Malin Olsson

Kontakt

090-785 16 21

Verksam som

Staff scientist vid Institutionen för folkhälsa och klinisk medicin

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.

Visa publikationer i DiVA

Forskargrupper

Gruppmedlem

Amyloidoscentrum

Forskningsprojekt

1 januari 2019

Patogenes, diagnostik och behandling av transtyretinamyloidos