"False"
Umeå University
printicon
Main menu hidden.
Staff photo Malin Olsson

Malin Olsson

Contact

E-mail
malin.olsson@umu.se
Phone
+46 90 785 16 21

Works at

Affiliation
Staff scientist at Department of Public Health and Clinical Medicine
Location
6M, Norrlands Universitetssjukhus, 5032 Umeå universitet, 901 85 Umeå
A multicentric study of the disease risks and first manifestations in Hereditary transthyretin amyloidosis (ATTRv): insights for an earlier diagnosis
Amyloid: Journal of Protein Folding Disorders, Taylor & Francis 2023, Vol. 30, (3) : 313-320
Planté-Bordeneuve, Violaine; Gorram, Farida; Olsson, Malin; et al.
New data on the genetic profile and penetrance of hereditary Val30Met transthyretin amyloidosis in Sweden
Amyloid: Journal of Protein Folding Disorders, Taylor & Francis 2021, Vol. 28, (2) : 84-90
Gorram, Farida; Olsson, Malin; Alarcon, Flora; et al.
Metabolomics analysis for diagnosis and biomarker discovery of transthyretin amyloidosis
Amyloid: Journal of Protein Folding Disorders, Taylor & Francis Group 2021, Vol. 28, (4) : 234-242
Olsson, Malin; Hellman, Urban; Wixner, Jonas; 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.
Non-parametric estimation of survival in age-dependent genetic disease and application to the transthyretin-related hereditary amyloidosis
PLOS ONE, Public Library Science 2018, Vol. 13, (9)
Alarcon, Flora; Plante-Bordeneuve, Violaine; Olsson, Malin; et al.
Variation of Penetrance estimates in a wide spectrum of TTR-FAP families: implication for management of carriers
Neurology, Lippincott Williams & Wilkins 2018, Vol. 90
Gorram, Farida; Olsson, Malin; Alarcon, Flora; et al.
Effect of doxycycline and ursodeoxycholic acid on transthyretin amyloidosis
Amyloid: Journal of Protein Folding Disorders, Vol. 24, (1) : 78-79
Wixner, Jonas; Pilebro, Bjorn; Lundgren, Hans-Erik; et al.
Gene expression profile in hereditary transthyretin amyloidosis: differences in targeted and source organs
Amyloid: Journal of Protein Folding Disorders, Vol. 21, (2) : 113-119
Norgren, Nina; Olsson, Malin; Nyström, Hanna; 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.
Allele specific expression of the transthyretin gene in Swedish patients with hereditary transthyretin amyloidosis (ATTR V30M) is similar between the two alleles
PLOS ONE, Vol. 7, (11) : e49981-
Norgren, Nina; Hellman, Urban; Ericzon, Bo Göran; et al.
TTR familial amyloid polyneuropathy: does a mitochondrial polymorphism entirely explain the parent-of-origin difference in penetrance?
European Journal of Human Genetics
Bonaïti, Bernard; Olsson, Malin; Hellman, Urban; et al.
Familial amyloidosis with polyneuropathy: studies of genetic factors modifying the phenotype of the disease
Umeå University medical dissertations, 1351
Olsson, Malin
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.
Mitochondrial haplogroup is associated with the phenotype of familial amyloidosis with polyneuropathy in Swedish and French patients
Clinical Genetics, Vol. 75, (2) : 163-168
Olsson, Malin; Hellman, Urban; Planté-Bordeneuve, V; et al.
Report of five rare or previously unknown amyloidogenic transthyretin mutations disclosed in Sweden.
Amyloid: Journal of Protein Folding Disorders, Vol. 16, (4) : 208-214
Suhr, Ole B; Andersen, Oluf; Aronsson, Thomas; et al.
Impact of serotonin transporter and catechol-O-methyl transferase genes polymorphism on gastrointestinal dysfunction in Swedish and Japanese familial amyloidotic polyneuropathy patients.
Clinica Chimica Acta, Vol. 398, (1-2) : 10-4
Obayashi, Konen; Olsson, Malin; Anan, Intissar; et al.
Genealogic studies of the Swedish hereditary transthyretin amyloidosis (ATTR V30M) population: differences in age at onset within the population
Norgren, Nina; Andersson Escher, Stefan; Lundgren, Hans-Erik; et al.
Distribution of mitochondrial DNA haplogroups in Portuguese familial amyloidosis with polyneuropathy (FAP) patients
Olsson, Malin; Norgren, Nina; Saraiva, Maria J; et al.
View publications in DiVA