Eva-Lena Stattin

937 total citations
6 papers, 301 citations indexed

About

Eva-Lena Stattin is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Eva-Lena Stattin has authored 6 papers receiving a total of 301 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Molecular Biology, 2 papers in Cardiology and Cardiovascular Medicine and 2 papers in Genetics. Recurrent topics in Eva-Lena Stattin's work include Cardiac electrophysiology and arrhythmias (2 papers), Cardiac Arrest and Resuscitation (2 papers) and Cardiovascular Effects of Exercise (2 papers). Eva-Lena Stattin is often cited by papers focused on Cardiac electrophysiology and arrhythmias (2 papers), Cardiac Arrest and Resuscitation (2 papers) and Cardiovascular Effects of Exercise (2 papers). Eva-Lena Stattin collaborates with scholars based in Sweden, United Kingdom and United States. Eva-Lena Stattin's co-authors include Aase Wisten, Peter Krantz, Martin Wehling, Jens Schuster, Bert Callewaert, Daniela Toniolo, Silvia Bione, Bart Loeys, Anne De Paepe and Paul Coucke and has published in prestigious journals such as Human Molecular Genetics, Resuscitation and International Journal of Cardiology.

In The Last Decade

Eva-Lena Stattin

6 papers receiving 297 citations

Peers

Eva-Lena Stattin
Claire Turner United Kingdom
K. Aisaka Japan
Sarah Lawson United States
Attila Tar Hungary
Claire Turner United Kingdom
Eva-Lena Stattin
Citations per year, relative to Eva-Lena Stattin Eva-Lena Stattin (= 1×) peers Claire Turner

Countries citing papers authored by Eva-Lena Stattin

Since Specialization
Citations

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

Fields of papers citing papers by Eva-Lena Stattin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eva-Lena Stattin. 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 Eva-Lena Stattin. The network helps show where Eva-Lena Stattin may publish in the future.

Co-authorship network of co-authors of Eva-Lena Stattin

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

All Works

6 of 6 papers shown
1.
Wisten, Aase, Mats Börjesson, Peter Krantz, & Eva-Lena Stattin. (2019). Exercise related sudden cardiac death (SCD) in the young — Pre-mortal characterization of a Swedish nationwide cohort, showing a decline in SCD among athletes. Resuscitation. 144. 99–105. 22 indexed citations
2.
Olsson, K. Sigvard, Maria Wilbe, Marie‐Louise Bondeson, et al.. (2017). Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 genes. Hereditas. 154(1). 16–16. 2 indexed citations
3.
Wisten, Aase, Peter Krantz, & Eva-Lena Stattin. (2016). Sudden cardiac death among the young in Sweden from 2000 to 2010: an autopsy-based study. EP Europace. 19(8). euw249–euw249. 29 indexed citations
4.
Stattin, Eva-Lena, Georgina Shaw, Dick Heinegård, et al.. (2016). Chondrocytes Derived From Mesenchymal Stromal Cells and Induced Pluripotent Cells of Patients With Familial Osteochondritis Dissecans Exhibit an Endoplasmic Reticulum Stress Response and Defective Matrix Assembly. Stem Cells Translational Medicine. 5(9). 1171–1181. 34 indexed citations
5.
Renard, Marjolijn, Bert Callewaert, Machteld Baetens, et al.. (2011). Novel MYH11 and ACTA2 mutations reveal a role for enhanced TGFβ signaling in FTAAD. International Journal of Cardiology. 165(2). 314–321. 115 indexed citations
6.
Mansouri, Mahmoud, Jens Schuster, Jitendra Badhai, et al.. (2008). Alterations in the expression, structure and function of progesterone receptor membrane component-1 (PGRMC1) in premature ovarian failure. Human Molecular Genetics. 17(23). 3776–3783. 99 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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