Jan Murken

3.3k total citations
51 papers, 1.1k citations indexed

About

Jan Murken is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Jan Murken has authored 51 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Genetics, 29 papers in Molecular Biology and 11 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Jan Murken's work include Genomic variations and chromosomal abnormalities (19 papers), Prenatal Screening and Diagnostics (9 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Jan Murken is often cited by papers focused on Genomic variations and chromosomal abnormalities (19 papers), Prenatal Screening and Diagnostics (9 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Jan Murken collaborates with scholars based in Germany, United Kingdom and Denmark. Jan Murken's co-authors include Thomas Meitinger, S. Stengel‐Rutkowski, Simone Schuffenhauer, Jon Stene, Alfons Meindl, Peer Bork, Martina Haasemann, Burkhard Rost, Chris Sander and A. Rodewald and has published in prestigious journals such as The Lancet, Nature Genetics and The American Journal of Human Genetics.

In The Last Decade

Jan Murken

51 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jan Murken Germany 17 633 535 265 261 84 51 1.1k
E. Boyd United Kingdom 22 804 1.3× 623 1.2× 233 0.9× 304 1.2× 35 0.4× 55 1.3k
P Jalbert France 19 1.1k 1.8× 735 1.4× 360 1.4× 263 1.0× 148 1.8× 59 1.7k
R. Sid Wilroy United States 21 778 1.2× 635 1.2× 275 1.0× 167 0.6× 54 0.6× 53 1.3k
Ellen Magenis United States 18 815 1.3× 694 1.3× 191 0.7× 154 0.6× 59 0.7× 31 1.4k
S. Stengel‐Rutkowski Germany 20 835 1.3× 609 1.1× 424 1.6× 253 1.0× 47 0.6× 50 1.3k
Jeanne Meck United States 22 725 1.1× 626 1.2× 380 1.4× 157 0.6× 85 1.0× 57 1.5k
Roberto Ciccone Italy 23 956 1.5× 681 1.3× 283 1.1× 270 1.0× 50 0.6× 51 1.4k
Udo Trautmann Germany 23 1.1k 1.7× 930 1.7× 328 1.2× 331 1.3× 50 0.6× 65 1.7k
Evica Rajcan‐Separovic Canada 24 770 1.2× 775 1.4× 386 1.5× 178 0.7× 71 0.8× 58 1.6k
Andreas Dufke Germany 22 865 1.4× 695 1.3× 351 1.3× 310 1.2× 109 1.3× 60 1.4k

