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Andreas Josef Forstner

Arzt

Name	Andreas Josef Forstner
Ort	Bonn (Geburtsort) Marburg (Wirkungsort) Deutschland
Geschlecht	männlich
Akademischer Grad bzw. Titel	Dr. (Univ. Bonn) (2014)
Beruf	Arzt (charakteristischer Beruf)
Variante	Andreas J. Forstner A. J. Forstner Andreas Forstner
Beziehung	Rheinische Friedrich-Wilhelms-Universität Bonn (2014) Philipps-Universität Marburg. Zentrum für Humangenetik (2018-) Psychologie (Thema)
Quelle	Loop-Profil: https://loop.frontiersin.org/people/99191/bio (Stand: 01.04.2020) ResearchGate-Profil: https://www.researchgate.net/profile/Andreas_Forstner (Stand: 01.04.2020)
Datensatztyp	Person
GND-Nummer	1064967531
Datensatz-ID	1064967531
Beteiligt an alle anzeigen A meta-analysis of genome-wide studies of resilience in the German population Factor analysis of lifetime psychopathology and its brain morphometric and genetic correlates in a transdiagnostic sample The interplay between polygenic score for tumor necrosis factor-α, brain structural connectivity, and processing speed in major depression Lithium response in bipolar disorder is associated with focal adhesion and PI3K-Akt networks: a multi-omics replication study White and gray matter alterations in bipolar I and bipolar II disorder subtypes compared with healthy controls – exploring associations with disease course and polygenic risk Fine-mapping genomic loci refines bipolar disorder risk genes Fine-mapping genomic loci refines bipolar disorder risk genes A systematic evaluation of machine learning-based biomarkers for major depressive disorder across modalities Genetic diversity enhances gene discovery for bipolar disorder Comparative serum proteomic analysis of a selected protein panel in individuals with schizophrenia and bipolar disorder and the impact of genetic risk burden on serum proteomic profiles Genetic and functional analyses implicate microRNA 499A in bipolar disorder development Correction: Combining schizophrenia and depression polygenic risk scores improves the genetic prediction of lithium response in bipolar disorder patients Combining schizophrenia and depression polygenic risk scores improves the genetic prediction of lithium response in bipolar disorder patients Dendritic Cells: Neglected Modulators of Peripheral Immune Responses and Neuroinflammation in Mood Disorders? Apolipoprotein E Homozygous ε4 Allele Status: A Deteriorating Effect on Visuospatial Working Memory and Global Brain Structure Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder Cortical surface area alterations shaped by genetic load for neuroticism Response to therapeutic sleep deprivation: a naturalistic study of clinical and genetic factors and post-treatment depressive symptom trajectory Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders Identification of shared risk loci and pathways for bipolar disorder and schizophrenia Identification of shared risk loci and pathways for bipolar disorder and schizophrenia Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia

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Katalog der Deutschen Nationalbibliothek

Andreas Josef Forstner

A meta-analysis of genome-wide studies of resilience in the German population

Factor analysis of lifetime psychopathology and its brain morphometric and genetic correlates in a transdiagnostic sample

The interplay between polygenic score for tumor necrosis factor-α, brain structural connectivity, and processing speed in major depression

Lithium response in bipolar disorder is associated with focal adhesion and PI3K-Akt networks: a multi-omics replication study

White and gray matter alterations in bipolar I and bipolar II disorder subtypes compared with healthy controls – exploring associations with disease course and polygenic risk

Fine-mapping genomic loci refines bipolar disorder risk genes

Fine-mapping genomic loci refines bipolar disorder risk genes

A systematic evaluation of machine learning-based biomarkers for major depressive disorder across modalities

Genetic diversity enhances gene discovery for bipolar disorder

Comparative serum proteomic analysis of a selected protein panel in individuals with schizophrenia and bipolar disorder and the impact of genetic risk burden on serum proteomic profiles

Genetic and functional analyses implicate microRNA 499A in bipolar disorder development

Correction: Combining schizophrenia and depression polygenic risk scores improves the genetic prediction of lithium response in bipolar disorder patients

Combining schizophrenia and depression polygenic risk scores improves the genetic prediction of lithium response in bipolar disorder patients

Dendritic Cells: Neglected Modulators of Peripheral Immune Responses and Neuroinflammation in Mood Disorders?

Apolipoprotein E Homozygous ε4 Allele Status: A Deteriorating Effect on Visuospatial Working Memory and Global Brain Structure

Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders

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

Cortical surface area alterations shaped by genetic load for neuroticism

Response to therapeutic sleep deprivation: a naturalistic study of clinical and genetic factors and post-treatment depressive symptom trajectory

Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders

Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders

Identification of shared risk loci and pathways for bipolar disorder and schizophrenia

Identification of shared risk loci and pathways for bipolar disorder and schizophrenia

Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia