Andersen PS - Search Results

1

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.

2

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

3

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

4

High-throughput single-strand conformation polymorphism analysis by automated capillary electrophoresis: robust multiplex analysis and pattern-based identification of allelic variants.

Larsen LA, Christiansen M, Vuust J, Andersen PS. Larsen LA, et al. Among authors: andersen ps. Hum Mutat. 1999;13(4):318-27. doi: 10.1002/(SICI)1098-1004(1999)13:4<318::AID-HUMU9>3.0.CO;2-F. Hum Mutat. 1999. PMID: 10220146

5

Familial hypertrophic cardiomyopathy associated with a novel missense mutation affecting the ATP-binding region of the cardiac beta-myosin heavy chain.

Bundgaard H, Havndrup O, Andersen PS, Larsen LA, Brandt NJ, Vuust J, Kjeldsen K, Christiansen M. Bundgaard H, et al. Among authors: andersen ps. J Mol Cell Cardiol. 1999 Apr;31(4):745-50. doi: 10.1006/jmcc.1998.0911. J Mol Cell Cardiol. 1999. PMID: 10329202

6

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

7

Adult-onset familial hypertrophic cardiomyopathy caused by a novel mutation, R694C, in the MYH7 gene.

Andersen PS, Havndrup O, Bundgaard H, Larsen LA, Vuust J, Kjeldsen K, Christiansen M. Andersen PS, et al. Clin Genet. 1999 Sep;56(3):244-6. doi: 10.1034/j.1399-0004.1999.560313.x. Clin Genet. 1999. PMID: 10563488 No abstract available.

8

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

9

High throughput mutation screening by automated capillary electrophoresis.

Larsen LA, Christiansen M, Vuust J, Andersen PS. Larsen LA, et al. Among authors: andersen ps. Comb Chem High Throughput Screen. 2000 Oct;3(5):393-409. doi: 10.2174/1386207003331508. Comb Chem High Throughput Screen. 2000. PMID: 11032956 Review.

10

Development and application of linkage analysis in genetic diagnosis of familial hypertrophic cardiomyopathy.

Mogensen J, Andersen PS, Steffensen U, Christiansen M, Egeblad H, Gregersen N, Børglum AD. Mogensen J, et al. Among authors: andersen ps. J Med Genet. 2001 Mar;38(3):193-8. doi: 10.1136/jmg.38.3.193. J Med Genet. 2001. PMID: 11303515 Free PMC article. No abstract available.

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