| 1 | MAOA, SYP
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| Interactions between MAOA and SYP polymorphisms were associated with symptoms of attention-deficit/hyperactivity disorder in Chinese Han subjects.
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| Gao Q, Liu L, Li HM, Tang YL, Wu ZM, Chen Y, Wang YF, Qian QJ.
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| Am J Med Genet B Neuropsychiatr Genet 168B(1):45-53. doi: 10.1002/ajmg.b.32273. Epub 2014 Dec 8.
2015
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| 2 | GATA2, MAOA, SP1, TBP
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| Molecular mechanism of monoamine oxidase A gene regulation under inflammation and ischemia-like conditions: key roles of the transcription factors GATA2, Sp1 and TBP.
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| Gupta V, Khan AA, Sasi BK, Mahapatra NR.
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| J Neurochem. Jul;134(1):21-38. doi: 10.1111/jnc.13099. Epub 2015 Apr 16 2015
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| 3 | HTR6, MAOA
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| Serotonin receptor 6 mediates defective brain development in monoamine oxidase A-deficient mouse embryos.
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| Wang CC, Man GC, Chu CY, Borchert A, Ugun-Klusek A, Billett EE, Kühn H, Ufer C.
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| J Biol Chem 289(12):8252-63. doi: 10.1074/jbc.M113.522094. Epub 2014 Feb 4.
2014
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| 4 | MAOA, MAOA/BD, MAOB
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| MAOA/B deletion syndrome in male siblings with severe developmental delay and sudden loss of muscle tonus.
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| Saito M, Yamagata T, Matsumoto A, Shiba Y, Nagashima M, Taniguchi S, Jimbo E, Momoi MY.
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| Brain Dev rain Dev. 2013 Feb 13. doi:pii: S0387-7604(13)00020-X. 10.1016/j.braindev.2013.01.004. [Epub ahead of print]
2013
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| 5 | MAOA
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| Early postnatal inhibition of serotonin synthesis results in long-term reductions of perseverative behaviors, but not aggression, in MAO A-deficient mice.
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| Bortolato M, Godar SC, Tambaro S, Li FG, Devoto P, Coba MP, Chen K, Shih JC.
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| Neuropharmacology 75:223-32. doi: 10.1016/j.neuropharm.2013.07.003. Epub 2013 Jul 16.
2013
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| 6 | AGTR2, ARHGEF6, MAGT1, MAOA, NXF5, SRPX2, ZNF41, ZNF674
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| XLID-causing mutations and associated genes challenged in light of data from large-scale human exome sequencing.
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| Piton A, Redin C, Mandel JL.
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| Am J Hum Genet 93(2):368-83. doi: 10.1016/j.ajhg.2013.06.013. Epub 2013 Jul 18. Erratum in: Am J Hum Genet. 2013 Aug 8;93(2):406.
2013
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| 7 | MAOA, TIEG2
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| Mechanistic role for a novel glucocorticoid-KLF11 (TIEG2) protein pathway in stress-induced monoamine oxidase A expression.
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| Grunewald M, Johnson S, Lu D, Wang Z, Lomberk G, Albert PR, Stockmeier CA, Meyer JH, Urrutia R, Miczek KA, Austin MC, Wang J, Paul IA, Woolverton WL, Seo S, Sittman DB, Ou XM.
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| J Biol Chem 287(29):24195-206. doi: 10.1074/jbc.M112.373936. Epub 2012 May 24.
2012
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| 8 | MAOA
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| Evidence that the methylation state of the monoamine oxidase A (MAOA) gene predicts brain activity of MAO A enzyme in healthy men.
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| Shumay E, Logan J, Volkow ND, Fowler JS.
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| Epigenetics 7(10):1151-60. doi: 10.4161/epi.21976. Epub 2012 Sep 4.
2012
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| 9 | MAOA
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| Association between a functional polymorphism in the MAOA gene and sudden infant death syndrome.
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| Klintschar M, Heimbold C.
