Jonathan J. Waters
Impact in
-
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 16
- Genomic variations and chromosomal abnormalities 15
- Genetics and Neurodevelopmental Disorders 3
-
- Prenatal Screening and Diagnostics 14
- Fetal and Pediatric Neurological Disorders 3
- Co-authors
- Lyn S. Chitty (3 shared papers)E Nacheva (1 shared paper)Thomas Boehm (1 shared paper)A. Förster (1 shared paper)Isabelle Lavenir (1 shared paper)Richard Baer (1 shared paper)Terence H. Rabbitts (1 shared paper)Caroline Mackie Ogilvie (4 shared papers)
- Journals
- Prenatal Diagnosis (8 papers)The EMBO Journal (2 papers)Cellular Reprogramming (1 paper)British Journal of Haematology (1 paper)Journal of Cellular Biochemistry (1 paper)
- Partner nations
- United KingdomUnited StatesAustralia
In The Last Decade
Jonathan J. Waters
32 papers receiving 955 citations
Peers
Comparison fields: 5 of 67
- Pediatrics, Perinatology and Child Health 410
- Genetics 439
- Hematology 127
- Genetics 58
- Molecular Biology 362
Countries citing papers authored by Jonathan J. Waters
This map shows the geographic impact of Jonathan J. Waters'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 Jonathan J. Waters with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jonathan J. Waters more than expected).
Fields of papers citing papers by Jonathan J. Waters
This network shows the impact of papers produced by Jonathan J. Waters. 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 Jonathan J. Waters. The network helps show where Jonathan J. Waters may publish in the future.
Co-authors
The 25 scholars most cited alongside Jonathan J. Waters, 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 32 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1988 | 200 | |
| 2 | Characterization of cryptic rearrangements and variant translocations in acute promyelocytic leukemia. | 1997 | 101 |
| 3 | 2005 | 91 | |
| 4 | 2010 | 57 | |
| 5 | 2006 | 53 | |
| 6 | 2005 | 51 | |
| 7 | 1989 | 51 | |
| 8 | 1991 | 48 | |
| 9 | 2004 | 39 | |
| 10 | 1987 | 37 | |
| 11 | 1988 | 29 | |
| 12 | 2007 | 27 | |
| 13 | 2012 | 24 | |
| 14 | 2011 | 24 | |
| 15 | 1996 | 21 | |
| 16 | 2003 | 19 | |
| 17 | 1999 | 19 | |
| 18 | 2006 | 14 | |
| 19 | 1990 | 12 | |
| 20 | 1990 | 12 |
About Jonathan J. Waters
Jonathan J. Waters is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Infectious Diseases and Plant Science, having authored 32 papers that have together received 1.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (15 papers), Prenatal Screening and Diagnostics (14 papers), Parvovirus B19 Infection Studies (5 papers), Genomics and Chromatin Dynamics (3 papers), Chromosomal and Genetic Variations (3 papers), Fetal and Pediatric Neurological Disorders (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Congenital heart defects research (3 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (410 citations), Genetics (439 citations), Hematology (127 citations), Genetics (58 citations) and Molecular Biology (362 citations). Jonathan J. Waters has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Lyn S. Chitty, E Nacheva, Thomas Boehm, A. Förster, Isabelle Lavenir, Richard Baer, Terence H. Rabbitts, Caroline Mackie Ogilvie, Pamela Rabbitts and John A. Crolla. Their work appears in journals such as Prenatal Diagnosis, The EMBO Journal, Cellular Reprogramming, British Journal of Haematology and Journal of Cellular Biochemistry.
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.