Manuel Antonio Rivas wetenschapper
Rivas, Manuel (Manuel A.)
VIAF ID: 11159999648030111447 (Personal)
Permalink: http://viaf.org/viaf/11159999648030111447
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Works
Title | Sources |
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Components of genetic associations across 2,138 phenotypes in the UK Biobank highlight adipocyte biology | |
Dopaminergic stimulants and risk of Parkinson’s disease | |
A fast and scalable framework for large-scale and ultrahigh-dimensional sparse regression with application to the UK Biobank | |
FasTag: Automatic text classification of unstructured medical narratives | |
A framework for variation discovery and genotyping using next-generation DNA sequencing data | |
Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's disease. | |
The genetic architecture of type 2 diabetes | |
Graphical analysis for phenome-wide causal discovery in genotyped population-scale biobanks | |
High-throughput SARS-CoV-2 and host genome sequencing from single nasopharyngeal swabs | |
Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population | |
Opportunities and challenges for transcriptome-wide association studies | |
A phenome-wide association study of 26 mendelian genes reveals phenotypic expressivity of common and rare variants within the general population | |
Polygenic risk modeling with latent trait-related genetic components | |
Race, Socioeconomic Deprivation, and Hospitalization for COVID-19 in English participants of a National Biobank | |
Rare protein-altering variants in ANGPTL7 lower intraocular pressure and protect against glaucoma | |
Sex-specific genetic effects across biomarkers | |
Significant sparse polygenic risk scores across 813 traits in UK Biobank |