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Items: 1 to 20 of 48


Pilot study indicate role of preferentially transmitted monoamine oxidase gene variants in behavioral problems of male ADHD probands.

Karmakar A, Goswami R, Saha T, Maitra S, Roychowdhury A, Panda CK, Sinha S, Ray A, Mohanakumar KP, Rajamma U, Mukhopadhyay K.

BMC Med Genet. 2017 Oct 5;18(1):109. doi: 10.1186/s12881-017-0469-5.


Association of Y-linked variants with impulsivity and aggression in boys with attention-deficit/hyperactivity disorder of Chinese Han descent.

Liu L, Cheng J, Li H, Su Y, Sun L, Yang L, Qian Q, Wang Y.

Psychiatry Res. 2017 Jun;252:185-187. doi: 10.1016/j.psychres.2017.02.055. Epub 2017 Feb 24.


Age-dependent role of pre- and perinatal factors in interaction with genes on ADHD symptoms across adolescence.

Brinksma DM, Hoekstra PJ, van den Hoofdakker B, de Bildt A, Buitelaar JK, Hartman CA, Dietrich A.

J Psychiatr Res. 2017 Jul;90:110-117. doi: 10.1016/j.jpsychires.2017.02.014. Epub 2017 Feb 21.


Common and specific genes and peripheral biomarkers in children and adults with attention-deficit/hyperactivity disorder.

Bonvicini C, Faraone SV, Scassellati C.

World J Biol Psychiatry. 2018 Mar;19(2):80-100. doi: 10.1080/15622975.2017.1282175. Epub 2017 Feb 24.


Monoamine oxidase B gene variants associated with attention deficit hyperactivity disorder in the Indo-Caucasoid population from West Bengal.

Karmakar A, Maitra S, Chakraborti B, Verma D, Sinha S, Mohanakumar KP, Rajamma U, Mukhopadhyay K.

BMC Genet. 2016 Jun 24;17(1):92. doi: 10.1186/s12863-016-0401-6.


Attention-deficit hyperactivity disorder in adults: A systematic review and meta-analysis of genetic, pharmacogenetic and biochemical studies.

Bonvicini C, Faraone SV, Scassellati C.

Mol Psychiatry. 2016 Jul;21(7):872-84. doi: 10.1038/mp.2016.74. Epub 2016 May 24. Review. Erratum in: Mol Psychiatry. 2016 Nov;21(11):1643.


Monoamine oxidase A polymorphism moderates stability of attention problems and susceptibility to life stress during adolescence.

Zohsel K, Bianchi V, Mascheretti S, Hohm E, Schmidt MH, Esser G, Brandeis D, Banaschewski T, Nobile M, Laucht M.

Genes Brain Behav. 2015 Nov;14(8):565-72. doi: 10.1111/gbb.12258. Epub 2015 Nov 5.


Impulsivity and Concussion in Juvenile Rats: Examining Molecular and Structural Aspects of the Frontostriatal Pathway.

Hehar H, Yeates K, Kolb B, Esser MJ, Mychasiuk R.

PLoS One. 2015 Oct 8;10(10):e0139842. doi: 10.1371/journal.pone.0139842. eCollection 2015.


Deficiency of Sustained Attention in ADHD and Its Potential Genetic Contributor MAOA.

Liu L, Cheng J, Su Y, Ji N, Gao Q, Li H, Yang L, Sun L, Qian Q, Wang Y.

J Atten Disord. 2018 Jul;22(9):878-885. doi: 10.1177/1087054715574832. Epub 2015 Mar 17.


The Altered Brain Activation of Phonological Working Memory, Dual Tasking, and Distraction Among Participants With Adult ADHD and the Effect of the MAOA Polymorphism.

Ko CH, Hsieh TJ, Wang PW, Lin WC, Chen CS, Yen JY.

J Atten Disord. 2018 Feb;22(3):240-249. doi: 10.1177/1087054715572609. Epub 2015 Mar 16.


Interactions between MAOA and SYP polymorphisms were associated with symptoms of attention-deficit/hyperactivity disorder in Chinese Han subjects.

Gao Q, Liu L, Li HM, Tang YL, Wu ZM, Chen Y, Wang YF, Qian QJ.

