A.-E. Lehesjoki

806 total citations
16 papers, 610 citations indexed

About

A.-E. Lehesjoki is a scholar working on Genetics, Rheumatology and Molecular Biology. According to data from OpenAlex, A.-E. Lehesjoki has authored 16 papers receiving a total of 610 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 9 papers in Rheumatology and 5 papers in Molecular Biology. Recurrent topics in A.-E. Lehesjoki's work include Glycogen Storage Diseases and Myoclonus (9 papers), Genetics and Neurodevelopmental Disorders (9 papers) and Amino Acid Enzymes and Metabolism (3 papers). A.-E. Lehesjoki is often cited by papers focused on Glycogen Storage Diseases and Myoclonus (9 papers), Genetics and Neurodevelopmental Disorders (9 papers) and Amino Acid Enzymes and Metabolism (3 papers). A.-E. Lehesjoki collaborates with scholars based in Finland, Hungary and United States. A.-E. Lehesjoki's co-authors include Albert de la Chapelle, P. Sistonen, Reijo Norio, Marjaleena Koskiniemi, Susanna Ranta, Johanna Hästbacka, Jinmin Miao, Holger Lerche, Eija Gaily and Snezana Maljevic and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The EMBO Journal and Neurology.

In The Last Decade

A.-E. Lehesjoki

16 papers receiving 579 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
A.-E. Lehesjoki Finland	12	310	241	199	133	128	16	610
Marta A. Bayly Australia	9	399 1.3×	181 0.8×	88 0.4×	140 1.1×	74 0.6×	11	588
Marcello Scala Italy	15	178 0.6×	207 0.9×	85 0.4×	91 0.7×	53 0.4×	61	513
Saadet Mercimek‐Andrews Canada	13	226 0.7×	276 1.1×	58 0.3×	63 0.5×	77 0.6×	52	623
M. A. Farnetani Italy	14	133 0.4×	137 0.6×	38 0.2×	109 0.8×	56 0.4×	24	447
Lemuel Racacho Canada	14	116 0.4×	262 1.1×	80 0.4×	20 0.2×	164 1.3×	18	547
Mar O’Callaghan Spain	12	98 0.3×	273 1.1×	30 0.2×	42 0.3×	80 0.6×	26	489
Shunling Guo United States	6	188 0.6×	199 0.8×	31 0.2×	176 1.3×	176 1.4×	6	533
Haruomi Nakamura Japan	11	64 0.2×	198 0.8×	49 0.2×	30 0.2×	117 0.9×	23	518
Parul Jayakar United States	15	217 0.7×	383 1.6×	44 0.2×	11 0.1×	99 0.8×	32	615
Pierre Cacciagli France	15	391 1.3×	410 1.7×	21 0.1×	104 0.8×	100 0.8×	25	739

Countries citing papers authored by A.-E. Lehesjoki

Since Specialization

Citations

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

Fields of papers citing papers by A.-E. Lehesjoki

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A.-E. Lehesjoki. 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 A.-E. Lehesjoki. The network helps show where A.-E. Lehesjoki may publish in the future.

Co-authorship network of co-authors of A.-E. Lehesjoki

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

All Works

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16 of 16 papers shown

Matur, Zeliha, Mikko Muona, Nerses Bebek, et al.. (2016). Progressive Myoclonic Epilepsy and NEU1 Mutation: A Different Phenotypic Case. Turkish Journal Of Neurology. 22(2). 84–87. 3 indexed citations

Schwarz, Niklas, Andreas Hahn, Thomas Bast, et al.. (2015). Mutations in the sodium channel gene SCN2A cause neonatal epilepsy with late-onset episodic ataxia. Journal of Neurology. 263(2). 334–343. 64 indexed citations

Liao, Yunxiang, Anna-Kaisa Anttonen, Esa Liukkonen, et al.. (2010). SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain. Neurology. 75(16). 1454–1458. 117 indexed citations

Koskenkorva, Päivi, Eini Niskanen, Mervi Könönen, et al.. (2009). Motor cortex and thalamic atrophy in Unverricht–Lundborg disease. Neurology. 73(8). 606–611. 43 indexed citations

Saarinen, Anne, Mervi K Mäyränpää, A.-E. Lehesjoki, & Outi Mäkitie. (2007). Heterozygous LRP5 mutations in children with fractures. Bone. 40(6). S74–S75. 1 indexed citations

Coppola, Giovanni, Chiara Criscuolo, Salvatore Striano, et al.. (2005). Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation. Journal of Neurology. 252(8). 897–900. 5 indexed citations

Haan, Gerrit‐Jan de, Dicky Halley, J.C. Doelman, et al.. (2004). Univerricht‐Lundborg Disease: Underdiagnosed in the Netherlands. Epilepsia. 45(9). 1061–1063. 23 indexed citations

Lehesjoki, A.-E.. (2003). NEW EMBO MEMBER'S REVIEW: Molecular background of progressive myoclonus epilepsy. The EMBO Journal. 22(14). 3473–3478. 44 indexed citations

Murphy, Kieran C., et al.. (2003). Efficacy of levetiracetam in a patient with Unverricht-Lundborg progressive myoclonic epilepsy. Neurology. 60(8). 1394–1395. 20 indexed citations

10.

Ranta, Susanna & A.-E. Lehesjoki. (2000). Northern epilepsy, a new member of the NCL family. Neurological Sciences. 21(0). S43–S47. 19 indexed citations

11.

Kolehmainen, Juha, et al.. (1998). Refined mapping of the Cohen syndrome gene by linkage disequilibrium.. PubMed. 5(4). 206–13. 30 indexed citations

12.

Ranta, Susanna, A.-E. Lehesjoki, Aune Hirvasniemi, et al.. (1996). Genetic and physical mapping of the progressive epilepsy with mental retardation (EPMR) locus on chromosome 8p.. Genome Research. 6(5). 351–360. 13 indexed citations

13.

Kääriäinen, H, et al.. (1994). Familial pericentric inversion inv(8)(p23q11).. Journal of Medical Genetics. 31(3). 201–205. 4 indexed citations

14.

Tahvanainen, Esa, Susanna Ranta, Aune Hirvasniemi, et al.. (1994). The gene for a recessively inherited human childhood progressive epilepsy with mental retardation maps to the distal short arm of chromosome 8.. Proceedings of the National Academy of Sciences. 91(15). 7267–7270. 68 indexed citations

15.

Lehesjoki, A.-E., Marjaleena Koskiniemi, Massimo Pandolfo, et al.. (1992). Linkage studies in progressive myoclonus epilepsy. Neurology. 42(8). 1545–1545. 38 indexed citations

16.

Lehesjoki, A.-E., Marjaleena Koskiniemi, P. Sistonen, et al.. (1991). Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22.. Proceedings of the National Academy of Sciences. 88(9). 3696–3699. 118 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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