Tarja Mononen

1.3k total citations
22 papers, 452 citations indexed

About

Tarja Mononen is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Tarja Mononen has authored 22 papers receiving a total of 452 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 5 papers in Molecular Biology and 5 papers in Physiology. Recurrent topics in Tarja Mononen's work include Lysosomal Storage Disorders Research (5 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Glycosylation and Glycoproteins Research (3 papers). Tarja Mononen is often cited by papers focused on Lysosomal Storage Disorders Research (5 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Glycosylation and Glycoproteins Research (3 papers). Tarja Mononen collaborates with scholars based in Finland, United States and Germany. Tarja Mononen's 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 and has published in prestigious journals such as Journal of Biological Chemistry, American Journal of Clinical Nutrition and Clinical Chemistry.

In The Last Decade

Tarja Mononen

22 papers receiving 424 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tarja Mononen Finland 12 179 176 85 76 57 22 452
Lindsay B. Henderson United States 13 216 1.2× 193 1.1× 40 0.5× 31 0.4× 33 0.6× 19 511
David W. Cooke United States 15 146 0.8× 302 1.7× 27 0.3× 143 1.9× 93 1.6× 30 589
J J Heinrich Argentina 13 134 0.7× 145 0.8× 51 0.6× 19 0.3× 43 0.8× 35 425
Marsha F. Browning United States 13 187 1.0× 221 1.3× 82 1.0× 122 1.6× 37 0.6× 15 704
Alba Pilotta Italy 15 268 1.5× 229 1.3× 86 1.0× 27 0.4× 63 1.1× 26 586
Masami Togawa Japan 9 58 0.3× 126 0.7× 38 0.4× 118 1.6× 27 0.5× 16 333
G. Fekete Hungary 12 173 1.0× 281 1.6× 75 0.9× 13 0.2× 39 0.7× 32 490
Marcos José Burle de Aguiar Brazil 19 152 0.8× 296 1.7× 127 1.5× 121 1.6× 160 2.8× 57 795
Li‐Ping Tsai Taiwan 13 284 1.6× 160 0.9× 91 1.1× 178 2.3× 17 0.3× 45 583
Yann Grattau France 5 100 0.6× 112 0.6× 51 0.6× 51 0.7× 28 0.5× 5 323

Countries citing papers authored by Tarja Mononen

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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 of co-authors of Tarja Mononen

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

All Works

20 of 20 papers shown
1.
Schilit, Samantha L.P., Benjamin Currall, Ruen Yao, et al.. (2016). Estrogen-related receptor gamma implicated in a phenotype including hearing loss and mild developmental delay. European Journal of Human Genetics. 24(11). 1622–1626. 14 indexed citations
2.
Mononen, Tarja, et al.. (2007). A novel duplication in the FMR1 gene: implications for molecular analysis in fragile X syndrome and repeat instability. Clinical Genetics. 72(6). 528–531. 10 indexed citations
3.
Herrgård, Eila, Tarja Mononen, Esa Mervaala, et al.. (2006). More severe epilepsy and cognitive impairment in the offspring of a mother with mosaicism for the ring 20 chromosome. Epilepsy Research. 73(1). 122–128. 31 indexed citations
4.
Casas, Kari, Tarja Mononen, Susan J. Hassed, et al.. (2004). Chromosome 2q terminal deletion: Report of 6 new patients and review of phenotype‐breakpoint correlations in 66 individuals. American Journal of Medical Genetics Part A. 130A(4). 331–339. 70 indexed citations
5.
Zerres, Klaus, Jan Senderek, Sabine Rudnik‐Schöneborn, et al.. (2004). New options for prenatal diagnosis in autosomal recessive polycystic kidney disease by mutation analysis of the PKHD1 gene. Clinical Genetics. 66(1). 53–57. 25 indexed citations
6.
Korppi, Matti, et al.. (2003). [Genetic fever--Internet consultation, mutation in the envelope].. PubMed. 119(16). 1567–71. 3 indexed citations
7.
Heinonen, Seppo, et al.. (2001). Risk of obstetric cholestasis in sisters of index patients. Clinical Genetics. 60(1). 42–45. 52 indexed citations
8.
Airaksinen, Eila, Riitta Matilainen, Tarja Mononen, et al.. (2000). A Population‐Based Study on Epilepsy in Mentally Retarded Children. Epilepsia. 41(9). 1214–1220. 44 indexed citations
9.
Mononen, Tarja, et al.. (1998). Molecular diagnosis of medium-chain acyl-CoA dehydrogenase deficiency by oligonucleotide ligation assay. Clinical Chemistry. 44(1). 68–71. 10 indexed citations
10.
Matilainen, Riitta, et al.. (1995). A population‐based study on the causes of mild and severe mental retardation. Acta Paediatrica. 84(3). 261–266. 40 indexed citations
11.
Mononen, Ilkka, et al.. (1994). Enzymatic diagnosis of aspartylglycosaminuria by fluorometric assay of glycosylasparaginase in serum, plasma, or lymphocytes. Clinical Chemistry. 40(3). 385–388. 11 indexed citations
12.
Mononen, Tarja, Pamela S. Karnes, Melvin O. Senac, & Rena E. Falk. (1992). New skeletal dysplasia with unique brachydactyly. American Journal of Medical Genetics. 42(5). 706–713. 2 indexed citations
13.
Mononen, Ilkka, Nora Heisterkamp, Vesa Kaartinen, et al.. (1992). Aspartylglycosaminuria in a non-Finnish patient caused by a donor splice mutation in the glycoasparaginase gene.. Journal of Biological Chemistry. 267(5). 3196–3199. 10 indexed citations
14.
Kaartinen, Vesa, Tarja Mononen, Reino Laatikainen, & Ilkka Mononen. (1992). Substrate specificity and reaction mechanism of human glycoasparaginase. The N-glycosidic linkage of various glycoasparagines is cleaved through a reaction mechanism similar to L-asparaginase.. Journal of Biological Chemistry. 267(10). 6855–6858. 32 indexed citations
15.
Mononen, Tarja, Ilkka Mononen, Riitta Matilainen, & Eila Airaksinen. (1991). High prevalence of aspartylglycosaminuria among school-age children in eastern Finland. Human Genetics. 87(3). 266–8. 24 indexed citations
16.
Mononen, Ilkka, Vesa Kaartinen, & Tarja Mononen. (1988). Laboratory detection of aspartylglycosaminuria. Scandinavian Journal of Clinical and Laboratory Investigation. 48(sup191). 7–11. 13 indexed citations
17.
Mononen, Ilkka, Vesa Kaartinen, & Tarja Mononen. (1987). Amniotic fluid glycoasparagines in fetal aspartylglycosaminuria. Journal of Inherited Metabolic Disease. 11(2). 194–198. 6 indexed citations
18.
Mononen, Tarja, Markku Parviainen, I Penttilä, & Ilkka Mononen. (1986). Liquid-chromatographic detection of aspartylglycosaminuria.. Clinical Chemistry. 32(3). 501–502. 11 indexed citations
19.
Heinonen, Kati, Ilkka Mononen, Tarja Mononen, et al.. (1986). Plasma vitamin C levels are low in premature infants fed human milk. American Journal of Clinical Nutrition. 43(6). 923–924. 13 indexed citations
20.
Mononen, Tarja, et al.. (1985). Isolation and partial characterization of keratan sulphate from human brain. Biochimica et Biophysica Acta (BBA) - General Subjects. 843(1-2). 155–158. 7 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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