Markus Nöthen

Professor, Director

University Hospital Bonn

Germany

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About

Markus Nöthen is a Professor and Director at the University Hospital of Bonn, Germany. His research focuses on neurobiological correlates of genetic risk factors for neuropsychiatric disorders, as well as the impacts of genetic polymorphisms on various health conditions. Recent publications include studies on schizophrenia, brain structure associations, genetic architecture of COVID-19, and mental health challenges linked to environmental factors.

Articles (18)

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2025

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2020

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2020

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2020

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2020

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2020

Collaborators (72)

Xavier Farré Ramon

Fundació Institut d'Investigació en Ciències de la Salut Germans Trias i Pujol

SPAIN

Markus Nöthen

Research Interests

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About

Articles (18)

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

Haplotype analysis identifies functional elements in monoclonal gammopathy of unknown significance

Genetic polymorphisms affecting telomere length and their association with cardiovascular disease in the Heinz-Nixdorf-Recall study

Associations between antagonistic SNPs for neuropsychiatric disorders and human brain structure

A second update on mapping the human genetic architecture of COVID-19.

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

Addressing Global Environmental Challenges to Mental Health Using Population Neuroscience: A Review.

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

GWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors.

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

Beyond the Global Brain Differences: Intra-individual Variability Differences in 1q21.1 Distal and 15q11.2 BP1-BP2 Deletion Carriers.

Genome-wide association study of antisocial personality disorder diagnostic criteria provides evidence for shared risk factors across disorders.

Hepatic Expression of the Na+-Taurocholate Cotransporting Polypeptide Is Independent from Genetic Variation

Risk prediction for coronary heart disease by a genetic risk score - results from the Heinz Nixdorf Recall study.

Childhood maltreatment and cognitive functioning: the role of depression, parental education, and polygenic predisposition.

Polygenic risk for schizophrenia and schizotypal traits in non-clinical subjects.

Insights Into the Biology of Persistent Chemotherapy-Induced Alopecia via Genomic Approaches-An Avenue to Clinical Translation?

Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder.

Collaborators (72)

Xavier Farré Ramon

Pär Ingemar Johansson

Andrea Ganna

Mario Caceres

Masaki Fukunaga

Alisha Silvia Mercedes Hall

Sugirthan Sivalingam

Mario Falchi

Spase Petkoski

Steven Jones

Yohei Mikami

André G Uitterlinden

Joscha Böhnlein

Ute Hofmann

Mattia Cordioli

Louise MacGillivray

MITSUHIRO YAMADA

Stuart Turvey

Jesus Vicente Torresano Lominchar

James Furniss

David Ellinghaus

Subhayan Chattopadhyay

Mari Kaunisto

Rosanna Asselta

Vincenzo Forgetta

Anthony Rostron

Eamon Raith

José Manuel Soria Fernández

Florian Büttner

Philip Jansen

Yasser El-Sherbiny

Anne T. Nies

Minttu Marttila

Caroline Cusick

Shea Andrews

Paul Dark

Khoa Manh Dinh

Per Hoffmann

Carlo Maj

Wei Wen

Antonio Espuela-Ortiz

Mathias Haag

Hauke Thomsen

Jolanta Lissowska

Derek Morris

Patrick Holt

Miguel E. Rentería

Gabriella Lindergard

Marc Moritz Berger

Tobias Kaufmann

Alessia Visconti

Pablo Minguez

Per Artursson

Angela Simpson

Giuseppe Citerio

Alfredo Ramirez