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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
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.
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.
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
Munch Andersen, Peter
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 (Baltimore, Md.), 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.
CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiency
Human Molecular Genetics, Oxford University Press 2018, Vol. 27, (4) : 706-715
Brockmann, Sarah J.; Freischmidt, Axel; Oeckl, Patrick; et al.
A novel p.Ser108LeufsTer15 SOD1 mutation leading to the formation of a premature stop codon in an apparently sporadic ALS patient: insights into the underlying pathomechanisms
Neurobiology of Aging, Elsevier 2018, Vol. 72
Canosa, Antonio; De Marco, Giovanni; Lomartire, Annarosa; et al.
Peripheral neuropathy in ALS: Phenotype association
Journal of the peripheral nervous system, John Wiley & Sons 2018, Vol. 23, (4) : 391-392
de Carvalho, Mamede; Pinto, Susana; Andersen, Peter; et al.
Mutant superoxide dismutase aggregates from human spinal cord transmit amyotrophic lateral sclerosis
Acta Neuropathologica, Springer 2018, Vol. 136, (6) : 939-953
Ekhtiari Bidhendi, Elaheh; Bergh, Johan; Zetterström, Per; et al.
Frequency of C9orf72 hexanucleotide repeat expansion and SOD1 mutations in Portuguese patients with amyotrophic lateral sclerosis
Neurobiology of Aging, Elsevier 2018, Vol. 70
Gromicho, Marta; Pinto, Susana; Gisca, Eugeniu; et al.
Dysregulation of a novel miR-1825/TBCB/TUBA4A pathway in sporadic and familial ALS
Cellular and Molecular Life Sciences (CMLS), Springer 2018, Vol. 75, (23) : 4301-4319
Helferich, Anika M.; Brockmann, Sarah J.; Reinders, Jörg; et al.
NEK1 loss-of-function mutation induces DNA damage accumulation in ALS patient-derived motoneurons
Stem Cell Research, Elsevier 2018, Vol. 30 : 150-162
Higelin, Julia; Catanese, Alberto; Semelink-Sedlacek, Lena Luisa; et al.
The Swedish motor neuron disease quality registry
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, Taylor & Francis 2018, Vol. 19, (7-8) : 528-537
Longinetti, Elisa; Regodón Wallin, Amanda; Samuelsson, Kristin; et al.
Comprehensive analysis of the mutation spectrum in 301 German ALS families
Journal of Neurology, Neurosurgery and Psychiatry, BMJ Publishing Group Ltd 2018, Vol. 89, (8) : 817-827
Mueller, Kathrin; Brenner, David; Weydt, Patrick; et al.
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene
Neuron, Cell Press 2018, Vol. 97, (6) : 1268-1283.e6
Nicolas, Aude; Kenna, Kevin P.; Renton, Alan E.; et al.
Reconsidering the causality of TIA1 mutations in ALS
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, TAYLOR & FRANCIS LTD 2018, Vol. 19, (1-2) : 1-3
Van Der Spek, Rick A.; Van Rheenen, Wouter; Pulit, Sara L.; et al.
Current knowledge and recent insights into the genetic basis of amyotrophic lateral sclerosis
Medizinische Genetik, Springer Berlin/Heidelberg 2018, Vol. 30, (2) : 252-258
Volk, Alexander E.; Weishaupt, Jochen H.; Andersen, Peter M.; et al.
July 2017 ENCALS statement on edaravone
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, Taylor & Francis 2017, Vol. 18, (7-8) : 471-474
Al-Chalabi, Ammar; Andersen, Peter M.; Chandran, Siddharthan; 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).