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Umeå universitet
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Huvudmenyn dold.

Nina Norgren

Kontakt

E-post
nina.norgren@umu.se
Telefon
090-785 67 60

Verksam vid

Anknytning
Första forskningsassistent vid Institutionen för molekylärbiologi Enhet: WABI, Wallenberg Advanced Bioinformatics Infrastructure
Plats
6K och 6L, Sjukhusområdet Umeå universitet, 901 87 Umeå
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.
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.
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