J. van Meurs

发表

Genome-wide analysis of constitutional DNA methylation in familial melanoma

A. Uitterlinden, M. Bonder, A. Zhernakova, 2020, Clinical Epigenetics.

Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss

M. P. Concas, M. Nalls, R. Mägi, 2022, American journal of human genetics.

Genome-wide identification of directed gene networks using large-scale population genomics data

A. Uitterlinden, M. Bonder, A. Zhernakova, 2017, bioRxiv.

Genome-wide characterization of circulating metabolic biomarkers reveals substantial pleiotropy and novel disease pathways

Pashupati P. Mishra, K. Kristiansson, M. Boehnke, 2022, medRxiv.

Population genomics in a disease targeted primary cell model.

Daniel Sinnett, Fernando Rivadeneira, Claes Ohlsson, 2009, Genome research.

Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation

Annelot M. Dekker, Walk, A. Caspi, 2021, Nature Genetics.

Genome-wide identification of directed gene networks using large-scale population genomics data

Peter A C 't Hoen, Cisca Wijmenga, Lude Franke, 2017, Nature Communications.

Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood

Sina A. Gharib, R. Marioni, P. Visscher, 2018, Nature Communications.

Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS

Annelot M. Dekker, N. Wray, A. McRae, 2022, Science Translational Medicine.

Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits

Zoltán Kutalik, Kaido Lepik, Alexandre Reymond, 2019, Nature Communications.

A linear mixed-model approach to study multivariate gene–environment interactions

Inês Barroso, Lude Franke, Oliver Stegle, 2018, Nature Genetics.

Skewed X-inactivation is common in the general female population

A. Uitterlinden, F. Hormozdiari, D. Cox, 2018, European Journal of Human Genetics.

Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour

M. P. Concas, Sina A. Gharib, C. Gieger, 2021, Nature Human Behaviour.

Target-selected gene inactivation in Caenorhabditis elegans by using a frozen transposon insertion mutant bank.

R. Plasterk, R. Zwaal, J. Groenen, 1993, Proceedings of the National Academy of Sciences of the United States of America.

Refined mapping of autoimmune disease associated genetic variants with gene expression suggests an important role for non-coding RNAs

A. Hofman, A. Uitterlinden, C. Wijmenga, 2016, Journal of autoimmunity.

Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation

C. Ward‐Caviness, M. Waldenberger, J. V. van Meurs, 2018, Nature Communications.

A linear mixed-model approach to study multivariate gene–environment interactions

M. Bonder, A. Zhernakova, C. Wijmenga, 2018, Nature Genetics.

GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures

A. Uitterlinden, J. V. van Meurs, E. Zeggini, 2019, Nature Communications.

Occupational exposure to gases/fumes and mineral dust affect DNA methylation levels of genes regulating expression

Cleo C. van Diemen, A. Uitterlinden, D. Postma, 2019, Human molecular genetics.

Stem Cell Derived Retinal Pigment Epithelium: The Role of Pigmentation as Maturation Marker and Gene Expression Profile Comparison with Human Endogenous Retinal Pigment Epithelium.

P. Moerland, T. Gorgels, A. Bergen, 2017, Stem Cell Reviews and Reports.

A characterization of cis- and trans-heritability of RNA-Seq-based gene expression

A. Uitterlinden, C. Wijmenga, B. Penninx, 2019, European Journal of Human Genetics.

Genome-wide analysis of constitutional DNA methylation in familial melanoma

A. Uitterlinden, M. Bonder, A. Zhernakova, 2020, Clinical Epigenetics.

Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood

Sina A. Gharib, R. Marioni, P. Visscher, 2018, Nature Communications.

Genome-wide identification of genes regulating DNA methylation using genetic anchors for causal inference

J. V. van Meurs, M. Bonder, C. Wijmenga, 2019, bioRxiv.

Correction for both common and rare cell types in blood is important to identify genes that correlate with age

M. Bonder, C. Wijmenga, D. Boomsma, 2020, BMC Genomics.

Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification

Clint L. Miller, M. Fornage, T. Assimes, 2023, Nature Genetics.

Improving Phenotypic Prediction by Combining Genetic and Epigenetic Associations

R. Marioni, L. Liang, P. Visscher, 2015, American journal of human genetics.

Genome-wide characterization of circulating metabolic biomarkers

Pashupati P. Mishra, J. Danesh, C. Gieger, 2024, Nature.

Comprehensive evaluation of smoking exposures and their interactions on DNA methylation

M. Bonder, G. Koppelman, D. Boomsma, 2024, EBioMedicine.

The Rotterdam Study. Design update and major findings between 2020 and 2024.

Brenda C T Kieboom, A. Luik, F. V. van Rooij, 2024, European journal of epidemiology.

Osmolarity‐Induced Altered Intracellular Molecular Crowding Drives Osteoarthritis Pathology

J. V. van Rooij, Y. Ramos, J. van Meurs, 2024, Advanced science.

Epigenome-wide association study on the plasma metabolome suggests self-regulation of the glycine and serine pathway through DNA methylation

M. Bonder, H. Westra, L. Franke, 2024, Clinical epigenetics.