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| Pediatrics 129(3):e756-61. doi: 10.1542/peds.2011-1642. Epub 2012 Feb 20.
2012
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| 10 | DUPXPP, MAOA, MAOB, NDP
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| Duplication of MAOA, MAOB, and NDP in a patient with mental retardation and epilepsy.
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| Klitten LL, Mĝller RS, Ravn K, Hjalgrim H, Tommerup N.
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| Eur J Hum Genet 19(1):1-2. Epub 2010 Sep 1. No abstract available. PMID: 20808325 2011
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| 11 | MAOA, MAOB
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| Behavioral outcomes of monoamine oxidase deficiency: preclinical and clinical evidence.
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| Bortolato M, Shih JC.
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| Int Rev Neurobiol 100:13-42. doi: 10.1016/B978-0-12-386467-3.00002-9. Review.
2011
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| 12 | MAOA, MAOB
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| Structural properties of human monoamine oxidases A and B.
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| Binda C, Mattevi A, Edmondson DE.
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| Int Rev Neurobiol 100:1-11. doi: 10.1016/B978-0-12-386467-3.00001-7. Review.
2011
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| 13 | MAOA, MAOB
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| Transcriptional regulation and multiple functions of MAO genes.
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| Shih JC, Wu JB, Chen K.
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| J Neural Transm 118(7):979-86. doi: 10.1007/s00702-010-0562-9. Epub 2011 Feb 27. Review.
2011
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| 14 | MAOA, MAOB, PRKN
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| Parkin degrades estrogen-related receptors to limit the expression of monoamine oxidases.
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| Ren Y, Jiang H, Ma D, Nakaso K, Feng J.
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| Hum Mol Genet 20(6):1074-83. doi: 10.1093/hmg/ddq550. Epub 2010 Dec 21. 2011
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| 15 | DELXP11, MAOA, MAOA/BD, MAOB
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| Deletion of MAOA and MAOB in a male patient causes severe developmental delay, intermittent hypotonia and stereotypical hand movements.
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| Whibley A, Urquhart J, Dore J, Willatt L, Parkin G, Gaunt L, Black G, Donnai D, Raymond FL.
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| Eur J Hum Genet 18(10):1095-9. Epub 2010 May 19.PMID: 20485326 [ 2010
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| 16 | DELXP11, MAOA, MAOB, ND, NDP
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| Co-segregation of Norrie disease and idiopathic pulmonary hypertension in a family with a microdeletion of the NDP region at Xp11.3-p11.4.
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| Staropoli JF, Xin W, Sims KB.
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| J Med Genet 47(11):786-90. Epub 2010 Aug 2.PMID: 20679667 2010
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| 17 | MAOA, SLC6A3, SLC6A3
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| Association of MAOA, 5-HTT, and NET promoter polymorphisms with gene expression and protein activity in human placentas.
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| Zhang H, Smith GN, Liu X, Holden JJ.
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| Physiol Genomics 42(1):85-92. Epub 2010 Mar 23.
2010
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| 18 | MAOA, MAOB
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| Monoamine oxidases regulate telencephalic neural progenitors in late embryonic and early postnatal development.
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| Cheng A, Scott AL, Ladenheim B, Chen K, Ouyang X, Lathia JD, Mughal M, Cadet JL, Mattson MP, Shih JC.
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| J Neurosci 30(32):10752-62. doi: 10.1523/JNEUROSCI.2037-10.2010.
2010
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| 19 | MAOA, MAOB
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| Platelet monoamine oxidase activity in children with attention-deficit/hyperactivity disorder.
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| Nedic G, Pivac N, Hercigonja DK, Jovancevic M, Curkovic KD, Muck-Seler D.
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| Psychiatry Res 175(3):252-5. doi: 10.1016/j.psychres.2009.08.013.
2010
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| 20 | HTR1E, HTR2B, HTR2A, HTR1A, MAOA, HTR4, HTR6, HTR7, HTR5A
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| Genetic evaluation of the serotonergic system in chronic fatigue syndrome.
