Filtros de búsqueda

Lista de obras de Thomas Werge

100 ancient genomes show repeated population turnovers in Neolithic Denmark

artículo científico publicado en 2024

22q11.2 Deletion Syndrome Is Associated With Impaired Auditory Steady-State Gamma Response

artículo científico publicado en 2017

3D facial landmarks: Inter-operator variability of manual annotation

artículo científico publicado en 2014

A comprehensive family-based replication study of schizophrenia genes

artículo científico publicado en 2013

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

A genetic deconstruction of neurocognitive traits in schizophrenia and bipolar disorder

artículo científico publicado en 2013

A genetic investigation of sex bias in the prevalence of attention deficit hyperactivity disorder

article

A genome-wide association study of shared risk across psychiatric disorders implicates gene regulation during fetal neurodevelopment

artículo científico publicado en 2019

A large population-based investigation into the genetics of susceptibility to gastrointestinal infections and the link between gastrointestinal infections and mental illness

artículo científico publicado en 2020

A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia

artículo científico publicado en 2010

A large-scale genome-wide association study meta-analysis of cannabis use disorder

artículo científico publicado en 2020

A large-scale genomic investigation of susceptibility to infection and its association with mental disorders in the Danish population

scientific article published on 11 November 2019

A major role for common genetic variation in anxiety disorders

artículo científico publicado en 2019

A polygenic resilience score moderates the genetic risk for schizophrenia

artículo científico publicado en 2019

A possible association between schizophrenia and GRIK3 polymorphisms in a multicenter sample of Scandinavian origin (SCOPE).

artículo científico publicado en 2008

A rare variant in MYH6 is associated with high risk of sick sinus syndrome

artículo científico publicado en 2011

A study of the genetic architecture of social responsiveness in families with parental schizophrenia or bipolar disorder and population-based controls

artículo científico publicado en 2023

AMPK signaling linked to the schizophrenia-associated 1q21.1 deletion is required for neuronal and sleep maintenance

artículo científico

ASD and ADHD have a similar burden of rare protein-truncating variants

ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties

scientific article published on 03 January 2017

Adolescent residential mobility, genetic liability and risk of schizophrenia, bipolar disorder and major depression

artículo científico publicado en 2020

Advice on the genotyping of CYP2C19: comments on a recent article

artículo científico publicado en 2008

Altered auditory processing and effective connectivity in 22q11.2 deletion syndrome

artículo científico publicado en 2018

An Empirical Bayes Mixture Model for Effect Size Distributions in Genome-Wide Association Studies

artículo científico publicado en 2015

An evaluation of the genetic-matched pair study design using genome-wide SNP data from the European population

artículo científico publicado en 2009

An exploratory model for G×E interaction on hippocampal volume in schizophrenia; obstetric complications and hypoxia-related genes

article

An intron 1 polymorphism in the cholecystokinin-A receptor gene associated with schizophrenia in males.

artículo científico publicado en 2009

Analysis of coding-polymorphisms in NOTCH-related genes reveals NUMBL poly-glutamine repeat to be associated with schizophrenia in Brazilian and Danish subjects

artículo científico publicado en 2006

Analysis of genes within the schizophrenia-linked 22q11.2 deletion identifies interaction of night owl/LZTR1 and NF1 in GABAergic sleep control

artículo científico publicado en 2020

Analysis of heterogeneity and epistasis in physiological mixed populations by combined structural equation modelling and latent class analysis

artículo científico publicado en 2008

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

Ancient genomes from Iceland reveal the making of a human population

artículo científico publicado en 2018

Antidepressive-drug-induced bodyweight gain is associated with polymorphisms in genes coding for COMT and TPH1.

artículo científico publicado en 2009

Antipsychotic-like effect of the muscarinic acetylcholine receptor agonist BuTAC in non-human primates

artículo científico publicado en 2015

Apolipoprotein D is associated with long-term outcome in patients with schizophrenia

artículo científico publicado en 2006

Association Between Childhood Green Space, Genetic Liability, and the Incidence of Schizophrenia

artículo científico publicado en 2020

Association Study of Nonsynonymous Single Nucleotide Polymorphisms in Schizophrenia

article by Noa Carrera et al published January 2012 in Biological Psychiatry

Association analysis of ANK3 gene variants in nordic bipolar disorder and schizophrenia case-control samples

article

Association analysis of PALB2 and BRCA2 in bipolar disorder and schizophrenia in a scandinavian case-control sample

article

Association analysis of schizophrenia on 18 genes involved in neuronal migration: MDGA1 as a new susceptibility gene

artículo científico publicado en 2008

Association between Mental Disorders and Subsequent Medical Conditions

artículo científico publicado en 2020

Association between a disrupted-in-schizophrenia 1 (DISC1) single nucleotide polymorphism and schizophrenia in a combined Scandinavian case-control sample.

