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Genetic Testing and Molecular Biomarkers|August 22, 2019
Detection of PMS2 Mutations by Screening Hereditary Nonpolyposis Colon Cancer Families from Denmark and SwedenHenrik Okkels, Kristina Lagerstedt-Robinsson, Friedrik P Wikman, et al.
Human Reproduction (Oxford, England)|August 20, 2019
Whole-exome sequencing identifies a GREB1L variant in a three-generation family with Müllerian and renal agenesis: a novel candidate gene in Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome. A case reportMorten K Herlin, Vang Q Le, Allan T Højland, et al.
Scandinavian Journal of Gastroenterology|May 13, 2010
Genetic variants of glutathione S-transferases mu, theta, and pi display no susceptibility to inflammatory bowel disease in the Danish populationAnja Ernst, Vibeke Andersen, Mette Østergaard, et al.
Applied Immunohistochemistry & Molecular Morphology : AIMM|April 13, 2012
MSH6 mutations are frequent in hereditary nonpolyposis colorectal cancer families with normal pMSH6 expression as detected by immunohistochemistryHenrik Okkels, Karen Lindorff-Larsen, Ole Thorlasius-Ussing, et al.
Scandinavian Journal of Gastroenterology|September 14, 2007
Mutations in CARD15 and smoking confer susceptibility to Crohn's disease in the Danish populationAnja Ernst, Bent Jacobsen, Mette Østergaard, et al.
Acta Obstetricia Et Gynecologica Scandinavica|February 11, 2020
A systematic review on concurrent aneuploidy screening and preimplantation genetic testing for hereditary disorders: What is the prevalence of aneuploidy and is there a clinical effect from aneuploidy screening?Christian Liebst Frisk Toft, Hans Jakob Ingerslev, Ulrik Schiøler Kesmodel, et al.
International Journal of Colorectal Disease|March 10, 2006
Polyposis and early cancer in a patient with low penetrant mutations in MSH6 and APC: hereditary colorectal cancer as a polygenic traitHenrik Okkels, Lone Sunde, Karen Lindorff-Larsen, et al.
BMC Medical Genetics|October 5, 2013
Functional examination of MLH1, MSH2, and MSH6 intronic mutations identified in Danish colorectal cancer patientsSanne M Petersen, Mette Dandanell, Lene J Rasmussen, et al.
Journal of Clinical Lipidology|July 23, 2023
Possible explanations for the common clinical familial hypercholesterolemia phenotypes in the Faroe IslandsSanna Á Borg, Albert Marni Joensen, Michael René Skjelbo Nielsen, et al.
Familial Cancer|June 21, 2008
Major contribution from recurrent alterations and MSH6 mutations in the Danish Lynch syndrome populationMef Nilbert, Friedrik P Wikman, Thomas V O Hansen, et al.
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