Litanja Lodder
Impact in
- Genetics top 5%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
-
- Childhood Cancer Survivors' Quality of Life
- Prenatal Screening and Diagnostics
Papers in
- Genetics 10
- BRCA gene mutations in cancer 10
- Nutrition, Genetics, and Disease 2
- Genomics and Rare Diseases 1
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- Family Support in Illness 6
- Co-authors
- Jan G.M. Klijn (6 shared papers)Aad Tibben (7 shared papers)Conny A. van der Meer (7 shared papers)R.W. Trijsburg (8 shared papers)E.J. Meijers-Heijboer (7 shared papers)Petra G. Frets (8 shared papers)Martinus F. Niermeijer (8 shared papers)Hugo J. Duivenvoorden (5 shared papers)
- Journals
- European Journal of Human Genetics (1 paper)Cognitive Therapy and Research (1 paper)Journal of Clinical Oncology (1 paper)Breast Cancer Research and Treatment (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- Netherlands
In The Last Decade
Litanja Lodder
11 papers receiving 779 citations
Peers
Comparison fields: 5 of 49
- Genetics 669
- Pediatrics, Perinatology and Child Health 133
- Sociology and Political Science 221
- Pathology and Forensic Medicine 75
- Reproductive Medicine 34
Countries citing papers authored by Litanja Lodder
This map shows the geographic impact of Litanja Lodder'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 Litanja Lodder with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Litanja Lodder more than expected).
Fields of papers citing papers by Litanja Lodder
This network shows the impact of papers produced by Litanja Lodder. 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 Litanja Lodder. The network helps show where Litanja Lodder may publish in the future.
Co-authors
The 25 scholars most cited alongside Litanja Lodder, 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 | 238 | |
| 2 | 2002 | 151 | |
| 3 | 2001 | 139 | |
| 4 | 2000 | 110 | |
| 5 | Presymptomatic testing for BRCA1 and BRCA2: how distressing are the pre-test weeks? Rotterdam/Leiden Genetics Working Group. | 1999 | 66 |
| 6 | 2001 | 47 | |
| 7 | 1998 | 39 | |
| 8 | 2002 | 29 | |
| 9 | 2001 | 4 | |
| 10 | 2000 | 2 | |
| 11 | 1999 | 1 | |
| 12 | Dealing with the Risk for Hereditary Breast and Ovarian Cancer | 2001 | 0 |
About Litanja Lodder
Litanja Lodder is a scholar working on Genetics, Sociology and Political Science, Public Health, Environmental and Occupational Health, Molecular Biology and Pediatrics, Perinatology and Child Health, having authored 12 papers that have together received 826 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (10 papers), Family Support in Illness (6 papers), DNA Repair Mechanisms (2 papers), Nutrition, Genetics, and Disease (2 papers), Patient Dignity and Privacy (2 papers), Genomics and Rare Diseases (1 paper), Biotechnology and Related Fields (1 paper) and Personality Disorders and Psychopathology (1 paper). The work is most often cited by research in Genetics (669 citations), Pediatrics, Perinatology and Child Health (133 citations), Sociology and Political Science (221 citations), Pathology and Forensic Medicine (75 citations) and Reproductive Medicine (34 citations). Litanja Lodder has collaborated with scholars based in Netherlands. Frequent co-authors include Jan G.M. Klijn, Aad Tibben, Conny A. van der Meer, R.W. Trijsburg, E.J. Meijers-Heijboer, Petra G. Frets, Martinus F. Niermeijer, Hugo J. Duivenvoorden, Caroline Seynaeve and Curt W. Burger. Their work appears in journals such as European Journal of Human Genetics, Cognitive Therapy and Research, Journal of Clinical Oncology, Breast Cancer Research and Treatment and Journal of Medical 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.