Regine Witköwski
Impact in
- Genetics top 5%
- Glioma Diagnosis and Treatment
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
-
- Cancer Genomics and Diagnostics
Papers in
- Genetics 8
- Glioma Diagnosis and Treatment 6
- Genomic variations and chromosomal abnormalities 4
- Digestive system and related health 3
- Co-authors
- Gundula ThielK VorpahlHubert MartinSiegfried VogelCatrin WernickeG JacobaschThomas RiedThomas Cremer
- 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
| # | Work | ||
|---|---|---|---|
| 1 | 2003 | 10 | |
| 2 | 1999 | 27 | |
| 3 | 1999 | 4 | |
| 4 | 1999 | 1 | |
| 5 | 1998 | 3 | |
| 6 | 1997 | 23 | |
| 7 | Somatic mutations in the neurofibromatosis 1 gene in gliomas and primitive neuroectodermal tumours. | 1996 | 15 |
| 8 | 1996 | 81 | |
| 9 | 1995 | 32 | |
| 10 | 1993 | 24 | |
| 11 | Chromosomal changes and correspondingly altered proto-oncogene expression in human gliomas. Value of combined cytogenetic and molecular genetic analysis. | 1993 | 11 |
| 12 | Phenotype and counseling in lacrimo-auriculo-dento-digital (LADD) syndrome. | 1993 | 7 |
| 13 | 1992 | 120 | |
| 14 | 1991 | 24 | |
| 15 | Sex-specific testosterone and FSH concentrations in amniotic fluids of mid-pregnancy. | 1977 | 3 |
| 16 | Genetik erblicher Syndrome und Missbildungen : Wörterbuch für die Familienberatung | 1976 | 4 |
| 17 | [Chromosome findings in melanoma cells]. | 1970 | 0 |
| 18 | Hereditary nephritis witj h perceptive deafness (Alport's syndrome). | 1969 | 1 |
| 19 | 1968 | 0 | |
| 20 | 1964 | 1 |
About Regine Witköwski
Regine Witköwski is a scholar working on Genetics, Genetics, Developmental Biology, Clinical Biochemistry and Cancer Research, 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), DNA Repair Mechanisms (3 papers), Metabolism and Genetic Disorders (3 papers), Microtubule and mitosis dynamics (3 papers) and Digestive system and related health (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 Ried, Thomas Cremer, Evelin Schröck and Stanislas du Manoir. 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.