Arthur Ko
Impact in
- Genetics top 0.5%
- Genetic Associations and Epidemiology
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Cognitive Neuroscience top 2%
- Autism Spectrum Disorder Research
Papers in
- Genetics 23
- Genetic Associations and Epidemiology 15
- Genomics and Rare Diseases 7
- Genomic variations and chromosomal abnormalities 2
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- Adipose Tissue and Metabolism 4
- Co-authors
- Päivi Pajukanta (14 shared papers)Marcus Alvarez (9 shared papers)Zong Miao (6 shared papers)Kristina M. Garske (5 shared papers)Elior Rahmani (2 shared papers)Kirsi Hannele Pietiläinen (2 shared papers)Brandon Jew (2 shared papers)Eran Halperin (2 shared papers)
- Journals
- Nature Communications (8 papers)The American Journal of Human Genetics (4 papers)Nature (2 papers)Nature Genetics (2 papers)PLoS Genetics (2 papers)
- Partner nations
- United StatesFinlandUnited Kingdom
In The Last Decade
Arthur Ko
38 papers receiving 5.2k citations
Arthur Ko's Hit Papers
Peers
Comparison fields: 5 of 121
- Genetics 2.9k
- Cognitive Neuroscience 766
- Molecular Biology 1.1k
- Developmental Neuroscience 52
- Psychiatry and Mental health 295
Countries citing papers authored by Arthur Ko
This map shows the geographic impact of Arthur Ko'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 Arthur Ko with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Arthur Ko more than expected).
Fields of papers citing papers by Arthur Ko
This network shows the impact of papers produced by Arthur Ko. 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 Arthur Ko. The network helps show where Arthur Ko may publish in the future.
Co-authors
The 25 scholars most cited alongside Arthur Ko, 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 40 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations Hit paper breakdown → | 2012 | 1739 |
| 2 | Integrative approaches for large-scale transcriptome-wide association studies Hit paper breakdown → | 2016 | 1641 |
| 3 | 2014 | 328 | |
| 4 | 2020 | 287 | |
| 5 | 2012 | 156 | |
| 6 | 2017 | 130 | |
| 7 | 2014 | 81 | |
| 8 | 2016 | 76 | |
| 9 | 2023 | 74 | |
| 10 | 2018 | 69 | |
| 11 | 2019 | 58 | |
| 12 | 2021 | 57 | |
| 13 | 2019 | 52 | |
| 14 | 2020 | 47 | |
| 15 | 2018 | 44 | |
| 16 | 2013 | 43 | |
| 17 | 2019 | 42 | |
| 18 | 2019 | 36 | |
| 19 | 2021 | 35 | |
| 20 | 2019 | 33 |
About Arthur Ko
Arthur Ko is a scholar working on Genetics, Physiology, Neurology, Epidemiology and Molecular Biology, having authored 40 papers that have together received 5.3k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (15 papers), Genomics and Rare Diseases (7 papers), Adipose Tissue and Metabolism (4 papers), Adipokines, Inflammation, and Metabolic Diseases (3 papers), Long-Term Effects of COVID-19 (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Genomics and Chromatin Dynamics (2 papers) and Genomics and Phylogenetic Studies (2 papers). The work is most often cited by research in Genetics (2.9k citations), Cognitive Neuroscience (766 citations), Molecular Biology (1.1k citations), Developmental Neuroscience (52 citations) and Psychiatry and Mental health (295 citations). Arthur Ko has collaborated with scholars based in United States, Finland and United Kingdom. Frequent co-authors include Päivi Pajukanta, Marcus Alvarez, Zong Miao, Kristina M. Garske, Elior Rahmani, Kirsi Hannele Pietiläinen, Brandon Jew, Eran Halperin, Jae Hoon Sul and Markku Laakso. Their work appears in journals such as Nature Communications, The American Journal of Human Genetics, Nature, Nature Genetics 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.