Margit Nõukas
Impact in
- Reproductive Medicine top 5%
- Endometriosis Research and Treatment
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genetic Associations and Epidemiology
Papers in
- Genetics 18
- Genomics and Rare Diseases 8
- Genomic variations and chromosomal abnormalities 7
- Genetic Associations and Epidemiology 6
- BRCA gene mutations in cancer 4
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- Cancer Genomics and Diagnostics 3
- Co-authors
- Mart Kals (6 shared papers)Katrin Õunap (7 shared papers)Andres Metspalu (8 shared papers)Tiit Nikopensius (5 shared papers)Olga Žilina (3 shared papers)Tiia Reimand (3 shared papers)Ants Kurg (3 shared papers)Tarmo Annilo (4 shared papers)
- Journals
- European Journal of Medical Genetics (3 papers)European Journal of Human Genetics (3 papers)Frontiers in Genetics (2 papers)Cell (2 papers)Nature Communications (2 papers)
- Partner nations
- EstoniaUnited StatesFinland
In The Last Decade
Margit Nõukas
27 papers receiving 979 citations
Margit Nõukas's Hit Papers
Peers
Comparison fields: 5 of 76
- Reproductive Medicine 159
- Genetics 440
- Obstetrics and Gynecology 67
- Pediatrics, Perinatology and Child Health 99
- Aging 9
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
Showing the 20 most-cited of 27 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A cross-disorder dosage sensitivity map of the human genome Hit paper breakdown → | 2022 | 197 |
| 2 | The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions Hit paper breakdown → | 2023 | 167 |
| 3 | 2015 | 144 | |
| 4 | 2020 | 71 | |
| 5 | 2017 | 65 | |
| 6 | 2013 | 58 | |
| 7 | 2016 | 49 | |
| 8 | 2019 | 42 | |
| 9 | 2018 | 27 | |
| 10 | 2015 | 25 | |
| 11 | 2025 | 23 | |
| 12 | 2014 | 18 | |
| 13 | 2015 | 13 | |
| 14 | 2023 | 13 | |
| 15 | 2016 | 13 | |
| 16 | 2015 | 11 | |
| 17 | 2022 | 10 | |
| 18 | 2022 | 10 | |
| 19 | 2022 | 9 | |
| 20 | 2015 | 8 |
About Margit Nõukas
Margit Nõukas is a scholar working on Genetics, Cancer Research, Clinical Biochemistry, Pathology and Forensic Medicine and Cardiology and Cardiovascular Medicine, having authored 27 papers that have together received 1.0k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (8 papers), Genomic variations and chromosomal abnormalities (7 papers), Genetic Associations and Epidemiology (6 papers), BRCA gene mutations in cancer (4 papers), Cancer Genomics and Diagnostics (3 papers), Genetic factors in colorectal cancer (2 papers), RNA regulation and disease (2 papers) and Metabolism and Genetic Disorders (2 papers). The work is most often cited by research in Reproductive Medicine (159 citations), Genetics (440 citations), Obstetrics and Gynecology (67 citations), Pediatrics, Perinatology and Child Health (99 citations) and Aging (9 citations). Margit Nõukas has collaborated with scholars based in Estonia, United States and Finland. Frequent co-authors include Mart Kals, Katrin Õunap, Andres Metspalu, Tiit Nikopensius, Olga Žilina, Tiia Reimand, Ants Kurg, Tarmo Annilo, Tiina Talvik and Reedik Mägi. Their work appears in journals such as European Journal of Medical Genetics, European Journal of Human Genetics, Frontiers in Genetics, Cell and Nature Communications.
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.