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Page 1
Platelet function is modified by common sequence variation in megakaryocyte super enhancers.
Petersen R, Lambourne JJ, Javierre BM, Grassi L, Kreuzhuber R, Ruklisa D, Rosa IM, Tomé AR, Elding H, van Geffen JP, Jiang T, Farrow S, Cairns J, Al-Subaie AM, Ashford S, Attwood A, Batista J, Bouman H, Burden F, Choudry FA, Clarke L, Flicek P, Garner SF, Haimel M, Kempster C, Ladopoulos V, Lenaerts AS, Materek PM, McKinney H, Meacham S, Mead D, Nagy M, Penkett CJ, Rendon A, Seyres D, Sun B, Tuna S, van der Weide ME, Wingett SW, Martens JH, Stegle O, Richardson S, Vallier L, Roberts DJ, Freson K, Wernisch L, Stunnenberg HG, Danesh J, Fraser P, Soranzo N, Butterworth AS, Heemskerk JW, Turro E, Spivakov M, Ouwehand WH, Astle WJ, Downes K, Kostadima M, Frontini M. Petersen R, et al. Among authors: lenaerts as. Nat Commun. 2017 Jul 13;8:16058. doi: 10.1038/ncomms16058. Nat Commun. 2017. PMID: 28703137 Free PMC article.
The SMAD2/3 interactome reveals that TGFβ controls m6A mRNA methylation in pluripotency.
Bertero A, Brown S, Madrigal P, Osnato A, Ortmann D, Yiangou L, Kadiwala J, Hubner NC, de Los Mozos IR, Sadée C, Lenaerts AS, Nakanoh S, Grandy R, Farnell E, Ule J, Stunnenberg HG, Mendjan S, Vallier L. Bertero A, et al. Among authors: lenaerts as. Nature. 2018 Mar 8;555(7695):256-259. doi: 10.1038/nature25784. Epub 2018 Feb 28. Nature. 2018. PMID: 29489750 Free PMC article.
Modeling PNPLA3-Associated NAFLD Using Human-Induced Pluripotent Stem Cells.
Tilson SG, Morell CM, Lenaerts AS, Park SB, Hu Z, Jenkins B, Koulman A, Liang TJ, Vallier L. Tilson SG, et al. Among authors: lenaerts as. Hepatology. 2021 Dec;74(6):2998-3017. doi: 10.1002/hep.32063. Epub 2021 Sep 27. Hepatology. 2021. PMID: 34288010 Free PMC article.
Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population.
Moens LN, De Rijk P, Reumers J, Van den Bossche MJ, Glassee W, De Zutter S, Lenaerts AS, Nordin A, Nilsson LG, Medina Castello I, Norrback KF, Goossens D, Van Steen K, Adolfsson R, Del-Favero J. Moens LN, et al. Among authors: lenaerts as. PLoS One. 2011;6(8):e23450. doi: 10.1371/journal.pone.0023450. Epub 2011 Aug 11. PLoS One. 2011. PMID: 21853134 Free PMC article.
Detailed analysis of the serotonin transporter gene (SLC6A4) shows no association with bipolar disorder in the Northern Swedish population.
Alaerts M, Ceulemans S, Forero D, Moens LN, De Zutter S, Heyrman L, Lenaerts AS, Norrback KF, Goossens D, De Rijk P, Nilsson LG, Adolfsson R, Del-Favero J. Alaerts M, et al. Among authors: lenaerts as. Am J Med Genet B Neuropsychiatr Genet. 2009 Jun 5;150B(4):585-92. doi: 10.1002/ajmg.b.30853. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 18792946
Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?
Van Den Bossche MJ, Johnstone M, Strazisar M, Pickard BS, Goossens D, Lenaerts AS, De Zutter S, Nordin A, Norrback KF, Mendlewicz J, Souery D, De Rijk P, Sabbe BG, Adolfsson R, Blackwood D, Del-Favero J. Van Den Bossche MJ, et al. Among authors: lenaerts as. Am J Med Genet B Neuropsychiatr Genet. 2012 Oct;159B(7):812-22. doi: 10.1002/ajmg.b.32088. Epub 2012 Aug 22. Am J Med Genet B Neuropsychiatr Genet. 2012. PMID: 22911887
Identification of rare copy number variants in high burden schizophrenia families.
Van Den Bossche MJ, Strazisar M, Cammaerts S, Liekens AM, Vandeweyer G, Depreeuw V, Mattheijssens M, Lenaerts AS, De Zutter S, De Rijk P, Sabbe B, Del-Favero J. Van Den Bossche MJ, et al. Among authors: lenaerts as. Am J Med Genet B Neuropsychiatr Genet. 2013 Apr;162B(3):273-82. doi: 10.1002/ajmg.b.32146. Epub 2013 Mar 15. Am J Med Genet B Neuropsychiatr Genet. 2013. PMID: 23505263
Identification of a CACNA2D4 deletion in late onset bipolar disorder patients and implications for the involvement of voltage-dependent calcium channels in psychiatric disorders.
Van Den Bossche MJ, Strazisar M, De Bruyne S, Bervoets C, Lenaerts AS, De Zutter S, Nordin A, Norrback KF, Goossens D, De Rijk P, Green EK, Grozeva D, Mendlewicz J, Craddock N, Sabbe BG, Adolfsson R, Souery D, Del-Favero J. Van Den Bossche MJ, et al. Among authors: lenaerts as. Am J Med Genet B Neuropsychiatr Genet. 2012 Jun;159B(4):465-75. doi: 10.1002/ajmg.b.32053. Epub 2012 Apr 9. Am J Med Genet B Neuropsychiatr Genet. 2012. PMID: 22488967
19 results