Bruce E. Hayward
Impact in
- Genetics top 1%
- Genetic Syndromes and Imprinting
- Genomics and Rare Diseases
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
Papers in
-
- Metabolism, Diabetes, and Cancer 8
- Epigenetics and DNA Methylation 8
- Genetics 34
- Genetics and Neurodevelopmental Disorders 19
- Genetic Syndromes and Imprinting 11
- Genomic variations and chromosomal abnormalities 7
- Co-authors
- David T. Bonthron (28 shared papers)Eamonn Sheridan (13 shared papers)Lisa Strain (3 shared papers)Veronica Moran (3 shared papers)Karen Usdin (20 shared papers)Ian Carr (8 shared papers)Michel De Vos (5 shared papers)Graham R. Taylor (7 shared papers)
- Journals
- Human Mutation (5 papers)Scientific Reports (4 papers)Human Molecular Genetics (3 papers)The American Journal of Human Genetics (3 papers)Nucleic Acids Research (3 papers)
- Partner nations
- United KingdomUnited StatesFrance
In The Last Decade
Bruce E. Hayward
53 papers receiving 2.9k citations
Peers
Comparison fields: 5 of 93
- Genetics 1.3k
- Cancer Research 418
- Molecular Biology 1.7k
- Pediatrics, Perinatology and Child Health 481
- Endocrinology, Diabetes and Metabolism 384
Countries citing papers authored by Bruce E. Hayward
This map shows the geographic impact of Bruce E. Hayward'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 Bruce E. Hayward with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bruce E. Hayward more than expected).
Fields of papers citing papers by Bruce E. Hayward
This network shows the impact of papers produced by Bruce E. Hayward. 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 Bruce E. Hayward. The network helps show where Bruce E. Hayward may publish in the future.
Co-authors
The 25 scholars most cited alongside Bruce E. Hayward, 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 54 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1998 | 239 | |
| 2 | 2001 | 231 | |
| 3 | 1998 | 218 | |
| 4 | 2011 | 174 | |
| 5 | 2002 | 170 | |
| 6 | 2009 | 139 | |
| 7 | 2004 | 136 | |
| 8 | 2000 | 133 | |
| 9 | 2013 | 123 | |
| 10 | 2009 | 122 | |
| 11 | 2009 | 88 | |
| 12 | 2010 | 83 | |
| 13 | 1986 | 83 | |
| 14 | 2012 | 76 | |
| 15 | 2003 | 73 | |
| 16 | 1998 | 66 | |
| 17 | 2006 | 63 | |
| 18 | 2010 | 62 | |
| 19 | 2000 | 58 | |
| 20 | 1997 | 44 |
About Bruce E. Hayward
Bruce E. Hayward is a scholar working on Molecular Biology, Genetics, Surgery, Pediatrics, Perinatology and Child Health and Pathology and Forensic Medicine, having authored 54 papers that have together received 2.9k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (19 papers), Genetic Syndromes and Imprinting (11 papers), Metabolism, Diabetes, and Cancer (8 papers), Prenatal Screening and Diagnostics (8 papers), Epigenetics and DNA Methylation (8 papers), Pancreatic function and diabetes (7 papers), Autism Spectrum Disorder Research (7 papers) and Genomic variations and chromosomal abnormalities (7 papers). The work is most often cited by research in Genetics (1.3k citations), Cancer Research (418 citations), Molecular Biology (1.7k citations), Pediatrics, Perinatology and Child Health (481 citations) and Endocrinology, Diabetes and Metabolism (384 citations). Bruce E. Hayward has collaborated with scholars based in United Kingdom, United States and France. Frequent co-authors include David T. Bonthron, Eamonn Sheridan, Lisa Strain, Veronica Moran, Karen Usdin, Ian Carr, Michel De Vos, Graham R. Taylor, Aruna Asipu and Christine P. Diggle. Their work appears in journals such as Human Mutation, Scientific Reports, Human Molecular Genetics, The American Journal of Human Genetics and Nucleic Acids Research.
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.