Associated Papers
Whole Exome Sequencing Study in Isolated South-Eastern Moravia (Czechia) Population Indicates Heterogenous Genetic Background for Parkinsonism Development.
Kolarikova K et al.
Frontiers in Neuroscience, 2022
Polymorphic variation at the serotonin 1-A receptor gene is associated with comorbid depression and generalized anxiety.
Molina E et al.
Psychiatric Genetics, 2011
Pharmacogenetics of antidepressants.
Crisafulli C et al.
Frontiers in Pharmacology, 2011
Lack of association between five serotonin metabolism-related genes and medication overuse headache.
Cevoli S et al.
The Journal of Headache and Pain, 2010
Transcriptional regulation at a HTR1A polymorphism associated with mental illness.
Le François B et al.
Neuropharmacology, 2008
5-HT1A gene variants and psychiatric disorders: a review of current literature and selection of SNPs for future studies.
Drago A et al.
The International Journal of Neuropsychopharmacology, 2008
Genetic variation in the HTR1A gene and sudden infant death syndrome.
Morley ME et al.
American Journal of Medical Genetics. Part A, 2008
Assessment of human serotonin 1A receptor polymorphisms and SSRI responsiveness.
Levin GM et al.
Molecular Diagnosis & Therapy, 2007
[Alcohol dependence and polymorphisms of serotonin-related genes].
Gorwood P et al.
Medecine Sciences : M/s, 2004
Pharmacology of polymorphic variants of the human 5-HT1A receptor.
Del Tredici AL et al.
Biochemical Pharmacology, 2004
Lack of an association between 5-HT1A receptor gene structural polymorphisms and suicide victims.
Nishiguchi N et al.
American Journal of Medical Genetics, 2002
Analysis of structural polymorphisms and C-1018G promoter variant of the 5-HT(1A) receptor gene as putative risk factors in major depression.
Arias B et al.
Molecular Psychiatry, 2002
Novel mutations in the promoter and coding region of the human 5-HT1A receptor gene and association analysis in schizophrenia.
Kawanishi Y et al.
American Journal of Medical Genetics, 1998
Mass allele detection (MAD) of rare 5-HT1A structural variants with allele-specific amplification and electrochemiluminescent detection.
Bergen A et al.
Human Mutation, 1996
Binding properties of the naturally occurring human 5-HT1A receptor variant with the Ile28Val substitution in the extracellular domain.
Brüss M et al.
Naunyn-schmiedeberg's Archives of Pharmacology, 1995