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Lista de obras de Thomas F. Hansen

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

artículo científico publicado en 2014

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

A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome

artículo científico publicado en 2022

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

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

Ancient human genome sequence of an extinct Palaeo-Eskimo

artículo científico publicado en 2010

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

artículo científico publicado en 2006

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

artículo científico publicado en 2010

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 a dopamine beta-hydroxylase gene variant with depression in elderly women possibly reflecting noradrenergic dysfunction

scientific article published on 14 August 2007

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

artículo científico publicado en 2010

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

artículo científico publicado en 2011

Attitudes of stakeholders in psychiatry towards the inclusion of children in genomic research

artículo científico publicado en 2018

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

Cancer predisposition in mice deficient for the metastasis-associated Mts1(S100A4) gene

artículo científico publicado en 2004

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

Characterization of Familial and Sporadic Migraine

artículo científico publicado en 2019

Cognitive performance in elderly women: significance of the 19bp insertion/deletion polymorphism in the 5' flank of the dopamine beta-hydroxylase gene, educational level, body fat measures, serum triglyceride, alcohol consumption and age.

artículo científico publicado en 2007

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

Combinations of self-reported rhinitis, conjunctivitis, and asthma predicts IgE sensitization in more than 25,000 Danes

artículo científico publicado en 2021

Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families

article by Padhraig Gormley et al published September 2018 in Neuron

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

artículo científico publicado en 2012

Common variants conferring risk of schizophrenia

artículo científico publicado en 2009

Comorbidity of migraine with ADHD in adults

artículo científico publicado en 2018

Comparing migraine with and without aura to healthy controls using RNA sequencing

scientific article published on 19 May 2019

Connection between genetic and clinical data in bipolar disorder

artículo científico publicado en 2012

Copy number variations in affective disorders and meta-analysis

artículo científico publicado en 2011

Cross-sectional study identifies lower risk of Staphylococcus aureus nasal colonization in Danish blood donors with hidradenitis suppurativa symptoms

artículo científico publicado en 2020

DBDS Genomic Cohort, a prospective and comprehensive resource for integrative and temporal analysis of genetic, environmental and lifestyle factors affecting health of blood donors

scientific article published on 09 June 2019

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

artículo científico publicado en 2007

Diastolic dysfunction predicts new-onset atrial fibrillation and cardiovascular events in patients with acute myocardial infarction and depressed left ventricular systolic function: a CARISMA substudy

artículo científico publicado en 2010

Digital questionnaire platform in the Danish Blood Donor Study.

artículo científico publicado en 2016

Disruption of the neurexin 1 gene is associated with schizophrenia

artículo científico publicado en 2009

Dual association of a TRKA polymorphism with schizophrenia.

artículo científico publicado en 2011

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

Estrogen receptor alpha and risk for cognitive impairment in postmenopausal women

artículo científico publicado en 2006

Evaluation of shared genetic susceptibility loci between autoimmune diseases and schizophrenia based on genome-wide association studies

artículo científico publicado en 2016

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

artículo científico publicado en 2009

Familial analysis reveals rare risk variants for migraine in regulatory regions

artículo científico publicado en 2020

Functional significance of metastasis-inducing S100A4(Mts1) in tumor-stroma interplay

artículo científico publicado en 2004

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 Susceptibility Loci in Genomewide Association Study of Cluster Headache

artículo científico publicado en 2021

Genetic analyses of the human eye colours using a novel objective method for eye colour classification

artículo científico publicado en 2013

Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease

artículo científico publicado en 2020

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

artículo científico publicado en 2013

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 identifies 16 genomic regions associated with circulating cytokines at birth

scientific article published on 23 November 2020

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

artículo científico publicado en 2020

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

artículo científico publicado en 2011

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

scientific article published on 11 November 2019

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

Herpes Simplex Virus Type 1 infection is associated with suicidal behavior and first registered psychiatric diagnosis in a healthy population

artículo científico publicado en 2019

Higher burden of rare frameshift indels in genes related to synaptic transmission separate familial hemiplegic migraine from common types of migraine

artículo científico publicado en 2020

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

artículo científico publicado en 2015

Investigation of SNP rs2060546 Immediately Upstream to NTN4 in a Danish Gilles de la Tourette Syndrome Cohort

artículo científico publicado en 2016

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

Large recurrent microdeletions associated with schizophrenia

artículo científico publicado en 2008

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

artículo científico publicado en 2015

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

artículo científico publicado en 2011

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

artículo científico publicado en 2016

Migraine polygenic risk score associates with efficacy of migraine-specific drugs

artículo científico publicado en 2019

Molecular genetic overlap between migraine and major depressive disorder

scholarly article by Yuanhao Yang et al published 11 July 2018 in European Journal of Human Genetics

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

artículo científico publicado en 2015

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

article

Nosographic analysis of osmophobia and field testing of diagnostic criteria including osmophobia

artículo científico publicado en 2018

Polygenic risk score: use in migraine research.

artículo científico publicado en 2018

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

Predicting treatment response using pharmacy register in migraine

scientific article published on 02 April 2019

Prevalence and socio-demographic characteristics of persons who have never had a headache among healthy voluntary blood donors - a population-based study

scientific article published on 20 April 2020

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

artículo científico publicado en 2011

Proposed new diagnostic criteria for chronic migraine

artículo científico publicado en 2019

RNA Sequencing of Trigeminal Ganglia in Rattus Norvegicus after Glyceryl Trinitrate Infusion with Relevance to Migraine

artículo científico publicado en 2016

Reliability of clinical ICD-10 schizophrenia diagnoses

artículo científico publicado en 2005

Self-reported restless legs syndrome and involuntary leg movements during sleep are associated with symptoms of attention deficit hyperactivity disorder

scientific article published on 11 February 2019

Sequence analysis of 17 NRXN1 deletions.

artículo científico publicado en 2013

Stakeholders in psychiatry and their attitudes toward receiving pertinent and incident findings in genomic research. ⬇️

artículo científico publicado en 2017

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

artículo científico publicado en 2015

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 first step towards personalized risk prediction for common epilepsies

artículo científico publicado en 2019

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 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 one and the many: effects of the cell adhesion molecule pathway on neuropsychological function in psychosis

artículo científico publicado en 2013

The preferences of potential stakeholders in psychiatric genomic research regarding consent procedures and information delivery

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

Transcriptomic profiling of trigeminal nucleus caudalis and spinal cord dorsal horn

scientific article published on 30 April 2018

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

artículo científico publicado en 2008

Tyrosine hydroxylase Val81Met polymorphism: lack of association with schizophrenia.

artículo científico publicado en 2009

UGT polymorphisms and lamotrigine clearance during pregnancy.

artículo científico publicado en 2018

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

artículo científico publicado en 2011

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

artículo científico publicado en 2008

Whole transcriptome expression of trigeminal ganglia compared to dorsal root ganglia in Rattus Norvegicus.

artículo científico publicado en 2017

[Submicroscopic chromosomal anomalies as a cause of schizophrenia]

artículo científico publicado en 2008

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