David E. Mutton
Impact in
-
- Prenatal Screening and Diagnostics
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic Syndromes and Imprinting
Papers in
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- Prenatal Screening and Diagnostics 22
- Genetics 13
- Genomic variations and chromosomal abnormalities 8
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Genetic Syndromes and Imprinting 4
- Co-authors
- Eva D. Alberman (19 shared papers)Joan K. Morris (12 shared papers)E B Hook (2 shared papers)Matteo Adinolfí (1 shared paper)Peter Johnson (1 shared paper)Martin Bobrow (7 shared papers)Paul Emanuel Polani (2 shared papers)Angela Elvira Covone (1 shared paper)
- Journals
- Journal of Medical Screening (5 papers)Prenatal Diagnosis (5 papers)The Lancet (3 papers)Archives of Disease in Childhood (2 papers)Clinical Genetics (2 papers)
- Partner nations
- United KingdomUnited StatesCanada
In The Last Decade
David E. Mutton
44 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 105
- Pediatrics, Perinatology and Child Health 910
- Genetics 560
- Obstetrics and Gynecology 92
- Developmental Biology 26
- Public Health, Environmental and Occupational Health 200
Countries citing papers authored by David E. Mutton
This map shows the geographic impact of David E. Mutton'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 David E. Mutton with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David E. Mutton more than expected).
Fields of papers citing papers by David E. Mutton
This network shows the impact of papers produced by David E. Mutton. 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 David E. Mutton. The network helps show where David E. Mutton may publish in the future.
Co-authors
The 25 scholars most cited alongside David E. Mutton, 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 46 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2002 | 228 | |
| 2 | 1984 | 166 | |
| 3 | 1996 | 141 | |
| 4 | 2006 | 99 | |
| 5 | 2003 | 91 | |
| 6 | 1971 | 83 | |
| 7 | The natural history of Down syndrome conceptuses diagnosed prenatally that are not electively terminated. | 1995 | 56 |
| 8 | 2005 | 55 | |
| 9 | 1963 | 53 | |
| 10 | 2005 | 50 | |
| 11 | 1991 | 49 | |
| 12 | 1962 | 49 | |
| 13 | 2005 | 47 | |
| 14 | 2012 | 47 | |
| 15 | 1973 | 41 | |
| 16 | 1973 | 37 | |
| 17 | 1993 | 35 | |
| 18 | 2003 | 30 | |
| 19 | 2012 | 30 | |
| 20 | 1998 | 29 |
About David E. Mutton
David E. Mutton is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Health Information Management, Plant Science and Obstetrics and Gynecology, having authored 46 papers that have together received 1.6k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (22 papers), Genomic variations and chromosomal abnormalities (8 papers), Chromosomal and Genetic Variations (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Genetic Syndromes and Imprinting (4 papers), Sexual Differentiation and Disorders (3 papers), Gestational Diabetes Research and Management (2 papers) and Medical Coding and Health Information (2 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (910 citations), Genetics (560 citations), Obstetrics and Gynecology (92 citations), Developmental Biology (26 citations) and Public Health, Environmental and Occupational Health (200 citations). David E. Mutton has collaborated with scholars based in United Kingdom, United States and Canada. Frequent co-authors include Eva D. Alberman, Joan K. Morris, E B Hook, Matteo Adinolfí, Peter Johnson, Martin Bobrow, Paul Emanuel Polani, Angela Elvira Covone, Nicholas Wald and George M. Savva. Their work appears in journals such as Journal of Medical Screening, Prenatal Diagnosis, The Lancet, Archives of Disease in Childhood 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.