Nina Norgren

Contact

nina.norgren@umu.se

+46 90 786 99 86, +46 90 785 67 60

Works as

Staff scientist at Department of Plant Physiology Section: Umeå Plant Science Centre - UmU

Fysiologihuset, Byggnad L, Artedigränd 7, Fysiologisk botanik, UPSC Umeå universitet, 901 87 Umeå

Other position at Department of Molecular Biology Section: WABI, Wallenberg Advanced Bioinformatics Infrastructure

6K och 6L, Sjukhusområdet Umeå universitet, 901 87 Umeå

Publications Publications

Whole genome case-control study of central nervous system toxicity due to antimicrobial drugs

PLOS ONE, Public Library of Science (PLoS) 2024, Vol. 19, (2)

Ås, Joel; Bertulyte, Ilma; Norgren, Nina; et al.

Python in a week: Conceptual tests for learning and course development

Proceedings of the International CDIO Conference, NTNU SEED 2023 : 470-480

Blöcker, Christopher; Mejtoft, Thomas; Norgren, Nina

Rare variants in the outcome of social skills group training for autism

Autism Research, John Wiley & Sons 2022, Vol. 15, (3) : 434-446

Li, Danyang; Choque Olsson, Nora; Becker, Martin; et al.

Transcriptomic analysis reveals proinflammatory signatures associated with acute myeloid leukemia progression

Blood Advances, American Society of Hematology 2022, Vol. 6, (1) : 152-164

Stratmann, Svea; Yones, Sara A.; Garbulowski, Mateusz; et al.

Genomic characterization of relapsed acute myeloid leukemia reveals novel putative therapeutic targets

Blood Advances, American Society of Hematology 2021, Vol. 5, (3) : 900-912

Stratmann, Svea; Yones, Sara A.; Mayrhofer, Markus; et al.

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

NPJ Genomic Medicine, Nature Publishing Group 2020, Vol. 5, (1)

Li, Danyang; Choque-Olsson, Nora; Jiao, Hong; et al.

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

Genome Biology, BMC 2019, Vol. 20, (1)

Franco, Irene; Helgadottir, Hafdis T.; Moggio, Aldo; et al.

Hereditary transthyretin amyloidosis (ATTR V30M): from genes to genealogy

Umeå University medical dissertations, 1622

Norgren, Nina

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

Amyloid: Journal of Protein Folding Disorders, Vol. 21, (2) : 113-119

Norgren, Nina; Olsson, Malin; Nyström, Hanna; et al.

Allele specific expression of the transthyretin gene in Swedish patients with hereditary transthyretin amyloidosis (ATTR V30M) is similar between the two alleles

PLOS ONE, Vol. 7, (11) : e49981-

Norgren, Nina; Hellman, Urban; Ericzon, Bo Göran; et al.

A high-penetrance form of late-onset torsion dystonia maps to a novel locus (DYT21) on chromosome 2q14.3-q21.3

Neurogenetics, Heidelberg: Springer Berlin/Heidelberg 2011, Vol. 12, (2) : 137-143

Norgren, Nina; Mattson, Emma; Forsgren, Lars; et al.

Transthyretin familial amyloid polyneuropathy: Delineating the individual disease risk to improve management of patients and carriers

Future Neurology, Future Medicine 2011, Vol. 6, (4) : 437-440

Planté-Bordeneuve, Violaine; Norgren, Nina

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

BMC Medical Genetics, Vol. 11 : 130-

Olsson, Malin; Norgren, Nina; Obayashi, Konen; et al.

Genealogic studies of the Swedish hereditary transthyretin amyloidosis (ATTR V30M) population: differences in age at onset within the population

Norgren, Nina; Andersson Escher, Stefan; Lundgren, Hans-Erik; et al.

Distribution of mitochondrial DNA haplogroups in Portuguese familial amyloidosis with polyneuropathy (FAP) patients

Olsson, Malin; Norgren, Nina; Saraiva, Maria J; et al.

View publications in DiVA