Comprehensive SNP array study of frequently used neuroblastoma cell lines; copy neutral loss of heterozygosity is common in the cell lines but uncommon in primary tumors

por Kryh, Hanna, Carén, Helena, Erichsen, Jennie, Sjöberg, Rose-Marie, Abrahamsson, Jonas, Kogner, Per, Martinsson, Tommy
Publicado 2011

High-resolution array copy number analyses for detection of deletion, gain, amplification and copy-neutral LOH in primary neuroblastoma tumors: Four cases of homozygous deletions o...

por Carén, Helena, Erichsen, Jennie, Olsson, Linda, Enerbäck, Charlotta, Sjöberg, Rose-Marie, Abrahamsson, Jonas, Kogner, Per, Martinsson, Tommy
Publicado 2008

Identification of epigenetically regulated genes that predict patient outcome in neuroblastoma

por Carén, Helena, Djos, Anna, Nethander, Maria, Sjöberg, Rose-Marie, Kogner, Per, Enström, Camilla, Nilsson, Staffan, Martinsson, Tommy
Publicado 2011

A cluster of genes located in 1p36 are down-regulated in neuroblastomas with poor prognosis, but not due to CpG island methylation

por Carén, Helena, Ejeskär, Katarina, Fransson, Susanne, Hesson, Luke, Latif, Farida, Sjöberg, Rose-Marie, Krona, Cecilia, Martinsson, Tommy
Publicado 2005

Low Frequency ALK Hotspots Mutations In Neuroblastoma Tumours Detected By Ultra-deep Sequencing: Implications For ALK Inhibitor Treatment

por Javanmardi, Niloufar, Fransson, Susanne, Djos, Anna, Sjöberg, Rose-Marie, Nilsson, Staffan, Truvé, Katarina, Kogner, Per, Martinsson, Tommy
Publicado 2019

Whole-genome sequencing of recurrent neuroblastoma reveals somatic mutations that affect key players in cancer progression and telomere maintenance

por Fransson, Susanne, Martinez-Monleon, Angela, Johansson, Mathias, Sjöberg, Rose-Marie, Björklund, Caroline, Ljungman, Gustaf, Ek, Torben, Kogner, Per, Martinsson, Tommy
Publicado 2020