Attention-deficit hyperactivity disorder (ADHD)
- Prosjektnummer
- 911393
- Ansvarlig person
- Jan Haavik
- Institusjon
- Universitetet i Bergen
- Prosjektkategori
- Forskningsprosjekt
- Helsekategori
- Mental Health
- Forskningsaktivitet
- 2. Aetiology
Clinical assessment and diagnosis of adults with attention-deficit/hyperactivity disorder.
Expert Rev Neurother 2010 Oct;10(10):1569-80.
PMID: 20925472
Attention-deficit/hyperactivity disorder symptoms in offspring of mothers with impaired serotonin production.
Arch Gen Psychiatry 2010 Oct;67(10):1033-43.
PMID: 20921119
No association between the serotonin transporter gene polymorphism 5-HTTLPR and cyclothymic temperament as measured by TEMPS-A.
J Affect Disord 2011 Mar;129(1-3):308-12. Epub 2010 sep 28
PMID: 20880592
A genome-wide association study of bipolar disorder and comorbid migraine.
Genes Brain Behav 2010 Oct;9(7):673-80. Epub 2010 jun 29
PMID: 20528957
Effect of pharmacological chaperones on brain tyrosine hydroxylase and tryptophan hydroxylase 2.
J Neurochem 2010 Aug;114(3):853-63. Epub 2010 mai 18
PMID: 20492352
Common variants in the TPH1 and TPH2 regions are not associated with persistent ADHD in a combined sample of 1,636 adult cases and 1,923 controls from four European populations.
Am J Med Genet B Neuropsychiatr Genet 2010 Jul;153B(5):1008-15.
PMID: 20213726
A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication.
Mol Psychiatry 2010 Nov;15(11):1053-66. Epub 2010 feb 16
PMID: 20157310
Bipolar symptoms in adult attention-deficit/hyperactivity disorder: a cross-sectional study of 510 clinically diagnosed patients and 417 population-based controls.
J Clin Psychiatry 2010 Jan;71(1):48-57.
PMID: 20129005
Multicenter analysis of the SLC6A3/DAT1 VNTR haplotype in persistent ADHD suggests differential involvement of the gene in childhood and persistent ADHD.
Neuropsychopharmacology 2010 Feb;35(3):656-64. Epub 2009 nov 4
PMID: 19890261
Meta-analysis of brain-derived neurotrophic factor p.Val66Met in adult ADHD in four European populations.
Am J Med Genet B Neuropsychiatr Genet 2010 Mar;153B(2):512-23.
PMID: 19603419
An international multicenter association study of the serotonin transporter gene in persistent ADHD.
Genes Brain Behav 2010 Jul;9(5):449-58. Epub 2010 jan 25
PMID: 20113357
Tryptophan as an evolutionarily conserved signal to brain serotonin: molecular evidence and psychiatric implications.
World J Biol Psychiatry 2009;10(4):258-68.
PMID: 19921967
Case-control study of six genes asymmetrically expressed in the two cerebral hemispheres: association of BAIAP2 with attention-deficit/hyperactivity disorder.
Biol Psychiatry 2009 Nov;66(10):926-34. Epub 2009 sep 5
PMID: 19733838
Three-way interaction between 14-3-3 proteins, the N-terminal region of tyrosine hydroxylase, and negatively charged membranes.
J Biol Chem 2009 Nov;284(47):32758-69. Epub 2009 sep 28
PMID: 19801645
Occupational outcome in adult ADHD: impact of symptom profile, comorbid psychiatric problems, and treatment: a cross-sectional study of 414 clinically diagnosed adult ADHD patients.
J Atten Disord 2009 Sep;13(2):175-87. Epub 2009 apr 16
PMID: 19372500
Functional properties of missense variants of human tryptophan hydroxylase 2.
Hum Mutat 2009 May;30(5):787-94.
PMID: 19319927
Association between catechol O-methyltransferase (COMT) haplotypes and severity of hyperactivity symptoms in adults.
Am J Med Genet B Neuropsychiatr Genet 2009 Apr;150B(3):403-10.
PMID: 18802928
Mutations in human monoamine-related neurotransmitter pathway genes.
Hum Mutat 2008 Jul;29(7):891-902.
PMID: 18444257
Tetrahydrobiopterin shows chaperone activity for tyrosine hydroxylase.
