Marcella Rietschel

Thomas G Schulze, Francis J McMahon, Sven Cichon, 2014, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.

Genetic predictors of response to antidepressants in the GENDEP project

Thomas G Schulze, Marcella Rietschel, Erik Roj Larsen, 2009, The Pharmacogenomics Journal.

Outgroup emotion processing in the vACC is modulated by childhood trauma and CACNA1C risk variant

Tilo Kircher, Axel Krug, Benjamin Straube, 2018, Social cognitive and affective neuroscience.

Association of rs1006737 in CACNA1C with alterations in prefrontal activation and fronto‐hippocampal connectivity

Tilo Kircher, Axel Krug, Marcella Rietschel, 2014, Human brain mapping.

Novel genetic loci associated with hippocampal volume

Benjamin S Aribisala, Wiro J Niessen, Peter Kochunov, 2017, Nature Communications.

Identification of gene ontologies linked to prefrontal–hippocampal functional coupling in the human brain

Henrik Walter, Manuel Mattheisen, Andreas Heinz, 2014, Proceedings of the National Academy of Sciences.

Relation between cerebrospinal fluid, gray matter and white matter changes in families with schizophrenia.

Michael Wagner, Kai Vogeley, Thomas G Schulze, 2006, Journal of psychiatric research.

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

Wei Cheng, Jianxin Shi, Elvira Bramon, 2016, Nature Genetics.

Unipolar depression and hippocampal volume: Impact of DNA sequence variants of the glucocorticoid receptor gene

Lukas Scheef, Marcella Rietschel, Wolfgang Block, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Phenotypic association analyses with copy number variation in recurrent depressive disorder

Florian Holsboer, Gerome Breen, Marcella Rietschel, 2015 .

A target sample of adolescents and reward processing: same neural and behavioral correlates engaged in common paradigms?

Christian Büchel, Andreas Heinz, Zdenka Pausova, 2012, Experimental Brain Research.

Variability of single trial brain activation predicts fluctuations in reaction time

Christoph Klein, Tobias Banaschewski, Stephan Bender, 2015, Biological Psychology.

Addiction Research Consortium: Losing and regaining control over drug intake (ReCoDe)—From trajectories to mechanisms and interventions

Daniel Durstewitz, Georgia Koppe, Peter Kirsch, 2019, Addiction biology.

Multiple Independent Loci at Chromosome 15q25.1 Affect Smoking Quantity: a Meta-Analysis and Comparison with Lung Cancer and COPD

William Wheeler, Peter Kraft, Tianhua Niu, 2010, PLoS genetics.

Investigation of the human serotonin receptor gene HTR3B in bipolar affective and schizophrenic patients

Margot Albus, Marcella Rietschel, Wolfgang Maier, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

City living and urban upbringing affect neural social stress processing in humans

Jens C. Pruessner, Peter Kirsch, Andreas Meyer-Lindenberg, 2011, Nature.

Novel genetic loci underlying human intracranial volume identified through genome-wide association

Benjamin S Aribisala, Wiro J Niessen, Peter Kochunov, 2016, Nature Neuroscience.

The genetic architecture of the human cerebral cortex

Anders M. Dale, Robert C. Green, Shannon L. Risacher, 2020, Science.

The IMAGEN study: a decade of imaging genetics in adolescents

Vincent Frouin, Semiha Aydin, Gareth J. Barker, 2020, Molecular Psychiatry.

Common structural correlates of trait impulsiveness and perceptual reasoning in adolescence

Christian Büchel, Jean-Baptiste Poline, Norbert Kathmann, 2013, Human brain mapping.

Brain function in carriers of a genome-wide supported bipolar disorder variant.

Peter Kirsch, Henrik Walter, Andreas Meyer-Lindenberg, 2010, Archives of general psychiatry.

Support for association of schizophrenia with genetic variation in the 6p22.3 gene, dysbindin, in sib-pair families with linkage and in an additional sample of triad families.

Margot Albus, Marcella Rietschel, Michael Knapp, 2003, American journal of human genetics.

Common variants on 8p12 and 1q24.2 confer risk of schizophrenia

Qi Xu, Peng Wang, Dengtang Liu, 2011, Nature Genetics.

Polygenic risk for schizophrenia affects working memory and its neural correlates in healthy subjects

Tilo Kircher, Bruno Dietsche, Axel Krug, 2018, Schizophrenia Research.

Genome‐wide significant association between alcohol dependence and a variant in the ADH gene cluster

Manuel Mattheisen, Bertram Müller-Myhsok, Karl Mann, 2012, Addiction biology.

FTO, obesity and the adolescent brain.

Vincent Frouin, Christian Büchel, Andreas Heinz, 2013, Human molecular genetics.

A genetic risk score combining 32 SNPs is associated with body mass index and improves obesity prediction in people with major depressive disorder

Sven Bergmann, Florian Holsboer, Bertram Müller-Myhsok, 2015, BMC Medicine.

