Author pages are created from data sourced from our academic publisher partnerships and public sources.
- Publications
- Influence
The A1 allele of the human D2 dopamine receptor gene predicts low D2 receptor availability in healthy volunteers
- T. Pohjalainen, J. Rinne, +4 authors J. Hietala
- Biology, Medicine
- Molecular Psychiatry
- 1 May 1998
Positron emission tomography (PET) studies have revealed significant interindividual variation in dopamine D2 receptor density in vivo in human striatum.1 Low D2 receptor binding in vivo has been… Expand
Sex differences in the striatal dopamine D2 receptor binding characteristics in vivo.
- T. Pohjalainen, J. Rinne, K. Någren, E. Syvälahti, J. Hietala
- Psychology, Medicine
- The American journal of psychiatry
- 1 June 1998
OBJECTIVE
The authors investigated whether striatal dopamine D2 receptor binding characteristics in vivo are similar in men and women and whether there are sex-related differences in the decline in… Expand
C957T polymorphism of the dopamine D2 receptor (DRD2) gene affects striatal DRD2 availability in vivo
- M. Hirvonen, A. Laakso, K. Någren, J. Rinne, T. Pohjalainen, J. Hietala
- Biology, Medicine
- Molecular Psychiatry
- 27 July 2004
C957T polymorphism of the dopamine D2 receptor (DRD2) gene affects striatal DRD2 availability in vivo
Association between low activity serotonin transporter promoter genotype and early onset alcoholism with habitual impulsive violent behavior
- T. Hallikainen, T. Saito, +7 authors J. Tiihonen
- Psychology, Medicine
- Molecular Psychiatry
- 1 July 1999
A common 44-base pair insertion/deletion polymorphism in the promoter region of the human serotonin transporter (5-HTT) gene has been observed to be associated with affective illness and… Expand
Age-related dopamine D2/D3 receptor loss in extrastriatal regions of the human brain
- V. Kaasinen, H. Vilkman, J. Hietala, K. Någren, J. Rinne
- Psychology, Medicine
- Neurobiology of Aging
- 1 September 2000
Loss of dopamine D2-like receptors in the striatum has been associated with both normal human aging and impairment of cognitive and motor functions in the elderly. To investigate whether there are… Expand
Comparison of the Transient Equilibrium and Continuous Infusion Method for Quantitative PET Analysis of [11C]Raclopride Binding
- H. Ito, J. Hietala, G. Blomqvist, C. Halldin, L. Farde
- Chemistry, Medicine
- Journal of cerebral blood flow and metabolism…
- 1 September 1998
Several approaches have been applied for quantification of D2 dopamine receptors in positron emission tomography studies using [11C]raclopride. Initial approaches were based on analyses of data… Expand
Mesolimbic dopamine release is linked to symptom severity in pathological gambling
- J. Joutsa, J. Johansson, +9 authors V. Kaasinen
- Medicine, Computer Science
- NeuroImage
- 1 May 2012
TLDR
C957T polymorphism of the human dopamine D2 receptor gene predicts extrastriatal dopamine receptor availability in vivo
- M. Hirvonen, V. Lumme, J. Hirvonen, U. Pesonen, J. Hietala
- Biology, Medicine
- Progress in Neuro-Psychopharmacology and…
- 15 June 2009
The C957T (rs6277) single nucleotide polymorphism (SNP) of the human dopamine D2 receptor (DRD2) gene (DRD2) affects DRD2 mRNA stability and has been shown to predict striatal DRD2 availability… Expand
Depressive symptoms and presynaptic dopamine function in neuroleptic-naive schizophrenia
- J. Hietala, E. Syvälahti, H. Vilkman, K. Vuorio, R. Salokangas
- Psychology, Medicine
- Schizophrenia Research
- 4 January 1999
We have previously reported aberrations in the striatal presynaptic dopamine function in neuroleptic-naive schizophrenic patients compared to healthy controls (Hietala, J., Syvälahti, E., Vuorio, K.… Expand
Association between the functional variant of the catechol-O-methyltransferase (COMT) gene and type 1 alcoholism
- J. Tiihonen, T. Hallikainen, +10 authors J. Hietala
- Psychology, Medicine
- Molecular Psychiatry
- 1 May 1999
Catechol-O-methyltransferase (COMT) is an enzyme which has a crucial role in the metabolism of dopamine. It has been suggested that a common functional genetic polymorphism in the COMT gene, which… Expand