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Markus Maria Nöthen

Arzt

Name	Markus Maria Nöthen
Time	2004- (Wirkungsdaten)
Place	Bonn (Wirkungsort) Deutschland
Gender	männlich
Academic degree	Prof. Dr.
Profession	Arzt (characteristic profession)
Variant	Markus M. Nöthen Markus Nöthen M. M. Nöthen M. Nöthen Markus M. Noethen Markus Noethen Markus M. Nothen Markus Nothen
Related	Institut für Humangenetik (Bonn) (Direktor) (01.04.2008-) Humangenetik (Thema)
Source	https://www.uni-bonn.de/de/forschung-lehre/forschungsprofil/transdisziplinaere-forschungsbereiche/tra-3-life-1/mitgliederverzeichnis/markus-noethen (Stand: 09.05.2023)
Record type	Person
GND-Identifier	1069221139
Record ID	1069221139
Involved in show all Exome sequencing points to pathogenic ATM variants in gastric cancer Within- and between-family genetic effects on educational achievement vary across countries and ages Author Correction: Fine-mapping genomic loci refines bipolar disorder risk genes Germany’s national genomDE strategy Implications of monogenic bicuspid aortic valve (BAV) forms among sporadic BAV patients Neurobiological correlates of schizophrenia-specific and highly pleiotropic genetic risk scores for neuropsychiatric disorders Fine-mapping genomic loci refines bipolar disorder risk genes Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings Evidence for a transgenerational mutational signature from ionizing radiation exposure in humans Genetisch informierte Therapie in der Psychiatrie: neue Dynamik durch APOE und Antikörpertherapie der Alzheimer-Krankheit Genetic and environmental contributions to epigenetic aging across adolescence and young adulthood GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets Ein Geburtstagsgruß für Thomas Cremer zum 80. Geburtstag Exemplar scoring identifies genetically separable phenotypes of lithium responsive bipolar disorder Genetische Diagnostik bei psychischen Erkrankungen im Erwachsenenalter = Genetic diagnostics of mental health disorders in adulthood Socioeconomic position interacts with the genetic effect of a CRP gene common variant to influence C-reactive protein values Longitudinal markers of cognitive procedural learning in fronto-striatal circuits and putative effects of a BDNF plasticity-related variant Genomic analysis of intracranial and subcortical brain volumes yields polygenic scores accounting for variation across ancestries Multi-omics profiling of DNA methylation and gene expression alterations in human cocaine use disorder Associations between antagonistic SNPs for neuropsychiatric disorders and human brain structure Multi-omics analyses of the environMENTAL project provide insights into mental health and disease Genetische Diagnostik bei psychischen Erkrankungen im Erwachsenenalter Haplotype analysis identifies functional elements in monoclonal gammopathy of unknown significance Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings Exploring the genetics of lithium response in bipolar disorders 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 Genetic associations of cardiovascular risk genes in European patients with coronary artery spasm Lithium response in bipolar disorder is associated with focal adhesion and PI3K-Akt networks: a multi-omics replication study Männlicher Haarausfall – was uns unsere Gene verraten Fine-mapping genomic loci refines bipolar disorder risk genes Fine-mapping genomic loci refines bipolar disorder risk genes GestaltMatcher Database - a FAIR database for medical imaging data of rare disorders Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings Evidence for a shared genetic contribution to loneliness and borderline personality disorder Abelson Helper Integration Site 1 haplotypes and peripheral blood expression associates with lithium response and immunomodulation in bipolar patients Deeplasia: deep learning for bone age assessment validated on skeletal dysplasias European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss Effects of urban living environments on mental health in adults Association between urinary iodine excretion, genetic disposition and fluid intelligence in children, adolescents and young adults: the DONALD study Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology A systematic evaluation of machine learning-based biomarkers for major depressive disorder across modalities Genetic, individual, and familial risk correlates of brain network controllability in major depressive disorder Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores IFN-γ secretion of PBMC from non-drug-allergic control persons: Considerations for the validity of a positive lymphocyte transformation test The co-localisation with specific neurotransmitter systems discriminates schizophrenia patients from healthy controls [Abstract] Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants 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 A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy Genetic and functional analyses implicate microRNA 499A in bipolar disorder development Analysis of associations between dietary patterns, genetic disposition, and cognitive function in data from UK Biobank The serotonin receptor 3E variant is a risk factor for female IBS-D Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers Behavioural and functional evidence revealing the role of RBFOX1 variation in multiple psychiatric disorders and traits Author Correction: LAMP-Seq enables sensitive, multiplexed COVID-19 diagnostics using molecular barcoding Correction: Combining schizophrenia and depression polygenic risk scores improves the genetic prediction of lithium response in bipolar disorder patients Borderline personality disorder and the big five: molecular genetic analyses indicate shared genetic architecture with neuroticism and openness Investigating the phenotypic and genetic associations between personality traits and suicidal behavior across major mental health diagnoses

