Nina Norgren
0000-0002-3823-1555
10 papers found
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Transcriptomic analysis reveals proinflammatory signatures associated with acute myeloid leukemia progression
Rare variants in the outcome of social skills group training for autism
Genomic characterization of relapsed acute myeloid leukemia reveals novel putative therapeutic targets
The influence of common polygenic risk and gene sets on social skills group training response in autism spectrum disorder
Whole genome DNA sequencing provides an atlas of somatic mutagenesis in healthy human cells and identifies a tumor-prone cell type
Common susceptibility variants are shared between schizophrenia and psoriasis in the Han Chinese population
Gene expression profile in hereditary transthyretin amyloidosis: differences in targeted and source organs
Allele specific expression of the transthyretin gene in Swedish patients with hereditary transthyretin amyloidosis (ATTR V30M) is similar between the two alleles
A high-penetrance form of late-onset torsion dystonia maps to a novel locus (DYT21) on chromosome 2q14.3-q21.3
A possible role for miRNA silencing in disease phenotype variation in Swedish transthyretin V30M carriers
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