Christiansen M - Search Results

1

Chromosome 22q11.2 duplication is rare in a population-based cohort of Danish children with cardiovascular malformations.

Agergaard P, Olesen C, Østergaard JR, Christiansen M, Sørensen KM. Agergaard P, et al. Among authors: christiansen m. Am J Med Genet A. 2012 Mar;158A(3):509-13. doi: 10.1002/ajmg.a.34441. Epub 2012 Feb 2. Am J Med Genet A. 2012. PMID: 22302736

2

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. Among authors: christiansen m. Hum Mutat. 2009 Mar;30(3):363-70. doi: 10.1002/humu.20862. Hum Mutat. 2009. PMID: 19035361

3

Detecting 22q11.2 deletions by use of multiplex ligation-dependent probe amplification on DNA from neonatal dried blood spot samples.

Sørensen KM, Agergaard P, Olesen C, Andersen PS, Larsen LA, Ostergaard JR, Schouten JP, Christiansen M. Sørensen KM, et al. Among authors: christiansen m. J Mol Diagn. 2010 Mar;12(2):147-51. doi: 10.2353/jmoldx.2010.090099. Epub 2010 Jan 14. J Mol Diagn. 2010. PMID: 20075206 Free PMC article.

4

The prevalence of chromosome 22q11.2 deletions in 2,478 children with cardiovascular malformations. A population-based study.

Agergaard P, Olesen C, Østergaard JR, Christiansen M, Sørensen KM. Agergaard P, et al. Among authors: christiansen m. Am J Med Genet A. 2012 Mar;158A(3):498-508. doi: 10.1002/ajmg.a.34250. Epub 2011 Dec 21. Am J Med Genet A. 2012. PMID: 22190294

5

Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2.

Christiansen M, Hedley PL, Theilade J, Stoevring B, Leren TP, Eschen O, Sørensen KM, Tybjærg-Hansen A, Ousager LB, Pedersen LN, Frikke-Schmidt R, Aidt FH, Hansen MG, Hansen J, Bloch Thomsen PE, Toft E, Henriksen FL, Bundgaard H, Jensen HK, Kanters JK. Christiansen M, et al. BMC Med Genet. 2014 Mar 7;15:31. doi: 10.1186/1471-2350-15-31. BMC Med Genet. 2014. PMID: 24606995 Free PMC article.

6

Mutations in calmodulin cause ventricular tachycardia and sudden cardiac death.

Nyegaard M, Overgaard MT, Søndergaard MT, Vranas M, Behr ER, Hildebrandt LL, Lund J, Hedley PL, Camm AJ, Wettrell G, Fosdal I, Christiansen M, Børglum AD. Nyegaard M, et al. Among authors: christiansen m. Am J Hum Genet. 2012 Oct 5;91(4):703-12. doi: 10.1016/j.ajhg.2012.08.015. Am J Hum Genet. 2012. PMID: 23040497 Free PMC article.

7

Co-occurring hydrocephalus in autism spectrum disorder: a Danish population-based cohort study.

Munch TN, Hedley PL, Hagen CM, Bækvad-Hansen M, Bybjerg-Grauholm J, Grove J, Nordentoft M, Børglum AD, Mortensen PB, Werge TM, Melbye M, Hougaard DM, Christiansen M. Munch TN, et al. Among authors: christiansen m. J Neurodev Disord. 2021 Apr 28;13(1):19. doi: 10.1186/s11689-021-09367-0. J Neurodev Disord. 2021. PMID: 33910498 Free PMC article.

8

Prenatal testing among women pregnant after assisted reproductive techniques in Denmark 1995-2000: a national cohort study.

Gjerris AC, Loft A, Pinborg A, Christiansen M, Tabor A. Gjerris AC, et al. Among authors: christiansen m. Hum Reprod. 2008 Jul;23(7):1545-52. doi: 10.1093/humrep/den103. Epub 2008 Apr 1. Hum Reprod. 2008. PMID: 18385126

9

[Quality control of prenatal screening].

Pihl K, Larsen T, Jønsson L, Hougaard D, Krebs L, Nørgaard-Pedersen B, Christiansen M. Pihl K, et al. Among authors: christiansen m. Ugeskr Laeger. 2008 Aug 25;170(35):2691-5. Ugeskr Laeger. 2008. PMID: 18761859 Danish.

10

First-trimester combined screening for Down syndrome: prediction of low birth weight, small for gestational age and pre-term delivery in a cohort of non-selected women.

Pihl K, Sørensen TL, Nørgaard-Pedersen B, Larsen SO, Nguyen TH, Krebs L, Larsen T, Christiansen M. Pihl K, et al. Among authors: christiansen m. Prenat Diagn. 2008 Mar;28(3):247-53. doi: 10.1002/pd.1946. Prenat Diagn. 2008. PMID: 18302310

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