Edward Blair
Impact in
-
- Cardiomyopathy and Myosin Studies
- Cardiovascular Effects of Exercise
- Cardiovascular Function and Risk Factors
- Viral Infections and Immunology Research
- Genetics top 1%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 24
- Genomic variations and chromosomal abnormalities 9
- Connective tissue disorders research 6
- Genomics and Rare Diseases 6
-
- Congenital heart defects research 6
- Co-authors
- Hugh Watkins (13 shared papers)Charles Redwood (4 shared papers)Houman Ashrafian (2 shared papers)Jenny C. Taylor (9 shared papers)Ingegerd Östman‐Smith (4 shared papers)Kate Thomson (4 shared papers)B. Rajagopalan (1 shared paper)Peter Styles (1 shared paper)
- Journals
- European Journal of Human Genetics (5 papers)Human Molecular Genetics (3 papers)Circulation Research (2 papers)Journal of Medical Genetics (2 papers)Genetics in Medicine (2 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Edward Blair
47 papers receiving 3.5k citations
Edward Blair's Hit Papers
Peers
Comparison fields: 5 of 134
- Cardiology and Cardiovascular Medicine 1.4k
- Genetics 1.1k
- Molecular Biology 1.4k
- Developmental Neuroscience 60
- Pediatrics, Perinatology and Child Health 201
Countries citing papers authored by Edward Blair
This map shows the geographic impact of Edward Blair'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 Edward Blair with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Edward Blair more than expected).
Fields of papers citing papers by Edward Blair
This network shows the impact of papers produced by Edward Blair. 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 Edward Blair. The network helps show where Edward Blair may publish in the future.
Co-authors
The 25 scholars most cited alongside Edward Blair, 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 47 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples Hit paper breakdown → | 2016 | 462 |
| 2 | 2006 | 428 | |
| 3 | 2001 | 373 | |
| 4 | 2003 | 330 | |
| 5 | 2003 | 254 | |
| 6 | 2008 | 161 | |
| 7 | 2006 | 117 | |
| 8 | Mutations in the gamma2 subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis. | 2001 | 115 |
| 9 | 2014 | 89 | |
| 10 | 2011 | 86 | |
| 11 | 2011 | 83 | |
| 12 | 2002 | 77 | |
| 13 | 2015 | 72 | |
| 14 | 2008 | 71 | |
| 15 | 2009 | 68 | |
| 16 | 2012 | 59 | |
| 17 | 2011 | 59 | |
| 18 | 2011 | 55 | |
| 19 | 2007 | 55 | |
| 20 | 2013 | 54 |
About Edward Blair
Edward Blair is a scholar working on Genetics, Molecular Biology, Cardiology and Cardiovascular Medicine, Pulmonary and Respiratory Medicine and Immunology, having authored 47 papers that have together received 3.6k indexed citations. Recurring topics across this work include Cardiomyopathy and Myosin Studies (11 papers), Genomic variations and chromosomal abnormalities (9 papers), Congenital heart defects research (6 papers), Connective tissue disorders research (6 papers), Genomics and Rare Diseases (6 papers), Cardiovascular Effects of Exercise (5 papers), Aortic Disease and Treatment Approaches (4 papers) and Cardiovascular Function and Risk Factors (4 papers). The work is most often cited by research in Cardiology and Cardiovascular Medicine (1.4k citations), Genetics (1.1k citations), Molecular Biology (1.4k citations), Developmental Neuroscience (60 citations) and Pediatrics, Perinatology and Child Health (201 citations). Edward Blair has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Hugh Watkins, Charles Redwood, Houman Ashrafian, Jenny C. Taylor, Ingegerd Östman‐Smith, Kate Thomson, B. Rajagopalan, Peter Styles, Kieran Clarke and Jenifer Crilley. Their work appears in journals such as European Journal of Human Genetics, Human Molecular Genetics, Circulation Research, Journal of Medical Genetics and Genetics in Medicine.
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.