Wibowo Arindrarto
Wibowo Arindrarto
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Cited by
Unraveling the polygenic architecture of complex traits using blood eQTL metaanalysis
U Vősa, A Claringbould, HJ Westra, MJ Bonder, P Deelen, B Zeng, ...
BioRxiv, 447367, 2018
Disease variants alter transcription factor levels and methylation of their binding sites
MJ Bonder, R Luijk, D Zhernakova, M Moed, P Deelen, M Vermaat, ...
Nature Genetics 49, 131-138, 2016
Identification of context-dependent expression quantitative trait loci in whole blood
DV Zhernakova, P Deelen, M Vermaat, M Van Iterson, M Van Galen, ...
Nature genetics 49 (1), 139-145, 2017
Genetic and environmental influences interact with age and sex in shaping the human methylome
J Van Dongen, MG Nivard, G Willemsen, JJ Hottenga, Q Helmer, ...
Nature communications 7 (1), 11115, 2016
Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression
U Vősa, A Claringbould, HJ Westra, MJ Bonder, P Deelen, B Zeng, ...
Nature genetics 53 (9), 1300-1310, 2021
Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits
E Porcu, S Rüeger, K Lepik, FA Santoni, A Reymond, Z Kutalik
Nature communications 10 (1), 3300, 2019
DNA methylation analysis identifies loci for blood pressure regulation
MA Richard, T Huan, S Ligthart, R Gondalia, MA Jhun, JA Brody, MR Irvin, ...
The American Journal of Human Genetics 101 (6), 888-902, 2017
Improving phenotypic prediction by combining genetic and epigenetic associations
S Shah, MJ Bonder, RE Marioni, Z Zhu, AF McRae, A Zhernakova, ...
The American Journal of Human Genetics 97 (1), 75-85, 2015
KeyGenes, a tool to probe tissue differentiation using a human fetal transcriptional atlas
MS Roost, L Van Iperen, Y Ariyurek, HP Buermans, W Arindrarto, ...
Stem cell reports 4 (6), 1112-1124, 2015
Refined mapping of autoimmune disease associated genetic variants with gene expression suggests an important role for non-coding RNAs
I Ricańo-Ponce, DV Zhernakova, P Deelen, O Luo, X Li, A Isaacs, ...
Journal of autoimmunity 68, 62-74, 2016
Uncoupling protein 2 gene polymorphisms are associated with obesity
S Oktavianthi, H Trimarsanto, CA Febinia, K Suastika, MR Saraswati, ...
Cardiovascular diabetology 11, 1-10, 2012
Parental haplotype-specific single-cell transcriptomics reveal incomplete epigenetic reprogramming in human female germ cells
Á Vértesy, W Arindrarto, MS Roost, B Reinius, V Torrens-Juaneda, ...
Nature Communications 9 (1), 1873, 2018
Transcriptional signatures of somatic neoblasts and germline cells in Macrostomum lignano
M Grudniewska, S Mouton, D Simanov, F Beltman, M Grelling, ...
eLife 5 (e20607), 2016
Epigenome-wide association study of attention-deficit/hyperactivity disorder symptoms in adults
J van Dongen, NR Zilhăo, K Sugden, BT Heijmans, P AC’t Hoen, ...
Biological psychiatry 86 (8), 599-607, 2019
Comprehensive diagnostics of acute myeloid leukemia by whole transcriptome RNA sequencing
W Arindrarto, DM Borrŕs, RAL de Groen, RR van den Berg, IJ Locher, ...
Leukemia 35 (1), 47-61, 2021
Annotating transcriptional effects of genetic variants in disease‐relevant tissue: transcriptome‐wide allelic imbalance in osteoarthritic cartilage
W den Hollander, I Pulyakhina, C Boer, N Bomer, R van der Breggen, ...
Arthritis & Rheumatology 71 (4), 561-570, 2019
Dynamic changes in Sox2 spatio-temporal expression promote the second cell fate decision through Fgf4/Fgfr2 signaling in preimplantation mouse embryos
TK Mistri, W Arindrarto, WP Ng, C Wang, LH Lim, L Sun, I Chambers, ...
Biochemical Journal 475 (6), 1075-1089, 2018
Genes associated with venous thromboembolism in colorectal cancer patients
B Ünlü, N Van Es, W Arindrarto, SM Kiełbasa, H Mei, J Westerga, ...
Journal of Thrombosis and Haemostasis 16 (2), 293-302, 2018
New function of the myostatin/activin type I receptor (ALK4) as a mediator of muscle atrophy and muscle regeneration
S Pasteuning-Vuhman, JW Boertje-van der Meulen, M Van Putten, ...
The FASEB Journal 31 (1), 238, 2017
Deep characterization of a common D4Z4 variant identifies biallelic DUX4 expression as a modifier for disease penetrance in FSHD2
RJLF Lemmers, PJ van der Vliet, J Balog, JJ Goeman, W Arindrarto, ...
European Journal of Human Genetics 26 (1), 94-106, 2018
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