Katrin Männik
Impact in
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- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
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- Language Development and Disorders
Papers in
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- Congenital heart defects research 2
- RNA modifications and cancer 1
- Ubiquitin and proteasome pathways 1
- Genetics 1
- Genetics and Neurodevelopmental Disorders 1
Katrin Männik
2 papers receiving 72 citations
Peers
Comparison fields: 5 of 25
- Genetics 42
- Developmental and Educational Psychology 12
- Developmental Biology 2
- Cell Biology 14
- Developmental Neuroscience 3
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 16 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
About Katrin Männik
Katrin Männik is a scholar working on Molecular Biology, Genetics, Developmental Neuroscience, Infectious Diseases and Organic Chemistry, having authored 2 papers that have together received 72 indexed citations. Recurring topics across this work include Congenital heart defects research (2 papers), Williams Syndrome Research (1 paper), Genetics and Neurodevelopmental Disorders (1 paper), RNA modifications and cancer (1 paper) and Ubiquitin and proteasome pathways (1 paper). The work is most often cited by research in Genetics (42 citations), Developmental and Educational Psychology (12 citations), Developmental Biology (2 citations), Cell Biology (14 citations) and Developmental Neuroscience (3 citations). Katrin Männik has collaborated with scholars based in Estonia, Italy and Belgium. Frequent co-authors include Katrin Õunap, Guy Froyen, Olga Žilina, Patrizia D’Adamo, Hilde Van Esch, Annick Vogels, Martine Raynaud, Tiia Reimand, Maila Giannandrea and Sylvain Briault. Their work appears in journals such as Human Mutation and American Journal of Medical Genetics Part A.
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.