Eija H. Seppälä

2.3k citations

34 papers · 1.1k indexed · h-index 17

Co-authors: Hannes Lohi Johanna Schleutker Teuvo L.J. Tammela Mika Matikainen Tarja Ikonen Ville Autio Nina Mononen Annika Rökman
Topics: Neurological diseases and metabolism (6 papers)Lysosomal Storage Disorders Research (4 papers)Veterinary Medicine and Surgery (4 papers)
Cited by: Clinical Biochemistry Genetics Neurology
Journals: Nature Genetics PLoS ONE JNCI Journal of the National Cancer Institute
Partner nations: Finland United States Sweden

In The Last Decade

Eija H. Seppälä

33 papers receiving 1.1k citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Fasting triglyceride concentrations are associated with markers of lipid metabolism and glucose homeostasis in healthy, non-obese dogs in lean and overweight condition 2024 ·Frontiers in Veterinary Science ·(unknown),Dominique Peeters,Frédéric Farnir,Katja Höglund,(unknown),Maria Wiberg,Jakob L. Willesen,Sofia Hanås,Kathleen Mc Entee,Laurent Tiret,Jens Häggström,Hannes Lohi,Valérie Chetboul,Merete Fredholm,Eija H. Seppälä,Anne‐Sophie Lequarré,Alexander J. German,Anne‐Christine Merveille	2
2	Next-generation sequencing in childhood-onset epilepsies: Diagnostic yield and impact on neuronal ceroid lipofuscinosis type 2 (CLN2) disease diagnosis 2021 ·PLoS ONE ·(unknown),Emanuela Izzo,Eija H. Seppälä,Kirsi Alakurtti,Lars‐Owe Koskinen,(unknown),(unknown),Samuel Myllykangas,Juha Koskenvuo,Tero‐Pekka Alastalo	6
3	Genome wide association study of 40 clinical measurements in eight dog breeds 2020 ·Scientific Reports ·Yukihide Momozawa,Anne‐Christine Merveille,(unknown),Maria Wiberg,J. Koch,Jakob L. Willesen,Helle Friis Proschowsky,Vassiliki Gouni,Valérie Chetboul,Laurent Tiret,Merete Fredholm,Eija H. Seppälä,Hannes Lohi,Michel Georges,Anne‐Sophie Lequarré	13
4	Interbreed variation of biomarkers of lipid and glucose metabolism in dogs 2018 ·Veterinary Clinical Pathology ·(unknown),Dominique Peeters,(unknown),Frédéric Farnir,Katja Höglund,Vassiliki Gouni,Maria Wiberg,Jakob L. Willesen,Sofia Hanås,Kathleen Mc Entee,Laurent Tiret,Jens Häggström,Hannes Lohi,Valérie Chetboul,Merete Fredholm,Eija H. Seppälä,Anne‐Sophie Lequarré,Anne‐Christine Merveille	5
5	Interbreed variation in serum serotonin (5-hydroxytryptamine) concentration in healthy dogs 2018 ·Journal of Veterinary Cardiology ·Katja Höglund,Jens Häggström,Sofia Hanås,Anne‐Christine Merveille,Vassiliki Gouni,Maria Wiberg,Jakob L. Willesen,Kathleen Mc Entee,(unknown),Laurent Tiret,Eija H. Seppälä,Hannes Lohi,Valérie Chetboul,Merete Fredholm,Anne‐Sophie Lequarré,Ingrid Ljungvall	14
6	Heterozygous junctophilin-2 (JPH2) p.(Thr161Lys) is a monogenic cause for HCM with heart failure 2018 ·PLoS ONE ·(unknown),(unknown),Eija H. Seppälä,Katriina Aalto‐Setälä,Olli Pitkänen,(unknown),(unknown),(unknown),Tero‐Pekka Alastalo,Samuel Myllykangas,Tiina Heliö,Juha Koskenvuo	34
7	ADAM23 is a common risk gene for canine idiopathic epilepsy 2017 ·BMC Genetics ·Lotta L. E. Koskinen,Eija H. Seppälä,(unknown),Tarja S. Jokinen,Ranno Viitmaa,(unknown),Pascale Quignon,Andrea Fischer,Catherine André,Hannes Lohi	20
8	Case reports of two pedigrees with recessive arrhythmogenic right ventricular cardiomyopathy associated with homozygous Thr335Ala variant in DSG2 2017 ·BMC Medical Genetics ·S. U. Qadri,Olli Anttonen,(unknown),Eija H. Seppälä,Samuel Myllykangas,Tero‐Pekka Alastalo,Miia Holmström,Tiina Heliö,Juha Koskenvuo	14
9	Behavioral Abnormalities in Lagotto Romagnolo Dogs with a History of Benign Familial Juvenile Epilepsy: A Long-Term Follow-Up Study 2015 ·Journal of Veterinary Internal Medicine ·Tarja S. Jokinen,Katriina Tiira,Liisa Metsähonkala,Eija H. Seppälä,Anna Hielm‐Björkman,Hannes Lohi,(unknown)	28
10	Identification of a common risk haplotype for canine idiopathic epilepsy in the ADAM23 gene 2015 ·BMC Genomics ·Lotta L. E. Koskinen,Eija H. Seppälä,Janelle M. Belanger,Meharji Arumilli,(unknown),Päivi Jokinen,Elisa Nevalainen,Ranno Viitmaa,Tarja S. Jokinen,Anita M. Oberbauer,Hannes Lohi	22
