Andersen PS - Search Results

1

Echocardiographic strain imaging to assess early and late consequences of sarcomere mutations in hypertrophic cardiomyopathy.

Ho CY, Carlsen C, Thune JJ, Havndrup O, Bundgaard H, Farrohi F, Rivero J, Cirino AL, Andersen PS, Christiansen M, Maron BJ, Orav EJ, Køber L. Ho CY, et al. Among authors: andersen ps. Circ Cardiovasc Genet. 2009 Aug;2(4):314-21. doi: 10.1161/CIRCGENETICS.109.862128. Epub 2009 Jun 19. Circ Cardiovasc Genet. 2009. PMID: 20031602 Free PMC article.

2

Penetrance of hypertrophic cardiomyopathy in children and adolescents: a 12-year follow-up study of clinical screening and predictive genetic testing.

Jensen MK, Havndrup O, Christiansen M, Andersen PS, Diness B, Axelsson A, Skovby F, Køber L, Bundgaard H. Jensen MK, et al. Among authors: andersen ps. Circulation. 2013 Jan 1;127(1):48-54. doi: 10.1161/CIRCULATIONAHA.111.090514. Epub 2012 Nov 28. Circulation. 2013. PMID: 23197161

3

Echocardiographic evaluation of pre-diagnostic development in young relatives genetically predisposed to hypertrophic cardiomyopathy.

Jensen MK, Havndrup O, Christiansen M, Andersen PS, Axelsson A, Køber L, Bundgaard H. Jensen MK, et al. Among authors: andersen ps. Int J Cardiovasc Imaging. 2015 Dec;31(8):1511-8. doi: 10.1007/s10554-015-0723-x. Epub 2015 Aug 1. Int J Cardiovasc Imaging. 2015. PMID: 26231341

4

Outcome of clinical versus genetic family screening in hypertrophic cardiomyopathy with focus on cardiac beta-myosin gene mutations.

Havndrup O, Bundgaard H, Andersen PS, Allan Larsen L, Vuust J, Kjeldsen K, Christiansen M. Havndrup O, et al. Among authors: andersen ps. Cardiovasc Res. 2003 Feb;57(2):347-57. doi: 10.1016/s0008-6363(02)00711-3. Cardiovasc Res. 2003. PMID: 12566107

5

One third of Danish hypertrophic cardiomyopathy patients with MYH7 mutations have mutations [corrected] in MYH7 rod region.

Hougs L, Havndrup O, Bundgaard H, Køber L, Vuust J, Larsen LA, Christiansen M, Andersen PS. Hougs L, et al. Among authors: andersen ps. Eur J Hum Genet. 2005 Feb;13(2):161-5. doi: 10.1038/sj.ejhg.5201310. Eur J Hum Genet. 2005. PMID: 15483641

6

Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relatives.

Andersen PS, Havndrup O, Hougs L, Sørensen KM, Jensen M, Larsen LA, Hedley P, Thomsen AR, Moolman-Smook J, Christiansen M, Bundgaard H. Andersen PS, et al. Hum Mutat. 2009 Mar;30(3):363-70. doi: 10.1002/humu.20862. Hum Mutat. 2009. PMID: 19035361

7

The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy.

Møller DV, Andersen PS, Hedley P, Ersbøll MK, Bundgaard H, Moolman-Smook J, Christiansen M, Køber L. Møller DV, et al. Among authors: andersen ps. Eur J Hum Genet. 2009 Oct;17(10):1241-9. doi: 10.1038/ejhg.2009.34. Epub 2009 Mar 18. Eur J Hum Genet. 2009. PMID: 19293840 Free PMC article.

8

Cardiac myosin binding protein-C mutations in families with hypertrophic cardiomyopathy: disease expression in relation to age, gender, and long term outcome.

Page SP, Kounas S, Syrris P, Christiansen M, Frank-Hansen R, Andersen PS, Elliott PM, McKenna WJ. Page SP, et al. Among authors: andersen ps. Circ Cardiovasc Genet. 2012 Apr 1;5(2):156-66. doi: 10.1161/CIRCGENETICS.111.960831. Epub 2012 Jan 20. Circ Cardiovasc Genet. 2012. PMID: 22267749

9

Fabry disease mimicking hypertrophic cardiomyopathy: genetic screening needed for establishing the diagnosis in women.

Havndrup O, Christiansen M, Stoevring B, Jensen M, Hoffman-Bang J, Andersen PS, Hasholt L, Nørremølle A, Feldt-Rasmussen U, Køber L, Bundgaard H. Havndrup O, et al. Among authors: andersen ps. Eur J Heart Fail. 2010 Jun;12(6):535-40. doi: 10.1093/eurjhf/hfq073. Eur J Heart Fail. 2010. PMID: 20498269 Free article.

10

Genetic and phenotypic characterization of mutations in myosin-binding protein C (MYBPC3) in 81 families with familial hypertrophic cardiomyopathy: total or partial haploinsufficiency.

Andersen PS, Havndrup O, Bundgaard H, Larsen LA, Vuust J, Pedersen AK, Kjeldsen K, Christiansen M. Andersen PS, et al. Eur J Hum Genet. 2004 Aug;12(8):673-7. doi: 10.1038/sj.ejhg.5201190. Eur J Hum Genet. 2004. PMID: 15114369

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