Mari Nelis

45.1k total citations
35 papers, 567 citations indexed

About

Mari Nelis is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Mari Nelis has authored 35 papers receiving a total of 567 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 10 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Mari Nelis's work include Genetic Associations and Epidemiology (10 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genomics and Rare Diseases (5 papers). Mari Nelis is often cited by papers focused on Genetic Associations and Epidemiology (10 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genomics and Rare Diseases (5 papers). Mari Nelis collaborates with scholars based in Estonia, Switzerland and United States. Mari Nelis's co-authors include Reedik Mägi, Andres Metspalu, Maido Remm, Tōnu Esko, Lili Milani, Georgi Hudjashov, Alexandre Montpetit, Bayazit Yunusbayev, Kumarasamy Thangaraj and Xiayi Ke and has published in prestigious journals such as Nature Medicine, Nature Communications and PLoS ONE.

In The Last Decade

Mari Nelis

32 papers receiving 555 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Mari Nelis Estonia 13 306 183 47 34 32 35 567
Adekunle Odunsi United States 11 370 1.2× 336 1.8× 47 1.0× 29 0.9× 26 0.8× 14 730
Christalena Sofocleous Greece 14 261 0.9× 218 1.2× 31 0.7× 81 2.4× 26 0.8× 45 459
Andrea Byrnes United States 5 390 1.3× 318 1.7× 24 0.5× 25 0.7× 26 0.8× 8 786
Marc Vía Spain 15 503 1.6× 198 1.1× 36 0.8× 25 0.7× 46 1.4× 48 848
Sebastian Schoenherr Austria 4 523 1.7× 290 1.6× 40 0.9× 47 1.4× 66 2.1× 5 902
Joelle Mbatchou United States 5 315 1.0× 171 0.9× 19 0.4× 26 0.8× 46 1.4× 10 693
Alessandro De Grandi Italy 14 301 1.0× 316 1.7× 27 0.6× 28 0.8× 53 1.7× 32 819
Fatih Temiz Türkiye 9 137 0.4× 238 1.3× 17 0.4× 19 0.6× 35 1.1× 35 563
Ewa Jamroz Poland 13 139 0.5× 241 1.3× 47 1.0× 83 2.4× 35 1.1× 52 529
Chaowei Tian China 7 161 0.5× 136 0.7× 19 0.4× 13 0.4× 37 1.2× 12 415

