Karin S. Graffmo

1.7k total citations
18 papers, 1.3k citations indexed

About

Karin S. Graffmo is a scholar working on Neurology, Genetics and Pharmacology. According to data from OpenAlex, Karin S. Graffmo has authored 18 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Neurology, 10 papers in Genetics and 5 papers in Pharmacology. Recurrent topics in Karin S. Graffmo's work include Amyotrophic Lateral Sclerosis Research (18 papers), Neurogenetic and Muscular Disorders Research (10 papers) and Cholinesterase and Neurodegenerative Diseases (5 papers). Karin S. Graffmo is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (18 papers), Neurogenetic and Muscular Disorders Research (10 papers) and Cholinesterase and Neurodegenerative Diseases (5 papers). Karin S. Graffmo collaborates with scholars based in Sweden, Denmark and Romania. Karin S. Graffmo's co-authors include Stefan L. Marklund, Thomas Brännström, Peter M. Andersen, P. Andreas Jonsson, Karin Forsberg, Daniel Bergemalm, Mikael Oliveberg, Per Zetterström, Mikael Lindberg and Magnus Hultdin and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Neuroscience.

In The Last Decade

Karin S. Graffmo

18 papers receiving 1.3k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Karin S. Graffmo Sweden	16	1.2k	590	425	204	201	18	1.3k
D. McKenna‐Yasek United States	15	1.1k 0.9×	656 1.1×	517 1.2×	354 1.7×	169 0.8×	19	1.4k
Mercedes Prudencio United States	25	1.3k 1.1×	610 1.0×	918 2.2×	269 1.3×	432 2.1×	47	1.9k
Jimei Tong United States	8	868 0.7×	410 0.7×	585 1.4×	147 0.7×	310 1.5×	10	1.2k
Melissa McAlonis‐Downes United States	16	1.3k 1.1×	793 1.3×	807 1.9×	327 1.6×	279 1.4×	18	1.8k
Kathryn Volkening Canada	22	1.1k 1.0×	694 1.2×	890 2.1×	226 1.1×	232 1.2×	44	1.7k
Edward Pokrishevsky Canada	9	671 0.6×	316 0.5×	570 1.3×	206 1.0×	191 1.0×	12	983
Iga Wegorzewska United States	11	750 0.6×	383 0.6×	889 2.1×	175 0.9×	222 1.1×	12	1.5k
Per Zetterström Sweden	12	621 0.5×	276 0.5×	312 0.7×	123 0.6×	134 0.7×	17	774
Peter C. Sapp United States	23	1.7k 1.5×	1.0k 1.7×	949 2.2×	520 2.5×	260 1.3×	33	2.2k
Anna M. Blokhuis Netherlands	7	655 0.6×	412 0.7×	451 1.1×	115 0.6×	152 0.8×	7	929

Countries citing papers authored by Karin S. Graffmo

Since Specialization

Citations

This map shows the geographic impact of Karin S. Graffmo's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Karin S. Graffmo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Karin S. Graffmo more than expected).

Fields of papers citing papers by Karin S. Graffmo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Karin S. Graffmo. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Karin S. Graffmo. The network helps show where Karin S. Graffmo may publish in the future.

Co-authorship network of co-authors of Karin S. Graffmo

This figure shows the co-authorship network connecting the top 25 collaborators of Karin S. Graffmo. A scholar is included among the top collaborators of Karin S. Graffmo based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Karin S. Graffmo. Karin S. Graffmo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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18 of 18 papers shown

Forsberg, Karin, et al.. (2022). Widespread CNS pathology in amyotrophic lateral sclerosis homozygous for the D90A SOD1 mutation. Acta Neuropathologica. 145(1). 13–28. 12 indexed citations

Forsberg, Karin, Karin S. Graffmo, Bente Pakkenberg, et al.. (2019). Misfolded SOD1 inclusions in patients with mutations in C9orf72 and other ALS/FTD-associated genes. Journal of Neurology Neurosurgery & Psychiatry. 90(8). 861–869. 70 indexed citations

Nordin, Angelica, Chizuru Akimoto, Anna Wuolikainen, et al.. (2015). Extensive size variability of the GGGGCC expansion in C9orf72 in both neuronal and non-neuronal tissues in 18 patients with ALS or FTD. Human Molecular Genetics. 24(11). 3133–3142. 76 indexed citations

Bergh, Johan, Per Zetterström, Peter M. Andersen, et al.. (2015). Structural and kinetic analysis of protein-aggregate strains in vivo using binary epitope mapping. Proceedings of the National Academy of Sciences. 112(14). 4489–4494. 62 indexed citations

