Eija H. Seppälä

2.3k total citations
34 papers, 1.1k citations indexed

About

Eija H. Seppälä is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Eija H. Seppälä has authored 34 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 11 papers in Genetics and 6 papers in Neurology. Recurrent topics in Eija H. Seppälä's work include Neurological diseases and metabolism (6 papers), Lysosomal Storage Disorders Research (4 papers) and Veterinary Medicine and Surgery (4 papers). Eija H. Seppälä is often cited by papers focused on Neurological diseases and metabolism (6 papers), Lysosomal Storage Disorders Research (4 papers) and Veterinary Medicine and Surgery (4 papers). Eija H. Seppälä collaborates with scholars based in Finland, United States and Sweden. Eija H. Seppälä's co-authors include Hannes Lohi, Johanna Schleutker, Teuvo L.J. Tammela, Tarja Ikonen, Mika Matikainen, Ville Autio, Nina Mononen, Annika Rökman, Kerstin Lindblad‐Toh and Olli Kallioniemi and has published in prestigious journals such as Nature Genetics, PLoS ONE and JNCI Journal of the National Cancer Institute.

In The Last Decade

Eija H. Seppälä

33 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
Eija H. Seppälä Finland 17 436 417 186 108 95 34 1.1k
Yulan Lu China 19 527 1.2× 314 0.8× 150 0.8× 67 0.6× 32 0.3× 83 1.2k
Carol Saunders United States 22 744 1.7× 635 1.5× 64 0.3× 130 1.2× 93 1.0× 59 1.3k
Asbjørg Stray‐Pedersen Norway 22 516 1.2× 371 0.9× 118 0.6× 26 0.2× 229 2.4× 55 1.9k
Férechté Encha‐Razavi France 21 870 2.0× 529 1.3× 33 0.2× 70 0.6× 215 2.3× 64 1.7k
Tomohide Goto Japan 18 602 1.4× 165 0.4× 38 0.2× 101 0.9× 328 3.5× 67 1.3k
L.‐C. Tsui Canada 26 1.3k 3.1× 547 1.3× 919 4.9× 71 0.7× 81 0.9× 50 2.5k
Louise Tee United Kingdom 18 801 1.8× 781 1.9× 51 0.3× 43 0.4× 107 1.1× 31 1.5k
Mitsunobu Shimadzu Japan 22 812 1.9× 195 0.5× 79 0.4× 370 3.4× 452 4.8× 43 1.7k
Maria Luisa Tenchini Italy 24 555 1.3× 198 0.5× 354 1.9× 32 0.3× 252 2.7× 74 1.6k
Agnieszka Pollak Poland 19 588 1.3× 202 0.5× 30 0.2× 158 1.5× 73 0.8× 83 1.2k

Countries citing papers authored by Eija H. Seppälä

Since Specialization
Citations

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

Fields of papers citing papers by Eija H. Seppälä

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eija H. Seppälä. 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 Eija H. Seppälä. The network helps show where Eija H. Seppälä may publish in the future.

