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Year Number of Results
2015 5
2016 3
2017 3
2019 1
2020 2
2022 1
2023 1
2024 0

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13 results

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Page 1
An exome-wide study of renal operational tolerance.
Massart A, Danger R, Olsen C, Emond MJ, Viklicky O, Jacquemin V, Soblet J, Duerinckx S, Croes D, Perazzolo C, Hruba P, Daneels D, Caljon B, Sever MS, Pascual J, Miglinas M; Renal Tolerance Investigators; Pirson I, Ghisdal L, Smits G, Giral M, Abramowicz D, Abramowicz M, Brouard S. Massart A, et al. Among authors: daneels d. Front Med (Lausanne). 2023 May 17;9:976248. doi: 10.3389/fmed.2022.976248. eCollection 2022. Front Med (Lausanne). 2023. PMID: 37265662 Free PMC article.
Understanding mutational effects in digenic diseases.
Gazzo A, Raimondi D, Daneels D, Moreau Y, Smits G, Van Dooren S, Lenaerts T. Gazzo A, et al. Among authors: daneels d. Nucleic Acids Res. 2017 Sep 6;45(15):e140. doi: 10.1093/nar/gkx557. Nucleic Acids Res. 2017. PMID: 28911095 Free PMC article.
DIDA: A curated and annotated digenic diseases database.
Gazzo AM, Daneels D, Cilia E, Bonduelle M, Abramowicz M, Van Dooren S, Smits G, Lenaerts T. Gazzo AM, et al. Among authors: daneels d. Nucleic Acids Res. 2016 Jan 4;44(D1):D900-7. doi: 10.1093/nar/gkv1068. Epub 2015 Oct 19. Nucleic Acids Res. 2016. PMID: 26481352 Free PMC article.
Contribution of Cardiac Sodium Channel β-Subunit Variants to Brugada Syndrome.
Peeters U, Scornik F, Riuró H, Pérez G, Komurcu-Bayrak E, Van Malderen S, Pappaert G, Tarradas A, Pagans S, Daneels D, Breckpot K, Brugada P, Bonduelle M, Brugada R, Van Dooren S. Peeters U, et al. Among authors: daneels d. Circ J. 2015;79(10):2118-29. doi: 10.1253/circj.CJ-15-0164. Epub 2015 Jul 15. Circ J. 2015. PMID: 26179811 Free article. Clinical Trial.
Accurate and comprehensive analysis of single nucleotide variants and large deletions of the human mitochondrial genome in DNA and single cells.
Zambelli F, Vancampenhout K, Daneels D, Brown D, Mertens J, Van Dooren S, Caljon B, Gianaroli L, Sermon K, Voet T, Seneca S, Spits C. Zambelli F, et al. Among authors: daneels d. Eur J Hum Genet. 2017 Nov;25(11):1229-1236. doi: 10.1038/ejhg.2017.129. Epub 2017 Aug 23. Eur J Hum Genet. 2017. PMID: 28832570 Free PMC article.
Novel inactivating follicle-stimulating hormone receptor mutations in a patient with premature ovarian insufficiency identified by next-generation sequencing gene panel analysis.
Sassi A, Désir J, Janssens V, Marangoni M, Daneels D, Gheldof A, Bonduelle M, Van Dooren S, Costagliola S, Delbaere A. Sassi A, et al. Among authors: daneels d. F S Rep. 2020 Aug 22;1(3):193-201. doi: 10.1016/j.xfre.2020.08.008. eCollection 2020 Dec. F S Rep. 2020. PMID: 34223243 Free PMC article.
13 results