Rayomand Press

2.6k total citations
65 papers, 1.5k citations indexed

About

Rayomand Press is a scholar working on Neurology, Cellular and Molecular Neuroscience and Pathology and Forensic Medicine. According to data from OpenAlex, Rayomand Press has authored 65 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Neurology, 28 papers in Cellular and Molecular Neuroscience and 10 papers in Pathology and Forensic Medicine. Recurrent topics in Rayomand Press's work include Peripheral Neuropathies and Disorders (27 papers), Hereditary Neurological Disorders (25 papers) and Amyotrophic Lateral Sclerosis Research (15 papers). Rayomand Press is often cited by papers focused on Peripheral Neuropathies and Disorders (27 papers), Hereditary Neurological Disorders (25 papers) and Amyotrophic Lateral Sclerosis Research (15 papers). Rayomand Press collaborates with scholars based in Sweden, United States and China. Rayomand Press's co-authors include Hans Link, Mathilde C.M. Kouwenhoven, Volkan Özenci, Anette Forsberg, Kristin Samuelsson, Lotta Widén Holmqvist, Мikhail Pashenkov, Caroline Ingre, Jesús de Pedro-Cuesta and Eng M. Tan and has published in prestigious journals such as The Lancet, Nature Communications and SHILAP Revista de lepidopterología.

In The Last Decade

Rayomand Press

65 papers receiving 1.4k citations

Peers

Rayomand Press
M. Carpo Italy
Susanna Ruggero Italy
Hannah Briemberg Canada
Matthew C. Garrett United States
Elia Sechi Italy
Kathy Alderson United States
Masamichi Tomonaga Japan
Helmar C. Lehmann Germany
Timothée Lenglet France
Fumiharu Kimura Japan
M. Carpo Italy
Rayomand Press
Citations per year, relative to Rayomand Press Rayomand Press (= 1×) peers M. Carpo

Countries citing papers authored by Rayomand Press

Since Specialization
Citations

This map shows the geographic impact of Rayomand Press'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 Rayomand Press with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rayomand Press more than expected).

Fields of papers citing papers by Rayomand Press

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rayomand Press. 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 Rayomand Press. The network helps show where Rayomand Press may publish in the future.

