Search Results - "Børglum, Anders Dupont"
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Analyzing the Role of MicroRNAs in Schizophrenia in the Context of Common Genetic Risk Variants
Published in JAMA psychiatry (Chicago, Ill.) (01-04-2016)“…The recent implication of 108 genomic loci in schizophrenia marked a great advancement in our understanding of the disease. Against the background of its…”
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Inactivation of the Schizophrenia-associated BRD1 gene in Brain Causes Failure-to-thrive, Seizure Susceptibility and Abnormal Histone H3 Acetylation and N-tail Clipping
Published in Molecular neurobiology (01-09-2021)“…Genetic studies have repeatedly shown that the Bromodomain containing 1 gene, BRD1 , is involved in determining mental health, and the importance of the BRD1…”
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Brain proteome changes in female Brd1+/− mice unmask dendritic spine pathology and show enrichment for schizophrenia risk
Published in Neurobiology of disease (01-04-2019)“…Genetic and molecular studies have implicated the Bromodomain containing 1 (BRD1) gene in the pathogenesis of schizophrenia and bipolar disorder. Accordingly,…”
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The psychiatric risk gene BRD1 modulates mitochondrial bioenergetics by transcriptional regulation
Published in Translational psychiatry (08-08-2022)“…Bromodomain containing 1 ( BRD1) encodes an epigenetic regulator that controls the expression of genetic networks linked to mental illness. BRD1 is essential…”
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High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA
Published in PloS one (18-04-2016)“…Stored neonatal dried blood spot (DBS) samples from neonatal screening programmes are a valuable diagnostic and research resource. Combined with information…”
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Quantitative assessment of methyl-esterification and other side reactions in a standard propionylation protocol for detection of histone modifications
Published in Proteomics (Weinheim) (01-07-2016)“…Histone modifications play an important role in regulating chromatin stability and gene expression, but to date, investigating them remains challenging. In…”
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DNA Methylation at the Neonatal State and at the Time of Diagnosis: Preliminary Support for an Association with the Estrogen Receptor 1, Gamma-Aminobutyric Acid B Receptor 1, and Myelin Oligodendrocyte Glycoprotein in Female Adolescent Patients with OCD
Published in Frontiers in psychiatry (18-03-2016)“…Obsessive-compulsive disorder (OCD) is a neuropsychiatric disorder. Non-genetic factors and their interaction with genes have attracted increasing attention…”
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Association of Childhood Exposure to Nitrogen Dioxide and Polygenic Risk Score for Schizophrenia With the Risk of Developing Schizophrenia
Published in JAMA network open (01-11-2019)“…Importance Schizophrenia is a highly heritable psychiatric disorder, and recent studies have suggested that exposure to nitrogen dioxide (NO2) during childhood…”
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Co-occurring hydrocephalus in autism spectrum disorder: a Danish population-based cohort study
Published in Journal of neurodevelopmental disorders (28-04-2021)“…The association between autism spectrum disorder and hydrocephalus is not well understood, despite demonstrated links between autism spectrum disorder and…”
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The Genome-Wide DNA Methylation Profile of Peripheral Blood Is Not Systematically Changed by Short-Time Storage at Room Temperature
Published in Epigenomes (01-12-2017)“…Background: Epigenetic epidemiology has proven an important research discipline in the delineation of diseases of complex etiology. The approach, in such…”
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Association Between Childhood Green Space, Genetic Liability, and the Incidence of Schizophrenia
Published in Schizophrenia bulletin (01-12-2020)“…Abstract Childhood exposure to green space has previously been associated with lower risk of developing schizophrenia later in life. It is unclear whether this…”
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The importance of data structure in statistical analysis of dendritic spine morphology
Published in Journal of neuroscience methods (15-02-2018)“…•Data collection for dendritic spine morphology often results in multilevel data structure.•The need for implementation of data structure in statistical models…”
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The Schizophrenia-Associated BRD1 Gene Regulates Behavior, Neurotransmission, and Expression of Schizophrenia Risk Enriched Gene Sets in Mice
Published in Biological psychiatry (1969) (01-07-2017)“…Abstract Background The schizophrenia-associated BRD1 gene encodes a transcriptional regulator whose comprehensive chromatin interactome is enriched with…”
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A genome-wide search for linkage to allergic rhinitis in Danish sib-pair families
Published in European journal of human genetics : EJHG (01-09-2012)“…Allergic rhinitis (AR) is a complex disorder with a polygenic, multifactorial aetiology. Twin studies have found the genetic contribution to be substantial. We…”
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A functional CD86 polymorphism associated with asthma and related allergic disorders
Published in Journal of medical genetics (01-08-2007)“…Background: Several studies have documented a substantial genetic component in the aetiology of allergic diseases and a number of atopy susceptibility loci…”
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Differential activity of transcribed enhancers in the prefrontal cortex of 537 cases with schizophrenia and controls
Published in Molecular psychiatry (01-11-2019)“…Transcription at enhancers is a widespread phenomenon which produces so-called enhancer RNA (eRNA) and occurs in an activity-dependent manner. However, the…”
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Schizophrenia risk variants affecting microRNA function and site-specific regulation of NT5C2 by miR-206
Published in European neuropsychopharmacology (01-09-2016)“…Abstract Despite the identification of numerous schizophrenia-associated genetic variants, few have been examined functionally to identify and characterize the…”
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Genomics of mental disorders
Published in Ugeskrift for læger (10-11-2014)“…The heritability of mental disorders is high, but it has been very difficult to unravel the genetic architecture. In the past five years, unprecedented…”
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Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations
Published in Journal of medical genetics (01-12-2001)“…Mutations in α-tropomyosin (TPM1), 5 troponin T (TNNT2), 5 6 troponin I (TNNI3), 6 cardiac α-actin (ACTC), 7 titin (TTN), 8 and the essential (MYL3) and the…”
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Development and application of linkage analysis in genetic diagnosis of familial hypertrophic cardiomyopathy
Published in Journal of medical genetics (01-03-2001)“…[...]the pathogenic impact of any amino acid variation identified needs to be based on substantial evidence since a genetic diagnosis may have profound…”
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