Andersen PS - Search Results

1

Novel donor splice site mutation in the KVLQT1 gene is associated with long QT syndrome.

Kanters JK, Larsen LA, Orholm M, Agner E, Andersen PS, Vuust J, Christiansen M. Kanters JK, et al. Among authors: andersen ps. J Cardiovasc Electrophysiol. 1998 Jun;9(6):620-4. doi: 10.1111/j.1540-8167.1998.tb00944.x. J Cardiovasc Electrophysiol. 1998. PMID: 9654228

2

A single strand conformation polymorphism/heteroduplex (SSCP/HD) method for detection of mutations in 15 exons of the KVLQT1 gene, associated with long QT syndrome.

Larsen LA, Andersen PS, Kanters JK, Jacobsen JR, Vuust J, Christiansen M. Larsen LA, et al. Among authors: andersen ps. Clin Chim Acta. 1999 Feb;280(1-2):113-25. doi: 10.1016/s0009-8981(98)00177-6. Clin Chim Acta. 1999. PMID: 10090529

3

Recessive Romano-Ward syndrome associated with compound heterozygosity for two mutations in the KVLQT1 gene.

Larsen LA, Fosdal I, Andersen PS, Kanters JK, Vuust J, Wettrell G, Christiansen M. Larsen LA, et al. Among authors: andersen ps. Eur J Hum Genet. 1999 Sep;7(6):724-8. doi: 10.1038/sj.ejhg.5200323. Eur J Hum Genet. 1999. PMID: 10482963

4

Long QT syndrome with a high mortality rate caused by a novel G572R missense mutation in KCNH2.

Larsen LA, Svendsen IH, Jensen AM, Kanters JK, Andersen PS, Møller M, Sørensen SA, Sandøe E, Jacobsen JR, Vuust J, Christiansen M. Larsen LA, et al. Among authors: andersen ps. Clin Genet. 2000 Feb;57(2):125-30. doi: 10.1034/j.1399-0004.2000.570206.x. Clin Genet. 2000. PMID: 10735633

5

A novel missense mutation, Leu390Val, in the cardiac beta-myosin heavy chain associated with pronounced septal hypertrophy in two families with hypertrophic cardiomyopathy.

Havndrup O, Bundgaard H, Andersen PS, Larsen LA, Vuust J, Kjeldsen K, Christiansen M. Havndrup O, et al. Among authors: andersen ps. Scand Cardiovasc J. 2000 Dec;34(6):558-63. doi: 10.1080/140174300750064477. Scand Cardiovasc J. 2000. PMID: 11214007 Free article.

6

Mutations in the genes KCND2 and KCND3 encoding the ion channels Kv4.2 and Kv4.3, conducting the cardiac fast transient outward current (ITO,f), are not a frequent cause of long QT syndrome.

Frank-Hansen R, Larsen LA, Andersen P, Jespersgaard C, Christiansen M. Frank-Hansen R, et al. Clin Chim Acta. 2005 Jan;351(1-2):95-100. doi: 10.1016/j.cccn.2004.08.017. Clin Chim Acta. 2005. PMID: 15563876

7

Mutations in the HERG K+-ion channel: a novel link between long QT syndrome and sudden infant death syndrome.

Christiansen M, Tønder N, Larsen LA, Andersen PS, Simonsen H, Oyen N, Kanters JK, Jacobsen JR, Fosdal I, Wettrell G, Kjeldsen K. Christiansen M, et al. Among authors: andersen ps. Am J Cardiol. 2005 Feb 1;95(3):433-4. doi: 10.1016/j.amjcard.2004.09.054. Am J Cardiol. 2005. PMID: 15670565

8

Mutations in the Kv1.5 channel gene KCNA5 in cardiac arrest patients.

Nielsen NH, Winkel BG, Kanters JK, Schmitt N, Hofman-Bang J, Jensen HS, Bentzen BH, Sigurd B, Larsen LA, Andersen PS, Haunsø S, Kjeldsen K, Grunnet M, Christiansen M, Olesen SP. Nielsen NH, et al. Among authors: andersen ps. Biochem Biophys Res Commun. 2007 Mar 16;354(3):776-82. doi: 10.1016/j.bbrc.2007.01.048. Epub 2007 Jan 18. Biochem Biophys Res Commun. 2007. PMID: 17266934

9

High-throughput single strand conformation polymorphism mutation detection by automated capillary array electrophoresis: validation of the method.

Andersen PS, Jespersgaard C, Vuust J, Christiansen M, Larsen LA. Andersen PS, et al. Hum Mutat. 2003 Feb;21(2):116-22. doi: 10.1002/humu.10161. Hum Mutat. 2003. PMID: 12552558

10

Capillary electrophoresis-based single strand DNA conformation analysis in high-throughput mutation screening.

Andersen PS, Jespersgaard C, Vuust J, Christiansen M, Larsen LA. Andersen PS, et al. Hum Mutat. 2003 May;21(5):455-65. doi: 10.1002/humu.10169. Hum Mutat. 2003. PMID: 12673787 Review.

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