Rita Teek
Impact in
- Sensory Systems top 10%
- Hearing, Cochlea, Tinnitus, Genetics
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- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic Syndromes and Imprinting
Papers in
-
- Connexins and lens biology 2
- Ion channel regulation and function 2
- Congenital heart defects research 2
- Epigenetics and DNA Methylation 2
- Genetics 8
- Genomic variations and chromosomal abnormalities 5
- Genetics and Neurodevelopmental Disorders 2
- Co-authors
- Katrin Õunap (13 shared papers)Tiia Reimand (8 shared papers)Eve Õiglane‐Shlik (4 shared papers)Inga Talvik (3 shared papers)Sander Pajusalu (3 shared papers)Tiiu Tomberg (2 shared papers)Ulvi Vaher (2 shared papers)Riina Žordania (6 shared papers)
- Journals
- International Journal of Pediatric Otorhinolaryngology (2 papers)European Journal of Human Genetics (1 paper)European Journal of Medical Genetics (1 paper)European Journal of Pediatrics (1 paper)European Journal of Paediatric Neurology (1 paper)
- Partner nations
- EstoniaUnited StatesSwitzerland
In The Last Decade
Rita Teek
14 papers receiving 208 citations
Peers
Comparison fields: 5 of 58
- Sensory Systems 27
- Genetics 124
- Otorhinolaryngology 9
- Cellular and Molecular Neuroscience 34
- Molecular Biology 126
Countries citing papers authored by Rita Teek
This map shows the geographic impact of Rita Teek'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 Rita Teek with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rita Teek more than expected).
Fields of papers citing papers by Rita Teek
This network shows the impact of papers produced by Rita Teek. 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 Rita Teek. The network helps show where Rita Teek may publish in the future.
Co-authors
The 25 scholars most cited alongside Rita Teek, 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 | 62 | |
| 2 | 2013 | 22 | |
| 3 | 2009 | 22 | |
| 4 | 2014 | 21 | |
| 5 | 2014 | 18 | |
| 6 | 2019 | 17 | |
| 7 | 2010 | 15 | |
| 8 | 2009 | 12 | |
| 9 | 2013 | 11 | |
| 10 | 2008 | 8 | |
| 11 | 2015 | 7 | |
| 12 | 2010 | 3 | |
| 13 | 2010 | 2 | |
| 14 | 2023 | 1 |
About Rita Teek
Rita Teek is a scholar working on Molecular Biology, Genetics, Sensory Systems, Pediatrics, Perinatology and Child Health and Otorhinolaryngology, having authored 14 papers that have together received 221 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Hearing, Cochlea, Tinnitus, Genetics (3 papers), Connexins and lens biology (2 papers), Ion channel regulation and function (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Prenatal Screening and Diagnostics (2 papers), Congenital heart defects research (2 papers) and Epigenetics and DNA Methylation (2 papers). The work is most often cited by research in Sensory Systems (27 citations), Genetics (124 citations), Otorhinolaryngology (9 citations), Cellular and Molecular Neuroscience (34 citations) and Molecular Biology (126 citations). Rita Teek has collaborated with scholars based in Estonia, United States and Switzerland. Frequent co-authors include Katrin Õunap, Tiia Reimand, Eve Õiglane‐Shlik, Inga Talvik, Sander Pajusalu, Tiiu Tomberg, Ulvi Vaher, Riina Žordania, Karit Reinson and Sanna Puusepp. Their work appears in journals such as International Journal of Pediatric Otorhinolaryngology, European Journal of Human Genetics, European Journal of Medical Genetics, European Journal of Pediatrics and European Journal of Paediatric Neurology.
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.