Konrad Rawlik
Impact in
- Genetics top 5%
- Genetic Associations and Epidemiology
- Genetic Mapping and Diversity in Plants and Animals
- Genetic and phenotypic traits in livestock
- Genomics and Rare Diseases
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- Epigenetics and DNA Methylation
- Bioinformatics and Genomic Networks
Papers in
- Genetics 16
- Genetic Associations and Epidemiology 13
- Genetic and phenotypic traits in livestock 7
- Genetic Mapping and Diversity in Plants and Animals 5
- Genetic Syndromes and Imprinting 3
-
- Epigenetics and DNA Methylation 7
- Co-authors
- Albert Tenesa (18 shared papers)Oriol Canela‐Xandri (12 shared papers)Sethu Vijayakumar (6 shared papers)Marc Toussaint (5 shared papers)Elena Bernabeu (1 shared paper)James Prendergast (1 shared paper)Andrea Talenti (1 shared paper)Chris Haley (4 shared papers)
- Journals
- Nature Genetics (3 papers)Human Molecular Genetics (2 papers)Genome biology (2 papers)Heredity (1 paper)PLoS Genetics (1 paper)
- Partner nations
- United KingdomGermanyChina
In The Last Decade
Konrad Rawlik
29 papers receiving 1.1k citations
Konrad Rawlik's Hit Papers
Peers
Comparison fields: 5 of 137
- Genetics 496
- Molecular Biology 360
- Aging 8
- Cell Biology 65
- Cancer Research 53
Countries citing papers authored by Konrad Rawlik
This map shows the geographic impact of Konrad Rawlik'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 Konrad Rawlik with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Konrad Rawlik more than expected).
Fields of papers citing papers by Konrad Rawlik
This network shows the impact of papers produced by Konrad Rawlik. 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 Konrad Rawlik. The network helps show where Konrad Rawlik may publish in the future.
Co-authors
The 25 scholars most cited alongside Konrad Rawlik, 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 30 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | An atlas of genetic associations in UK Biobank Hit paper breakdown → | 2018 | 387 |
| 2 | 2021 | 95 | |
| 3 | 2018 | 81 | |
| 4 | International Joint Conference in Artificial Intelligence (IJCAI) | 2013 | 71 |
| 5 | 2016 | 64 | |
| 6 | 2016 | 63 | |
| 7 | 2012 | 49 | |
| 8 | 2021 | 35 | |
| 9 | 2015 | 29 | |
| 10 | 2020 | 21 | |
| 11 | An Approximate Inference Approach to Temporal Optimization in Optimal Control | 2010 | 21 |
| 12 | 2020 | 20 | |
| 13 | 2019 | 19 | |
| 14 | 2020 | 18 | |
| 15 | 2011 | 18 | |
| 16 | 2020 | 16 | |
| 17 | 2019 | 15 | |
| 18 | 2016 | 14 | |
| 19 | 2012 | 11 | |
| 20 | 2016 | 10 |
About Konrad Rawlik
Konrad Rawlik is a scholar working on Genetics, Molecular Biology, Control and Systems Engineering, Artificial Intelligence and Epidemiology, having authored 30 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (13 papers), Genetic and phenotypic traits in livestock (7 papers), Epigenetics and DNA Methylation (7 papers), Genetic Mapping and Diversity in Plants and Animals (5 papers), Genetic Syndromes and Imprinting (3 papers), Robot Manipulation and Learning (2 papers), Reinforcement Learning in Robotics (2 papers) and Control Systems and Identification (2 papers). The work is most often cited by research in Genetics (496 citations), Molecular Biology (360 citations), Aging (8 citations), Cell Biology (65 citations) and Cancer Research (53 citations). Konrad Rawlik has collaborated with scholars based in United Kingdom, Germany and China. Frequent co-authors include Albert Tenesa, Oriol Canela‐Xandri, Sethu Vijayakumar, Marc Toussaint, Elena Bernabeu, James Prendergast, Andrea Talenti, Chris Haley, María Muñoz and Ricardo Pong‐Wong. Their work appears in journals such as Nature Genetics, Human Molecular Genetics, Genome biology, Heredity and PLoS 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.