Julie Maynard
Impact in
-
- Genetic factors in colorectal cancer
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
Papers in
-
- Genetic factors in colorectal cancer 9
-
- DNA Repair Mechanisms 3
- Co-authors
- Julian R. Sampson (11 shared papers)Jeremy P. Cheadle (11 shared papers)Angela Hodges (2 shared papers)Nada Al Tassan (2 shared papers)Geraint T. Williams (2 shared papers)D. Rhodri Davies (1 shared paper)Nicholas I. Fleming (1 shared paper)Sheila S. David (1 shared paper)
- Journals
- Human Genetics (5 papers)Journal of Medical Genetics (3 papers)Human Mutation (3 papers)Clinical Cancer Research (1 paper)Nature Genetics (1 paper)
- Partner nations
- United KingdomUnited StatesSingapore
In The Last Decade
Julie Maynard
24 papers receiving 1.9k citations
Julie Maynard's Hit Papers
Peers
Comparison fields: 5 of 77
- Pathology and Forensic Medicine 1.1k
- Cancer Research 460
- Oncology 701
- Neurology 319
- Molecular Biology 829
Countries citing papers authored by Julie Maynard
This map shows the geographic impact of Julie Maynard'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 Julie Maynard with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Julie Maynard more than expected).
Fields of papers citing papers by Julie Maynard
This network shows the impact of papers produced by Julie Maynard. 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 Julie Maynard. The network helps show where Julie Maynard may publish in the future.
Co-authors
The 25 scholars most cited alongside Julie Maynard, 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 24 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Inherited variants of MYH associated with somatic G:C→T:A mutations in colorectal tumors Hit paper breakdown → | 2002 | 980 |
| 2 | 2003 | 307 | |
| 3 | 1998 | 117 | |
| 4 | 1996 | 85 | |
| 5 | 1992 | 58 | |
| 6 | 2003 | 37 | |
| 7 | 1995 | 35 | |
| 8 | 2004 | 34 | |
| 9 | 2000 | 32 | |
| 10 | 2015 | 32 | |
| 11 | 1996 | 30 | |
| 12 | 1995 | 29 | |
| 13 | 2018 | 28 | |
| 14 | 1996 | 24 | |
| 15 | 1997 | 21 | |
| 16 | 2017 | 19 | |
| 17 | 1997 | 12 | |
| 18 | 1998 | 6 | |
| 19 | 2005 | 5 | |
| 20 | 2005 | 4 |
About Julie Maynard
Julie Maynard is a scholar working on Pathology and Forensic Medicine, Molecular Biology, Neurology, Oncology and Pulmonary and Respiratory Medicine, having authored 24 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (9 papers), Neurofibromatosis and Schwannoma Cases (8 papers), Colorectal Cancer Treatments and Studies (6 papers), Cancer Genomics and Diagnostics (5 papers), Sarcoma Diagnosis and Treatment (3 papers), Meningioma and schwannoma management (3 papers), Vascular Malformations Diagnosis and Treatment (3 papers) and DNA Repair Mechanisms (3 papers). The work is most often cited by research in Pathology and Forensic Medicine (1.1k citations), Cancer Research (460 citations), Oncology (701 citations), Neurology (319 citations) and Molecular Biology (829 citations). Julie Maynard has collaborated with scholars based in United Kingdom, United States and Singapore. Frequent co-authors include Julian R. Sampson, Jeremy P. Cheadle, Angela Hodges, Nada Al Tassan, Geraint T. Williams, D. Rhodri Davies, Nicholas I. Fleming, Sheila S. David, Nikolas H. Chmiel and Alison L. Livingston. Their work appears in journals such as Human Genetics, Journal of Medical Genetics, Human Mutation, Clinical Cancer Research 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.