His primary areas of study are Genetics, Genome-wide association study, Disease, Genetic association and Genome. All of his Genetics and Genomics, Candidate gene, Gene and Human genome investigations are sub-components of the entire Genetics study. His study connects Computational biology and Genomics.
His Computational biology study incorporates themes from Exome sequencing, Genetic variation and Human genetic variation. Kasper Lage integrates many fields, such as Genome-wide association study, Allele and Bioinformatics, in his works. His study in Disease is interdisciplinary in nature, drawing from both Phenotype, Proteomics and Gene expression.
His primary scientific interests are in Genetics, Gene, Computational biology, Genome-wide association study and Candidate gene. His study in the field of Allele, Exome and Zebrafish also crosses realms of Congenital diaphragmatic hernia. In his research on the topic of Gene, Mutation is strongly related with Cancer.
His Computational biology study integrates concerns from other disciplines, such as Genomics, Disease, Missense mutation and Protein–protein interaction. His Genetic association research extends to Genome-wide association study, which is thematically connected. His Candidate gene study combines topics in areas such as Internal medicine, QRS complex and Gene expression profiling.
His scientific interests lie mostly in Gene, Computational biology, Protein–protein interaction, Disease and Haploinsufficiency. In his study, Embedding, Identification and Leverage is strongly linked to Cancer, which falls under the umbrella field of Gene. His studies deal with areas such as Missense mutation, CRISPR, Mutagenesis, Interaction network and Protein structure as well as Computational biology.
His studies in Haploinsufficiency integrate themes in fields like Cerebral cortex and Human brain. His Mutation research includes themes of Class, Biological network and Mutation. His Phenotype research is classified as research in Genetics.
Kasper Lage focuses on Gene, Computational biology, Mutagenesis, Point mutation and Amino acid. His study on Mutation is often connected to Key as part of broader study in Gene. In his papers, Kasper Lage integrates diverse fields, such as Computational biology and Alternative splicing.
His Mutagenesis research incorporates elements of Protein structure and Missense mutation.
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.
A global reference for human genetic variation.
Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin.
(2015)
A global reference for human genetic variation
Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin.
PMC (2015)
A human phenome-interactome network of protein complexes implicated in genetic disorders
Kasper Lage;E Olof Karlberg;Zenia M Størling;Páll Í Ólason.
Nature Biotechnology (2007)
Sequencing Chromosomal Abnormalities Reveals Neurodevelopmental Loci that Confer Risk across Diagnostic Boundaries
Michael E. Talkowski;Jill A. Rosenfeld;Ian Blumenthal;Vamsee Pillalamarri.
Cell (2012)
Pervasive sharing of genetic effects in autoimmune disease.
Chris Cotsapas;Benjamin F. Voight;Benjamin F. Voight;Elizabeth Rossin;Kasper Lage;Kasper Lage;Kasper Lage.
PLOS Genetics (2011)
Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biology
Elizabeth J. Rossin;Kasper Lage;Soumya Raychaudhuri;Soumya Raychaudhuri;Soumya Raychaudhuri;Ramnik J. Xavier;Ramnik J. Xavier.
PLOS Genetics (2011)
Proteomic analysis of lysine acetylation sites in rat tissues reveals organ specificity and subcellular patterns
Alicia Lundby;Alicia Lundby;Alicia Lundby;Kasper Lage;Brian T. Weinert;Dorte B. Bekker-Jensen.
Cell Reports (2012)
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge.
Catherine A. Brownstein;Alan H. Beggs;Nils Homer;Barry Merriman.
(2014)
Integrative Annotation of Variants from 1092 Humans: Application to Cancer Genomics
Ekta Khurana;Yao Fu;Vincenza Colonna;Vincenza Colonna;Xinmeng Jasmine Mu.
Science (2013)
Genome-wide meta-analysis identifies new susceptibility loci for migraine
Verneri Anttila;Bendik S. Winsvold;Bendik S. Winsvold;Padhraig Gormley;Tobias Kurth.
Nature Genetics (2013)
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