Anders O.H. Nygren
Impact in
- Oncology top 2%
- PARP inhibition in cancer therapy
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
Papers in
-
- Epigenetics and DNA Methylation 8
- DNA Repair Mechanisms 7
- Advanced biosensing and bioanalysis techniques 5
- Genetics 15
- Genomic variations and chromosomal abnormalities 6
- Genetic Syndromes and Imprinting 4
- Genetics and Neurodevelopmental Disorders 3
- Co-authors
- Jos Jonkers (4 shared papers)Piet Borst (4 shared papers)Sven Rottenberg (4 shared papers)Eline van der Burg (3 shared papers)Ariena Kersbergen (3 shared papers)Mark J. O’Connor (3 shared papers)Aaron Cranston (3 shared papers)Alan Lau (3 shared papers)
- Journals
- European Journal of Human Genetics (3 papers)Cancer Research (3 papers)Journal of Molecular Diagnostics (2 papers)Proceedings of the National Academy of Sciences (2 papers)Human Mutation (2 papers)
- Partner nations
- NetherlandsGermanyUnited States
In The Last Decade
Anders O.H. Nygren
38 papers receiving 3.2k citations
Anders O.H. Nygren's Hit Papers
Peers
Comparison fields: 5 of 110
- Oncology 1.1k
- Cancer Research 453
- Pediatrics, Perinatology and Child Health 506
- Molecular Biology 1.7k
- Genetics 614
Countries citing papers authored by Anders O.H. Nygren
This map shows the geographic impact of Anders O.H. Nygren'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 Anders O.H. Nygren with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anders O.H. Nygren more than expected).
Fields of papers citing papers by Anders O.H. Nygren
This network shows the impact of papers produced by Anders O.H. Nygren. 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 Anders O.H. Nygren. The network helps show where Anders O.H. Nygren may publish in the future.
Co-authors
The 25 scholars most cited alongside Anders O.H. Nygren, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 38 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | High sensitivity of BRCA1-deficient mammary tumors to the PARP inhibitor AZD2281 alone and in combination with platinum drugs Hit paper breakdown → | 2008 | 771 |
| 2 | Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting Hit paper breakdown → | 2011 | 372 |
| 3 | 2005 | 304 | |
| 4 | 2004 | 255 | |
| 5 | 2007 | 220 | |
| 6 | 2007 | 125 | |
| 7 | 2010 | 112 | |
| 8 | 2006 | 105 | |
| 9 | 2007 | 102 | |
| 10 | 2009 | 95 | |
| 11 | 2009 | 77 | |
| 12 | 2006 | 73 | |
| 13 | 2015 | 68 | |
| 14 | 2010 | 67 | |
| 15 | 2007 | 55 | |
| 16 | 2008 | 50 | |
| 17 | 2007 | 47 | |
| 18 | 2005 | 36 | |
| 19 | 2008 | 35 | |
| 20 | 2010 | 29 |
About Anders O.H. Nygren
Anders O.H. Nygren is a scholar working on Molecular Biology, Genetics, Oncology, Pediatrics, Perinatology and Child Health and Pathology and Forensic Medicine, having authored 38 papers that have together received 3.3k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (8 papers), DNA Repair Mechanisms (7 papers), Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (5 papers), Advanced biosensing and bioanalysis techniques (5 papers), PARP inhibition in cancer therapy (4 papers), Genetic Syndromes and Imprinting (4 papers) and Genetics and Neurodevelopmental Disorders (3 papers). The work is most often cited by research in Oncology (1.1k citations), Cancer Research (453 citations), Pediatrics, Perinatology and Child Health (506 citations), Molecular Biology (1.7k citations) and Genetics (614 citations). Anders O.H. Nygren has collaborated with scholars based in Netherlands, Germany and United States. Frequent co-authors include Jos Jonkers, Piet Borst, Sven Rottenberg, Eline van der Burg, Ariena Kersbergen, Mark J. O’Connor, Aaron Cranston, Alan Lau, Niall M.B. Martin and Jan P. Schouten. Their work appears in journals such as European Journal of Human Genetics, Cancer Research, Journal of Molecular Diagnostics, Proceedings of the National Academy of Sciences and Human Mutation.
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.