Stefan L. Marklund
Active 1974–2024
- 100
- Papers
- 29,029
- Citations
- 85
- h-index
- 100
- i10-index
Citations
Citation sources
Countries
Institutions
- Umeå University1%
- Beni-Suef University0.7%
- Inserm0.6%
- King Saud University0.6%
- Al-Azhar University0.6%
- Harvard University0.6%
- Other95.9%
Fields
- Medicine47%
- Biochemistry, Genetics and Molecular Biology25%
- Agricultural and Biological Sciences6.2%
- Nursing5.2%
- Environmental Science4.1%
- Neuroscience3.9%
- Other8.6%
Topics
- Amyotrophic Lateral Sclerosis Research5.2%
- Neurogenetic and Muscular Disorders Research2.6%
- Parkinson's Disease Mechanisms and Treatments1.9%
- Nitric Oxide and Endothelin Effects1.7%
- Alzheimer's disease research and treatments1.5%
- Mitochondrial Function and Pathology1.5%
- Other85.6%
Coauthors
- Peter M. Andersen27
- Thomas Brännström18
- Kurt Karlsson10
- Per Zetterström10
- Karin S. Graffmo9
- Karin Forsberg8
- P. Andreas Jonsson8
- Helena Edlund7
- Leif Andersson7
- Peter Nilsson6
- Ulrika Nordström6
- Henrik Antti5
- Mikael Oliveberg5
- Pär Jonsson5
- Thomas Möritz5
- Daniel Bergemalm4
- Hans Ellegren4
- Johan Bergh4
- Johan Sandström4
- Jonathan D. Gilthorpe4
- Lars Forsgren4
- Pontus Strålin4
- Anna Wuolikainen3
- James Kijas3
All papers
- Involvement of the Superoxide Anion Radical in the Autoxidation of Pyrogallol and a Convenient Assay for Superoxide Dismutase
Authors: Stefan L. Marklund, Gudrun MARKLUND - European Journal of Biochemistry 1974 cited by 10,276
- Misfolded SOD1 pathology in sporadic Amyotrophic Lateral Sclerosis
Authors: Bastien Paré, Manuela Lehmann, Marie Beaudin, Ulrika Nordström, Stéphan Saïkali, Jean‐Pierre Julien, Jonathan D. Gilthorpe, Stefan L. Marklund, Neil R. Cashman, Peter M. Andersen, Karin Forsberg, Nicolas Dupré, Peter V. Gould, Thomas Brännström, François Gros‐Louis - Scientific Reports 2018 cited by 152
- Superoxide dismutase isoenzymes in tissues and plasma from New Zealand black mice, nude mice and normal BALB/c mice
Authors: Stefan L. Marklund - Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 1985 cited by 254
- Phenotype in an Infant with SOD1 Homozygous Truncating Mutation
Authors: Peter M. Andersen, Ulrika Nordström, Konstantinos Tsiakas, Jessika Johannsen, Alexander E. Volk, Tatjana Bierhals, Per Zetterström, Stefan L. Marklund, Maja Hempel, René Santer - New England Journal of Medicine 2019 cited by 61
- Extraction and GC/MS Analysis of the Human Blood Plasma Metabolome
Authors: Jiye Aa, Johan Trygg, Jonas Gullberg, Annika Johansson, Pär Jonsson, Henrik Antti, Stefan L. Marklund, Thomas Möritz - Analytical Chemistry 2005 cited by 535
- Glial nuclear aggregates of superoxide dismutase-1 are regularly present in patients with amyotrophic lateral sclerosis
Authors: Karin Forsberg, Peter M. Andersen, Stefan L. Marklund, Thomas Brännström - Acta Neuropathologica 2011 cited by 195
- Novel Antibodies Reveal Inclusions Containing Non-Native SOD1 in Sporadic ALS Patients
Authors: Karin Forsberg, P. Andreas Jonsson, Peter M. Andersen, Daniel Bergemalm, Karin S. Graffmo, Magnus Hultdin, Johan Jacobsson, Roland Rosquist, Stefan L. Marklund, Thomas Brännström - PLoS ONE 2010 cited by 321
- Mutant superoxide dismutase aggregates from human spinal cord transmit amyotrophic lateral sclerosis
Authors: Elaheh Ekhtiari Bidhendi, Johan Bergh, Per Zetterström, Karin Forsberg, Bente Pakkenberg, Peter M. Andersen, Stefan L. Marklund, Thomas Brännström - Acta Neuropathologica 2018 cited by 88
- Alteration of Mitochondrial Integrity as Upstream Event in the Pathophysiology of SOD1-ALS
Authors: René Günther, Arun Pal, Chloe Williams, Vitaly Zimyanin, Maria Liehr, Cläre von Neubeck, Mechthild Krause, Mrudula G. Parab, Susanne Petri, Norman Kalmbach, Stefan L. Marklund, Jared Sterneckert, Peter M. Andersen, Florian Wegner, Jonathan D. Gilthorpe, Andreas Hermann - Cells 2022 cited by 30
- The motor system is exceptionally vulnerable to absence of the ubiquitously expressed superoxide dismutase-1
Authors: Julien H. Park, Ulrika Nordström, Konstantinos Tsiakas, Isil Keskin, Christiane Elpers, Manoj Mannil, Raoul Heller, Melinda Nolan, Salam Alburaiky, Per Zetterström, Maja Hempel, Ulrike Schara‐Schmidt, Saskia Biskup, Petra Steinacker, Markus Otto, Jochen H. Weishaupt, Andreas Hahn, René Santer, Thorsten Marquardt, Stefan L. Marklund, Peter M. Andersen - Brain Communications 2022 cited by 20
- Product of extracellular‐superoxide dismutase catalysis
