K Loggenberg
Impact in
- Genetics top 10%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Nutrition, Genetics, and Disease
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- Ovarian cancer diagnosis and treatment
Papers in
- Genetics 6
- BRCA gene mutations in cancer 5
- Genomics and Rare Diseases 1
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- Parvovirus B19 Infection Studies 2
- Co-authors
- Sue Gessler (6 shared papers)Uziel Beller (6 shared papers)Matthew Burnell (5 shared papers)Huw Dorkins (5 shared papers)Yvonne Wallis (5 shared papers)Saskia C. Sanderson (6 shared papers)Usha Menon (6 shared papers)Ian Tomlinson (6 shared papers)
- Journals
- BJOG An International Journal of Obstetrics & Gynaecology (4 papers)Frontiers in Genetics (1 paper)Molecular Cytogenetics (1 paper)JNCI Journal of the National Cancer Institute (1 paper)UCL Discovery (University College London) (1 paper)
- Partner nations
- AustraliaUnited KingdomIsrael
In The Last Decade
K Loggenberg
8 papers receiving 237 citations
Peers
Comparison fields: 5 of 25
- Genetics 200
- Reproductive Medicine 29
- Cancer Research 34
- Pediatrics, Perinatology and Child Health 30
- Pathology and Forensic Medicine 23
Countries citing papers authored by K Loggenberg
This map shows the geographic impact of K Loggenberg'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 K Loggenberg with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites K Loggenberg more than expected).
Fields of papers citing papers by K Loggenberg
This network shows the impact of papers produced by K Loggenberg. 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 K Loggenberg. The network helps show where K Loggenberg may publish in the future.
Co-authors
The 25 scholars most cited alongside K Loggenberg, 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 | 2014 | 139 | |
| 2 | 2019 | 47 | |
| 3 | 2019 | 23 | |
| 4 | 2022 | 16 | |
| 5 | 2022 | 5 | |
| 6 | 2024 | 4 | |
| 7 | 2021 | 4 | |
| 8 | Population based testing for high-penetrance dominant gene mutations: initial results from the pilot phase of GCaPPS | 2012 | 2 |
About K Loggenberg
K Loggenberg is a scholar working on Genetics, Infectious Diseases, Pediatrics, Perinatology and Child Health, Molecular Biology and Public Health, Environmental and Occupational Health, having authored 8 papers that have together received 240 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (5 papers), Parvovirus B19 Infection Studies (2 papers), Prenatal Screening and Diagnostics (2 papers), Genomics and Rare Diseases (1 paper), Gestational Trophoblastic Disease Studies (1 paper), Molecular Biology Techniques and Applications (1 paper) and Fetal and Pediatric Neurological Disorders (1 paper). The work is most often cited by research in Genetics (200 citations), Reproductive Medicine (29 citations), Cancer Research (34 citations), Pediatrics, Perinatology and Child Health (30 citations) and Pathology and Forensic Medicine (23 citations). K Loggenberg has collaborated with scholars based in Australia, United Kingdom and Israel. Frequent co-authors include Sue Gessler, Uziel Beller, Matthew Burnell, Huw Dorkins, Yvonne Wallis, Saskia C. Sanderson, Usha Menon, Ian Tomlinson, Chris Jacobs and Lucy Side. Their work appears in journals such as BJOG An International Journal of Obstetrics & Gynaecology, Frontiers in Genetics, Molecular Cytogenetics, JNCI Journal of the National Cancer Institute and UCL Discovery (University College London).
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.