John Attia
Impact in
- Biological Psychiatry top 0.5%
- Tryptophan and brain disorders
- Genetics top 0.2%
- Genetic Associations and Epidemiology
Papers in
- Genetics 79
- Genetic Associations and Epidemiology 64
- Epidemiology 86
- Acute Ischemic Stroke Management 37
- Substance Abuse Treatment and Outcomes 19
- Co-authors
- Ammarin Thakkinstian (154 shared papers)Mark McEvoy (133 shared papers)Catherine Anne D’Este (36 shared papers)Patrick McElduff (33 shared papers)Christopher J. Oldmeadow (98 shared papers)Sarah A. Hiles (8 shared papers)Cosetta Minelli (12 shared papers)Christopher Royce Levi (38 shared papers)
- Journals
- The Medical Journal of Australia (20 papers)BMJ Open (18 papers)PLoS ONE (14 papers)Scientific Reports (13 papers)Nature Genetics (12 papers)
- Partner nations
- AustraliaUnited KingdomThailand
In The Last Decade
John Attia
824 papers receiving 39.0k citations
John Attia's Hit Papers
Peers
Comparison fields: 5 of 219
- Biological Psychiatry 768
- Genetics 6.5k
- Internal Medicine 777
- Rehabilitation 1.0k
- Nephrology 1.1k
Countries citing papers authored by John Attia
This map shows the geographic impact of John Attia'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 John Attia with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites John Attia more than expected).
Fields of papers citing papers by John Attia
This network shows the impact of papers produced by John Attia. 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 John Attia. The network helps show where John Attia may publish in the future.
Co-authors
The 25 scholars most cited alongside John Attia, 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 859 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Analysis of shared heritability in common disorders of the brain Hit paper breakdown → | 2018 | 1441 |
| 2 | Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes Hit paper breakdown → | 2018 | 1188 |
| 3 | Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits Hit paper breakdown → | 2018 | 990 |
| 4 | Genome-wide association study identifies 74 loci associated with educational attainment Hit paper breakdown → | 2016 | 914 |
| 5 | Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses Hit paper breakdown → | 2016 | 742 |
| 6 | Genome-Wide Association Study of Retinopathy in Individuals without Diabetes Hit paper breakdown → | 2013 | 735 |
| 7 | Genome-wide association analyses identify 18 new loci associated with serum urate concentrations Hit paper breakdown → | 2012 | 666 |
| 8 | A systematic review and meta-analysis of dietary patterns and depression in community-dwelling adults Hit paper breakdown → | 2013 | 611 |
| 9 | GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment Hit paper breakdown → | 2013 | 607 |
| 10 | The power of genetic diversity in genome-wide association studies of lipids Hit paper breakdown → | 2021 | 583 |
| 11 | 2004 | 541 | |
| 12 | Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function Hit paper breakdown → | 2018 | 469 |
| 13 | A saturated map of common genetic variants associated with human height Hit paper breakdown → | 2022 | 456 |
| 14 | Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function Hit paper breakdown → | 2016 | 426 |
| 15 | Extending thrombolysis to 4·5–9 h and wake-up stroke using perfusion imaging: a systematic review and meta-analysis of individual patient data Hit paper breakdown → | 2019 | 384 |
| 16 | Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals Hit paper breakdown → | 2022 | 380 |
| 17 | Stroke genetics informs drug discovery and risk prediction across ancestries Hit paper breakdown → | 2022 | 355 |
| 18 | 2012 | 353 | |
| 19 | 2005 | 329 | |
| 20 | Imaging features and safety and efficacy of endovascular stroke treatment: a meta-analysis of individual patient-level data Hit paper breakdown → | 2018 | 316 |
About John Attia
John Attia is a scholar working on Genetics, Epidemiology, Public Health, Environmental and Occupational Health, Cardiology and Cardiovascular Medicine and Physiology, having authored 859 papers that have together received 40.4k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (64 papers), Acute Ischemic Stroke Management (37 papers), Substance Abuse Treatment and Outcomes (19 papers), Stroke Rehabilitation and Recovery (18 papers), Birth, Development, and Health (17 papers), Retinal Diseases and Treatments (16 papers), Smoking Behavior and Cessation (14 papers) and Pregnancy and Medication Impact (13 papers). The work is most often cited by research in Biological Psychiatry (768 citations), Genetics (6.5k citations), Internal Medicine (777 citations), Rehabilitation (1.0k citations) and Nephrology (1.1k citations). John Attia has collaborated with scholars based in Australia, United Kingdom and Thailand. Frequent co-authors include Ammarin Thakkinstian, Mark McEvoy, Catherine Anne D’Este, Patrick McElduff, Christopher J. Oldmeadow, Sarah A. Hiles, Cosetta Minelli, Christopher Royce Levi, Rodney J. Scott and Thunyarat Anothaisintawee. Their work appears in journals such as The Medical Journal of Australia, BMJ Open, PLoS ONE, Scientific Reports and Nature 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.