about
The prevalence of metabolic syndrome and metabolically healthy obesity in Europe: a collaborative analysis of ten large cohort studiesOntoCAT--simple ontology search and integration in Java, R and REST/JavaScriptGenetic studies of body mass index yield new insights for obesity biologyPyPedia: using the wiki paradigm as crowd sourcing environment for bioinformatics protocolsThe FAIR Guiding Principles for scientific data management and stewardshipThe ARVD/C genetic variants database: 2014 updateMutation update on the CHD7 gene involved in CHARGE syndromeMeta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levelsGenome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levelsThe Genome of the Netherlands: design, and project goalsVarioML framework for comprehensive variation data representation and exchangeBioinformatics tools and database resources for systems genetics analysis in mice--a short review and an evaluation of future needsTowards the integration of mouse databases - definition and implementation of solutions to two use-cases in mouse functional genomicsInteroperability and FAIRness through a novel combination of Web technologiesGenome-wide analysis identifies 12 loci influencing human reproductive behavior.Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.Lessons learned from whole exome sequencing in multiplex families affected by a complex genetic disorder, intracranial aneurysm.Deleterious alleles in the human genome are on average younger than neutral alleles of the same frequency.Cafe Variome: general-purpose software for making genotype-phenotype data discoverable in restricted or open access contexts.WormQTL--public archive and analysis web portal for natural variation data in Caenorhabditis spp.WormQTLHD--a web database for linking human disease to natural variation data in C. elegans.BiobankConnect: software to rapidly connect data elements for pooled analysis across biobanks using ontological and lexical indexing.Calling genotypes from public RNA-sequencing data enables identification of genetic variants that affect gene-expression levelsDiagnostic interpretation of array data using public databases and internet sources.CoNVaDING: Single Exon Variation Detection in Targeted NGS Data.Toward Global Biobank Integration by Implementation of the Minimum Information About BIobank Data Sharing (MIABIS 2.0 Core).MOLGENIS/connect: a system for semi-automatic integration of heterogeneous phenotype data with applications in biobanks.Solutions for data integration in functional genomics: a critical assessment and case study.Complex nature of SNP genotype effects on gene expression in primary human leucocytesdesignGG: an R-package and web tool for the optimal design of genetical genomics experiments.XGAP: a uniform and extensible data model and software platform for genotype and phenotype experimentsA reference panel of 64,976 haplotypes for genotype imputation.1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.The MOLGENIS toolkit: rapid prototyping of biosoftware at the push of a button.A high-throughput processing service for retention time alignment of complex proteomics and metabolomics LC-MS data.PeakML/mzMatch: a file format, Java library, R library, and tool-chain for mass spectrometry data analysis.Fine mapping the CETP region reveals a common intronic insertion associated to HDL-CModifiers of mutant huntingtin aggregation: functional conservation of C. elegans-modifiers of polyglutamine aggregation.Global genetic robustness of the alternative splicing machinery in Caenorhabditis elegans.Molecular Genetics Information System (MOLGENIS): alternatives in developing local experimental genomics databases.
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Morris A Swertz
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Morris A Swertz
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Morris A Swertz
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Morris A Swertz
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Morris A Swertz
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Morris A Swertz
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Morris A Swertz
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Morris A Swertz
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Morris A. Swertz
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Morris A Swertz
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Morris A Swertz
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Morris A Swertz
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Morris A Swertz
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0000-0002-0979-3401