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Cancer Genetics|November 26, 2016
Differences in global DNA methylation of testicular seminoma are not associated with changes in histone modifications, clinical prognosis, BRAF mutations or gene expressionLouise Holm Pedersen, John E Nielsen, Gedske Daugaard, et al.
The Journal of Molecular Diagnostics : JMD|August 21, 2017
Next-Generation Sequencing-Based Detection of Germline Copy Number Variations in BRCA1/BRCA2: Validation of a One-Step Diagnostic WorkflowAne Y Schmidt, Thomas V O Hansen, Lise B Ahlborn, et al.
BMC Cancer|February 7, 2015
High-density SNP arrays improve detection of HER2 amplification and polyploidy in breast tumorsThomas V O Hansen, Jonas Vikesaa, Sine S Buhl, et al.
The EMBO Journal|March 17, 2006
RNA-binding IMPs promote cell adhesion and invadopodia formationJonas Vikesaa, Thomas V O Hansen, Lars Jønson, et al.
Neuroreport|July 7, 2009
Neuropeptide Y infusion into the shell region of the rat nucleus accumbens increases extracellular levels of dopamineGunnar Sørensen, Gregers Wegener, Jørgen Hasselstrøm, et al.
Familial Cancer|June 22, 2012
Novel germline c-MET mutation in a family with hereditary papillary renal carcinomaKarin A W Wadt, Anne-Marie Gerdes, Thomas V O Hansen, et al.
Breast Cancer Research and Treatment|May 4, 2010
Identification of a novel BRCA1 nucleotide 4803delCC/c.4684delCC mutation and a nucleotide 249T>A/c.130T>A (p.Cys44Ser) mutation in two Greenlandic Inuit families: implications for genetic screening of Greenlandic Inuit families with high risk for breast and/or ovarian cancerThomas V O Hansen, Lars Jønson, Anders Albrechtsen, et al.
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.
Familial Cancer|August 27, 2014
Identification of a breast cancer family double heterozygote for RAD51C and BRCA2 gene mutationsLise B Ahlborn, Ane Y Steffensen, Lars Jønson, et al.
BMC Medical Genetics|July 4, 2008
Novel de novo BRCA2 mutation in a patient with a family history of breast cancerThomas V O Hansen, Marie Luise Bisgaard, Lars Jønson, et al.
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