Loeys BL - Search Results

1

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: loeys bl. 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.

2

Applying massive parallel sequencing to molecular diagnosis of Marfan and Loeys-Dietz syndromes.

Baetens M, Van Laer L, De Leeneer K, Hellemans J, De Schrijver J, Van De Voorde H, Renard M, Dietz H, Lacro RV, Menten B, Van Criekinge W, De Backer J, De Paepe A, Loeys B, Coucke PJ. Baetens M, et al. Hum Mutat. 2011 Sep;32(9):1053-62. doi: 10.1002/humu.21525. Epub 2011 Jul 20. Hum Mutat. 2011. PMID: 21542060

3

Marfan syndrome: from gene to therapy.

Bolar N, Van Laer L, Loeys BL. Bolar N, et al. Among authors: loeys bl. Curr Opin Pediatr. 2012 Aug;24(4):498-504. doi: 10.1097/MOP.0b013e3283557d4c. Curr Opin Pediatr. 2012. PMID: 22705998 Review.

4

Educational paper. Connective tissue disorders with vascular involvement: from gene to therapy.

Van Laer L, Proost D, Loeys BL. Van Laer L, et al. Among authors: loeys bl. Eur J Pediatr. 2013 Aug;172(8):997-1005. doi: 10.1007/s00431-012-1773-x. Epub 2012 Jul 17. Eur J Pediatr. 2013. PMID: 22801769 Free PMC article. Review.

5

Mutation of the iron-sulfur cluster assembly gene IBA57 causes severe myopathy and encephalopathy.

Ajit Bolar N, Vanlander AV, Wilbrecht C, Van der Aa N, Smet J, De Paepe B, Vandeweyer G, Kooy F, Eyskens F, De Latter E, Delanghe G, Govaert P, Leroy JG, Loeys B, Lill R, Van Laer L, Van Coster R. Ajit Bolar N, et al. Hum Mol Genet. 2013 Jul 1;22(13):2590-602. doi: 10.1093/hmg/ddt107. Epub 2013 Mar 5. Hum Mol Genet. 2013. PMID: 23462291

6

Genetics of thoracic aortic aneurysm: at the crossroad of transforming growth factor-β signaling and vascular smooth muscle cell contractility.

Gillis E, Van Laer L, Loeys BL. Gillis E, et al. Among authors: loeys bl. Circ Res. 2013 Jul 19;113(3):327-40. doi: 10.1161/CIRCRESAHA.113.300675. Circ Res. 2013. PMID: 23868829 Review.

7

Loeys-Dietz syndrome.

Van Laer L, Dietz H, Loeys B. Van Laer L, et al. Adv Exp Med Biol. 2014;802:95-105. doi: 10.1007/978-94-007-7893-1_7. Adv Exp Med Biol. 2014. PMID: 24443023 Review.

8

An FBN1 deep intronic mutation in a familial case of Marfan syndrome: an explanation for genetically unsolved cases?

Gillis E, Kempers M, Salemink S, Timmermans J, Cheriex EC, Bekkers SC, Fransen E, De Die-Smulders CE, Loeys BL, Van Laer L. Gillis E, et al. Among authors: loeys bl. Hum Mutat. 2014 May;35(5):571-4. doi: 10.1002/humu.22540. Epub 2014 Apr 7. Hum Mutat. 2014. PMID: 24610719

9

Genetics of sudden cardiac death in the young.

Saenen JB, Van Craenenbroeck EM, Proost D, Marchau F, Van Laer L, Vrints CJ, Loeys BL. Saenen JB, et al. Among authors: loeys bl. Clin Genet. 2015 Aug;88(2):101-13. doi: 10.1111/cge.12519. Epub 2014 Nov 22. Clin Genet. 2015. PMID: 25307320 Review.

10

VariantDB: a flexible annotation and filtering portal for next generation sequencing data.

Vandeweyer G, Van Laer L, Loeys B, Van den Bulcke T, Kooy RF. Vandeweyer G, et al. Genome Med. 2014 Oct 2;6(10):74. doi: 10.1186/s13073-014-0074-6. eCollection 2014. Genome Med. 2014. PMID: 25352915 Free PMC article.

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