Alvarez, Susana, et al.. (2013). Peripheral motor axons of SOD1G127X mutant mice are susceptible to activity-dependent degeneration. Neuroscience. 241. 239–249. 7 indexed citations

Zetterström, Per, Karin S. Graffmo, Peter M. Andersen, Thomas Brännström, & Stefan L. Marklund. (2012). Composition of Soluble Misfolded Superoxide Dismutase-1 in Murine Models of Amyotrophic Lateral Sclerosis. NeuroMolecular Medicine. 15(1). 147–158. 27 indexed citations

Graffmo, Karin S., Karin Forsberg, Johan Bergh, et al.. (2012). Expression of wild-type human superoxide dismutase-1 in mice causes amyotrophic lateral sclerosis. Human Molecular Genetics. 22(1). 51–60. 117 indexed citations

Moldovan, Mihai, et al.. (2011). Nerve excitability changes related to axonal degeneration in amyotrophic lateral sclerosis: Insights from the transgenic SOD1G127X mouse model. Experimental Neurology. 233(1). 408–420. 24 indexed citations

Zetterström, Per, Karin S. Graffmo, Peter M. Andersen, Thomas Brännström, & Stefan L. Marklund. (2011). Proteins That Bind to Misfolded Mutant Superoxide Dismutase-1 in Spinal Cords from Transgenic Amyotrophic Lateral Sclerosis (ALS) Model Mice. Journal of Biological Chemistry. 286(23). 20130–20136. 38 indexed citations

10.

Bergemalm, Daniel, Karin Forsberg, Vaibhav Srivastava, et al.. (2010). Superoxide dismutase‐1 and other proteins in inclusions from transgenic amyotrophic lateral sclerosis model mice. Journal of Neurochemistry. 114(2). 408–418. 37 indexed citations

11.

Meehan, Claire Francesca, Mihai Moldovan, Stefan L. Marklund, et al.. (2010). Intrinsic properties of lumbar motor neurones in the adult G127insTGGG superoxide dismutase‐1 mutant mouse in vivo: evidence for increased persistent inward currents. Acta Physiologica. 200(4). 361–376. 53 indexed citations

12.

Forsberg, Karin, P. Andreas Jonsson, Peter M. Andersen, et al.. (2010). Novel Antibodies Reveal Inclusions Containing Non-Native SOD1 in Sporadic ALS Patients. PLoS ONE. 5(7). e11552–e11552. 262 indexed citations

13.

Bergemalm, Daniel, Karin Forsberg, P. Andreas Jonsson, et al.. (2009). Changes in the Spinal Cord Proteome of an Amyotrophic Lateral Sclerosis Murine Model Determined by Differential In-gel Electrophoresis. Molecular & Cellular Proteomics. 8(6). 1306–1317. 23 indexed citations

14.

Jonsson, P. Andreas, Karin S. Graffmo, Peter M. Andersen, Stefan L. Marklund, & Thomas Brännström. (2009). Superoxide dismutase in amyotrophic lateral sclerosis patients homozygous for the D90A mutation. Neurobiology of Disease. 36(3). 421–424. 18 indexed citations

15.

Zetterström, Per, Heather Stewart, Daniel Bergemalm, et al.. (2007). Soluble misfolded subfractions of mutant superoxide dismutase-1s are enriched in spinal cords throughout life in murine ALS models. Proceedings of the National Academy of Sciences. 104(35). 14157–14162. 131 indexed citations

16.

Jonsson, P. Andreas, Karin S. Graffmo, Thomas Brännström, et al.. (2006). Motor Neuron Disease in Mice Expressing the Wild Type-Like D90A Mutant Superoxide Dismutase-1. Journal of Neuropathology & Experimental Neurology. 65(12). 1126–1136. 85 indexed citations

17.

Bergemalm, Daniel, P. Andreas Jonsson, Karin S. Graffmo, et al.. (2006). Overloading of Stable and Exclusion of Unstable Human Superoxide Dismutase-1 Variants in Mitochondria of Murine Amyotrophic Lateral Sclerosis Models. Journal of Neuroscience. 26(16). 4147–4154. 89 indexed citations

18.

Jonsson, P. Andreas, Karin S. Graffmo, Peter M. Andersen, et al.. (2005). Disulphide-reduced superoxide dismutase-1 in CNS of transgenic amyotrophic lateral sclerosis models. Brain. 129(2). 451–464. 196 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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