Lista de obras - Tiina Paunio - Dominio Público Uruguay

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation

artículo científico publicado en 2013

A genome-wide screen for acrophobia susceptibility loci in a Finnish isolate

artículo científico publicado en 2016

A population-based association study of candidate genes for depression and sleep disturbance.

artículo científico publicado en 2010

A population-specific HTR2B stop codon predisposes to severe impulsivity

artículo científico publicado en 2010

AMIGO-Kv2.1 Potassium Channel Complex Is Associated With Schizophrenia-Related Phenotypes

artículo científico publicado en 2015

An association between both low and high birth weight and increased disorganized and negative symptom severity in schizophrenia and other psychoses

artículo científico publicado en 2012

An association between high birth weight and schizophrenia in a Finnish schizophrenia family study sample

artículo científico publicado en 2011

An interaction between NDE1 and high birth weight increases schizophrenia susceptibility

artículo científico publicado en 2015

Analysis of detailed phenotype profiles reveals CHRNA5-CHRNA3-CHRNB4 gene cluster association with several nicotine dependence traits

artículo científico publicado en 2012

Association between Dopamine Receptor D2 (DRD2) Variations rs6277 and rs1800497 and Cognitive Performance According to Risk Type for Psychosis: A Nested Case Control Study in a Finnish Population Sample

artículo científico publicado en 2015

Association of AKT1 with verbal learning, verbal memory, and regional cortical gray matter density in twins

artículo científico publicado en 2009

Association of a nonsynonymous variant of DAOA with visuospatial ability in a bipolar family sample

artículo científico publicado en 2008

CRY2 is associated with depression

artículo científico publicado en 2010

Childhood adversities and quality of sleep in adulthood: A population-based study of 26,000 Finns

artículo científico publicado en 2009

Circadian clock-related polymorphisms in seasonal affective disorder and their relevance to diurnal preference

artículo científico publicado en 2002

Common Genetic Variation Near Melatonin Receptor 1A Gene Linked to Job-Related Exhaustion in Shift Workers

artículo científico publicado en 2017

Common variants at VRK2 and TCF4 conferring risk of schizophrenia

artículo científico publicado en 2011

Common variants conferring risk of schizophrenia

artículo científico publicado en 2009

Comparing cognitive-behavioural psychotherapy and psychoeducation for non-specific symptoms associated with indoor air: a randomised control trial protocol

artículo científico publicado en 2016

Contribution of adenosine related genes to the risk of depression with disturbed sleep

artículo científico publicado en 2010

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

artículo científico publicado en 2016

DISC1 Gene Network Mutations In Major Mental Illness

article

Data on schizotypy and affective scales are gender and education dependent--study in the Northern Finland 1966 Birth Cohort

artículo científico publicado en 2010

Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders

scientific article published on 04 August 2013

Development of sleep-wake rhythms during the first year of age

scientific article published on 08 September 2019

Differences and similarities of risk factors for suicidal ideation and attempts among patients with depressive or bipolar disorders

artículo científico publicado en 2016

Early age at onset of bipolar disorder is associated with more severe clinical features but delayed treatment seeking

artículo científico publicado en 2007

Early environment and neurobehavioral development predict adult temperament clusters

artículo científico publicado en 2012

Environmental stress affects DNA methylation of a CpG rich promoter region of serotonin transporter gene in a nurse cohort

artículo científico publicado en 2012

Epigenetic dysregulation of genes related to synaptic long-term depression among adolescents with depressive disorder and sleep symptoms

artículo científico publicado en 2019

Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1.

