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Nina Norgren · SciRah

Researcher profile · Semantic Scholar

Nina Norgren

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Nina Norgren — researcher profile on SciRah

h-index: 10
Works: 18
Citations: 312

Most-cited papers

Whole genome DNA sequencing provides an atlas of somatic mutagenesis in healthy human cells and identifies a tumor-prone cell type
Irene Franco, H. Helgadóttir, Aldo Moggio, M. Larsson +11 more
2019Genome Biology76 citations Open access
Semantic Scholar
Genomic characterization of relapsed acute myeloid leukemia reveals novel putative therapeutic targets.
Svea Stratmann, S. Yones, M. Mayrhofer, Nina Norgren +16 more
2021Blood Advances51 citations Open access
Semantic Scholar
A high-penetrance form of late-onset torsion dystonia maps to a novel locus (DYT21) on chromosome 2q14.3-q21.3
Nina Norgren, E. Mattson, L. Forsgren, M. Holmberg
2011Neurogenetics36 citations
Semantic Scholar
Transcriptomic analysis reveals proinflammatory signatures associated with acute myeloid leukemia progression
Svea Stratmann, S. Yones, Mateusz Garbulowski, Ji-Tong Sun +16 more
2021Blood Advances35 citations Open access
Semantic Scholar
A possible role for miRNA silencing in disease phenotype variation in Swedish transthyretin V30M carriers
M. Olsson, Nina Norgren, K. Obayashi, V. Planté-Bordeneuve +3 more
2010BMC Medical Genetics35 citations Open access
Semantic Scholar
Common susceptibility variants are shared between schizophrenia and psoriasis in the Han Chinese population.
Xian-Yong Yin, Nathan E. Wineinger, Kai Wang, W. Yue +27 more
2016Journal of Psychiatry & Neuroscience23 citations Open access
Semantic Scholar
Gene expression profile in hereditary transthyretin amyloidosis: differences in targeted and source organs
Nina Norgren, M. Olsson, Hanna Nyström, B. Ericzon +4 more
2014Amyloid: Journal of Protein Folding Disorders14 citations Open access
Semantic Scholar
The influence of common polygenic risk and gene sets on social skills group training response in autism spectrum disorder
Danyang Li, Nora Choque-Olsson, H. Jiao, Nina Norgren +3 more
2019npj Genomic Medicine13 citations Open access
Semantic Scholar
Allele Specific Expression of the Transthyretin Gene in Swedish Patients with Hereditary Transthyretin Amyloidosis (ATTR V30M) Is Similar between the Two Alleles
Nina Norgren, U. Hellman, B. Ericzon, M. Olsson +1 more
2012PLoS ONE13 citations Open access
Semantic Scholar
Rare variants in the outcome of social skills group training for autism
Danyang Li, Nora Choque Olsson, M. Becker, Abishek Arora +5 more
2021medRxiv12 citations Open access
Semantic Scholar
Genomic and Transcriptomic Characterization of Adult and Pediatric Relapsed Acute Myeloid Leukemia Reveals Novel Therapeutic Targets
Svea Stratmann, S. Yones, Ji-Tong Sun, A. Skaftason +10 more
2020Blood1 citations Open access
Semantic Scholar
Hereditary transthyretin amyloidosis (ATTR V30M) : from genes to genealogy
Nina Norgren
20141 citations
Semantic Scholar
Genealogic studies of the Swedish hereditary transthyretin amyloidosis (ATTR V30M) population : differences in age at onset within the population
Nina Norgren, S. A. Escher, H. Lundgren, O. Suhr +1 more
20141 citations
Semantic Scholar
Transthyretin familial amyloid polyneuropathy: delineating the individual disease risk to improve management of patients and carriers
V. Planté-Bordeneuve, Nina Norgren
20111 citations Open access
Semantic Scholar
Whole genome case-control study of central nervous system toxicity due to antimicrobial drugs
Joel Ås, I. Bertulyte, Nina Norgren, Anna C. V. Johansson +4 more
2024PLoS ONE0 citations Open access
Semantic Scholar
SO042WHOLE GENOME SEQUENCING OF HUMAN KIDNEY PROGENITORS IDENTIFIES A MUTATION-PRONE CELL TYPE IN THE PROXIMAL TUBULE
Irene Franco, H. Helgadóttir, Aldo Moggio, M. Larsson +11 more
2020Nephrology, Dialysis and Transplantation0 citations
Semantic Scholar
Distribution of mitochondrial DNA haplogroups in Portuguese familial amyloidosis with polyneuropathy (FAP) patients
M. Olsson, Nina Norgren, M. J. Saraiva, K. Cederquist +2 more
20100 citations
Semantic Scholar
Title : A possible role for miRNA silencing in disease phenotype variation in Swedish transthyretin V 30 M carriers
M. Olsson, Nina Norgren, V. Planté-Bordeneuve, O. Suhr +3 more
20100 citations
Semantic Scholar

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