R. Hanke
Impact in
- Immunology and Allergy top 10%
- Cell Adhesion Molecules Research
-
- Metabolism and Genetic Disorders
Papers in
-
- Muscle Physiology and Disorders 10
- RNA modifications and cancer 3
- RNA Research and Splicing 3
- Congenital heart defects research 2
- Genetics 6
- Neurogenetic and Muscular Disorders Research 6
- Co-authors
- Astrid Speer (3 shared papers)Uwe Lenk (4 shared papers)Hannelore Thiele (1 shared paper)Andreas Speer (15 shared papers)Katrin Wenzel (2 shared papers)F. X. Kleber (1 shared paper)Christiane Gläser (1 shared paper)Klaus Rohde (1 shared paper)
- Journals
- Journal of Medical Genetics (4 papers)Human Genetics (2 papers)Nucleic Acids Research (2 papers)Prenatal Diagnosis (2 papers)Clinical Genetics (1 paper)
- Partner nations
- GermanyAustraliaUnited Kingdom
In The Last Decade
R. Hanke
19 papers receiving 351 citations
Peers
Comparison fields: 5 of 57
- Immunology and Allergy 47
- Clinical Biochemistry 33
- Aging 8
- Molecular Biology 256
- Genetics 38
Countries citing papers authored by R. Hanke
This map shows the geographic impact of R. Hanke'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 R. Hanke with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites R. Hanke more than expected).
Fields of papers citing papers by R. Hanke
This network shows the impact of papers produced by R. Hanke. 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 R. Hanke. The network helps show where R. Hanke may publish in the future.
Co-authors
The 25 scholars most cited alongside R. Hanke, 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 | 1993 | 102 | |
| 2 | 1997 | 50 | |
| 3 | 1985 | 48 | |
| 4 | 1994 | 37 | |
| 5 | 2003 | 17 | |
| 6 | Typing of families with classical phenylketonuria using three alleles of the Hindiii linked restriction fragment polymorphism, detectable with a phenylalanine hydroxylase cDNA probe. Family typing for PKU by linked HindIII RFLP. | 1986 | 17 |
| 7 | 1989 | 15 | |
| 8 | 1993 | 13 | |
| 9 | 1994 | 12 | |
| 10 | 1989 | 11 | |
| 11 | 1986 | 9 | |
| 12 | 1986 | 7 | |
| 13 | 1993 | 6 | |
| 14 | 1990 | 4 | |
| 15 | 2002 | 2 | |
| 16 | 1987 | 2 | |
| 17 | Possibilities and problems in genomic diagnosis of Duchenne muscular dystrophy with molecular probes. | 1986 | 2 |
| 18 | 1993 | 1 | |
| 19 | Pre-mRNA from erythroid enriched bone marrow cells of the rabbit. | 1979 | 1 |
About R. Hanke
R. Hanke is a scholar working on Molecular Biology, Genetics, Genetics, Physiology and Clinical Biochemistry, having authored 19 papers that have together received 356 indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (10 papers), Neurogenetic and Muscular Disorders Research (6 papers), Metabolism and Genetic Disorders (3 papers), RNA modifications and cancer (3 papers), RNA Research and Splicing (3 papers), Telomeres, Telomerase, and Senescence (2 papers), Congenital heart defects research (2 papers) and Folate and B Vitamins Research (2 papers). The work is most often cited by research in Immunology and Allergy (47 citations), Clinical Biochemistry (33 citations), Aging (8 citations), Molecular Biology (256 citations) and Genetics (38 citations). R. Hanke has collaborated with scholars based in Germany, Australia and United Kingdom. Frequent co-authors include Astrid Speer, Uwe Lenk, Hannelore Thiele, Andreas Speer, Katrin Wenzel, F. X. Kleber, Christiane Gläser, Klaus Rohde, Stephan B. Felix and Anneke C. Blackburn. Their work appears in journals such as Journal of Medical Genetics, Human Genetics, Nucleic Acids Research, Prenatal Diagnosis and Clinical Genetics.
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.