Rita Teek
Impact in
- Sensory Systems top 10%
- Hearing, Cochlea, Tinnitus, Genetics
-
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic Syndromes and Imprinting
Papers in
- Genetics 8
- Genomic variations and chromosomal abnormalities 5
- Genetic Syndromes and Imprinting 2
- Genomics and Rare Diseases 2
- Genetics and Neurodevelopmental Disorders 2
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
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- Hearing, Cochlea, Tinnitus, Genetics 3
- Co-authors
- Katrin Õunap (14 shared papers)Tiia Reimand (8 shared papers)Eve Õiglane‐Shlik (4 shared papers)Olga Žilina (4 shared papers)Sanna Puusepp (3 shared papers)Riina Žordania (6 shared papers)Inga Talvik (3 shared papers)Sander Pajusalu (3 shared papers)
- Journals
- European Journal of Medical Genetics (2 papers)International Journal of Pediatric Otorhinolaryngology (2 papers)European Journal of Paediatric Neurology (1 paper)European Journal of Pediatrics (1 paper)European Journal of Human Genetics (1 paper)
- Partner nations
- EstoniaUnited StatesBulgaria
In The Last Decade
Rita Teek
15 papers receiving 255 citations
Peers
Comparison fields: 5 of 56
- Sensory Systems 29
- Genetics 136
- Cellular and Molecular Neuroscience 37
- Molecular Biology 123
- Pediatrics, Perinatology and Child Health 30
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 | 67 | |
| 2 | 2009 | 26 | |
| 3 | 2008 | 25 | |
| 4 | 2013 | 25 | |
| 5 | 2014 | 23 | |
| 6 | 2019 | 22 | |
| 7 | 2014 | 18 | |
| 8 | 2010 | 16 | |
| 9 | 2009 | 14 | |
| 10 | 2013 | 11 | |
| 11 | 2008 | 9 | |
| 12 | 2015 | 8 | |
| 13 | 2010 | 4 | |
| 14 | 2023 | 3 | |
| 15 | 2010 | 2 |
About Rita Teek
Rita Teek is a scholar working on Genetics, Sensory Systems, Molecular Biology, Genetics and Neurology, having authored 15 papers that have together received 273 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Hearing, Cochlea, Tinnitus, Genetics (3 papers), Congenital heart defects research (2 papers), Genetic Syndromes and Imprinting (2 papers), Genomics and Rare Diseases (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper) and RNA modifications and cancer (1 paper). The work is most often cited by research in Sensory Systems (29 citations), Genetics (136 citations), Cellular and Molecular Neuroscience (37 citations), Molecular Biology (123 citations) and Pediatrics, Perinatology and Child Health (30 citations). Rita Teek has collaborated with scholars based in Estonia, United States and Bulgaria. Frequent co-authors include Katrin Õunap, Tiia Reimand, Eve Õiglane‐Shlik, Olga Žilina, Sanna Puusepp, Riina Žordania, Inga Talvik, Sander Pajusalu, Karit Reinson and Tiiu Tomberg. Their work appears in journals such as European Journal of Medical Genetics, International Journal of Pediatric Otorhinolaryngology, European Journal of Paediatric Neurology, European Journal of Pediatrics and European Journal of Human 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.