Tarja Mononen
Impact in
- Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Papers in
-
- Metabolism and Genetic Disorders 2
- Co-authors
- Ilkka MononenRiitta MatilainenVesa KaartinenSeppo HeinonenSirkku T. SaarikoskiEila AiraksinenK LaunialaJohn J. Mulvihill
- Journals
- Clinical Chemistry (4 papers)Clinical Genetics (3 papers)Acta Paediatrica (2 papers)Journal of Biological Chemistry (2 papers)Journal of Inherited Metabolic Disease (1 paper)
- Partner nations
- FinlandUnited StatesGermany
In The Last Decade
Tarja Mononen
22 papers receiving 424 citations
Peers
Comparison fields: 5 of 74
- Genetics 179
- Pediatrics, Perinatology and Child Health 85
- Clinical Biochemistry 21
- Physiology 76
- Cognitive Neuroscience 55
Countries citing papers authored by Tarja Mononen
This map shows the geographic impact of Tarja Mononen'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 Tarja Mononen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tarja Mononen more than expected).
Fields of papers citing papers by Tarja Mononen
This network shows the impact of papers produced by Tarja Mononen. 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 Tarja Mononen. The network helps show where Tarja Mononen may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Tarja Mononen, 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 | 2016 | 14 | |
| 2 | 2007 | 10 | |
| 3 | 2006 | 31 | |
| 4 | 2004 | 70 | |
| 5 | 2004 | 25 | |
| 6 | [Genetic fever--Internet consultation, mutation in the envelope]. | 2003 | 3 |
| 7 | 2001 | 52 | |
| 8 | 2000 | 44 | |
| 9 | 1998 | 10 | |
| 10 | 1995 | 40 | |
| 11 | 1994 | 11 | |
| 12 | 1992 | 2 | |
| 13 | 1992 | 10 | |
| 14 | 1992 | 32 | |
| 15 | 1991 | 24 | |
| 16 | 1988 | 13 | |
| 17 | 1987 | 6 | |
| 18 | 1986 | 11 | |
| 19 | 1986 | 13 | |
| 20 | 1985 | 7 |
About Tarja Mononen
Tarja Mononen is a scholar working on Developmental Biology, Clinical Biochemistry, Genetics, Cell Biology and Physiology, having authored 22 papers that have together received 452 indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Glycosylation and Glycoproteins Research (3 papers), Genomics and Rare Diseases (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Folate and B Vitamins Research (3 papers), Metabolism and Genetic Disorders (2 papers) and Cellular transport and secretion (2 papers). The work is most often cited by research in Genetics (179 citations), Pediatrics, Perinatology and Child Health (85 citations), Clinical Biochemistry (21 citations), Physiology (76 citations) and Cognitive Neuroscience (55 citations). Tarja Mononen has collaborated with scholars based in Finland, United States and Germany. Frequent co-authors include Ilkka Mononen, Riitta Matilainen, Vesa Kaartinen, Seppo Heinonen, Sirkku T. Saarikoski, Eila Airaksinen, K Launiala, John J. Mulvihill, Henry J. Lin and Susan J. Hassed. Their work appears in journals such as Clinical Chemistry, Clinical Genetics, Acta Paediatrica, Journal of Biological Chemistry 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.