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Genome-Wide Copy Number Variation Scan Identifies Complement Component C4 as Novel Susceptibility Gene for Crohn's Disease.
Cleynen I, Konings P, Robberecht C, Laukens D, Amininejad L, Théâtre E, Machiels K, Arijs I, Rutgeerts P, Louis E, Franchimont D, De Vos M, Van Steen K, Georges M, Moreau Y, Vermeesch J, Vermeire S. Cleynen I, et al. Inflamm Bowel Dis. 2016 Mar;22(3):505-15. doi: 10.1097/MIB.0000000000000623. Inflamm Bowel Dis. 2016. PMID: 26595553
Genetics of inflammatory bowel disease: beyond NOD2.
Mirkov MU, Verstockt B, Cleynen I. Mirkov MU, et al. Among authors: cleynen i. Lancet Gastroenterol Hepatol. 2017 Mar;2(3):224-234. doi: 10.1016/S2468-1253(16)30111-X. Epub 2017 Feb 9. Lancet Gastroenterol Hepatol. 2017. PMID: 28404137 Review.
The genetics of non-monogenic IBD.
Jans D, Cleynen I. Jans D, et al. Among authors: cleynen i. Hum Genet. 2023 May;142(5):669-682. doi: 10.1007/s00439-023-02521-9. Epub 2023 Jan 31. Hum Genet. 2023. PMID: 36720734 Review.
91 results