David Peakman
Impact in
- Hematology top 5%
- Acute Myeloid Leukemia Research
- Hematopoietic Stem Cell Transplantation
- Chronic Myeloid Leukemia Treatments
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Chronic Lymphocytic Leukemia Research
Papers in
- Genetics 13
- Genomic variations and chromosomal abnormalities 10
- Genetic Syndromes and Imprinting 3
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
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- Prenatal Screening and Diagnostics 10
- Co-authors
- Arthur Robinson (19 shared papers)Helvise G. Morse (6 shared papers)Taru Hays (4 shared papers)Frederick Hecht (3 shared papers)Brahma S. Sharma (1 shared paper)F. L. Johnson (1 shared paper)Barbara Rose (2 shared papers)B. Kaiser McCaw (2 shared papers)
- Journals
- Human Genetics (4 papers)The Journal of Pediatrics (2 papers)Cancer (2 papers)Journal of Medical Genetics (2 papers)Pediatric Research (2 papers)
- Partner nations
- United States
In The Last Decade
David Peakman
29 papers receiving 583 citations
Peers
Comparison fields: 5 of 61
- Hematology 227
- Genetics 278
- Pediatrics, Perinatology and Child Health 192
- Genetics 97
- Immunology 110
Countries citing papers authored by David Peakman
This map shows the geographic impact of David Peakman'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 Peakman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David Peakman more than expected).
Fields of papers citing papers by David Peakman
This network shows the impact of papers produced by David Peakman. 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 Peakman. The network helps show where David Peakman may publish in the future.
Co-authors
The 25 scholars most cited alongside David Peakman, 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 30 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1978 | 115 | |
| 2 | 1979 | 49 | |
| 3 | Chromosomal mosaicism in amniotic fluid cell cultures. | 1979 | 48 |
| 4 | 1977 | 42 | |
| 5 | 1975 | 41 | |
| 6 | 1978 | 40 | |
| 7 | 1988 | 38 | |
| 8 | Isolated severe gamma A deficiency: immunoglobulin levels, clinical disorders, and chromosome studies. | 1970 | 38 |
| 9 | 1978 | 26 | |
| 10 | 1981 | 24 | |
| 11 | 1978 | 20 | |
| 12 | 1976 | 18 | |
| 13 | 1971 | 17 | |
| 14 | 1979 | 16 | |
| 15 | 1975 | 15 | |
| 16 | 1981 | 13 | |
| 17 | 1970 | 12 | |
| 18 | 1977 | 12 | |
| 19 | 1979 | 9 | |
| 20 | 1971 | 8 |
About David Peakman
David Peakman is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Hematology, Molecular Biology and Public Health, Environmental and Occupational Health, having authored 30 papers that have together received 636 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (10 papers), Genomic variations and chromosomal abnormalities (10 papers), Acute Myeloid Leukemia Research (8 papers), Acute Lymphoblastic Leukemia research (5 papers), Chronic Myeloid Leukemia Treatments (5 papers), Congenital Anomalies and Fetal Surgery (4 papers), Genetic Syndromes and Imprinting (3 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). The work is most often cited by research in Hematology (227 citations), Genetics (278 citations), Pediatrics, Perinatology and Child Health (192 citations), Genetics (97 citations) and Immunology (110 citations). David Peakman has collaborated with scholars based in United States. Frequent co-authors include Arthur Robinson, Helvise G. Morse, Taru Hays, Frederick Hecht, Brahma S. Sharma, F. L. Johnson, Barbara Rose, B. Kaiser McCaw, Alexander Robinson and James R. Humbert. Their work appears in journals such as Human Genetics, The Journal of Pediatrics, Cancer, Journal of Medical Genetics and Pediatric Research.
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.