artículo científico publicado en 2008

Association between a genetic variant in the serotonin transporter gene (SLC6A4) and suicidal behavior in patients with schizophrenia

artículo científico publicado en 2012

Association between methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and age of onset in schizophrenia

artículo científico publicado en 2010

Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large European Cohort

artículo científico publicado en 2015

Association of Childhood Exposure to Nitrogen Dioxide and Polygenic Risk Score for Schizophrenia With the Risk of Developing Schizophrenia

scientific article published on 01 November 2019

Association of GRIN1 and GRIN2A-D with schizophrenia and genetic interaction with maternal herpes simplex virus-2 infection affecting disease risk

artículo científico publicado en 2011

Association of MCTP2 gene variants with schizophrenia in three independent samples of Scandinavian origin (SCOPE).

artículo científico publicado en 2009

Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank

scholarly article by Miruna C. Barbu et al published July 2018 in Biological Psychiatry: Cognitive Neuroscience and Neuroimaging

Association of the 120-bp duplication in the dopamine D4 receptor gene and schizophrenia in a sample of Danish subjects

artículo científico publicado en 2005

Association of the leucine-7 to proline-7 variation in the signal sequence of neuropeptide Y with major depression

artículo científico publicado en 2012

Association study of PDE4B gene variants in Scandinavian schizophrenia and bipolar disorder multicenter case-control samples

artículo científico publicado en 2010

Associations between social cognition, skills, and function and subclinical negative and positive symptoms in 22q11.2 deletion syndrome

artículo científico publicado en 2016

At-risk variant in TCF7L2 for type II diabetes increases risk of schizophrenia.

artículo científico publicado en 2011

Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants

artículo científico publicado en 2019

Brain expressed microRNAs implicated in schizophrenia etiology

artículo científico publicado en 2007

CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits

artículo científico publicado en 2017

CYP2D6 genotype predicts antipsychotic side effects in schizophrenia inpatients: a retrospective matched case-control study

artículo científico publicado en 2009

Candidate gene analysis of the human natural killer-1 carbohydrate pathway and perineuronal nets in schizophrenia: B3GAT2 is associated with disease risk and cortical surface area

artículo científico publicado en 2010

Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles

artículo científico publicado en 2014

Cognitive impairment in elderly women: the relative importance of selected genes, lifestyle factors, and comorbidities

scientific article published on June 2006

Combinations of Genetic Data Present in Bipolar Patients, but Absent in Control Persons

artículo científico publicado en 2015

Combinations of SNPs related to signal transduction in bipolar disorder

artículo científico publicado en 2011

Common risk variants identified in autism spectrum disorder

Common variant at 16p11.2 conferring risk of psychosis.

artículo científico publicado en 2012

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

Common variants on 8p12 and 1q24.2 confer risk of schizophrenia

artículo científico publicado en 2011

Comorbidities to restless legs syndrome – results from the Danish blood donor study

Complex spatio-temporal distribution and genogeographic affinity of mitochondrial DNA haplogroups in 24,216 Danes

Complex spatio-temporal distribution and genomic ancestry of mitochondrial DNA haplogroups in 24,216 Danes

scientific article published in PLoS ONE

Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci

artículo científico publicado en 2022

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

artículo científico publicado en 2016

Copy number variations in affective disorders and meta-analysis.