11	Multiple Changes of Gene Expression and Function Reveal Genomic and Phenotypic Complexity in SLE-like Disease 2015 ·PLoS Genetics ·Maria Wilbe,Sergey V. Kozyrev,Fabiana Farias,(unknown),(unknown),Gerli Pielberg,Eija H. Seppälä,Ulla Gustafson,Hannes Lohi,Örjan Carlborg,Göran Andersson,Helene Hansson‐Hamlin,Kerstin Lindblad‐Toh	21
12	A Nonsense Mutation in the Acid α-Glucosidase Gene Causes Pompe Disease in Finnish and Swedish Lapphunds 2013 ·PLoS ONE ·Eija H. Seppälä,Arnold Reuser,Hannes Lohi	24
13	Phenotype, inheritance characteristics, and risk factors for idiopathic epilepsy in Finnish Spitz dogs 2013 ·Journal of the American Veterinary Medical Association ·Ranno Viitmaa,Sigitas Čižinauskas,Toomas Orro,(unknown),(unknown),Hannes Lohi,Eija H. Seppälä,(unknown),Marjatta Snellman	12
14	Identification of a Novel Idiopathic Epilepsy Locus in Belgian Shepherd Dogs 2012 ·PLoS ONE ·Eija H. Seppälä,Lotta L. E. Koskinen,(unknown),Päivi Jokinen,Peter Karlskov‐Mortensen,(unknown),Izabella Baranowska Körberg,Sigitas Čižinauskas,Anita M. Oberbauer,Mette Berendt,Merete Fredholm,Hannes Lohi	39
15	A SEL1L Mutation Links a Canine Progressive Early-Onset Cerebellar Ataxia to the Endoplasmic Reticulum–Associated Protein Degradation (ERAD) Machinery 2012 ·PLoS Genetics ·Kaisa Kyöstilä,Sigitas Čižinauskas,Eija H. Seppälä,E. Suhonen,(unknown),Antti Sukura,Pernilla Syrjä,Hannes Lohi	56
16	A truncating mutation in ATP13A2 is responsible for adult-onset neuronal ceroid lipofuscinosis in Tibetan terriers 2011 ·Neurobiology of Disease ·Fabiana Farias,Rong Zeng,Gary S. Johnson,Fred A. Wininger,Jeremy F. Taylor,Robert D. Schnabel,Stephanie McKay,Douglas N. Sanders,Hannes Lohi,Eija H. Seppälä,Claire M. Wade,Kerstin Lindblad‐Toh,Dennis P. O’Brien,Martin L. Katz	100
17	Segregation of point mutation heteroplasmy in the control region of dog mtDNA studied systematically in deep generation pedigrees 2010 ·International Journal of Legal Medicine ·Cornelya F. C. Klütsch,Eija H. Seppälä,Mathias Uhlén,Hannes Lohi,Peter Savolainen	7
18	Regional occurrence, high frequency but low diversity of mitochondrial DNA haplogroup d1 suggests a recent dog-wolf hybridization in Scandinavia 2010 ·Animal Genetics ·Cornelya F. C. Klütsch,Eija H. Seppälä,Tove Fall,Mathias Uhlén,Åke Hedhammar,Hannes Lohi,Peter Savolainen	33
19	Genome-wide association mapping identifies multiple loci for a canine SLE-related disease complex 2010 ·Nature Genetics ·Maria Wilbe,Päivi Jokinen,Katarina Truvé,Eija H. Seppälä,Elinor K. Karlsson,Tara Biagi,Angela M. Hughes,Danika L. Bannasch,Göran Andersson,Helene Hansson‐Hamlin,Hannes Lohi,Kerstin Lindblad‐Toh	90
20	KLF6 IVS1 -27G>A Variant and the Risk of Prostate Cancer in Finland 2006 ·European Urology ·Eija H. Seppälä,Ville Autio,Priya Duggal,Tarja Ikonen,Ulf‐Håkan Stenman,Anssi Auvinen,Joan E. Bailey‐Wilson,Teuvo L.J. Tammela,Johanna Schleutker	10

About Eija H. Seppälä

Eija H. Seppälä is a scholar working on Neurology, Equine and Small Animals, having authored 34 papers that have together received 1.1k indexed citations. Recurring topics across this work include Neurological diseases and metabolism (6 papers), Lysosomal Storage Disorders Research (4 papers) and Veterinary Medicine and Surgery (4 papers). The work is most often cited by research in Clinical Biochemistry (108 citations), Genetics (417 citations) and Neurology (92 citations). Eija H. Seppälä has collaborated with scholars based in Finland, United States and Sweden. Frequent co-authors include Hannes Lohi, Johanna Schleutker, Teuvo L.J. Tammela, Mika Matikainen, Tarja Ikonen, Ville Autio, Nina Mononen, Annika Rökman, Olli Kallioniemi and Kerstin Lindblad‐Toh. Their work appears in journals such as Nature Genetics, PLoS ONE and JNCI Journal of the National Cancer Institute.

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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