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Marcella Rietschel (1957-)

Ärztin

Name	Marcella Rietschel
Zeit	1957- (Lebensdaten)
Ort	Stuttgart (Geburtsort) Mannheim (Wirkungsort) Heidelberg (Wirkungsort) Deutschland
Geschlecht	weiblich
Akademischer Grad bzw. Titel	Prof. Dr.
Beruf	Ärztin (charakteristischer Beruf) Hochschullehrerin
Variante	Marcella Michel (früherer Name) M. Rietschel Marcela Rietschel Marcela D. C. Rietschel
Beziehung	Zentralinstitut für Seelische Gesundheit. Abteilung Genetische Epidemiologie in der Psychiatrie (Wissenschaftliche Direktorin) (2002-) Deutsche Akademie der Naturforscher Leopoldina (Mitglied, Matrikelnummer 07440) (2011-)
Themengebiet	Personen zu Medizin, Tiermedizin
Weitere Angaben	Leiterin der Abteilung "Genetische Epidemiologie in der Psychiatrie" am Zentralinstitut für Seelische Gesundheit in Mannheim; Ärztin für Psychiatrie und Psychotherapie sowie medizinische Genetik; IZN, Central Research Institutions, Universität Heidelberg
Quelle	Landesbibliographie Baden-Württemberg
Datensatztyp	Person
GND-Nummer	112785751
Datensatz-ID	112785751
Beteiligt an alle anzeigen Factor analysis of lifetime psychopathology and its brain morphometric and genetic correlates in a transdiagnostic sample The interplay between polygenic score for tumor necrosis factor-α, brain structural connectivity, and processing speed in major depression Lithium response in bipolar disorder is associated with focal adhesion and PI3K-Akt networks: a multi-omics replication study Fine-mapping genomic loci refines bipolar disorder risk genes Fine-mapping genomic loci refines bipolar disorder risk genes Genetic variation in TERT modifies the risk of hepatocellular carcinoma in alcohol-related cirrhosis : results from a genome-wide case-control study Longitudinal Investigation of Phenotypic, Genetic and Epigenetic Factors in Mood Disorders Stress in pregnancy - implications for fetal BDNF in amniotic fluid at birth Evidence for a shared genetic contribution to loneliness and borderline personality disorder A systematic evaluation of machine learning-based biomarkers for major depressive disorder across modalities Lifetime and current depression in the German National Cohort (NAKO) The interplay of family history of depression and early trauma: associations with lifetime and current depression in the German national cohort (NAKO) Comparative serum proteomic analysis of a selected protein panel in individuals with schizophrenia and bipolar disorder and the impact of genetic risk burden on serum proteomic profiles Genetic and functional analyses implicate microRNA 499A in bipolar disorder development Depression and bipolar disorder subtypes differ in their genetic correlations with biological rhythms Behavioural and functional evidence revealing the role of RBFOX1 variation in multiple psychiatric disorders and traits Correction: Combining schizophrenia and depression polygenic risk scores improves the genetic prediction of lithium response in bipolar disorder patients Epigenetic signatures in antidepressant treatment response: a methylome-wide association study in the EMC trial Association of polygenic risk for schizophrenia with fast sleep spindle density depends on pro-cognitive variants Borderline personality disorder and the big five: molecular genetic analyses indicate shared genetic architecture with neuroticism and openness Investigating the phenotypic and genetic associations between personality traits and suicidal behavior across major mental health diagnoses Behavioural and functional evidence revealing the role of RBFOX1 variation in multiple psychiatric disorders and traits Urbanicity, behavior problems and HPA axis regulation in preschoolers Combining schizophrenia and depression polygenic risk scores improves the genetic prediction of lithium response in bipolar disorder patients Einsamkeit während der ersten Welle der SARS-CoV-2-Pandemie – Ergebnisse der NAKO-Gesundheitsstudie Prediction of lithium response using genomic data Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders Effects of high-frequency prefrontal rTMS on heart frequency rates and blood pressure in schizophrenia HLA-DRB1 and HLA-DQB1 genetic diversity modulates response to lithium in bipolar affective disorders Interplay between the genetics of personality traits, severe psychiatric disorders and COVID-19 host genetics in the susceptibility to SARS-CoV-2 infection Expanding the genetic architecture of nicotine dependence and its shared genetics with multiple traits Apolipoprotein E Homozygous ε4 Allele Status: A Deteriorating Effect on Visuospatial Working Memory and Global Brain Structure A functional variant in the serotonin receptor 7 gene (HTR7), rs7905446, is associated with good response to SSRIs in bipolar and unipolar depression Genetik in Neurologie und Psychiatrie Reproducible grey matter patterns index a multivariate, global alteration of brain structure in schizophrenia and bipolar disorder Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders Efficacy of high-frequency repetitive transcranial magnetic stimulation in schizophrenia patients with treatment-resistant negative symptoms treated with clozapine Interaction of the Psychiatric Risk Gene Cacna1c With Post-weaning Social Isolation or Environmental Enrichment Does Not Affect Brain Mitochondrial Bioenergetics in Rats Nutzung genomweiter Daten zum besseren Verständnis der molekulargenetischen Basis von Schizophrenie und Alkoholabhängigkeit Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders Detecting significant genotype–phenotype association rules in bipolar disorder: market research meets complex genetics Effects of BDNF Val66Met genotype and schizophrenia familial risk on a neural functional network for cognitive control in humans Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder Cortical surface area alterations shaped by genetic load for neuroticism Genes associated with anhedonia: a new analysis in a large clinical trial (GENDEP) Response to therapeutic sleep deprivation: a naturalistic study of clinical and genetic factors and post-treatment depressive symptom trajectory Risk-seeking for losses is associated with 5-HTTLPR, but not with transient changes in 5-HT levels Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression Response to the letter by Esteves et al Impact on birth weight of maternal smoking throughout pregnancy mediated by DNA methylation Antidepressant drug-specific prediction of depression treatment outcomes from genetic and clinical variables Impact of prenatal stress on mother-infant dyadic behavior during the still-face paradigm Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders Exome sequencing in large, multiplex bipolar disorder families from Cuba Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes Study protocol of the ASD-Net, the German research consortium for the study of Autism Spectrum Disorder across the lifespan: from a better etiological understanding, through valid diagnosis, to more effective health care The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders Epigenome-wide DNA methylation analysis in siblings and monozygotic twins discordant for sporadic Parkinson’s disease revealed different epigenetic patterns in peripheral blood mononuclear cells Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1

