The scientist’s investigation covers issues in Genome-wide association study, Genetics, Heritability, Genetic association and Bioinformatics. Hilary K. Finucane has researched Genome-wide association study in several fields, including Major depressive disorder, Bipolar disorder, Sample size determination and Genetic correlation. Her work on Linkage disequilibrium and Single-nucleotide polymorphism as part of general Genetics research is often related to Risk assessment and Maximal information coefficient, thus linking different fields of science.
Hilary K. Finucane works mostly in the field of Heritability, limiting it down to concerns involving SNP and, occasionally, Medical research, Epidemiology of cancer and Data science. The various areas that Hilary K. Finucane examines in her Genetic association study include Genetic predisposition, Medical genetics, Locus, Breast cancer and Genetic variation. The study incorporates disciplines such as Statistics, Reference values, Haplotype and Genetic architecture in addition to Bioinformatics.
Hilary K. Finucane focuses on Genome-wide association study, Heritability, Genetics, Computational biology and Genetic association. Her research in Genome-wide association study intersects with topics in Quantitative trait locus, Breast cancer, Genetic correlation and Genomics. She interconnects SNP, Single-nucleotide polymorphism, Linkage disequilibrium and Regression in the investigation of issues within Heritability.
Her study on Genotype, Expression quantitative trait loci and Locus is often connected to Mendelian randomization as part of broader study in Genetics. The concepts of her Computational biology study are interwoven with issues in Chromatin and Genome. Her Genetic association study integrates concerns from other disciplines, such as Regression analysis, Genetic variation and Major histocompatibility complex.
Hilary K. Finucane mainly investigates Computational biology, Genome-wide association study, Genetic association, Gene and Genome. Her Computational biology research includes themes of Biobank and Heritability. In her articles, Hilary K. Finucane combines various disciplines, including Genome-wide association study and Human leukocyte antigen.
Her research in Genetic association focuses on subjects like Haplotype, which are connected to Locus, Genetic variation and Odds ratio. Her study with Locus involves better knowledge in Genetics. Her studies in Genome integrate themes in fields like Phenotype and CRISPR.
Hilary K. Finucane spends much of her time researching Computational biology, Single-nucleotide polymorphism, Trait, Genetic association and Heritability. Her research integrates issues of Biological pathway, Novel gene, Gene expression, Gene and Gene prioritization in her study of Computational biology. Her Genetic association research is multidisciplinary, incorporating perspectives in Genome-wide association study and Haplotype.
In her papers, she integrates diverse fields, such as Genome-wide association study and Human leukocyte antigen. Haplotype is a subfield of Genetics that she investigates. Her Heritability research incorporates themes from SNP, Biobank and Human genetics.
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LD score regression distinguishes confounding from polygenicity in genome-wide association studies :
Brendan K Bulik-Sullivan;Po-Ru Loh;Hilary K Finucane;Stephan Ripke.
Nature Genetics (2015)
An atlas of genetic correlations across human diseases and traits.
Brendan Bulik-Sullivan;Brendan Bulik-Sullivan;Hilary K Finucane;Verneri Anttila;Verneri Anttila;Alexander Gusev.
Nature Genetics (2015)
Detecting Novel Associations in Large Data Sets
David N. Reshef;David N. Reshef;David N. Reshef;Yakir A. Reshef;Yakir A. Reshef;Hilary K. Finucane;Sharon R. Grossman;Sharon R. Grossman.
Science (2011)
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)
Partitioning heritability by functional annotation using genome-wide association summary statistics.
Hilary K Finucane;Hilary K Finucane;Brendan Bulik-Sullivan;Brendan Bulik-Sullivan;Alexander Gusev;Gosia Trynka.
Nature Genetics (2015)
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)
Efficient Bayesian mixed-model analysis increases association power in large cohorts
Po-Ru Loh;George Tucker;Brendan K Bulik-Sullivan;Bjarni J Vilhjálmsson;Bjarni J Vilhjálmsson.
Nature Genetics (2015)
LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis
Jie Zheng;Mesut A. Erzurumluoglu;Benjamin L. Elsworth;John P. Kemp.
Bioinformatics (2017)
Reference-based phasing using the Haplotype Reference Consortium panel.
Po-Ru Loh;Po-Ru Loh;Petr Danecek;Pier Francesco Palamara;Pier Francesco Palamara;Christian Fuchsberger;Christian Fuchsberger.
Nature Genetics (2016)
Association analysis identifies 65 new breast cancer risk loci
Kyriaki Michailidou;Kyriaki Michailidou;Sara Lindström;Sara Lindström;Joe Dennis;Jonathan Beesley.
Nature (2017)
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