J Neurochem 2008 Jul;106(2):672-81. Epub 2008 apr 14
PMID: 18419768
Endogenous tetrahydroisoquinolines associated with Parkinson's disease mimic the feedback inhibition of tyrosine hydroxylase by catecholamines.
FEBS J 2008 May;275(9):2109-21. Epub 2008 mar 19
PMID: 18355318
A loss-of-function mutation in tryptophan hydroxylase 2 segregating with attention-deficit/hyperactivity disorder.
Mol Psychiatry 2008 Apr;13(4):365-7.
PMID: 18347598
Genetic analyses of dopamine related genes in adult ADHD patients suggest an association with the DRD5-microsatellite repeat, but not with DRD4 or SLC6A3 VNTRs.
Am J Med Genet B Neuropsychiatr Genet 2008 Dec;147B(8):1470-5.
PMID: 18081165
Activation and stabilization of human tryptophan hydroxylase 2 by phosphorylation and 14-3-3 binding.
Biochem J 2008 Feb;410(1):195-204.
PMID: 17973628
Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5'-region are associated with bipolar affective disorder.
Hum Mol Genet 2008 Jan;17(1):87-97. Epub 2007 sep 27
PMID: 17905754
Oxygen dependence of tyrosine hydroxylase.
Amino Acids 2008 Apr;34(3):455-64. Epub 2007 mai 23
PMID: 17520326
ADHD and bipolar disorder in a lifetime perspective.
Nordic psychiatric academy Copenhagen, Denmark, January 14-16 2010
ADHD in adults – genetic and clinical findings
SCNP 51st Annual Meeting, Gothenburg, SwedenApril 12. 2010
Long term consequences of an impaired serotonin production on the developing human brain
WCPG, Athens, Greece October 3.-7. 2010
Risk alleles from GWAS of bipolar disorder in adult ADHD patients
WCPG, Athens, Greece.October 3.-7. 2010
Mavroconstanti T, Johansson S., Winge I, Knappskog P.M. Haavik J.
WCPG, Athens, Greece. October 3.-7. 2010
Impaired serotonin production in mothers with TPH1 mutations may have long term effects on brain development in their offspring
Cambridge, UK. March 2010
DISC1 as a novel candidate gene in ADHD – association between rs1538979 and ADHD in a Norwegian sample of adult ADHD patients
Amsterdam, The Netherlands.May 25th 2010
Functional characterization of ADHD candidate genes. The role of exon & exome sequencing
11th Annual Meeting of the ADHD Molecular Genetics Network. Dec. 13, 2010
Impaired serotonin production in mothers with TPH1 mutations may have long term effects on brain development in their offspring
NeuroNor, Bergen, NorwayMay 27.-28 2010
From synthesis to reuptake: Serotonergic genes and ADHD
22. ECNP congress Istanbul, Turkey
ADHD hos voksne : genetikk og diagnostikk
ADHD konferanse, Sykehuset Østfold, Fredrikstad.
Functional studies on ADHD candidate genes
World Congress of Biological Psychiatry (WCBP), Paris, France
ADHD: Fra klinisk karakterisering til molekylære mekanismer
MoodNet Annual Meeting, Bergen.
Bipolar Disorder in Adult Patients with Attention Deficit Hyperactivity Disorder (ADHD)
2. International ADHD congress, Vienna, Austria.
Pre- og perinatale risikofaktorer ved persisterende ADHD
Norwegian Research Network on AD/HD Solstrand, Norway.
ADHD: from functional characterization to molecular mechanisms
Norwegian Research Network on AD/HD Solstrand, Norway.
ADHD in adults: from functional characterization to molecular mechanisms.
2. IMpACT meeting, Nijmegen, The Netherlands.
Common variants in the TPH1 and TPH2 regions are not associated with persistent ADHD in 3559 individuals from four European popu
WCPG, San Diego, USA
Meta-analysis of brain-derived neurotrophic factor p.val66met in adult adhd in four European populations
WCPG, San Diego, USA.
Case-control study of six genes asymmetrically expressed in the two cerebral hemispheres: association of baiap2 with ADHD.
WCPG, San Diego, USA.
eRapport er utarbeidet av Sølvi Lerfald og Reidar Thorstensen, Regionalt kompetansesenter for klinisk forskning, Helse Vest RHF, og videreutvikles av de fire RHF-ene i fellesskap, med støtte fra Helse Vest IKT
Alle henvendelser rettes til Faglig rapportering, Helse Vest