Erna Claes
Impact in
- Genetics top 5%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
-
- Childhood Cancer Survivors' Quality of Life
Papers in ⓘ
- Genetics 14
- BRCA gene mutations in cancer 14
- Nutrition, Genetics, and Disease 2
- Genomics and Rare Diseases 1
- Co-authors
- Gerry Evers‐Kiebooms (12 shared papers)Lieve Denayer (12 shared papers)Eric Legius (9 shared papers)Andrea Boogaerts (7 shared papers)Marleen Decruyenaere (8 shared papers)Myriam Welkenhuysen (5 shared papers)Koenraad Devriendt (1 shared paper)Sabine Tejpar (1 shared paper)
- Journals
- Psycho-Oncology (3 papers)European Journal of Human Genetics (1 paper)Social Science & Medicine (1 paper)Disease Markers (1 paper)Patient Education and Counseling (1 paper)
- Partner nations
- BelgiumUnited States
In The Last Decade
Erna Claes
13 papers receiving 605 citations
Peers
Comparison fields: 5 of 57
- Genetics 507
- Pediatrics, Perinatology and Child Health 160
- Pathology and Forensic Medicine 118
- Sociology and Political Science 207
- Applied Psychology 22
Countries citing papers authored by Erna Claes
This map shows the geographic impact of Erna Claes'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 Erna Claes with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Erna Claes more than expected).
Fields of papers citing papers by Erna Claes
This network shows the impact of papers produced by Erna Claes. 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 Erna Claes. The network helps show where Erna Claes may publish in the future.
Co-authors
The 10 scholars most cited alongside Erna Claes, 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 | 2002 | 194 | |
| 2 | 2000 | 84 | |
| 3 | 2000 | 74 | |
| 4 | 2004 | 65 | |
| 5 | 2005 | 56 | |
| 6 | 2005 | 52 | |
| 7 | 2004 | 39 | |
| 8 | 2005 | 32 | |
| 9 | 2000 | 25 | |
| 10 | 2000 | 6 | |
| 11 | Psychological implications of living with familial adenomatous polyposis. | 2011 | 4 |
| 12 | 1999 | 2 | |
| 13 | Genetic testing for hereditary breast and ovarian cancer in cancer patients: family communication and knowledge | 2001 | 1 |
| 14 | A psychological perspective on genetic testing for hereditary cancers: Psychological aspects of uptake and impact of genetic testing for hereditary breast and ovarian cancer and hereditary nonpolyposis colorectal cancer. | 2005 | 1 |
About Erna Claes
Erna Claes is a scholar working on Genetics, Applied Psychology, Pathology and Forensic Medicine, Sociology and Political Science and Pediatrics, Perinatology and Child Health, having authored 14 papers that have together received 635 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (14 papers), Family Support in Illness (7 papers), Genetic factors in colorectal cancer (3 papers), Childhood Cancer Survivors' Quality of Life (3 papers), Nutrition, Genetics, and Disease (2 papers), Genomics and Rare Diseases (1 paper), Global Cancer Incidence and Screening (1 paper) and Genetic Neurodegenerative Diseases (1 paper). The work is most often cited by research in Genetics (507 citations), Pediatrics, Perinatology and Child Health (160 citations), Pathology and Forensic Medicine (118 citations), Sociology and Political Science (207 citations) and Applied Psychology (22 citations). Erna Claes has collaborated with scholars based in Belgium and United States. Frequent co-authors include Gerry Evers‐Kiebooms, Lieve Denayer, Eric Legius, Andrea Boogaerts, Marleen Decruyenaere, Myriam Welkenhuysen, Koenraad Devriendt, Sabine Tejpar, Koen Demyttenaere and Alex Kartheuser. Their work appears in journals such as Psycho-Oncology, European Journal of Human Genetics, Social Science & Medicine, Disease Markers and Patient Education and Counseling.
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.