Katrin Männik
Impact in
- Genetics top 1%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
Papers in
- Genetics 24
- Genomic variations and chromosomal abnormalities 23
- Genomics and Rare Diseases 7
- Genetics and Neurodevelopmental Disorders 4
- Genetic Associations and Epidemiology 3
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- Congenital heart defects research 4
- Gene expression and cancer classification 3
- Glycosylation and Glycoproteins Research 1
- Co-authors
- Ants Kurg (8 shared papers)Sébastien Jacquemont (2 shared papers)Anne Manuela Maillard (2 shared papers)Alexandre Reymond (2 shared papers)Carlotta Ferrari (1 shared paper)Philippe P. Maeder (1 shared paper)Nouchine K. Hadjikhani (1 shared paper)Stanisław Adaszewski (1 shared paper)
- Journals
- European Journal of Medical Genetics (3 papers)Biological Psychiatry (2 papers)Molecular Psychiatry (2 papers)Nature (2 papers)European Journal of Human Genetics (1 paper)
- Partner nations
- SwitzerlandEstoniaUnited States
In The Last Decade
Katrin Männik
27 papers receiving 2.5k citations
Katrin Männik's Hit Papers
Peers
Comparison fields: 5 of 88
- Genetics 1.7k
- Endocrine and Autonomic Systems 127
- Cognitive Neuroscience 379
- Clinical Psychology 302
- Molecular Biology 967
Countries citing papers authored by Katrin Männik
This map shows the geographic impact of Katrin Männik'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 Katrin Männik with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Katrin Männik more than expected).
Fields of papers citing papers by Katrin Männik
This network shows the impact of papers produced by Katrin Männik. 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 Katrin Männik. The network helps show where Katrin Männik may publish in the future.
Co-authors
The 25 scholars most cited alongside Katrin Männik, 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 | 2010 | 420 | |
| 2 | Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa Hit paper breakdown → | 2017 | 388 |
| 3 | 2011 | 372 | |
| 4 | 2012 | 240 | |
| 5 | 2015 | 188 | |
| 6 | 2014 | 167 | |
| 7 | 2015 | 144 | |
| 8 | 2018 | 133 | |
| 9 | 2016 | 80 | |
| 10 | 2015 | 75 | |
| 11 | 2017 | 65 | |
| 12 | 2014 | 57 | |
| 13 | 2019 | 55 | |
| 14 | 2015 | 44 | |
| 15 | 2013 | 35 | |
| 16 | 2013 | 35 | |
| 17 | 2015 | 34 | |
| 18 | 2005 | 13 | |
| 19 | 2016 | 13 | |
| 20 | 2012 | 12 |
About Katrin Männik
Katrin Männik is a scholar working on Genetics, Molecular Biology, Plant Science, Cancer Research and Pediatrics, Perinatology and Child Health, having authored 27 papers that have together received 2.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (23 papers), Genomics and Rare Diseases (7 papers), Chromosomal and Genetic Variations (5 papers), Congenital heart defects research (4 papers), Genetics and Neurodevelopmental Disorders (4 papers), Gene expression and cancer classification (3 papers), Genetic Associations and Epidemiology (3 papers) and Glycosylation and Glycoproteins Research (1 paper). The work is most often cited by research in Genetics (1.7k citations), Endocrine and Autonomic Systems (127 citations), Cognitive Neuroscience (379 citations), Clinical Psychology (302 citations) and Molecular Biology (967 citations). Katrin Männik has collaborated with scholars based in Switzerland, Estonia and United States. Frequent co-authors include Ants Kurg, Sébastien Jacquemont, Anne Manuela Maillard, Alexandre Reymond, Carlotta Ferrari, Philippe P. Maeder, Nouchine K. Hadjikhani, Stanisław Adaszewski, Zoltán Kutalik and Bogdan Draganski. Their work appears in journals such as European Journal of Medical Genetics, Biological Psychiatry, Molecular Psychiatry, Nature 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.