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

por Sandgren, Johanna, Holm, Stefan, Marino, Ana Maria, Asmundsson, Jurate, Grillner, Pernilla, Nistér, Monica, Díaz de Ståhl, Teresita
Publicado 2015

Age dependence of tumor genetics in unfavorable neuroblastoma: arrayCGH profiles of 34 consecutive cases, using a Swedish 25-year neuroblastoma cohort for validation

por Cetinkaya, Cihan, Martinsson, Tommy, Sandgren, Johanna, Träger, Catarina, Kogner, Per, Dumanski, Jan, Díaz de Ståhl, Teresita, Hedborg, Fredrik
Publicado 2013

Sarek: A portable workflow for whole-genome sequencing analysis of germline and somatic variants

por Garcia, Maxime, Juhos, Szilveszter, Larsson, Malin, Olason, Pall I., Martin, Marcel, Eisfeldt, Jesper, DiLorenzo, Sebastian, Sandgren, Johanna, Díaz De Ståhl, Teresita, Ewels, Philip, Wirta, Valtteri, Nistér, Monica, Käller, Max, Nystedt, Björn
Publicado 2020

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

por 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
Publicado 2023

The Swedish childhood tumor biobank: systematic collection and molecular characterization of all pediatric CNS and other solid tumors in Sweden

por Díaz de Ståhl, Teresita, Shamikh, Alia, Mayrhofer, Markus, Juhos, Szilvester, Basmaci, Elisa, Prochazka, Gabriela, Garcia, Maxime, Somarajan, Praveen Raj, Zielinska-Chomej, Katarzyna, Illies, Christopher, Øra, Ingrid, Siesjö, Peter, Sandström, Per-Erik, Stenman, Jakob, Sabel, Magnus, Gustavsson, Bengt, Kogner, Per, Pfeifer, Susan, Ljungman, Gustaf, Sandgren, Johanna, Nistér, Monica
Publicado 2023

Spatially resolved clonal copy number alterations in benign and malignant tissue

por 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
Publicado 2022

Diagnostic Yield From a Nationwide Implementation of Precision Medicine for all Children With Cancer

por 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
Publicado 2023