Kirsi Auro

9.0k total citations
17 papers, 431 citations indexed

About

Kirsi Auro is a scholar working on Genetics, Obstetrics and Gynecology and Hematology. According to data from OpenAlex, Kirsi Auro has authored 17 papers receiving a total of 431 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Obstetrics and Gynecology and 4 papers in Hematology. Recurrent topics in Kirsi Auro's work include Genetic Associations and Epidemiology (6 papers), Pregnancy and preeclampsia studies (5 papers) and Blood Coagulation and Thrombosis Mechanisms (4 papers). Kirsi Auro is often cited by papers focused on Genetic Associations and Epidemiology (6 papers), Pregnancy and preeclampsia studies (5 papers) and Blood Coagulation and Thrombosis Mechanisms (4 papers). Kirsi Auro collaborates with scholars based in Finland, United States and Sweden. Kirsi Auro's co-authors include Markus Perola, Leena Peltonen, Kaisa Silander, Mervi Alanne, Veikko Salomaa, Kari Kuulasmaa, Kati Kristiansson, Sangita Kulathinal, Pekka Ellonen and Janna Saarela and has published in prestigious journals such as PLoS ONE, Hypertension and Arteriosclerosis Thrombosis and Vascular Biology.

In The Last Decade

Kirsi Auro

17 papers receiving 421 citations

Peers

Kirsi Auro

GENET

CCM

IMMUN

Shufei Zeng China

Danuta Lipińska Poland

R U Simpson United States

Zari Dastani Canada

Wendy Beattie United Kingdom

Víctor Barrientos Chile

Hongfang Shao China

Joong-Yeon Lim South Korea

Jovana Kaludjerovic Canada

Małgorzata Marchelek‐Myśliwiec Poland

Shufei Zeng China

Kirsi Auro

145 ×1.4

65 ×0.6

GENET

42 ×0.4

28 ×0.5

CCM

25 ×0.5

IMMUN

Citations per year, relative to Kirsi Auro Kirsi Auro (= 1×) peers Shufei Zeng

Countries citing papers authored by Kirsi Auro

Since Specialization

Citations

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

Fields of papers citing papers by Kirsi Auro

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kirsi Auro

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

All Works

Sort: Min cites: Since: Top N: Style:

17 of 17 papers shown

Lokki, A. Inkeri, Michael Triebwasser, Emma Daly, et al.. (2024). Understanding rare genetic variants within the terminal pathway of complement system in preeclampsia. Genes and Immunity. 26(1). 22–26. 2 indexed citations

Auro, Kirsi, et al.. (2024). Attention-Deficit/Hyperactivity Disorder Diagnoses in Finland During the COVID-19 Pandemic. JAMA Network Open. 7(6). e2418204–e2418204. 8 indexed citations

Haapanen, Aleksi, et al.. (2023). Psychiatric disorders and interventions in patients sustaining facial fractures from interpersonal violence. Head & Face Medicine. 19(1). 45–45. 2 indexed citations

Lokki, A. Inkeri, Zhen Ren, Michael Triebwasser, et al.. (2023). Identification of complement factor H variants that predispose to pre‐eclampsia: A genetic and functional study. BJOG An International Journal of Obstetrics & Gynaecology. 130(12). 1473–1482. 13 indexed citations

Lappalainen, Olli-Pekka, et al.. (2022). Psychiatric morbidity is common in orthognathic surgery patients—a retrospective study. Oral Surgery Oral Medicine Oral Pathology and Oral Radiology. 135(6). 716–723. 3 indexed citations

Marttila, M., Teemu Paajanen, Minna Brunfeldt, et al.. (2021). A Web Portal for Communicating Polygenic Risk Score Results for Health Care Use—The P5 Study. Frontiers in Genetics. 12. 763159–763159. 13 indexed citations

Lokki, A. Inkeri, Laura Teirilä, Michael Triebwasser, et al.. (2021). Dysfunction of complement receptors CR3 (CD11b/18) and CR4 (CD11c/18) in pre‐eclampsia: a genetic and functional study. BJOG An International Journal of Obstetrics & Gynaecology. 128(8). 1282–1291. 15 indexed citations

Lokki, A. Inkeri, Michael Triebwasser, Emma Daly, et al.. (2018). Rare mutations in factor H predispose to severe preeclampsia. Molecular Immunology. 102. 184–185. 1 indexed citations

Lokki, A. Inkeri, Emma Daly, Michael Triebwasser, et al.. (2017). Protective Low-Frequency Variants for Preeclampsia in the Fms Related Tyrosine Kinase 1 Gene in the Finnish Population. Hypertension. 70(2). 365–371. 17 indexed citations

10.

Silander, Kaisa, Mervi Alanne, Kati Kristiansson, et al.. (2008). Gender Differences in Genetic Risk Profiles for Cardiovascular Disease. PLoS ONE. 3(10). e3615–e3615. 105 indexed citations

11.

Saarinen, Anne, Ville‐Valtteri Välimäki, Matti Välimäki, et al.. (2007). The A1330V polymorphism of the low-density lipoprotein receptor-related protein 5 gene (LRP5) associates with low peak bone mass in young healthy men. Bone. 40(4). 1006–1012. 60 indexed citations

12.

Auro, Kirsi, Kati Kristiansson, Björn Zethelius, et al.. (2007). USF1 gene variants contribute to metabolic traits in men in a longitudinal 32-year follow-up study. Diabetologia. 51(3). 464–472. 15 indexed citations

13.

Auro, Kirsi, Mervi Alanne, Kati Kristiansson, et al.. (2007). Combined Effects of Thrombosis Pathway Gene Variants Predict Cardiovascular Events. PLoS Genetics. 3(7). e120–e120. 22 indexed citations

14.

Alanne, Mervi, Kati Kristiansson, Kirsi Auro, et al.. (2007). Variation in the selenoprotein S gene locus is associated with coronary heart disease and ischemic stroke in two independent Finnish cohorts. Human Genetics. 122(3-4). 355–365. 87 indexed citations

15.

Alanne, Mervi, Kirsi Auro, Riika Kilpikari, et al.. (2006). Risk Alleles of USF1 Gene Predict Cardiovascular Disease of Women in Two Prospective Studies. PLoS Genetics. 2(5). e69–e69. 49 indexed citations

16.

Auro, Kirsi, Mervi Alanne, Kaisa Silander, et al.. (2006). Thrombomodulin Gene Polymorphisms and Haplotypes and the Risk of Cardiovascular Events. Arteriosclerosis Thrombosis and Vascular Biology. 26(4). 942–947. 17 indexed citations

17.

Alanne, Mervi, Kirsi Auro, Riika Kilpikari, et al.. (2005). Risk Alleles of USF1 -Gene Predict Cardiovascular Disease of Women in Two Prospective Studies. PLoS Genetics. preprint(2006). e69–e69. 2 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.

Explore authors with similar magnitude of impact