Katrin Männik
Impact in
-
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
-
- Autism Spectrum Disorder Research
Papers in
- Genetics 9
- Genomic variations and chromosomal abnormalities 9
- Genomics and Rare Diseases 4
- Genetics and Neurodevelopmental Disorders 2
- BRCA gene mutations in cancer 1
-
- Gene expression and cancer classification 2
- Congenital heart defects research 1
- Advanced biosensing and bioanalysis techniques 1
- Co-authors
- Ants Kurg (7 shared papers)Nouchine Hadjikhani (1 shared paper)Carlotta Ferrari (1 shared paper)Marianna Zazhytska (1 shared paper)Zoltán Kutalik (1 shared paper)Sébastien Jacquemont (2 shared papers)Stanisław Adaszewski (1 shared paper)Juergen Dukart (1 shared paper)
- Journals
- European Journal of Medical Genetics (3 papers)Nature Protocols (1 paper)European Journal of Human Genetics (1 paper)Twin Research and Human Genetics (1 paper)Molecular Psychiatry (1 paper)
- Partner nations
- EstoniaCyprusSwitzerland
In The Last Decade
Katrin Männik
9 papers receiving 207 citations
Peers
Comparison fields: 5 of 43
- Genetics 163
- Cognitive Neuroscience 41
- Molecular Biology 124
- Developmental Neuroscience 6
- Genetics 15
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
| # | Work | ||
|---|---|---|---|
| 1 | 2014 | 134 | |
| 2 | 2013 | 32 | |
| 3 | 2005 | 12 | |
| 4 | 2012 | 11 | |
| 5 | 2006 | 9 | |
| 6 | 2016 | 8 | |
| 7 | 2008 | 7 | |
| 8 | 2010 | 6 | |
| 9 | 2014 | 3 |
About Katrin Männik
Katrin Männik is a scholar working on Genetics, Molecular Biology, Plant Science, Pediatrics, Perinatology and Child Health and Cognitive Neuroscience, having authored 9 papers that have together received 222 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Genomics and Rare Diseases (4 papers), Chromosomal and Genetic Variations (3 papers), Gene expression and cancer classification (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Congenital heart defects research (1 paper), Advanced biosensing and bioanalysis techniques (1 paper) and BRCA gene mutations in cancer (1 paper). The work is most often cited by research in Genetics (163 citations), Cognitive Neuroscience (41 citations), Molecular Biology (124 citations), Developmental Neuroscience (6 citations) and Genetics (15 citations). Katrin Männik has collaborated with scholars based in Estonia, Cyprus and Switzerland. Frequent co-authors include Ants Kurg, Nouchine Hadjikhani, Carlotta Ferrari, Marianna Zazhytska, Zoltán Kutalik, Sébastien Jacquemont, Stanisław Adaszewski, Juergen Dukart, Philippe Maeder and Bogdan Draganski. Their work appears in journals such as European Journal of Medical Genetics, Nature Protocols, European Journal of Human Genetics, Twin Research and Human Genetics and Molecular Psychiatry.
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.