artículo científico publicado en 2011

Copy number variations of chromosome 16p13.1 region associated with schizophrenia

artículo científico publicado en 2009

Correction: Immunity and mental illness: findings from a Danish population-based immunogenetic study of seven psychiatric and neurodevelopmental disorder

artículo científico publicado en 2020

Correction: Improved Detection of Common Variants Associated with Schizophrenia and Bipolar Disorder Using Pleiotropy-Informed Conditional False Discovery Rate

artículo científico publicado en 2015

Correlation between genetic and geographic structure in Europe

artículo científico publicado en 2008

D-amino acid oxidase activator gene (DAOA) variation affects cerebrospinal fluid homovanillic acid concentrations in healthy Caucasians

artículo científico publicado en 2012

DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder

artículo científico publicado en 2012

DTNBP1, NRG1, DAOA, DAO and GRM3 polymorphisms and schizophrenia: an association study

artículo científico publicado en 2009

Diagnostic agreement of schizophrenia spectrum disorders among chronic patients with functional psychoses

artículo científico publicado en 2006

Diagnostic stability among chronic patients with functional psychoses: an epidemiological and clinical study

artículo científico publicado en 2007

Differential DNA methylation at birth associated with mental disorder in individuals with 22q11.2 deletion syndrome

artículo científico

Discovery Of The First Genome-Wide Significant Risk Loci For ADHD

scholarly article published 3 June 2017

Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

artículo científico publicado en 2018

Disruption of the neurexin 1 gene is associated with schizophrenia

artículo científico publicado en 2009

Does pharmacogenetic testing for CYP450 2D6 and 2C19 among patients with diagnoses within the schizophrenic spectrum reduce treatment costs?

artículo científico publicado en 2013

Dose-Specific Adverse Drug Reaction Identification in Electronic Patient Records: Temporal Data Mining in an Inpatient Psychiatric Population

artículo científico publicado en 2014

Dual association of a TRKA polymorphism with schizophrenia.

artículo científico publicado en 2011

Dysbindin and d-amino-acid-oxidase gene polymorphisms associated with positive and negative symptoms in schizophrenia

artículo científico publicado en 2009

Dystrobrevin-binding protein 1 gene (DTNBP1) variants associated with cerebrospinal fluid homovanillic acid and 5-hydroxyindoleacetic acid concentrations in healthy volunteers

article

Effects of cannabinoid CB1 receptor agonism and antagonism on SKF81297-induced dyskinesia and haloperidol-induced dystonia in Cebus apella monkeys ⬇️

artículo científico publicado el 26 de octubre de 2010

Effects of postnatal anoxia on striatal dopamine metabolism and prepulse inhibition in rats

artículo científico publicado en 2004

Effects of prenatal exposure to chronic mild stress and toluene in rats

artículo científico publicado en 2005

Effects of the cannabinoid CB1 receptor agonist CP55,940 and antagonist SR141716A on d-amphetamine-induced behaviours in Cebus monkeys

artículo científico publicado en 2006

Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder

article

Elevated polygenic burden for autism is associated with differential DNA methylation at birth.

artículo científico publicado en 2018

Erratum to: Dose-Specific Adverse Drug Reaction Identification in Electronic Patient Records: Temporal Data Mining in an Inpatient Psychiatric Population

artículo científico publicado en 2014

Erratum: Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

artículo científico publicado en 2016

Erratum: Sequence analysis of 17 NRXN1 deletions

scholarly article published in American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Estimating Effect Sizes and Expected Replication Probabilities from GWAS Summary Statistics

artículo científico publicado en 2016

Estrogen receptor alpha and risk for cognitive impairment in postmenopausal women.

artículo científico publicado en 2006

Evaluating historical candidate genes for schizophrenia

artículo científico publicado en 2015

Evidence for a possible association of neurotrophin receptor (NTRK-3) gene polymorphisms with hippocampal function and schizophrenia

artículo científico publicado en 2009

Examining Sex-Differentiated Genetic Effects Across Neuropsychiatric and Behavioral Traits

artículo científico publicado en 2021

Expanding the range of ZNF804A variants conferring risk of psychosis

artículo científico publicado en 2010

Exploring Comorbidity Within Mental Disorders Among a Danish National Population

artículo científico publicado en 2019

FUT2-ABO epistasis increases the risk of early childhood asthma and Streptococcus pneumoniae respiratory illnesses

artículo científico publicado en 2020

GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia

artículo científico publicado en 2010

GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores.

