Mari Nelis
Impact in
- Genetics top 10%
- Genetic Associations and Epidemiology
- Forensic and Genetic Research
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genetic diversity and population structure
- Genetic Mapping and Diversity in Plants and Animals
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- Epilepsy research and treatment
Papers in
- Genetics 18
- Genetic Associations and Epidemiology 10
- Genomic variations and chromosomal abnormalities 6
- Genomics and Rare Diseases 5
- Forensic and Genetic Research 3
- Genetics and Neurodevelopmental Disorders 3
- Genetic and phenotypic traits in livestock 2
- Co-authors
- Reedik Mägi (24 shared papers)Andres Metspalu (26 shared papers)Maido Remm (7 shared papers)Tōnu Esko (23 shared papers)Lili Milani (21 shared papers)Georgi Hudjashov (15 shared papers)Alexandre Montpetit (3 shared papers)Bayazit Yunusbayev (4 shared papers)
- Journals
- Nature Communications (4 papers)The American Journal of Human Genetics (3 papers)Scientific Reports (2 papers)PLoS Genetics (2 papers)PLoS ONE (2 papers)
- Partner nations
- EstoniaSwitzerlandUnited States
In The Last Decade
Mari Nelis
32 papers receiving 555 citations
Peers
Comparison fields: 5 of 118
- Genetics 306
- Psychiatry and Mental health 47
- Molecular Biology 183
- Endocrine and Autonomic Systems 15
- Archeology 22
Countries citing papers authored by Mari Nelis
This map shows the geographic impact of Mari Nelis'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 Mari Nelis with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mari Nelis more than expected).
Fields of papers citing papers by Mari Nelis
This network shows the impact of papers produced by Mari Nelis. 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 Mari Nelis. The network helps show where Mari Nelis may publish in the future.
Co-authors
The 25 scholars most cited alongside Mari Nelis, 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 35 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 110 | |
| 2 | 2006 | 72 | |
| 3 | 2013 | 52 | |
| 4 | 2013 | 41 | |
| 5 | 2022 | 35 | |
| 6 | 2021 | 31 | |
| 7 | 2023 | 23 | |
| 8 | 2023 | 23 | |
| 9 | 2022 | 21 | |
| 10 | 2016 | 20 | |
| 11 | 2007 | 19 | |
| 12 | 2024 | 15 | |
| 13 | 2022 | 14 | |
| 14 | 2013 | 11 | |
| 15 | 2022 | 9 | |
| 16 | 2022 | 9 | |
| 17 | 2011 | 8 | |
| 18 | 2022 | 7 | |
| 19 | 2015 | 7 | |
| 20 | 2012 | 6 |
About Mari Nelis
Mari Nelis is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Epidemiology and Physiology, having authored 35 papers that have together received 567 indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (10 papers), Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (5 papers), Prenatal Screening and Diagnostics (4 papers), Forensic and Genetic Research (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genetic and phenotypic traits in livestock (2 papers) and Diet and metabolism studies (2 papers). The work is most often cited by research in Genetics (306 citations), Psychiatry and Mental health (47 citations), Molecular Biology (183 citations), Endocrine and Autonomic Systems (15 citations) and Archeology (22 citations). Mari Nelis has collaborated with scholars based in Estonia, Switzerland and United States. Frequent co-authors include Reedik Mägi, Andres Metspalu, Maido Remm, Tōnu Esko, Lili Milani, Georgi Hudjashov, Alexandre Montpetit, Bayazit Yunusbayev, Xiayi Ke and Ramasamy Pitchappan. Their work appears in journals such as Nature Communications, The American Journal of Human Genetics, Scientific Reports, PLoS Genetics and PLoS ONE.
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.