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American Journal of Medical Genetics. Part A|November 12, 2005
Neurofibromatosis von Recklinghausen type I phenotype and early onset of cancers in siblings compound heterozygous for mutations in MSH6John R Ostergaard, Lone Sunde, Henrik Okkels
Scandinavian Journal of Gastroenterology|April 26, 2006
Geographical clustering and maintained health in individuals harbouring the mutation for Greenland familial cholestasis: A population-based studyStig Andersen, Henrik Okkels, Henrik Krarup, et al.
International Journal of Systematic and Evolutionary Microbiology|May 15, 2004
Delineation of the genus Actinobacillus by comparison of partial infB sequencesNiels Nørskov-Lauritsen, Henrik Christensen, Henrik Okkels, et al.
The American Journal of Surgical Pathology|August 13, 2011
Challenges in the identification of MSH6-associated colorectal cancer: rectal location, less typical histology, and a subset with retained mismatch repair functionLouise Klarskov, Susanne Holck, Inge Bernstein, et al.
Microbiology (Reading, England)|September 6, 2001
Phylogeny of the genus Haemophilus as determined by comparison of partial infB sequencesJakob Hedegaard, Henrik Okkels, Brita Bruun, et al.
Molecular Genetics & Genomic Medicine|March 5, 2021
First reported CABP2-related non-syndromic hearing loss in Northern EuropeInger Norlyk Sheyanth, Allan Thomas Højland, Henrik Okkels, et al.
Scandinavian Journal of Gastroenterology|February 13, 2008
Benign course of long-standing hepatitis B virus infection among Greenland Inuit?Henrik Bygum Krarup, Stig Andersen, Poul Henning Madsen, et al.
Molecular Genetics & Genomic Medicine|March 10, 2021
First reported case of Doyne honeycomb retinal dystrophy (Malattia Leventinese/autosomal dominant drusen) in ScandinaviaInger Norlyk Sheyanth, Ihab Bishara Lolas, Henrik Okkels, et al.
American Journal of Medical Genetics. Part A|November 22, 2018
First reported adult patient with TARP syndrome: A case reportAllan T Højland, Ihab Lolas, Henrik Okkels, et al.
European Journal of Gastroenterology & Hepatology|January 14, 2011
Common polymorphisms in the microsomal epoxide hydrolase and N-acetyltransferase 2 genes in association with inflammatory bowel disease in the Danish populationAnja Ernst, Vibeke Andersen, Mette Ostergaard, et al.
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