Malin Olsson

Kontakt

malin.olsson@umu.se

090-785 16 21

Verksam vid

Första forskningsingenjör vid Institutionen för folkhälsa och klinisk medicin Enhet: Avdelningen för medicin

6M, Norrlands Universitetssjukhus, 5032 Umeå universitet, by1a, B41, NUS, 901 85 Umeå

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