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Jianxin Shi, Susmita Datta, Aribert Rothenberger, 2013, Nature Genetics.

Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder

Jakob Grove, Esben Agerbo, Andres Metspalu, 2017, bioRxiv.

A systems medicine research approach for studying alcohol addiction

Klaus Obermayer, Daniel Durstewitz, Henrik Walter, 2013, Addiction biology.

Edinburgh Research Explorer Association of Mouse Dlg4 (PSD-95) Gene Deletion and Human DLG4 Gene Variation With Phenotypes Relevant to Autism Spectrum Disorders and Williams' Syndrome

Peter Kirsch, Henrik Walter, Reza Momenan, 2022 .

A genome-wide association study of alcohol dependence

Laura J. Bierut, Karl Mann, Markus M. Nöthen, 2010, Proceedings of the National Academy of Sciences.

DCLK1 Variants Are Associated across Schizophrenia and Attention Deficit/Hyperactivity Disorder

Ole A. Andreassen, Vidar M. Steen, Manuel Mattheisen, 2012, PloS one.

Genetic Determinants of Cortical Structure (Thickness, Surface Area and Volumes) among Disease Free Adults in the CHARGE Consortium

Anders M. Dale, Robert C. Green, Shannon L. Risacher, 2018, bioRxiv.

Genome‐wide gene‐environment interaction in depression: A systematic evaluation of candidate genes

Alexander Teumer, Niamh Mullins, Stephan Ripke, 2018, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Disruption of the neurexin 1 gene is associated with schizophrenia.

Elvira Bramon, Chiara Sabatti, Kari Stefansson, 2009, Human molecular genetics.

Genetic variation in the schizophrenia‐risk gene neuregulin 1 correlates with brain activation and impaired speech production in a verbal fluency task in healthy individuals

Nadim Jon Shah, Tilo Kircher, Axel Krug, 2009, Human brain mapping.

Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.

Stephan Ripke, Steven P. Hamilton, Florian Holsboer, 2013, The American journal of psychiatry.

Hippocampal and Frontolimbic Function as Intermediate Phenotype for Psychosis: Evidence from Healthy Relatives and a Common Risk Variant in CACNA1C

Peter Kirsch, Henrik Walter, Andreas Meyer-Lindenberg, 2014, Biological Psychiatry.

Mechanisms of disturbed emotion processing and social interaction in borderline personality disorder: state of knowledge and research agenda of the German Clinical Research Unit

Peter Kirsch, Stefanie Lis, Rolf-Detlef Treede, 2014, Borderline Personality Disorder and Emotion Dysregulation.

Common Genetic Variants and Gene-Expression Changes Associated with Bipolar Disorder Are Over-Represented in Brain Signaling Pathway Genes

Gerome Breen, Inti Pedroso, Markus M. Nöthen, 2012, Biological Psychiatry.

Association of the functional V158M catechol-O-methyl-transferase polymorphism with panic disorder in women.

Katharina Domschke, Marcella Rietschel, Rolf Fimmers, 2004, The international journal of neuropsychopharmacology.

Genetic variation in the PNPLA3 gene is associated with alcoholic liver injury in caucasians

Michael Krawczak, Thomas Berg, Henry Völzke, 2010, Hepatology.

Genome-wide association study identifies five new schizophrenia loci

Anders D. Børglum, Peter Donnelly, Jianxin Shi, 2011, Nature Genetics.

An integrated genome research network for studying the genetics of alcohol addiction

Roland Eils, Henrik Walter, Andreas Heinz, 2010, Addiction biology.

Genome‐wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness

Stephan Ripke, Andrew McQuillin, Hugh Gurling, 2016, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Partial support for ZNF804A genotype‐dependent alterations in prefrontal connectivity

Tilo Kircher, Axel Krug, Marcella Rietschel, 2013, Human brain mapping.

Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort.

Elvira Bramon, Leena Peltonen, Morten Mattingsdal, 2010, Journal of psychiatric research.

Interaction between the 5-HTTLPR serotonin transporter polymorphism and environmental adversity for mood and anxiety psychopathology: evidence from a high-risk community sample of young adults.

Martin H. Schmidt, Tobias Banaschewski, Marcella Rietschel, 2009, The international journal of neuropsychopharmacology.

Genomewide Association Scan of Suicidal Thoughts and Behaviour in Major Depression

Bertram Müller-Myhsok, Gerome Breen, Michael Gill, 2011, PloS one.

Association of the alcohol dehydrogenase gene polymorphism rs1789891 with gray matter brain volume, alcohol consumption, alcohol craving and relapse risk

Henrik Walter, Anne Beck, Andreas Heinz, 2019, Addiction biology.

Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

Laura J. Scott, Naomi R. Wray, Margaret A. Pericak-Vance, 2015, Nature Neuroscience.