artículo científico publicado en 2019

Gene-based analysis of regionally enriched cortical genes in GWAS data sets of cognitive traits and psychiatric disorders

artículo científico publicado en 2012

Genetic Markers of Human Evolution Are Enriched in Schizophrenia

artículo científico publicado en 2015

Genetic Variants Associated With Anxiety and Stress-Related Disorders: A Genome-Wide Association Study and Mouse-Model Study

scientific article published on 22 May 2019

Genetic factors underlying the bidirectional relationship between autoimmune and mental disorders - findings from a Danish population-based study

artículo científico publicado en 2020

Genetic liability to ADHD and substance use disorders in individuals with ADHD

artículo científico publicado en 2019

Genetic liability to major depression and risk of childhood asthma

artículo científico publicado en 2020

Genetic predictors of educational attainment and intelligence test performance predict voter turnout

scientific article published on 09 November 2020

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

artículo científico publicado en 2013

Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

artículo científico publicado en 2016

Genetic risk scores for major psychiatric disorders and the risk of postpartum psychiatric disorders

scientific article published on 11 November 2019

Genetic stratification of depression in UK Biobank

scientific article published on 24 May 2020

Genetic susceptibility factors for multiple chemical sensitivity revisited

artículo científico publicado en 2010

Genetics of suicide attempts in individuals with and without mental disorders: a population-based genome-wide association study

article

Genome-Wide Association Study of Genetic Variants in LPS-Stimulated IL-6, IL-8, IL-10, IL-1ra and TNF-α Cytokine Response in a Danish Cohort

artículo científico publicado en 2013

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.

artículo científico publicado en 2018

Genome-wide association study across pediatric central nervous system tumors implicates shared predisposition and points to 1q25.2 (PAPPA2) and 11p12 (LRRC4C) as novel candidate susceptibility loci

artículo científico publicado en 2020

Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth

scientific article published on 23 November 2020

Genome-wide association study identifies 30 loci associated with bipolar disorder.

artículo científico publicado en 2019

Genome-wide association study identifies 48 common genetic variants associated with handedness

artículo científico publicado en 2020

Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa.

artículo científico publicado en 2019

Genome-wide association study identifies four loci associated with eruption of permanent teeth

artículo científico publicado en 2011

Genome-wide association study implicates CHRNA2 in cannabis use disorder

artículo científico publicado en 2019

Genome-wide association study implicatesCHRNA2in cannabis use disorder

Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.

artículo científico publicado en 2010

Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

artículo científico publicado en 2021

Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression

scientific article published on 11 November 2019

Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness

artículo científico publicado en 2015

Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity

artículo científico publicado en 2017

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals

artículo científico publicado en 2020

Genotyping of the 19-bp insertion/deletion polymorphism in the 5' flank of beta-hydroxylase gene by dissociation analysis of allele-specific PCR products

artículo científico publicado en 2005

Gestational age-dependent development of the neonatal metabolome

scientific article published on 17 September 2020

Heritability of Schizophrenia and Schizophrenia Spectrum Based on the Nationwide Danish Twin Register

artículo científico publicado en 2017

High loading of polygenic risk in cases with chronic schizophrenia

artículo científico publicado en 2015

Identification and characterization of a tandem repeat in exon III of the dopamine receptor D4 (DRD4) gene in cetaceans

artículo científico publicado en 2006

Identification and characterization of tandem repeats in exon III of dopamine receptor D4 (DRD4) genes from different mammalian species

artículo científico publicado en 2005

Identification of common genetic risk variants for autism spectrum disorder

artículo científico publicado en 2019

Identification of rare high-risk copy number variants affecting the dopamine transporter gene in mental disorders

artículo científico publicado en 2015

Immunity and mental illness: findings from a Danish population-based immunogenetic study of seven psychiatric and neurodevelopmental disorders

artículo científico publicado en 2019

Impaired glutathione synthesis in schizophrenia: convergent genetic and functional evidence

artículo científico publicado en 2007

Improved detection of common variants associated with schizophrenia and bipolar disorder using pleiotropy-informed conditional false discovery rate

artículo científico publicado en 2013

Improved detection of common variants associated with schizophrenia by leveraging pleiotropy with cardiovascular-disease risk factors

artículo científico publicado en 2013

Individualization of treatments with drugs metabolized by CES1: combining genetics and metabolomics.

artículo científico publicado en 2015

Interaction between genetic polymorphisms and stressful life events in first episode depression

artículo científico publicado en 2009

International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci

scientific article published on 08 October 2019

Is an Early Age at Illness Onset in Schizophrenia Associated With Increased Genetic Susceptibility? Analysis of Data From the Nationwide Danish Twin Register

artículo científico publicado en 2017

Kynurenine 3-monooxygenase (KMO) polymorphisms in schizophrenia: An association study