Co-authorship network of co-authors of Eija H. Seppälä

This figure shows the co-authorship network connecting the top 25 collaborators of Eija H. Seppälä. A scholar is included among the top collaborators of Eija H. Seppälä 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 Eija H. Seppälä. Eija H. Seppälä 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.
Peeters, Dominique, Frédéric Farnir, Katja Höglund, et al.. (2024). Fasting triglyceride concentrations are associated with markers of lipid metabolism and glucose homeostasis in healthy, non-obese dogs in lean and overweight condition. Frontiers in Veterinary Science. 11. 1406322–1406322. 2 indexed citations
2.
Izzo, Emanuela, Eija H. Seppälä, Kirsi Alakurtti, et al.. (2021). Next-generation sequencing in childhood-onset epilepsies: Diagnostic yield and impact on neuronal ceroid lipofuscinosis type 2 (CLN2) disease diagnosis. PLoS ONE. 16(9). e0255933–e0255933. 6 indexed citations
3.
Momozawa, Yukihide, Anne‐Christine Merveille, Maria Wiberg, et al.. (2020). Genome wide association study of 40 clinical measurements in eight dog breeds. Scientific Reports. 10(1). 6520–6520. 13 indexed citations
4.
Höglund, Katja, Jens Häggström, Sofia Hanås, et al.. (2018). Interbreed variation in serum serotonin (5-hydroxytryptamine) concentration in healthy dogs. Journal of Veterinary Cardiology. 20(4). 244–253. 14 indexed citations
5.
Peeters, Dominique, Frédéric Farnir, Katja Höglund, et al.. (2018). Interbreed variation of biomarkers of lipid and glucose metabolism in dogs. Veterinary Clinical Pathology. 47(4). 582–588. 5 indexed citations
6.
Seppälä, Eija H., Katriina Aalto‐Setälä, Olli Pitkänen, et al.. (2018). Heterozygous junctophilin-2 (JPH2) p.(Thr161Lys) is a monogenic cause for HCM with heart failure. PLoS ONE. 13(9). e0203422–e0203422. 34 indexed citations
7.
Koskinen, Lotta L. E., Eija H. Seppälä, Tarja S. Jokinen, et al.. (2017). ADAM23 is a common risk gene for canine idiopathic epilepsy. BMC Genetics. 18(1). 8–8. 20 indexed citations
8.
Qadri, S. U., Olli Anttonen, Eija H. Seppälä, et al.. (2017). Case reports of two pedigrees with recessive arrhythmogenic right ventricular cardiomyopathy associated with homozygous Thr335Ala variant in DSG2. BMC Medical Genetics. 18(1). 86–86. 14 indexed citations
9.
Jokinen, Tarja S., Katriina Tiira, Liisa Metsähonkala, et al.. (2015). Behavioral Abnormalities in Lagotto Romagnolo Dogs with a History of Benign Familial Juvenile Epilepsy: A Long-Term Follow-Up Study. Journal of Veterinary Internal Medicine. 29(4). 1081–1087. 28 indexed citations
10.
Koskinen, Lotta L. E., Eija H. Seppälä, Janelle M. Belanger, et al.. (2015). Identification of a common risk haplotype for canine idiopathic epilepsy in the ADAM23 gene. BMC Genomics. 16(1). 465–465. 22 indexed citations
11.
Ahonen, Saija, Meharji Arumilli, Eija H. Seppälä, et al.. (2014). Increased Expression of MERTK is Associated with a Unique Form of Canine Retinopathy. PLoS ONE. 9(12). e114552–e114552. 8 indexed citations
12.
Viitmaa, Ranno, Sigitas Čižinauskas, Toomas Orro, et al.. (2013). Phenotype, inheritance characteristics, and risk factors for idiopathic epilepsy in Finnish Spitz dogs. Journal of the American Veterinary Medical Association. 243(7). 1001–1009. 12 indexed citations
13.
Seppälä, Eija H., Lotta L. E. Koskinen, Päivi Jokinen, et al.. (2012). Identification of a Novel Idiopathic Epilepsy Locus in Belgian Shepherd Dogs. PLoS ONE. 7(3). e33549–e33549. 39 indexed citations
14.
Kyöstilä, Kaisa, Sigitas Čižinauskas, Eija H. Seppälä, et al.. (2012). A SEL1L Mutation Links a Canine Progressive Early-Onset Cerebellar Ataxia to the Endoplasmic Reticulum–Associated Protein Degradation (ERAD) Machinery. PLoS Genetics. 8(6). e1002759–e1002759. 56 indexed citations
15.
Farias, Fabiana, Rong Zeng, Gary S. Johnson, et al.. (2011). A truncating mutation in ATP13A2 is responsible for adult-onset neuronal ceroid lipofuscinosis in Tibetan terriers. Neurobiology of Disease. 42(3). 468–474. 100 indexed citations
16.
Klütsch, Cornelya F. C., Eija H. Seppälä, Tove Fall, et al.. (2010). Regional occurrence, high frequency but low diversity of mitochondrial DNA haplogroup d1 suggests a recent dog-wolf hybridization in Scandinavia. Animal Genetics. 42(1). 100–103. 33 indexed citations
17.
Klütsch, Cornelya F. C., Eija H. Seppälä, Mathias Uhlén, Hannes Lohi, & Peter Savolainen. (2010). Segregation of point mutation heteroplasmy in the control region of dog mtDNA studied systematically in deep generation pedigrees. International Journal of Legal Medicine. 125(4). 527–535. 7 indexed citations
18.
Seppälä, Eija H., Ville Autio, Priya Duggal, et al.. (2006). KLF6 IVS1 -27G>A Variant and the Risk of Prostate Cancer in Finland. European Urology. 52(4). 1076–1081. 10 indexed citations
19.
Seppälä, Eija H., Tarja Ikonen, Nina Mononen, et al.. (2003). CHEK2 variants associate with hereditary prostate cancer. British Journal of Cancer. 89(10). 1966–1970. 108 indexed citations
20.
Rökman, Annika, Tarja Ikonen, Eija H. Seppälä, et al.. (2002). Germline Alterations of the RNASEL Gene, a Candidate HPC1 Gene at 1q25, in Patients and Families with Prostate Cancer. The American Journal of Human Genetics. 70(5). 1299–1304. 174 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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