Jón J. Jónsson
Impact in
- Genetics top 5%
- Genetic and Kidney Cyst Diseases
- Genetic Syndromes and Imprinting
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- Renal and related cancers
- Microbial Metabolic Engineering and Bioproduction
- Peroxisome Proliferator-Activated Receptors
Papers in
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- DNA and Nucleic Acid Chemistry 4
- Renal and related cancers 3
- RNA Research and Splicing 3
- Genetics 20
- BRCA gene mutations in cancer 6
- Genomic variations and chromosomal abnormalities 4
- Co-authors
- Ines Thiele (2 shared papers)Swagatika Sahoo (2 shared papers)Martin I. Sigurðsson (4 shared papers)Hans T. Björnsson (5 shared papers)Maike K. Aurich (1 shared paper)Albert V. Smith (3 shared papers)Francesca Vitelli (3 shared papers)Alessandra Renieri (3 shared papers)
- Journals
- Nucleic Acids Research (3 papers)Gene (2 papers)European Journal of Human Genetics (2 papers)Genomics (2 papers)Apmis (1 paper)
- Partner nations
- IcelandUnited StatesUnited Kingdom
In The Last Decade
Jón J. Jónsson
45 papers receiving 989 citations
Peers
Comparison fields: 5 of 101
- Genetics 351
- Molecular Biology 561
- Clinical Biochemistry 44
- Biochemistry 43
- Pediatrics, Perinatology and Child Health 93
Countries citing papers authored by Jón J. Jónsson
This map shows the geographic impact of Jón J. Jónsson'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 Jón J. Jónsson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jón J. Jónsson more than expected).
Fields of papers citing papers by Jón J. Jónsson
This network shows the impact of papers produced by Jón J. Jónsson. 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 Jón J. Jónsson. The network helps show where Jón J. Jónsson may publish in the future.
Co-authors
The 25 scholars most cited alongside Jón J. Jónsson, 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 47 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 162 | |
| 2 | 1998 | 94 | |
| 3 | 2014 | 72 | |
| 4 | 1992 | 64 | |
| 5 | 2012 | 49 | |
| 6 | 2009 | 49 | |
| 7 | 1991 | 39 | |
| 8 | 1998 | 38 | |
| 9 | Molecular diagnosis of mucopolysaccharidosis type II (Hunter syndrome) by automated sequencing and computer-assisted interpretation: toward mutation mapping of the iduronate-2-sulfatase gene. | 1995 | 37 |
| 10 | 1996 | 36 | |
| 11 | Molecular characterization of patients with 18q23 deletions. | 1997 | 32 |
| 12 | 2006 | 30 | |
| 13 | 1999 | 26 | |
| 14 | 2010 | 21 | |
| 15 | 2007 | 21 | |
| 16 | 2013 | 19 | |
| 17 | 1995 | 19 | |
| 18 | 2005 | 19 | |
| 19 | 2009 | 17 | |
| 20 | 2010 | 16 |
About Jón J. Jónsson
Jón J. Jónsson is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health and Physiology, having authored 47 papers that have together received 1.0k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (6 papers), Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Chromosomal and Genetic Variations (4 papers), DNA and Nucleic Acid Chemistry (4 papers), Renal and related cancers (3 papers), RNA Research and Splicing (3 papers) and Lysosomal Storage Disorders Research (3 papers). The work is most often cited by research in Genetics (351 citations), Molecular Biology (561 citations), Clinical Biochemistry (44 citations), Biochemistry (43 citations) and Pediatrics, Perinatology and Child Health (93 citations). Jón J. Jónsson has collaborated with scholars based in Iceland, United States and United Kingdom. Frequent co-authors include Ines Thiele, Swagatika Sahoo, Martin I. Sigurðsson, Hans T. Björnsson, Maike K. Aurich, Albert V. Smith, Francesca Vitelli, Alessandra Renieri, Stephen E. Braun and Barbara R. Pober. Their work appears in journals such as Nucleic Acids Research, Gene, European Journal of Human Genetics, Genomics and Apmis.
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.