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| Smith AK, Dimulescu I, Falkenberg VR, Narasimhan S, Heim C, Vernon SD, Rajeevan MS.
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| Psychoneuroendocrinology 33(2):188-97. 2008
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| 21 | MAOA
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| The VNTR 2 repeat in MAOA and delinquent behavior in adolescence and young adulthood: associations and MAOA promoter activity.
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| Guo G, Ou XM, Roettger M, Shih JC.
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| Eur J Hum Genet 16(5):626-34. Epub 2008 Jan 23. 2008
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| 22 | MAOA, SLC6A2
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| An interaction between the norepinephrine transporter and monoamine oxidase A polymorphisms, and novelty-seeking personality traits in Korean females.
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| Lee BC, Yang JW, Lee SH, Kim SH, Joe SH, Jung IK, Choi IG, Ham BJ.
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| Prog Neuropsychopharmacol Biol Psychiatry 32(1):238-42. Epub 2007 Aug 22.
2008
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| 23 | DELXP11, EFHC2, MAOA, MAOB, ND, NDP
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| Contiguous deletion of the NDP, MAOA, MAOB, and EFHC2 genes in a patient with Norrie disease, severe psychomotor retardation and myoclonic epilepsy.
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| Rodriguez-Revenga L, Madrigal I, Alkhalidi LS, Armengol L, González E, Badenas C, Estivill X, Milà M.
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| Am J Med Genet A 143A(9):916-20.PMID: 17431911 2007
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| 24 | CDCA7, CDCA7L, MAOA
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| Monoamine oxidase A and repressor R1 are involved in apoptotic signaling pathway.
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| Ou XM, Chen K, Shih JC.
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| Proc Natl Acad Sci U S A 103(29):10923-8. Epub 2006 Jul 7. 2006
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| 25 | MAOA, MAOB
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| Association of variations in monoamine oxidases A and B with Parkinson's disease subgroups.
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| Parsian A, Racette B, Zhang ZH, Rundle M, Perlmutter JS.
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| Genomics 83(3):454-60. 2004
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| 26 | MAOA
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| Excess of high activity monoamine oxidase A gene promoter alleles in female patients with panic disorder.
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| Deckert J, et al.
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| Hum Mol Genet 8(4):621-4. 1999
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| 27 | MAOA
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| A functional polymorphism in the monoamine oxidase A gene promoter.
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| Sabol SZ, et al.
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| Hum Genet 103 : 273-279. 1998
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| 28 | MAOA, MAOB, MRIB
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| Specific genetic deficiencies of the A and B isoenzymes of monoamine oxidase are characterized by distinct neurochemical and clinical phenotypes.
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| Lenders JWM, et al.
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| J Clin Invest 97 : 1010-1019. 1996
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| 29 | MAOA
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| Genetic association between monoamine oxidase A microsatellite and RFLP alleles and bipolar affective disorder : analysis and meta-analysis.
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| Rubinsztein DC, et al.
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| Hum Mol Genet 5 : 779-782. 1996
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| 30 | MAOA
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| Mutational analysis of the human MAOA gene.
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| Tivol EA, et al.
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| Am J Med Genet 67 : 92-97. 1996
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| 31 | MAOA, MRIB
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| Aggressive behavior and altered amounts of brain serotonin and norepinephrine in mice lacking MAOA.
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| Cases O, Seif I, Grimsby J, Gaspar P, Chen K, Pournin S, Müller U, Aguet M, Babinet C, Shih JC, et al.
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| Science 268(5218):1763-6.
1995
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| 32 | MAOA, MAOB
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| Linkage analysis of the monoamine A and B genes using newly-defined polymorphisms.
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| Harris BD, et al.
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| Cytogenet Cell Genet 62 : 236-237. 1993
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| 33 | MAOA
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| Characterization of a highly polymorphic region near the first exon of the human MAOA gene containing a GT dinucleotide and a novel VNTR motif.
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| Hinds HL, et al.
