Lista de obras -

5-HTR1A, 5-HTR2A, 5-HTR6, TPH1 and TPH2 polymorphisms and major depression.

artículo científico publicado en 2009

A catalog of genetic loci associated with kidney function from analyses of a million individuals

scientific article published on 31 May 2019

A genome-wide expression quantitative trait loci analysis of proprotein convertase subtilisin/kexin enzymes identifies a novel regulatory gene variant for FURIN expression and blood pressure

artículo científico publicado en 2015

Activated immune-inflammatory pathways are associated with long-standing depressive symptoms: Evidence from gene-set enrichment analyses in the Young Finns Study

artículo científico publicado en 2015

Adult-type hypolactasia is not a predisposing factor for the early functional and structural changes of atherosclerosis: the Cardiovascular Risk in Young Finns Study

artículo científico publicado en 2008

Androgen receptor CAG polymorphism and prostate cancer risk

scholarly article by Nina Mononen et al published 3 July 2002 in Human Genetics

Associations of functional alanine-glyoxylate aminotransferase 2 gene variants with atrial fibrillation and ischemic stroke

artículo científico publicado en 2016

BDNF and NRG1 polymorphisms and temperament in selective serotonin reuptake inhibitor-treated patients with major depression

artículo científico publicado en 2018

BDNF polymorphism rs11030101 is associated with the efficacy of electroconvulsive therapy in treatment-resistant depression

artículo científico publicado en 2013

Blood pathway analyses reveal differences between prediabetic subjects with or without dyslipidaemia. The Cardiovascular Risk in Young Finns Study

artículo científico publicado en 2017

CYP1A2 polymorphism -1545C > T (rs2470890) is associated with increased side effects to clozapine

artículo científico publicado en 2014

Catechol-O-methyltransferase val108/158met genotype, major depressive disorder and response to selective serotonin reuptake inhibitors in major depressive disorder

artículo científico publicado en 2010

Differentially expressed genes and canonical pathway expression in human atherosclerotic plaques - Tampere Vascular Study

artículo científico publicado en 2017

Differentially expressed genes and canonical pathways in the ascending thoracic aortic aneurysm - The Tampere Vascular Study

artículo científico publicado en 2017

Dopamine 2 receptor C957T and catechol-o-methyltransferase Val158Met polymorphisms are associated with treatment response in electroconvulsive therapy

artículo científico publicado en 2008

Erratum: Genetic loci associated with heart rate variability and their effects on cardiac disease risk

artículo científico publicado en 2017

Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

artículo científico publicado en 2016

ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals

Genetic Polymorphisms Associated With Constipation and Anticholinergic Symptoms in Patients Receiving Clozapine

artículo científico publicado en 2018

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

artículo científico publicado en 2014

Genetic loci associated with heart rate variability and their effects on cardiac disease risk

artículo científico publicado en 2017

Genetic profiling using genome-wide significant coronary artery disease risk variants does not improve the prediction of subclinical atherosclerosis: the Cardiovascular Risk in Young Finns Study, the Bogalusa Heart Study and the Health 2000 Survey--

artículo científico publicado en 2012

Genetic variants and their interactions in the prediction of increased pre-clinical carotid atherosclerosis: the cardiovascular risk in young Finns study

artículo científico publicado en 2010

Genetic variation in the hTAS2R38 taste receptor and food consumption among Finnish adults

artículo científico publicado en 2014

Germ-line alterations in MSR1 gene and prostate cancer risk

artículo científico publicado en 2003

Germline alterations of the RNASEL gene, a candidate HPC1 gene at 1q25, in patients and families with prostate cancer

artículo científico publicado en 2002

Histaminergic gene polymorphisms associated with sedation in clozapine-treated patients

artículo científico publicado en 2017

INSIG2 polymorphism and weight gain, dyslipidemia and serum adiponectin in Finnish patients with schizophrenia treated with clozapine

artículo científico publicado en 2016

Interaction between two HTR2A polymorphisms and gender is associated with treatment response in MDD.

artículo científico publicado en 2011

Is 5-HTTLPR linked to the response of selective serotonin reuptake inhibitors in MDD?

artículo científico publicado en 2010

Melatonin pathway genes are associated with progressive subtypes and disability status in multiple sclerosis among Finnish patients

artículo científico publicado en 2012

Mitochondrial diabetes is associated with insulin resistance in subcutaneous adipose tissue but not with increased liver fat content

artículo científico publicado en 2011

Motherhood and oxytocin receptor genetic variation are associated with selective changes in electrocortical responses to infant facial expressions.

