Unidade de investigación
Servicio
Leiden University Medical Center
Leiden, HolandaPublicacións en colaboración con investigadores/as de Leiden University Medical Center (19)
2024
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Evolution and advancements in genomics and epigenomics in OA research: How far we have come
Osteoarthritis and Cartilage
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Minimal information for studies of extracellular vesicles (MISEV2023): From basic to advanced approaches
Journal of Extracellular Vesicles, Vol. 13, Núm. 2
2023
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Genetic analysis of blood molecular phenotypes reveals common properties in the regulatory networks affecting complex traits
Nature Communications, Vol. 14, Núm. 1
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Meta-analysis of erosive hand osteoarthritis identifies four common variants that associate with relatively large effect
Annals of the Rheumatic Diseases, Vol. 82, Núm. 6, pp. 873-880
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Pharmacogenomics of GLP-1 receptor agonists: a genome-wide analysis of observational data and large randomised controlled trials
The Lancet Diabetes and Endocrinology, Vol. 11, Núm. 1, pp. 33-41
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Three decades of advancements in osteoarthritis research: insights from transcriptomic, proteomic, and metabolomic studies
Osteoarthritis and Cartilage
2021
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Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
Autophagy, Vol. 17, Núm. 1, pp. 1-382
2020
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A reference map of potential determinants for the human serum metabolome
Nature, Vol. 588, Núm. 7836, pp. 135-140
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Predicting and elucidating the etiology of fatty liver disease: A machine learning modeling and validation study in the IMI DIRECT cohorts
PLoS Medicine, Vol. 17, Núm. 6
2019
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Genetic studies of abdominal MRI data identify genes regulating hepcidin as major determinants of liver iron concentration
Journal of Hepatology, Vol. 71, Núm. 3, pp. 594-602
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Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
Nature Genetics, Vol. 51, Núm. 5, pp. 804-814
2016
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Genome-wide associations for birth weight and correlations with adult disease
Nature, Vol. 538, Núm. 7624, pp. 248-252
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Variations in the Genome: The Mutation Detection 2015 Meeting on Detection, Genome Sequencing, and Interpretation
Human Mutation, Vol. 37, Núm. 10, pp. 1106-1109
2015
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Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation
PLoS Genetics, Vol. 11, Núm. 7
2011
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Call for participation in the neurogenetics consortium within the Human Variome Project
Neurogenetics, Vol. 12, Núm. 3, pp. 169-173
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Insights into the genetic architecture of osteoarthritis from stage 1 of the arcOGEN study
Annals of the Rheumatic Diseases, Vol. 70, Núm. 5, pp. 864-867
2010
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How to catch all those mutations-the report of the third human variome project meeting, UNESCO Paris, May 2010
Human Mutation, Vol. 31, Núm. 12, pp. 1374-1381
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Practical guidelines addressing ethical issues pertaining to the curation of human locus-specific variation databases (LSDBs)
Human Mutation, Vol. 31, Núm. 11, pp. 1179-1184
1988
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Molecular analysis of HLA-A2.4 functional variant KLO: close structural and evolutionary relatedness to the HLA-A2.2 subtype
Immunogenetics, Vol. 28, Núm. 3, pp. 143-152