Am J Med Genet B Neuropsychiatr Genet. 2015 Jan;168B(1):45-53. doi: 10.1002/ajmg.b.32273. Epub 2014 Dec 8.


Differential associations of dopamine-related polymorphisms with discrete components of reaction time variability: relevance for attention deficit/hyperactivity disorder.

Grant P, Kuepper Y, Wielpuetz C, Hennig J.

Neuropsychobiology. 2014;69(4):220-6. doi: 10.1159/000360367. Epub 2014 Jun 18.


Potential contribution of monoamine oxidase a gene variants in ADHD and behavioral co-morbidities: scenario in eastern Indian probands.

Karmakar A, Maitra S, Verma D, Chakraborti B, Goswami R, Ghosh P, Sinha S, Mohanakumar KP, Usha R, Mukhopadhyay K.

Neurochem Res. 2014 May;39(5):843-52. doi: 10.1007/s11064-014-1276-4. Epub 2014 Mar 21.


Significance of Dopaminergic Gene Variants in the Male Biasness of ADHD.

Das Bhowmik A, Sarkar K, Ghosh P, Das M, Bhaduri N, Sarkar K, Ray A, Sinha S, Mukhopadhyay K.

J Atten Disord. 2017 Feb;21(3):200-208. doi: 10.1177/1087054713494004. Epub 2016 Jul 28.


Positive effects of methylphenidate on hyperactivity are moderated by monoaminergic gene variants in children with autism spectrum disorders.

McCracken JT, Badashova KK, Posey DJ, Aman MG, Scahill L, Tierney E, Arnold LE, Vitiello B, Whelan F, Chuang SZ, Davies M, Shah B, McDougle CJ, Nurmi EL.

Pharmacogenomics J. 2014 Jun;14(3):295-302. doi: 10.1038/tpj.2013.23. Epub 2013 Jul 16.


Neural mechanisms of attention-deficit/hyperactivity disorder symptoms are stratified by MAOA genotype.

Nymberg C, Jia T, Lubbe S, Ruggeri B, Desrivieres S, Barker G, Büchel C, Fauth-Buehler M, Cattrell A, Conrod P, Flor H, Gallinat J, Garavan H, Heinz A, Ittermann B, Lawrence C, Mann K, Nees F, Salatino-Oliveira A, Paillère Martinot ML, Paus T, Rietschel M, Robbins T, Smolka M, Banaschewski T, Rubia K, Loth E, Schumann G; IMAGEN Consortium.

Biol Psychiatry. 2013 Oct 15;74(8):607-14. doi: 10.1016/j.biopsych.2013.03.027. Epub 2013 Jun 5.


Association study between the dopamine-related candidate gene polymorphisms and ADHD among Saudi Arabia population via PCR technique.

El-Tarras AE, Alsulaimani AA, Awad NS, Mitwaly N, Said MM, Sabry AM.

Mol Biol Rep. 2012 Dec;39(12):11081-6. doi: 10.1007/s11033-012-2012-2. Epub 2012 Oct 18.


A preliminary analysis of interactions between genotype, retrospective ADHD symptoms, and initial reactions to smoking in a sample of young adults.

Bidwell LC, Garrett ME, McClernon FJ, Fuemmeler BF, Williams RB, Ashley-Koch AE, Kollins SH.

Nicotine Tob Res. 2012 Feb;14(2):229-33. doi: 10.1093/ntr/ntr125. Epub 2011 Jul 20.


Association analyses of MAOA in Chinese Han subjects with attention-deficit/hyperactivity disorder: family-based association test, case-control study, and quantitative traits of impulsivity.

Liu L, Guan LL, Chen Y, Ji N, Li HM, Li ZH, Qian QJ, Yang L, Glatt SJ, Faraone SV, Wang YF.

Am J Med Genet B Neuropsychiatr Genet. 2011 Sep;156B(6):737-48. doi: 10.1002/ajmg.b.31217. Epub 2011 Jul 14.


Associations of MAOA-VNTR or 5HTT-LPR alleles with attention-deficit hyperactivity disorder symptoms are moderated by platelet monoamine oxidase B activity.

Wargelius HL, Malmberg K, Larsson JO, Oreland L.

Psychiatr Genet. 2012 Feb;22(1):42-5. doi: 10.1097/YPG.0b013e328347c1ab.


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