Umeå universitet
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Personalbild Peter Andersen

Peter Andersen

Jag är professor och överläkare i neurologi och började forska om ALS 1992. Jag forskar om orsaken till ALS/FTD och leder även läkemedelsstudier där vi utvärderar nya läkemedel.

Kontakt

E-post
peter.andersen@umu.se
Telefon
090-786 55 00

Verksam vid

Anknytning
Professor, överläkare vid Institutionen för klinisk vetenskap Enhet: Neurovetenskaper
Plats
Norrlands universitetssjukhus, Umeå universitet, Klinisk vetenskap Umeå universitet, Klinisk vetenskap, 901 85 Umeå
SOD1 mutations associated with amyotrophic lateral sclerosis analysis of variant severity
Scientific Reports, Nature Publishing Group 2022, Vol. 12, (1)
Berdynski, Mariusz; Miszta, Przemysław; Safranow, Krzysztof; et al.
Alteration of Mitochondrial Integrity as Upstream Event in the Pathophysiology of SOD1-ALS
Cells, MDPI 2022, Vol. 11, (7)
Günther, René; Pal, Arun; Williams, Chloe; et al.
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS
Science Translational Medicine, American Association for the Advancement of Science 2022, Vol. 14, (633)
Hop, Paul J.; Zwamborn, Ramona A.J.; Hannon, Eilis; et al.
Clinical trials in pediatric ALS: a TRICALS feasibility study
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
Kliest, Tessa; Van Eijk, Ruben P.A.; Al-Chalabi, Ammar; et al.
Respiratory onset of amyotrophic lateral sclerosis in a pregnant woman with a novel SOD1 mutation
European Journal of Neurology, John Wiley & Sons 2022, Vol. 29, (4) : 1279-1283
Masrori, Pegah; Ospitalieri, Simona; Forsberg, Karin; et al.
Heterozygous DHTKD1 Variants in Two European Cohorts of Amyotrophic Lateral Sclerosis Patients
Genes, MDPI 2022, Vol. 13, (1)
Osmanovic, Alma; Gogol, Isabel; Martens, Helge; et al.
Caregivers’ divergent perspectives on patients’ well-being and attitudes towards hastened death in Germany, Poland and Sweden
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
Andersen, Peter M.; Kuźma-Kozakiewicz, Magdalena; Keller, Jürgen; et al.
Neurofilaments can differentiate ALS subgroups and ALS from common diagnostic mimics
Scientific Reports, Nature Publishing Group 2021, Vol. 11, (1)
Behzadi, Arvin; Pujol-Calderón, Fani; Tjust, Anton E.; et al.
FUS mutations dominate TBK1 mutations in FUS/TBK1 double-mutant ALS/FTD pedigrees
Neurogenetics
Brenner, David; Müller, Kathrin; Lattante, Serena; et al.
Safety and efficacy of oral levosimendan in people with amyotrophic lateral sclerosis (the REFALS study): a randomised, double-blind, placebo-controlled phase 3 trial
Lancet Neurology, Elsevier 2021, Vol. 20, (10) : 821-831
Cudkowicz, Merit; Genge, Angela; Maragakis, Nicholas; et al.
A serum microRNA sequence reveals fragile X protein pathology in amyotrophic lateral sclerosis
Brain, Oxford University Press 2021, Vol. 144, (4) : 1214-1229
Freischmidt, Axel; Goswami, Anand; Limm, Katharina; et al.
Motor neuron disease beginning with frontotemporal dementia: clinical features and progression
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, Taylor & Francis 2021, Vol. 22, (7-8) : 508-516
Gromicho, Marta; Kuzma-Kozakiewicz, Magdalena; Szacka, Katarzyna; et al.
SCFD1 expression quantitative trait loci in amyotrophic lateral sclerosis are differentially expressed
Brain Communications, Oxford University Press 2021, Vol. 3, (4)
Iacoangeli, Alfredo; Fogh, Isabella; Selvackadunco, Sashika; et al.
Peripheral administration of SOD1 aggregates does not transmit pathogenic aggregation to the CNS of SOD1 transgenic mice
Acta neuropathologica communications, BioMed Central 2021, Vol. 9, (1)
Keskin, Isil; Ekhtiari Bidhendi, Elaheh; Marklund, Matthew; et al.
Putative founder effect in the Polish, Iranian and United States populations for the L144SSOD1mutation associated with slowly uniform phenotype of amyotrophic lateral sclerosis
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, Taylor & Francis 2021, Vol. 22, (1-2) : 80-85
Kuzma-Kozakiewicz, Magdalena; Andersen, Peter M.; Elahi, Elahe; et al.
The Effect of SMN Gene Dosage on ALS Risk and Disease Severity
