Anna Rautanen

14.2k total citations · 1 hit paper
28 papers, 1.2k citations indexed

About

Anna Rautanen is a scholar working on Immunology, Epidemiology and Molecular Biology. According to data from OpenAlex, Anna Rautanen has authored 28 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Immunology, 9 papers in Epidemiology and 7 papers in Molecular Biology. Recurrent topics in Anna Rautanen's work include Pregnancy and preeclampsia studies (5 papers), Blood Coagulation and Thrombosis Mechanisms (4 papers) and Immune Response and Inflammation (4 papers). Anna Rautanen is often cited by papers focused on Pregnancy and preeclampsia studies (5 papers), Blood Coagulation and Thrombosis Mechanisms (4 papers) and Immune Response and Inflammation (4 papers). Anna Rautanen collaborates with scholars based in United Kingdom, Finland and Sweden. Anna Rautanen's co-authors include Adrian V. S. Hill, Tara C. Mills, Charles Hinds, Christopher S. Garrard, Anthony Gordon, Paula Hutton, Emma E. Davenport, Katie L. Burnham, Peter Humburg and Jayachandran Radhakrishnan and has published in prestigious journals such as The Lancet, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Anna Rautanen

28 papers receiving 1.2k citations

Hit Papers

Genomic landscape of the individual host response and out... 2016 2026 2019 2022 2016 100 200 300 400

Peers

Anna Rautanen
Anna Rautanen
Citations per year, relative to Anna Rautanen Anna Rautanen (= 1×) peers Stefan Rußwurm

Countries citing papers authored by Anna Rautanen

Since Specialization
Citations

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

Fields of papers citing papers by Anna Rautanen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Rautanen

This figure shows the co-authorship network connecting the top 25 collaborators of Anna Rautanen. A scholar is included among the top collaborators of Anna Rautanen 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 Anna Rautanen. Anna Rautanen 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.
Lad, Eleonora M., Michel Tessier, Anna Rautanen, et al.. (2022). Longitudinal Evaluation of Visual Function Impairments in Early and Intermediate Age-Related Macular Degeneration Patients. SHILAP Revista de lepidopterología. 2(3). 100173–100173. 8 indexed citations
2.
Scherag, André, Miriam Kesselmeier, Stefan Taudien, et al.. (2016). Genetic Factors of the Disease Course after Sepsis: A Genome-Wide Study for 28 Day Mortality. EBioMedicine. 12. 239–246. 35 indexed citations
3.
Mackinnon, Margaret J., Carolyne Ndila, Sophie Uyoga, et al.. (2016). Environmental Correlation Analysis for Genes Associated with Protection against Malaria. Molecular Biology and Evolution. 33(5). 1188–1204. 17 indexed citations
4.
Gilchrist, James J., Tara C. Mills, Vivek Naranbhai, et al.. (2015). Genetic variants associated with non-typhoidal Salmonella bacteraemia in African children. The Lancet. 385. S13–S13. 3 indexed citations
5.
Mills, Tara C., S. Jonathan Chapman, Paula Hutton, et al.. (2015). Variants in the Mannose-binding Lectin GeneMBL2do not Associate With Sepsis Susceptibility or Survival in a Large European Cohort. Clinical Infectious Diseases. 61(5). 695–703. 17 indexed citations
6.
Ellis, Magda, Katherine S. Elliott, Anna Rautanen, et al.. (2015). Rare Variants in MYD88, IRAK4 and IKBKG and Susceptibility to Invasive Pneumococcal Disease: A Population-Based Case-Control Study. PLoS ONE. 10(4). e0123532–e0123532. 3 indexed citations
7.
Mills, Tara C., Anna Rautanen, Tom Parks, et al.. (2013). IFITM3 and Susceptibility to Respiratory Viral Infections in the Community. The Journal of Infectious Diseases. 209(7). 1028–1031. 63 indexed citations
8.
George, Julie, Andriy V. Kubarenko, Anna Rautanen, et al.. (2010). MyD88 Adaptor-Like D96N Is a Naturally Occurring Loss-of-Function Variant of TIRAP. The Journal of Immunology. 184(6). 3025–3032. 27 indexed citations
9.
Hiltunen, Leena, Hannele Laivuori, Anna Rautanen, et al.. (2010). Factor V Leiden as a risk factor for preterm birth – a population‐based nested case–control study. Journal of Thrombosis and Haemostasis. 9(1). 71–78. 23 indexed citations
10.
Kubarenko, Andriy V., Satish Ranjan, Anna Rautanen, et al.. (2010). A Naturally Occurring Variant in Human TLR9, P99L, Is Associated with Loss of CpG Oligonucleotide Responsiveness. Journal of Biological Chemistry. 285(47). 36486–36494. 25 indexed citations
11.
Chapman, S. Jonathan, Fredrik Vannberg, Chiea Chuen Khor, et al.. (2010). Mannose-binding lectin genotypes: lack of association with susceptibility to thoracic empyema. BMC Medical Genetics. 11(1). 5–5. 7 indexed citations
12.
George, Julie, Hui Wang, Andriy V. Kubarenko, et al.. (2010). Two Human MYD88 Variants, S34Y and R98C, Interfere with MyD88-IRAK4-Myddosome Assembly. Journal of Biological Chemistry. 286(2). 1341–1353. 50 indexed citations
13.
Chapman, S. Jonathan, Chiea Chuen Khor, Fredrik Vannberg, et al.. (2010). Common NFKBIL2 polymorphisms and susceptibility to pneumococcal disease: a genetic association study. Critical Care. 14(6). R227–R227. 17 indexed citations
14.
Chapman, S. Jonathan, Chiea Chuen Khor, Fredrik Vannberg, et al.. (2009). NFKBIZ polymorphisms and susceptibility to pneumococcal disease in European and African populations. Genes and Immunity. 11(4). 319–325. 27 indexed citations
15.
Hiltunen, Leena, Hannele Laivuori, Anna Rautanen, et al.. (2009). Factor V Leiden as risk factor for unexplained stillbirth – a population-based nested case-control study. Thrombosis Research. 125(6). 505–510. 13 indexed citations
16.
Hiltunen, Leena, Hannele Laivuori, Anna Rautanen, et al.. (2008). Blood group AB and factor V Leiden as risk factors for pre-eclampsia: A population-based nested case-control study. Thrombosis Research. 124(2). 167–173. 52 indexed citations
17.
Rautanen, Anna. (2007). GENOTYPING FOR GENETIC ASSOCIATION STUDIES: METHODS AND APPLICATIONS. Työväentutkimus Vuosikirja. 1 indexed citations
18.
Rautanen, Anna, Johan G. Eriksson, Juha Kere, et al.. (2006). Associations of Body Size at Birth with Late-Life Cortisol Concentrations and Glucose Tolerance Are Modified by Haplotypes of the Glucocorticoid Receptor Gene. The Journal of Clinical Endocrinology & Metabolism. 91(11). 4544–4551. 38 indexed citations
19.
Ulander, Veli‐Matti, Ulla Wartiovaara, Leena Hiltunen, Anna Rautanen, & Risto Kaaja. (2006). Thrombophilia: A new potential risk factor for cervical insufficiency. Thrombosis Research. 118(6). 705–708. 4 indexed citations
20.
Rautanen, Anna, Marco Zucchelli, Siru Mäkelä, & Juha Kere. (2005). Gene mapping with pooled samples on three genotyping platforms. Molecular and Cellular Probes. 19(6). 408–416. 5 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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