A-C Syvänen

1.9k total citations
29 papers, 1.1k citations indexed

About

A-C Syvänen is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, A-C Syvänen has authored 29 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 9 papers in Genetics and 7 papers in Rheumatology. Recurrent topics in A-C Syvänen's work include Systemic Lupus Erythematosus Research (6 papers), Cytokine Signaling Pathways and Interactions (5 papers) and Advanced biosensing and bioanalysis techniques (4 papers). A-C Syvänen is often cited by papers focused on Systemic Lupus Erythematosus Research (6 papers), Cytokine Signaling Pathways and Interactions (5 papers) and Advanced biosensing and bioanalysis techniques (4 papers). A-C Syvänen collaborates with scholars based in Sweden, Finland and United Kingdom. A-C Syvänen's co-authors include Laura‐Maria Peltonen, Elina Ikonen, Gerli Pielberg, Leif Andersson, Christian Olsson, Marina Bengtström, Snævar Sigurðsson, Guðrún Kristjánsdóttir, Gunnel Nordmark and Lennart Truedsson and has published in prestigious journals such as The EMBO Journal, Biochemical Journal and Genetics.

In The Last Decade

A-C Syvänen

28 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
A-C Syvänen Sweden 17 442 339 323 251 234 29 1.1k
Cecilia Soh United Kingdom 12 416 0.9× 291 0.9× 254 0.8× 53 0.2× 186 0.8× 16 840
Stephen Demczuk Switzerland 9 409 0.9× 139 0.4× 393 1.2× 233 0.9× 55 0.2× 16 1.2k
Diego G. Silva Australia 15 485 1.1× 198 0.6× 677 2.1× 89 0.4× 51 0.2× 22 1.3k
Masaaki Honda Japan 16 334 0.8× 91 0.3× 578 1.8× 154 0.6× 168 0.7× 47 1.4k
S L Woo United States 16 698 1.6× 567 1.7× 182 0.6× 126 0.5× 52 0.2× 23 1.4k
Shigeki Miyawaki Japan 17 323 0.7× 79 0.2× 660 2.0× 92 0.4× 219 0.9× 31 1.3k
María Ángeles García-López Spain 13 254 0.6× 88 0.3× 546 1.7× 78 0.3× 67 0.3× 20 1.0k
Julie Carman United States 19 441 1.0× 79 0.2× 772 2.4× 129 0.5× 103 0.4× 32 1.4k
Y Mory Israel 17 731 1.7× 209 0.6× 309 1.0× 46 0.2× 95 0.4× 26 1.5k
Toshihide Akasaka Japan 19 346 0.8× 141 0.4× 95 0.3× 84 0.3× 64 0.3× 72 1.0k

Countries citing papers authored by A-C Syvänen

Since Specialization
Citations

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

Fields of papers citing papers by A-C Syvänen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A-C Syvänen. 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 A-C Syvänen. The network helps show where A-C Syvänen may publish in the future.