artículo científico publicado en 2006

Frontal Cortex Myo-Inositol Is Associated with Sleep and Depression in Adolescents: A Proton Magnetic Resonance Spectroscopy Study

artículo científico publicado en 2017

Gene expression patterns in a rodent model for depression

artículo científico

Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia

artículo científico publicado en 2003

Genome-wide scan of job-related exhaustion with three replication studies implicate a susceptibility variant at the UST gene locus

artículo científico publicado en 2013

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

artículo científico publicado en 2017

Haplotype analysis and identification of genes for a complex trait: examples from schizophrenia

artículo científico publicado en 2004

Haplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effects

artículo científico publicado en 2003

Helsinki alert of biodiversity and health

artículo científico publicado en 2015

Heritability and number of quantitative trait loci of neurocognitive functions in families with schizophrenia

artículo científico publicado en 2002

Heritability of cognitive functions in families with bipolar disorder

artículo científico publicado en 2007

Identification of NCAN as a candidate gene for developmental dyslexia

artículo científico

Identifying Schizophrenia and Other Psychoses With Psychological Scales in the General Population

Impact of temperament on depression and anxiety symptoms and depressive disorder in a population-based birth cohort

artículo científico publicado en 2011

Inter-tissue Networks Between the Basal Forebrain, Hippocampus, and Prefrontal Cortex in a Model for Depression Caused by Disturbed Sleep ⬇️

artículo científico publicado el 11 de julio de 2012

Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

artículo científico publicado en 2022

Interaction between compound genetic risk for schizophrenia and high birth weight contributes to social anhedonia and schizophrenia in women

artículo científico publicado en 2017

Interaction of early environment, gender and genes of monoamine neurotransmission in the aetiology of depression in a large population-based Finnish birth cohort

artículo científico publicado en 2011

Large recurrent microdeletions associated with schizophrenia

artículo científico publicado en 2008

Linkage analysis of schizophrenia controlling for population substructure

artículo científico publicado en 2009

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

artículo científico publicado en 2022

Maternal and paternal sleep during pregnancy in the Child-sleep birth cohort

artículo científico publicado en 2016

Mixture model clustering of phenotype features reveals evidence for association of DTNBP1 to a specific subtype of schizophrenia

artículo científico publicado en 2009

Neuregulin-1 genotype is associated with structural differences in the normal human brain

artículo científico publicado en 2011

Nightmares as predictors of suicide: an extension study including war veterans

scientific article published on 15 March 2017

Nightmares: Prevalence among the Finnish General Adult Population and War Veterans during 1972-2007.

artículo científico publicado en 2013

Nightmares: risk factors among the Finnish general adult population

artículo científico publicado en 2015

No association of COMT (Val158Met) genotype with brain structure differences between men and women

artículo científico publicado en 2012

Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant

scientific article published on 18 July 2018

Normal sleep development in infants: findings from two large birth cohorts

artículo científico publicado en 2020

Parent-reported early sleep problems and internalising, externalising and dysregulation symptoms in toddlers

scientific article published on 10 March 2020

Partial sleep restriction activates immune response-related gene expression pathways: experimental and epidemiological studies in humans

artículo científico publicado en 2013

Phenotype mining in CNV carriers from a population cohort

artículo científico publicado en 2011

Phenotypic Translation of the Disc1 Network Highlights the Role of the Nde1 Locus, with Pharmacological Implications

scholarly article by William Hennah et al published 2017 in European Neuropsychopharmacology

Poor sleep predicts symptoms of depression and disability retirement due to depression

artículo científico publicado en 2014

Predicting depression with psychopathology and temperament traits: the northern Finland 1966 birth cohort

artículo científico publicado en 2012

Prolonged sleep restriction induces changes in pathways involved in cholesterol metabolism and inflammatory responses

artículo científico publicado en 2016

RHD maternal-fetal genotype incompatibility and schizophrenia: extending the MFG test to include multiple siblings and birth order

artículo científico publicado en 2004

RHD maternal-fetal genotype incompatibility increases schizophrenia susceptibility

artículo científico publicado en 2002

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.

artículo científico publicado en 2016

Replication of association between working memory and Reelin, a potential modifier gene in schizophrenia

artículo científico publicado en 2010

Role of nicotine dependence in the association between the dopamine receptor gene DRD3 and major depressive disorder

artículo científico publicado en 2014

Role of proprotein convertases in the pathogenic processing of the amyloidosis-associated form of secretory gelsolin

artículo científico publicado en 2002

Search for cognitive trait components of schizophrenia reveals a locus for verbal learning and memory on 4q and for visual working memory on 2q.

