Hereditary breast and ovarian cancer: new genes in confined pathways von Nielsen, Finn Cilius, van Overeem Hansen, Thomas, Sørensen, Claus Storgaard

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Exploring the hereditary background of renal cancer in Denmark von Christensen, Maria Bejerholm, Wadt, Karin, Jensen, Uffe Birk, Lautrup, Charlotte Kvist, Bojesen, Anders, Krogh, Lotte Nylandsted, Overeem Hansen, Thomas van, Gerdes, Anne-Marie

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Clinical characteristics and registry-validated extended pedigrees of germline TP53 mutation carriers in Denmark von Stoltze, Ulrik, Skytte, Anne-Bine, Roed, Henriette, Hasle, Henrik, Ejlertsen, Bent, Overeem Hansen, Thomas van, Schmiegelow, Kjeld, Gerdes, Anne-Marie, Wadt, Karin

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A complex of BRCA2 and PP2A-B56 is required for DNA repair by homologous recombination von Ambjørn, Sara M., Duxin, Julien P., Hertz, Emil P. T., Nasa, Isha, Duro, Joana, Kruse, Thomas, Lopez-Mendez, Blanca, Rymarczyk, Beata, Cressey, Lauren E., van Overeem Hansen, Thomas, Kettenbach, Arminja N., Oestergaard, Vibe H., Lisby, Michael, Nilsson, Jakob

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Molecular reclassification reveals low prevalence of germline predisposition in children with ependymoma von Foss-Skiftesvik, Jon, Mathiasen, René, van Overeem Hansen, Thomas, Wadt, Karin, Schmiegelow, Kjeld, Stoltze, Ulrik Kristoffer

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Redefining germline predisposition in children with molecularly characterized ependymoma: a population-based 20-year cohort von Foss-Skiftesvik, Jon, Stoltze, Ulrik Kristoffer, van Overeem Hansen, Thomas, Ahlborn, Lise Barlebo, Sørensen, Erik, Ostrowski, Sisse Rye, Kullegaard, Solvej Margrete Aldringer, Laspiur, Adrian Otamendi, Melchior, Linea Cecilie, Scheie, David, Kristensen, Bjarne Winther, Skjøth-Rasmussen, Jane, Schmiegelow, Kjeld, Wadt, Karin, Mathiasen, René

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New Pathogenic Germline Variants in Very Early Onset and Familial Colorectal Cancer Patients von Djursby, Malene, Madsen, Majbritt B., Frederiksen, Jane H., Berchtold, Lukas A., Therkildsen, Christina, Willemoe, Gro L., Hasselby, Jane P., Wikman, Friedrik, Okkels, Henrik, Skytte, Anne-Bine, Nilbert, Mef, Wadt, Karin, Gerdes, Anne-Marie, van Overeem Hansen, Thomas

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The effect of a single SMARCA4 exon deletion on RNA splicing: Implications for variant classification von Byrjalsen, Anna, Stoltze, Ulrik, Mehrjouy, Mana, Frederiksen, Jane Hübertz, Bak, Mads, Birkedal, Ulf, Hasle, Henrik, Gerdes, Anne-Marie, Schmiegelow, Kjeld, Wadt, Karin, Hansen, Thomas van Overeem

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TINF2 is a major susceptibility gene in Danish patients with multiple primary melanoma von Jensen, Marlene Richter, Jelsig, Anne Marie, Gerdes, Anne-Marie, Hölmich, Lisbet Rosenkrantz, Kainu, Kati Hannele, Lorentzen, Henrik Frank, Hansen, Mary Højgaard, Bak, Mads, Johansson, Peter A., Hayward, Nicholas K., Van Overeem Hansen, Thomas, Wadt, Karin A.W.

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Continuing rise in oropharyngeal cancer in a high HPV prevalence area: A Danish population-based study from 2011 to 2014 von Carlander, Amanda-Louise Fenger, Grønhøj Larsen, Christian, Jensen, David Hebbelstrup, Garnæs, Emilie, Kiss, Katalin, Andersen, Luise, Olsen, Caroline Holkmann, Franzmann, Maria, Høgdall, Estrid, Kjær, Susanne K, Norrild, Bodil, Specht, Lena, Andersen, Elo, van Overeem Hansen, Thomas, Nielsen, Finn Cilius, von Buchwald, Christian

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Novel Alu insertion in the ZEB2 gene causing Mowat‐Wilson syndrome von Barington, Maria, Bak, Mads, Kjartansdóttir, Kristín Rós, Hansen, Thomas van Overeem, Birkedal, Ulf, Østergaard, Elsebet, Hove, Hanne Buciek

