Mosaic loss of chromosome Y in peripheral blood is associated with shorter survival and higher risk of cancer von Forsberg, Lars A, Rasi, Chiara, Malmqvist, Niklas, Davies, Hanna, Pasupulati, Saichand, Pakalapati, Geeta, Sandgren, Johanna, de Ståhl, Teresita Diaz, Zaghlool, Ammar, Giedraitis, Vilmantas, Lannfelt, Lars, Score, Joannah, Cross, Nicholas C P, Absher, Devin, Janson, Eva Tiensuu, Lindgren, Cecilia M, Morris, Andrew P, Ingelsson, Erik, Lind, Lars, Dumanski, Jan P

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Somatic mosaicism for copy number variation in differentiated human tissues von Piotrowski, Arkadiusz, Bruder, Carl E.G, Andersson, Robin, de Ståhl, Teresita Diaz, Menzel, Uwe, Sandgren, Johanna, Poplawski, Andrzej, von Tell, Desiree, Crasto, Chiquito, Bogdan, Adam, Bartoszewski, Rafal, Bebok, Zsuzsa, Krzyzanowski, Maciej, Jankowski, Zbigniew, Partridge, E. Christopher, Komorowski, Jan, Dumanski, Jan P

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Phenotypically Concordant and Discordant Monozygotic Twins Display Different DNA Copy-Number-Variation Profiles von Bruder, Carl E.G., Piotrowski, Arkadiusz, Gijsbers, Antoinet A.C.J., Andersson, Robin, Erickson, Stephen, Diaz de Ståhl, Teresita, Menzel, Uwe, Sandgren, Johanna, von Tell, Desiree, Poplawski, Andrzej, Crowley, Michael, Crasto, Chiquito, Partridge, E. Christopher, Tiwari, Hemant, Allison, David B., Komorowski, Jan, van Ommen, Gert-Jan B., Boomsma, Dorret I., Pedersen, Nancy L., den Dunnen, Johan T., Wirdefeldt, Karin, Dumanski, Jan P.

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Human cytomegalovirus tegument protein pp65 is detected in all intra- and extra-axial brain tumours independent of the tumour type or grade von Libard, Sylwia, Popova, Svetlana N, Amini, Rose-Marie, Kärjä, Vesa, Pietiläinen, Timo, Hämäläinen, Kirsi M, Sundström, Christer, Hesselager, Göran, Bergqvist, Michael, Ekman, Simon, Zetterling, Maria, Smits, Anja, Nilsson, Pelle, Pfeifer, Susan, de Ståhl, Teresita Diaz, Enblad, Gunilla, Ponten, Fredrik, Alafuzoff, Irina

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Cytotoxicity of poly-guanidine in medulloblastoma cell lines von Gallo-Oller, Gabriel, de Ståhl, Teresita Díaz, Alaiya, Ayodele, Nilsson, Sten, Holmberg, Anders R., Márquez-Méndez, Marcela

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Register-based and genetic studies of Prader-Willi syndrome show a high frequency of gonadal tumors and a possible mechanism for tumorigenesis through imprinting relaxation von Maya-González, Carolina, Wessman, Sandra, Lagerstedt-Robinson, Kristina, Taylan, Fulya, Tesi, Bianca, Kuchinskaya, Ekaterina, McCluggage, W Glenn, Poluha, Anna, Holm, Stefan, Nergårdh, Ricard, Díaz De Ståhl, Teresita, Höybye, Charlotte, Tettamanti, Giorgio, Delgado-Vega, Angelica Maria, Skarin Nordenvall, Anna, Nordgren, Ann

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Diagnostic Yield From a Nationwide Implementation of Precision Medicine for all Children With Cancer von Wadensten, Elisabeth, Wessman, Sandra, Abel, Frida, Diaz De Ståhl, Teresita, Tesi, Bianca, Orsmark Pietras, Christina, Arvidsson, Linda, Taylan, Fulya, Fransson, Susanne, Vogt, Hartmut, Poluha, Anna, Pradhananga, Sailendra, Hellberg, Maria, Lagerstedt-Robinson, Kristina, Raj Somarajan, Praveen, Samuelsson, Sofie, Orrsjö, Sara, Maqbool, Khurram, Henning, Karin, Strid, Tobias, Ek, Torben, Fagman, Henrik, Olsson Bontell, Thomas, Martinsson, Tommy, Puls, Florian, Kogner, Per, Wirta, Valtteri, Pronk, Cornelis Jan, Wille, Joakim, Rosenquist, Richard, Nistér, Monica, Mertens, Fredrik, Sabel, Magnus, Norén-Nyström, Ulrika, Grillner, Pernilla, Nordgren, Ann, Ljungman, Gustaf, Sandgren, Johanna, Gisselsson, David

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Somatic mosaicism for chromosome X and Y aneuploidies in monozygotic twins heterozygous for sickle cell disease mutation von Razzaghian, Hamid Reza, Shahi, Mehdi Hayat, Forsberg, Lars A., de Ståhl, Teresita Diaz, Absher, Devin, Dahl, Niklas, Westerman, Maxwell P., Dumanski, Jan P.