Kynurenine 3-monooxygenase polymorphisms: relevance for kynurenic acid synthesis in patients with schizophrenia and healthy controls

artículo científico publicado en 2012

Lack of association between the regulator of G-protein signaling 4 (RGS4) rs951436 polymorphism and schizophrenia.

artículo científico publicado en 2012

Lack of association between two dopamine D2 receptor gene polymorphisms and schizophrenia

article

Lack of association of the serotonin transporter gene promoter region polymorphism, 5-HTTLPR, including rs25531 with cigarette smoking and alcohol consumption.

artículo científico publicado en 2009

Large recurrent microdeletions associated with schizophrenia

artículo científico publicado en 2008

Large-scale genome-wide association meta-analysis of endometriosis reveals 13 novel loci and genetically-associated comorbidity with other pain conditions

Largest genome-wide association study for PTSD identifies genetic risk loci in European and African ancestries and implicates novel biological pathways

article published in 2018

Lessons to be Learned From 22q2.11 Syndromes-Reply

artículo científico publicado en 2017

Leveraging Genomic Annotations and Pleiotropic Enrichment for Improved Replication Rates in Schizophrenia GWAS.

artículo científico publicado en 2016

Leveraging both individual-level genetic data and GWAS summary statistics increases polygenic prediction

artículo científico publicado en 2020

Linkage and whole genome sequencing identify a locus on 6q25-26 for formal thought disorder and implicate MEF2A regulation

artículo científico publicado en 2015

Links between cardiovascular disease and osteoporosis in postmenopausal women: serum lipids or atherosclerosis per se?

artículo científico publicado en 2006

Low frequency and rare coding variation contributes to multiple sclerosis risk

Maternal pregnancy-related infections and autism spectrum disorder—the genetic perspective

scientific article published in 2022

Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness

artículo científico publicado en 2011

Meta-analysis of heterogeneous data sources for genome-scale identification of risk genes in complex phenotypes

artículo científico publicado en 2011

Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and age at onset of schizophrenia: no consistent evidence for an association in the Nordic population

scientific article published on 17 October 2012

MicroRNAs show mutually exclusive expression patterns in the brain of adult male rats

artículo científico publicado en 2009

Mining of hospital laboratory information systems: a model study defining age- and gender-specific reference intervals and trajectories for plasma creatinine in a pediatric population

artículo científico publicado en 2015

Mitochondrial DNA SNPs associated with Schizophrenia exhibit Highly Variable Inter-allelic Haplogroup Affiliation and Nuclear Genogeographic Affinity: Bi-Genomic Linkage Disequilibrium raises Major Concerns for Link to Disease

Mutation screening of the glutamate cysteine ligase modifier (GCLM) gene in patients with schizophrenia.

artículo científico publicado en 2009

Mutations in NRXN1 in a family multiply affected with brain disorders: NRXN1 mutations and brain disorders

artículo científico publicado en 2012

Negation scope and spelling variation for text-mining of Danish electronic patient records ⬇️

artículo científico publicado en 2014

Neuropeptide Y genes and suicidal behaviour among schizophrenic patients

artículo científico publicado en 2013

New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis

artículo científico publicado en 2015

No association between DGKH and bipolar disorder in a Scandinavian case–control sample

No association between the -399 C > T polymorphism of the neuropeptide Y gene and schizophrenia, unipolar depression or panic disorder in a Danish population

artículo científico publicado en 2006

No association of polymorphisms in human endogenous retrovirus K18 and CD48 with schizophrenia

article

No influence of the polymorphisms CYP2C19 and CYP2D6 on the efficacy of cyclophosphamide, thalidomide, and bortezomib in patients with Multiple Myeloma

artículo científico publicado en 2010

No interactions between genetic polymorphisms and stressful life events on outcome of antidepressant treatment

artículo científico publicado en 2010

No significant association of the 5' end of neuregulin 1 and schizophrenia in a large Danish sample

artículo científico publicado en 2006

Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk

article

O4.6. GENOME-WIDE ASSOCIATION STUDY, HERITABILITY ESTIMATION AND POLYGENIC RISK ANALYSIS OF SUSCEPTIBILITY TO INFECTIONS IN 65,534 INDIVIDUALS WITH SEVERE MENTAL DISORDERS AND POPULATION CONTROLS.

