Eino Palin

527 total citations
9 papers, 284 citations indexed

About

Eino Palin is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Eino Palin has authored 9 papers receiving a total of 284 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Cellular and Molecular Neuroscience and 2 papers in Genetics. Recurrent topics in Eino Palin's work include Mitochondrial Function and Pathology (4 papers), Genetic Neurodegenerative Diseases (4 papers) and DNA Repair Mechanisms (3 papers). Eino Palin is often cited by papers focused on Mitochondrial Function and Pathology (4 papers), Genetic Neurodegenerative Diseases (4 papers) and DNA Repair Mechanisms (3 papers). Eino Palin collaborates with scholars based in Finland, United Kingdom and Sweden. Eino Palin's co-authors include Anu Suomalainen, Anders Paetau, Liliya Euro, Laurie S. Kaguni, G.A. Farnum, Virginia Brilhante, Christopher J. Carroll, Jouko Lohi, Tiina Tyni and Eero Jokinen and has published in prestigious journals such as Nucleic Acids Research, Journal of the American College of Cardiology and Brain.

In The Last Decade

Eino Palin

9 papers receiving 281 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Eino Palin Finland	8	218	65	63	50	34	9	284
Hannah E. Steele United Kingdom	9	180 0.8×	53 0.8×	14 0.2×	77 1.5×	30 0.9×	14	275
Martino Montomoli Italy	8	166 0.8×	87 1.3×	15 0.2×	39 0.8×	91 2.7×	11	299
Satu Sandell Finland	10	232 1.1×	14 0.2×	114 1.8×	89 1.8×	18 0.5×	21	313
Giovanni Matteo Fratta Italy	7	422 1.9×	211 3.2×	34 0.5×	74 1.5×	32 0.9×	8	463
Rebecca C. Adikes United States	5	194 0.9×	39 0.6×	30 0.5×	53 1.1×	6 0.2×	9	248
Ilaria D’Amato Italy	6	236 1.1×	88 1.4×	9 0.1×	68 1.4×	39 1.1×	8	320
Günther Metz Germany	4	404 1.9×	106 1.6×	9 0.1×	69 1.4×	9 0.3×	6	433
Eduardo Calpena Spain	11	153 0.7×	20 0.3×	11 0.2×	114 2.3×	42 1.2×	21	272
Marie‐France Rioux Canada	6	140 0.6×	37 0.6×	7 0.1×	117 2.3×	38 1.1×	8	270
B. Halliger–Keller Germany	6	249 1.1×	28 0.4×	127 2.0×	70 1.4×	58 1.7×	8	324

Countries citing papers authored by Eino Palin

Since Specialization

Citations

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

Fields of papers citing papers by Eino Palin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eino Palin

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

All Works

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9 of 9 papers shown

Isohanni, Pirjo, Päivi Lahermo, Virginia Brilhante, et al.. (2020). Genetic background of ataxia in children younger than 5 years in Finland. Neurology Genetics. 6(4). e444–e444. 5 indexed citations

Vasilescu, Catalina, Tiina Ojala, Virginia Brilhante, et al.. (2018). Genetic Basis of Severe Childhood-Onset Cardiomyopathies. Journal of the American College of Cardiology. 72(19). 2324–2338. 100 indexed citations

Cooper, Helen, Yang Yang, Emil Ylikallio, et al.. (2017). ATPase-deficient mitochondrial inner membrane protein ATAD3A disturbs mitochondrial dynamics in dominant hereditary spastic paraplegia. Human Molecular Genetics. 26(8). 1432–1443. 53 indexed citations

Pasanen, Petra, Eino Palin, Minna Pöyhönen, et al.. (2016). SNCA mutation p.Ala53Glu is derived from a common founder in the Finnish population. Neurobiology of Aging. 50. 168.e5–168.e8. 8 indexed citations

Suriyanarayanan, Saranya, Mari Auranen, Jussi Toppila, et al.. (2015). The Variant p.(Arg183Trp) in SPTLC2 Causes Late-Onset Hereditary Sensory Neuropathy. NeuroMolecular Medicine. 18(1). 81–90. 19 indexed citations

Palin, Eino, Anders Paetau, & Anu Suomalainen. (2013). Mesencephalic complex I deficiency does not correlate with parkinsonism in mitochondrial DNA maintenance disorders. Brain. 136(8). 2379–2392. 37 indexed citations

Palin, Eino, et al.. (2011). Mitochondrial recessive ataxia syndrome mimicking dominant spinocerebellar ataxia. Journal of the Neurological Sciences. 315(1-2). 160–163. 14 indexed citations

Euro, Liliya, G.A. Farnum, Eino Palin, Anu Suomalainen, & Laurie S. Kaguni. (2011). Clustering of Alpers disease mutations and catalytic defects in biochemical variants reveal new features of molecular mechanism of the human mitochondrial replicase, Pol γ. Nucleic Acids Research. 39(21). 9072–9084. 40 indexed citations

Palin, Eino, et al.. (2010). Functional analysis of H. sapiens DNA polymerase γ spacer mutation W748S with and without common variant E1143G. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1802(6). 545–551. 8 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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