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A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies.
Turro E, Greene D, Wijgaerts A, Thys C, Lentaigne C, Bariana TK, Westbury SK, Kelly AM, Selleslag D, Stephens JC, Papadia S, Simeoni I, Penkett CJ, Ashford S, Attwood A, Austin S, Bakchoul T, Collins P, Deevi SV, Favier R, Kostadima M, Lambert MP, Mathias M, Millar CM, Peerlinck K, Perry DJ, Schulman S, Whitehorn D, Wittevrongel C; BRIDGE-BPD Consortium; De Maeyer M, Rendon A, Gomez K, Erber WN, Mumford AD, Nurden P, Stirrups K, Bradley JR, Raymond FL, Laffan MA, Van Geet C, Richardson S, Freson K, Ouwehand WH. Turro E, et al. Among authors: wijgaerts a. Sci Transl Med. 2016 Mar 2;8(328):328ra30. doi: 10.1126/scitranslmed.aad7666. Epub 2016 Mar 2. Sci Transl Med. 2016. PMID: 26936507 Free PMC article.
GATA1 gene variants associated with thrombocytopenia and anemia.
Freson K, Wijgaerts A, Van Geet C. Freson K, et al. Among authors: wijgaerts a. Platelets. 2017 Nov;28(7):731-734. doi: 10.1080/09537104.2017.1361525. Epub 2017 Sep 12. Platelets. 2017. PMID: 28895773 Review. No abstract available.
Unravelling the disease mechanism for TSPYL1 deficiency.
Buyse G, Di Michele M, Wijgaerts A, Louwette S, Wittevrongel C, Thys C, Downes K, Ceulemans B, Van Esch H, Van Geet C, Freson K. Buyse G, et al. Among authors: wijgaerts a. Hum Mol Genet. 2020 Dec 18;29(20):3431-3442. doi: 10.1093/hmg/ddaa233. Hum Mol Genet. 2020. PMID: 33075815
Differentiation between chemo- and radiotoxicity of 137Cs and 60Co on Lemna minor.
Van Dyck I, Vanhoudt N, Vives I Batlle J, Vargas CS, Horemans N, Van Gompel A, Nauts R, Wijgaerts A, Marchal W, Claesen J, Vangronsveld J. Van Dyck I, et al. Among authors: wijgaerts a. J Environ Radioact. 2024 Feb;272:107351. doi: 10.1016/j.jenvrad.2023.107351. Epub 2023 Dec 7. J Environ Radioact. 2024. PMID: 38064934