Karina Meden Sørensen

Responsibilities

• General management and head of the biobank laboratory
• Management and coordination of projects in the biobank
• Scientific content of research projects
• Economics and administration
• Quality assurance

Publications

• Karina Meden Sørensen, Milad El‐Segaier, Eva Fernlund, Ab Errami, Patrice Bouvagnet, Nancy Nehme, Jesper Steensberg, Vibeke Hjortdal, Maria Soller, Mohaddeseh Behjati, Thomas Werge, Maria Kirchoff, Jan Schouten, Niels Tommerup, Paal Skytt Andersen, Lars Allan Larsen. Screening of congenital heart disease patients using multiplex ligation‐dependent probe amplification: Early diagnosis of syndromic patients. American Journal of Medical Genetics. Volume158A, Issue4, April 2012, Pages 720-725
• Peter Agergaard, Charlotte Olesen, John Rosendahl Østergaard, Michael Christiansen, Karina Meden Sørensen. The prevalence of chromosome 22q11.2 deletions in 2,478 children with cardiovascular malformations. A population‐based study. American Journal of Medical Genetics, Volume158A, Issue3, March 2012, Pages 498-508
• Sorensen KM., Agergaard P, Olesen C, Andersen PS, Larsen LA, Ostergaard JR, Schouten JP, Christiansen M. Detecting 22q11.2 deletions by use of multiplex ligation-dependent probe amplification on DNA from neonatal dried blood spot samples. J Mol Diagn. 2010 Mar;12(2):147-51.
• Sørensen KM, Andersen PS, Larsen LA, Schwartz M, Schouten JP, Nygren AO. Multiplex ligation-dependent probe amplification technique for copy number analysis on small amounts of DNA material. Anal Chem. 2008 Dec 1;80(23):9363-8.
• Sørensen KM, Jespersgaard C, Vuust J, Hougaard D, Nørgaard-Pedersen B, Andersen PS. Whole genome amplification on DNA from filter paper blood spot samples: an evaluation of selected systems. Genet Test. 2007 Spring;11(1):65-71.