Annals of Neurology, John Wiley & Sons 2021, Vol. 89, (4) : 686-697
Moisse, Matthieu; Zwamborn, Ramona A. J.; van Vugt, Joke; et al.
Extensive heterogeneity in patients with ALS with mutations in SOD1 in France
Journal of Neurology, Neurosurgery and Psychiatry, BMJ Publishing Group Ltd 2021, Vol. 92, (9) : 914-914
Munch Andersen, Peter
De novo mutations in SOD1 are a cause of ALS
Journal of Neurology, Neurosurgery and Psychiatry
Müller, Kathrin; Oh, Ki-Wook; Nordin, Angelica; et al.
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
Nature Genetics, Nature Publishing Group 2021, Vol. 53, (12) : 1636-1648
van Rheenen, Wouter; van der Spek, Rick A. A.; Bakker, Mark K.; et al.
Impact of comorbidities and co-medication on disease onset and progression in a large German ALS patient group
Journal of Neurology, Springer 2020, Vol. 267, (7) : 2130-2141
Diekmann, Kristin; Kuzma-Kozakiewicz, Magdalena; Piotrkiewicz, Maria; et al.
ALS kan vara en prionsjukdom: Inklusioner av felvecklat SOD1-protein tycks finnas hos patienter med alla typer av ALS
Läkartidningen, Läkartidningen Förlag AB 2020, Vol. 117
Forsberg, Karin; Tjust, Anton E.; Zetterström, Per; et al.
Commentary: Effects of ALS-associated TANK binding kinase 1 mutations on protein-protein interactions and kinase activity
Frontiers in Neuroscience, Frontiers Media S.A. 2020, Vol. 14
Freischmidt, Axel; Brenner, David; Ludolph, Albert C.; et al.
Rare heterozygous DHTKD1 variants in patients with amyotrophic lateral sclerosis
European Journal of Human Genetics, Springer Nature 2020, Vol. 28 : 428-429
Gogol, I.; Osmanovic, A.; Martens, H.; et al.
Potential Preventive Strategies for Amyotrophic Lateral Sclerosis
Frontiers in Neuroscience, Frontiers Media S.A. 2020, Vol. 14
Kuraszkiewicz, B.; Goszczynska, H.; Podsiadly-Marczykowska, T.; et al.
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome
Circulation, Lippincott Williams & Wilkins 2020, Vol. 142, (4) : 324-338
Lahrouchi, Najim; Tadros, Rafik; Crotti, Lia; et al.
Aggregate-selective antibody attenuates seeded aggregation but not spontaneously evolving disease in SOD1 ALS model mice
Acta neuropathologica communications, BMC 2020, Vol. 8, (1)
Lehmann, Manuela; Marklund, Matthew; Bolender, Anna-Lena; et al.
Deficits in verbal fluency in presymptomatic C9orf72 mutation gene carriers-a developmental disorder
Journal of Neurology, Neurosurgery and Psychiatry, BMJ Publishing Group Ltd 2020, Vol. 91, (11) : 1195-1200
Lulé, Dorothée E.; Müller, Hans-Peter; Finsel, Julia; et al.
Phase 1-2 Trial of Antisense Oligonucleotide Tofersen for SOD1 ALS
New England Journal of Medicine, Massachusetts Medical Society 2020, Vol. 383, (2) : 109-119
Miller, Timothy; Cudkowicz, Merit; Shaw, Pamela J.; et al.
Inflammatory profiles relate to survival in subtypes of amyotrophic lateral sclerosis
Neurology: Neuroimmunology and neuroinflammation, Wolters Kluwer 2020, Vol. 7, (3)
Olesen, Mads Nikolaj; Wuolikainen, Anna; Nilsson, Anna Christine; et al.
Gut microbiota-specific IgA+ B cells traffic to the CNS in active multiple sclerosis
Science immunology, American Association for the Advancement of Science 2020, Vol. 5, (53)
Pröbstel, Anne-Katrin; Zhou, Xiaoyuan; Baumann, Ryan; et al.
SQSTM1/p62 variants in 486 patients with familial ALS from Germany and Sweden
Neurobiology of Aging, ELSEVIER SCIENCE INC 2020, Vol. 87 : 139.e9-139.e15
Yilmaz, Rüstem; Müller, Kathrin; Brenner, David; et al.
Phenotype in an Infant with SOD1 Homozygous Truncating Mutation
New England Journal of Medicine, Massachusetts Medical Society 2019, Vol. 381, (5) : 486-488
Andersen, Peter M.; Hempel, Maja; Santer, René; et al.
Neurofilaments in pre-symptomatic ALS and the impact of genotype
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, Taylor & Francis 2019, Vol. 20, (7-8) : 538-548
Benatar, Michael; Wuu, Joanne; Lombardi, Vittoria; et al.
Mutant SOD1 aggregates from human ventral horn transmit templated aggregation and fatal ALS-like disease
Brain Pathology, John Wiley & Sons 2019, Vol. 29 : 90-90
Brännström, Thomas; Andersen, Peter M.; Bergh, Johan; et al.
