Jan Murken
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 32
- Genomic variations and chromosomal abnormalities 19
- Genetics and Neurodevelopmental Disorders 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
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- Sexual Differentiation and Disorders 4
- RNA modifications and cancer 3
- Congenital heart defects research 3
- Co-authors
- Thomas Meitinger (12 shared papers)S. Stengel‐Rutkowski (8 shared papers)Simone Schuffenhauer (11 shared papers)Jon Stene (4 shared papers)Alfons Meindl (2 shared papers)Peer Bork (1 shared paper)Martina Haasemann (1 shared paper)Chris Sander (1 shared paper)
- Journals
- Human Genetics (8 papers)European Journal of Pediatrics (7 papers)European Journal of Human Genetics (2 papers)Journal of Medical Genetics (2 papers)Clinical Genetics (2 papers)
- Partner nations
- GermanyUnited KingdomDenmark
In The Last Decade
Jan Murken
51 papers receiving 1.0k citations
Peers
Comparison fields: 5 of 84
- Genetics 633
- Pediatrics, Perinatology and Child Health 265
- Developmental Biology 22
- Molecular Biology 535
- Reproductive Medicine 63
Countries citing papers authored by Jan Murken
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
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-authors
The 25 scholars most cited alongside Jan Murken, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 51 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1993 | 146 | |
| 2 | 2001 | 82 | |
| 3 | 1990 | 76 | |
| 4 | 1999 | 72 | |
| 5 | 1977 | 68 | |
| 6 | 1981 | 66 | |
| 7 | 1998 | 64 | |
| 8 | Definitive localization of X-linked Kallman syndrome (hypogonadotropic hypogonadism and anosmia) to Xp22.3: close linkage to the hypervariable repeat sequence CRI-S232. | 1990 | 53 |
| 9 | 1981 | 44 | |
| 10 | 1999 | 39 | |
| 11 | 1997 | 33 | |
| 12 | 1970 | 32 | |
| 13 | 1979 | 27 | |
| 14 | 1970 | 27 | |
| 15 | DiGeorge syndrome and partial monosomy 10p: case report and review. | 1995 | 23 |
| 16 | 1974 | 19 | |
| 17 | 1994 | 16 | |
| 18 | 1989 | 16 | |
| 19 | 2001 | 16 | |
| 20 | 1981 | 15 |
About Jan Murken
Jan Murken is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Genetics, having authored 51 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (19 papers), Prenatal Screening and Diagnostics (9 papers), Chromosomal and Genetic Variations (6 papers), Genetics and Neurodevelopmental Disorders (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Sexual Differentiation and Disorders (4 papers), RNA modifications and cancer (3 papers) and Congenital heart defects research (3 papers). The work is most often cited by research in Genetics (633 citations), Pediatrics, Perinatology and Child Health (265 citations), Developmental Biology (22 citations), Molecular Biology (535 citations) and Reproductive Medicine (63 citations). Jan Murken has collaborated with scholars based in Germany, United Kingdom and Denmark. Frequent co-authors include Thomas Meitinger, S. Stengel‐Rutkowski, Simone Schuffenhauer, Jon Stene, Alfons Meindl, Peer Bork, Martina Haasemann, Chris Sander, Burkhard Rost and A. Rodewald. Their work appears in journals such as Human Genetics, European Journal of Pediatrics, European Journal of Human Genetics, Journal of Medical Genetics 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.