The G72/G30 gene locus in psychiatric disorders: a challenge to diagnostic boundaries?

Sven Cichon, Marcella Rietschel, Johannes Schumacher, 2005, Schizophrenia bulletin.

SCN1A Affects Brain Structure and the Neural Activity of the Aging Brain

Vanessa Nieratschker, Gabriele Ende, Marcella Rietschel, 2012, Biological Psychiatry.

Association between a serotonin transporter length polymorphism and primary insomnia.

Thomas G Schulze, Andreas Meyer-Lindenberg, Marcella Rietschel, 2010, Sleep.

Pharmacogenetics of Tardive Dyskinesia: Combined Analysis of 780 Patients Supports Association with Dopamine D3 Receptor Gene Ser9Gly Polymorphism

Fabio Macciardi, Marcella Rietschel, Heiner Fangerau, 2002, Neuropsychopharmacology.

The impact of dystrobrevin‐binding protein 1 (DTNBP1) on neural correlates of episodic memory encoding and retrieval

Nadim Jon Shah, Tilo Kircher, Axel Krug, 2009, Human brain mapping.

Integrated Pathway-Based Approach Identifies Association between Genomic Regions at CTCF and CACNB2 and Schizophrenia

Christoph Lange, Manuel Mattheisen, Stephan Ripke, 2014, PLoS genetics.

A genome-wide supported variant in CACNA1C influences hippocampal activation during episodic memory encoding and retrieval

Tilo Kircher, Bruno Dietsche, Heidelore Backes, 2014, European Archives of Psychiatry and Clinical Neuroscience.

Linkage-disequilibrium-based binning affects the interpretation of GWASs.

Inge Jonassen, Manuel Mattheisen, Morten Mattingsdal, 2012, American journal of human genetics.

The Complement Control-Related Genes CSMD1 and CSMD2 Associate to Schizophrenia

Vidar M. Steen, Marcella Rietschel, Stephanie Le Hellard, 2011, Biological Psychiatry.

Decreased frontal lobe ratio of N-acetyl aspartate to choline in familial schizophrenia: a proton magnetic resonance spectroscopy study

Thomas G Schulze, Peter Falkai, Marcella Rietschel, 2000, Neuroscience Letters.

Candidate Gene Analysis of the Human Natural Killer-1 Carbohydrate Pathway and Perineuronal Nets in Schizophrenia: B3GAT2 Is Associated with Disease Risk and Cortical Surface Area

Anders M. Dale, Elvira Bramon, Ole A. Andreassen, 2011, Biological Psychiatry.

Neuroimaging evidence for a role of neural social stress processing in ethnic minority-associated environmental risk.

Peter Kirsch, Andreas Meyer-Lindenberg, Marcella Rietschel, 2014, JAMA psychiatry.

Functional Connectivity Analyses in Imaging Genetics: Considerations on Methods and Data Interpretation

Tilo Kircher, Axel Krug, Marcella Rietschel, 2011, PloS one.

Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

Michael W. Weiner, Anders M. Dale, Robert C. Green, 2017, bioRxiv.

Reduction of the Internal Capsule in Families Affected with Schizophrenia

Michael Wagner, Kai Vogeley, Peter Falkai, 2008, Biological Psychiatry.

Adverse reactions to antidepressants.

Marcella Rietschel, Erik Roj Larsen, Peter McGuffin, 2009, The British journal of psychiatry : the journal of mental science.

The hippocampus in families with schizophrenia in relation to obstetric complications

Michael Wagner, Peter Falkai, Marcella Rietschel, 2008, Schizophrenia Research.

Altered Functional Subnetwork During Emotional Face Processing: A Potential Intermediate Phenotype for Schizophrenia.

Henrik Walter, Manuel Mattheisen, Andreas Heinz, 2016, JAMA psychiatry.

ADH1B Arg48His Allele Frequency Map: Filling in the Gap for Central Europe

Marcella Rietschel, Jens Treutlein, Falk Kiefer, 2014, Biological Psychiatry.

Neurobiology of the major psychoses: a translational perspective on brain structure and function—the FOR2107 consortium

Tilo Kircher, Axel Krug, Tim Hahn, 2018, European Archives of Psychiatry and Clinical Neuroscience.

Early Cannabis Use, Polygenic Risk Score for Schizophrenia and Brain Maturation in Adolescence.

Vincent Frouin, Henrik Walter, Andreas Heinz, 2015, JAMA psychiatry.

The 5-HTTLPR Polymorphism Affects Network-Based Functional Connectivity in the Visual-Limbic System in Healthy Adults

Henrik Walter, Manuel Mattheisen, Thomas Mühleisen, 2018, Neuropsychopharmacology.

Prefrontal-temporal gray matter deficits in bipolar disorder patients with persecutory delusions.

Thomas G Schulze, Andreas Meyer-Lindenberg, Gabriele Ende, 2010, Journal of affective disorders.