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Katalog der Deutschen Nationalbibliothek

Marcella Rietschel (1957-)

Factor analysis of lifetime psychopathology and its brain morphometric and genetic correlates in a transdiagnostic sample

The interplay between polygenic score for tumor necrosis factor-α, brain structural connectivity, and processing speed in major depression

Lithium response in bipolar disorder is associated with focal adhesion and PI3K-Akt networks: a multi-omics replication study

Fine-mapping genomic loci refines bipolar disorder risk genes

Fine-mapping genomic loci refines bipolar disorder risk genes

Genetic variation in TERT modifies the risk of hepatocellular carcinoma in alcohol-related cirrhosis : results from a genome-wide case-control study

Longitudinal Investigation of Phenotypic, Genetic and Epigenetic Factors in Mood Disorders

Stress in pregnancy - implications for fetal BDNF in amniotic fluid at birth

Evidence for a shared genetic contribution to loneliness and borderline personality disorder

A systematic evaluation of machine learning-based biomarkers for major depressive disorder across modalities

Lifetime and current depression in the German National Cohort (NAKO)

The interplay of family history of depression and early trauma: associations with lifetime and current depression in the German national cohort (NAKO)

Comparative serum proteomic analysis of a selected protein panel in individuals with schizophrenia and bipolar disorder and the impact of genetic risk burden on serum proteomic profiles

