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Author Details
Full Name
Jens Treutlein
Affiliation
Heidelberg University
ORCID
Career Start Year
2001
Papers
104
H Index
38
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
32064741
Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies.
Addict Biol
2021
34786613
The German research consortium for the study of bipolar disorder (BipoLife): a magnetic resonance imaging study protocol.
Int J Bipolar Disord
2021
31712721
Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders.
Mol Psychiatry
2021
32080920
Acute alcohol withdrawal and recovery in men lead to profound changes in DNA methylation profiles: a longitudinal clinical study.
Addiction
2020
29058369
Association of the alcohol dehydrogenase gene polymorphism rs1789891 with gray matter brain volume, alcohol consumption, alcohol craving and relapse risk.
Addict Biol
2019
31852885
Longitudinal transcriptome-wide gene expression analysis of sleep deprivation treatment shows involvement of circadian genes and immune pathways.
Transl Psychiatry
2019
30507021
Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy.
Am J Med Genet B Neuropsychiatr Genet
2019
30503783
Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder.
Eur Neuropsychopharmacol
2019
29197740
Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder.
J Affect Disord
2018
29985185
Glutamate concentration in the anterior cingulate cortex in alcohol dependence: association with alcohol withdrawal and exploration of contribution from glutamatergic candidate genes.
Psychiatr Genet
2018
29901528
Shared genetic etiology between alcohol dependence and major depressive disorder.
Psychiatr Genet
2018
29872112
Response to therapeutic sleep deprivation: a naturalistic study of clinical and genetic factors and post-treatment depressive symptom trajectory.
Neuropsychopharmacology
2018
30482948
Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders.
Nat Neurosci
2018
30415424
Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics.
Int J Bipolar Disord
2018
29700475
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.
Nat Genet
2018
29695247
Impact on birth weight of maternal smoking throughout pregnancy mediated by DNA methylation.
BMC Genomics
2018
29325115
Fast sleep spindle density is associated with rs4680 (Val108/158Met) genotype of catechol-O-methyltransferase (COMT).
Sleep
2018
27584037
Association between neuropeptide Y receptor Y2 promoter variant rs6857715 and major depressive disorder.
Psychiatr Genet
2017
28166306
Identification of shared risk loci and pathways for bipolar disorder and schizophrenia.
PLoS One
2017
28350396
Genetic effects influencing risk for major depressive disorder in China and Europe.
Transl Psychiatry
2017
29198511
Preliminary Evidence for an Association Between Variants of the Catechol-O-Methyltransferase (COMT) Gene and Premature Ejaculation.
J Sex Med
2017
28731911
Expert and self-assessment of lifetime symptoms and diagnosis of major depressive disorder in large-scale genetic studies in the general population: comparison of a clinical interview and a self-administered checklist.
Psychiatr Genet
2017
28714907
Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis.
Genes (Basel)
2017
28632202
Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia.
Transl Psychiatry
2017
26879624
Interaction between COMT Val(158)Met polymorphism and childhood adversity affects reward processing in adulthood.
Neuroimage
2016
26392368
Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts.
Behav Genet
2016
27397865
GATA4 variant interaction with brain limbic structure and relapse risk: A voxel-based morphometry study.
Eur Neuropsychopharmacol
2016
27374936
Analysis of Rare Variants in the Alcohol Dependence Candidate Gene GATA4.
Alcohol Clin Exp Res
2016
27459726
A gene-by-sex interaction for nicotine reward: evidence from humanized mice and epidemiology.
Transl Psychiatry
2016
25031104
Genetic variation in the G72 gene is associated with increased frontotemporal fiber tract integrity.
Eur Arch Psychiatry Clin Neurosci
2015
26401310
New-born females show higher stress- and genotype-independent methylation of SLC6A4 than males.
Borderline Personal Disord Emot Dysregul
2015
26556287
Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder.
Transl Psychiatry
2015
26475575
A common risk variant in CACNA1C supports a sex-dependent effect on longitudinal functioning and functional recovery from episodes of schizophrenia-spectrum but not bipolar disorder.
Eur Neuropsychopharmacol
2015
25894927
Alterations of Glucocorticoid Receptor Gene Methylation in Externalizing Disorders During Childhood and Adolescence.
Behav Genet
2015
25724484
Association of norepinephrine transporter (NET, SLC6A2) genotype with ADHD-related phenotypes: findings of a longitudinal study from birth to adolescence.
Psychiatry Res
2015
25801500
NCAN Cross-Disorder Risk Variant Is Associated With Limbic Gray Matter Deficits in Healthy Subjects and Major Depression.
Neuropsychopharmacology
2015
25035082
XRCC5 as a risk gene for alcohol dependence: evidence from a genome-wide gene-set-based analysis and follow-up studies in Drosophila and humans.
Neuropsychopharmacology
2015
24011820
ADH1B Arg48His allele frequency map: filling in the gap for Central Europe.
Biol Psychiatry
2014
25304227
Analysis of genome-wide significant bipolar disorder genes in borderline personality disorder.
Psychiatr Genet
2014
25017620
Association between dopa decarboxylase gene variants and borderline personality disorder.
Psychiatry Res
2014
25144209
Smoking behaviour: investigation of the coaction of environmental and genetic risk factors.
Psychiatr Genet
2014
25136889
Investigation of manic and euthymic episodes identifies state- and trait-specific gene expression and STAB1 as a new candidate gene for bipolar disorder.
Transl Psychiatry
2014
24800784
A functional variant in the neuropeptide S receptor 1 gene moderates the influence of urban upbringing on stress processing in the amygdala.
Stress
2014
24901509
Integrated pathway-based approach identifies association between genomic regions at CTCF and CACNB2 and schizophrenia.
PLoS Genet
2014
24553580
Interaction between prenatal stress and dopamine D4 receptor genotype in predicting aggression and cortisol levels in young adults.
Psychopharmacology (Berl)
2014
24618891
Genome-wide association study reveals two new risk loci for bipolar disorder.
Nat Commun
2014
24683514
A Neuregulin-1 schizophrenia susceptibility variant causes perihippocampal fiber tract anomalies in healthy young subjects.
Brain Behav
2014
24314346
Genetic variation in the atrial natriuretic peptide transcription factor GATA4 modulates amygdala responsiveness in alcohol dependence.
Biol Psychiatry
2014
22424243
Gene expression of glutamate transporters SLC1A1, SLC1A3 and SLC1A6 in the cerebellar subregions of elderly schizophrenia patients and effects of antipsychotic treatment.
World J Biol Psychiatry
2013
23933821
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.
Nat Genet
2013
1 - 50 of 104
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University of Duisburg-Essen
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Jana Strohmaier
Central Institute of Mental Health, University of Heidelberg
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Thomas G Schulze
SUNY Upstate Medical University
Co-authored papers
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Stefan Herms
Institute of Human Genetics, University of Bonn
Co-authored papers
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Wolfgang Maier
University Hospital Bonn
Co-authored papers
21
Bertram M??ller-Myhsok
Max Planck Institute of Psychiatry
Co-authored papers
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Fabian Streit
Central Institute of Mental Health, Heidelberg University
Co-authored papers
21
Manuel Mattheisen
Dalhousie University
Co-authored papers
20
Thomas W M??hleisen
Institute of Neuroscience and Medicine (INM-1), Research Center Juelich
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19
Andreas J Forstner
University of Bonn, School of Medicine & University Hospital Bonn.
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Per Hoffmann
Institute of Human Genetics, University of Bonn and University Hospital Bonn
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Nicholas G Martin
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