D Donnai

1.8k total citations
22 papers, 1.2k citations indexed

About

D Donnai is a scholar working on Genetics, Surgery and Rheumatology. According to data from OpenAlex, D Donnai has authored 22 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 4 papers in Surgery and 4 papers in Rheumatology. Recurrent topics in D Donnai's work include Genetic and rare skin diseases. (3 papers), Congenital limb and hand anomalies (2 papers) and Connective tissue disorders research (2 papers). D Donnai is often cited by papers focused on Genetic and rare skin diseases. (3 papers), Congenital limb and hand anomalies (2 papers) and Connective tissue disorders research (2 papers). D Donnai collaborates with scholars based in United Kingdom, South Africa and United States. D Donnai's co-authors include Sara Landy, Andrew Read, Thomy de Ravel, Conny M.A. van Ravenswaaij, R.J.C. Admiraal, Lies H. Hoefsloot, Bert B.A. de Vries, Han G. Brunner, Johanna M. van Hagen and Lisenka E.L.M. Vissers and has published in prestigious journals such as Ophthalmology, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

D Donnai

21 papers receiving 1.2k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
D Donnai United Kingdom 14 576 447 266 225 216 22 1.2k
H D Flad Germany 6 124 0.2× 462 1.0× 89 0.3× 195 0.9× 237 1.1× 6 1.3k
Elena Belloni Italy 20 971 1.7× 2.0k 4.5× 203 0.8× 448 2.0× 236 1.1× 41 2.8k
S Nishikawa Japan 15 185 0.3× 739 1.7× 179 0.7× 115 0.5× 78 0.4× 30 2.2k
Hardeep Singh Mudhar United Kingdom 21 125 0.2× 563 1.3× 116 0.4× 216 1.0× 92 0.4× 122 2.0k
Gopalrao V.N. Velagaleti United States 17 507 0.9× 594 1.3× 512 1.9× 355 1.6× 103 0.5× 74 1.5k
Chester J. Herman United States 18 109 0.2× 496 1.1× 60 0.2× 280 1.2× 248 1.1× 35 1.5k
Anne Hing United States 26 1.6k 2.8× 1.3k 2.9× 261 1.0× 614 2.7× 268 1.2× 56 2.7k
C McKeown United Kingdom 13 551 1.0× 735 1.6× 59 0.2× 168 0.7× 79 0.4× 25 1.3k
Mahin Golabi United States 26 1.2k 2.0× 1.3k 2.9× 107 0.4× 470 2.1× 146 0.7× 59 2.4k
Holger Kulessa United States 13 190 0.3× 1.2k 2.6× 117 0.4× 144 0.6× 97 0.4× 13 1.7k

Countries citing papers authored by D Donnai

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of D Donnai

This figure shows the co-authorship network connecting the top 25 collaborators of D Donnai. A scholar is included among the top collaborators of D Donnai based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with D Donnai. D Donnai is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Admiraal, R.J.C., Lisenka E.L.M. Vissers, Annette F. Baas, et al.. (2005). CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene. Journal of Medical Genetics. 43(4). 306–314. 301 indexed citations
2.
Elanko, Navaratnam, et al.. (2001). A survey of TWIST for mutations in craniosynostosis reveals a variable length polyglycine tract in asymptomatic individuals.. The American Journal of Human Genetics. 69. 653–653. 2 indexed citations
3.
Tassabehji, Mayada, Kay Metcalfe, Annette Karmiloff‐Smith, et al.. (1999). Williams Syndrome: Use of Chromosomal Microdeletions as a Tool to Dissect Cognitive and Physical Phenotypes. The American Journal of Human Genetics. 64(1). 118–125. 166 indexed citations
4.
5.
Lloyd, I. Christopher, Jill Clayton‐Smith, Peter T. Clayton, et al.. (1997). Anterior segment dysgenesis in mosaic Turner syndrome. British Journal of Ophthalmology. 81(8). 639–643. 17 indexed citations
6.
McGaughran, Julie, Lorraine Gaunt, J. F. Doré, et al.. (1996). Rubinstein-Taybi syndrome with deletions of FISH probe RT1 at 16p13.3: two UK patients.. Journal of Medical Genetics. 33(1). 82–83. 12 indexed citations
7.
Dennis, N R, et al.. (1994). Anencephaly with spinal dysraphism, cleft lip and palate and limb reduction defects. Clinical Dysmorphology. 3(3). 270–270. 1 indexed citations
8.
Landy, Sara & D Donnai. (1993). Incontinentia pigmenti (Bloch-Sulzberger syndrome).. Journal of Medical Genetics. 30(1). 53–59. 258 indexed citations
9.
Sims, Katherine B., Michel P. Coleman, D Donnai, et al.. (1992). Characterization of a YAC containing part or all of the Norrie disease locus. Human Molecular Genetics. 1(3). 161–164. 12 indexed citations
10.
Donnai, D. (1992). Chromosome Anomalies and Prenatal Development: An Atlas. Journal of Medical Genetics. 29(4). 288.2–288. 39 indexed citations
11.
Norman, Andrew, S. Rimmer, Sara Landy, & D Donnai. (1992). Thanatophoric dysplasia of the straight-bone type (type 2). Clinical Dysmorphology. 1(2). 115???120–115???120. 17 indexed citations
12.
Colley, Andrew, et al.. (1992). Unbalanced 13;18 translocation and Williams syndrome.. Journal of Medical Genetics. 29(1). 63–65. 14 indexed citations
13.
Norman, Andrew, et al.. (1992). Fetus with unbalanced translocation involving chromosomes 2 and 11. Clinical Dysmorphology. 1(1). 53???56–53???56. 2 indexed citations
14.
Colley, Andrew, et al.. (1991). Ectopia lentis et pupillae: the genetic aspects and differential diagnosis.. Journal of Medical Genetics. 28(11). 791–794. 20 indexed citations
15.
Donnai, D. (1991). Multiple Congenital Anomalies. Archives of Disease in Childhood. 66(10). 1264–1264. 1 indexed citations
16.
Evans, D. Gareth, et al.. (1990). Ankyloblepharon filiforme adnatum in trisomy 18 Edwards syndrome.. Journal of Medical Genetics. 27(11). 720–721. 6 indexed citations
17.
Clayton‐Smith, Jill & D Donnai. (1989). A new recessive syndrome of unusual facies, digital abnormalities, and ichthyosis.. Journal of Medical Genetics. 26(5). 339–342. 3 indexed citations
18.
Donnai, D, Andrew Read, C McKeown, & Tony Andrews. (1988). Hypomelanosis of Ito: a manifestation of mosaicism or chimerism.. Journal of Medical Genetics. 25(12). 809–818. 77 indexed citations
19.
Thompson, Elizabeth M., D Donnai, M Baraitser, et al.. (1987). Multiple pterygium syndrome: evolution of the phenotype.. Journal of Medical Genetics. 24(12). 733–749. 44 indexed citations
20.
Clark, Robin D., D Donnai, John Rogers, et al.. (1987). Proteus syndrome: An expanded phenotype. American Journal of Medical Genetics. 27(1). 99–117. 87 indexed citations

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.

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