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Umeå University
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Jenni Jonasson

Contact

E-mail
jenni.jonasson@umu.se
Phone

Works at

Affiliation
Affiliated as research fellow at Department of Medical Biosciences Section: Pathology
Location
By 6M, Sjukhusområdet Umeå universitet, 901 85 Umeå
Should variants of unknown significance (VUS) be disclosed to patients in cardiogenetics or not; only in case of high suspicion of pathogenicity?
European Journal of Human Genetics, Springer Nature 2022, Vol. 30 : 1208-1210
van der Crabben, Saskia N.; Mörner, Stellan; Lundström, Anna; et al.
Transthyretin Glu54Leu - an unknown mutation within the Swedish population associated with amyloid cardiomyopathy and a unique fibril type
Scandinavian Journal of Clinical and Laboratory Investigation, Taylor & Francis 2019, Vol. 79, (6) : 372-376
Hellman, Urban; Lång, Kenneth; Ihse, Elisabet; et al.
Genetic screening in sudden cardiac death in the young can save future lives
International journal of legal medicine, Vol. 130, (1) : 59-66
Stattin, Eva-Lena; Westin, Ida Maria; Cederquist, Kristina; et al.
Frequency of the transthyretin Val30Met mutation in the northern Swedish population
Amyloid: Journal of Protein Folding Disorders, Vol. 21, (1) : 18-20
Olsson, Malin; Jonasson, Jenni; Cederquist, Kristina; et al.
Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing
BMC Cardiovascular Disorders, BioMed Central 2012, Vol. 12 : 95-
Stattin, Eva-Lena; Boström, Ida Maria; Winbo, Annika; et al.
A possible role for miRNA silencing in disease phenotype variation in Swedish transthyretin V30M carriers
BMC Medical Genetics, Vol. 11 : 130-
Olsson, Malin; Norgren, Nina; Obayashi, Konen; et al.
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