artículo científico

Seasonal affective disorder and the G-protein beta-3-subunit C825T polymorphism

artículo científico publicado en 2004

Seasonal variation in affective and other clinical symptoms among high-risk families for bipolar disorders in an Arctic population

artículo científico publicado en 2015

Shared genetic background for regulation of mood and sleep: association of GRIA3 with sleep duration in healthy Finnish women

artículo científico publicado en 2011

Sleep and Behavior in Cross-Fostering Rats: Developmental and Sex Aspects

scientific article published on 09 September 2016

Sleep modifies metabolism

artículo científico publicado en 2012

Substance Use and Sleep Problems in Patients With Psychotic Disorders

artículo científico publicado en 2022

Systematic analysis of circadian genes in a population-based sample reveals association of TIMELESS with depression and sleep disturbance

artículo científico publicado en 2010

Temperament clusters in a normal population: implications for health and disease

artículo científico publicado en 2012

The NDE1 genomic locus can affect treatment of psychiatric illness through gene expression changes related to microRNA-484.

artículo científico publicado en 2017

The Val66Met polymorphism in the BDNF gene is associated with epilepsy in fragile X syndrome.

artículo científico publicado en 2009

The genome-wide patterns of variation expose significant substructure in a founder population

artículo científico publicado en 2008

Three circadian clock genes Per2, Arntl, and Npas2 contribute to winter depression

artículo científico publicado en 2007

Truncating mutations in RBM12 are associated with psychosis

artículo científico publicado en 2017

Variants in calcium voltage-gated channel subunit Alpha1 C-gene (CACNA1C) are associated with sleep latency in infants

artículo científico publicado en 2017

Variants in regulatory elements of PDE4D associate with Major Mental Illness in the Finnish population

Variation near MTNR1A associates with early development and interacts with seasons

scientific article published on 07 October 2019

Winter is coming: nightmares and sleep problems during seasonal affective disorder

artículo científico publicado en 2016

Lista de obras de Tiina Paunio

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation

A genome-wide screen for acrophobia susceptibility loci in a Finnish isolate

A population-based association study of candidate genes for depression and sleep disturbance.

A population-specific HTR2B stop codon predisposes to severe impulsivity

AMIGO-Kv2.1 Potassium Channel Complex Is Associated With Schizophrenia-Related Phenotypes

An association between both low and high birth weight and increased disorganized and negative symptom severity in schizophrenia and other psychoses

An association between high birth weight and schizophrenia in a Finnish schizophrenia family study sample

An interaction between NDE1 and high birth weight increases schizophrenia susceptibility

Analysis of detailed phenotype profiles reveals CHRNA5-CHRNA3-CHRNB4 gene cluster association with several nicotine dependence traits

Association between Dopamine Receptor D2 (DRD2) Variations rs6277 and rs1800497 and Cognitive Performance According to Risk Type for Psychosis: A Nested Case Control Study in a Finnish Population Sample

Association of AKT1 with verbal learning, verbal memory, and regional cortical gray matter density in twins

Association of a nonsynonymous variant of DAOA with visuospatial ability in a bipolar family sample

CRY2 is associated with depression

Childhood adversities and quality of sleep in adulthood: A population-based study of 26,000 Finns

Circadian clock-related polymorphisms in seasonal affective disorder and their relevance to diurnal preference

Common Genetic Variation Near Melatonin Receptor 1A Gene Linked to Job-Related Exhaustion in Shift Workers

Common variants at VRK2 and TCF4 conferring risk of schizophrenia

Common variants conferring risk of schizophrenia

Comparing cognitive-behavioural psychotherapy and psychoeducation for non-specific symptoms associated with indoor air: a randomised control trial protocol

Contribution of adenosine related genes to the risk of depression with disturbed sleep

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

DISC1 Gene Network Mutations In Major Mental Illness

Data on schizotypy and affective scales are gender and education dependent--study in the Northern Finland 1966 Birth Cohort

Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders

Development of sleep-wake rhythms during the first year of age

Differences and similarities of risk factors for suicidal ideation and attempts among patients with depressive or bipolar disorders

Early age at onset of bipolar disorder is associated with more severe clinical features but delayed treatment seeking

Early environment and neurobehavioral development predict adult temperament clusters

Environmental stress affects DNA methylation of a CpG rich promoter region of serotonin transporter gene in a nurse cohort

Epigenetic dysregulation of genes related to synaptic long-term depression among adolescents with depressive disorder and sleep symptoms

Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1.

