Robert Winqvist
Impact in
- Cancer Research top 2%
- Cancer Genomics and Diagnostics
- Genetics top 2%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
Papers in
-
- DNA Repair Mechanisms 33
- RNA modifications and cancer 12
- Genomics and Chromatin Dynamics 8
- Genetics 39
- BRCA gene mutations in cancer 33
- Co-authors
- Katri Pylkäs (38 shared papers)Kari Alitalo (9 shared papers)Arja Jukkola‐Vuorinen (8 shared papers)Irene Newsham (4 shared papers)Albert de la Chapelle (3 shared papers)Virpi Launonen (8 shared papers)Katrin Rapakko (12 shared papers)Sanna‐Maria Karppinen (10 shared papers)
- Journals
- Human Genetics (6 papers)European Journal of Cancer (5 papers)Cancer Letters (5 papers)Breast Cancer Research and Treatment (4 papers)BMC Cancer (4 papers)
- Partner nations
- FinlandUnited StatesGermany
In The Last Decade
Robert Winqvist
87 papers receiving 3.1k citations
Peers
Comparison fields: 5 of 98
- Cancer Research 716
- Genetics 1.0k
- Oncology 827
- Molecular Biology 1.8k
- Pathology and Forensic Medicine 420
Countries citing papers authored by Robert Winqvist
This map shows the geographic impact of Robert Winqvist'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 Robert Winqvist with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Robert Winqvist more than expected).
Fields of papers citing papers by Robert Winqvist
This network shows the impact of papers produced by Robert Winqvist. 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 Robert Winqvist. The network helps show where Robert Winqvist may publish in the future.
Co-authors
The 25 scholars most cited alongside Robert Winqvist, 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 90 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 456 | |
| 2 | 1984 | 159 | |
| 3 | 1987 | 127 | |
| 4 | Loss of heterozygosity in sporadic human breast carcinoma: a common region between 11q22 and 11q23.3. | 1994 | 118 |
| 5 | 1987 | 112 | |
| 6 | Loss of heterozygosity for chromosome 11 in primary human breast tumors is associated with poor survival after metastasis. | 1995 | 109 |
| 7 | 1992 | 89 | |
| 8 | 1989 | 86 | |
| 9 | 2008 | 81 | |
| 10 | 1985 | 79 | |
| 11 | 2002 | 72 | |
| 12 | 1989 | 70 | |
| 13 | 2001 | 68 | |
| 14 | 1996 | 66 | |
| 15 | Refinement of regional loss of heterozygosity for chromosome 11p15.5 in human breast tumors. | 1993 | 63 |
| 16 | 2009 | 57 | |
| 17 | 2013 | 51 | |
| 18 | 2018 | 51 | |
| 19 | 1994 | 51 | |
| 20 | 2012 | 50 |
About Robert Winqvist
Robert Winqvist is a scholar working on Molecular Biology, Genetics, Oncology, Pathology and Forensic Medicine and Cancer Research, having authored 90 papers that have together received 3.3k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (33 papers), BRCA gene mutations in cancer (33 papers), Cancer-related Molecular Pathways (13 papers), Genetic factors in colorectal cancer (13 papers), RNA modifications and cancer (12 papers), Cancer Genomics and Diagnostics (8 papers), Genomics and Chromatin Dynamics (8 papers) and Neuroblastoma Research and Treatments (5 papers). The work is most often cited by research in Cancer Research (716 citations), Genetics (1.0k citations), Oncology (827 citations), Molecular Biology (1.8k citations) and Pathology and Forensic Medicine (420 citations). Robert Winqvist has collaborated with scholars based in Finland, United States and Germany. Frequent co-authors include Katri Pylkäs, Kari Alitalo, Arja Jukkola‐Vuorinen, Irene Newsham, Albert de la Chapelle, Virpi Launonen, Katrin Rapakko, Sanna‐Maria Karppinen, Kalle Saksela and Minna Allinen. Their work appears in journals such as Human Genetics, European Journal of Cancer, Cancer Letters, Breast Cancer Research and Treatment and BMC Cancer.
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.