Anders O.H. Nygren
Impact in
- Oncology top 2%
- PARP inhibition in cancer therapy
-
- Prenatal Screening and Diagnostics
Papers in
- Genetics 13
- Genomic variations and chromosomal abnormalities 5
- Genetic Syndromes and Imprinting 5
- Genomics and Rare Diseases 3
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- Hereditary Neurological Disorders 6
- Co-authors
- Jos Jonkers (4 shared papers)Sven Rottenberg (4 shared papers)Piet Borst (4 shared papers)Ariena J. Kersbergen (3 shared papers)Eline van der Burg (3 shared papers)Mark J. O’Connor (3 shared papers)Niall M.B. Martin (3 shared papers)Alan Lau (3 shared papers)
- Journals
- Human Mutation (3 papers)European Journal of Human Genetics (3 papers)Cancer Research (3 papers)Brain (2 papers)Journal of Molecular Diagnostics (2 papers)
- Partner nations
- GermanyUnited StatesUnited Kingdom
In The Last Decade
Anders O.H. Nygren
43 papers receiving 3.9k citations
Anders O.H. Nygren's Hit Papers
Peers
Comparison fields: 5 of 98
- Oncology 937
- Pediatrics, Perinatology and Child Health 492
- Cancer Research 349
- Genetics 635
- Molecular Biology 1.2k
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 43 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 | 826 |
| 2 | Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting Hit paper breakdown → | 2011 | 399 |
| 3 | 2005 | 334 | |
| 4 | 2004 | 273 | |
| 5 | 2016 | 271 | |
| 6 | 2007 | 255 | |
| 7 | 2008 | 152 | |
| 8 | 2007 | 136 | |
| 9 | 2006 | 121 | |
| 10 | 2010 | 119 | |
| 11 | 2007 | 110 | |
| 12 | 2009 | 100 | |
| 13 | 2007 | 94 | |
| 14 | 2009 | 86 | |
| 15 | 2006 | 75 | |
| 16 | 2010 | 73 | |
| 17 | 2015 | 71 | |
| 18 | 2007 | 66 | |
| 19 | 2007 | 55 | |
| 20 | 2008 | 50 |
About Anders O.H. Nygren
Anders O.H. Nygren is a scholar working on Genetics, Cellular and Molecular Neuroscience, Oncology, Molecular Biology and Pediatrics, Perinatology and Child Health, having authored 43 papers that have together received 4.1k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (6 papers), Hereditary Neurological Disorders (6 papers), Genomic variations and chromosomal abnormalities (5 papers), Genetic Syndromes and Imprinting (5 papers), PARP inhibition in cancer therapy (4 papers), Genomics and Rare Diseases (3 papers), Molecular Biology Techniques and Applications (3 papers) and Prenatal Screening and Diagnostics (3 papers). The work is most often cited by research in Oncology (937 citations), Pediatrics, Perinatology and Child Health (492 citations), Cancer Research (349 citations), Genetics (635 citations) and Molecular Biology (1.2k citations). Anders O.H. Nygren has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Jos Jonkers, Sven Rottenberg, Piet Borst, Ariena J. Kersbergen, Eline van der Burg, Mark J. O’Connor, Niall M.B. Martin, Alan Lau, Aaron N. Cranston and Serge A.L. Zander. Their work appears in journals such as Human Mutation, European Journal of Human Genetics, Cancer Research, Brain and Journal of Molecular Diagnostics.
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.