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 *

154 related articles for article (PubMed ID: 35553330)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Association between catechol O-methyltransferase (COMT) haplotypes and severity of hyperactivity symptoms in adults.
    Halleland H; Lundervold AJ; Halmøy A; Haavik J; Johansson S
    Am J Med Genet B Neuropsychiatr Genet; 2009 Apr; 150B(3):403-10. PubMed ID: 18802928
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Haplotype relative risk study of catechol-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD): association of the high-enzyme activity Val allele with ADHD impulsive-hyperactive phenotype.
    Eisenberg J; Mei-Tal G; Steinberg A; Tartakovsky E; Zohar A; Gritsenko I; Nemanov L; Ebstein RP
    Am J Med Genet; 1999 Oct; 88(5):497-502. PubMed ID: 10490706
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Candidate genetic pathways for attention-deficit/hyperactivity disorder (ADHD) show association to hyperactive/impulsive symptoms in children with ADHD.
    Bralten J; Franke B; Waldman I; Rommelse N; Hartman C; Asherson P; Banaschewski T; Ebstein RP; Gill M; Miranda A; Oades RD; Roeyers H; Rothenberger A; Sergeant JA; Oosterlaan J; Sonuga-Barke E; Steinhausen HC; Faraone SV; Buitelaar JK; Arias-Vásquez A
    J Am Acad Child Adolesc Psychiatry; 2013 Nov; 52(11):1204-1212.e1. PubMed ID: 24157394
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Catechol-O-methyltransferase Val158Met polymorphism is associated with methylphenidate response in ADHD children.
    Kereszturi E; Tarnok Z; Bognar E; Lakatos K; Farkas L; Gadoros J; Sasvari-Szekely M; Nemoda Z
    Am J Med Genet B Neuropsychiatr Genet; 2008 Dec; 147B(8):1431-5. PubMed ID: 18214865
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Influence of DAT1 and COMT variants on neural activation during response inhibition in adolescents with attention-deficit/hyperactivity disorder and healthy controls.
    van Rooij D; Hoekstra PJ; Bralten J; Hakobjan M; Oosterlaan J; Franke B; Rommelse N; Buitelaar JK; Hartman CA
    Psychol Med; 2015 Nov; 45(15):3159-70. PubMed ID: 26073896
    [TBL] [Abstract][Full Text] [Related]  

  • 14. DAT1 and COMT effects on delay discounting and trait impulsivity in male adolescents with attention deficit/hyperactivity disorder and healthy controls.
    Paloyelis Y; Asherson P; Mehta MA; Faraone SV; Kuntsi J
    Neuropsychopharmacology; 2010 Nov; 35(12):2414-26. PubMed ID: 20736997
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A pilot study on the contribution of folate gene variants in the cognitive function of ADHD probands.
    Saha T; Dutta S; Rajamma U; Sinha S; Mukhopadhyay K
    Neurochem Res; 2014 Nov; 39(11):2058-67. PubMed ID: 25079255
    [TBL] [Abstract][Full Text] [Related]  

  • 16. COMT Val158Met variant and functional haplotypes associated with childhood ADHD history in women with bulimia nervosa.
    Yilmaz Z; Kaplan AS; Zai CC; Levitan RD; Kennedy JL
    Prog Neuropsychopharmacol Biol Psychiatry; 2011 Jun; 35(4):948-52. PubMed ID: 21300128
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Parental age and developmental milestones: pilot study indicated a role in understanding ADHD severity in Indian probands.
    Maitra S; Mukhopadhyay K
    BMC Pediatr; 2019 Apr; 19(1):117. PubMed ID: 31010429
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The methionine allele of the COMT polymorphism impairs prefrontal cognition in children and adolescents with ADHD.
    Bellgrove MA; Domschke K; Hawi Z; Kirley A; Mullins C; Robertson IH; Gill M
    Exp Brain Res; 2005 Jun; 163(3):352-60. PubMed ID: 15654584
    [TBL] [Abstract][Full Text] [Related]  

  • 19. No association between catechol-O-methyltransferase (COMT) gene polymorphism and attention deficit hyperactivity disorder (ADHD) in an Irish sample.
    Hawi Z; Millar N; Daly G; Fitzgerald M; Gill M
    Am J Med Genet; 2000 Jun; 96(3):282-4. PubMed ID: 10898900
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The dopamine transporter gene and the impulsivity phenotype in attention deficit hyperactivity disorder: a case-control association study in a Korean sample.
    Kim JW; Kim BN; Cho SC
    J Psychiatr Res; 2006 Dec; 40(8):730-7. PubMed ID: 16368111
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.