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16 February, 2022Analysing sperm can detect rare genetic variants
Researchers from Karolinska Institutet have analysed blood and sperm samples from healthy parents to children with genetic syndromes and the results indicate that germline mosaicism is underestimated as a cause to syndromes and that the level of the genetic variant is higher in sperm than in blood. The study was recently published in Molecular Genetics & Genomic Medicine.
25 November, 2021Rare diseases the central topic of Spanish state visit
On November 24, H.M. Queen Letizia of Spain, H.M. Queen Silvia and H.R.H. Crown Princess Victoria Karolinska Institutet and Karolinska University Hospital.
1 November, 202120 MSEK from the Swedish Research Council to MMK
Congratulations to five researchers at the Department of Molecular Medicine and Surgery who received funding from the Swedish Research Council within the field Medicine and Health at the dividend on October 28, 2021.
30 September, 2021Major investment on precision medicine and its clinical application
The government is set to invest through the innovation authority Vinnova another SEK 96 million on Genomic Medicine Sweden (GMS), a national organisation led from Karolinska Institutet. Regions and universities are also putting up SEK 124 million, making a total of SEK 220 million that will make it possible to continue introducing precision medicine into Swedish healthcare.
24 February, 2021Genetic cause of severe liver disease discovered
Liver transplantation is currently the only treatment available for the severe liver disease PSC. Now, however, researchers at Karolinska Institutet and Oslo University have discovered the first reported genetic mutation that causes PSC. The study, which is published in Science Translational Medicine, opens new paths to future treatments.
2 February, 2021Study offers hope of new treatment for accelerated aging in children
Researchers from Karolinska Institutet and Gothenburg University have investigated a potential new drug target for the rare genetic disorder Hutchinson-Gilford progeria syndrome that causes accelerated aging in children. The findings in mice are published in the scientific journal eLife and may aid in the development of more effective treatments for this fatal condition.
11 February, 2019DNA puzzle uncovers rare chromosome defects
Using puzzle pieces from four different DNA analyses, researchers at Karolinska Institutet have been able to map three extremely complex chromosome aberrations. This has given families answers about the cause of their children’s serious symptoms. The study was published in the scientific journal PLOS Genetics and the goal is to produce a test to be used in the clinic.