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Molecular and Cellular Biology|May 4, 2004
Dwarfism and impaired gut development in insulin-like growth factor II mRNA-binding protein 1-deficient miceThomas V O Hansen, Niels A Hammer, Jacob Nielsen, et al.
Familial Cancer|February 15, 2011
Screening of 1331 Danish breast and/or ovarian cancer families identified 40 novel BRCA1 and BRCA2 mutationsThomas V O Hansen, Lars Jønson, Ane Y Steffensen, et al.
Familial Cancer|January 21, 2015
Germline RAD51B truncating mutation in a family with cutaneous melanomaKarin A W Wadt, Lauren G Aoude, Lisa Golmard, et al.
Familial Cancer|March 25, 2011
A putative Lynch syndrome family carrying MSH2 and MSH6 variants of uncertain significance-functional analysis reveals the pathogenic oneJukka Kantelinen, Thomas V O Hansen, Minttu Kansikas, et al.
Hereditary Cancer in Clinical Practice|June 10, 2016
Identification of eight novel SDHB, SDHC, SDHD germline variants in Danish pheochromocytoma/paraganglioma patientsMarc Bennedbæk, Maria Rossing, Åse K Rasmussen, et al.
Breast Cancer Research and Treatment|January 8, 2016
Identification of six pathogenic RAD51C mutations via mutational screening of 1228 Danish individuals with increased risk of hereditary breast and/or ovarian cancerLars Jønson, Lise B Ahlborn, Ane Y Steffensen, et al.
Clinical Genetics|January 10, 2025
A Novel Case of Biallelic MLH3 Variants in a Patient With Rectal Cancer and PolypsKatrine M Johannesen, John Gásdal Karstensen, Andreas Ørslev Rasmussen, et al.
Familial Cancer|February 3, 2016
BRCA1/BRCA2 founder mutations and cancer risks: impact in the western Danish populationHenriette Roed Nielsen, Mef Nilbert, Janne Petersen, et al.
Hereditary Cancer in Clinical Practice|April 16, 2020
A rare missense variant in APC interrupts splicing and causes AFAP in two Danish familiesMalene Djursby, Karin Wadt, Jane Hübertz Frederiksen, et al.
JIMD Reports|September 9, 2016
Leukoencephalopathy due to Complex II Deficiency and Bi-Allelic SDHB Mutations: Further Cases and Implications for Genetic CounsellingSabine Grønborg, Niklas Darin, Maria J Miranda, et al.
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