V. Proud
Impact in
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- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- DNA Repair Mechanisms
- Renal and related cancers
- CRISPR and Genetic Engineering
Papers in
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- Genetics, Bioinformatics, and Biomedical Research 1
- Epigenetics and DNA Methylation 1
- DNA Repair Mechanisms 1
- Genetics 5
- BRCA gene mutations in cancer 2
- Genomic variations and chromosomal abnormalities 2
- Genomics and Rare Diseases 1
- Animal Genetics and Reproduction 1
- Co-authors
- E. Diane Johnson (4 shared papers)Brendan Mullaney (1 shared paper)Sat Dev Batish (1 shared paper)Mark E. Robson (1 shared paper)Helmut Hanenberg (1 shared paper)Arleen D. Auerbach (1 shared paper)Kandice Mah (1 shared paper)Khédoudja Nafa (1 shared paper)
- Journals
- Human Molecular Genetics (1 paper)Academic Medicine (1 paper)JNCI Journal of the National Cancer Institute (1 paper)Genomics (1 paper)Mayo Clinic Proceedings (1 paper)
- Partner nations
- United StatesFranceUnited Kingdom
In The Last Decade
V. Proud
10 papers receiving 328 citations
Peers
Comparison fields: 5 of 62
- Genetics 165
- Molecular Biology 218
- Genetics 31
- Cancer Research 41
- Issues, ethics and legal aspects 3
Countries citing papers authored by V. Proud
This map shows the geographic impact of V. Proud'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 V. Proud with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites V. Proud more than expected).
Fields of papers citing papers by V. Proud
This network shows the impact of papers produced by V. Proud. 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 V. Proud. The network helps show where V. Proud may publish in the future.
Co-authors
The 25 scholars most cited alongside V. Proud, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2003 | 144 | |
| 2 | 1997 | 54 | |
| 3 | 2001 | 34 | |
| 4 | 1997 | 31 | |
| 5 | 2007 | 24 | |
| 6 | 1992 | 17 | |
| 7 | 1990 | 12 | |
| 8 | 1991 | 12 | |
| 9 | Teaching human genetics in biochemistry by computer literature searching. | 1989 | 11 |
| 10 | Students online: learning medical genetics. | 1993 | 6 |
About V. Proud
V. Proud is a scholar working on Molecular Biology, Genetics, General Health Professions, Communication and Health, having authored 10 papers that have together received 345 indexed citations. Recurring topics across this work include Health Sciences Research and Education (3 papers), BRCA gene mutations in cancer (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Genetics, Bioinformatics, and Biomedical Research (1 paper), Genomics and Rare Diseases (1 paper), Epigenetics and DNA Methylation (1 paper), DNA Repair Mechanisms (1 paper) and Animal Genetics and Reproduction (1 paper). The work is most often cited by research in Genetics (165 citations), Molecular Biology (218 citations), Genetics (31 citations), Cancer Research (41 citations) and Issues, ethics and legal aspects (3 citations). V. Proud has collaborated with scholars based in United States, France and United Kingdom. Frequent co-authors include E. Diane Johnson, Brendan Mullaney, Sat Dev Batish, Mark E. Robson, Helmut Hanenberg, Arleen D. Auerbach, Kandice Mah, Khédoudja Nafa, Orna Levran and Amie M. Deffenbaugh. Their work appears in journals such as Human Molecular Genetics, Academic Medicine, JNCI Journal of the National Cancer Institute, Genomics and Mayo Clinic Proceedings.
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.