Peter Seranski

1.2k total citations
8 papers, 208 citations indexed

About

Peter Seranski is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Peter Seranski has authored 8 papers receiving a total of 208 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Genetics. Recurrent topics in Peter Seranski's work include RNA Research and Splicing (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Sarcoma Diagnosis and Treatment (2 papers). Peter Seranski is often cited by papers focused on RNA Research and Splicing (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Sarcoma Diagnosis and Treatment (2 papers). Peter Seranski collaborates with scholars based in Germany, United States and United Kingdom. Peter Seranski's co-authors include Annemarie Poustka, Klaus K. Wilgenbus, Steffen Hennig, Uwe Radelof, Richard Reinhardt, Wolfram Scheurlen, Céline Hoff, Nina S. Heiss, Peter Lichter and Niels Sörensen and has published in prestigious journals such as Nucleic Acids Research, Gene and Genomics.

In The Last Decade

Peter Seranski

8 papers receiving 204 citations

Peers

Peter Seranski

MB

GENET

CR

PFM

Martje Tönjes Germany

Carmelo Laganà Italy

Alain Zasadzinski France

Julie Skotte Denmark

J.G. Dauwerse Netherlands

Yongji Wu China

Asif H. Chowdhury United States

Katarzyna Borg Poland

Martina Kreiß‐Nachtsheim Germany

V Murday United Kingdom

Martje Tönjes Germany

Peter Seranski

381 ×2.6

MB

63 ×0.7

GENET

26 ×0.5

GENET

49 ×2.1

CR

14 ×0.7

PFM

Citations per year, relative to Peter Seranski Peter Seranski (= 1×) peers Martje Tönjes

Countries citing papers authored by Peter Seranski

Since Specialization

Citations

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

Fields of papers citing papers by Peter Seranski

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Peter Seranski

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

All Works

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8 of 8 papers shown

1.

Steinfath, Markus, Peter Seranski, Surjit Singh, et al.. (2002). Evidence for a spontaneous C1840-T mutation in the RYR1 gene after DNA fingerprinting in a malignant hyperthermia susceptible family. Naunyn-Schmiedeberg s Archives of Pharmacology. 366(4). 372–375. 4 indexed citations

2.

Seranski, Peter, Céline Hoff, Uwe Radelof, et al.. (2001). RAI1 is a novel polyglutamine encoding gene that is deleted in Smith–Magenis syndrome patients. Gene. 270(1-2). 69–76. 29 indexed citations

3.

Hoff, Céline, Peter Seranski, Jan Mollenhauer, et al.. (2000). Physical and Transcriptional Mapping of the 17p13.3 Region That Is Frequently Deleted in Human Cancer. Genomics. 70(1). 26–33. 15 indexed citations

4.

Seranski, Peter, Nina S. Heiss, Sophie Dhorne‐Pollet, et al.. (1999). Transcription Mapping in a Medulloblastoma Breakpoint Interval and Smith–Magenis Syndrome Candidate Region: Identification of 53 Transcriptional Units and New Candidate Genes. Genomics. 56(1). 1–11. 24 indexed citations

5.

Scheurlen, Wolfram, Georg C. Schwabe, Peter Seranski, et al.. (1999). Mapping of the breakpoints on the short arm of chromosome 17 in neoplasms with an i(17q). Genes Chromosomes and Cancer. 25(3). 230–240. 35 indexed citations

6.

Radelof, Uwe, Steffen Hennig, Juliane Ramser, et al.. (1998). Preselection of shotgun clones by oligonucleotide fingerprinting: an efficient and high throughput strategy to reduce redundancy in large-scale sequencing projects. Nucleic Acids Research. 26(23). 5358–5364. 29 indexed citations

7.

Wilgenbus, Klaus K., Peter Seranski, Angela Brown, et al.. (1997). Molecular Characterization of a Genetically Unstable Region Containing the SMS Critical Area and a Breakpoint Cluster for Human PNETs. Genomics. 42(1). 1–10. 25 indexed citations

8.

Scheurlen, Wolfram, Peter Seranski, Joachim Kühl, et al.. (1997). High-resolution deletion mapping of chromosome arm 17p in childhood primitive neuroectodermal tumors reveals a common chromosomal disruption within the Smith-Magenis region, an unstable region in chromosome band 17p11.2. Genes Chromosomes and Cancer. 18(1). 50–58. 47 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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