Kai Muru
Impact in
- Clinical Biochemistry top 10%
- Metabolism and Genetic Disorders
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- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Papers in
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- Congenital heart defects research 2
- RNA modifications and cancer 2
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- Prenatal Screening and Diagnostics 4
- Neonatal Health and Biochemistry 2
- Co-authors
- Katrin Õunap (16 shared papers)Mari‐Anne Vals (4 shared papers)Karit Reinson (6 shared papers)Tiina Kahre (7 shared papers)Gunnar Tasa (1 shared paper)A. Lang (1 shared paper)Sander Pajusalu (7 shared papers)Jaak Kals (1 shared paper)
- Journals
- European Journal of Pediatrics (2 papers)Frontiers in Genetics (1 paper)The Journal of Maternal-Fetal & Neonatal Medicine (1 paper)Frontiers in Neurology (1 paper)European Journal of Medical Genetics (1 paper)
- Partner nations
- EstoniaUnited StatesNetherlands
In The Last Decade
Kai Muru
19 papers receiving 162 citations
Peers
Comparison fields: 5 of 45
- Clinical Biochemistry 37
- Genetics 55
- Rheumatology 25
- Pediatrics, Perinatology and Child Health 31
- Genetics 9
Countries citing papers authored by Kai Muru
This map shows the geographic impact of Kai Muru'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 Kai Muru with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kai Muru more than expected).
Fields of papers citing papers by Kai Muru
This network shows the impact of papers produced by Kai Muru. 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 Kai Muru. The network helps show where Kai Muru may publish in the future.
Co-authors
The 25 scholars most cited alongside Kai Muru, 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 | A novel mutation in the M1S1 gene responsible for gelatinous droplike corneal dystrophy. | 2001 | 41 |
| 2 | 2015 | 26 | |
| 3 | 2018 | 22 | |
| 4 | 2021 | 16 | |
| 5 | 2019 | 15 | |
| 6 | 2009 | 13 | |
| 7 | 2022 | 8 | |
| 8 | 2015 | 8 | |
| 9 | 2021 | 7 | |
| 10 | 2014 | 6 | |
| 11 | 2019 | 5 | |
| 12 | 2021 | 4 | |
| 13 | 2019 | 4 | |
| 14 | 2017 | 4 | |
| 15 | 2023 | 3 | |
| 16 | 2010 | 3 | |
| 17 | 2010 | 3 | |
| 18 | 2025 | 1 | |
| 19 | 2023 | 1 | |
| 20 | 2014 | 0 |
About Kai Muru
Kai Muru is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health, Clinical Biochemistry, Genetics and Physiology, having authored 20 papers that have together received 190 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (5 papers), Prenatal Screening and Diagnostics (4 papers), Folate and B Vitamins Research (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Genetic Syndromes and Imprinting (2 papers), Congenital heart defects research (2 papers), Neonatal Health and Biochemistry (2 papers) and RNA modifications and cancer (2 papers). The work is most often cited by research in Clinical Biochemistry (37 citations), Genetics (55 citations), Rheumatology (25 citations), Pediatrics, Perinatology and Child Health (31 citations) and Genetics (9 citations). Kai Muru has collaborated with scholars based in Estonia, United States and Netherlands. Frequent co-authors include Katrin Õunap, Mari‐Anne Vals, Karit Reinson, Tiina Kahre, Gunnar Tasa, A. Lang, Sander Pajusalu, Jaak Kals, Erkki Juronen and Andres Piirsoo. Their work appears in journals such as European Journal of Pediatrics, Frontiers in Genetics, The Journal of Maternal-Fetal & Neonatal Medicine, Frontiers in Neurology and European Journal of Medical Genetics.
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.