R. Hanke

407 total citations
19 papers, 356 citations indexed

About

R. Hanke is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, R. Hanke has authored 19 papers receiving a total of 356 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Genetics. Recurrent topics in R. Hanke's work include Muscle Physiology and Disorders (10 papers), Neurogenetic and Muscular Disorders Research (6 papers) and RNA modifications and cancer (3 papers). R. Hanke is often cited by papers focused on Muscle Physiology and Disorders (10 papers), Neurogenetic and Muscular Disorders Research (6 papers) and RNA modifications and cancer (3 papers). R. Hanke collaborates with scholars based in Germany, Australia and United Kingdom. R. Hanke's co-authors include Astrid Speer, Uwe Lenk, Hannelore Thiele, Andreas Speer, Katrin Wenzel, Anneke C. Blackburn, Christiane Gläser, Klaus Rohde, Gert Baumann and F. X. Kleber and has published in prestigious journals such as Nucleic Acids Research, Analytical Biochemistry and Human Molecular Genetics.

In The Last Decade

R. Hanke

19 papers receiving 351 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
R. Hanke Germany 10 256 67 66 60 47 19 356
Margherita Verardo Italy 12 316 1.2× 62 0.9× 60 0.9× 39 0.7× 21 0.4× 20 442
Annette Düwel Spain 10 397 1.6× 43 0.6× 43 0.7× 92 1.5× 20 0.4× 13 575
Suna Önengüt United States 11 396 1.5× 52 0.8× 31 0.5× 120 2.0× 6 0.1× 11 551
Yalda Nilipour Iran 12 219 0.9× 71 1.1× 64 1.0× 68 1.1× 10 0.2× 61 426
Loïc Van Den Berghe France 13 275 1.1× 27 0.4× 32 0.5× 37 0.6× 32 0.7× 21 461
Ilana Talior‐Volodarsky Canada 10 237 0.9× 61 0.9× 77 1.2× 30 0.5× 63 1.3× 12 448
Martin A. Haagmans Netherlands 7 157 0.6× 41 0.6× 28 0.4× 43 0.7× 17 0.4× 11 301
Ying Zhang Chen Japan 7 159 0.6× 26 0.4× 27 0.4× 49 0.8× 11 0.2× 7 313
Andriani Margariti United Kingdom 7 265 1.0× 56 0.8× 30 0.5× 19 0.3× 23 0.5× 7 404
Robyn E. Rennick Australia 8 157 0.6× 47 0.7× 59 0.9× 32 0.5× 72 1.5× 9 386

Countries citing papers authored by R. Hanke

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of R. Hanke

This figure shows the co-authorship network connecting the top 25 collaborators of R. Hanke. A scholar is included among the top collaborators of R. Hanke based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with R. Hanke. R. Hanke is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Sifringer, Marco, Birgit Uhlenberg, R. Hanke, et al.. (2003). Identification of transcripts from a subtraction library which might be responsible for the mild phenotype in an intrafamilially variable course of Duchenne muscular dystrophy. Human Genetics. 114(2). 149–156. 17 indexed citations
2.
Spitzer, E., et al.. (2002). Identification of a new cystic fibrosis transmembrane regulator mutation in a severely affected patient. European Respiratory Journal. 19(2). 374–376. 2 indexed citations
3.
Wenzel, Katrin, Anneke C. Blackburn, R. Hanke, et al.. (1997). Relationship of polymorphisms in the renin-angiotensin system and in E-selectin of patients with early severe coronary heart disease. Journal of Molecular Medicine. 75(1). 57–61. 50 indexed citations
4.
Wenzel, Katrin, R. Hanke, & Astrid Speer. (1994). Polymorphism in the human E-selectin gene detected by PCR-SSCP. Human Genetics. 94(4). 452–3. 37 indexed citations
5.
Lenk, Uwe, R. Hanke, & Andreas Speer. (1994). Carrier detection in DMD families with point mutations, using PCR-SSCP and direct sequencing. Neuromuscular Disorders. 4(5-6). 411–418. 12 indexed citations
6.
Lenk, Uwe, R. Hanke, Hannelore Thiele, & Astrid Speer. (1993). Point mutations at the carboxy terminus of the human dystrophin gene: implications for an association with mental retardation in DMD patients. Human Molecular Genetics. 2(11). 1877–1881. 102 indexed citations
7.
8.
Lenk, Uwe, et al.. (1993). Non-isotopic analysis of single strand conformation polymorphism (SSCP) in the exon 13 region of the human dystrophin gene.. Journal of Medical Genetics. 30(11). 951–954. 13 indexed citations
9.
Lenk, Uwe, et al.. (1993). Alternative splicing of dystrophin mRNA complicates carrier determination: report of a DMD family.. Journal of Medical Genetics. 30(3). 206–209. 6 indexed citations
10.
Speer, Andreas, R. Hanke, K. Wulff, et al.. (1990). Deletion analysis of DMD/BMD families from the German Democratic Republic and selected regions of Czechoslovakia and Hungary.. Journal of Medical Genetics. 27(11). 679–682. 4 indexed citations
11.
Speer, Andreas, et al.. (1989). DNA amplification of a further exon of Duchenne muscular dystrophy locus increase possibilities for deletion screening. Nucleic Acids Research. 17(12). 4892–4892. 11 indexed citations
12.
Speer, Andreas, R. Hanke, S. M. Forrest, et al.. (1989). Possibilities and limitation of prenatal diagnosis and carrier determination for Duchenne and Becker muscular dystrophy using cDNA probes.. Journal of Medical Genetics. 26(1). 1–5. 15 indexed citations
13.
14.
Speer, Andreas, et al.. (1986). Prenatal diagnosis of classical phenylketonuria by linked restriction fragment length polymorphism analysis. Prenatal Diagnosis. 6(6). 447–450. 7 indexed citations
15.
Speer, Andreas, K E Davies, R. Hanke, et al.. (1986). Possibilities and problems in genomic diagnosis of Duchenne muscular dystrophy with molecular probes.. PubMed. 45(7). K19–27. 2 indexed citations
16.
17.
Speer, Andreas, et al.. (1986). 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.. PubMed. 29(6). 491–5. 17 indexed citations
18.
Davies, Kay E., Andreas Speer, F. H. Herrmann, et al.. (1985). Human X chromosome markers and Duchenne muscular dystrophy. Nucleic Acids Research. 13(10). 3419–3426. 48 indexed citations
19.
Speer, Andreas, et al.. (1979). Pre-mRNA from erythroid enriched bone marrow cells of the rabbit.. PubMed. 38(11-12). 1555–63. 1 indexed citations

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.

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