Allele Specific Expression of the Transthyretin Gene in Swedish Patients with Hereditary Transthyretin Amyloidosis (ATTR V30M) Is Similar between the Two Alleles

por Norgren, Nina, Hellman, Urban, Ericzon, Bo Göran, Olsson, Malin, Suhr, Ole B.
Publicado 2012

The influence of common polygenic risk and gene sets on social skills group training response in autism spectrum disorder

por Li, Danyang, Choque-Olsson, Nora, Jiao, Hong, Norgren, Nina, Jonsson, Ulf, Bölte, Sven, Tammimies, Kristiina
Publicado 2020

A possible role for miRNA silencing in disease phenotype variation in Swedish transthyretin V30M carriers

por Olsson, Malin, Norgren, Nina, Obayashi, Konen, Plante-Bordeneuve, Violaine, Suhr, Ole B, Cederquist, Kristina, Jonasson, Jenni
Publicado 2010

Gene expression profile in hereditary transthyretin amyloidosis: differences in targeted and source organs

por Norgren, Nina, Olsson, Malin, Nyström, Hanna, Ericzon, Bo Göran, de Tayrac, Marie, Genin, Emmanuelle, Planté-Bordeneuve, Violaine, Suhr, Ole B
Publicado 2014

Whole genome DNA sequencing provides an atlas of somatic mutagenesis in healthy human cells and identifies a tumor-prone cell type

por Franco, Irene, Helgadottir, Hafdis T., Moggio, Aldo, Larsson, Malin, Vrtačnik, Peter, Johansson, Anna, Norgren, Nina, Lundin, Pär, Mas-Ponte, David, Nordström, Johan, Lundgren, Torbjörn, Stenvinkel, Peter, Wennberg, Lars, Supek, Fran, Eriksson, Maria
Publicado 2019

Transcriptomic analysis reveals proinflammatory signatures associated with acute myeloid leukemia progression

por Stratmann, Svea, Yones, Sara A., Garbulowski, Mateusz, Sun, Jitong, Skaftason, Aron, Mayrhofer, Markus, Norgren, Nina, Herlin, Morten Krogh, Sundström, Christer, Eriksson, Anna, Höglund, Martin, Palle, Josefine, Abrahamsson, Jonas, Jahnukainen, Kirsi, Munthe-Kaas, Monica Cheng, Zeller, Bernward, Tamm, Katja Pokrovskaja, Cavelier, Lucia, Komorowski, Jan, Holmfeldt, Linda
Publicado 2022