artículo científico publicado en 2014

Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

scientific article published on 21 May 2020

No association of nineteen COX-2 gene variants to preclinical markers of atherosclerosis The Cardiovascular Risk in Young Finns Study

artículo científico publicado en 2012

No support for a role for BDNF gene polymorphisms rs11030101 and rs61888800 in major depressive disorder or antidepressant response in patients of Finnish origin

artículo científico publicado en 2013

Obesity accelerates epigenetic aging in middle-aged but not in elderly individuals

scientific article published on 14 February 2017

P2RX7 polymorphisms Gln460Arg and His155Tyr are not associated with major depressive disorder or remission after SSRI or ECT.

artículo científico publicado en 2011

Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals

artículo científico publicado en 2016

Polymorphism in alpha 2A adrenergic receptor gene is associated with sialorrhea in schizophrenia patients on clozapine treatment

artículo científico publicado en 2014

Polymorphism in the IL10 promoter region and early markers of atherosclerosis: the Cardiovascular Risk in Young Finns Study

artículo científico publicado en 2009

Polymorphism in the IL6 promoter region is associated with the risk factors and markers of subclinical atherosclerosis in men: The Cardiovascular Risk in Young Finns Study

artículo científico publicado en 2008

Polymorphisms in genes involved in androgen pathways as risk factors for prostate cancer

artículo científico publicado en 2009

Predicting sudden cardiac death using common genetic risk variants for coronary artery disease

artículo científico publicado en 2015

Profiling Genetic Variation along the Androgen Biosynthesis and Metabolism Pathways Implicates Several Single Nucleotide Polymorphisms and Their Combinations as Prostate Cancer Risk Factors

scholarly article by Nina Mononen et al published 15 January 2006 in Cancer Research

Regulatory variant of the TPH2 gene and early life stress are associated with heightened attention to social signals of fear in infants

artículo científico publicado en 2013

SERT and NET polymorphisms, temperament and antidepressant response

artículo científico publicado en 2015

Serotonin transporter (5-HTTLPR) and norepinephrine transporter (NET) gene polymorphisms: susceptibility and treatment response of electroconvulsive therapy in treatment resistant depression

artículo científico publicado en 2015

TPH1 218A/C polymorphism is associated with major depressive disorder and its treatment response

artículo científico publicado en 2009

TPH1 A218C polymorphism and temperament in major depression

artículo científico publicado en 2013

Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels

artículo científico publicado en 2019

Temperament profiles, 5-HT2A genotype, and response to treatment with SSRIs in major depression

artículo científico publicado en 2010

The APOE -219G/T and +113G/C polymorphisms affect insulin resistance among Turks

artículo científico publicado en 2010

The SGLT2 Inhibitor Dapagliflozin Reduces Liver Fat but Does Not Affect Tissue Insulin Sensitivity: A Randomized, Double-Blind, Placebo-Controlled Study With 8-Week Treatment in Type 2 Diabetes Patients

artículo científico publicado en 2019

Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation

artículo científico publicado en 2015

Vascular cell adhesion molecule 1, soluble Fas and hepatocyte growth factor as predictors of mortality in nonagenarians: the Vitality 90+ study

artículo científico publicado en 2013

Vascular endothelial growth factor (VEGF) polymorphism is associated with treatment resistant depression

artículo científico publicado en 2010

Lista de obras de

5-HTR1A, 5-HTR2A, 5-HTR6, TPH1 and TPH2 polymorphisms and major depression.

A catalog of genetic loci associated with kidney function from analyses of a million individuals

A genome-wide expression quantitative trait loci analysis of proprotein convertase subtilisin/kexin enzymes identifies a novel regulatory gene variant for FURIN expression and blood pressure

Activated immune-inflammatory pathways are associated with long-standing depressive symptoms: Evidence from gene-set enrichment analyses in the Young Finns Study

Adult-type hypolactasia is not a predisposing factor for the early functional and structural changes of atherosclerosis: the Cardiovascular Risk in Young Finns Study

Androgen receptor CAG polymorphism and prostate cancer risk

Associations of functional alanine-glyoxylate aminotransferase 2 gene variants with atrial fibrillation and ischemic stroke

BDNF and NRG1 polymorphisms and temperament in selective serotonin reuptake inhibitor-treated patients with major depression

BDNF polymorphism rs11030101 is associated with the efficacy of electroconvulsive therapy in treatment-resistant depression

Blood pathway analyses reveal differences between prediabetic subjects with or without dyslipidaemia. The Cardiovascular Risk in Young Finns Study

CYP1A2 polymorphism -1545C > T (rs2470890) is associated with increased side effects to clozapine

