Regine Witköwski
Impact in
- Genetics top 5%
- Glioma Diagnosis and Treatment
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
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- Cancer Genomics and Diagnostics
Papers in
-
- DNA Repair Mechanisms 3
- Genomics and Chromatin Dynamics 3
- Genetics 14
- Glioma Diagnosis and Treatment 6
- Genomic variations and chromosomal abnormalities 4
- Co-authors
- Gundula Thiel (9 shared papers)K Vorpahl (1 shared paper)Hubert Martin (1 shared paper)Siegfried Vogel (3 shared papers)Catrin Wernicke (2 shared papers)G Jacobasch (2 shared papers)Thomas Cremer (1 shared paper)Thomas Ried (1 shared paper)
- Journals
- Human Genetics (6 papers)Genes Chromosomes and Cancer (3 papers)Archives of Gynecology and Obstetrics (1 paper)Journal of Molecular Medicine (1 paper)Acta Haematologica (1 paper)
- Partner nations
- GermanyUnited StatesAustralia
In The Last Decade
Regine Witköwski
38 papers receiving 512 citations
Peers
Comparison fields: 5 of 65
- Genetics 209
- Cancer Research 124
- Developmental Biology 16
- Genetics 203
- Neurology 72
Countries citing papers authored by Regine Witköwski
This map shows the geographic impact of Regine Witköwski'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 Regine Witköwski with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Regine Witköwski more than expected).
Fields of papers citing papers by Regine Witköwski
This network shows the impact of papers produced by Regine Witköwski. 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 Regine Witköwski. The network helps show where Regine Witköwski may publish in the future.
Co-authors
The 25 scholars most cited alongside Regine Witköwski, 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 | 1992 | 120 | |
| 2 | 1996 | 81 | |
| 3 | 1983 | 47 | |
| 4 | 1995 | 32 | |
| 5 | 1999 | 27 | |
| 6 | 1991 | 24 | |
| 7 | 1993 | 24 | |
| 8 | 1997 | 23 | |
| 9 | Chromosomal aberrations and abnormalities of red-cell metabolism in a case of Fanconi's anaemia before and after development of leukaemia. | 1968 | 18 |
| 10 | Somatic mutations in the neurofibromatosis 1 gene in gliomas and primitive neuroectodermal tumours. | 1996 | 15 |
| 11 | 1968 | 15 | |
| 12 | 1967 | 13 | |
| 13 | Chromosomal changes and correspondingly altered proto-oncogene expression in human gliomas. Value of combined cytogenetic and molecular genetic analysis. | 1993 | 11 |
| 14 | 2003 | 10 | |
| 15 | 1998 | 9 | |
| 16 | 1978 | 8 | |
| 17 | Phenotype and counseling in lacrimo-auriculo-dento-digital (LADD) syndrome. | 1993 | 7 |
| 18 | The XX male -- report on a child and an adult. | 1980 | 5 |
| 19 | 1986 | 5 | |
| 20 | 1999 | 4 |
About Regine Witköwski
Regine Witköwski is a scholar working on Molecular Biology, Genetics, Genetics, Cancer Research and Plant Science, having authored 43 papers that have together received 539 indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (6 papers), Cancer Genomics and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Chromosomal and Genetic Variations (4 papers), Microtubule and mitosis dynamics (3 papers), DNA Repair Mechanisms (3 papers), Metabolism and Genetic Disorders (3 papers) and Genomics and Chromatin Dynamics (3 papers). The work is most often cited by research in Genetics (209 citations), Cancer Research (124 citations), Developmental Biology (16 citations), Genetics (203 citations) and Neurology (72 citations). Regine Witköwski has collaborated with scholars based in Germany, United States and Australia. Frequent co-authors include Gundula Thiel, K Vorpahl, Hubert Martin, Siegfried Vogel, Catrin Wernicke, G Jacobasch, Thomas Cremer, Thomas Ried, Marika Kiessling and Evelin Schröck. Their work appears in journals such as Human Genetics, Genes Chromosomes and Cancer, Archives of Gynecology and Obstetrics, Journal of Molecular Medicine and Acta Haematologica.
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.