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Survival, surveillance, and genetics in patients with Peutz–Jeghers syndrome: A nationwide study von Jelsig, Anne Marie, Overeem Hansen, Thomas, Gede, Lene Bjerring, Qvist, Niels, Christensen, Lise‐Lotte, Lautrup, Charlotte Kvist, Frederiksen, Jane Hübertz, Sunde, Lone, Ousager, Lilian Bomme, Ljungmann, Ken, Bertelsen, Birgitte, Karstensen, John Gásdal

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Aortic dissection in a young male with persistent ductus arteriosus and a novel variant in MYLK von Boelman, Maria Bejerholm, Hansen, Thomas van Overeem, Smith, Matthias Nybro, Hammer‐Hansen, Sophia, Christensen, Alex Hørby, Diness, Birgitte Rode

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The evolutionary impact of childhood cancer on the human gene pool von Stoltze, Ulrik Kristoffer, Foss-Skiftesvik, Jon, Hansen, Thomas van Overeem, Rasmussen, Simon, Karczewski, Konrad J., Wadt, Karin A. W., Schmiegelow, Kjeld

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Genetic predisposition and evolutionary traces of pediatric cancer risk: a prospective 5-year population-based genome sequencing study of children with CNS tumors von Stoltze, Ulrik Kristoffer, Foss-Skiftesvik, Jon, van Overeem Hansen, Thomas, Byrjalsen, Anna, Sehested, Astrid, Scheie, David, Stamm Mikkelsen, Torben, Rasmussen, Simon, Bak, Mads, Okkels, Henrik, Thude Callesen, Michael, Skjøth-Rasmussen, Jane, Gerdes, Anne-Marie, Schmiegelow, Kjeld, Mathiasen, René, Wadt, Karin

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Rare germline chromosome 1 duplication identified in young male with colon cancer: a case report investigating causality von Byrjalsen, Anna, Garcia, Sara L, Borgwardt, Line, Wadt, Karin, Gerdes, Anne Marie, van Overeem Hansen, Thomas

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Predicting the impact of rare variants on RNA splicing in CAGI6 von Lord, Jenny, Oquendo, Carolina Jaramillo, Wai, Htoo A, Douglas, Andrew G L, Bunyan, David J, Wang, Yaqiong, Hu, Zhiqiang, Zeng, Zishuo, Danis, Daniel, Katsonis, Panagiotis, Williams, Amanda, Lichtarge, Olivier, Chang, Yuchen, Bagnall, Richard D, Mount, Stephen M, Matthiasardottir, Brynja, Lin, Chiaofeng, Hansen, Thomas van Overeem, Leman, Raphael, Martins, Alexandra, Houdayer, Claude, Krieger, Sophie, Bakolitsa, Constantina, Peng, Yisu, Kamandula, Akash, Radivojac, Predrag, Baralle, Diana

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Whole genome sequencing and disease pattern in patients with juvenile polyposis syndrome: a nationwide study von Jelsig, Anne Marie, van Overeem Hansen, Thomas, Gede, Lene Bjerring, Qvist, Niels, Christensen, Lise-Lotte, Lautrup, Charlotte Kvist, Ljungmann, Ken, Christensen, Louise Torp, Rønlund, Karina, Tørring, Pernille Mathiesen, Bertelsen, Birgitte, Sunde, Lone, Karstensen, John Gásdal

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Selection criteria for assembling a pediatric cancer predisposition syndrome gene panel von Byrjalsen, Anna, Diets, Illja J., Bakhuizen, Jette, Hansen, Thomas van Overeem, Schmiegelow, Kjeld, Gerdes, Anne-Marie, Stoltze, Ulrik, Kuiper, Roland P., Merks, Johannes H. M., Wadt, Karin, Jongmans, Marjolijn

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Distribution of RET Mutations in Multiple Endocrine Neoplasia 2 in Denmark 1994–2014: A Nationwide Study von Mathiesen, Jes Sloth, Kroustrup, Jens Peter, Vestergaard, Peter, Stochholm, Kirstine, Poulsen, Per Løgstrup, Rasmussen, Åse Krogh, Feldt-Rasmussen, Ulla, Gaustadnes, Mette, Ørntoft, Torben Falck, van Overeem Hansen, Thomas, Nielsen, Finn Cilius, Brixen, Kim, Godballe, Christian, Frederiksen, Anja Lisbeth

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