A. Westerveld
Impact in
- Molecular Biology top 1%
- DNA Repair Mechanisms
- CRISPR and Genetic Engineering
- Retinal Development and Disorders
- Genomics and Chromatin Dynamics
- Epigenetics and DNA Methylation
- Neurology top 1%
- Neuroblastoma Research and Treatments
Papers in
- Genetics 51
- Virus-based gene therapy research 14
- Genetic Syndromes and Imprinting 11
-
- DNA Repair Mechanisms 29
- CRISPR and Genetic Engineering 20
- Biochemical and Molecular Research 13
- Epigenetics and DNA Methylation 12
- Co-authors
- D. BootsmaJan H.J. HoeijmakersHanny OdijkRosalyn SlaterP. Meera KhanRogier VersteegJan de WitS. van Soest
- Journals
- Cytogenetic and Genome Research (24 papers)Human Genetics (18 papers)Genes Chromosomes and Cancer (13 papers)Experimental Cell Research (9 papers)Genomics (8 papers)
- Partner nations
- NetherlandsUnited KingdomUnited States
In The Last Decade
A. Westerveld
152 papers receiving 5.8k citations
Peers
Comparison fields: 5 of 130
- Molecular Biology 4.3k
- Neurology 931
- Cancer Research 876
- Genetics 1.4k
- Cell Biology 500
Countries citing papers authored by A. Westerveld
This map shows the geographic impact of A. Westerveld'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 A. Westerveld with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A. Westerveld more than expected).
Fields of papers citing papers by A. Westerveld
This network shows the impact of papers produced by A. Westerveld. 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 A. Westerveld. The network helps show where A. Westerveld may publish in the future.
Co-authorship network
The 25 scholars most cited alongside A. Westerveld, 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 | 2001 | 63 | |
| 2 | 2000 | 40 | |
| 3 | 1999 | 18 | |
| 4 | 1997 | 69 | |
| 5 | A constitutional balanced 1;17 neuroblastoma translocation | 1997 | 1 |
| 6 | 1991 | 19 | |
| 7 | 1990 | 27 | |
| 8 | The cloned human DNA excision repair gene ERCC-1 fails to correct xeroderma pigmentosum complementation groups A through I. | 1989 | 64 |
| 9 | 1988 | 125 | |
| 10 | 1987 | 20 | |
| 11 | 1980 | 46 | |
| 12 | 1978 | 13 | |
| 13 | 1978 | 3 | |
| 14 | 1976 | 16 | |
| 15 | Human gene mapping 2 : Rotterdam Conference (1974) | 1975 | 2 |
| 16 | 1975 | 3 | |
| 17 | 1975 | 12 | |
| 18 | 1974 | 14 | |
| 19 | 1974 | 16 | |
| 20 | Mammalian cell hybridization | 1973 | 1 |
About A. Westerveld
A. Westerveld is a scholar working on Genetics, Molecular Biology, Neurology, Cancer Research and Clinical Biochemistry, having authored 153 papers that have together received 6.1k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (29 papers), CRISPR and Genetic Engineering (20 papers), Virus-based gene therapy research (14 papers), Biochemical and Molecular Research (13 papers), Epigenetics and DNA Methylation (12 papers), Genetic Syndromes and Imprinting (11 papers), Lysosomal Storage Disorders Research (11 papers) and Neuroblastoma Research and Treatments (10 papers). The work is most often cited by research in Molecular Biology (4.3k citations), Neurology (931 citations), Cancer Research (876 citations), Genetics (1.4k citations) and Cell Biology (500 citations). A. Westerveld has collaborated with scholars based in Netherlands, United Kingdom and United States. Frequent co-authors include D. Bootsma, Jan H.J. Hoeijmakers, Hanny Odijk, Rosalyn Slater, P. Meera Khan, Rogier Versteeg, Jan de Wit, S. van Soest, Arthur A. Bergen and Theo J.M. Hulsebos. Their work appears in journals such as Cytogenetic and Genome Research, Human Genetics, Genes Chromosomes and Cancer, Experimental Cell Research and Genomics.
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.