artículo científico publicado en 2018

PCM1 is necessary for focal ciliary integrity and is a candidate for severe schizophrenia

artículo científico publicado en 2020

Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders.

artículo científico publicado en 2016

Pharmacogenetic genotype and phenotype frequencies in a large Danish population-based case-cohort sample

artículo científico publicado en 2021

Polygenic Risk and Progression to Bipolar or Psychotic Disorders Among Individuals Diagnosed With Unipolar Depression in Early Life

artículo científico publicado en 2020

Polygenic risk score, psychosocial environment and the risk of attention-deficit/hyperactivity disorder

artículo científico publicado en 2020

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

article

Polymorphisms in SREBF1 and SREBF2, two antipsychotic-activated transcription factors controlling cellular lipogenesis, are associated with schizophrenia in German and Scandinavian samples

artículo científico publicado en 2008

Polymorphisms of serotonin receptor 2A and 2C genes and COMT in relation to obesity and type 2 diabetes

artículo científico publicado en 2009

Population genomics of post-glacial western Eurasia

artículo científico publicado en 2024

Population genomics of the Viking world

scientific article published on 16 September 2020

Poster #64 RECRUITMENT STATUS OF THE TEA TRIAL: TOLERANCE AND EFFECT OF ANTIPSYCHOTICS IN CHILDREN AND ADOLESCENTS WITH PSYCHOSIS. AN INVESTIGATOR-INITIATED, PHASE IV, RANDOMISED DOUBLE-BLIND MULTI-CENTRE TRIAL OF THE BENEFITS AND HARMS OF ARIPIPRAZO

article by Anne K. Pagsberg et al published April 2012 in Schizophrenia Research

Postpartum and non-postpartum depression: a population-based matched case-control study comparing polygenic risk scores for severe mental disorders

Prenatal stress may increase vulnerability to life events: comparison with the effects of prenatal dexamethasone

artículo científico publicado en 2005

Prevalence of rearrangements in the 22q11.2 region and population-based risk of neuropsychiatric and developmental disorders in a Danish population: a case-cohort study

scientific article published on 07 June 2018

Prevalence of restless legs syndrome and associated factors in an otherwise healthy population: results from the Danish Blood Donor Study

artículo científico publicado en 2017

Promoter variants in IL18 are associated with onset of depression in patients previously exposed to stressful-life events

artículo científico publicado en 2011

Psychiatric research ought to be central to long-term plans for psychiatry

artículo científico publicado en 2013

Psychopharmacology in a genomic perspective

artículo científico publicado en 2005

Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum

Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum

Redox dysregulation in the pathophysiology of schizophrenia and bipolar disorder: insights from animal models

artículo científico

Reduced neonatal brain-derived neurotrophic factor is associated with autism spectrum disorders

artículo científico publicado en 2019

Reliability of clinical ICD-10 schizophrenia diagnoses

artículo científico publicado en 2005

Replication and meta-analysis of common variants identifies a genome-wide significant locus in migraine.

artículo científico publicado en 2013

Replication study and meta-analysis in European samples supports association of the 3p21.1 locus with bipolar disorder

artículo científico publicado en 2012

Response to Boot et al. Letter

Risk of Psychiatric Disorders Among Individuals With the 22q11.2 Deletion or Duplication: A Danish Nationwide, Register-Based Study

artículo científico publicado en 2017

Roadmap for a precision-medicine initiative in the Nordic region

artículo científico publicado en 2019

Schizophrenia Spectrum Disorders in a Danish 22q11.2 Deletion Syndrome Cohort Compared to the Total Danish Population--A Nationwide Register Study

artículo científico publicado en 2016

Schizophrenia and oxidative stress: glutamate cysteine ligase modifier as a susceptibility gene

artículo científico publicado en 2006

Schizophrenia-associated mt-DNA SNPs exhibit highly variable haplogroup affiliation and nuclear ancestry: Bi-genomic dependence raises major concerns for link to disease

artículo científico publicado en 2018

Screening of congenital heart disease patients using multiplex ligation-dependent probe amplification: Early diagnosis of syndromic patients

Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction

artículo científico publicado en 2009

Serotonin transporter: evolution and impact of polymorphic transcriptional regulation

artículo científico publicado en 2005

Severe Parkinsonism and Creatine Kinase Increase After Low-Dose Aripiprazole Treatment in a Patient of African Descent

artículo científico publicado en 2017

Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders

artículo científico publicado en 2022

Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies

artículo científico publicado en 2020

Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap.

