Maria Johansson Soller
1 – 10 of 45
      - show: 10
- |
- sort: year (new to old)
        Close
        
            
    
    Embed this list
<iframe src=""
              width=""
              height=""
              allowtransparency="true"
              frameborder="0">
            </iframe>
        - 2024
- 
                        Mark
        Malignant hyperthermia safety - A nationwide survey of publicly funded Swedish healthcare
    
    - Contribution to journal › Article
 
- 2022
- 
                        Mark
        Implementing precision medicine in a regionally organized healthcare system in Sweden
    
    - Contribution to journal › Letter
 
- 2020
- 
                        Mark
        Whole-Exome Sequencing in 22 Young Ischemic Stroke Patients With Familial Clustering of Stroke
    
    - Contribution to journal › Article
 
- 2019
- 
                        Mark
        A stroke gene panel for whole-exome sequencing
    
    - Contribution to journal › Article
 
- 
                        Mark
        Low prevalence of known pathogenic mutations in dominant PD genes : A Swedish multicenter study
    
    - Contribution to journal › Article
 
- 2017
- 
                        Mark
        Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU
    
    - Contribution to journal › Article
 
- 
                        Mark
        Respiratory chain complex III deficiency due to mutated BCS1L : A novel phenotype with encephalomyopathy, partially phenocopied in a Bcs1l mutant mouse model
    
    - Contribution to journal › Article
 
- 2016
- 
                        Mark
        Familial aggregation of stroke amongst young patients in Lund Stroke Register.
    
    - Contribution to journal › Article
 
- 
                        Mark
        The fetal thymus has a unique genomic copy number profile resulting from physiological T cell receptor gene rearrangement
    
    - Contribution to journal › Article
 
- 
                        Mark
        No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer
    
    - Contribution to journal › Article
 
