Jon Stene
Impact in
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- Prenatal Screening and Diagnostics
- Assisted Reproductive Technology and Twin Pregnancy
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetic Associations and Epidemiology
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomics and Rare Diseases
Papers in
- Genetics 15
- Genomic variations and chromosomal abnormalities 12
- Forensic and Genetic Research 2
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- Prenatal Screening and Diagnostics 12
- Co-authors
- Eeva Stene (9 shared papers)S. Stengel‐Rutkowski (10 shared papers)Newton E. Morton (1 shared paper)Margareta Mikkelsen (7 shared papers)Jan Murken (4 shared papers)Margaret A. Lennox‐Buchthal (1 shared paper)Alina T. Midro (1 shared paper)E Frantzen (1 shared paper)
- Journals
- Annals of Human Genetics (12 papers)Biometrics (7 papers)Human Genetics (7 papers)Human Heredity (3 papers)Clinical Genetics (3 papers)
- Partner nations
- DenmarkGermanyUnited States
In The Last Decade
Jon Stene
47 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 101
- Pediatrics, Perinatology and Child Health 650
- Genetics 739
- Developmental Biology 32
- Statistics and Probability 67
- Plant Science 272
Countries citing papers authored by Jon Stene
This map shows the geographic impact of Jon Stene'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 Jon Stene with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jon Stene more than expected).
Fields of papers citing papers by Jon Stene
This network shows the impact of papers produced by Jon Stene. 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 Jon Stene. The network helps show where Jon Stene may publish in the future.
Co-authors
The 25 scholars most cited alongside Jon Stene, 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 49 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1983 | 186 | |
| 2 | 1977 | 105 | |
| 3 | 1970 | 95 | |
| 4 | 1984 | 84 | |
| 5 | 1976 | 77 | |
| 6 | 1992 | 72 | |
| 7 | 1981 | 71 | |
| 8 | 1977 | 69 | |
| 9 | 1970 | 60 | |
| 10 | 1979 | 58 | |
| 11 | 1984 | 51 | |
| 12 | 1981 | 44 | |
| 13 | 1977 | 39 | |
| 14 | 1987 | 36 | |
| 15 | 1986 | 35 | |
| 16 | 1977 | 33 | |
| 17 | 1970 | 30 | |
| 18 | 1982 | 29 | |
| 19 | 1977 | 28 | |
| 20 | 1984 | 27 |
About Jon Stene
Jon Stene is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Statistics and Probability and Plant Science, having authored 49 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (12 papers), Demographic Trends and Gender Preferences (3 papers), Statistical Methods and Bayesian Inference (3 papers), Chromosomal and Genetic Variations (3 papers), Forensic and Genetic Research (2 papers), Metabolism and Genetic Disorders (2 papers) and Insurance, Mortality, Demography, Risk Management (2 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (650 citations), Genetics (739 citations), Developmental Biology (32 citations), Statistics and Probability (67 citations) and Plant Science (272 citations). Jon Stene has collaborated with scholars based in Denmark, Germany and United States. Frequent co-authors include Eeva Stene, S. Stengel‐Rutkowski, Newton E. Morton, Margareta Mikkelsen, Jan Murken, Margaret A. Lennox‐Buchthal, Alina T. Midro, E Frantzen, Erik Petersen and A. Rodewald. Their work appears in journals such as Annals of Human Genetics, Biometrics, Human Genetics, Human Heredity 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.