Child Adolesc Psychiatry 2010;19:237-57.
    • (2010) Eur Child Adolesc Psychiatry , vol.19 , pp. 237-257
    • Banaschewski, T.1    Becker, K.2    Scherag, S.3
  • 6
    • 28144455908 scopus 로고    scopus 로고
    • Preferential transmission of paternal alleles at risk genes in attention-deficit/hyperactivity disorder
    • Hawi Z, Segurado R, Conroy J, et al. Preferential transmission of paternal alleles at risk genes in attention-deficit/hyperactivity disorder. Am J Hum Genet 2005;77:958-65.
    • (2005) Am J Hum Genet , vol.77 , pp. 958-965
    • Hawi, Z.1    Segurado, R.2    Conroy, J.3
  • 7
    • 27144502791 scopus 로고    scopus 로고
    • Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD
    • Kent L, Green E, Hawi Z, et al. Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD. Mol Psychiatry 2005;10:939-43.
    • (2005) Mol Psychiatry , vol.10 , pp. 939-943
    • Kent, L.1    Green, E.2    Hawi, Z.3
  • 8
    • 73949144020 scopus 로고    scopus 로고
    • ADHD and DAT1: Further evidence of paternal over-transmission of risk alleles and haplotype
    • Hawi Z, Kent L, Hill M, et al. ADHD and DAT1: further evidence of paternal over-transmission of risk alleles and haplotype. Am J Med Genet B Neuropsychiatr Genet 2010;153B:97-102.
    • (2010) Am J Med Genet B Neuropsychiatr Genet , vol.153 B , pp. 97-102
    • Hawi, Z.1    Kent, L.2    Hill, M.3
  • 9
    • 0034989797 scopus 로고    scopus 로고
    • Dopa decarboxylase gene polymorphisms and attention deficit hyperactivity disorder (ADHD): No evidence for association in the Irish population
    • Hawi Z, Foley D, Kirley A, et al. Dopa decarboxylase gene polymorphisms and attention deficit hyperactivity disorder (ADHD): no evidence for association in the Irish population. Mol Psychiatry 2001; 6:420-4.
    • (2001) Mol Psychiatry , vol.6 , pp. 420-424
    • Hawi, Z.1    Foley, D.2    Kirley, A.3
  • 10
    • 57349170939 scopus 로고    scopus 로고
    • Parent of origin effects in attention/deficit hyperactivity disorder (ADHD): Analysis of data from the international multicenter ADHD genetics (IMAGE) program
    • Anney RJ, Hawi Z, Sheehan K, et al. Parent of origin effects in attention/deficit hyperactivity disorder (ADHD): analysis of data from the international multicenter ADHD genetics (IMAGE) program. Am J Med Genet B Neuropsychiatr Genet 2008;147B:1495-500.
    • (2008) Am J Med Genet B Neuropsychiatr Genet , vol.147 B , pp. 1495-1500
    • Anney, R.J.1    Hawi, Z.2    Sheehan, K.3
  • 11
    • 35848936058 scopus 로고    scopus 로고
    • Investigation of the G protein subunit Galphaolf gene (GNAL) in attention deficit/ hyperactivity disorder
    • Laurin N, Ickowicz A, Pathare T, et al. Investigation of the G protein subunit Galphaolf gene (GNAL) in attention deficit/ hyperactivity disorder. J Psychiatr Res 2008;42:117-24.
    • (2008) J Psychiatr Res , vol.42 , pp. 117-124
    • Laurin, N.1    Ickowicz, A.2    Pathare, T.3
  • 12
    • 0036364966 scopus 로고    scopus 로고
    • Serotonergic system and attention deficit hyperactivity disorder (ADHD): A potential susceptibility locus at the 5-HT(1B) receptor gene in 273 nuclear families from a multi-centre sample
    • Hawi Z, Dring M, Kirley A, et al. Serotonergic system and attention deficit hyperactivity disorder (ADHD): a potential susceptibility locus at the 5-HT(1B) receptor gene in 273 nuclear families from a multi-centre sample. Mol Psychiatry 2002;7:718-25.
    • (2002) Mol Psychiatry , vol.7 , pp. 718-725
    • Hawi, Z.1    Dring, M.2    Kirley, A.3
  • 13
    • 33745028902 scopus 로고    scopus 로고
    • A family-based study of Indian subjects from Kolkata reveals allelic association of the serotonin transporter intron-2 (STin2) polymorphism and attention-deficithyperactivity disorder (ADHD)
    • Banerjee E, Sinha S, Chatterjee A, et al. A family-based study of Indian subjects from Kolkata reveals allelic association of the serotonin transporter intron-2 (STin2) polymorphism and attention-deficithyperactivity disorder (ADHD). Am J Med Genet B Neuropsychiatr Genet 2006;141B:361-6.
