J. Vesa

665 total citations
12 papers, 563 citations indexed

About

J. Vesa is a scholar working on Molecular Biology, Physiology and Epidemiology. According to data from OpenAlex, J. Vesa has authored 12 papers receiving a total of 563 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Physiology and 5 papers in Epidemiology. Recurrent topics in J. Vesa's work include Lysosomal Storage Disorders Research (6 papers), Genetic Neurodegenerative Diseases (3 papers) and Trypanosoma species research and implications (2 papers). J. Vesa is often cited by papers focused on Lysosomal Storage Disorders Research (6 papers), Genetic Neurodegenerative Diseases (3 papers) and Trypanosoma species research and implications (2 papers). J. Vesa collaborates with scholars based in Finland, United States and Japan. J. Vesa's co-authors include Elina Hellsten, Laura‐Maria Peltonen, Anu Jalanko, Vesa M. Olkkonen, Leena Peltonen, Tomi P. Mäkelä, Kari Alitalo, Maria Anvret, Susan E. Andrew and E. Almqvist and has published in prestigious journals such as The EMBO Journal, Human Molecular Genetics and Genomics.

In The Last Decade

J. Vesa

12 papers receiving 551 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
J. Vesa Finland 11 349 226 173 131 108 12 563
Akira Tokuda Japan 12 490 1.4× 141 0.6× 175 1.0× 179 1.4× 101 0.9× 29 743
Mónica Tomás Spain 15 308 0.9× 144 0.6× 73 0.4× 320 2.4× 62 0.6× 23 635
S. Treiber-Held Germany 10 184 0.5× 89 0.4× 187 1.1× 196 1.5× 36 0.3× 11 502
Toshka A. Abrams United States 14 470 1.3× 105 0.5× 126 0.7× 48 0.4× 24 0.2× 20 738
Veronica Colomer United States 8 647 1.9× 363 1.6× 93 0.5× 306 2.3× 98 0.9× 11 818
Nina Aula Finland 8 258 0.7× 72 0.3× 353 2.0× 208 1.6× 24 0.2× 10 616
Stéphanie Bigou France 12 303 0.9× 86 0.4× 294 1.7× 174 1.3× 125 1.2× 16 583
Anna-Elina Lehesjoki Finland 10 395 1.1× 92 0.4× 345 2.0× 172 1.3× 67 0.6× 10 768
Thomas L. Shirley United States 8 611 1.8× 402 1.8× 32 0.2× 38 0.3× 125 1.2× 8 722
Timothy A. Bolger United States 13 782 2.2× 121 0.5× 61 0.4× 52 0.4× 58 0.5× 16 915

Countries citing papers authored by J. Vesa

Since Specialization
Citations

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

Fields of papers citing papers by J. Vesa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J. Vesa

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

All Works

12 of 12 papers shown
1.
Fabritius, Anna‐Liisa, et al.. (2014). Neuronal ceroid lipofuscinosis genes, CLN2, CLN3 and CLN5 are spatially and temporally co-expressed in a developing mouse brain. Experimental and Molecular Pathology. 97(3). 484–491. 19 indexed citations
2.
Miettinen, Päivi J., J. Vesa, Arto Orpana, et al.. (2004). Novel splice site CACNA1A mutation causing episodic ataxia type 2. Neurogenetics. 5(1). 69–73. 24 indexed citations
3.
Syvänen, Ann-Christine, et al.. (1997). DNA Diagnosis and Identification of Carriers of Infantile and Juvenile Neuronal Ceroid Lipofuscinoses. Neuropediatrics. 28(1). 63–66. 12 indexed citations
4.
Hellsten, Elina, J. Vesa, Vesa M. Olkkonen, Anu Jalanko, & Laura‐Maria Peltonen. (1996). Human palmitoyl protein thioesterase: evidence for lysosomal targeting of the enzyme and disturbed cellular routing in infantile neuronal ceroid lipofuscinosis.. The EMBO Journal. 15(19). 5240–5245. 155 indexed citations
5.
6.
Hellsten, Elina, J. Vesa, Mervi Heiskanen, et al.. (1995). Identification of YAC clones for human chromosome 1p32 and physical mapping of the infantile neuronal ceroid lipofuscinosis (INCL) locus. Genomics. 25(2). 404–412. 24 indexed citations
7.
Mäkelä, Tomi P., Elina Hellsten, J. Vesa, et al.. (1995). The rearranged L-myc fusion gene (RLF) encodes a Zn-15 related zinc finger protein.. PubMed. 11(12). 2699–704. 17 indexed citations
8.
Squitieri, Ferdinando, Susan E. Andrew, Y. Paul Goldberg, et al.. (1994). DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence. Human Molecular Genetics. 3(12). 2103–2114. 148 indexed citations
9.
Vesa, J., Elina Hellsten, Tomi P. Mäkelä, et al.. (1993). A Single PCR Marker in Strong Allelic Association with the Infantile Form of Neuronal Ceroid Lipofuscinosis Facilitates Reliable Prenatal Diagnostics and Disease Carrier Identification. European Journal of Human Genetics. 1(2). 125–132. 17 indexed citations
10.
Hellsten, Elina, J. Vesa, Irma Järvelä, et al.. (1993). Refined assignment of the infantile neuronal ceroid‐lipofuscinosis (INCL) locus at 1p32 and the current status of prenatal and carrier diagnostics. Journal of Inherited Metabolic Disease. 16(2). 335–338. 7 indexed citations
11.
Vesa, J., et al.. (1992). Massive renal infarction due to mucormycosis in an AIDS patient. Infection. 20(4). 234–236. 34 indexed citations
12.
Mäkelä, Tomi P., Elina Hellsten, J. Vesa, Kari Alitalo, & Leena Peltonen. (1992). An Alu variable polyA repeat polymorphism upstream of L-myc at 1p32. Human Molecular Genetics. 1(3). 217–217. 47 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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