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Author Details

Thomas W M??hleisen
Institute of Neuroscience and Medicine (INM-1), Research Center Juelich
2004
118
49
PMIDPaper TitleJournal TitlePublished Year
35172679Associations of common genetic risk variants of the muscarinic acetylcholine receptor M2 with cardiac autonomic dysfunction in patients with schizophrenia.World J Biol Psychiatry2023
37030412Relationships between neurotransmitter receptor densities and expression levels of their corresponding genes in the human hippocampus.Neuroimage2023
35172679Associations of common genetic risk variants of the muscarinic acetylcholine receptor M2 with cardiac autonomic dysfunction in patients with schizophrenia.World J Biol Psychiatry2023
37030412Relationships between neurotransmitter receptor densities and expression levels of their corresponding genes in the human hippocampus.Neuroimage2023
33615640Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs.Hum Brain Mapp2022
36421807Analysis of <i>CACNA1C</i> and <i>KCNH2</i> Risk Variants on Cardiac Autonomic Function in Patients with Schizophrenia.Genes (Basel)2022
33615640Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs.Hum Brain Mapp2022
36421807Analysis of <i>CACNA1C</i> and <i>KCNH2</i> Risk Variants on Cardiac Autonomic Function in Patients with Schizophrenia.Genes (Basel)2022
33221148A common variation in HCN1 is associated with heart rate variability in schizophrenia.Schizophr Res2021
34002096Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology.Nat Genet2021
33782385Genetic factors influencing a neurobiological substrate for psychiatric disorders.Transl Psychiatry2021
33221148A common variation in HCN1 is associated with heart rate variability in schizophrenia.Schizophr Res2021
34653833A 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 Neuropsychopharmacol2021
34539327Identification of Phonology-Related Genes and Functional Characterization of Broca's and Wernicke's Regions in Language and Learning Disorders.Front Neurosci2021
33782385Genetic factors influencing a neurobiological substrate for psychiatric disorders.Transl Psychiatry2021
34539327Identification of Phonology-Related Genes and Functional Characterization of Broca's and Wernicke's Regions in Language and Learning Disorders.Front Neurosci2021
34653833A 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 Neuropsychopharmacol2021
34002096Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology.Nat Genet2021
30705424Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia.Mol Psychiatry2020
31665216Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition.JAMA Psychiatry2020
30705424Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia.Mol Psychiatry2020
31402375Pathway-Specific Genetic Risk for Alzheimer's Disease Differentiates Regional Patterns of Cortical Atrophy in Older Adults.Cereb Cortex2020
31665216Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition.JAMA Psychiatry2020
31402375Pathway-Specific Genetic Risk for Alzheimer's Disease Differentiates Regional Patterns of Cortical Atrophy in Older Adults.Cereb Cortex2020
30503783Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder.Eur Neuropsychopharmacol2019
30554862Leptin gene polymorphisms are associated with weight gain during lithium augmentation in patients with major depression.Eur Neuropsychopharmacol2019
30503783Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder.Eur Neuropsychopharmacol2019
30375508Effects of BDNF Val<sup>66</sup>Met genotype and schizophrenia familial risk on a neural functional network for cognitive control in humans.Neuropsychopharmacology2019
30728360Combining lifestyle risks to disentangle brain structure and functional connectivity differences in older adults.Nat Commun2019
30728360Combining lifestyle risks to disentangle brain structure and functional connectivity differences in older adults.Nat Commun2019
30554862Leptin gene polymorphisms are associated with weight gain during lithium augmentation in patients with major depression.Eur Neuropsychopharmacol2019
30375508Effects of BDNF Val<sup>66</sup>Met genotype and schizophrenia familial risk on a neural functional network for cognitive control in humans.Neuropsychopharmacology2019
28589968The 5-HTTLPR Polymorphism Affects Network-Based Functional Connectivity in the Visual-Limbic System in Healthy Adults.Neuropsychopharmacology2018
28589968The 5-HTTLPR Polymorphism Affects Network-Based Functional Connectivity in the Visual-Limbic System in Healthy Adults.Neuropsychopharmacology2018
29930110Analysis of shared heritability in common disorders of the brain.Science2018
30415424Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics.Int J Bipolar Disord2018
29478144Integration of transcriptomic and cytoarchitectonic data implicates a role for MAOA and TAC1 in the limbic-cortical network.Brain Struct Funct2018
29730826Using coordinate-based meta-analyses to explore structural imaging genetics.Brain Struct Funct2018
29197740Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder.J Affect Disord2018
29930110Analysis of shared heritability in common disorders of the brain.Science2018
30415424Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics.Int J Bipolar Disord2018
29730826Using coordinate-based meta-analyses to explore structural imaging genetics.Brain Struct Funct2018
29478144Integration of transcriptomic and cytoarchitectonic data implicates a role for MAOA and TAC1 in the limbic-cortical network.Brain Struct Funct2018
29197740Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder.J Affect Disord2018
28072415Functional neuroimaging effects of recently discovered genetic risk loci for schizophrenia and polygenic risk profile in five RDoC subdomains.Transl Psychiatry2017
28632202Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia.Transl Psychiatry2017
28566273An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.Diabetes2017
28072415Functional neuroimaging effects of recently discovered genetic risk loci for schizophrenia and polygenic risk profile in five RDoC subdomains.Transl Psychiatry2017
28166306Identification of shared risk loci and pathways for bipolar disorder and schizophrenia.PLoS One2017
28098162Novel genetic loci associated with hippocampal volume.Nat Commun2017
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Central Institute of Mental Health, University of Mannheim
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Co-authored papers 29
Co-authored papers 29
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Co-authored papers 29
University Hospital Bonn
Co-authored papers 26
Central Institute of Mental Health, Medical Faculty Mannheim/Heidelberg University
Co-authored papers 22
Oslo University Hospital & Institute of Clinical Medicine, University of Oslo
Co-authored papers 20
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Heidelberg University
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Max Planck Institute of Psychiatry
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Oslo University Hospital
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Alexandru Obregia Clinical Psychiatric Hospital.
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The Lundbeck Foundation Initiative for Integrative Psychiatric Research
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Central Institute of Mental Health, Heidelberg University
Co-authored papers 14
University of Bonn, School of Medicine & University Hospital Bonn.
Co-authored papers 13
Poznan University of Medical Sciences
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