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Author Details
Full Name
Bertram M??ller-Myhsok
Affiliation
Max Planck Institute of Psychiatry
ORCID
Career Start Year
1989
Papers
375
H Index
84
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35987817
Genetic and modifiable risk factors combine multiplicatively in common disease.
Clin Res Cardiol
2023
37533333
Burnout and secondary traumatic stress in staff working with people with intellectual disabilities: The role of adverse childhood experiences, resilience and trauma-informed organisational climate.
J Appl Res Intellect Disabil
2023
37214898
Distinct genetic liability profiles define clinically relevant patient strata across common diseases.
medRxiv
2023
37205363
netMUG: a novel network-guided multi-view clustering workflow for dissecting genetic and facial heterogeneity.
bioRxiv
2023
37435051
High genetic risk for depression as an independent risk factor for mortality in patients referred for coronary angiography.
Front Cardiovasc Med
2023
37225062
Advancing social behavioral neuroscience by integrating ethology and comparative psychology methods through machine learning.
Neurosci Biobehav Rev
2023
37461564
Genetic structure of major depression symptoms across clinical and community cohorts.
medRxiv
2023
36639510
Genetic, individual, and familial risk correlates of brain network controllability in major depressive disorder.
Mol Psychiatry
2023
32758327
Polygenic risk for schizophrenia and schizotypal traits in non-clinical subjects.
Psychol Med
2022
35836174
Creating sparser prediction models of treatment outcome in depression: a proof-of-concept study using simultaneous feature selection and hyperparameter tuning.
BMC Med Inform Decis Mak
2022
35396580
Mapping genomic loci implicates genes and synaptic biology in schizophrenia.
Nature
2022
35489115
ExomeChip-based rare variant association study in restless legs syndrome.
Sleep Med
2022
35998220
Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people.
Proc Natl Acad Sci U S A
2022
33878186
Cis-epistasis at the LPA locus and risk of cardiovascular diseases.
Cardiovasc Res
2022
35046466
Genome and transcriptome profiling of spontaneous preterm birth phenotypes.
Sci Rep
2022
35105937
Publisher Correction: Genome and transcriptome profiling of spontaneous preterm birth phenotypes.
Sci Rep
2022
35105872
DNA-methylation dynamics across short-term, exposure-containing CBT in patients with panic disorder.
Transl Psychiatry
2022
34542150
GWAS meta-analysis followed by Mendelian randomization revealed potential control mechanisms for circulating α-Klotho levels.
Hum Mol Genet
2022
34099189
Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.
Biol Psychiatry
2022
33201861
Congenital heart disease risk loci identified by genome-wide association study in European patients.
J Clin Invest
2021
33827729
Effects of polygenic risk for major mental disorders and cross-disorder on cortical complexity.
Psychol Med
2021
33742474
Plasma long-chain omega-3 fatty acid status and risk of recurrent early spontaneous preterm birth: a prospective observational study.
Acta Obstet Gynecol Scand
2021
33590662
"The Heidelberg Five" personality dimensions: Genome-wide associations, polygenic risk for neuroticism, and psychopathology 20â¿¿years after assessment.
Am J Med Genet B Neuropsychiatr Genet
2021
33782385
Genetic factors influencing a neurobiological substrate for psychiatric disorders.
Transl Psychiatry
2021
33721783
The association between genetically determined ABO blood types and major depressive disorder.
Psychiatry Res
2021
34903727
Sex differences in the genetic regulation of the blood transcriptome response to glucocorticoid receptor activation.
Transl Psychiatry
2021
35048876
Characterisation of age and polarity at onset in bipolar disorder.
Br J Psychiatry
2021
34402867
Metabolic profiling of maternal serum of women at high-risk of spontaneous preterm birth using NMR and MGWAS approach.
Biosci Rep
2021
34744805
Systematic Review of Functional MRI Applications for Psychiatric Disease Subtyping.
Front Psychiatry
2021
34534736
Maternal selenium levels and whole genome screen in recurrent spontaneous preterm birth population: A nested case control study.
Eur J Obstet Gynecol Reprod Biol
2021
34127797
Identification of transdiagnostic psychiatric disorder subtypes using unsupervised learning.
Neuropsychopharmacology
2021
34215153
Interaction of developmental factors and ordinary stressful life events on brain structure in adults.
Neuroimage Clin
2021
34086673
Novel EDGE encoding method enhances ability to identify genetic interactions.
PLoS Genet
2021
34002096
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology.
Nat Genet
2021
31712721
Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders.
Mol Psychiatry
2021
31712720
Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression.
Mol Psychiatry
2021
32064741
Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies.
Addict Biol
2021
33407710
Adapting the randomised controlled trial (RCT) for precision medicine: introducing the nested-precision RCT (npRCT).
Trials
2021
33376202
Sunlight exposure exerts immunomodulatory effects to reduce multiple sclerosis severity.
Proc Natl Acad Sci U S A
2021
33057169
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia.
Mol Psychiatry
2021
31630246
A different view on fine-scale population structure in Western African populations.
Hum Genet
2020
31788832
Identification of Restless Legs Syndrome Genes by Mutational Load Analysis.
Ann Neurol
2020
31922285
Polygenic risk scores outperform machine learning methods in predicting coronary artery disease status.
Genet Epidemiol
2020
32012148
DeepWAS: Multivariate genotype-phenotype associations by directly integrating regulatory information using deep learning.
PLoS Comput Biol
2020
33172359
A Novel Locus and Candidate Gene for Familial Developmental Dyslexia on Chromosome 4q.
Z Kinder Jugendpsychiatr Psychother
2020
33170024
Population Bias in Polygenic Risk Prediction Models for Coronary Artery Disease.
Circ Genom Precis Med
2020
33143745
Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS.
BMC Med
2020
33072080
Gene Expression in Spontaneous Experimental Autoimmune Encephalomyelitis Is Linked to Human Multiple Sclerosis Risk Genes.
Front Immunol
2020
32915819
Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study.
PLoS One
2020
32681593
Genetic comorbidity between major depression and cardio-metabolic traits, stratified by age at onset of major depression.
Am J Med Genet B Neuropsychiatr Genet
2020
1 - 50 of 375
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Dorret I Boomsma
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Franziska Degenhardt
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Stephanie H Witt
Central Institute of Mental Health, Heidelberg University
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Jana Strohmaier
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Gerome Breen
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