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Phenotypic spectrum of the first Belgian MYBPC3 founder: a large multi-exon deletion with a varying phenotype.
Boen HM, Alaerts M, Van Laer L, Saenen JB, Goovaerts I, Bastianen J, Koopman P, Vanduynhoven P, De Vuyst E, Rosseel M, Heidbuchel H, Van Craenenbroeck EM, Loeys B. Boen HM, et al. Among authors: van laer l. Front Genet. 2024 May 21;15:1392527. doi: 10.3389/fgene.2024.1392527. eCollection 2024. Front Genet. 2024. PMID: 38836037 Free PMC article.
Left ventricular non-compaction with Ebstein anomaly attributed to a TPM1 mutation.
Nijak A, Alaerts M, Kuiperi C, Corveleyn A, Suys B, Paelinck B, Saenen J, Van Craenenbroeck E, Van Laer L, Loeys B, Verstraeten A. Nijak A, et al. Among authors: van craenenbroeck e, van laer l. Eur J Med Genet. 2018 Jan;61(1):8-10. doi: 10.1016/j.ejmg.2017.10.003. Epub 2017 Oct 9. Eur J Med Genet. 2018. PMID: 29024827
Compound Heterozygous SCN5A Mutations in Severe Sodium Channelopathy With Brugada Syndrome: A Case Report.
Nijak A, Labro AJ, De Wilde H, Dewals W, Peigneur S, Tytgat J, Snyders D, Sieliwonczyk E, Simons E, Van Craenenbroeck E, Schepers D, Van Laer L, Saenen J, Loeys B, Alaerts M. Nijak A, et al. Among authors: van craenenbroeck e, van laer l. Front Cardiovasc Med. 2020 Jul 24;7:117. doi: 10.3389/fcvm.2020.00117. eCollection 2020. Front Cardiovasc Med. 2020. PMID: 32850980 Free PMC article.
Clinical characterization of the first Belgian SCN5A founder mutation cohort.
Sieliwonczyk E, Alaerts M, Robyns T, Schepers D, Claes C, Corveleyn A, Willems R, Van Craenenbroeck EM, Simons E, Nijak A, Vandendriessche B, Mortier G, Vrints C, Koopman P, Heidbuchel H, Van Laer L, Saenen J, Loeys B. Sieliwonczyk E, et al. Among authors: van craenenbroeck em, van laer l. Europace. 2021 Jun 7;23(6):918-927. doi: 10.1093/europace/euaa305. Europace. 2021. PMID: 33221854
Molecular autopsy and subsequent functional analysis reveal de novo DSG2 mutation as cause of sudden death.
Simons E, Labro A, Saenen J, Nijak A, Sieliwonczyk E, Vandendriessche B, Dąbrowska M, Van Craenenbroeck EM, Schepers D, Van Laer L, Loeys BL, Alaerts M. Simons E, et al. Among authors: van craenenbroeck em, van laer l. Eur J Med Genet. 2021 Nov;64(11):104322. doi: 10.1016/j.ejmg.2021.104322. Epub 2021 Aug 23. Eur J Med Genet. 2021. PMID: 34438094
Diagnostic yield of genetic testing in heart transplant recipients with prior cardiomyopathy.
Boen HM, Loeys BL, Alaerts M, Saenen JB, Goovaerts I, Van Laer L, Vorlat A, Vermeulen T, Franssen C, Pauwels P, Rodrigus I, Heidbuchel H, Van Craenenbroeck EM. Boen HM, et al. Among authors: van craenenbroeck em, van laer l. J Heart Lung Transplant. 2022 Sep;41(9):1218-1227. doi: 10.1016/j.healun.2022.03.020. Epub 2022 Apr 9. J Heart Lung Transplant. 2022. PMID: 35581137 Free PMC article.
Targeted Next-Generation Sequencing of 51 Genes Involved in Primary Electrical Disease.
Proost D, Saenen J, Vandeweyer G, Rotthier A, Alaerts M, Van Craenenbroeck EM, Van Crombruggen J, Mortier G, Wuyts W, Vrints C, Del Favero J, Loeys B, Van Laer L. Proost D, et al. Among authors: van craenenbroeck em, van crombruggen j, van laer l. J Mol Diagn. 2017 May;19(3):445-459. doi: 10.1016/j.jmoldx.2017.01.010. Epub 2017 Mar 22. J Mol Diagn. 2017. PMID: 28341588 Free article.
Cardiogeneticsbank@UZA: A Collection of DNA, Tissues, and Cell Lines as a Translational Tool.
Alaerts M, van de Beek G, Luyckx I, Meester J, Schepers D, Verstraeten A, Saenen J, Van Craenenbroeck E, Goovaerts I, Rodrigus I, Laga S, Hendriks J, Goethals S, De Wilde A, Smits E, Jorens P, Huizing M, Van Laer L, Loeys B. Alaerts M, et al. Among authors: van craenenbroeck e, van de beek g, van laer l. Front Med (Lausanne). 2019 Sep 6;6:198. doi: 10.3389/fmed.2019.00198. eCollection 2019. Front Med (Lausanne). 2019. PMID: 31555651 Free PMC article.
175 results