Cargando…

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

Mental disorders have for the majority of cases an unknown etiology, but several studies indicate that neurodevelopmental changes happen in utero or early after birth. We performed a nested case–control study of the relation between blood levels of neuro-developmental (S100B, BDNF, and VEGF-A) and i...

Descripción completa

Detalles Bibliográficos
Autores principales:	Skogstrand, Kristin, Hagen, Christian Munch, Borbye-Lorenzen, Nis, Christiansen, Michael, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Werge, Thomas, Børglum, Anders, Mors, Ole, Nordentoft, Merethe, Mortensen, Preben Bo, Hougaard, David Michael
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group UK 2019
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6779749/ https://www.ncbi.nlm.nih.gov/pubmed/31591381 http://dx.doi.org/10.1038/s41398-019-0587-2

Ejemplares similares

Co-occurring hydrocephalus in autism spectrum disorder: a Danish population-based cohort study
por: Munch, Tina Nørgaard, et al.
Publicado: (2021)

Pharmacogenetic genotype and phenotype frequencies in a large Danish population-based case-cohort sample
por: Lunenburg, Carin A. T. C., et al.
Publicado: (2021)

Editorial: Biomarkers to predict, prevent and find the appropriate treatments of disorders in childhood
por: Skogstrand, Kristin, et al.
Publicado: (2022)

Schizophrenia-associated mt-DNA SNPs exhibit highly variable haplogroup affiliation and nuclear ancestry: Bi-genomic dependence raises major concerns for link to disease
por: Hagen, Christian M., et al.
Publicado: (2018)

Complex spatio-temporal distribution and genomic ancestry of mitochondrial DNA haplogroups in 24,216 Danes
por: Bybjerg-Grauholm, Jonas, et al.
Publicado: (2018)

Elevated polygenic burden for autism is associated with differential DNA methylation at birth
por: Hannon, Eilis, et al.
Publicado: (2018)

The genetic background of hydrocephalus in a population-based cohort: implication of ciliary involvement
por: Munch, Tina N, et al.
Publicado: (2023)

Polygenic risk score, psychosocial environment and the risk of attention-deficit/hyperactivity disorder
por: Østergaard, Søren D., et al.
Publicado: (2020)

Polygenic Heterogeneity Across Obsessive-Compulsive Disorder Subgroups Defined by a Comorbid Diagnosis
por: Strom, Nora I., et al.
Publicado: (2021)

Accuracy of haplotype estimation and whole genome imputation affects complex trait analyses in complex biobanks
por: Appadurai, Vivek, et al.
Publicado: (2023)

High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA
por: Poulsen, Jesper Buchhave, et al.
Publicado: (2016)

A large population-based investigation into the genetics of susceptibility to gastrointestinal infections and the link between gastrointestinal infections and mental illness
por: Nudel, Ron, et al.
Publicado: (2020)

Autism spectrum disorder (ASD) and attention-deficit/hyperactivity disorder (ADHD) have a similar burden of rare protein-truncating variants
por: Satterstrom, F. Kyle, et al.
Publicado: (2019)

Maternal pregnancy-related infections and autism spectrum disorder—the genetic perspective
por: Nudel, Ron, et al.
Publicado: (2022)

A large-scale genomic investigation of susceptibility to infection and its association with mental disorders in the Danish population
por: Nudel, Ron, et al.
Publicado: (2019)

Immunity and mental illness: findings from a Danish population-based immunogenetic study of seven psychiatric and neurodevelopmental disorders
por: Nudel, Ron, et al.
Publicado: (2019)

Correction: Immunity and mental illness: findings from a Danish population-based immunogenetic study of seven psychiatric and neurodevelopmental disorder
por: Nudel, Ron, et al.
Publicado: (2020)

Author Correction: Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder
por: Demontis, Ditte, et al.
Publicado: (2021)

Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder
por: Demontis, Ditte, et al.
Publicado: (2021)

Genome-wide by Environment Interaction Study of Stressful Life Events and Hospital-Treated Depression in the iPSYCH2012 Sample
por: Suppli, Nis P., et al.
Publicado: (2021)

Implementation of SCID Screening in Denmark
por: Bækvad-Hansen, Marie, et al.
Publicado: (2021)

RNA sequencing of archived neonatal dried blood spots
por: Bybjerg-Grauholm, Jonas, et al.
Publicado: (2016)

Accounting for age of onset and family history improves power in genome-wide association studies
por: Pedersen, Emil M., et al.
Publicado: (2022)

Genetic correlates of vitamin D-binding protein and 25-hydroxyvitamin D in neonatal dried blood spots
por: Albiñana, Clara, et al.
Publicado: (2023)

Delivery Modality Affect Neonatal Levels of Inflammation, Stress, and Growth Factors
por: Kiilerich, Pia, et al.
Publicado: (2021)

Genome-wide association study of school grades identifies genetic overlap between language ability, psychopathology and creativity
por: Rajagopal, Veera M., et al.
Publicado: (2023)

The Duffy-null genotype and risk of infection
por: Legge, Sophie E, et al.
Publicado: (2020)

The iPSYCH2012 case–cohort sample: new directions for unravelling genetic and environmental architectures of severe mental disorders
por: Pedersen, C B, et al.
Publicado: (2018)

Genome-wide scans using archived neonatal dried blood spot samples
por: Hollegaard, Mads V, et al.
Publicado: (2009)

Comparisons of 25 cerebrospinal fluid cytokines in a case–control study of 106 patients with recent-onset depression and 106 individually matched healthy subjects
por: Sørensen, Nina Vindegaard, et al.
Publicado: (2023)

A polygenic resilience score moderates the genetic risk for schizophrenia
por: Hess, Jonathan L., et al.
Publicado: (2019)

Associations between patterns in comorbid diagnostic trajectories of individuals with schizophrenia and etiological factors
por: Krebs, Morten Dybdahl, et al.
Publicado: (2021)

A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder
por: Martin, Joanna, et al.
Publicado: (2018)

Evaluation of whole genome amplified DNA to decrease material expenditure and increase quality
por: Bækvad-Hansen, Marie, et al.
Publicado: (2017)

Differential DNA methylation at birth associated with mental disorder in individuals with 22q11.2 deletion syndrome
por: Starnawska, A, et al.
Publicado: (2017)

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders
por: Weiner, Daniel J., et al.
Publicado: (2017)

Postpartum and non-postpartum depression: a population-based matched case-control study comparing polygenic risk scores for severe mental disorders
por: Munk-Olsen, Trine, et al.
Publicado: (2023)

Exploring Cuba’s population structure and demographic history using genome-wide data
por: Fortes-Lima, Cesar, et al.
Publicado: (2018)

Combinatorial batching of DNA for ultralow-cost detection of pathogenic variants
por: Stoltze, Ulrik Kristoffer, et al.
Publicado: (2023)

Language deficits in specific language impairment, attention deficit/hyperactivity disorder, and autism spectrum disorder: An analysis of polygenic risk
por: Nudel, Ron, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_hetclpls8i9co1vvt6cdk0k86h