Eva‐Lena Stattin

467 total citations
11 papers, 307 citations indexed

About

Eva‐Lena Stattin is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Eva‐Lena Stattin has authored 11 papers receiving a total of 307 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 2 papers in Genetics and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Eva‐Lena Stattin's work include Genetic Neurodegenerative Diseases (2 papers), RNA modifications and cancer (2 papers) and Mitochondrial Function and Pathology (2 papers). Eva‐Lena Stattin is often cited by papers focused on Genetic Neurodegenerative Diseases (2 papers), RNA modifications and cancer (2 papers) and Mitochondrial Function and Pathology (2 papers). Eva‐Lena Stattin collaborates with scholars based in Sweden, United Kingdom and Australia. Eva‐Lena Stattin's co-authors include Niklas Dahl, Adam Ameur, Takako Sasaki, Karin Lindblom, Fredrik Wiklund, Yelverton Tegner, Björn‐Anders Jonsson, Stefan Lohmander, Anders Aspberg and Dick Heinegård and has published in prestigious journals such as Scientific Reports, The American Journal of Human Genetics and Human Mutation.

In The Last Decade

Eva‐Lena Stattin

11 papers receiving 302 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eva‐Lena Stattin Sweden 8 175 133 53 39 33 11 307
Lisette Nevarez United States 9 264 1.5× 242 1.8× 52 1.0× 36 0.9× 40 1.2× 13 542
Alison M. Muir United States 10 145 0.8× 85 0.6× 45 0.8× 23 0.6× 38 1.2× 14 267
Renata Pellegrino da Silva United States 7 134 0.8× 91 0.7× 98 1.8× 27 0.7× 18 0.5× 9 284
Ted Choi United States 6 252 1.4× 216 1.6× 55 1.0× 23 0.6× 20 0.6× 7 389
Alice Costantini Sweden 13 255 1.5× 263 2.0× 65 1.2× 91 2.3× 25 0.8× 28 430
Ewelina Bukowska‐Olech Poland 11 157 0.9× 147 1.1× 33 0.6× 22 0.6× 20 0.6× 41 273
Dwi U. Kemaladewi Netherlands 11 515 2.9× 164 1.2× 51 1.0× 18 0.5× 35 1.1× 16 609
Florian Witte Germany 12 525 3.0× 158 1.2× 66 1.2× 24 0.6× 70 2.1× 12 620
Wenyi Wu China 13 352 2.0× 77 0.6× 21 0.4× 35 0.9× 29 0.9× 38 537
Robea Ballo South Africa 7 137 0.8× 79 0.6× 37 0.7× 31 0.8× 13 0.4× 19 281

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

11 of 11 papers shown
1.
Stattin, Eva‐Lena, Karin Lindblom, André Struglics, et al.. (2022). Novel missense ACAN gene variants linked to familial osteochondritis dissecans cluster in the C-terminal globular domain of aggrecan. Scientific Reports. 12(1). 5215–5215. 7 indexed citations
2.
Sundblom, Jimmy, et al.. (2020). High frequency of intermediary alleles in the HTT gene in Northern Sweden - The Swedish Huntingtin Alleles and Phenotype (SHAPE) study. Scientific Reports. 10(1). 9853–9853. 4 indexed citations
3.
Angius, Andrea, Paolo Uva, Manuela Oppo, et al.. (2019). Exome sequencing in Crisponi/cold‐induced sweating syndrome–like individuals reveals unpredicted alternative diagnoses. Clinical Genetics. 95(5). 607–614. 9 indexed citations
4.
Stattin, Eva‐Lena, Sanna Gudmundsson, Adam Ameur, et al.. (2018). A novel ECEL1 mutation expands the phenotype of distal arthrogryposis multiplex congenita type 5D to include pretibial vertical skin creases. American Journal of Medical Genetics Part A. 176(6). 1405–1410. 8 indexed citations
5.
Höijer, Ida, Yu‐Chih Tsai, Tyson A. Clark, et al.. (2018). Detailed analysis of HTT repeat elements in human blood using targeted amplification-free long-read sequencing. Human Mutation. 39(9). 1262–1272. 58 indexed citations
6.
Wilbe, Maria, Sanna Gudmundsson, Adam Ameur, et al.. (2017). A novel approach using long‐read sequencing and ddPCR to investigate gonadal mosaicism and estimate recurrence risk in two families with developmental disorders. Prenatal Diagnosis. 37(11). 1146–1154. 20 indexed citations
7.
8.
Stattin, Eva‐Lena, Petra Henning, Joakim Klar, et al.. (2017). SNX10 gene mutation leading to osteopetrosis with dysfunctional osteoclasts. Scientific Reports. 7(1). 3012–3012. 36 indexed citations
9.
Lombardi, Maria, Saskia Bulk, Jacopo Celli, et al.. (2011). Mutation update for the PORCN gene. Human Mutation. 32(7). 723–728. 44 indexed citations
10.
Stattin, Eva‐Lena, Fredrik Wiklund, Karin Lindblom, et al.. (2010). A Missense Mutation in the Aggrecan C-type Lectin Domain Disrupts Extracellular Matrix Interactions and Causes Dominant Familial Osteochondritis Dissecans. The American Journal of Human Genetics. 86(2). 126–137. 114 indexed citations
11.
Jensen, Steen M., Eva‐Lena Stattin, & Annika Rydberg. (2007). [Long QT syndrome can be effectively treated. Important to identify mutation carriers].. PubMed. 104(40). 2866–70. 1 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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