The scientist’s investigation covers issues in Genome-wide association study, Genetics, Single-nucleotide polymorphism, Locus and Internal medicine. His Genome-wide association study research is multidisciplinary, incorporating elements of Schizophrenia, Bioinformatics, Bipolar disorder, Case-control study and Major depressive disorder. The various areas that he examines in his Major depressive disorder study include Meta-analysis, Genetic heterogeneity and Heritability.
Bertram Müller-Myhsok interconnects Hippocampal formation and Age of onset in the investigation of issues within Genetics. His biological study deals with issues like Breast cancer, which deal with fields such as Genotyping and Mutation. His Internal medicine research is multidisciplinary, relying on both Antidepressant, Endocrinology and Oncology.
Bertram Müller-Myhsok spends much of his time researching Genetics, Genome-wide association study, Single-nucleotide polymorphism, Internal medicine and Genetic association. His study involves Locus, Gene, Genetic linkage, Linkage disequilibrium and Candidate gene, a branch of Genetics. Bertram Müller-Myhsok combines subjects such as Odds ratio, Genetic predisposition, Bipolar disorder, Psychiatry and Major depressive disorder with his study of Genome-wide association study.
The Bipolar disorder study combines topics in areas such as Schizophrenia and Disease. His Single-nucleotide polymorphism research is multidisciplinary, incorporating perspectives in Allele, Haplotype and Bioinformatics. In his research on the topic of Internal medicine, Pharmacology is strongly related with Antidepressant.
His primary areas of study are Genome-wide association study, Major depressive disorder, Schizophrenia, Bipolar disorder and Genetics. The subject of his Genome-wide association study research is within the realm of Single-nucleotide polymorphism. His Major depressive disorder study also includes
His Schizophrenia research incorporates elements of Psychosis, Clinical psychology, Disease and Depression. His study looks at the relationship between Bipolar disorder and topics such as Mood, which overlap with Genomics. As part of the same scientific family, Bertram Müller-Myhsok usually focuses on Genetics, concentrating on Dyslexia and intersecting with Attention deficit hyperactivity disorder and Polymorphism.
Bertram Müller-Myhsok focuses on Genome-wide association study, Major depressive disorder, Schizophrenia, Bipolar disorder and Genetic association. His biological study spans a wide range of topics, including Genetic predisposition, Dyslexia, Heritability, Genetic architecture and Attention deficit hyperactivity disorder. His studies in Major depressive disorder integrate themes in fields like Imputation, Clinical psychology, Disease and Cohort.
His Schizophrenia study combines topics from a wide range of disciplines, such as Bulimia nervosa and Comorbidity. His work on Genetics expands to the thematically related Bipolar disorder. His Genetic heterogeneity study in the realm of Genetics interacts with subjects such as Bipolar I disorder.
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.
Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology
Alexander Zimprich;Alexander Zimprich;Saskia Biskup;Petra Leitner;Peter Lichtner.
Neuron (2004)
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)
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)
Large-scale genotyping identifies 41 new loci associated with breast cancer risk
Kyriaki Michailidou;Per Hall;Anna Gonzalez-Neira;Maya Ghoussaini.
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)
Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatment
Elisabeth B Binder;Daria Salyakina;Peter Lichtner;Gabriele M Wochnik.
Nature Genetics (2004)
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)
Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene
Alfons Meindl;Heide Hellebrand;Constanze Wiek;Verena Erven.
Nature Genetics (2010)
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions
Juliane Winkelmann;Barbara Schormair;Peter Lichtner;Stephan Ripke.
Nature Genetics (2007)
A susceptibility locus for Parkinson's disease maps to chromosome 2p13
Thomas Gasser;Bertram Müller-Myhsok;Zbigniew K. Wszolek;Ralph Oehlmann.
Nature Genetics (1998)
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