Rainer Fislage

494 total citations
14 papers, 312 citations indexed

About

Rainer Fislage is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Genetics. According to data from OpenAlex, Rainer Fislage has authored 14 papers receiving a total of 312 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Pulmonary and Respiratory Medicine and 3 papers in Genetics. Recurrent topics in Rainer Fislage's work include Cystic Fibrosis Research Advances (5 papers), RNA and protein synthesis mechanisms (4 papers) and RNA modifications and cancer (2 papers). Rainer Fislage is often cited by papers focused on Cystic Fibrosis Research Advances (5 papers), RNA and protein synthesis mechanisms (4 papers) and RNA modifications and cancer (2 papers). Rainer Fislage collaborates with scholars based in Germany. Rainer Fislage's co-authors include Brigitte Wulf, Thomas Neumann, Burkhard Tümmler, Maria Wendt, Thilo Dörk, Burkhard TÃ ⁄ mmler, Meinhard Hahn, Alfred Pingoud, Walter Sierralta and Frauke Mekus and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Human Molecular Genetics.

In The Last Decade

Rainer Fislage

14 papers receiving 299 citations

Peers

Countries citing papers authored by Rainer Fislage

Since Specialization

Citations

This map shows the geographic impact of Rainer Fislage'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 Rainer Fislage with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rainer Fislage more than expected).

Fields of papers citing papers by Rainer Fislage

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rainer Fislage. 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 Rainer Fislage. The network helps show where Rainer Fislage may publish in the future.

Co-authorship network of co-authors of Rainer Fislage

This figure shows the co-authorship network connecting the top 25 collaborators of Rainer Fislage. A scholar is included among the top collaborators of Rainer Fislage 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 Rainer Fislage. Rainer Fislage is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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14 of 14 papers shown

#	Work	Indexed citations
1	Detection of nucleic acid sequences from bacterial species with molecular genetic methods 2000 ·Transfusion Science ·Eduard K. Petershofen, Rainer Fislage, René Fáber, (unknown), W. Kurt Roth, Erhard Seifried	20
2	Effect of Surface Modifications of Intraocular Lenses on the Adherence of Staphylococcus epidermidis 1998 ·Zentralblatt für Bakteriologie ·(unknown), (unknown), Rainer Fislage, (unknown), Rudolf Guthoff	18
3	Differential display approach to quantitation of environmental stimuli on bacterial gene expression (minireview) 1998 ·Electrophoresis ·Rainer Fislage	12
4	Primer design for a prokaryotic differential display RT-PCR 1997 ·Nucleic Acids Research ·Rainer Fislage, (unknown), (unknown), Maria Wendt, (unknown)	55
5	Localization of the Iodomycin Binding Site in Hamster P-glycoprotein 1997 ·Journal of Biological Chemistry ·(unknown), Hubert Thole, (unknown), (unknown), Manfred Raida, Rainer Fislage, Burkhard Tümmler	32
6	Comparison of type IV-pilin genes ofPseudomonas aeruginosaof various habitats has uncovered a novel unusual sequence 1995 ·FEMS Microbiology Letters ·(unknown), Rainer Fislage, Walter Sierralta, Burkhard TÃ ⁄ mmler, (unknown)	28
7	Polymorphism of the pentanucleotide repeat d(AAAAT) within intron 1 of the human tumor suppressor gene p53 (17p13.1) 1995 ·Human Genetics ·Meinhard Hahn, Rainer Fislage, Alfred Pingoud	18
8	[Theory and practice of macrorestriction analysis for the clonal analysis of pathogens]. 1995 ·PubMed ·Ute Römling, Rainer Fislage, (unknown)	2
9	Detection of more than 50 different CFTR mutations in a large group of German cystic fibrosis patients 1994 ·Human Genetics ·Thilo Dörk, Frauke Mekus, Karen Schmidt, (unknown), Rainer Fislage, (unknown), (unknown), Thomas Neumann, Nanette Kälin, Ulrich Wulbrand, Brigitte Wulf, H. von der Hardt, (unknown), Burkhard Tümmler	71
10	Exon 9 of the CFTR gene: splice site haplotypes and cystic fibrosis mutations 1994 ·Human Genetics ·(unknown), Rainer Fislage, Thomas Neumann, Brigitte Wulf, (unknown)	41
11	Cystic fibrosis: the impact of analytical technology for genotype-phenotype studies 1993 ·Clinica Chimica Acta ·Burkhard Tümmler, Thilo Dörk, (unknown), Rainer Fislage, Nanette Kälin, Thomas Neumann, Ulrich Wulbrand, Brigitte Wulf, Gratiana Steinkamp, H. von der Hardt	3
12	Complex mutation 4114 ATA → TT in Exon 22 of the cystic fibrosis gene CFTR 1993 ·Human Mutation ·Thilo Dörk, Rainer Fislage, Burkhard Tümmler	2
13	Severe splice site mutation preceding exon 9 of the CFTR gene 1993 ·Human Molecular Genetics ·Thilo Dörk, Rainer Fislage, (unknown), Burkhard Tümmler	5
14	Primary sequence of the human ribosomal protein L37a 1992 ·Nucleic Acids Research ·(unknown), Rainer Fislage, Burkhard Tümmler	5

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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