Frontal Cortex Myo-Inositol Is Associated with Sleep and Depression in Adolescents: A Proton Magnetic Resonance Spectroscopy Study

Gene expression patterns in a rodent model for depression

Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia

Genome-wide scan of job-related exhaustion with three replication studies implicate a susceptibility variant at the UST gene locus

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

Haplotype analysis and identification of genes for a complex trait: examples from schizophrenia

Haplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effects

Helsinki alert of biodiversity and health

Heritability and number of quantitative trait loci of neurocognitive functions in families with schizophrenia

Heritability of cognitive functions in families with bipolar disorder

Identification of NCAN as a candidate gene for developmental dyslexia

Identifying Schizophrenia and Other Psychoses With Psychological Scales in the General Population

Impact of temperament on depression and anxiety symptoms and depressive disorder in a population-based birth cohort

Inter-tissue Networks Between the Basal Forebrain, Hippocampus, and Prefrontal Cortex in a Model for Depression Caused by Disturbed Sleep ⬇️

Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

Interaction between compound genetic risk for schizophrenia and high birth weight contributes to social anhedonia and schizophrenia in women

Interaction of early environment, gender and genes of monoamine neurotransmission in the aetiology of depression in a large population-based Finnish birth cohort

Large recurrent microdeletions associated with schizophrenia

Linkage analysis of schizophrenia controlling for population substructure

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

Maternal and paternal sleep during pregnancy in the Child-sleep birth cohort

Mixture model clustering of phenotype features reveals evidence for association of DTNBP1 to a specific subtype of schizophrenia

Neuregulin-1 genotype is associated with structural differences in the normal human brain

Nightmares as predictors of suicide: an extension study including war veterans

Nightmares: Prevalence among the Finnish General Adult Population and War Veterans during 1972-2007.

Nightmares: risk factors among the Finnish general adult population

No association of COMT (Val158Met) genotype with brain structure differences between men and women

Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant

Normal sleep development in infants: findings from two large birth cohorts

Parent-reported early sleep problems and internalising, externalising and dysregulation symptoms in toddlers

Partial sleep restriction activates immune response-related gene expression pathways: experimental and epidemiological studies in humans

Phenotype mining in CNV carriers from a population cohort

Phenotypic Translation of the Disc1 Network Highlights the Role of the Nde1 Locus, with Pharmacological Implications

Poor sleep predicts symptoms of depression and disability retirement due to depression

Predicting depression with psychopathology and temperament traits: the northern Finland 1966 birth cohort

Prolonged sleep restriction induces changes in pathways involved in cholesterol metabolism and inflammatory responses

RHD maternal-fetal genotype incompatibility and schizophrenia: extending the MFG test to include multiple siblings and birth order

RHD maternal-fetal genotype incompatibility increases schizophrenia susceptibility

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.

Replication of association between working memory and Reelin, a potential modifier gene in schizophrenia

Role of nicotine dependence in the association between the dopamine receptor gene DRD3 and major depressive disorder

Role of proprotein convertases in the pathogenic processing of the amyloidosis-associated form of secretory gelsolin

Search for cognitive trait components of schizophrenia reveals a locus for verbal learning and memory on 4q and for visual working memory on 2q.

Seasonal affective disorder and the G-protein beta-3-subunit C825T polymorphism

Seasonal variation in affective and other clinical symptoms among high-risk families for bipolar disorders in an Arctic population

Shared genetic background for regulation of mood and sleep: association of GRIA3 with sleep duration in healthy Finnish women