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A segmental maximum a posteriori approach to genome-wide copy number profiling von Andersson, Robin, Bruder, Carl E. G., Piotrowski, Arkadiusz, Menzel, Uwe, Nord, Helena, Sandgren, Johanna, Hvidsten, Torgeir R., Diaz de Ståhl, Teresita, Dumanski, Jan P., Komorowski, Jan

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Spatially resolved clonal copy number alterations in benign and malignant tissue von Erickson, Andrew, He, Mengxiao, Berglund, Emelie, Marklund, Maja, Mirzazadeh, Reza, Schultz, Niklas, Kvastad, Linda, Andersson, Alma, Bergenstråhle, Ludvig, Bergenstråhle, Joseph, Larsson, Ludvig, Alonso Galicia, Leire, Shamikh, Alia, Basmaci, Elisa, Díaz De Ståhl, Teresita, Rajakumar, Timothy, Doultsinos, Dimitrios, Thrane, Kim, Ji, Andrew L., Khavari, Paul A., Tarish, Firaz, Tanoglidi, Anna, Maaskola, Jonas, Colling, Richard, Mirtti, Tuomas, Hamdy, Freddie C., Woodcock, Dan J., Helleday, Thomas, Mills, Ian G., Lamb, Alastair D., Lundeberg, Joakim

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Whole Exome- and mRNA-Sequencing of an AT/RT Case Reveals Few Somatic Mutations and Several Deregulated Signalling Pathways in the Context of SMARCB1 Deficiency von Díaz de Ståhl, Teresita, Grillner, Pernilla, Asmundsson, Jurate, Marino, Ana Maria, Holm, Stefan, Sandgren, Johanna, Nistér, Monica

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Recurrent genomic alterations in benign and malignant pheochromocytomas and paragangliomas revealed by whole-genome array comparative genomic hybridization analysis von Sandgren, Johanna, Diaz de Ståhl, Teresita, Andersson, Robin, Menzel, Uwe, Piotrowski, Arkadiusz, Nord, Helena, Bäckdahl, Martin, Kiss, Nimrod B, Brauckhoff, Michael, Komorowski, Jan, Dralle, Henning, Hessman, Ola, Larsson, Catharina, Åkerström, Göran, Bruder, Carl, Dumanski, Jan P, Westin, Gunnar

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Enhanced susceptibility to low-dose collagen-induced arthritis in CR1/2-deficient female mice--possible role of estrogen on CR1 expression von Nilsson, Kajsa E, Andrén, Maria, de Ståhl, Teresita Diaz, Kleinau, Sandra

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Distal 22q11.2 microduplication encompassing the BCR gene von Descartes, Maria, Franklin, Judy, de Ståhl, Teresita Diaz, Piotrowski, Arkadiusz, Bruder, Carl E.G., Dumanski, Jan P., Carroll, Andrew J., Mikhail, Fady M.

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Efficient IgG-Mediated Suppression of Primary Antibody Responses in Fcγ Receptor-Deficient Mice von Mikael C. I. Karlsson, Wernersson, Sara, de Stahl, Teresita Diaz, Gustavsson, Susanne, Heyman, Birgitta

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Novel amplifications in pediatric medulloblastoma identified by genome-wide copy number profiling von Nord, Helena, Pfeifer, Susan, Nilsson, Pelle, Sandgren, Johanna, Popova, Svetlana, Strömberg, Bo, Alafuzoff, Irina, Nistér, Monica, Díaz de Ståhl, Teresita

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Simultaneous Ultra-Sensitive Detection of Structural and Single Nucleotide Variants Using Multiplex Droplet Digital PCR in Liquid Biopsies from Children with Medulloblastoma von Arthur, Cecilia, Jylhä, Cecilia, de Ståhl, Teresita Díaz, Shamikh, Alia, Sandgren, Johanna, Rosenquist, Richard, Nordenskjöld, Magnus, Harila, Arja, Barbany, Gisela, Sandvik, Ulrika, Tham, Emma

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Occurrence of cancer in Marfan syndrome: Report of two patients with neuroblastoma and review of the literature von Maya‐González, Carolina, Delgado‐Vega, Angelica Maria, Taylan, Fulya, Lagerstedt Robinson, Kristina, Hansson, Lina, Pal, Niklas, Fagman, Henrik, Puls, Florian, Wessman, Sandra, Stenman, Jakob, Georgantzi, Kleopatra, Fransson, Susanne, Díaz De Ståhl, Teresita, Ek, Torben, Palmer, Ruth, Tesi, Bianca, Kogner, Per, Martinsson, Tommy, Nordgren, Ann

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A previously unrecognized microdeletion syndrome on chromosome 22 band q11.2 encompassing the BCR gene von Mikhail, Fady M., Descartes, Maria, Piotrowski, Arkadiusz, Andersson, Robin, Diaz de Ståhl, Teresita, Komorowski, Jan, Bruder, Carl E.G., Dumanski, Jan P., Carroll, Andrew J.

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Frequent genetic differences between matched primary and metastatic breast cancer provide an approach to identification of biomarkers for disease progression von Popławski, Andrzej B, Jankowski, Michał, Erickson, Stephen W, Díaz de Ståhl, Teresita, Partridge, E Christopher, Crasto, Chiquito, Guo, Jingyu, Gibson, John, Menzel, Uwe, Bruder, Carl EG, Kaczmarczyk, Aneta, Benetkiewicz, Magdalena, Andersson, Robin, Sandgren, Johanna, Zegarska, Barbara, Bała, Dariusz, Śrutek, Ewa, Allison, David B, Piotrowski, Arkadiusz, Zegarski, Wojciech, Dumanski, Jan P

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