Loeys B - Search Results

1

Toward reporting standards for the pathogenicity of variant combinations involved in multilocus/oligogenic diseases.

Papadimitriou S, Gravel B, Nachtegael C, De Baere E, Loeys B, Vikkula M, Smits G, Lenaerts T. Papadimitriou S, et al. Among authors: loeys b. HGG Adv. 2022 Dec 2;4(1):100165. doi: 10.1016/j.xhgg.2022.100165. eCollection 2023 Jan 12. HGG Adv. 2022. PMID: 36578772 Free PMC article. Review.

2

A generated induced pluripotent stem cell (iPSC) line (CMGANTi005-A) of a Marfan syndrome patient with an FBN1 c.7754T > C (p.Ile2585Thr) variation.

Van Den Heuvel LJF, Peeters S, Meester JAN, Perik M, Coucke P, Loeys BL. Van Den Heuvel LJF, et al. Stem Cell Res. 2023 Mar;67:103032. doi: 10.1016/j.scr.2023.103032. Epub 2023 Jan 23. Stem Cell Res. 2023. PMID: 36708686 Free article.

3

Structural genomic variants in thoracic aortic disease.

Meester JAN, Hebert A, Loeys BL. Meester JAN, et al. Curr Opin Cardiol. 2023 May 1;38(3):157-161. doi: 10.1097/HCO.0000000000001030. Epub 2023 Mar 17. Curr Opin Cardiol. 2023. PMID: 36795406 Free PMC article. Review.

4

varAmpliCNV: analyzing variance of amplicons to detect CNVs in targeted NGS data.

Kumar AA, Loeys B, Van De Beek G, Peeters N, Wuyts W, Van Laer L, Vandeweyer G, Alaerts M. Kumar AA, et al. Among authors: loeys b. Bioinformatics. 2023 Jan 1;39(1):btac756. doi: 10.1093/bioinformatics/btac756. Bioinformatics. 2023. PMID: 36440912 Free PMC article.

5

Clinical and functional characterisation of a recurrent KCNQ1 variant in the Belgian population.

Sieliwonczyk E, Alaerts M, Simons E, Snyders D, Nijak A, Vandendriessche B, Schepers D, Akdeniz D, Van Craenenbroeck E, Knaepen K, Rabaut L, Heidbuchel H, Van Laer L, Saenen J, Labro AJ, Loeys B. Sieliwonczyk E, et al. Among authors: loeys b. Orphanet J Rare Dis. 2023 Jan 31;18(1):23. doi: 10.1186/s13023-023-02618-4. Orphanet J Rare Dis. 2023. PMID: 36721196 Free PMC article.

6

Variants in structural cardiac genes in patients with cancer therapy-related cardiac dysfunction after anthracycline chemotherapy: a case control study.

Boen HM, Alaerts M, Goovaerts I, Saenen JB, Franssen C, Vorlat A, Vermeulen T, Heidbuchel H, Van Laer L, Loeys B, Van Craenenbroeck EM. Boen HM, et al. Among authors: loeys b. Cardiooncology. 2024 Apr 30;10(1):26. doi: 10.1186/s40959-024-00231-3. Cardiooncology. 2024. PMID: 38689299 Free PMC article.

7

Flemish network on rare connective tissue diseases (CTD): patient pathways in systemic sclerosis. First steps taken.

Piette Y, Van den Bossche F, Aerts J, Aerts N, Ajeganova S, Badot V, Berghen N, Blockmans D, Brusselle G, Caeyers N, De Decker M, De Haes P, De Cock C, De Keyser F, De Langhe E, Delcroix M, De Nutte H, De Pauw M, Depicker A, De Sutter A, De Sutter J, Du Four T, Frank C, Goubau J, Guiot J, Gutermuth J, Heeman L, Houssiau F, Hennes I, Lenaerts J, Lintermans A, Loeys B, Luyten H, Maeyaert B, Malfait F, Moeyersoons A, Mostmans Y, Nijs J, Poppe B, Polfliet K, Ruttens D, Sabato V, Schoeters E, Slabbynck H, Stuer A, Tamirou F, Thevissen K, Van Kersschaever G, Vanneuville B, Van Offel J, Vanthuyne M, Van Wabeke J, Verbist C, Vos I, Westhovens R, Wuyts W, Yserbyt J, Smith V. Piette Y, et al. Among authors: loeys b. Acta Clin Belg. 2024 Feb;79(1):26-33. doi: 10.1080/17843286.2023.2280737. Epub 2024 Jan 2. Acta Clin Belg. 2024. PMID: 38108332 Free article.

8

Variable clinical expression of a Belgian TGFB3 founder variant suggests the presence of a genetic modifier.

Perik MHAM, Govaerts E, Laga S, Goovaerts I, Saenen J, Van Craenenbroeck E, Meester JAN, Luyckx I, Rodrigus I, Verstraeten A, Van Laer L, Loeys BL. Perik MHAM, et al. Among authors: loeys bl. Front Genet. 2023 Aug 31;14:1251675. doi: 10.3389/fgene.2023.1251675. eCollection 2023. Front Genet. 2023. PMID: 37719708 Free PMC article.

9

Growth charts for Marfan syndrome in the Netherlands and analysis of genotype-phenotype relationships.

Lauffer P, Pals G, Zwinderman AH, Postema FAM, Baars MJH, Dulfer E, Hilhorst-Hofstee Y, Houweling AC, Kempers M, Krapels IPC, van de Laar IMBH, Loeys B, Spaans AMJ, Warnink-Kavelaars J, de Waard V, Wit JM, Menke LA. Lauffer P, et al. Among authors: loeys b. Am J Med Genet A. 2023 Feb;191(2):479-489. doi: 10.1002/ajmg.a.63047. Epub 2022 Nov 15. Am J Med Genet A. 2023. PMID: 36380655 Free PMC article.

10

IPSC reprogramming of two patients with spondyloepimetaphyseal dysplasia (SEMD, biglycan type).

De Kinderen P, Peeters S, Rabaut L, Mortier G, Ponsaerts P, Loeys B, Verstraeten A, Meester JAN. De Kinderen P, et al. Among authors: loeys b. Stem Cell Res. 2023 Mar;67:103024. doi: 10.1016/j.scr.2023.103024. Epub 2023 Jan 6. Stem Cell Res. 2023. PMID: 36640472 Free PMC article.

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