Genetic and functional analyses implicate microRNA 499A in bipolar disorder development

Depression and bipolar disorder subtypes differ in their genetic correlations with biological rhythms

Behavioural and functional evidence revealing the role of RBFOX1 variation in multiple psychiatric disorders and traits

Correction: Combining schizophrenia and depression polygenic risk scores improves the genetic prediction of lithium response in bipolar disorder patients

Epigenetic signatures in antidepressant treatment response: a methylome-wide association study in the EMC trial

Association of polygenic risk for schizophrenia with fast sleep spindle density depends on pro-cognitive variants

Borderline personality disorder and the big five: molecular genetic analyses indicate shared genetic architecture with neuroticism and openness

Investigating the phenotypic and genetic associations between personality traits and suicidal behavior across major mental health diagnoses

Behavioural and functional evidence revealing the role of RBFOX1 variation in multiple psychiatric disorders and traits

Urbanicity, behavior problems and HPA axis regulation in preschoolers

Combining schizophrenia and depression polygenic risk scores improves the genetic prediction of lithium response in bipolar disorder patients

Einsamkeit während der ersten Welle der SARS-CoV-2-Pandemie – Ergebnisse der NAKO-Gesundheitsstudie

Prediction of lithium response using genomic data

Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders

Effects of high-frequency prefrontal rTMS on heart frequency rates and blood pressure in schizophrenia

HLA-DRB1 and HLA-DQB1 genetic diversity modulates response to lithium in bipolar affective disorders

Interplay between the genetics of personality traits, severe psychiatric disorders and COVID-19 host genetics in the susceptibility to SARS-CoV-2 infection

Expanding the genetic architecture of nicotine dependence and its shared genetics with multiple traits

Apolipoprotein E Homozygous ε4 Allele Status: A Deteriorating Effect on Visuospatial Working Memory and Global Brain Structure

A functional variant in the serotonin receptor 7 gene (HTR7), rs7905446, is associated with good response to SSRIs in bipolar and unipolar depression

Genetik in Neurologie und Psychiatrie

Reproducible grey matter patterns index a multivariate, global alteration of brain structure in schizophrenia and bipolar disorder

Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders

Efficacy of high-frequency repetitive transcranial magnetic stimulation in schizophrenia patients with treatment-resistant negative symptoms treated with clozapine

Interaction of the Psychiatric Risk Gene Cacna1c With Post-weaning Social Isolation or Environmental Enrichment Does Not Affect Brain Mitochondrial Bioenergetics in Rats

Nutzung genomweiter Daten zum besseren Verständnis der molekulargenetischen Basis von Schizophrenie und Alkoholabhängigkeit

Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

Detecting significant genotype–phenotype association rules in bipolar disorder: market research meets complex genetics

Effects of BDNF Val66Met genotype and schizophrenia familial risk on a neural functional network for cognitive control in humans

Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder

Cortical surface area alterations shaped by genetic load for neuroticism

Genes associated with anhedonia: a new analysis in a large clinical trial (GENDEP)

Response to therapeutic sleep deprivation: a naturalistic study of clinical and genetic factors and post-treatment depressive symptom trajectory

Risk-seeking for losses is associated with 5-HTTLPR, but not with transient changes in 5-HT levels

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

Response to the letter by Esteves et al

Impact on birth weight of maternal smoking throughout pregnancy mediated by DNA methylation

Antidepressant drug-specific prediction of depression treatment outcomes from genetic and clinical variables

Impact of prenatal stress on mother-infant dyadic behavior during the still-face paradigm

Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders

Exome sequencing in large, multiplex bipolar disorder families from Cuba

Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders

Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes

Study protocol of the ASD-Net, the German research consortium for the study of Autism Spectrum Disorder across the lifespan: from a better etiological understanding, through valid diagnosis, to more effective health care

The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders

Epigenome-wide DNA methylation analysis in siblings and monozygotic twins discordant for sporadic Parkinson’s disease revealed different epigenetic patterns in peripheral blood mononuclear cells

Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1