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Predicting disease-causing variant combinations.
Proc Natl Acad Sci U S A. 2019 Jun 11;116(24):11878-11887. doi: 10.1073/pnas.1815601116. Epub 2019 May 24.
Proc Natl Acad Sci U S A. 2019.
PMID: 31127050
Free PMC article.
ORVAL: a novel platform for the prediction and exploration of disease-causing oligogenic variant combinations.
Renaux A, Papadimitriou S, Versbraegen N, Nachtegael C, Boutry S, Nowé A, Smits G, Lenaerts T.
Renaux A, et al. Among authors: versbraegen n.
Nucleic Acids Res. 2019 Jul 2;47(W1):W93-W98. doi: 10.1093/nar/gkz437.
Nucleic Acids Res. 2019.
PMID: 31147699
Free PMC article.
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Using game theory and decision decomposition to effectively discern and characterise bi-locus diseases.
Versbraegen N, Fouché A, Nachtegael C, Papadimitriou S, Gazzo A, Smits G, Lenaerts T.
Versbraegen N, et al.
Artif Intell Med. 2019 Aug;99:101690. doi: 10.1016/j.artmed.2019.06.006. Epub 2019 Jul 23.
Artif Intell Med. 2019.
PMID: 31606112
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Undiagnosed RASopathies in infertile men.
Juchnewitsch AG, Pomm K, Dutta A, Tamp E, Valkna A, Lillepea K, Mahyari E, Tjagur S, Belova G, Kübarsepp V, Castillo-Madeen H, Riera-Escamilla A, Põlluaas L, Nagirnaja L, Poolamets O, Vihljajev V, Sütt M, Versbraegen N, Papadimitriou S, McLachlan RI, Jarvi KA, Schlegel PN, Tennisberg S, Korrovits P, Vigh-Conrad K, O'Bryan MK, Aston KI, Lenaerts T, Conrad DF, Kasak L, Punab M, Laan M.
Juchnewitsch AG, et al. Among authors: versbraegen n.
Front Endocrinol (Lausanne). 2024 Apr 9;15:1312357. doi: 10.3389/fendo.2024.1312357. eCollection 2024.
Front Endocrinol (Lausanne). 2024.
PMID: 38654924
Free PMC article.
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Toward clinical exomes in diagnostics and management of male infertility.
Lillepea K, Juchnewitsch AG, Kasak L, Valkna A, Dutta A, Pomm K, Poolamets O, Nagirnaja L, Tamp E, Mahyari E, Vihljajev V, Tjagur S, Papadimitriou S, Riera-Escamilla A, Versbraegen N, Farnetani G, Castillo-Madeen H, Sütt M, Kübarsepp V, Tennisberg S, Korrovits P, Krausz C, Aston KI, Lenaerts T, Conrad DF, Punab M, Laan M.
Lillepea K, et al. Among authors: versbraegen n.
Am J Hum Genet. 2024 May 2;111(5):877-895. doi: 10.1016/j.ajhg.2024.03.013. Epub 2024 Apr 12.
Am J Hum Genet. 2024.
PMID: 38614076
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Faster and more accurate pathogenic combination predictions with VarCoPP2.0.
Versbraegen N, Gravel B, Nachtegael C, Renaux A, Verkinderen E, Nowé A, Lenaerts T, Papadimitriou S.
Versbraegen N, et al.
BMC Bioinformatics. 2023 May 1;24(1):179. doi: 10.1186/s12859-023-05291-3.
BMC Bioinformatics. 2023.
PMID: 37127601
Free PMC article.
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Congenital hydrocephalus: new Mendelian mutations and evidence for oligogenic inheritance.
Jacquemin V, Versbraegen N, Duerinckx S, Massart A, Soblet J, Perazzolo C, Deconinck N, Brischoux-Boucher E, De Leener A, Revencu N, Janssens S, Moorgat S, Blaumeiser B, Avela K, Touraine R, Abou Jaoude I, Keymolen K, Saugier-Veber P, Lenaerts T, Abramowicz M, Pirson I.
Jacquemin V, et al. Among authors: versbraegen n.
Hum Genomics. 2023 Mar 2;17(1):16. doi: 10.1186/s40246-023-00464-w.
Hum Genomics. 2023.
PMID: 36859317
Free PMC article.
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