M D Crawfurd
Impact in
- Developmental Biology top 10%
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 15
- Genomic variations and chromosomal abnormalities 4
- Genomics and Rare Diseases 3
- Ocular Disorders and Treatments 2
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- Biochemical and Molecular Research 4
- Co-authors
- P J Toghill (2 shared papers)Stephen H. Morgan (2 shared papers)Elizabeth A. Holly (1 shared paper)R. Bannister (1 shared paper)Elisabeth Young (1 shared paper)Stuart Smith (1 shared paper)B. E. Kendall (1 shared paper)R M Winter (1 shared paper)
- Journals
- Journal of Medical Genetics (8 papers)The Lancet (7 papers)Annals of Human Genetics (2 papers)Clinical Genetics (2 papers)Brain (1 paper)
- Partner nations
- United KingdomJamaicaSouth Africa
In The Last Decade
M D Crawfurd
32 papers receiving 606 citations
Peers
Comparison fields: 5 of 73
- Developmental Biology 28
- Genetics 290
- Immunology and Allergy 59
- Pediatrics, Perinatology and Child Health 129
- Rheumatology 86
Countries citing papers authored by M D Crawfurd
This map shows the geographic impact of M D Crawfurd'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 M D Crawfurd with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M D Crawfurd more than expected).
Fields of papers citing papers by M D Crawfurd
This network shows the impact of papers produced by M D Crawfurd. 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 M D Crawfurd. The network helps show where M D Crawfurd may publish in the future.
Co-authors
The 25 scholars most cited alongside M D Crawfurd, 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 33 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1990 | 91 | |
| 2 | 1966 | 73 | |
| 3 | 1961 | 54 | |
| 4 | Alport's syndrome of hereditary nephritis and deafness. | 1968 | 43 |
| 5 | 1990 | 37 | |
| 6 | 1979 | 31 | |
| 7 | 1981 | 30 | |
| 8 | 1980 | 29 | |
| 9 | 1984 | 27 | |
| 10 | 1973 | 27 | |
| 11 | 1971 | 25 | |
| 12 | 1978 | 21 | |
| 13 | 1978 | 21 | |
| 14 | 1965 | 19 | |
| 15 | 1966 | 18 | |
| 16 | 1991 | 17 | |
| 17 | 1990 | 17 | |
| 18 | 1964 | 17 | |
| 19 | 1979 | 17 | |
| 20 | 1961 | 15 |
About M D Crawfurd
M D Crawfurd is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Physiology, having authored 33 papers that have together received 705 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (5 papers), Biochemical and Molecular Research (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Lysosomal Storage Disorders Research (3 papers), Metabolism and Genetic Disorders (3 papers), Genomics and Rare Diseases (3 papers), Ocular Disorders and Treatments (2 papers) and Esophageal and GI Pathology (2 papers). The work is most often cited by research in Developmental Biology (28 citations), Genetics (290 citations), Immunology and Allergy (59 citations), Pediatrics, Perinatology and Child Health (129 citations) and Rheumatology (86 citations). M D Crawfurd has collaborated with scholars based in United Kingdom, Jamaica and South Africa. Frequent co-authors include P J Toghill, Stephen H. Morgan, Elizabeth A. Holly, R. Bannister, Elisabeth Young, Stuart Smith, B. E. Kendall, R M Winter, Dian Donnai and A.M. Bronstein. Their work appears in journals such as Journal of Medical Genetics, The Lancet, Annals of Human Genetics, Clinical Genetics and Brain.
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.