Jonathan Marchini
- Genetics top 0.02%
- Genetic Associations and Epidemiology 38
- Genetic Mapping and Diversity in Plants and Animals 29
- Genetic and phenotypic traits in livestock 21
- Genomics and Rare Diseases 6
- Genomic variations and chromosomal abnormalities 6
- Computational Mathematics top 2%
- Molecular Biology top 1%
- Gene expression and cancer classification 10
- Cancer Research top 2%
- Biological Psychiatry top 2%
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- Advanced MRI Techniques and Applications 4
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- Functional Brain Connectivity Studies 4
- Co-authors
- Bryan HowiePeter DonnellyOlivier DelaneauGil McVeanJean‐François ZaguryLon R. CardonMatthew StephensSimon Myers
- Journals
- Nature Genetics (14 papers)The American Journal of Human Genetics (5 papers)Bioinformatics (4 papers)
- Partner nations
- United KingdomUnited StatesSwitzerland
In The Last Decade
Jonathan Marchini
52 papers receiving 16.8k citations
Hit Papers
Peers
Comparison fields: 5 of 184
- Genetics 10.3k
- Computational Mathematics 51
- Molecular Biology 5.7k
- Cancer Research 1.1k
- Biological Psychiatry 157
Countries citing papers authored by Jonathan Marchini
This map shows the geographic impact of Jonathan Marchini'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 Jonathan Marchini with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jonathan Marchini more than expected).
Fields of papers citing papers by Jonathan Marchini
This network shows the impact of papers produced by Jonathan Marchini. 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 Jonathan Marchini. The network helps show where Jonathan Marchini may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Jonathan Marchini, 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 | 2025 | 0 | |
| 2 | 2025 | 11 | |
| 3 | 2024 | 9 | |
| 4 | 2024 | 6 | |
| 5 | 2024 | 4 | |
| 6 | 2021 | 43 | |
| 7 | 2020 | 9 | |
| 8 | 2019 | 99 | |
| 9 | 2019 | 39 | |
| 10 | 2018 | 56 | |
| 11 | The UK Biobank resource with deep phenotyping and genomic databreakdown → | 2018 | 4399 |
| 12 | 2012 | 39 | |
| 13 | Fast and accurate genotype imputation in genome-wide association studies through pre-phasingbreakdown → | 2012 | 990 |
| 14 | 2011 | 9 | |
| 15 | A linear complexity phasing method for thousands of genomesbreakdown → | 2011 | 1014 |
| 16 | A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studiesbreakdown → | 2009 | 2337 |
| 17 | Genome-wide strategies for detecting multiple loci that influence complex diseasesbreakdown → | 2005 | 677 |
| 18 | 2003 | 52 | |
| 19 | Assessing population structure and its effects on association studies in a genome wide SNP dataset. | 2002 | 1 |
| 20 | 1997 | 48 |
About Jonathan Marchini
Jonathan Marchini is a scholar working on Genetics, Anatomy and Cognitive Neuroscience, having authored 53 papers that have together received 17.0k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (38 papers), Genetic Mapping and Diversity in Plants and Animals (29 papers), Genetic and phenotypic traits in livestock (21 papers), Gene expression and cancer classification (10 papers), Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Advanced MRI Techniques and Applications (4 papers) and Functional Brain Connectivity Studies (4 papers). The work is most often cited by research in Genetics (10.3k citations), Computational Mathematics (51 citations) and Molecular Biology (5.7k citations). Jonathan Marchini has collaborated with scholars based in United Kingdom, United States and Switzerland. Frequent co-authors include Bryan Howie, Peter Donnelly, Olivier Delaneau, Gil McVean, Jean‐François Zagury, Lon R. Cardon, Matthew Stephens, Simon Myers, Kevin Sharp and Lloyd T. Elliott. Their work appears in journals such as Nature Genetics, The American Journal of Human Genetics, Bioinformatics, PLoS Genetics and NeuroImage.
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.