These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

197 related articles for article (PubMed ID: 27341797)

  • 1. 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; 17(1):92. PubMed ID: 27341797
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 18(1):109. PubMed ID: 28982350
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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. PubMed ID: 24652311
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Adhesion G protein-coupled receptor L3 gene variants: Statistically significant association observed in the male Indo-caucasoid Attention deficit hyperactivity disorder probands.
    Chatterjee M; Saha S; Shom S; Sinha S; Mukhopadhyay K
    Mol Biol Rep; 2021 Apr; 48(4):3213-3222. PubMed ID: 33914279
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Catecholaminergic gene variants: contribution in ADHD and associated comorbid attributes in the eastern Indian probands.
    Ghosh P; Sarkar K; Bhaduri N; Ray A; Sarkar K; Sinha S; Mukhopadhyay K
    Biomed Res Int; 2013; 2013():918410. PubMed ID: 24163823
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Linkage studies between attention-deficit hyperactivity disorder and the monoamine oxidase genes.
    Jiang S; Xin R; Lin S; Qian Y; Tang G; Wang D; Wu X
    Am J Med Genet; 2001 Dec; 105(8):783-8. PubMed ID: 11803531
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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. PubMed ID: 21761555
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Dopaminergic gene analysis indicates influence of inattention but not IQ in executive dysfunction of Indian ADHD probands.
    Maitra S; Chatterjee M; Sinha S; Mukhopadhyay K
    J Neurogenet; 2019 Dec; 33(4):209-217. PubMed ID: 31663399
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Role of gene-gene/gene-environment interaction in the etiology of eastern Indian ADHD probands.
    Das M; Das Bhowmik A; Bhaduri N; Sarkar K; Ghosh P; Sinha S; Ray A; Chatterjee A; Mukhopadhyay K
    Prog Neuropsychopharmacol Biol Psychiatry; 2011 Mar; 35(2):577-87. PubMed ID: 21216270
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Potential contribution of dopaminergic gene variants in ADHD core traits and co-morbidity: a study on eastern Indian probands.
    Maitra S; Sarkar K; Ghosh P; Karmakar A; Bhattacharjee A; Sinha S; Mukhopadhyay K
    Cell Mol Neurobiol; 2014 May; 34(4):549-64. PubMed ID: 24585059
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The monoamine oxidase B gene exhibits significant association to ADHD.
    Li J; Wang Y; Hu S; Zhou R; Yu X; Wang B; Guan L; Yang L; Zhang F; Faraone SV
    Am J Med Genet B Neuropsychiatr Genet; 2008 Apr; 147(3):370-4. PubMed ID: 17918234
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Specific dopaminergic genetic variants influence impulsivity, cognitive deficit, and disease severity of Indian ADHD probands.
    Maitra S; Chatterjee M; Roychowdhury A; Panda CK; Sinha S; Mukhopadhyay K
    Mol Biol Rep; 2022 Aug; 49(8):7315-7325. PubMed ID: 35553330
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Association analysis of the monoamine oxidase A and B genes with attention deficit hyperactivity disorder (ADHD) in an Irish sample: preferential transmission of the MAO-A 941G allele to affected children.
    Domschke K; Sheehan K; Lowe N; Kirley A; Mullins C; O'sullivan R; Freitag C; Becker T; Conroy J; Fitzgerald M; Gill M; Hawi Z
    Am J Med Genet B Neuropsychiatr Genet; 2005 Apr; 134B(1):110-4. PubMed ID: 15717295
    [TBL] [Abstract][Full Text] [Related]  

  • 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. PubMed ID: 21610556
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Association of Monoamine Oxidase A (MAOA) Gene uVNTR and rs6323 Polymorphisms with Attention Deficit and Hyperactivity Disorder in Korean Children.
    Hwang IW; Lim MH; Kwon HJ; Jin HJ
    Medicina (Kaunas); 2018 May; 54(3):. PubMed ID: 30344263
    [No Abstract]   [Full Text] [Related]  

  • 16. Association analysis of monoamine oxidase A and attention deficit hyperactivity disorder.
    Lawson DC; Turic D; Langley K; Pay HM; Govan CF; Norton N; Hamshere ML; Owen MJ; O'Donovan MC; Thapar A
    Am J Med Genet B Neuropsychiatr Genet; 2003 Jan; 116B(1):84-9. PubMed ID: 12497620
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic variants of MAOB affect serotonin level and specific behavioral attributes to increase autism spectrum disorder (ASD) susceptibility in males.
    Chakraborti B; Verma D; Karmakar A; Jaiswal P; Sanyal A; Paul D; Sinha S; Singh AS; Guhathakurta S; Roychowdhury A; Panda CK; Ghosh S; Mohanakumar KP; Mukhophadhyay K; Rajamma U
    Prog Neuropsychopharmacol Biol Psychiatry; 2016 Nov; 71():123-36. PubMed ID: 27381555
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Association study between the monoamine oxidase A gene and attention deficit hyperactivity disorder in Taiwanese samples.
    Xu X; Brookes K; Chen CK; Huang YS; Wu YY; Asherson P
    BMC Psychiatry; 2007 Feb; 7():10. PubMed ID: 17328795
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Study on DBH genetic polymorphisms and plasma activity in attention deficit hyperactivity disorder patients from Eastern India.
    Bhaduri N; Sarkar K; Sinha S; Chattopadhyay A; Mukhopadhyay K
    Cell Mol Neurobiol; 2010 Mar; 30(2):265-74. PubMed ID: 19757024
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Association between attention deficit hyperactivity disorder and the DXS7 locus.
    Jiang S; Xin R; Wu X; Lin S; Qian Y; Ren D; Tang G; Wang D
    Am J Med Genet; 2000 Jun; 96(3):289-92. PubMed ID: 10898902
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.