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Page 1
Transcriptomic fingerprints in human peripheral blood mononuclear cells indicative of genotoxic and non-genotoxic carcinogenic exposure.
Hochstenbach K, van Leeuwen DM, Gottschalk RW, Gmuender H, Stølevik SB, Nygaard UC, Løvik M, Granum B, Namork E, van Loveren H, van Delft JH. Hochstenbach K, et al. Among authors: gottschalk rw. Mutat Res. 2012 Aug 15;746(2):124-34. doi: 10.1016/j.mrgentox.2012.01.002. Epub 2012 Jan 16. Mutat Res. 2012. PMID: 22269147
Global gene expression analysis in cord blood reveals gender-specific differences in response to carcinogenic exposure in utero.
Hochstenbach K, van Leeuwen DM, Gmuender H, Gottschalk RW, Løvik M, Granum B, Nygaard U, Namork E, Kirsch-Volders M, Decordier I, Vande Loock K, Besselink H, Törnqvist M, von Stedingk H, Rydberg P, Kleinjans JC, van Loveren H, van Delft JH. Hochstenbach K, et al. Among authors: gottschalk rw. Cancer Epidemiol Biomarkers Prev. 2012 Oct;21(10):1756-67. doi: 10.1158/1055-9965.EPI-12-0304. Epub 2012 Aug 9. Cancer Epidemiol Biomarkers Prev. 2012. PMID: 22879202
Toxicogenomic profiles in relation to maternal immunotoxic exposure and immune functionality in newborns.
Hochstenbach K, van Leeuwen DM, Gmuender H, Gottschalk RW, Stølevik SB, Nygaard UC, Løvik M, Granum B, Namork E, Meltzer HM, Kleinjans JC, van Delft JH, van Loveren H. Hochstenbach K, et al. Among authors: gottschalk rw. Toxicol Sci. 2012 Oct;129(2):315-24. doi: 10.1093/toxsci/kfs214. Epub 2012 Jun 27. Toxicol Sci. 2012. PMID: 22738990 Free PMC article.
Whole Exome Sequencing Is the Preferred Strategy to Identify the Genetic Defect in Patients With a Probable or Possible Mitochondrial Cause.
Theunissen TEJ, Nguyen M, Kamps R, Hendrickx AT, Sallevelt SCEH, Gottschalk RWH, Calis CM, Stassen APM, de Koning B, Mulder-Den Hartog ENM, Schoonderwoerd K, Fuchs SA, Hilhorst-Hofstee Y, de Visser M, Vanoevelen J, Szklarczyk R, Gerards M, de Coo IFM, Hellebrekers DMEI, Smeets HJM. Theunissen TEJ, et al. Among authors: gottschalk rwh. Front Genet. 2018 Oct 12;9:400. doi: 10.3389/fgene.2018.00400. eCollection 2018. Front Genet. 2018. PMID: 30369941 Free PMC article.
Novel SLC25A32 mutation in a patient with a severe neuromuscular phenotype.
Hellebrekers DMEI, Sallevelt SCEH, Theunissen TEJ, Hendrickx ATM, Gottschalk RW, Hoeijmakers JGJ, Habets DD, Bierau J, Schoonderwoerd KG, Smeets HJM. Hellebrekers DMEI, et al. Among authors: gottschalk rw. Eur J Hum Genet. 2017 Jun;25(7):886-888. doi: 10.1038/ejhg.2017.62. Epub 2017 Apr 26. Eur J Hum Genet. 2017. PMID: 28443623 Free PMC article.
Polyhydramnios and cerebellar atrophy: a prenatal presentation of mitochondrial encephalomyopathy caused by mutations in the FBXL4 gene.
van Rij MC, Jansen FA, Hellebrekers DM, Onkenhout W, Smeets HJ, Hendrickx AT, Gottschalk RW, Steggerda SJ, Peeters-Scholte CM, Haak MC, Hilhorst-Hofstee Y. van Rij MC, et al. Among authors: gottschalk rw. Clin Case Rep. 2016 Mar 16;4(4):425-8. doi: 10.1002/ccr3.511. eCollection 2016 Apr. Clin Case Rep. 2016. PMID: 27099744 Free PMC article.
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