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194 related items for PubMed ID: 25744621

  • 1. Further evidence for the association of the NPSR1 gene A/T polymorphism (Asn107Ile) with impulsivity and hyperactivity.
    Laas K, Eensoo D, Paaver M, Lesch KP, Reif A, Harro J.
    J Psychopharmacol; 2015 Aug; 29(8):878-83. PubMed ID: 25744621
    [Abstract] [Full Text] [Related]

  • 2. A functional NPSR1 gene variant and environment shape personality and impulsive action: a longitudinal study.
    Laas K, Reif A, Kiive E, Domschke K, Lesch KP, Veidebaum T, Harro J.
    J Psychopharmacol; 2014 Mar; 28(3):227-36. PubMed ID: 23325374
    [Abstract] [Full Text] [Related]

  • 3. Interaction of the neuropeptide S receptor gene Asn¹⁰⁷Ile variant and environment: contribution to affective and anxiety disorders, and suicidal behaviour.
    Laas K, Reif A, Akkermann K, Kiive E, Domschke K, Lesch KP, Veidebaum T, Harro J.
    Int J Neuropsychopharmacol; 2014 Apr; 17(4):541-52. PubMed ID: 24331455
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  • 5. Neuropeptide S receptor gene Asn107 polymorphism in obese male individuals in Pakistan.
    Ahmad A, Almsned F, Ghazal P, Ahmed MW, Jafri MS, Bokhari H.
    PLoS One; 2020 Apr; 15(12):e0243205. PubMed ID: 33332443
    [Abstract] [Full Text] [Related]

  • 6. The functional coding variant Asn107Ile of the neuropeptide S receptor gene (NPSR1) is associated with schizophrenia and modulates verbal memory and the acoustic startle response.
    Lennertz L, Quednow BB, Schuhmacher A, Petrovsky N, Frommann I, Schulze-Rauschenbach S, Landsberg MW, Steinbrecher A, Höfels S, Pukrop R, Klosterkötter J, Franke PE, Wölwer W, Gaebel W, Häfner H, Maier W, Wagner M, Mössner R.
    Int J Neuropsychopharmacol; 2012 Oct; 15(9):1205-15. PubMed ID: 22078257
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  • 7. The functional coding variant Asn107Ile of the neuropeptide S receptor gene (NPSR1) influences age at onset of obsessive-compulsive disorder.
    Lennertz L, Franke PE, Grabe HJ, Rampacher F, Schulze-Rauschenbach S, Guttenthaler V, Ruhrmann S, Pukrop R, Klosterkötter J, Falkai P, Maier W, Wagner M, Mössner R.
    Int J Neuropsychopharmacol; 2013 Oct; 16(9):1951-8. PubMed ID: 23680103
    [Abstract] [Full Text] [Related]

  • 8. Neuropeptide S receptor (NPSR1) gene variation modulates response inhibition and error monitoring.
    Beste C, Konrad C, Uhlmann C, Arolt V, Zwanzger P, Domschke K.
    Neuroimage; 2013 May 01; 71():1-9. PubMed ID: 23319044
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  • 9. Driving risks of young drivers with symptoms of attention deficit hyperactivity disorder: association with the dopamine transporter gene VNTR polymorphism.
    Tokko T, Miškinyte G, Eensoo D, Harro J.
    Nord J Psychiatry; 2022 Nov 01; 76(8):575-583. PubMed ID: 35130472
    [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 01; 52(11):1204-1212.e1. PubMed ID: 24157394
    [Abstract] [Full Text] [Related]

  • 11. Sex-specific association between functional neuropeptide S receptor gene (NPSR1) variants and cortisol and central stress responses.
    Streit F, Akdeniz C, Haddad L, Kumsta R, Entringer S, Frank J, Yim IS, Zänkert S, Witt SH, Kirsch P, Rietschel M, Wüst S.
    Psychoneuroendocrinology; 2017 Feb 01; 76():49-56. PubMed ID: 27883964
    [Abstract] [Full Text] [Related]

  • 12. Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits.
    Ebejer JL, Duffy DL, van der Werf J, Wright MJ, Montgomery G, Gillespie NA, Hickie IB, Martin NG, Medland SE.
    Twin Res Hum Genet; 2013 Apr 01; 16(2):560-74. PubMed ID: 23527680
    [Abstract] [Full Text] [Related]

  • 13. Relapse of drunk driving and association with traffic accidents, alcohol-related problems and biomarkers of impulsivity.
    Tokko T, Eensoo D, Vaht M, Lesch KP, Reif A, Harro J.
    Acta Neuropsychiatr; 2019 Apr 01; 31(2):84-92. PubMed ID: 30472966
    [Abstract] [Full Text] [Related]

  • 14. Investigating the Contribution of NPSR1, IL-6 and BDNF Polymorphisms to Depressive and Anxiety Symptoms in Hemodialysis Patients.
    Alshogran OY, Al-Eitan LN, Altawalbeh SM, Khalil AA, Alqudah MAY, Oweis AO, Aman HA, Alhawari HH.
    Prog Neuropsychopharmacol Biol Psychiatry; 2019 Aug 30; 94():109657. PubMed ID: 31132388
    [Abstract] [Full Text] [Related]

  • 15. Nitric oxide synthase genotype modulation of impulsivity and ventral striatal activity in adult ADHD patients and healthy comparison subjects.
    Hoogman M, Aarts E, Zwiers M, Slaats-Willemse D, Naber M, Onnink M, Cools R, Kan C, Buitelaar J, Franke B.
    Am J Psychiatry; 2011 Oct 30; 168(10):1099-106. PubMed ID: 21724667
    [Abstract] [Full Text] [Related]

  • 16. Gender-specific association of a functional coding polymorphism in the Neuropeptide S receptor gene with panic disorder but not with schizophrenia or attention-deficit/hyperactivity disorder.
    Okamura N, Hashimoto K, Iyo M, Shimizu E, Dempfle A, Friedel S, Reinscheid RK.
    Prog Neuropsychopharmacol Biol Psychiatry; 2007 Oct 01; 31(7):1444-8. PubMed ID: 17669576
    [Abstract] [Full Text] [Related]

  • 17. Study on the possible association of brain-derived neurotrophic factor polymorphism with the developmental course of symptoms of attention deficit and hyperactivity.
    Bergman O, Westberg L, Lichtenstein P, Eriksson E, Larsson H.
    Int J Neuropsychopharmacol; 2011 Nov 01; 14(10):1367-76. PubMed ID: 21466746
    [Abstract] [Full Text] [Related]

  • 18. Inferring candidate genes for attention deficit hyperactivity disorder (ADHD) assessed by the World Health Organization Adult ADHD Self-Report Scale (ASRS).
    Reuter M, Kirsch P, Hennig J.
    J Neural Transm (Vienna); 2006 Jul 01; 113(7):929-38. PubMed ID: 16362639
    [Abstract] [Full Text] [Related]

  • 19. A Population-Based Imaging Genetics Study of Inattention/Hyperactivity: Basal Ganglia and Genetic Pathways.
    Mous SE, Hammerschlag AR, Polderman TJ, Verhulst FC, Tiemeier H, van der Lugt A, Jaddoe VW, Hofman A, White T, Posthuma D.
    J Am Acad Child Adolesc Psychiatry; 2015 Sep 01; 54(9):745-52. PubMed ID: 26299296
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