Anna Wedell
Stockholm, AB 17176, Sweden
Last Updated: 09/26/2026
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Found 98 publications
Genomic Medicine Sweden: Advancing precision medicine at the national level.
Journal: Journal of internal medicine
Published: July 07, 2026
MitoSAM-dependent lipoylation controls postnatal heart development via metabolic remodeling.
Journal: bioRxiv : the preprint server for biology
Published: May 04, 2026
Neonatal Screening for CAH in Sweden-Results of Implementing Second-Tier Testing.
Journal: International journal of neonatal screening
Published: March 04, 2026
Extracting homogenous data from heterogenous diseases: RaraSwed, the Swedish national rare disease quality registry.
Journal: BMC global and public health
Published: December 27, 2025
MRPS22 variants alter mitochondrial ribosome assembly in patients with leukodystrophy, movement disorder and intellectual impairment.
Journal: Human molecular genetics
Published: December 09, 2025
Advancing a sensitive method for measuring mitochondrial ATP production in small muscle biopsy samples.
Journal: Analytical biochemistry
Published: September 03, 2025
Biallelic variants in RNU2-2 cause a remarkably frequent developmental and epileptic encephalopathy.
Biallelic variants in RNU2-2 cause a remarkably frequent developmental and epileptic encephalopathy.
Journal: Nature genetics
Published: September 02, 2025
Next-Generation Sequencing in the Diagnostic Workup of Neonatal Dried Blood Spot Screening in Sweden 2015-2023.
Journal: International journal of neonatal screening
Published: July 22, 2025
The genomic medicine center Karolinska 10-year report on genome sequencing for rare diseases and a strategy for stepwise clinical implementation.
Journal: Genome medicine
Published: May 31, 2025
Precision Omics Initiative Sweden (PROMISE) will integrate research with healthcare.
Journal: Nature medicine
Published: April 04, 2025
Last Updated: 09/26/2026