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 *

123 related articles for article (PubMed ID: 19757024)

  • 21. Attention deficit hyperactivity disorder and the gene for dopamine Beta-hydroxylase.
    Wigg K; Zai G; Schachar R; Tannock R; Roberts W; Malone M; Kennedy JL; Barr CL
    Am J Psychiatry; 2002 Jun; 159(6):1046-8. PubMed ID: 12042196
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Dopamine β-hydroxylase gene associates with stroop color-word task performance in Han Chinese children with attention deficit/hyperactivity disorder.
    Ji N; Shuai L; Chen Y; Liu L; Li HM; Li ZH; Yang L; Qian QJ; Tang YL; Cubells JF; Wang YF
    Am J Med Genet B Neuropsychiatr Genet; 2011 Sep; 156B(6):730-6. PubMed ID: 21761554
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A haplotype at the DBH locus, associated with low plasma dopamine beta-hydroxylase activity, also associates with cocaine-induced paranoia.
    Cubells JF; Kranzler HR; McCance-Katz E; Anderson GM; Malison RT; Price LH; Gelernter J
    Mol Psychiatry; 2000 Jan; 5(1):56-63. PubMed ID: 10673769
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Dopamine β hydroxylase (DBH) polymorphisms do not contribute towards the clinical course of Wilson's disease in Indian patients.
    Roy S; Ghosh S; Bhattacharya S; Saha A; Das SK; Gangopadhyay PK; Bavdekar A; Ray K; Sengupta M; Ray J
    J Gene Med; 2019 Sep; 21(9):e3109. PubMed ID: 31265749
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. [Association of dopamine beta-hydroxylase polymorphism with attention deficit hyperactivity disorder in children].
    Zhang HB; Wang YF; Li J; Wang B; Yang L
    Beijing Da Xue Xue Bao Yi Xue Ban; 2004 Jun; 36(3):290-3. PubMed ID: 15205702
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Association between tryptophan hydroxylase gene polymorphisms and attention deficit hyperactivity disorder in Chinese Han population.
    Li J; Wang Y; Zhou R; Zhang H; Yang L; Wang B; Faraone SV
    Am J Med Genet B Neuropsychiatr Genet; 2006 Mar; 141B(2):126-9. PubMed ID: 16389593
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Polymorphisms of dopamine-beta-hydroxylase in ADHD children.
    Kopecková M; Paclt I; Goetz P
    Folia Biol (Praha); 2006; 52(6):194-201. PubMed ID: 17184598
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Haplotype study of three polymorphisms at the dopamine transporter locus confirm linkage to attention-deficit/hyperactivity disorder.
    Barr CL; Xu C; Kroft J; Feng Y; Wigg K; Zai G; Tannock R; Schachar R; Malone M; Roberts W; Nöthen MM; Grünhage F; Vandenbergh DJ; Uhl G; Sunohara G; King N; Kennedy JL
    Biol Psychiatry; 2001 Feb; 49(4):333-9. PubMed ID: 11239904
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Association between serotonin 2C gene polymorphisms and attention deficit hyperactivity disorder in children with or without comorbidity of disruptive behavior disorder].
    Li J; Wang YF; Zhou RL; Yang L; Zhang HB; Wang B
    Zhonghua Er Ke Za Zhi; 2007 May; 45(5):374-7. PubMed ID: 17697626
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The cognitive genetics of attention deficit hyperactivity disorder (ADHD): sustained attention as a candidate phenotype.
    Bellgrove MA; Hawi Z; Gill M; Robertson IH
    Cortex; 2006 Aug; 42(6):838-45. PubMed ID: 17131588
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Linkage disequilibrium analysis of the dopamine beta-hydroxylase gene in persistent attention deficit hyperactivity disorder.
    Inkster B; Muglia P; Jain U; Kennedy JL
    Psychiatr Genet; 2004 Jun; 14(2):117-20. PubMed ID: 15167700
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Role of SNAP25 explored in eastern Indian attention deficit hyperactivity disorder probands.
    Sarkar K; Bhaduri N; Ghosh P; Sinha S; Ray A; Chatterjee A; Mukhopadhyay K
    Neurochem Res; 2012 Feb; 37(2):349-57. PubMed ID: 21996783
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Associations between the DBH gene, plasma dopamine β-hydroxylase activity and cognitive measures in Han Chinese patients with schizophrenia.
    Sun Z; Ma Y; Li W; He J; Li J; Yang X; Mao P; Cubells JF; Tang YL
    Schizophr Res; 2018 Mar; 193():58-63. PubMed ID: 28647493
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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. PubMed ID: 23881560
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Association between serotonin 2C gene polymorphisms and attention deficit hyperactivity disorder comorbid or not comorbid with learning disorder].
    Li J; Wang YF; Zhou RL; Zhang HB; Wang B; Yang L
    Beijing Da Xue Xue Bao Yi Xue Ban; 2004 Aug; 36(4):366-9. PubMed ID: 15303127
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A haplotype of the norepinephrine transporter gene (SLC6A2) is associated with visual memory in attention-deficit/hyperactivity disorder.
    Shang CY; Chiang HL; Gau SS
    Prog Neuropsychopharmacol Biol Psychiatry; 2015 Apr; 58():89-96. PubMed ID: 25554436
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A common haplotype at the dopamine transporter gene 5' region is associated with attention-deficit/hyperactivity disorder.
    Genro JP; Polanczyk GV; Zeni C; Oliveira AS; Roman T; Rohde LA; Hutz MH
    Am J Med Genet B Neuropsychiatr Genet; 2008 Dec; 147B(8):1568-75. PubMed ID: 18802919
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.