artículo científico publicado en 2018

Soluble urokinase-type plasminogen activator receptor levels in patients with schizophrenia

artículo científico publicado en 2014

Spatial fine-mapping for gene-by-environment effects identifies risk hot spots for schizophrenia

scientific article published in Nature Communications

The Anorexia Nervosa Genetics Initiative: Overview and Methods

article

The Danish 22q11 research initiative

artículo científico publicado en 2015

The Duffy-null genotype and risk of infection

artículo científico publicado en 2020

The acetylcholinesterase inhibitor galantamine inhibits d-amphetamine-induced psychotic-like behavior in Cebus monkeys

artículo científico publicado en 2007

The association between candidate migraine susceptibility loci and severe migraine phenotype in a clinical sample

artículo científico publicado en 2015

The catechol-O-methyltransferase (COMT) Val158Met genotype modulates working memory-related dorsolateral prefrontal response and performance in bipolar disorder.

artículo científico publicado en 2017

The complement control-related genes CSMD1 and CSMD2 associate to schizophrenia

artículo científico publicado en 2011

The estrogen hypothesis of schizophrenia implicates glucose metabolism: association study in three independent samples

artículo científico publicado en 2008

The gene encoding the melanin-concentrating hormone receptor 1 is associated with schizophrenia in a Danish case-control sample

artículo científico publicado en 2012

The genetic architecture of sporadic and multiple consecutive miscarriage

scientific article published on 25 November 2020

The iPSYCH2012 case-cohort sample: New directions for unravelling genetic and environmental architectures of severe mental disorders

The iPSYCH2012 case-cohort sample: new directions for unravelling genetic and environmental architectures of severe mental disorders.

artículo científico publicado en 2017

The impact of CYP2D6 and CYP2C19 polymorphisms on suicidal behavior and substance abuse disorder among patients with schizophrenia: a retrospective study.

artículo científico publicado en 2008

The influence of genetic constitution on migraine drug responses

artículo científico publicado en 2015

The muscarinic M1/M4 receptor agonist xanomeline exhibits antipsychotic-like activity in Cebus apella monkeys

artículo científico publicado en 2003

The selection landscape and genetic legacy of ancient Eurasians

artículo científico publicado en 2024

The tachykinin tale: molecular recognition in a historical perspective

artículo científico publicado en 2007

The tryptophan hydroxylase 1 (TPH1) gene, schizophrenia susceptibility, and suicidal behavior: a multi-centre case-control study and meta-analysis

artículo científico publicado en 2010

Three-cohort targeted gene screening reveals a non-synonymous TRKA polymorphism associated with schizophrenia

artículo científico publicado en 2009

Triton X-100 inhibits agonist-induced currents and suppresses benzodiazepine modulation of GABA(A) receptors in Xenopus oocytes

artículo científico publicado en 2009

Tryptophan hydroxylase gene 1 (TPH1) variants associated with cerebrospinal fluid 5-hydroxyindole acetic acid and homovanillic acid concentrations in healthy volunteers

artículo científico publicado en 2010

Two methylenetetrahydrofolate reductase gene (MTHFR) polymorphisms, schizophrenia and bipolar disorder: an association study

artículo científico publicado en 2008

Two rare deletions upstream of the NRXN1 gene (2p16.3) affecting the non-coding mRNA AK127244 segregate with diverse psychopathological phenotypes in a family

artículo científico publicado en 2015

Tyrosine hydroxylase Val81Met polymorphism: lack of association with schizophrenia.

artículo científico publicado en 2009

Using Electronic Patient Records to Discover Disease Correlations and Stratify Patient Cohorts

artículo científico publicado en 2011

Utility and adoption of CYP2D6 and CYP2C19 genotyping and its translation into psychiatric clinical practice

artículo científico publicado en 2011

Variable DNA methylation in neonates mediates the association between prenatal smoking and birth weight

Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 are associated with gestational duration

article

Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration

artículo científico publicado en 2019

Variation in the purinergic P2RX(7) receptor gene and schizophrenia

artículo científico publicado en 2008

Dominio Público Uruguay está sostenido por:

Acerca de Dominio Público Uruguay

Ayuda