D Donnai
Impact in
- Developmental Neuroscience top 5%
- Williams Syndrome Research
- Genetics top 5%
- Genetic and rare skin diseases.
- Congenital Ear and Nasal Anomalies
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 8
- Craniofacial Disorders and Treatments 2
- Congenital Ear and Nasal Anomalies 2
- Connective tissue disorders research 2
- Genetic and rare skin diseases. 2
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- Dupuytren's Contracture and Treatments 2
- Co-authors
- Sara Landy (2 shared papers)Andrew Read (3 shared papers)Livia Kapusta (1 shared paper)Thomy de Ravel (1 shared paper)Conny M.A. van Ravenswaaij (1 shared paper)Bert B.A. de Vries (1 shared paper)Lies H. Hoefsloot (1 shared paper)Lisenka E.L.M. Vissers (1 shared paper)
- Journals
- Journal of Medical Genetics (10 papers)The American Journal of Human Genetics (2 papers)Human Molecular Genetics (1 paper)British Journal of Ophthalmology (1 paper)Archives of Disease in Childhood (1 paper)
- Partner nations
- United KingdomSouth AfricaUnited States
In The Last Decade
D Donnai
21 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 70
- Developmental Neuroscience 160
- Genetics 273
- Genetics 581
- Dermatology 115
- Developmental Biology 20
Countries citing papers authored by D Donnai
This map shows the geographic impact of D Donnai'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 D Donnai with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites D Donnai more than expected).
Fields of papers citing papers by D Donnai
This network shows the impact of papers produced by D Donnai. 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 D Donnai. The network helps show where D Donnai may publish in the future.
Co-authors
The 25 scholars most cited alongside D Donnai, 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 22 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2005 | 341 | |
| 2 | 1993 | 283 | |
| 3 | 1999 | 180 | |
| 4 | 1987 | 98 | |
| 5 | 1999 | 88 | |
| 6 | 1988 | 83 | |
| 7 | 1992 | 50 | |
| 8 | 1987 | 49 | |
| 9 | The expression of CD18 is increased on Trisomy 21 (Down syndrome) lymphoblastoid cells. | 1988 | 30 |
| 10 | 1992 | 24 | |
| 11 | 1991 | 22 | |
| 12 | 1997 | 18 | |
| 13 | 1992 | 18 | |
| 14 | 1992 | 15 | |
| 15 | 1992 | 14 | |
| 16 | 1996 | 12 | |
| 17 | 1990 | 7 | |
| 18 | 1989 | 3 | |
| 19 | A survey of TWIST for mutations in craniosynostosis reveals a variable length polyglycine tract in asymptomatic individuals. | 2001 | 2 |
| 20 | 1992 | 2 |
About D Donnai
D Donnai is a scholar working on Genetics, Rheumatology, Surgery, Molecular Biology and Genetics, having authored 22 papers that have together received 1.3k indexed citations. Recurring topics across this work include Williams Syndrome Research (2 papers), Craniofacial Disorders and Treatments (2 papers), Congenital Ear and Nasal Anomalies (2 papers), Connective tissue disorders research (2 papers), Genetic and rare skin diseases. (2 papers), Prenatal Screening and Diagnostics (2 papers), Congenital limb and hand anomalies (2 papers) and Dupuytren's Contracture and Treatments (2 papers). The work is most often cited by research in Developmental Neuroscience (160 citations), Genetics (273 citations), Genetics (581 citations), Dermatology (115 citations) and Developmental Biology (20 citations). D Donnai has collaborated with scholars based in United Kingdom, South Africa and United States. Frequent co-authors include Sara Landy, Andrew Read, Livia Kapusta, Thomy de Ravel, Conny M.A. van Ravenswaaij, Bert B.A. de Vries, Lies H. Hoefsloot, Lisenka E.L.M. Vissers, Johanna M. van Hagen and R.J.C. Admiraal. Their work appears in journals such as Journal of Medical Genetics, The American Journal of Human Genetics, Human Molecular Genetics, British Journal of Ophthalmology and Archives of Disease in Childhood.
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.