A method for detecting IBD regions simultaneously in multiple individuals—with applications to disease genetics

par Moltke, Ida, Albrechtsen, Anders, Hansen, Thomas v.O., Nielsen, Finn C., Nielsen, Rasmus
Publié 2011

Identification of 3 novel VHL germ-line mutations in Danish VHL patients

par Dandanell, Mette, Friis-Hansen, Lennart, Sunde, Lone, Nielsen, Finn C, Hansen, Thomas v O
Publié 2012

Classification of the spliceogenic BRCA1 c.4096+3A>G variant as likely benign based on cosegregation data and identification of a healthy homozygous carrier

par Byrjalsen, Anna, Steffensen, Ane Y., Hansen, Thomas v. O., Wadt, Karin, Gerdes, Anne‐Marie
Publié dans Clin Case Rep (2017)

Human insulin-like growth factor II leader 2 mediates internal initiation of translation.

par Pedersen, Susanne K, Christiansen, Jan, Hansen, Thomas v O, Larsen, Martin R, Nielsen, Finn C
Publié 2002

Control of Fetal Growth and Neonatal Survival by the RasGAP-Associated Endoribonuclease G3BP

par Zekri, Latifa, Chebli, Karim, Tourrière, Hélène, Nielsen, Finn C., Hansen, Thomas V. O., Rami, Abdelhaq, Tazi, Jamal
Publié 2005

Identification of a Danish breast/ovarian cancer family double heterozygote for BRCA1 and BRCA2 mutations

par Steffensen, Ane Y., Jønson, Lars, Ejlertsen, Bent, Gerdes, Anne-Marie, Nielsen, Finn C., Hansen, Thomas V. O.
Publié 2010

High-density SNP arrays improve detection of HER2 amplification and polyploidy in breast tumors

par Hansen, Thomas v O, Vikesaa, Jonas, Buhl, Sine S, Rossing, Henrik H, Timmermans-Wielenga, Vera, Nielsen, Finn C
Publié dans BMC Cancer (2015)

Splicing analysis of 14 BRCA1 missense variants classifies nine variants as pathogenic

par Ahlborn, Lise B., Dandanell, Mette, Steffensen, Ane Y., Jønson, Lars, Nielsen, Finn C., Hansen, Thomas v. O.
Publié dans Breast Cancer Res Treat (2015)

RNA-binding IMPs promote cell adhesion and invadopodia formation

par Vikesaa, Jonas, Hansen, Thomas V O, Jønson, Lars, Borup, Rehannah, Wewer, Ulla M, Christiansen, Jan, Nielsen, Finn C
Publié 2006

Functional characterization of BRCA1 gene variants by mini-gene splicing assay

par Steffensen, Ane Y, Dandanell, Mette, Jønson, Lars, Ejlertsen, Bent, Gerdes, Anne-Marie, Nielsen, Finn C, Hansen, Thomas vO
Publié dans Eur J Hum Genet (2014)

Dwarfism and Impaired Gut Development in Insulin-Like Growth Factor II mRNA-Binding Protein 1-Deficient Mice

par Hansen, Thomas V. O., Hammer, Niels A., Nielsen, Jacob, Madsen, Mette, Dalbaeck, Charlotte, Wewer, Ulla M., Christiansen, Jan, Nielsen, Finn C.
Publié 2004

Novel de novo BRCA2 mutation in a patient with a family history of breast cancer

par Hansen, Thomas V O, Bisgaard, Marie Luise, Jønson, Lars, Albrechtsen, Anders, Filtenborg-Barnkob, Bettina, Eiberg, Hans, Ejlertsen, Bent, Nielsen, Finn C
Publié 2008

Identification of eight novel SDHB, SDHC, SDHD germline variants in Danish pheochromocytoma/paraganglioma patients

par Bennedbæk, Marc, Rossing, Maria, Rasmussen, Åse K., Gerdes, Anne-Marie, Skytte, Anne-Bine, Jensen, Uffe B., Nielsen, Finn C., Hansen, Thomas v. O.
Publié dans Hered Cancer Clin Pract (2016)

Leukoencephalopathy due to Complex II Deficiency and Bi-Allelic SDHB Mutations: Further Cases and Implications for Genetic Counselling

par Grønborg, Sabine, Darin, Niklas, Miranda, Maria J., Damgaard, Bodil, Cayuela, Jorge Asin, Oldfors, Anders, Kollberg, Gittan, Hansen, Thomas V. O., Ravn, Kirstine, Wibrand, Flemming, Østergaard, Elsebet
Publié dans JIMD Rep (2016)

A rare missense variant in APC interrupts splicing and causes AFAP in two Danish families

par Djursby, Malene, Wadt, Karin, Frederiksen, Jane Hübertz, Madsen, Majbritt Busk, Berchtold, Lukas Adrian, Hasselby, Jane Preuss, Willemoe, Gro Linno, Hansen, Thomas v. O., Gerdes, Anne-Marie
Publié dans Hered Cancer Clin Pract (2020)

Functional examination of MLH1, MSH2, and MSH6 intronic mutations identified in Danish colorectal cancer patients

par Petersen, Sanne M, Dandanell, Mette, Rasmussen, Lene J, Gerdes, Anne-Marie, Krogh, Lotte N, Bernstein, Inge, Okkels, Henrik, Wikman, Friedrik, Nielsen, Finn C, Hansen, Thomas v O
Publié 2013

Functional assays for analysis of variants of uncertain significance in BRCA2

par Guidugli, Lucia, Carreira, Aura, Caputo, Sandrine M., Ehlen, Asa, Galli, Alvaro, Monteiro, Alvaro N.A., Neuhausen, Susan L., Hansen, Thomas V.O., Couch, Fergus J., Vreeswijk, Maaike P.G.
Publié 2013

Classifications within Molecular Subtypes Enables Identification of BRCA1/BRCA2 Mutation Carriers by RNA Tumor Profiling

par Larsen, Martin J., Kruse, Torben A., Tan, Qihua, Lænkholm, Anne-Vibeke, Bak, Martin, Lykkesfeldt, Anne E., Sørensen, Kristina P., Hansen, Thomas v. O., Ejlertsen, Bent, Gerdes, Anne-Marie, Thomassen, Mads
Publié 2013

A Guide for Functional Analysis of BRCA1 Variants of Uncertain Significance (VUS)

par Millot, Gaël, Carvalho, Marcelo A., Caputo, Sandrine M, Vreeswijk, Maaike P.G., Brown, Melissa A, Webb, Michelle, Rouleau, Etienne, Neuhausen, Susan L., Hansen, Thomas v. O., Galli, Alvaro, Brandão, Rita D, Blok, Marinus J., Velkova, Aneliya, Couch, Fergus J., Monteiro, Alvaro N.A.
Publié 2012

Molecular Characterization of Melanoma Cases in Denmark Suspected of Genetic Predisposition

par Wadt, Karin A. W., Aoude, Lauren G., Krogh, Lotte, Sunde, Lone, Bojesen, Anders, Grønskov, Karen, Wartacz, Nine, Ek, Jakob, Tolstrup-Andersen, Morten, Klarskov-Andersen, Mette, Borg, Åke, Heegaard, Steffen, Kiilgaard, Jens F., Hansen, Thomas V. O., Klein, Kerenaftali, Jönsson, Göran, Drzewiecki, Krzysztof T., Dunø, Morten, Hayward, Nicholas K., Gerdes, Anne-Marie
Publié dans PLoS One (2015)