John Barnard
Impact in
- Genetics top 0.1%
- Genetic Associations and Epidemiology
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Forensic and Genetic Research
- Genetics and Neurodevelopmental Disorders
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- Atrial Fibrillation Management and Outcomes
- Cardiac electrophysiology and arrhythmias
Papers in
- Hematology 38
- Acute Myeloid Leukemia Research 35
- Genetics 58
- Genetic Associations and Epidemiology 51
- Genomics and Rare Diseases 8
- Co-authors
- Xiao‐Li Meng (1 shared paper)Mina K. Chung (23 shared papers)Gudrun Maria Jonsdottir (2 shared papers)Kāri Stefánsson (2 shared papers)Thorgeir Elís Thorgeirsson (2 shared papers)Jeffrey R. Gulcher (2 shared papers)Michael L. Frigge (2 shared papers)Daniel Fannar Gudbjartsson (2 shared papers)
- Journals
- Blood (18 papers)Nature Genetics (15 papers)Circulation Arrhythmia and Electrophysiology (9 papers)Nature Communications (9 papers)Nature (8 papers)
- Partner nations
- United StatesGermanyNetherlands
In The Last Decade
John Barnard
169 papers receiving 22.4k citations
John Barnard's Hit Papers
Peers
Comparison fields: 5 of 190
- Genetics 8.6k
- Cardiology and Cardiovascular Medicine 3.9k
- Hematology 1.5k
- Clinical Biochemistry 291
- Molecular Biology 3.3k
Countries citing papers authored by John Barnard
This map shows the geographic impact of John Barnard'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 Barnard with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites John Barnard more than expected).
Fields of papers citing papers by John Barnard
This network shows the impact of papers produced by John Barnard. 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 Barnard. The network helps show where John Barnard may publish in the future.
Co-authors
The 25 scholars most cited alongside John Barnard, 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 181 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The mutational constraint spectrum quantified from variation in 141,456 humans Hit paper breakdown → | 2020 | 6789 |
| 2 | A high-resolution recombination map of the human genome Hit paper breakdown → | 2002 | 1395 |
| 3 | Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program Hit paper breakdown → | 2021 | 1363 |
| 4 | A genomic mutational constraint map using variation in 76,156 human genomes Hit paper breakdown → | 2023 | 966 |
| 5 | A common inversion under selection in Europeans Hit paper breakdown → | 2005 | 638 |
| 6 | GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment Hit paper breakdown → | 2013 | 625 |
| 7 | 2007 | 602 | |
| 8 | 1999 | 597 | |
| 9 | Multi-ethnic genome-wide association study for atrial fibrillation Hit paper breakdown → | 2018 | 570 |
| 10 | Inherited causes of clonal haematopoiesis in 97,691 whole genomes Hit paper breakdown → | 2020 | 555 |
| 11 | Meta-analysis identifies six new susceptibility loci for atrial fibrillation Hit paper breakdown → | 2012 | 493 |
| 12 | 2010 | 418 | |
| 13 | 2010 | 361 | |
| 14 | 2021 | 285 | |
| 15 | 1999 | 272 | |
| 16 | 2017 | 270 | |
| 17 | Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data Hit paper breakdown → | 2022 | 229 |
| 18 | 2012 | 224 | |
| 19 | 2012 | 201 | |
| 20 | 2003 | 193 |
About John Barnard
John Barnard is a scholar working on Hematology, Genetics, Cardiology and Cardiovascular Medicine, Statistics and Probability and Pulmonary and Respiratory Medicine, having authored 181 papers that have together received 22.9k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (51 papers), Acute Myeloid Leukemia Research (35 papers), Atrial Fibrillation Management and Outcomes (28 papers), Cardiac electrophysiology and arrhythmias (27 papers), Pulmonary Hypertension Research and Treatments (10 papers), Genomics and Rare Diseases (8 papers), Science Education and Pedagogy (7 papers) and Statistical Methods and Bayesian Inference (6 papers). The work is most often cited by research in Genetics (8.6k citations), Cardiology and Cardiovascular Medicine (3.9k citations), Hematology (1.5k citations), Clinical Biochemistry (291 citations) and Molecular Biology (3.3k citations). John Barnard has collaborated with scholars based in United States, Germany and Netherlands. Frequent co-authors include Xiao‐Li Meng, Mina K. Chung, Gudrun Maria Jonsdottir, Kāri Stefánsson, Thorgeir Elís Thorgeirsson, Jeffrey R. Gulcher, Michael L. Frigge, Daniel Fannar Gudbjartsson, Sigrun Laufey Sigurdardottir and Augustine Kong. Their work appears in journals such as Blood, Nature Genetics, Circulation Arrhythmia and Electrophysiology, Nature Communications and Nature.
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.