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| Genomics 13 : 896-897. 1992
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| 34 | MAOA
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| Organization of the human monoamine oxidase genes and long-range physical mapping around them.
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| Chen ZY, et al.
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| Genomics 14 : 75-82. 1992
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| 35 | MAOA
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| An X chromosome inactivation assay based on differential methylation of a CpG island coupled to a VNTR polymorphism at the 5' end of the monoamine oxidase A gene.
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| Hendriks RW, et al.
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| Hum Mol Genet 1 : 187-194. 1992
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| 36 | DELXP11, MAOA, MAOB, ND, NDP
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| Clinical, biochemical, and neuropsychiatric evaluation of a patient with a contiguous gene syndrome due to a microdeletion Xp11.3 including the Norrie disease locus and monoamine oxidase (MAOA and MAOB) genes.
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| Collins FA, Murphy DL, Reiss AL, Sims KB, Lewis JG, Freund L, Karoum F, Zhu D, Maumenee IH, Antonarakis SE.
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| Am J Med Genet 42(1):127-34.PMID: 1308352 [ 1992
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| 37 | MAOA, MAOB
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| Long range physical mapping and organisation of the region including the genes for monoamine oxidase A and B, (MAOA & MAOB).
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| Chen ZY, et al.
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| (HGM11) Cytogenet Cell Genet 58 : 2059. 1991
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| 38 | DXS7, MAOA, MAOB
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| Characterisation of a 650 kb yeast artificial chromosome (YAC) containing DXS7, MAOA and MAOB loci implications for the isolation of the Norrie disease locus.
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| Chen ZY, et al.
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| (HGM11) Cytogenet Cell Genet 58 : 2060. 1991
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| 39 | MAOA
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| Dinucleotide repeat polymorphism at the MAOA locus.
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| Black GCM, et al.
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| Nucleic Acids Res 19 : 689. 1991
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| 40 | MAOA, MAOB, ND, NDP
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| Human monoamine oxidase A and B genes map to Xp11.23 and are deleted in a patient with Norrie disease.
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| Lan NC, Heinzmann C, Gal A, Klisak I, Orth U, Lai E, Grimsby J, Sparkes RS, Mohandas T, Shih JC.
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| Genomics 4 : 552-559. 1989
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| 41 | MAOA
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| Localization of human monoamine oxidase-A gene to Xp11.23-11.4 by in situ hybridization : implications for Norrie disease.
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| Levy ER, Powell JF, Buckle VJ, Hsu YP, Breakefield XO, Craig IW.
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| Genomics 5 : 368-370. 1989
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| 42 | NDP, MAOA
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| Norrie disease gene is distinct from the monoamine oxidase genes.
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| Sims KB, et al.
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| Am J Hum Genet 45 : 424-434. 1989
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| 43 | MAOA
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| MspI RFLP for human MAOA gene.
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| Ozelius L, et al.
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| Nucleic Acids Res 17 : 10516. 1989
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| 44 | MAOA, MAOB
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| cDNA cloning of human liver monoamine oxidase A and B: Molecular basis of differences in enzymatic properties.
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| Bach AWJ, et al.
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| Proc Natl Acad Sci U S A 85 : 4934-4938. 1988
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| 45 | MAOA, MAOB
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| X-linked monoamine oxidase deficiency in humans.
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| Breakefield XO, et al.
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| Am J Hum Genet 43 : A178. 1988
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| 46 | MAOA
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| Human monoamine oxidase gene (MAOA) : chromosome position (Xp21-p11) and DNA polymorphism.
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| Ozelius L, et al.
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| Genomics 3 : 53-58. 1988
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| 47 | MAOA
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| Gene for A form of human monoamine oxidase (MAOA) maps to Xp21-p11.
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| Ozelius L, et al.
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| (HGM9) Cytogenet Cell Genet 46 : 674. 1987
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| 48 | MAOA
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| Gene for monoamine oxidase type A assigned to the human X chromosome.
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| Pintar JE, et al.
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| J Neurosci 1 : 166-175. 1981
|