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Author Details
Full Name
Thomas W M??hleisen
Affiliation
Institute of Neuroscience and Medicine (INM-1), Research Center Juelich
ORCID
Career Start Year
2004
Papers
118
H Index
49
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35172679
Associations of common genetic risk variants of the muscarinic acetylcholine receptor M2 with cardiac autonomic dysfunction in patients with schizophrenia.
World J Biol Psychiatry
2023
37030412
Relationships between neurotransmitter receptor densities and expression levels of their corresponding genes in the human hippocampus.
Neuroimage
2023
35172679
Associations of common genetic risk variants of the muscarinic acetylcholine receptor M2 with cardiac autonomic dysfunction in patients with schizophrenia.
World J Biol Psychiatry
2023
37030412
Relationships between neurotransmitter receptor densities and expression levels of their corresponding genes in the human hippocampus.
Neuroimage
2023
33615640
Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs.
Hum Brain Mapp
2022
36421807
Analysis of <i>CACNA1C</i> and <i>KCNH2</i> Risk Variants on Cardiac Autonomic Function in Patients with Schizophrenia.
Genes (Basel)
2022
33615640
Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs.
Hum Brain Mapp
2022
36421807
Analysis of <i>CACNA1C</i> and <i>KCNH2</i> Risk Variants on Cardiac Autonomic Function in Patients with Schizophrenia.
Genes (Basel)
2022
33221148
A common variation in HCN1 is associated with heart rate variability in schizophrenia.
Schizophr Res
2021
34002096
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology.
Nat Genet
2021
33782385
Genetic factors influencing a neurobiological substrate for psychiatric disorders.
Transl Psychiatry
2021
33221148
A common variation in HCN1 is associated with heart rate variability in schizophrenia.
Schizophr Res
2021
34653833
A GWAS top hit for circulating leptin is associated with weight gain but not with leptin protein levels in lithium-augmented patients with major depression.
Eur Neuropsychopharmacol
2021
34539327
Identification of Phonology-Related Genes and Functional Characterization of Broca's and Wernicke's Regions in Language and Learning Disorders.
Front Neurosci
2021
33782385
Genetic factors influencing a neurobiological substrate for psychiatric disorders.
Transl Psychiatry
2021
34539327
Identification of Phonology-Related Genes and Functional Characterization of Broca's and Wernicke's Regions in Language and Learning Disorders.
Front Neurosci
2021
34653833
A GWAS top hit for circulating leptin is associated with weight gain but not with leptin protein levels in lithium-augmented patients with major depression.
Eur Neuropsychopharmacol
2021
34002096
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology.
Nat Genet
2021
30705424
Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia.
Mol Psychiatry
2020
31665216
Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition.
JAMA Psychiatry
2020
30705424
Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia.
Mol Psychiatry
2020
31402375
Pathway-Specific Genetic Risk for Alzheimer's Disease Differentiates Regional Patterns of Cortical Atrophy in Older Adults.
Cereb Cortex
2020
31665216
Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition.
JAMA Psychiatry
2020
31402375
Pathway-Specific Genetic Risk for Alzheimer's Disease Differentiates Regional Patterns of Cortical Atrophy in Older Adults.
Cereb Cortex
2020
30503783
Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder.
Eur Neuropsychopharmacol
2019
30554862
Leptin gene polymorphisms are associated with weight gain during lithium augmentation in patients with major depression.
Eur Neuropsychopharmacol
2019
30503783
Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder.
Eur Neuropsychopharmacol
2019
30375508
Effects of BDNF Val<sup>66</sup>Met genotype and schizophrenia familial risk on a neural functional network for cognitive control in humans.
Neuropsychopharmacology
2019
30728360
Combining lifestyle risks to disentangle brain structure and functional connectivity differences in older adults.
Nat Commun
2019
30728360
Combining lifestyle risks to disentangle brain structure and functional connectivity differences in older adults.
Nat Commun
2019
30554862
Leptin gene polymorphisms are associated with weight gain during lithium augmentation in patients with major depression.
Eur Neuropsychopharmacol
2019
30375508
Effects of BDNF Val<sup>66</sup>Met genotype and schizophrenia familial risk on a neural functional network for cognitive control in humans.
Neuropsychopharmacology
2019
28589968
The 5-HTTLPR Polymorphism Affects Network-Based Functional Connectivity in the Visual-Limbic System in Healthy Adults.
Neuropsychopharmacology
2018
28589968
The 5-HTTLPR Polymorphism Affects Network-Based Functional Connectivity in the Visual-Limbic System in Healthy Adults.
Neuropsychopharmacology
2018
29930110
Analysis of shared heritability in common disorders of the brain.
Science
2018
30415424
Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics.
Int J Bipolar Disord
2018
29478144
Integration of transcriptomic and cytoarchitectonic data implicates a role for MAOA and TAC1 in the limbic-cortical network.
Brain Struct Funct
2018
29730826
Using coordinate-based meta-analyses to explore structural imaging genetics.
Brain Struct Funct
2018
29197740
Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder.
J Affect Disord
2018
29930110
Analysis of shared heritability in common disorders of the brain.
Science
2018
30415424
Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics.
Int J Bipolar Disord
2018
29730826
Using coordinate-based meta-analyses to explore structural imaging genetics.
Brain Struct Funct
2018
29478144
Integration of transcriptomic and cytoarchitectonic data implicates a role for MAOA and TAC1 in the limbic-cortical network.
Brain Struct Funct
2018
29197740
Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder.
J Affect Disord
2018
28072415
Functional neuroimaging effects of recently discovered genetic risk loci for schizophrenia and polygenic risk profile in five RDoC subdomains.
Transl Psychiatry
2017
28632202
Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia.
Transl Psychiatry
2017
28566273
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.
Diabetes
2017
28072415
Functional neuroimaging effects of recently discovered genetic risk loci for schizophrenia and polygenic risk profile in five RDoC subdomains.
Transl Psychiatry
2017
28166306
Identification of shared risk loci and pathways for bipolar disorder and schizophrenia.
PLoS One
2017
28098162
Novel genetic loci associated with hippocampal volume.
Nat Commun
2017
1 - 50 of 236
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Central Institute of Mental Health, Heidelberg University
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Co-authored papers
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Wolfgang Maier
University Hospital Bonn
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Ren?? Breuer
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22
Ole A Andreassen
Oslo University Hospital & Institute of Clinical Medicine, University of Oslo
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Sarah E Medland
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Jens Treutlein
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Bertram M??ller-Myhsok
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