    • (2006) Am J Med Genet B Neuropsychiatr Genet , vol.141 B , pp. 361-366
    • Banerjee, E.1    Sinha, S.2    Chatterjee, A.3
  • 14
    • 4243158485 scopus 로고    scopus 로고
    • Haplotype analysis of SNAP-25 suggests a role in the aetiology of ADHD
    • Mill J, Richards S, Knight J, et al. Haplotype analysis of SNAP-25 suggests a role in the aetiology of ADHD. Mol Psychiatry 2004; 9: 801-10.
    • (2004) Mol Psychiatry , vol.9 , pp. 801-810
    • Mill, J.1    Richards, S.2    Knight, J.3
  • 16
    • 33847331198 scopus 로고    scopus 로고
    • No preferential transmission of paternal alleles at risk genes in attention-deficit hyperactivity disorder
    • Laurin N, Feng Y, Ickowicz A, et al. No preferential transmission of paternal alleles at risk genes in attention-deficit hyperactivity disorder. Mol Psychiatry 2007;12:226-9.
    • (2007) Mol Psychiatry , vol.12 , pp. 226-229
    • Laurin, N.1    Feng, Y.2    Ickowicz, A.3
  • 17
    • 84969213492 scopus 로고    scopus 로고
    • Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
    • Wellcome Trust Case Control Consortium
    • Wellcome Trust Case Control Consortium. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 2007;447:661-78.
    • (2007) Nature , vol.447 , pp. 661-678
  • 18
    • 67651113905 scopus 로고    scopus 로고
    • Genome-wide association studies in ADHD
    • Franke B, Neale BM, Faraone SV. Genome-wide association studies in ADHD. Hum Genet 2009;126:13-50.
    • (2009) Hum Genet , vol.126 , pp. 13-50
    • Franke, B.1    Neale, B.M.2    Faraone, S.V.3
  • 19
    • 57349166006 scopus 로고    scopus 로고
    • Genome-wide association scan of attention deficit hyperactivity disorder
    • Neale BM, Lasky-Su J, Anney R, et al. Genome-wide association scan of attention deficit hyperactivity disorder. Am J Med Genet B Neuropsychiatr Genet 2008;147B:1337-44.
    • (2008) Am J Med Genet B Neuropsychiatr Genet , vol.147 B , pp. 1337-1344
    • Neale, B.M.1    Lasky-Su, J.2    Anney, R.3
  • 20
    • 84870465485 scopus 로고
    • American Psychiatric Association, 4th ed. Washington: The Association
    • American Psychiatric Association. Diagnostic and statistical manual of mental disorders. 4th ed. Washington: The Association; 1994.
    • (1994) Diagnostic and Statistical Manual of Mental Disorders
  • 21
    • 34548292504 scopus 로고    scopus 로고
    • PLINK: A tool set for whole-genome association and population-based linkage analyses
    • Purcell S, Neale B, Todd-Brown K, et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 2007;81:559-75.
    • (2007) Am J Hum Genet , vol.81 , pp. 559-575
    • Purcell, S.1    Neale, B.2    Todd-Brown, K.3
  • 22
    • 0027377799 scopus 로고
    • Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM)
    • Spielman RS, McGinnis RE, Ewens WJ. Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM). Am J Hum Genet 1993;52:506-16.
    • (1993) Am J Hum Genet , vol.52 , pp. 506-516
    • Spielman, R.S.1    McGinnis, R.E.2    Ewens, W.J.3
  • 23
    • 13444269543 scopus 로고    scopus 로고
    • Haploview: Analysis and visualization of LD and haplotype maps
    • Barrett JC, Fry B, Maller J, et al. Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics 2005;21:263-5.
    • (2005) Bioinformatics , vol.21 , pp. 263-265
    • Barrett, J.C.1    Fry, B.2    Maller, J.3
  • 24
    • 0041857847 scopus 로고    scopus 로고
    • Pedigree disequilibrium tests for multilocus haplotypes
    • Dudbridge F. Pedigree disequilibrium tests for multilocus haplotypes. Genet Epidemiol 2003;25:115-21.
