His primary areas of study are Genome-wide association study, Genetics, Schizophrenia, Bipolar disorder and Case-control study. His work carried out in the field of Genome-wide association study brings together such families of science as Psychiatry, Comorbidity, Disease, Genetic association and Genetic architecture. His work on Genotype, Locus and Copy-number variation as part of general Genetics research is frequently linked to IRF6, bridging the gap between disciplines.
His Schizophrenia research includes elements of Major depressive disorder, Psychosis and Allele. His Major depressive disorder research integrates issues from Meta-analysis and Genetic heterogeneity. His biological study spans a wide range of topics, including Single-nucleotide polymorphism and Age of onset.
His primary areas of investigation include Genetics, Genome-wide association study, Bipolar disorder, Schizophrenia and Genetic association. His research integrates issues of Odds ratio, Internal medicine, Case-control study, Major depressive disorder and Genetic architecture in his study of Genome-wide association study. The study incorporates disciplines such as Clinical psychology and Bioinformatics in addition to Major depressive disorder.
His Bipolar disorder research incorporates elements of Lithium, Mental illness and Age of onset. He does research in Schizophrenia, focusing on Psychiatric genetics specifically. His Genetic association research is multidisciplinary, incorporating perspectives in Neuroscience, Disease, Inbreeding and Heritability.
Stefan Herms mainly investigates Genome-wide association study, Bipolar disorder, Genetics, Schizophrenia and Major depressive disorder. His Genome-wide association study study combines topics in areas such as Genetic correlation, Genetic predisposition, Eating disorders, Genetic association and Genetic architecture. His Bipolar disorder study combines topics from a wide range of disciplines, such as Internal medicine and Multiplex.
His Genetics study frequently involves adjacent topics like Bipolar II disorder. The Schizophrenia study which covers Disease that intersects with Atrophy and Borderline personality disorder. His study focuses on the intersection of Major depressive disorder and fields such as SNP with connections in the field of Locus.
Genome-wide association study, Bipolar disorder, Genetic architecture, Schizophrenia and Psychiatry are his primary areas of study. His Genome-wide association study study incorporates themes from Cerebral cortex, Neuroscience, Cortex and Genetic association. His Bipolar disorder study integrates concerns from other disciplines, such as Genetics, Internal medicine, Cohort and Gene expression.
His Genetic architecture research is multidisciplinary, relying on both Attention deficit hyperactivity disorder, Glycemic, Genetic variation, Brain mapping and Comorbidity. Specifically, his work in Schizophrenia is concerned with the study of Psychiatric genetics. The Psychiatry study combines topics in areas such as Body mass index, Case-control study and Disease.
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)
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
S. Hong Lee;Stephan Ripke;Stephan Ripke;Benjamin M. Neale;Benjamin M. Neale;Stephen V. Faraone.
Nature Genetics (2013)
A mega-analysis of genome-wide association studies for major depressive disorder
Stephan Ripke;Naomi R Wray;Cathryn M Lewis;Steven P Hamilton.
Molecular Psychiatry (2013)
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)
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
Naomi R. Wray;Stephan Ripke;Stephan Ripke;Stephan Ripke;Manuel Mattheisen;MacIej Trzaskowski.
Nature Genetics (2018)
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)
Direct Conversion of Fibroblasts into Stably Expandable Neural Stem Cells
Marc Thier;Philipp Wörsdörfer;Yenal B. Lakes;Raphaela Gorris.
Cell Stem Cell (2012)
Genome-wide association study identifies 30 loci associated with bipolar disorder
Eli A. Stahl;Eli A. Stahl;Gerome Breen;Andreas J. Forstner;Andrew McQuillin.
Nature Genetics (2019)
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
Colm O'Dushlaine;Lizzy Rossin;Phil H. Lee;Laramie Duncan;Laramie Duncan.
Nature Neuroscience (2015)
Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24
Stefanie Birnbaum;Stefanie Birnbaum;Kerstin U Ludwig;Heiko Reutter;Stefan Herms.
Nature Genetics (2009)
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