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Author Details

Morris A Swertz
University of Groningen, University Medical Center Groningen
2004
158
54
Timothy Clark (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
35957574Life course of retrospective harmonization initiatives: key elements to consider.J Dev Orig Health Dis2023
35957574Life course of retrospective harmonization initiatives: key elements to consider.J Dev Orig Health Dis2023
37781402Curation and expansion of the Human Phenotype Ontology for systemic autoinflammatory diseases improves phenotype-driven disease-matching.Front Immunol2023
37768885Ten quick tips for building FAIR workflows.PLoS Comput Biol2023
36964621The phenotypic spectrum of terminal and subterminal 6p deletions based on a social media-derived cohort and literature review.Orphanet J Rare Dis2023
36474914Altered and allele-specific open chromatin landscape reveals epigenetic and genetic regulators of innate immunity in COVID-19.Cell Genom2023
36935495Parent-reported phenotype data on chromosome 6 aberrations collected via an online questionnaire: data consistency and data availability.Orphanet J Rare Dis2023
37114804Semi-automatic translation of medicine usage data (in Dutch, free-text) from Lifelines COVID-19 questionnaires to ATC codes.Database (Oxford)2023
37047868The Impact of Mode of Birth, and Episiotomy, on Postpartum Sexual Function in the Medium- and Longer-Term: An Integrative Systematic Review.Int J Environ Res Public Health2023
37781402Curation and expansion of the Human Phenotype Ontology for systemic autoinflammatory diseases improves phenotype-driven disease-matching.Front Immunol2023
37768885Ten quick tips for building FAIR workflows.PLoS Comput Biol2023
37047868The Impact of Mode of Birth, and Episiotomy, on Postpartum Sexual Function in the Medium- and Longer-Term: An Integrative Systematic Review.Int J Environ Res Public Health2023
37114804Semi-automatic translation of medicine usage data (in Dutch, free-text) from Lifelines COVID-19 questionnaires to ATC codes.Database (Oxford)2023
36964621The phenotypic spectrum of terminal and subterminal 6p deletions based on a social media-derived cohort and literature review.Orphanet J Rare Dis2023
36474914Altered and allele-specific open chromatin landscape reveals epigenetic and genetic regulators of innate immunity in COVID-19.Cell Genom2023
36935495Parent-reported phenotype data on chromosome 6 aberrations collected via an online questionnaire: data consistency and data availability.Orphanet J Rare Dis2023
34826340From Inception to ConcePTION: Genesis of a Network to Support Better Monitoring and Communication of Medication Safety During Pregnancy and Breastfeeding.Clin Pharmacol Ther2022
35505836Road to FAIR genomes: a gap analysis of NGS data generation and sharing in the Netherlands.BMJ Open Sci2022
35418585FAIR Genomes metadata schema promoting Next Generation Sequencing data reuse in Dutch healthcare and research.Sci Data2022
36517834Towards FAIRification of sensitive and fragmented rare disease patient data: challenges and solutions in European reference network registries.Orphanet J Rare Dis2022
36463884Towards an Interoperable Ecosystem of Research Cohort and Real-world Data Catalogues Enabling Multi-center Studies.Yearb Med Inform2022
35292119Semantic modelling of common data elements for rare disease registries, and a prototype workflow for their deployment over registry data.J Biomed Semantics2022
35150722Associations of early-life pet ownership with asthma and allergic sensitization: A meta-analysis of more than 77,000 children from the EU Child Cohort Network.J Allergy Clin Immunol2022
34826340From Inception to ConcePTION: Genesis of a Network to Support Better Monitoring and Communication of Medication Safety During Pregnancy and Breastfeeding.Clin Pharmacol Ther2022
35505836Road to FAIR genomes: a gap analysis of NGS data generation and sharing in the Netherlands.BMJ Open Sci2022
35418585FAIR Genomes metadata schema promoting Next Generation Sequencing data reuse in Dutch healthcare and research.Sci Data2022
36517834Towards FAIRification of sensitive and fragmented rare disease patient data: challenges and solutions in European reference network registries.Orphanet J Rare Dis2022
36463884Towards an Interoperable Ecosystem of Research Cohort and Real-world Data Catalogues Enabling Multi-center Studies.Yearb Med Inform2022
35292119Semantic modelling of common data elements for rare disease registries, and a prototype workflow for their deployment over registry data.J Biomed Semantics2022
35150722Associations of early-life pet ownership with asthma and allergic sensitization: A meta-analysis of more than 77,000 children from the EU Child Cohort Network.J Allergy Clin Immunol2022
32333097Habitual dietary intake of IBD patients differs from population controls: a case-control study.Eur J Nutr2021
32333097Habitual dietary intake of IBD patients differs from population controls: a case-control study.Eur J Nutr2021
34012022Feasibility of predicting allele specific expression from DNA sequencing using machine learning.Sci Rep2021
33737436Lifelines COVID-19 cohort: investigating COVID-19 infection and its health and societal impacts in a Dutch population-based cohort.BMJ Open2021
33884544The EU Child Cohort Network's core data: establishing a set of findable, accessible, interoperable and re-usable (FAIR) variables.Eur J Epidemiol2021
34136434Strategies in Rapid Genetic Diagnostics of Critically Ill Children: Experiences From a Dutch University Hospital.Front Pediatr2021
34781942IRF7 and RNH1 are modifying factors of HIV-1 reservoirs: a genome-wide association analysis.BMC Med2021
35169663LongITools: Dynamic longitudinal exposome trajectories in cardiovascular and metabolic noncommunicable diseases.Environ Epidemiol2021
34820659The Data Use Ontology to streamline responsible access to human biomedical datasets.Cell Genom2021
34934888Advancing tools for human early lifecourse exposome research and translation (ATHLETE): Project overview.Environ Epidemiol2021
34475573Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression.Nat Genet2021
33737436Lifelines COVID-19 cohort: investigating COVID-19 infection and its health and societal impacts in a Dutch population-based cohort.BMJ Open2021
33884544The EU Child Cohort Network's core data: establishing a set of findable, accessible, interoperable and re-usable (FAIR) variables.Eur J Epidemiol2021
34934888Advancing tools for human early lifecourse exposome research and translation (ATHLETE): Project overview.Environ Epidemiol2021
35169663LongITools: Dynamic longitudinal exposome trajectories in cardiovascular and metabolic noncommunicable diseases.Environ Epidemiol2021
34820659The Data Use Ontology to streamline responsible access to human biomedical datasets.Cell Genom2021
34781942IRF7 and RNH1 are modifying factors of HIV-1 reservoirs: a genome-wide association analysis.BMC Med2021
34475573Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression.Nat Genet2021
34012022Feasibility of predicting allele specific expression from DNA sequencing using machine learning.Sci Rep2021
34136434Strategies in Rapid Genetic Diagnostics of Critically Ill Children: Experiences From a Dutch University Hospital.Front Pediatr2021
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University of Lausanne
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Lee Kong Chian School of Medicine, Nanyang Technological University
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Vertex Pharmaceuticals
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London NorthWest Healthcare NHS Trust
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National Institute on Aging
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Imperial College London
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University Medical Center Groningen, University of Groningen
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