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Markus Maria Nöthen

Exome sequencing points to pathogenic ATM variants in gastric cancer

Within- and between-family genetic effects on educational achievement vary across countries and ages

Author Correction: Fine-mapping genomic loci refines bipolar disorder risk genes

Germany’s national genomDE strategy

Implications of monogenic bicuspid aortic valve (BAV) forms among sporadic BAV patients

Neurobiological correlates of schizophrenia-specific and highly pleiotropic genetic risk scores for neuropsychiatric disorders

Fine-mapping genomic loci refines bipolar disorder risk genes

Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings

Evidence for a transgenerational mutational signature from ionizing radiation exposure in humans

Genetisch informierte Therapie in der Psychiatrie: neue Dynamik durch APOE und Antikörpertherapie der Alzheimer-Krankheit

Genetic and environmental contributions to epigenetic aging across adolescence and young adulthood

GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets

Ein Geburtstagsgruß für Thomas Cremer zum 80. Geburtstag

Exemplar scoring identifies genetically separable phenotypes of lithium responsive bipolar disorder

Genetische Diagnostik bei psychischen Erkrankungen im Erwachsenenalter = Genetic diagnostics of mental health disorders in adulthood

Socioeconomic position interacts with the genetic effect of a CRP gene common variant to influence C-reactive protein values

Longitudinal markers of cognitive procedural learning in fronto-striatal circuits and putative effects of a BDNF plasticity-related variant

Genomic analysis of intracranial and subcortical brain volumes yields polygenic scores accounting for variation across ancestries

Multi-omics profiling of DNA methylation and gene expression alterations in human cocaine use disorder

Associations between antagonistic SNPs for neuropsychiatric disorders and human brain structure

Multi-omics analyses of the environMENTAL project provide insights into mental health and disease

Genetische Diagnostik bei psychischen Erkrankungen im Erwachsenenalter

Haplotype analysis identifies functional elements in monoclonal gammopathy of unknown significance

Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings

Exploring the genetics of lithium response in bipolar disorders

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

Genetic associations of cardiovascular risk genes in European patients with coronary artery spasm

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

Männlicher Haarausfall – was uns unsere Gene verraten

Fine-mapping genomic loci refines bipolar disorder risk genes

Fine-mapping genomic loci refines bipolar disorder risk genes

GestaltMatcher Database - a FAIR database for medical imaging data of rare disorders

Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings

Evidence for a shared genetic contribution to loneliness and borderline personality disorder

Abelson Helper Integration Site 1 haplotypes and peripheral blood expression associates with lithium response and immunomodulation in bipolar patients

Deeplasia: deep learning for bone age assessment validated on skeletal dysplasias

European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation

Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss

Effects of urban living environments on mental health in adults

Association between urinary iodine excretion, genetic disposition and fluid intelligence in children, adolescents and young adults: the DONALD study

Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence

Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology

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

Genetic, individual, and familial risk correlates of brain network controllability in major depressive disorder

Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores

IFN-γ secretion of PBMC from non-drug-allergic control persons: Considerations for the validity of a positive lymphocyte transformation test

The co-localisation with specific neurotransmitter systems discriminates schizophrenia patients from healthy controls [Abstract]

Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

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

A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy

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

Analysis of associations between dietary patterns, genetic disposition, and cognitive function in data from UK Biobank

The serotonin receptor 3E variant is a risk factor for female IBS-D

Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers

Behavioural and functional evidence revealing the role of RBFOX1 variation in multiple psychiatric disorders and traits

Author Correction: LAMP-Seq enables sensitive, multiplexed COVID-19 diagnostics using molecular barcoding

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

Borderline personality disorder and the big five: molecular genetic analyses indicate shared genetic architecture with neuroticism and openness

Investigating the phenotypic and genetic associations between personality traits and suicidal behavior across major mental health diagnoses