Kuiperi C - Search Results

1

Repeat genetic testing with targeted capture sequencing in primary arrhythmia syndrome and cardiomyopathy.

Robyns T, Kuiperi C, Breckpot J, Devriendt K, Souche E, Van Cleemput J, Willems R, Nuyens D, Matthijs G, Corveleyn A. Robyns T, et al. Among authors: kuiperi c. Eur J Hum Genet. 2017 Dec;25(12):1313-1323. doi: 10.1038/s41431-017-0004-3. Epub 2017 Oct 10. Eur J Hum Genet. 2017. PMID: 29255176 Free PMC article.

2

Clinical and ECG variables to predict the outcome of genetic testing in hypertrophic cardiomyopathy.

Robyns T, Breckpot J, Nuyens D, Vandenberk B, Corveleyn A, Kuiperi C, Van Aelst L, Van Cleemput J, Willems R. Robyns T, et al. Among authors: kuiperi c. Eur J Med Genet. 2020 Mar;63(3):103754. doi: 10.1016/j.ejmg.2019.103754. Epub 2019 Sep 9. Eur J Med Genet. 2020. PMID: 31513939

3

Individualized corrected QT interval is superior to QT interval corrected using the Bazett formula in predicting mutation carriage in families with long QT syndrome.

Robyns T, Willems R, Vandenberk B, Ector J, Garweg C, Kuiperi C, Breckpot J, Corveleyn A, Janssens S, Heidbuchel H, Nuyens D. Robyns T, et al. Among authors: kuiperi c. Heart Rhythm. 2017 Mar;14(3):376-382. doi: 10.1016/j.hrthm.2016.11.034. Heart Rhythm. 2017. PMID: 28212739

4

Genotype-phenotype relationship and risk stratification in loss-of-function SCN5A mutation carriers.

Robyns T, Nuyens D, Vandenberk B, Kuiperi C, Corveleyn A, Breckpot J, Garweg C, Ector J, Willems R. Robyns T, et al. Among authors: kuiperi c. Ann Noninvasive Electrocardiol. 2018 Sep;23(5):e12548. doi: 10.1111/anec.12548. Epub 2018 Apr 30. Ann Noninvasive Electrocardiol. 2018. PMID: 29709101 Free PMC article.

5

Targeted capture sequencing in a large LQTS family reveals a new pathogenic mutation c.2038delG in KCNH2 initially missed due to allelic dropout.

Robyns T, Kuiperi C, Willems R, Corveleyn A, Nuyens D. Robyns T, et al. Among authors: kuiperi c. Acta Cardiol. 2015 Dec;70(6):747-9. doi: 10.2143/AC.70.6.3120197. Acta Cardiol. 2015. PMID: 26717233

6

Lower than expected desmosomal gene mutation prevalence in endurance athletes with complex ventricular arrhythmias of right ventricular origin.

La Gerche A, Robberecht C, Kuiperi C, Nuyens D, Willems R, de Ravel T, Matthijs G, Heidbüchel H. La Gerche A, et al. Among authors: kuiperi c. Heart. 2010 Aug;96(16):1268-74. doi: 10.1136/hrt.2009.189621. Epub 2010 Jun 4. Heart. 2010. PMID: 20525856

7

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: kuiperi c. 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

8

Unconventional intronic splice site mutation in SCN5A associates with cardiac sodium channelopathy.

Rossenbacker T, Schollen E, Kuipéri C, de Ravel TJ, Devriendt K, Matthijs G, Collen D, Heidbüchel H, Carmeliet P. Rossenbacker T, et al. Among authors: kuiperi c. J Med Genet. 2005 May;42(5):e29. doi: 10.1136/jmg.2004.029058. J Med Genet. 2005. PMID: 15863661 Free PMC article.

9

Prominent cerebral amyloid angiopathy in transgenic mice overexpressing the london mutant of human APP in neurons.

Van Dorpe J, Smeijers L, Dewachter I, Nuyens D, Spittaels K, Van Den Haute C, Mercken M, Moechars D, Laenen I, Kuiperi C, Bruynseels K, Tesseur I, Loos R, Vanderstichele H, Checler F, Sciot R, Van Leuven F. Van Dorpe J, et al. Among authors: kuiperi c. Am J Pathol. 2000 Oct;157(4):1283-98. doi: 10.1016/S0002-9440(10)64644-5. Am J Pathol. 2000. PMID: 11021833 Free PMC article.

10

Novel pore mutation in SCN5A manifests as a spectrum of phenotypes ranging from atrial flutter, conduction disease, and Brugada syndrome to sudden cardiac death.

Rossenbacker T, Carroll SJ, Liu H, Kuipéri C, de Ravel TJ, Devriendt K, Carmeliet P, Kass RS, Heidbüchel H. Rossenbacker T, et al. Among authors: kuiperi c. Heart Rhythm. 2004 Nov;1(5):610-5. doi: 10.1016/j.hrthm.2004.07.001. Heart Rhythm. 2004. PMID: 15851228

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