Catechol-O-methyltransferase val108/158met genotype, major depressive disorder and response to selective serotonin reuptake inhibitors in major depressive disorder

Differentially expressed genes and canonical pathway expression in human atherosclerotic plaques - Tampere Vascular Study

Differentially expressed genes and canonical pathways in the ascending thoracic aortic aneurysm - The Tampere Vascular Study

Dopamine 2 receptor C957T and catechol-o-methyltransferase Val158Met polymorphisms are associated with treatment response in electroconvulsive therapy

Erratum: Genetic loci associated with heart rate variability and their effects on cardiac disease risk

Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals

Genetic Polymorphisms Associated With Constipation and Anticholinergic Symptoms in Patients Receiving Clozapine

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

Genetic loci associated with heart rate variability and their effects on cardiac disease risk

Genetic profiling using genome-wide significant coronary artery disease risk variants does not improve the prediction of subclinical atherosclerosis: the Cardiovascular Risk in Young Finns Study, the Bogalusa Heart Study and the Health 2000 Survey--

Genetic variants and their interactions in the prediction of increased pre-clinical carotid atherosclerosis: the cardiovascular risk in young Finns study

Genetic variation in the hTAS2R38 taste receptor and food consumption among Finnish adults

Germ-line alterations in MSR1 gene and prostate cancer risk

Germline alterations of the RNASEL gene, a candidate HPC1 gene at 1q25, in patients and families with prostate cancer

Histaminergic gene polymorphisms associated with sedation in clozapine-treated patients

INSIG2 polymorphism and weight gain, dyslipidemia and serum adiponectin in Finnish patients with schizophrenia treated with clozapine

Interaction between two HTR2A polymorphisms and gender is associated with treatment response in MDD.

Is 5-HTTLPR linked to the response of selective serotonin reuptake inhibitors in MDD?

Melatonin pathway genes are associated with progressive subtypes and disability status in multiple sclerosis among Finnish patients

Mitochondrial diabetes is associated with insulin resistance in subcutaneous adipose tissue but not with increased liver fat content

Motherhood and oxytocin receptor genetic variation are associated with selective changes in electrocortical responses to infant facial expressions.

Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

No association of nineteen COX-2 gene variants to preclinical markers of atherosclerosis The Cardiovascular Risk in Young Finns Study

No support for a role for BDNF gene polymorphisms rs11030101 and rs61888800 in major depressive disorder or antidepressant response in patients of Finnish origin

Obesity accelerates epigenetic aging in middle-aged but not in elderly individuals

P2RX7 polymorphisms Gln460Arg and His155Tyr are not associated with major depressive disorder or remission after SSRI or ECT.

Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals

Polymorphism in alpha 2A adrenergic receptor gene is associated with sialorrhea in schizophrenia patients on clozapine treatment

Polymorphism in the IL10 promoter region and early markers of atherosclerosis: the Cardiovascular Risk in Young Finns Study

Polymorphism in the IL6 promoter region is associated with the risk factors and markers of subclinical atherosclerosis in men: The Cardiovascular Risk in Young Finns Study

Polymorphisms in genes involved in androgen pathways as risk factors for prostate cancer

Predicting sudden cardiac death using common genetic risk variants for coronary artery disease

Profiling Genetic Variation along the Androgen Biosynthesis and Metabolism Pathways Implicates Several Single Nucleotide Polymorphisms and Their Combinations as Prostate Cancer Risk Factors

Regulatory variant of the TPH2 gene and early life stress are associated with heightened attention to social signals of fear in infants

SERT and NET polymorphisms, temperament and antidepressant response

Serotonin transporter (5-HTTLPR) and norepinephrine transporter (NET) gene polymorphisms: susceptibility and treatment response of electroconvulsive therapy in treatment resistant depression

TPH1 218A/C polymorphism is associated with major depressive disorder and its treatment response

TPH1 A218C polymorphism and temperament in major depression

Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels

Temperament profiles, 5-HT2A genotype, and response to treatment with SSRIs in major depression

The APOE -219G/T and +113G/C polymorphisms affect insulin resistance among Turks

The SGLT2 Inhibitor Dapagliflozin Reduces Liver Fat but Does Not Affect Tissue Insulin Sensitivity: A Randomized, Double-Blind, Placebo-Controlled Study With 8-Week Treatment in Type 2 Diabetes Patients

Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation

Vascular cell adhesion molecule 1, soluble Fas and hepatocyte growth factor as predictors of mortality in nonagenarians: the Vitality 90+ study

Vascular endothelial growth factor (VEGF) polymorphism is associated with treatment resistant depression