Elina Hellsten
Impact in
- Physiology top 5%
- Lysosomal Storage Disorders Research
- Calcium signaling and nucleotide metabolism
- Cell Biology top 5%
- Cellular transport and secretion
Papers in
-
- Glycosylation and Glycoproteins Research 3
- RNA regulation and disease 3
- RNA modifications and cancer 2
- Biochemical and Molecular Research 2
- Physiology 10
- Lysosomal Storage Disorders Research 10
- Co-authors
- Jouni Vesa (6 shared papers)Pirkko Santavuori (4 shared papers)Leena Peltonen (2 shared papers)Sandra L. Hofmann (1 shared paper)Linda A. Verkruyse (1 shared paper)Juhani Rapola (1 shared paper)J. Vesa (6 shared papers)Laura‐Maria Peltonen (4 shared papers)
- Journals
- Genomics (3 papers)Human Molecular Genetics (2 papers)Genome Research (2 papers)European Journal of Human Genetics (1 paper)Journal of Inherited Metabolic Disease (1 paper)
- Partner nations
- FinlandUnited StatesPoland
In The Last Decade
Elina Hellsten
18 papers receiving 1.3k citations
Elina Hellsten's Hit Papers
Peers
Comparison fields: 5 of 78
- Physiology 648
- Cell Biology 408
- Physiology 110
- Molecular Biology 691
- Genetics 265
Countries citing papers authored by Elina Hellsten
This map shows the geographic impact of Elina Hellsten'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 Elina Hellsten with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Elina Hellsten more than expected).
Fields of papers citing papers by Elina Hellsten
This network shows the impact of papers produced by Elina Hellsten. 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 Elina Hellsten. The network helps show where Elina Hellsten may publish in the future.
Co-authors
The 25 scholars most cited alongside Elina Hellsten, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis Hit paper breakdown → | 1995 | 638 |
| 2 | 1996 | 164 | |
| 3 | High resolution mapping using fluorescence in situ hybridization to extended DNA fibers prepared from agarose-embedded cells. | 1994 | 91 |
| 4 | 1995 | 75 | |
| 5 | 1993 | 60 | |
| 6 | 1992 | 47 | |
| 7 | 2002 | 42 | |
| 8 | 2001 | 42 | |
| 9 | 1995 | 33 | |
| 10 | 1995 | 24 | |
| 11 | Genetic heterogeneity in neuronal ceroid lipofuscinosis (NCL): evidence that the late-infantile subtype (Jansky-Bielschowsky disease; CLN2) is not an allelic form of the juvenile or infantile subtypes. | 1993 | 23 |
| 12 | 1992 | 22 | |
| 13 | The rearranged L-myc fusion gene (RLF) encodes a Zn-15 related zinc finger protein. | 1995 | 19 |
| 14 | 1993 | 17 | |
| 15 | 1998 | 14 | |
| 16 | 1994 | 10 | |
| 17 | 1993 | 7 | |
| 18 | 1997 | 7 |
About Elina Hellsten
Elina Hellsten is a scholar working on Molecular Biology, Physiology, Epidemiology, Cell Biology and Genetics, having authored 18 papers that have together received 1.3k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (10 papers), Glycosylation and Glycoproteins Research (3 papers), Cellular transport and secretion (3 papers), RNA regulation and disease (3 papers), Trypanosoma species research and implications (2 papers), RNA modifications and cancer (2 papers), Sperm and Testicular Function (2 papers) and Biochemical and Molecular Research (2 papers). The work is most often cited by research in Physiology (648 citations), Cell Biology (408 citations), Physiology (110 citations), Molecular Biology (691 citations) and Genetics (265 citations). Elina Hellsten has collaborated with scholars based in Finland, United States and Poland. Frequent co-authors include Jouni Vesa, Pirkko Santavuori, Leena Peltonen, Sandra L. Hofmann, Linda A. Verkruyse, Juhani Rapola, J. Vesa, Laura‐Maria Peltonen, Kari Alitalo and Anu Jalanko. Their work appears in journals such as Genomics, Human Molecular Genetics, Genome Research, European Journal of Human Genetics and Journal of Inherited Metabolic Disease.
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.