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Nina Norgren
Contact
E-mail
nina.norgren@umu.se
Phone
+46 90 786 99 86
,
+46 90 785 67 60
Works at
Affiliation
Staff scientist at
Department of Plant Physiology
Section: Umeå Plant Science Centre - UmU
Location
Fysiologihuset, Byggnad L, Artedigränd 7, Fysiologisk botanik, UPSC
Umeå universitet, 901 87 Umeå
Affiliation
Affiliated as other position at
Department of Molecular Biology
Section: WABI, Wallenberg Advanced Bioinformatics Infrastructure
Location
6K och 6L, Sjukhusområdet
Umeå universitet, 901 87 Umeå
Publications
Publications
2024
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.
2023
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
2022
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.
2022
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.
2021
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.
2020
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.
2019
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.
2014
Hereditary transthyretin amyloidosis (ATTR V30M): from genes to genealogy
Umeå University medical dissertations
, 1622
Norgren, Nina
2014
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.
2012
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.
2011
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.
2011
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
2010
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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