Co-authorship network of co-authors of A-C Syvänen

This figure shows the co-authorship network connecting the top 25 collaborators of A-C Syvänen. A scholar is included among the top collaborators of A-C Syvänen 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 A-C Syvänen. A-C Syvänen 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.
Svenungsson, Elisabet, Andreas Jönsen, Dag Leonard, et al.. (2017). 237 Ischaemic stroke in systemic lupus erythematosus, -distribution of subtypes and a risk genotype in the stat4 gene. A108.3–A109.
2.
Berggren, Olof, Andrei Alexsson, David L. Morris, et al.. (2015). IFN-  production by plasmacytoid dendritic cell associations with polymorphisms in gene loci related to autoimmune and inflammatory diseases. Human Molecular Genetics. 24(12). 3571–3581. 26 indexed citations
3.
Berggren, Olof, Andrei Alexsson, Karolina Tandre, et al.. (2014). Effect of single-nucleotide polymorphisms on type I interferon production by plasmacytoid dendritic cells stimulated with SLE-associated immune complexes. Scandinavian Journal of Rheumatology. 43. 92–92. 1 indexed citations
4.
Nordlund, Jessica, Anna Kiialainen, Olof Karlberg, et al.. (2011). Digital gene expression profiling of primary acute lymphoblastic leukemia cells. Leukemia. 26(6). 1218–1227. 18 indexed citations
5.
Edvardsen, Hege, Paal Brunsvig, Hiroko Kato Solvang, et al.. (2010). SNPs in genes coding for ROS metabolism and signalling in association with docetaxel clearance. The Pharmacogenomics Journal. 10(6). 513–523. 18 indexed citations
6.
Hellquist, Anna, Johanna K. Sandling, Sari Koskenmies, et al.. (2009). Variation in STAT4 is associated with systemic lupus erythematosus in a Finnish family cohort. Annals of the Rheumatic Diseases. 69(5). 883–886. 16 indexed citations
7.
López‐Giráldez, Francesc, et al.. (2009). First generation microarray-system for identification of primate species subject to bushmeat trade. Endangered Species Research. 9. 133–142. 7 indexed citations
8.
9.
Nordmark, Gunnel, Guðrún Kristjánsdóttir, Elke Theander, et al.. (2008). Additive effects of the major risk alleles of IRF5 and STAT4 in primary Sjögren's syndrome. Genes and Immunity. 10(1). 68–76. 122 indexed citations
10.
Sigurðsson, Snævar, Gunnel Nordmark, Sophie Garnier, et al.. (2008). A risk haplotype of STAT4 for systemic lupus erythematosus is over-expressed, correlates with anti-dsDNA and shows additive effects with two risk alleles of IRF5. Human Molecular Genetics. 17(18). 2868–2876. 159 indexed citations
11.
Dideberg, Vinciane, Guðrún Kristjánsdóttir, Lili Milani, et al.. (2007). An insertion deletion polymorphism in the Interferon Regulatory Factor 5 (IRF5) gene confers risk of inflammatory bowel diseases. Human Molecular Genetics. 16(24). 3008–3016. 138 indexed citations
12.
Dahlgren, Atti‐La, Björn Zethelius, Karin Jensevik, A-C Syvänen, & Christian Berne. (2007). Variants of the TCF7L2 gene are associated with beta cell dysfunction and confer an increased risk of type 2 diabetes mellitus in the ULSAM cohort of Swedish elderly men. Diabetologia. 50(9). 1852–1857. 41 indexed citations
13.
Sigurðsson, Snævar, et al.. (2006). A microarray system for genotyping 150 single nucleotide polymorphisms in the coding region of human mitochondrial DNA. Genomics. 87(4). 534–542. 19 indexed citations
14.
15.
Heiskanen, Mervi, et al.. (1994). A novel method to quantitate methylation of specific genomic regions.. Genome Research. 4(1). 26–30. 6 indexed citations
16.
Syvänen, A-C, Antti Sajantila, & Matti Lukka. (1993). Forensic DNA typing by the solid-phase minisequencing method. Birkhäuser Basel eBooks. 67. 275–282. 2 indexed citations
17.
Jalanko, Anu, Juha Kere, Erkki Savilahti, et al.. (1992). SCREENING FOR DEFINED CYSTIC-FIBROSIS MUTATIONS BY SOLID-PHASE MINISEQUENCING. Advances in clinical chemistry. 1992(38). 39–43. 2 indexed citations
18.
Syvänen, A-C, Elina Ikonen, Tuula Manninen, et al.. (1992). Convenient and quantitative determination of the frequency of a mutant allele using solid-phase minisequencing: Application to aspartylglucosaminuria in Finland. Genomics. 12(3). 590–595. 113 indexed citations
19.
Vikkula, Miikka, Marjo Metsäranta, A-C Syvänen, et al.. (1992). Structural analysis of the regulatory elements of the type-II procollagen gene. Conservation of promoter and first intron sequences between human and mouse. Biochemical Journal. 285(1). 287–294. 28 indexed citations
20.
Ikonen, Elina, et al.. (1991). [Molecular genetics of aspartylglucosaminuria].. PubMed. 107(23-24). 1916–25. 4 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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