Ilse M. van der Werf
- Genetics
- Molecular Biology
- Pediatrics, Perinatology and Child Health
- Cancer Research
- Pathology and Forensic Medicine
- Co-authors
- R. Frank KooyGeert VandeweyerGeert MortierEdwin ReyniersHermann‐Josef LüdeckeBernhard HorsthemkeKarin BuitingDagmar Wieczorek
- Topics
- Genetic Syndromes and Imprinting (3 papers)Genomics and Rare Diseases (3 papers)Genetics and Neurodevelopmental Disorders (3 papers)
- Partner nations
- BelgiumNetherlandsGermany
In The Last Decade
Ilse M. van der Werf
8 papers receiving 130 citations
Peers
Comparison fields: 5 of 39
- Genetics 111
- Molecular Biology 79
- Pediatrics, Perinatology and Child Health 32
- Cancer Research 18
- Pathology and Forensic Medicine 14
Countries citing papers authored by Ilse M. van der Werf
This map shows the geographic impact of Ilse M. van der Werf'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 Ilse M. van der Werf with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ilse M. van der Werf more than expected).
Fields of papers citing papers by Ilse M. van der Werf
This network shows the impact of papers produced by Ilse M. van der Werf. 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 Ilse M. van der Werf. The network helps show where Ilse M. van der Werf may publish in the future.
Co-authorship network of co-authors of Ilse M. van der Werf
This figure shows the co-authorship network connecting the top 25 collaborators of Ilse M. van der Werf. A scholar is included among the top collaborators of Ilse M. van der Werf based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Ilse M. van der Werf. Ilse M. van der Werf is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 4 | |
| 2 | 12 | |
| 3 | 31 | |
| 4 | 17 | |
| 5 | 21 | |
| 6 | 36 | |
| 7 | 13 | |
| 8 | 21 |
About Ilse M. van der Werf
Ilse M. van der Werf is a scholar working on Genetics, Developmental Neuroscience and Cognitive Neuroscience, having authored 8 papers that have together received 155 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (3 papers), Genomics and Rare Diseases (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). The work is most often cited by research in Genetics (111 citations), Pediatrics, Perinatology and Child Health (32 citations) and Biological Psychiatry (3 citations). Ilse M. van der Werf has collaborated with scholars based in Belgium, Netherlands and Germany. Frequent co-authors include R. Frank Kooy, Geert Vandeweyer, Geert Mortier, Edwin Reyniers, Hermann‐Josef Lüdecke, Bernhard Horsthemke, Karin Buiting, Dagmar Wieczorek, Johanna Christina Czeschik and Piet Vanhaesebrouck. Their work appears in journals such as PLoS ONE, Gene and Behavioural Brain Research.
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.