Miko Valori

1.3k total citations
18 papers, 192 citations indexed

About

Miko Valori is a scholar working on Genetics, Molecular Biology and Neurology. According to data from OpenAlex, Miko Valori has authored 18 papers receiving a total of 192 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Molecular Biology and 5 papers in Neurology. Recurrent topics in Miko Valori's work include Chronic Lymphocytic Leukemia Research (4 papers), Immunodeficiency and Autoimmune Disorders (3 papers) and Alzheimer's disease research and treatments (2 papers). Miko Valori is often cited by papers focused on Chronic Lymphocytic Leukemia Research (4 papers), Immunodeficiency and Autoimmune Disorders (3 papers) and Alzheimer's disease research and treatments (2 papers). Miko Valori collaborates with scholars based in Finland, United States and United Kingdom. Miko Valori's co-authors include Pentti J. Tienari, Lilja Jansson, Sampsa Hautaniemi, Ville Rantanen, Liisa Myllykangas, Erkki Savilahti, Satu Mustjoki, Gustavo Giménez, Ludmilla Bardina and Mikael Kuitunen and has published in prestigious journals such as PLoS ONE, Neurobiology of Aging and Journal of Neuroimmunology.

In The Last Decade

Miko Valori

16 papers receiving 191 citations

Peers

Miko Valori
Miko Valori
Citations per year, relative to Miko Valori Miko Valori (= 1×) peers Sina Mersmann

Countries citing papers authored by Miko Valori

Since Specialization
Citations

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

Fields of papers citing papers by Miko Valori

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Miko Valori

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

All Works

18 of 18 papers shown
1.
Jahromi, Behnam Rezai, Miko Valori, Riikka Tulamo, et al.. (2024). Cancer-type somatic mutations in saccular cerebral aneurysms. European Journal of Human Genetics. 33(8). 1076–1079.
2.
Järvinen, Elina, Fumi Suomi, James B. Stewart, et al.. (2023). Cultured lymphocytes’ mitochondrial genome integrity is not altered by cladribine. Clinical & Experimental Immunology. 214(3). 304–313. 1 indexed citations
3.
Valori, Miko, et al.. (2023). High Epstein-Barr virus capsid antigen IgG level associates with the carriership of CD8+ T cell somatic mutations in the STAT3 SH2 domain. Clinical Immunology. 255. 109733–109733. 1 indexed citations
4.
5.
Valori, Miko, Lilja Jansson, & Pentti J. Tienari. (2021). CD8+ cell somatic mutations in multiple sclerosis patients and controls—Enrichment of mutations in STAT3 and other genes implicated in hematological malignancies. PLoS ONE. 16(12). e0261002–e0261002. 16 indexed citations
6.
Jahromi, Behnam Rezai, Miko Valori, Riikka Tulamo, et al.. (2021). Cancer-Type Somatic Mutations in Saccular Cerebral Aneurysms. SSRN Electronic Journal. 1 indexed citations
7.
Kaivola, Karri, Hannu Laaksovirta, Manu Jokela, et al.. (2019). Oligogenic basis of sporadic ALS. Neurology Genetics. 5(3). e335–e335. 15 indexed citations
8.
Guidugli, Lucia, Miika Mehine, Sari Tuupanen, et al.. (2019). Characterization of copy number variants (CNVs) identified by genetic testing of inherited retinal disorders. 60(9). 2944–2944.
9.
Kaivola, Karri, Miko Valori, Anders Paetau, et al.. (2018). Alzheimer risk loci and associated neuropathology in a population-based study (Vantaa 85+). Neurology Genetics. 4(1). e211–e211. 14 indexed citations
10.
Valori, Miko, et al.. (2017). Common origin of the gelsolin gene variant in 62 Finnish AGel amyloidosis families. European Journal of Human Genetics. 26(1). 117–123. 5 indexed citations
11.
Valori, Miko, Lilja Jansson, Kimmo Porkka, et al.. (2016). Lymphoid somatic mutations in multiple sclerosis. Multiple Sclerosis Journal. 22. 170–171. 2 indexed citations
12.
Valori, Miko, Lilja Jansson, Pekka Ellonen, et al.. (2016). A novel class of somatic mutations in blood detected preferentially in CD8 + cells. Clinical Immunology. 175. 75–81. 31 indexed citations
13.
Pasanen, Petra, Jussi Mäkinen, Liisa Myllykangas, et al.. (2016). Primary familial brain calcification linked to deletion of 5’ noncoding region of SLC20A2. Acta Neurologica Scandinavica. 136(1). 59–63. 11 indexed citations
14.
Valori, Miko, Tero Kivelä, Kirsi Setälä, et al.. (2015). Exome and regulatory element sequencing of neuromyelitis optica patients. Journal of Neuroimmunology. 289. 139–142. 6 indexed citations
15.
Peuralinna, Terhi, Liisa Myllykangas, Minna Oinas, et al.. (2015). Genome‐wide association study of neocortical Lewy‐related pathology. Annals of Clinical and Translational Neurology. 2(9). 920–931. 23 indexed citations
16.
Rantanen, Ville, Miko Valori, & Sampsa Hautaniemi. (2014). Anima: Modular Workflow System for Comprehensive Image Data Analysis. Frontiers in Bioengineering and Biotechnology. 2. 25–25. 10 indexed citations
17.
Solje, Eino, Päivi Hartikainen, Miko Valori, et al.. (2014). The C9ORF72 expansion does not affect the phenotype in Nasu-Hakola disease with the DAP12 mutation. Neurobiology of Aging. 35(7). 1780.e13–1780.e17. 2 indexed citations
18.
Savilahti, E, Mikael Kuitunen, Miko Valori, et al.. (2014). Use of IgE and IgG4 epitope binding to predict the outcome of oral immunotherapy in cow's milk allergy. Pediatric Allergy and Immunology. 25(3). 227–235. 49 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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