Authors: Stefan L. Marklund - FEBS Letters 1985 cited by 125
- Dysregulation of intracellular copper homeostasis is common to transgenic mice expressing human mutant superoxide dismutase-1s regardless of their copper-binding abilities
Authors: Eiichi Tokuda, Eriko Okawa, Shunsuke Watanabe, Shin-ichi Ono, Stefan L. Marklund - Neurobiology of Disease 2013 cited by 82
- CuZn-superoxide dismutase, Mn-superoxide dismutase, catalase and glutathione peroxidase in pancreatic islets and other tissues in the mouse
Authors: Kjell Grankvist, Stefan L. Marklund, I.‐B. Täljedal - Biochemical Journal 1981 cited by 508
- Analysis of proteome-wide degradation dynamics in ALS SOD1 iPSC-derived patient neurons reveals disrupted VCP homeostasis
Authors: Konstantinos Tsioras, Kevin C. Smith, Seby Edassery, Mehraveh Garjani, Yichen Li, Chloe Williams, Elizabeth D. McKenna, Wenxuan Guo, Anika P. Wilen, Timothy J. Hark, Stefan L. Marklund, Lyle W. Ostrow, Jonathan D. Gilthorpe, Justin K. Ichida, Robert G. Kalb, Jeffrey N. Savas, Evangelos Kiskinis - Cell Reports 2023 cited by 20
- Toxicity of Familial ALS-Linked SOD1 Mutants from Selective Recruitment to Spinal Mitochondria
Authors: Jian Liu, Concepción Lillo, P. Andreas Jonsson, Christine Vande Velde, Christopher M. Ward, Timothy M. Miller, Jamuna R. Subramaniam, Jeffery D. Rothstein, Stefan L. Marklund, Peter M. Andersen, Thomas Brännström, Ole Gredal, Philip C. Wong, David S. Williams, Don W. Cleveland - Neuron 2004 cited by 497
- High-Throughput Data Analysis for Detecting and Identifying Differences between Samples in GC/MS-Based Metabolomic Analyses
Authors: Pär Jonsson, Annika Johansson, Jonas Gullberg, Johan Trygg, Jiye Aa, Bjørn Grung, Stefan L. Marklund, Michael Sjöstróm, Henrik Antti, Thomas Möritz - Analytical Chemistry 2005 cited by 429
- Amyotrophic lateral sclerosis associated with homozygosity for an Asp90Ala mutation in CuZn-superoxide dismutase
Authors: Peter M. Andersen, Peter Nilsson, V. Ala‐Hurula, Marja-Leena Keränen, Ilkka Tarvainen, Tuula Haltia, Lotta Nilsson, Michael Binzer, Lars Forsgren, Stefan L. Marklund - Nature Genetics 1995 cited by 319
- Multi-platform mass spectrometry analysis of the CSF and plasma metabolomes of rigorously matched amyotrophic lateral sclerosis, Parkinson's disease and control subjects
Authors: Anna Wuolikainen, Pär Jonsson, Maria Ahnlund, Henrik Antti, Stefan L. Marklund, Thomas Möritz, Lars Forsgren, Peter M. Andersen, Miles Trupp - Molecular BioSystems 2016 cited by 139
- Human copper-containing superoxide dismutase of high molecular weight.
Authors: Stefan L. Marklund - National Academy of Sciences, Proceedings of the National Academy of Sciences 1982 cited by 753
- Superoxide dismutase in extracellular fluids
Authors: Stefan L. Marklund, Elisabeth Holme, L. Hellner - Clinica Chimica Acta 1982 cited by 436
- Extracellular superoxide dismutase in human tissues and human cell lines.
Authors: Stefan L. Marklund - Journal of Clinical Investigation 1984 cited by 430
- Extensive size variability of the GGGGCC expansion in C9orf72 in both neuronal and non-neuronal tissues in 18 patients with ALS or FTD
Authors: Angelica Nordin, Chizuru Akimoto, Anna Wuolikainen, Helena Alstermark, Pär Jonsson, Anna Birve, Stefan L. Marklund, Karin S. Graffmo, Karin Forsberg, Thomas Brännström, Peter M. Andersen - Human Molecular Genetics 2015 cited by 120
- Infantile SOD1 deficiency syndrome caused by a homozygous SOD1 variant with absence of enzyme activity
Authors: Shlomit Ezer, Muhannad Daana, Julien H. Park, Shira Yanovsky‐Dagan, Ulrika Nordström, Adily Basal, Simon Edvardson, Ann Saada, Markus Otto, Vardiella Meiner, Stefan L. Marklund, Peter M. Andersen, Tamar Harel - Brain 2021 cited by 27
- VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death
Authors: Diether Lambrechts, Erik Storkebaum, Masafumi Morimoto, Jurgen Del‐Favero, Frederik Desmet, Stefan L. Marklund, Sabine Wyns, Vincent Thijs, Jörgen Andersson, Ingrid van Marion, Ammar Al‐Chalabi, Stéphanie Bornes, Rhiannon Musson, Valerie K. Hansen, L. Beckman, Rolf Adolfsson, Hardev Pall, Hervé Prats, Séverine Vermeire, Paul Rutgeerts, Shigehiro Katayama, Takuya Awata, Nigel Leigh, Loı̈c Lang-Lazdunski, Mieke Dewerchin, Christopher E. Shaw, Lieve Moons, Robert Vlietinck, Karen Morrison, Wim Robberecht, Christine Van Broeckhoven, Désiré Collen, Peter M. Andersen, Peter Carmeliet - Nature Genetics 2003 cited by 860