Countries citing papers authored by Jan Murken

Since Specialization
Citations

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

Fields of papers citing papers by Jan Murken

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jan Murken

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

All Works

20 of 20 papers shown
1.
Schmidt, U., Jan Murken, & Volker Klauß. (2008). Wandel der Blindheitsursachen im Kindesalter. Klinische Monatsblätter für Augenheilkunde. 193(11). 457–464. 2 indexed citations
2.
Golla, Astrid, et al.. (2002). MRX42: Two linkage intervals, one in the pericentromeric region and one in Xq26, and the impact for carrier risk estimation. American Journal of Medical Genetics. 107(1). 18–25. 2 indexed citations
3.
Holinski‐Feder, Elke, Waltraut Friedl, Gabriela Möslein, et al.. (2001). DHPLC mutation analysis of the hereditary nonpolyposis colon cancer (HNPCC) genes hMLH1 and hMSH2. Journal of Biochemical and Biophysical Methods. 47(1-2). 21–32. 82 indexed citations
4.
Langer, Sabine, Christine Fauth, Mariano Rocchi, Jan Murken, & Michael R. Speicher. (2001). AcroM fluorescent in situ hybridization analyses of marker chromosomes. Human Genetics. 109(2). 152–158. 16 indexed citations
5.
Uhrig, Sabine, Simone Schuffenhauer, Christine Fauth, et al.. (1999). Multiplex-FISH for Pre- and Postnatal Diagnostic Applications. The American Journal of Human Genetics. 65(2). 448–462. 72 indexed citations
6.
Holinski‐Feder, Elke, Olaf Rittinger, Kerry Baldwin Jedele, et al.. (1999). Nonsyndromic X-linked mental retardation: Mapping of MRX58 to the pericentromeric region. American Journal of Medical Genetics. 86(2). 102–106. 9 indexed citations
7.
Murken, Jan. (1999). Ethische Probleme im Kontext genetischer Beratung und Diagnostik. Der Internist. 40(3). 286–293. 2 indexed citations
8.
Schuffenhauer, Simone, Peter Lichtner, Jan Murken, et al.. (1998). Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2). European Journal of Human Genetics. 6(3). 213–225. 64 indexed citations
9.
Baretton, Gustavo, Michael Müller, Antje Wirtz, Jan Murken, & H Arnholdt. (1998). Numerische Chromosomenaberrationen in Abortmaterial. Der Pathologe. 19(2). 120–128. 7 indexed citations
10.
Jedele, Kerry Baldwin, et al.. (1998). Spinal and bulbar muscular atrophy (SBMA): Somatic stability of an expanded CAG repeat in fetal tissues. Clinical Genetics. 54(2). 148–151. 5 indexed citations
11.
Brandau, Oliver, Gerald Nyakatura, Kerry Baldwin Jedele, et al.. (1998). UHX1 and PCTK1: precise characterisation and localisation within a gene-rich region in Xp11.23 and evaluation as candidate genes for retinal diseases mapped to Xp21.1–p11.2. European Journal of Human Genetics. 6(5). 459–466. 6 indexed citations
12.
Schuffenhauer, Simone, Astrid Golla, Peter Lichtner, et al.. (1996). Craniosynostosis suggestive of Saethre-Chotzen syndrome: Clinical description of a large kindred and exclusion of candidate regions on 7p. American Journal of Medical Genetics. 63(1). 177–184. 14 indexed citations
13.
Schuffenhauer, Simone, et al.. (1996). Interstitial deletion 5p accompanied by dicentric ring formation of the deleted segment resulting in trisomy 5p13-cen. American Journal of Medical Genetics. 65(1). 56–59. 13 indexed citations
14.
Rudolph, Günter, Werner Blum, M. Schöning, et al.. (1994). Growth hormone (GH), insulin‐like growth factors (IGFs), and IGF‐binding protein‐3 (IGFBP‐3) in a child with Proteus syndrome. American Journal of Medical Genetics. 50(2). 204–210. 16 indexed citations
15.
Meitinger, Thomas, Alfons Meindl, Peer Bork, et al.. (1993). Molecular modelling of the Norrie disease protein predicts a cystine knot growth factor tertiary structure. Nature Genetics. 5(4). 376–380. 146 indexed citations
16.
Schuffenhauer, Simone, et al.. (1992). De novo interstitial deletion 16(q12. 1q13) of paternal origin in a 10‐year‐old boy. Clinical Genetics. 42(5). 246–250. 12 indexed citations
17.
Murken, Jan, et al.. (1991). Trisomy 18 in chorionic villus sampling: Problems and consequences. Prenatal Diagnosis. 11(8). 563–567. 10 indexed citations
18.
Meitinger, Thomas, et al.. (1989). Linkage of X-linked retinitis pigmentosa to the hypervariable DNA marker M27? (DXS255). Human Genetics. 81(3). 283–6. 16 indexed citations
19.
Rodewald, A., Astrid Wirtz, Jan Murken, et al.. (1980). A (1;21) balanced translocation in a male with mucopolysaccharidosis type IIIA. Cytogenetic and Genome Research. 27(4). 267–267. 2 indexed citations
20.
Murken, Jan & W. Scholz. (1967). Serologische Klärung der Herkunft der überzähligen X-Chromosomen beim XXXXY-Syndrom. Annals of Hematology. 16(3). 164–168. 8 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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