Genotypes of amyotrophic lateral sclerosis in Mongolia
Journal of Neurology, Neurosurgery and Psychiatry, BMJ Publishing Group Ltd 2019, Vol. 90, (11) : 1300-1302
Daria, Tselmen; Müller, Kathrin; Oidovdorj, Gansuvd; et al.
Misfolded SOD1 inclusions in patients with mutations in C9orf72 and other ALS/FTD-associated genes
Journal of Neurology, Neurosurgery and Psychiatry, BMJ Publishing Group Ltd 2019, Vol. 90, (8) : 861-869
Forsberg, Karin; Graffmo, Karin Sixtensdotter; Pakkenberg, Bente; et al.
The molecular pathogenesis of superoxide dismutase 1-linked ALS is promoted by low oxygen tension
Acta Neuropathologica, New York: Springer 2019, Vol. 138, (1) : 85-101
Keskin, Isil; Forsgren, Elin; Lehmann, Manuela; et al.
Influence of Environment and Lifestyle on Incidence and Progress of Amyotrophic Lateral Sclerosis in A German ALS Population
Aging and Disease, Fort Worth: International Society on Aging & Disease 2019, Vol. 10, (2) : 205-216
Korner, Sonja; Kammeyer, Johanna; Zapf, Antonia; et al.
An observational study on quality of life and preferences to sustain life in locked-in state
Neurology, Wolters Kluwer 2019, Vol. 93, (10) : E938-E945
Kuzma-Kozakiewicz, Magdalena; Andersen, Peter M.; Ciecwierska, Katarzyna; et al.
C9orf72 expansion is associated with accelerated decline of respiratory function and decreased survival in amyotrophic lateral sclerosis
Journal of Neurology, Neurosurgery and Psychiatry, BMJ Publishing Group Ltd 2019, Vol. 90, (1) : 118-120
Miltenberger-Miltenyi, Gabriel; Conceicao, Vasco A.; Gromicho, Marta; et al.
C9orf72 expansion is associated with accelerated decline of respiratory function and decreased survival in amyotrophic lateral sclerosis
Medicine, Lippincott Williams & Wilkins 2019, Vol. 98, (26)
Miltenberger-Miltenyi, Gabriel; Conceicao, Vasco A.; Gromicho, Marta; et al.
Phenotypes and malignancy risk of different FUS mutations in genetic amyotrophic lateral sclerosis
Annals of Clinical and Translational Neurology, John Wiley & Sons 2019, Vol. 6, (12) : 2384-2394
Naumann, Marcel; Peikert, Kevin; Guenther, Rene; et al.
Different neuroinflammatory profile in amyotrophic lateral sclerosis and frontotemporal dementia is linked to the clinical phase
Journal of Neurology, Neurosurgery and Psychiatry, BMJ Publishing Group Ltd 2019, Vol. 90, (1) : 4-10
Oeckl, Patrick; Weydt, Patrick; Steinacker, Petra; et al.
Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohort
Neurobiology of Aging, Elsevier 2019, Vol. 74 : 234.e9-234.e15
Tazelaar, Gijs H. P.; Dekker, Annelot M.; van Vugt, Joke J. F. A.; et al.
Revised Airlie House consensus guidelines for design and implementation of ALS clinical trials
Neurology, Wolters Kluwer 2019, Vol. 92, (14) : E1610-E1623
van den Berg, Leonard H.; Sorenson, Eric; Gronseth, Gary; et al.
Targeted Multiple Reaction Monitoring Analysis of CSF Identifies UCHL1 and GPNMB as Candidate Biomarkers for ALS
Journal of Molecular Neuroscience, Springer 2019, Vol. 69, (4) : 643-657
Zhu, Shaochun; Wuolikainen, Anna; Wu, Junfang; et al.
Therapeutic decisions in ALS patients: cross-cultural differences and clinical implications
Journal of Neurology, Springer Berlin/Heidelberg 2018, Vol. 265, (7) : 1600-1606
Andersen, Peter M.; Kuzma-Kozakiewicz, Magdalena; Keller, Jürgen; et al.
Randomized, double-blind, placebo-controlled trial of arimoclomol in rapidly progressive SOD1 ALS
Neurology, Lippincott Williams & Wilkins 2018, Vol. 90, (7) : E565-E574
Benatar, Michael; Wuu, Joanne; Andersen, Peter M.; et al.
Neurofilament light: a candidate biomarker of presymptomatic amyotrophic lateral sclerosis and phenoconversion
Annals of Neurology, John Wiley & Sons 2018, Vol. 84, (1) : 130-139
Benatar, Michael; Wuu, Joanne; Andersen, Peter M.; et al.
Hot-spot KIF5A mutations cause familial ALS
Brain, Oxford University Press 2018, Vol. 141 : 688-697
Brenner, David; Yilmaz, Rüstem; Müller, Kathrin; et al.
Visa publikationer i DiVA

Forskargrupper

Forskningsledare
ALS forskning i Umeå
Forskningsledare
Peter Andersen

Undervisar läkarstuderande på termin 9 och termin 10 i neurologi (nervsystemets sjukdomar).