    • (2003) Genet Epidemiol , vol.25 , pp. 115-121
    • Dudbridge, F.1
  • 25
    • 41849094449 scopus 로고    scopus 로고
    • HLA-DQ and susceptibility to celiac disease: Evidence for gender differences and parent-oforigin effects
    • Megiorni F, Mora B, Bonamico M, et al. HLA-DQ and susceptibility to celiac disease: evidence for gender differences and parent-oforigin effects. Am J Gastroenterol 2008;103:997-1003.
    • (2008) Am J Gastroenterol , vol.103 , pp. 997-1003
    • Megiorni, F.1    Mora, B.2    Bonamico, M.3
  • 26
    • 0036228660 scopus 로고    scopus 로고
    • The transmission disequilibrium test suggests that HLA-DR4 and DR13 are linked to autism spectrum disorder
    • Torres AR, Maciulis A, Stubbs EG, et al. The transmission disequilibrium test suggests that HLA-DR4 and DR13 are linked to autism spectrum disorder. Hum Immunol 2002;63:311-6.
    • (2002) Hum Immunol , vol.63 , pp. 311-316
    • Torres, A.R.1    Maciulis, A.2    Stubbs, E.G.3
  • 27
    • 20144388362 scopus 로고    scopus 로고
    • A high-resolution linkagedisequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms
    • Miretti MM, Walsh EC, Ke X, et al. A high-resolution linkagedisequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms. Am J Hum Genet 2005;76:634-46.
    • (2005) Am J Hum Genet , vol.76 , pp. 634-646
    • Miretti, M.M.1    Walsh, E.C.2    Ke, X.3
  • 28
    • 33750444938 scopus 로고    scopus 로고
    • Polymorphisms of fas gene: Relationship with Alzheimer's disease and cognitive decline
    • Chiappelli M, Nasi M, Cossarizza A, et al. Polymorphisms of fas gene: relationship with Alzheimer's disease and cognitive decline. Dement Geriatr Cogn Disord 2006;22:296-300.
    • (2006) Dement Geriatr Cogn Disord , vol.22 , pp. 296-300
    • Chiappelli, M.1    Nasi, M.2    Cossarizza, A.3
  • 29
    • 77949338415 scopus 로고    scopus 로고
    • The FAS gene, brain volume, and disease progression in Alzheimer's disease
    • Erten-Lyons D, Jacobson A, Kramer P, et al. The FAS gene, brain volume, and disease progression in Alzheimer's disease. Alzheimers Dement 2010;6:118-24.
    • (2010) Alzheimers Dement , vol.6 , pp. 118-124
    • Erten-Lyons, D.1    Jacobson, A.2    Kramer, P.3
  • 30
    • 34447650841 scopus 로고    scopus 로고
    • Fas antigen and sporadic Alzheimer's disease in Southern Italy: Evaluation of two polymorphisms in the TNFRSF6 gene
    • Andreoli V, Nicoletti G, Romeo N, et al. Fas antigen and sporadic Alzheimer's disease in Southern Italy: evaluation of two polymorphisms in the TNFRSF6 gene. Neurochem Res 2007;32:1445-9.
    • (2007) Neurochem Res , vol.32 , pp. 1445-1449
    • Andreoli, V.1    Nicoletti, G.2    Romeo, N.3
  • 31
    • 29244448999 scopus 로고    scopus 로고
    • A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease
    • Grupe A, Li Y, Rowland C, et al. A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease. Am J Hum Genet 2006;78:78-88.
    • (2006) Am J Hum Genet , vol.78 , pp. 78-88
    • Grupe, A.1    Li, Y.2    Rowland, C.3
  • 32
    • 70350568168 scopus 로고    scopus 로고
    • Transcriptomic and genetic studies identify IL-33 as a candidate gene for Alzheimer's disease
    • Chapuis J, Hot D, Hansmannel F, et al. Transcriptomic and genetic studies identify IL-33 as a candidate gene for Alzheimer's disease. Mol Psychiatry 2009;14:1004-16.
    • (2009) Mol Psychiatry , vol.14 , pp. 1004-1016
    • Chapuis, J.1    Hot, D.2    Hansmannel, F.3
  • 33
    • 70349915913 scopus 로고    scopus 로고
    • Characterization of CLP36/ Elfin/ PDLIM1 in the nervous system
    • Ohno K, Kato H, Funahashi S, et al. Characterization of CLP36/ Elfin/ PDLIM1 in the nervous system. J Neurochem 2009; 111:790-800.
