Margit Nõukas
Impact in
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- Metabolism and Genetic Disorders
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- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
- Genetics 10
- Genomics and Rare Diseases 7
- Genomic variations and chromosomal abnormalities 4
- BRCA gene mutations in cancer 2
- Genetic Associations and Epidemiology 2
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- Kruppel-like factors research 1
- Co-authors
- Mart Kals (6 shared papers)Katrin Õunap (7 shared papers)Andres Metspalu (8 shared papers)Tiia Reimand (3 shared papers)Ants Kurg (3 shared papers)Tiit Nikopensius (5 shared papers)Olga Žilina (3 shared papers)Olga Tšuiko (1 shared paper)
In The Last Decade
Margit Nõukas
15 papers receiving 214 citations
Peers
Comparison fields: 5 of 50
- Clinical Biochemistry 31
- Genetics 111
- Psychiatry and Mental health 39
- Cellular and Molecular Neuroscience 31
- Biochemistry 12
Countries citing papers authored by Margit Nõukas
This map shows the geographic impact of Margit Nõukas'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 Margit Nõukas with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Margit Nõukas more than expected).
Fields of papers citing papers by Margit Nõukas
This network shows the impact of papers produced by Margit Nõukas. 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 Margit Nõukas. The network helps show where Margit Nõukas may publish in the future.
Co-authors
The 25 scholars most cited alongside Margit Nõukas, 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 | 2013 | 52 | |
| 2 | 2016 | 41 | |
| 3 | 2018 | 23 | |
| 4 | 2015 | 22 | |
| 5 | 2014 | 15 | |
| 6 | 2015 | 12 | |
| 7 | 2015 | 10 | |
| 8 | 2015 | 8 | |
| 9 | 2016 | 8 | |
| 10 | 2010 | 6 | |
| 11 | 2022 | 5 | |
| 12 | 2022 | 5 | |
| 13 | 2016 | 4 | |
| 14 | 2023 | 3 | |
| 15 | 2022 | 2 | |
| 16 | 2024 | 0 |
About Margit Nõukas
Margit Nõukas is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Clinical Biochemistry and Cancer Research, having authored 16 papers that have together received 216 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (7 papers), Genomic variations and chromosomal abnormalities (4 papers), Metabolism and Genetic Disorders (3 papers), Genetic factors in colorectal cancer (2 papers), BRCA gene mutations in cancer (2 papers), Cancer Genomics and Diagnostics (2 papers), Genetic Associations and Epidemiology (2 papers) and Kruppel-like factors research (1 paper). The work is most often cited by research in Clinical Biochemistry (31 citations), Genetics (111 citations), Psychiatry and Mental health (39 citations), Cellular and Molecular Neuroscience (31 citations) and Biochemistry (12 citations). Margit Nõukas has collaborated with scholars based in Estonia, Finland and Germany. Frequent co-authors include Mart Kals, Katrin Õunap, Andres Metspalu, Tiia Reimand, Ants Kurg, Tiit Nikopensius, Olga Žilina, Olga Tšuiko, Inga Talvik and Sander Pajusalu. Their work appears in journals such as European Journal of Medical Genetics, European Journal of Human Genetics, Cancers, Human Genetics and Genomics Advances and Gene.
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.