Paulussen AD - Search Results

1

Pharmacogenomics and acquired long QT syndrome.

Aerssens J, Paulussen AD. Aerssens J, et al. Among authors: paulussen ad. Pharmacogenomics. 2005 Apr;6(3):259-70. doi: 10.1517/14622416.6.3.259. Pharmacogenomics. 2005. PMID: 16013957 Review.

2

A novel mutation (T65P) in the PAS domain of the human potassium channel HERG results in the long QT syndrome by trafficking deficiency.

Paulussen A, Raes A, Matthijs G, Snyders DJ, Cohen N, Aerssens J. Paulussen A, et al. J Biol Chem. 2002 Dec 13;277(50):48610-6. doi: 10.1074/jbc.M206569200. Epub 2002 Sep 26. J Biol Chem. 2002. PMID: 12354768 Free article.

3

Mutation analysis in congenital Long QT Syndrome--a case with missense mutations in KCNQ1 and SCN5A.

Paulussen A, Matthijs G, Gewillig M, Verhasselt P, Cohen N, Aerssens J. Paulussen A, et al. Genet Test. 2003 Spring;7(1):57-61. doi: 10.1089/109065703321560958. Genet Test. 2003. PMID: 12820704

4

Genetic variations of KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced long QT syndrome patients.

Paulussen AD, Gilissen RA, Armstrong M, Doevendans PA, Verhasselt P, Smeets HJ, Schulze-Bahr E, Haverkamp W, Breithardt G, Cohen N, Aerssens J. Paulussen AD, et al. J Mol Med (Berl). 2004 Mar;82(3):182-8. doi: 10.1007/s00109-003-0522-z. Epub 2004 Feb 4. J Mol Med (Berl). 2004. PMID: 14760488

5

A single hERG mutation underlying a spectrum of acquired and congenital long QT syndrome phenotypes.

Saenen JB, Paulussen AD, Jongbloed RJ, Marcelis CL, Gilissen RA, Aerssens J, Snyders DJ, Raes AL. Saenen JB, et al. Among authors: paulussen ad. J Mol Cell Cardiol. 2007 Jul;43(1):63-72. doi: 10.1016/j.yjmcc.2007.04.012. Epub 2007 May 4. J Mol Cell Cardiol. 2007. PMID: 17531263

6

Risk factors for drug-induced long-QT syndrome.

Paulussen AD, Aerssens J. Paulussen AD, et al. Neth Heart J. 2005 Feb;13(2):47-56. Neth Heart J. 2005. PMID: 25696450 Free PMC article. Review.

7

HERG mutation predicts short QT based on channel kinetics but causes long QT by heterotetrameric trafficking deficiency.

Paulussen AD, Raes A, Jongbloed RJ, Gilissen RA, Wilde AA, Snyders DJ, Smeets HJ, Aerssens J. Paulussen AD, et al. Cardiovasc Res. 2005 Aug 15;67(3):467-75. doi: 10.1016/j.cardiores.2005.05.017. Cardiovasc Res. 2005. PMID: 15958262

8

Anthropometry, carbohydrate and lipid metabolism in the East Flanders Prospective Twin Survey: linkage of candidate genes using two sib-pair based variance components analyses.

Souren NY, Zeegers MP, Janssen RG, Steyls A, Gielen M, Loos RJ, Beunen G, Fagard R, Stassen AP, Aerssens J, Derom C, Vlietinck R, Paulussen AD. Souren NY, et al. Among authors: paulussen ad. Twin Res Hum Genet. 2008 Oct;11(5):505-16. doi: 10.1375/twin.11.5.505. Twin Res Hum Genet. 2008. PMID: 18828733

9

Analysis of the human KCNH2(HERG) gene: identification and characterization of a novel mutation Y667X associated with long QT syndrome and a non-pathological 9 bp insertion.

Paulussen A, Yang P, Pangalos M, Verhasselt P, Marrannes R, Verfaille C, Vandenberk I, Crabbe R, Konings F, Luyten W, Armstrong M. Paulussen A, et al. Hum Mutat. 2000 May;15(5):483. doi: 10.1002/(SICI)1098-1004(200005)15:5<483::AID-HUMU18>3.0.CO;2-T. Hum Mutat. 2000. PMID: 10790218

10

Genetic basis of drug-induced arrhythmias.

Vos MA, Paulussen AD. Vos MA, et al. Among authors: paulussen ad. Ann Med. 2004;36 Suppl 1:35-40. doi: 10.1080/17431380410032634. Ann Med. 2004. PMID: 15176422 Review.

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