Countries citing papers authored by Mari Nelis

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Mari Nelis

This figure shows the co-authorship network connecting the top 25 collaborators of Mari Nelis. A scholar is included among the top collaborators of Mari Nelis based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Mari Nelis. Mari Nelis is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Pujol‐Gualdo, Natàlia, Maire Peters, Andres Metspalu, et al.. (2025). A large-scale genome-wide association study on female genital tract polyps highlights role of DNA repair, cell proliferation, and cell growth. Human Reproduction. 40(4). 750–763. 1 indexed citations
2.
Reigo, Anu, Tarmo Annilo, Toomas Toomsoo, et al.. (2024). Use of Estonian Biobank data and participant recall to improve Wilson’s disease management. European Journal of Human Genetics. 33(11). 1499–1508.
3.
Cordioli, Mattia, Sakari Jukarainen, Tuomo Kiiskinen, et al.. (2024). Socio-demographic and genetic risk factors for drug adherence and persistence across 5 common medication classes. Nature Communications. 15(1). 9156–9156. 4 indexed citations
4.
Jaagura, Madis, Jaanika Kronberg, Anu Reigo, et al.. (2024). Comorbidities confound metabolomics studies of human disease. Scientific Reports. 14(1). 24810–24810. 2 indexed citations
5.
Kalnapenkis, Anette, Kaido Lepik, Mart Kals, et al.. (2024). Genetic determinants of plasma protein levels in the Estonian population. Scientific Reports. 14(1). 7694–7694. 2 indexed citations
6.
Hartonen, Tuomo, Bradley Jermy, Kristi Krebs, et al.. (2023). Nationwide health, socio-economic and genetic predictors of COVID-19 vaccination status in Finland. Nature Human Behaviour. 7(7). 1069–1083. 23 indexed citations
7.
Uusküla, Anneli, Kristi Läll, Andres Metspalu, et al.. (2023). Polygenic risk scores for cervical HPV infection, neoplasia and cancer show potential for personalised screening: comparison of two methods. Infectious Agents and Cancer. 18(1). 82–82. 1 indexed citations
8.
Peters, Maire, Merli Saare, Andres Metspalu, et al.. (2022). Endometriosis and irritable bowel syndrome: similarities and differences in the spectrum of comorbidities. Human Reproduction. 37(9). 2186–2196. 9 indexed citations
9.
Alver, Maris, Valentina Mancini, Kristi Läll, et al.. (2022). Contribution of schizophrenia polygenic burden to longitudinal phenotypic variance in 22q11.2 deletion syndrome. Molecular Psychiatry. 27(10). 4191–4200. 7 indexed citations
10.
Metspalu, Andres, Mari Nelis, Lili Milani, et al.. (2022). Prioritizing autoimmunity risk variants for functional analyses by fine-mapping mutations under natural selection. Nature Communications. 13(1). 7069–7069. 5 indexed citations
11.
Abroi, Aare, Ulvi Gerst Talas, Tuuli Reisberg, et al.. (2022). SARS-CoV-2 dual infection with Delta and Omicron variants in an immunocompetent host: a case report. International Journal of Infectious Diseases. 124. 41–44. 1 indexed citations
12.
Dannemann, Michael, Yuri Milaneschi, Danat Yermakovich, et al.. (2022). Neandertal introgression partitions the genetic landscape of neuropsychiatric disorders and associated behavioral phenotypes. Translational Psychiatry. 12(1). 433–433. 9 indexed citations
13.
Nethander, Maria, Eivind Coward, Ene Reimann, et al.. (2022). Assessment of the genetic and clinical determinants of hip fracture risk: Genome-wide association and Mendelian randomization study. Cell Reports Medicine. 3(10). 100776–100776. 21 indexed citations
14.
Pujol‐Gualdo, Natàlia, Kristi Läll, Maarja Lepamets, et al.. (2022). Advancing our understanding of genetic risk factors and potential personalized strategies for pelvic organ prolapse. Nature Communications. 13(1). 3584–3584. 14 indexed citations
15.
Шадрина, М. И., S. A. Klyushnikov, Tiit Nikopensius, et al.. (2016). ITPR1 gene p.Val1553Met mutation in Russian family with mild Spinocerebellar ataxia. PubMed. 3(1). 2–2. 20 indexed citations
16.
Palta, Priit, Lauris Kaplinski, Liina Nagirnaja, et al.. (2015). Haplotype Phasing and Inheritance of Copy Number Variants in Nuclear Families. PLoS ONE. 10(4). e0122713–e0122713. 7 indexed citations
17.
Metspalu, Mait, Irene Gallego Romero, Bayazit Yunusbayev, et al.. (2012). Shared and Unique Components of Human Population Structure and Genome-Wide Signals of Positive Selection in South Asia. The American Journal of Human Genetics. 90(2). 378–379. 6 indexed citations
18.
Nelis, Mari, et al.. (2011). Balanced reciprocal translocation t(5;13)(q33;q12) and 9q31.1 microduplication in a man suffering from infertility and pollinosis. Journal of Applied Genetics. 53(1). 93–97. 8 indexed citations
19.
Metspalu, Mait, Irene Gallego Romero, Bayazit Yunusbayev, et al.. (2011). Shared and Unique Components of Human Population Structure and Genome-Wide Signals of Positive Selection in South Asia. The American Journal of Human Genetics. 89(6). 731–744. 110 indexed citations
20.
Männik, Katrin, Sven Parkel, Priit Palta, et al.. (2010). A parallel SNP array study of genomic aberrations associated with mental retardation in patients and general population in Estonia. European Journal of Medical Genetics. 54(2). 136–143. 6 indexed citations

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.

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