Peter E. Thijssen
Peter E. Thijssen
PhD Student LUMC
Verified email at lumc.nl
Title
Cited by
Cited by
Year
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
3612014
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
1792013
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
1672009
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
1092013
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
862014
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
832013
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
812013
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
802015
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
512012
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
482015
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
382013
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
292016
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
282015
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
242013
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
242011
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
212014
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
172017
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
132014
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
62017
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
52016
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