Sally Davies

3.3k total citations
16 papers, 937 citations indexed

About

Sally Davies is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Sally Davies has authored 16 papers receiving a total of 937 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 5 papers in Molecular Biology and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Sally Davies's work include Genetic Syndromes and Imprinting (3 papers), Genetic factors in colorectal cancer (3 papers) and Genomics and Rare Diseases (2 papers). Sally Davies is often cited by papers focused on Genetic Syndromes and Imprinting (3 papers), Genetic factors in colorectal cancer (3 papers) and Genomics and Rare Diseases (2 papers). Sally Davies collaborates with scholars based in United Kingdom, Italy and Malaysia. Sally Davies's co-authors include Helen E. Hughes, Elizabeth D. Williams, David W. Williams, Gareth Williams, David F. Griffiths, Alexandra Murray, Nazneen Rahman, Jenny Douglas, Susan Tomkins and Sandra Hanks and has published in prestigious journals such as Nature, The Lancet and Circulation.

In The Last Decade

Sally Davies

16 papers receiving 911 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sally Davies United Kingdom	12	563	536	108	101	97	16	937
Louise C. Wilson United Kingdom	20	638 1.1×	629 1.2×	53 0.5×	178 1.8×	71 0.7×	46	1.2k
Jane E. Brissenden Canada	13	329 0.6×	479 0.9×	88 0.8×	84 0.8×	40 0.4×	20	815
Francesca Romana Lepri Italy	18	429 0.8×	608 1.1×	86 0.8×	74 0.7×	45 0.5×	62	972
Siddharth Banka United Kingdom	18	480 0.9×	339 0.6×	55 0.5×	104 1.0×	52 0.5×	55	991
Pamela S. Karnes United States	17	199 0.4×	430 0.8×	80 0.7×	200 2.0×	86 0.9×	29	992
Alicja Waliszewska United States	7	622 1.1×	241 0.4×	62 0.6×	66 0.7×	120 1.2×	9	1.0k
Julie Neidich United States	17	231 0.4×	270 0.5×	73 0.7×	97 1.0×	57 0.6×	42	698
Cynthia L. Neben United States	14	407 0.7×	325 0.6×	63 0.6×	114 1.1×	101 1.0×	20	791
Sevilhan Artan Türkiye	18	187 0.3×	308 0.6×	69 0.6×	81 0.8×	61 0.6×	84	760
Adriano Angioni Italy	21	435 0.8×	739 1.4×	120 1.1×	176 1.7×	57 0.6×	56	1.3k

Countries citing papers authored by Sally Davies

Since Specialization

Citations

This map shows the geographic impact of Sally Davies'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 Sally Davies with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sally Davies more than expected).

Fields of papers citing papers by Sally Davies

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sally Davies. 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 Sally Davies. The network helps show where Sally Davies may publish in the future.

Co-authorship network of co-authors of Sally Davies

This figure shows the co-authorship network connecting the top 25 collaborators of Sally Davies. A scholar is included among the top collaborators of Sally Davies 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 Sally Davies. Sally Davies is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Williamson, Anne, Rebecca Forman, Natasha Azzopardi‐Muscat, et al.. (2022). Effective post-pandemic governance must focus on shared challenges. The Lancet. 399(10340). 1999–2001. 9 indexed citations

Hassan, Mohamed Ibrahim Abu, et al.. (2021). A comparison of different standard‐setting methods for professional qualifying dental examination. Journal of Dental Education. 85(7). 1210–1216. 5 indexed citations

Davies, Sally, et al.. (2014). Training for the future NHS: training junior doctors in the United Kingdom within the 48-hour European working time directive. BMC Medical Education. 14(S1). S12–S12. 34 indexed citations

Pottinger, Caroline, et al.. (2009). Further evidence of dominant inheritance of Kabuki syndrome. Clinical Dysmorphology. 18(4). 215–217. 2 indexed citations

Mavrogiannis, Lampros A., Indira B. Taylor, Sally Davies, et al.. (2005). Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype. European Journal of Human Genetics. 14(2). 151–158. 52 indexed citations

Lewis, Mark, Martin Horan, John W Gregory, et al.. (2003). Novel mutations of the growth hormone 1 (GH1) gene disclosed by modulation of the clinical selection criteria for individuals with short stature. Human Mutation. 21(4). 424–440. 75 indexed citations

Douglas, Jenny, Sandra Hanks, I. Karen Temple, et al.. (2003). NSD1 Mutations Are the Major Cause of Sotos Syndrome and Occur in Some Cases of Weaver Syndrome but Are Rare in Other Overgrowth Phenotypes. The American Journal of Human Genetics. 72(1). 132–143. 210 indexed citations

Nigro, Cristiana Lo, Roberto Cusano, R. Cinti, et al.. (2000). A refined physical and transcriptional map of the SPG9 locus on 10q23.3–q24.2. European Journal of Human Genetics. 8(10). 777–782. 10 indexed citations

Churchman, Michael, Egle Avizienyte, C. McKeown, et al.. (1999). Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patients. Journal of Medical Genetics. 36(5). 365–368. 46 indexed citations

10.

Tischkowitz, Marc, et al.. (1999). Amelogenesis imperfecta, sensorineural hearing loss, and Beau's lines: a second case report of Heimler's syndrome. Journal of Medical Genetics. 36(12). 942–943. 14 indexed citations

11.

Wilson, Dirk G., Michael Bellamy, Mark Ramsey, et al.. (1999). Endothelial Function in Marfan Syndrome. Circulation. 99(7). 909–915. 59 indexed citations

12.

Davies, Sally. (1996). Dermatology and the New Genetics. Journal of Medical Genetics. 33(2). 176–176. 13 indexed citations

13.

Davies, Sally. (1996). Developmental Mechanisms of Heart Disease. Journal of Medical Genetics. 33(1). 86.3–87. 29 indexed citations

14.

Davies, Sally & Helen E. Hughes. (1994). Costello syndrome: natural history and differential diagnosis of cutis laxa.. Journal of Medical Genetics. 31(6). 486–489. 29 indexed citations

15.

Davies, Sally & Helen E. Hughes. (1993). Imprinting in Albright's hereditary osteodystrophy.. Journal of Medical Genetics. 30(2). 101–103. 211 indexed citations

16.

Griffiths, David F., Sally Davies, David W. Williams, Gareth Williams, & Elizabeth D. Williams. (1988). Demonstration of somatic mutation and colonic crypt clonality by X-linked enzyme histochemistry. Nature. 333(6172). 461–463. 139 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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