    • (2009) J Neurochem , vol.111 , pp. 790-800
    • Ohno, K.1    Kato, H.2    Funahashi, S.3
  • 34
    • 35248822612 scopus 로고    scopus 로고
    • Association of the trace amine associated receptor 6 (TAAR6) gene with schizophrenia and bipolar disorder in a Korean case control sample
    • Pae CU, Yu HS, Amann D, et al. Association of the trace amine associated receptor 6 (TAAR6) gene with schizophrenia and bipolar disorder in a Korean case control sample. J Psychiatr Res 2008;42:35-40.
    • (2008) J Psychiatr Res , vol.42 , pp. 35-40
    • Pae, C.U.1    Yu, H.S.2    Amann, D.3
  • 35
    • 34548303922 scopus 로고    scopus 로고
    • A region of 35 kb containing the trace amine associate receptor 6 (TAAR6) gene is associated with schizophrenia in the Irish study of high-density schizophrenia families
    • Vladimirov V, Thiselton DL, Kuo PH, et al. A region of 35 kb containing the trace amine associate receptor 6 (TAAR6) gene is associated with schizophrenia in the Irish study of high-density schizophrenia families. Mol Psychiatry 2007;12:842-53.
    • (2007) Mol Psychiatry , vol.12 , pp. 842-853
    • Vladimirov, V.1    Thiselton, D.L.2    Kuo, P.H.3
  • 36
    • 34147144860 scopus 로고    scopus 로고
    • Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease
    • Wang L, Hauser ER, Shah SH, et al. Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease. Am J Hum Genet 2007;80:650-63.
    • (2007) Am J Hum Genet , vol.80 , pp. 650-663
    • Wang, L.1    Hauser, E.R.2    Shah, S.H.3
  • 37
    • 70350537083 scopus 로고    scopus 로고
    • Validation study of genetic associations with coronary artery disease on chromosome 3q13-21 and potential effect modification by smoking
    • Horne BD, Hauser ER, Wang L, et al. Validation study of genetic associations with coronary artery disease on chromosome 3q13-21 and potential effect modification by smoking. Ann Hum Genet 2009; 73:551-8.
    • (2009) Ann Hum Genet , vol.73 , pp. 551-558
    • Horne, B.D.1    Hauser, E.R.2    Wang, L.3
  • 38
    • 71349088574 scopus 로고    scopus 로고
    • Modifier gene study of meconium ileus in cystic fibrosis: Statistical considerations and gene mapping results
    • Aug. 7. [Epub ahead of print]
    • Dorfman R, Li W, Sun L, et al. Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping results. Hum Genet 2009 Aug. 7. [Epub ahead of print].
    • (2009) Hum Genet
    • Dorfman, R.1    Li, W.2    Sun, L.3
  • 40
    • 84857503883 scopus 로고    scopus 로고
    • Jirtle Laboratory at Duke University, Available, accessed 2011 June 3
    • Jirtle Laboratory at Duke University. In: Geneimprint. Available: www.geneimprint.com (accessed 2011 June 3).
    • Geneimprint
  • 41
    • 33645533945 scopus 로고    scopus 로고
    • The biology of human sex differences
    • Federman DD. The biology of human sex differences. N Engl J Med 2006;354:1507-14.
    • (2006) N Engl J Med , vol.354 , pp. 1507-1514
    • Federman, D.D.1
  • 42
    • 4344708984 scopus 로고    scopus 로고
    • The parent-oforigin effect of 10q22 in pre-eclamptic females coincides with two regions clustered for genes with down-regulated expression in androgenetic placentas
    • Oudejans CB, Mulders J, Lachmeijer AM, et al. The parent-oforigin effect of 10q22 in pre-eclamptic females coincides with two regions clustered for genes with down-regulated expression in androgenetic placentas. Mol Hum Reprod 2004;10:589-98.
    • (2004) Mol Hum Reprod , vol.10 , pp. 589-598
    • Oudejans, C.B.1    Mulders, J.2    Lachmeijer, A.M.3
  • 43
    • 0033362236 scopus 로고    scopus 로고
    • Methods for detection of parent-of-origin effects in genetic studies of case-parents triads
    • Weinberg CR. Methods for detection of parent-of-origin effects in genetic studies of case-parents triads. Am J Hum Genet 1999;65: 229-35.
    • (1999) Am J Hum Genet , vol.65 , pp. 229-235
    • Weinberg, C.R.1


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