Genetics, Genome-wide association study, Genetic linkage, Linkage disequilibrium and Schizophrenia are her primary areas of study. Genetics is represented through her Allele, Chromosome, Genetic marker, Linkage and Genotype research. The concepts of her Genome-wide association study study are interwoven with issues in Bipolar disorder, Genetic association and Copy-number variation.
Her studies deal with areas such as Pedigree chart, Locus and Genome Scan as well as Genetic linkage. Her Linkage disequilibrium study is concerned with the larger field of Haplotype. In her study, Multifactorial Inheritance is inextricably linked to Disease, which falls within the broad field of Schizophrenia.
Sibylle G. Schwab spends much of her time researching Genetics, Haplotype, Schizophrenia, Allele and Single-nucleotide polymorphism. Her studies link Psychosis with Genetics. Her Haplotype study integrates concerns from other disciplines, such as Genetic variation and Substance dependence.
The Schizophrenia study combines topics in areas such as Genome-wide association study, Phenotype, Bipolar disorder, Age of onset and Neuroscience. Her Allele research integrates issues from Genotype and Exon. In the field of Single-nucleotide polymorphism, her study on SNP overlaps with subjects such as Heroin.
Her main research concerns Schizophrenia, Evolutionary biology, Psychiatry, Genome-wide association study and Genetic association. Her Genome-wide association study research incorporates elements of Bipolar disorder, Schizophrenia, Psychiatric genetics and Autism spectrum disorder. Her Schizophrenia study combines topics from a wide range of disciplines, such as Mental health, Disease, Age of onset and Copy-number variation.
In her research, Haplotype, Genetic variation, Single-nucleotide polymorphism and Quantitative trait locus is intimately related to Heritability, which falls under the overarching field of Genetic association. Her research on Haplotype concerns the broader Genetics. Sibylle G. Schwab has included themes like Psychosis and Substance dependence in her Genetics study.
Her primary areas of study are Genome-wide association study, Bipolar disorder, Lifetime risk, Schizophrenia and Case-control study. Her study in Genome-wide association study is interdisciplinary in nature, drawing from both Schizophrenia, Comorbidity, Tourette syndrome and Age of onset. Her work in Comorbidity covers topics such as Risk factor which are related to areas like Genetic association.
Her Tourette syndrome research includes elements of Pleiotropy, Psychiatric genetics, Autism spectrum disorder and Genetic architecture. Her Age of onset research incorporates themes from Multifactorial Inheritance, Psychosis, Genetics and Copy-number variation. Her Lifetime risk research includes themes of Evolutionary biology and Polygenic risk score.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Biological insights from 108 schizophrenia-associated genetic loci
Stephan Ripke;Stephan Ripke;Benjamin M. Neale;Benjamin M. Neale;Aiden Corvin;James T. R. Walters.
Nature (2014)
Genome-wide association study identifies five new schizophrenia loci
Stephan Ripke;Alan R. Sanders;Kenneth S. Kendler;Douglas F. Levinson.
Nature Genetics (2011)
Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part II: Schizophrenia
Cathryn M. Lewis;Douglas F. Levinson;Lesley H. Wise;Lynn E. DeLisi.
American Journal of Human Genetics (2003)
Analysis of shared heritability in common disorders of the brain
Verneri Anttila;Verneri Anttila;Brendan Bulik-Sullivan;Brendan Bulik-Sullivan;Hilary K. Finucane;Raymond K. Walters;Raymond K. Walters.
Science (2018)
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores
Bjarni J. Vilhjálmsson;Jian Yang;Hilary K. Finucane;Alexander Gusev.
American Journal of Human Genetics (2015)
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
Christian R Marshall;Daniel P Howrigan;Daniel P Howrigan;Daniele Merico;Bhooma Thiruvahindrapuram.
Nature Genetics (2017)
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders
Phil H. Lee;Verneri Anttila;Hyejung Won;Yen-Chen A. Feng.
Cell (2019)
Genomewide association studies: history, rationale, and prospects for psychiatric disorders.
Sven Cichon;Nick Craddock;Mark Daly;Mark Daly;Stephen V. Faraone.
American Journal of Psychiatry (2009)
Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes
Douglas M. Ruderfer;Stephan Ripke;Stephan Ripke;Stephan Ripke;Andrew McQuillin;James Boocock.
Cell (2018)
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
Sibylle G. Schwab;Michael Knapp;Stephanie Mondabon;Joachim Hallmayer.
American Journal of Human Genetics (2003)
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