Peter E. Thijssen
Peter E. Thijssen
PhD Student LUMC
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Cited by
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DNA methylation signatures link prenatal famine exposure to growth and metabolism
EW Tobi, JJ Goeman, R Monajemi, H Gu, H Putter, Y Zhang, RC Slieker, ...
Nature communications 5 (1), 1-14, 2014
MuSK IgG4 autoantibodies cause myasthenia gravis by inhibiting binding between MuSK and Lrp4
MG Huijbers, W Zhang, R Klooster, EH Niks, MB Friese, KR Straasheijm, ...
Proceedings of the National Academy of Sciences 110 (51), 20783-20788, 2013
SOX antibodies in small-cell lung cancer and Lambert-Eaton myasthenic syndrome: frequency and relation with survival
MJ Titulaer, R Klooster, M Potman, L Sabater, F Graus, IM Hegeman, ...
Journal of Clinical Oncology 27 (26), 4260-4267, 2009
Gene set analysis of GWAS data for human longevity highlights the relevance of the insulin/IGF-1 signaling and telomere maintenance pathways
J Deelen, HW Uh, R Monajemi, D van Heemst, PE Thijssen, S Böhringer, ...
Age 35 (1), 235-249, 2013
Mutations in CDCA7 and HELLS cause immunodeficiency–centromeric instability–facial anomalies syndrome
PE Thijssen, Y Ito, G Grillo, J Wang, G Velasco, H Nitta, M Unoki, ...
Nature communications 6 (1), 1-8, 2015
Intrinsic epigenetic regulation of the D4Z4 macrosatellite repeat in a transgenic mouse model for FSHD
YD Krom, PE Thijssen, JM Young, B den Hamer, J Balog, Z Yao, L Maves, ...
PLoS genet 9 (4), e1003415, 2013
Leukocyte telomere length associates with prospective mortality independent of immune-related parameters and known genetic markers
J Deelen, M Beekman, V Codd, S Trompet, L Broer, S Hägg, K Fischer, ...
International journal of epidemiology 43 (3), 878-886, 2014
Heterogeneous clinical presentation in ICF syndrome: correlation with underlying gene defects
CMR Weemaes, MJ Van Tol, J Wang, MM van Ostaijen-Ten Dam, ...
European Journal of Human Genetics 21 (11), 1219-1225, 2013
Correlation analysis of clinical parameters with epigenetic modifications in the DUX4 promoter in FSHD
J Balog, PE Thijssen, JC de Greef, B Shah, BGM van Engelen, ...
Epigenetics 7 (6), 579-584, 2012
The de-ubiquitylating enzymes USP26 and USP37 regulate homologous recombination by counteracting RAP80
D Typas, MS Luijsterburg, WW Wiegant, M Diakatou, A Helfricht, ...
Nucleic acids research 43 (14), 6919-6933, 2015
Remodeling and spacing factor 1 (RSF1) deposits centromere proteins at DNA double-strand breaks to promote non-homologous end-joining
A Helfricht, W Wiegant, P Thijssen, A Vertegaal, M Luijsterburg, ...
Cell cycle 12 (18), 3070-3082, 2013
Increased DUX4 expression during muscle differentiation correlates with decreased SMCHD1 protein levels at D4Z4
J Balog, PE Thijssen, S Shadle, KR Straasheijm, PJ van der Vliet, ...
Epigenetics 10 (12), 1133-1142, 2015
Converging disease genes in ICF syndrome: ZBTB24 controls expression of CDCA7 in mammals
H Wu, PE Thijssen, E de Klerk, KKD Vonk, J Wang, B den Hamer, ...
Human molecular genetics 25 (18), 4041-4051, 2016
Chromatin remodeling of human subtelomeres and TERRA promoters upon cellular senescence: commonalities and differences between chromosomes
PE Thijssen, EW Tobi, J Balog, SG Schouten, D Kremer, F El Bouazzaoui, ...
Epigenetics 8 (5), 512-521, 2013
Adipocyte telomere length associates negatively with adipocyte size, whereas adipose tissue telomere length associates negatively with the extent of fibrosis in severely obese …
F El Bouazzaoui, P Henneman, P Thijssen, A Visser, F Koning, MA Lips, ...
International Journal of Obesity 38 (5), 746-749, 2014
Genetic variation in PCAF, a key mediator in epigenetics, is associated with reduced vascular morbidity and mortality: evidence for a new concept from three independent …
D Pons, S Trompet, AJM de Craen, PE Thijssen, PHA Quax, MR de Vries, ...
Heart 97 (2), 143-150, 2011
Expanding the mutation spectrum in ICF syndrome: Evidence for a gender bias in ICF2
ML Van den Boogaard, PE Thijssen, C Aytekin, F Licciardi, AA Kıykım, ...
Clinical Genetics 92 (4), 380-387, 2017
DUX4 promotes transcription of FRG2 by directly activating its promoter in facioscapulohumeral muscular dystrophy
PE Thijssen, J Balog, Z Yao, TP Pham, R Tawil, SJ Tapscott, ...
Skeletal muscle 4 (1), 1-9, 2014
The role of muscle imaging in the diagnosis and assessment of children with genetic muscle disease
JW Chardon, V Straub
Neuropediatrics 48 (04), 233-241, 2017
Hematopoietic stem cell transplantation in a patient with ICF2 syndrome presenting with EBV-induced hemophagocytic lymphohystiocytosis
E Harnisch, EP Buddingh, PE Thijssen, AS Brooks, GJ Driessen, ...
Transplantation 100 (7), e35-e36, 2016
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