Co-authorship network of co-authors of Rayomand Press

This figure shows the co-authorship network connecting the top 25 collaborators of Rayomand Press. A scholar is included among the top collaborators of Rayomand Press 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 Rayomand Press. Rayomand Press is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
2.
Seitz, Christina, Anikó Lovik, Lu Pan, et al.. (2024). Lifestyle and medical conditions in relation to ALS risk and progression—an introduction to the Swedish ALSrisc Study. Journal of Neurology. 271(8). 5447–5459. 2 indexed citations
3.
Gustafsson, Rasmus, Katharina Fink, Anders Svenningsson, et al.. (2023). Validation of elevated levels of interleukin-8 in the cerebrospinal fluid, and discovery of new biomarkers in patients with GBS and CIDP using a proximity extension assay. Frontiers in Immunology. 14. 1241199–1241199. 2 indexed citations
4.
Sennfält, Stefan, Anikó Lovik, Anja Finn, et al.. (2023). Neurodegenerative biomarkers outperform neuroinflammatory biomarkers in amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 25(1-2). 150–161. 7 indexed citations
5.
Nilsson, Daniel, Martin Engvall, Helena Malmgren, et al.. (2023). Genome sequencing with comprehensive variant calling identifies structural variants and repeat expansions in a large fraction of individuals with ataxia and/or neuromuscular disorders. Frontiers in Neurology. 14. 1170005–1170005. 4 indexed citations
6.
Seitz, Christina, Can Cui, Anikó Lovik, et al.. (2022). T cell responses at diagnosis of amyotrophic lateral sclerosis predict disease progression. Nature Communications. 13(1). 6733–6733. 51 indexed citations
7.
Shen, Qing, Anja Finn, Björn Evertsson, et al.. (2021). Cardiac troponin T is elevated and increases longitudinally in ALS patients. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 23(1-2). 58–65. 17 indexed citations
8.
Samuelsson, Kristin, Per Svenningsson, Helena Malmgren, et al.. (2019). The cerebellar phenotype of Charcot-Marie-Tooth neuropathy type 4C. SHILAP Revista de lepidopterología. 6(1). 9–9. 9 indexed citations
9.
Feresiadou, Amalia, Kenneth Nilsson, Martin Ingelsson, et al.. (2019). Measurement of sCD27 in the cerebrospinal fluid identifies patients with neuroinflammatory disease. Journal of Neuroimmunology. 332. 31–36. 10 indexed citations
10.
Eimer, Johannes, Jan Vesterbacka, Irina Savitcheva, et al.. (2018). Nonopportunistic infection leading to rapidly progressive dementia in a patient with HIV/AIDS. Medicine. 97(12). e0162–e0162. 6 indexed citations
11.
Ingre, Caroline, Susana Pinto, Anna Birve, et al.. (2013). No association between VAPB mutations and familial or sporadic ALS in Sweden, Portugal and Iceland. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 14(7-8). 620–627. 10 indexed citations
12.
Forsberg, Anette, Rayomand Press, & Lotta Widén Holmqvist. (2012). Residual disability 10years after falling ill in Guillain–Barré syndrome: A prospective follow-up study. Journal of the Neurological Sciences. 317(1-2). 74–79. 29 indexed citations
13.
Yang, Xin, Tao Jin, Rayomand Press, et al.. (2008). The expression of TNF-α receptors 1 and 2 on peripheral blood mononuclear cells in chronic inflammatory demyelinating polyneuropathy. Journal of Neuroimmunology. 200(1-2). 129–132. 6 indexed citations
14.
Forsberg, Anette, et al.. (2008). Disability and health status in patients with chronic inflammatory demyelinating polyneuropathy. Disability and Rehabilitation. 31(9). 720–725. 26 indexed citations
15.
Forsberg, Anette, Rayomand Press, Ulrika Einarsson, Jesús de Pedro-Cuesta, & Lotta Widén Holmqvist. (2005). Disability and health-related quality of life in Guillain-Barré syndrome during the first two years after onset: a prospective study. Clinical Rehabilitation. 19(8). 900–909. 42 indexed citations
16.
Press, Rayomand, Inger Nennesmo, Mathilde C.M. Kouwenhoven, et al.. (2005). Dendritic cells in the cerebrospinal fluid and peripheral nerves in Guillain-Barré syndrome and chronic inflammatory demyelinating polyradiculoneuropathy. Journal of Neuroimmunology. 159(1-2). 165–176. 31 indexed citations
17.
Özenci, Volkan, Mathilde C.M. Kouwenhoven, Rayomand Press, Hans Link, & Yu-Min Huang. (2000). IL-12 ELISPOT ASSAYS TO DETECT AND ENUMERATE IL-12 SECRETING CELLS. Cytokine. 12(8). 1218–1224. 10 indexed citations
18.
Dahle, Charlotte, Maha Mustafa, Rayomand Press, et al.. (1998). Recovery from Guillain–Barré Syndrome Is Associated with Increased Levels of Neutralizing Autoantibodies to Interferon-γ. Clinical Immunology and Immunopathology. 88(3). 241–248. 18 indexed citations
19.
Fong, Jill, et al.. (1996). Prevention of maternal hypotension by epidural administration of ephedrine sulfate during lumbar epidural anesthesia for cesarean section. American Journal of Obstetrics and Gynecology. 175(4). 985–990. 9 indexed citations
20.
Press, Rayomand, Carol Peebles, Robert Ochs, Eng M. Tan, & Yasuo Kumagai. (1992). Antinuclear autoantibodies in women with silicone breast implants. The Lancet. 340(8831). 1304–1307. 97 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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