Molecular Composition of IMP1 Ribonucleoprotein Granules von J⊘nson, Lars, Vikesaa, Jonas, Krogh, Anders, Nielsen, Lars K., Hansen, Thomas vO, Borup, Rehannah, Johnsen, Anders H., Christiansen, Jan, Nielsen, Finn C.

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Birt-Hogg-Dubé syndrome: diagnosis and management von Menko, Fred H, Dr, van Steensel, Maurice AM, MD, Giraud, Sophie, MD, Friis-Hansen, Lennart, MD, Richard, Stéphane, Prof, Ungari, Silvana, MD, Nordenskjöld, Magnus, Prof, Hansen, Thomas vO, MSc, Solly, John, PhD, Maher, Eamonn R, Prof

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Genetic screening of the FLCN gene identify six novel variants and a Danish founder mutation von Rossing, Maria, Albrechtsen, Anders, Skytte, Anne-Bine, Jensen, Uffe B, Ousager, Lilian B, Gerdes, Anne-Marie, Nielsen, Finn C, Hansen, Thomas vO

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Functional Assays for Analysis of Variants of Uncertain Significance in BRCA2 von 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.

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Collection of Blood, Saliva, and Buccal Cell Samples in a Pilot Study on the Danish Nurse Cohort: Comparison of the Response Rate and Quality of Genomic DNA von HANSEN, Thomas V. O, SIMONSEN, Mette K, NIELSEN, Finn C, ANDERSEN HUNDRUP, Yrsa

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Functional characterization of BRCA1 gene variants by mini-gene splicing assay von Steffensen, Ane Y, Dandanell, Mette, Jønson, Lars, Ejlertsen, Bent, Gerdes, Anne-Marie, Nielsen, Finn C, Hansen, Thomas vO

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A guide for functional analysis of BRCA1 variants of uncertain significance von Millot, Gaël A., 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.

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Interferon-γ inhibits ghrelin expression and secretion via a somatostatin-mediated mechanism von Strickertsson, Jesper A B, Døssing, Kristina B V, Aabakke, Anna J M, Nilsson, Hans-Olof, Hansen, Thomas V O, Knigge, Ulrich, Kjær, Andreas, Wadström, Torkel, Friis-Hansen, Lennart

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RNA-binding IMPs promote cell adhesion and invadopodia formation von Vikesaa, Jonas, Hansen, Thomas VO, Jønson, Lars, Borup, Rehannah, Wewer, Ulla M, Christiansen, Jan, Nielsen, Finn C

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Identification of six pathogenic RAD51C mutations via mutational screening of 1228 Danish individuals with increased risk of hereditary breast and/or ovarian cancer von Jønson, Lars, Ahlborn, Lise B., Steffensen, Ane Y., Djursby, Malene, Ejlertsen, Bent, Timshel, Susanne, Nielsen, Finn C., Gerdes, Anne-Marie, Hansen, Thomas V. O.

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Characterization of BRCA1 and BRCA2 splicing variants: a collaborative report by ENIGMA consortium members von Thomassen, Mads, Blanco, Ana, Montagna, Marco, Hansen, Thomas V. O., Pedersen, Inge S., Gutiérrez-Enríquez, Sara, Menéndez, Mireia, Fachal, Laura, Santamariña, Marta, Steffensen, Ane Y., Jønson, Lars, Agata, Simona, Whiley, Phillip, Tognazzo, Silvia, Tornero, Eva, Jensen, Uffe B., Balmaña, Judith, Kruse, Torben A., Goldgar, David E., Lázaro, Conxi, Diez, Orland, Spurdle, Amanda B., Vega, Ana

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A method for detecting IBD regions simultaneously in multiple individuals--with applications to disease genetics von Moltke, Ida, Albrechtsen, Anders, Hansen, Thomas V O, Nielsen, Finn C, Nielsen, Rasmus

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Adeno-associated viral vector-induced overexpression of neuropeptide Y Y2 receptors in the hippocampus suppresses seizures von Woldbye, David P. D., Ängehagen, Mikael, Gøtzsche, Casper R., Elbrønd-Bek, Heidi, Sørensen, Andreas T., Christiansen, Søren H., Olesen, Mikkel V., Nikitidou, Litsa, Hansen, Thomas v. O., Kanter-Schlifke, Irene, Kokaia, Merab

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Evaluation of a 5-Tier Scheme Proposed for Classification of Sequence Variants Using Bioinformatic and Splicing Assay Data: Inter-Reviewer Variability and Promotion of Minimum Repo... von Walker, Logan C., Whiley, Phillip J., Houdayer, Claude, Hansen, Thomas V. O., Vega, Ana, Santamarina, Marta, Blanco, Ana, Fachal, Laura, Southey, Melissa C., Lafferty, Alan, Colombo, Mara, De Vecchi, Giovanna, Radice, Paolo, Spurdle, Amanda B.

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Large BRCA1 and BRCA2 genomic rearrangements in Danish high risk breast-ovarian cancer families von Hansen, Thomas v. O, Jønson, Lars, Albrechtsen, Anders, Andersen, Mette K, Ejlertsen, Bent, Nielsen, Finn C

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Prophylactic total gastrectomy in hereditary diffuse gastric cancer: identification of two novel CDH1 gene mutations—a clinical observational study von Bardram, Linda, Hansen, Thomas V. O., Gerdes, Anne-Marie, Timshel, Susanne, Friis-Hansen, Lennart, Federspiel, Birgitte

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Detection of PMS2 Mutations by Screening Hereditary Nonpolyposis Colon Cancer Families from Denmark and Sweden von Okkels, Henrik, Lagerstedt-Robinsson, Kristina, Wikman, Friedrik P, Hansen, Thomas V O, Lolas, Ihab, Lindberg, Lars Joachim, Krarup, Henrik B

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IMP3 RNP Safe Houses Prevent miRNA-Directed HMGA2 mRNA Decay in Cancer and Development von Jønson, Lars, Christiansen, Jan, Hansen, Thomas V.O., Vikeså, Jonas, Yamamoto, Yohei, Nielsen, Finn C.

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BRCA1/BRCA2 founder mutations and cancer risks: impact in the western Danish population von Nielsen, Henriette Roed, Nilbert, Mef, Petersen, Janne, Ladelund, Steen, Thomassen, Mads, Pedersen, Inge Søkilde, Hansen, Thomas V. O., Skytte, Anne-Bine, Borg, Åke, Therkildsen, Christina

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Identification of a breast cancer family double heterozygote for RAD51C and BRCA2 gene mutations von Ahlborn, Lise B., Steffensen, Ane Y., Jønson, Lars, Djursby, Malene, Nielsen, Finn C., Gerdes, Anne-Marie, Hansen, Thomas V. O.

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