Jonathan J. Waters
Impact in
-
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
- Hematology top 10%
- Acute Myeloid Leukemia Research
Papers in
-
- Prenatal Screening and Diagnostics 14
- Genetics 12
- Genomic variations and chromosomal abnormalities 11
- Genetics and Neurodevelopmental Disorders 3
- Co-authors
- Lyn S. Chitty (3 shared papers)A. Förster (1 shared paper)Richard Baer (1 shared paper)E Nacheva (1 shared paper)Terence H. Rabbitts (1 shared paper)Isabelle Lavenir (1 shared paper)Thomas Boehm (1 shared paper)Caroline Mackie Ogilvie (4 shared papers)
- Journals
- Prenatal Diagnosis (8 papers)The EMBO Journal (2 papers)European Journal of Medical Genetics (1 paper)Pediatric Nephrology (1 paper)Genes Chromosomes and Cancer (1 paper)
- Partner nations
- United KingdomUnited StatesAustralia
In The Last Decade
Jonathan J. Waters
32 papers receiving 956 citations
Peers
Comparison fields: 5 of 64
- Pediatrics, Perinatology and Child Health 395
- Hematology 120
- Genetics 278
- Genetics 54
- Immunology 106
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 | 25 | |
| 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 Pediatrics, Perinatology and Child Health, Genetics, Molecular Biology, Plant Science and Oncology, having authored 32 papers that have together received 1.0k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (14 papers), Genomic variations and chromosomal abnormalities (11 papers), Genetics and Neurodevelopmental Disorders (3 papers), Chromosomal and Genetic Variations (3 papers), Genomics and Chromatin Dynamics (3 papers), Alzheimer's disease research and treatments (2 papers), Congenital heart defects research (2 papers) and Lung Cancer Research Studies (2 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (395 citations), Hematology (120 citations), Genetics (278 citations), Genetics (54 citations) and Immunology (106 citations). Jonathan J. Waters has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Lyn S. Chitty, A. Förster, Richard Baer, E Nacheva, Terence H. Rabbitts, Isabelle Lavenir, Thomas Boehm, Caroline Mackie Ogilvie, Pamela Rabbitts and A. Caine. Their work appears in journals such as Prenatal Diagnosis, The EMBO Journal, European Journal of Medical Genetics, Pediatric Nephrology and Genes Chromosomes and Cancer.
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.