Sally Feather

3.3k total citations
27 papers, 1.4k citations indexed

About

Sally Feather is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Sally Feather has authored 27 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 10 papers in Genetics and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Sally Feather's work include Renal and related cancers (13 papers), Genetic and Kidney Cyst Diseases (8 papers) and Pediatric Urology and Nephrology Studies (7 papers). Sally Feather is often cited by papers focused on Renal and related cancers (13 papers), Genetic and Kidney Cyst Diseases (8 papers) and Pediatric Urology and Nephrology Studies (7 papers). Sally Feather collaborates with scholars based in United Kingdom, India and Greece. Sally Feather's co-authors include Adrian S. Woolf, Sue Malcolm, Paul J.D. Winyard, Victoria Wright, Leila Romio, David F. Thomas, Brunella Franco, Giovanna Giorgio, Andrew M. Fry and Andrea Ballabio and has published in prestigious journals such as The Lancet, The Journal of Physiology and Journal of the American Society of Nephrology.

In The Last Decade

Sally Feather

26 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sally Feather United Kingdom 19 825 591 389 320 235 27 1.4k
Boris Utsch Germany 20 596 0.7× 391 0.7× 224 0.6× 115 0.4× 116 0.5× 32 951
Bree Rumballe Australia 16 1.1k 1.3× 245 0.4× 275 0.7× 95 0.3× 98 0.4× 20 1.3k
Nicholas J Shaw United Kingdom 14 386 0.5× 355 0.6× 75 0.2× 29 0.1× 96 0.4× 18 1.0k
Marie Gonzalès France 14 348 0.4× 207 0.4× 353 0.9× 22 0.1× 25 0.1× 33 883
Hatice Akay Türkiye 18 229 0.3× 92 0.2× 95 0.2× 30 0.1× 127 0.5× 66 1.0k
Adel Shalata Israel 15 706 0.9× 212 0.4× 89 0.2× 51 0.2× 12 0.1× 42 1.2k
Shu Feng United States 23 393 0.5× 125 0.2× 66 0.2× 72 0.2× 35 0.1× 41 1.5k
Sirpa Ala‐Mello Finland 17 498 0.6× 468 0.8× 212 0.5× 7 0.0× 69 0.3× 29 1.2k
Robert Wallerstein United States 17 410 0.5× 399 0.7× 180 0.5× 39 0.1× 7 0.0× 66 924
Vincenzo Antona Italy 19 428 0.5× 307 0.5× 145 0.4× 29 0.1× 12 0.1× 57 821

Countries citing papers authored by Sally Feather

Since Specialization
Citations

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

Fields of papers citing papers by Sally Feather

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sally Feather

This figure shows the co-authorship network connecting the top 25 collaborators of Sally Feather. A scholar is included among the top collaborators of Sally Feather 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 Feather. Sally Feather 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.
McCarthy, Hugh J., Agnieszka Bierżyńska, Miloš Ognjanović, et al.. (2013). Simultaneous Sequencing of 24 Genes Associated with Steroid-Resistant Nephrotic Syndrome. Clinical Journal of the American Society of Nephrology. 8(4). 637–648. 122 indexed citations
2.
Thompson, Dorothy, Sally Feather, Horia Stanescu, et al.. (2011). Altered electroretinograms in patients with KCNJ10 mutations and EAST syndrome. The Journal of Physiology. 589(7). 1681–1689. 61 indexed citations
3.
Lambert, H, Ambrose Gullett, Heather J. Cordell, et al.. (2011). Primary, Nonsyndromic Vesicoureteric Reflux and Nephropathy in Sibling Pairs. Clinical Journal of the American Society of Nephrology. 6(4). 760–766. 7 indexed citations
4.
Smith, Nicholas, Claire L. Varley, Ian Eardley, et al.. (2011). Toll-Like Receptor Responses of Normal Human Urothelial Cells to Bacterial Flagellin and Lipopolysaccharide. The Journal of Urology. 186(3). 1084–1092. 25 indexed citations
5.
Cordell, Heather J., Rebecca Darlay, Pimphen Charoen, et al.. (2009). Whole-Genome Linkage and Association Scan in Primary, Nonsyndromic Vesicoureteric Reflux. Journal of the American Society of Nephrology. 21(1). 113–123. 42 indexed citations
6.
Rubenwolf, Peter, Nikolaos T. Georgopoulos, Lisa Clements, et al.. (2008). Expression and Localisation of Aquaporin Water Channels in Human Urothelium In Situ and In Vitro. European Urology. 56(6). 1013–1024. 55 indexed citations
7.
Thomas, David F., et al.. (2008). The long‐term outcome of prenatally detected posterior urethral valves: a 10 to 23‐year follow‐up study. British Journal of Urology. 102(8). 1020–1024. 59 indexed citations
8.
Shroff, Rukshana, Ann E. Donald, Melanie P. Hiorns, et al.. (2007). Mineral Metabolism and Vascular Damage in Children on Dialysis. Journal of the American Society of Nephrology. 18(11). 2996–3003. 152 indexed citations
9.
Subramaniam, Ramnath, et al.. (2007). Influence of gender on the outcome of endoscopic correction in vesicoureteric reflux. Journal of Pediatric Urology. 3. S16–S16.
10.
Jenkins, Dagan, Maria Bitner‐Glindzicz, S Malcolm, et al.. (2006). Mutation analyses of Uroplakin II in children with renal tract malformations. Nephrology Dialysis Transplantation. 21(12). 3415–3421. 21 indexed citations
11.
Jenkins, Dagan, Maria Bitner‐Glindzicz, Sue Malcolm, et al.. (2006). Mutational analyses of UPIIIA, SHH, EFNB2, and HNF1β in persistent cloaca and associated kidney malformations. Journal of Pediatric Urology. 3(1). 2–9. 22 indexed citations
12.
Jenkins, Dagan, Maria Bitner‐Glindzicz, Sue Malcolm, et al.. (2005). De Novo Uroplakin IIIa Heterozygous Mutations Cause Human Renal Adysplasia Leading to Severe Kidney Failure. Journal of the American Society of Nephrology. 16(7). 2141–2149. 86 indexed citations
13.
Romio, Leila, Andrew M. Fry, Paul J.D. Winyard, et al.. (2004). OFD1 Is a Centrosomal/Basal Body Protein Expressed during Mesenchymal-Epithelial Transition in Human Nephrogenesis. Journal of the American Society of Nephrology. 15(10). 2556–2568. 121 indexed citations
14.
Nowaczyk, Małgorzata J.M., Susan Zeesman, Donald T. Whelan, Victoria Wright, & Sally Feather. (2003). Oral‐facial‐digital syndrome VII is oral‐facial‐digital syndrome I: A clarification. American Journal of Medical Genetics Part A. 123A(2). 179–182. 9 indexed citations
15.
Woolf, Adrian S., Sally Feather, & Coralie Bingham. (2002). Recent insights into kidney diseases associated with glomerular cysts. Pediatric Nephrology. 17(4). 229–235. 22 indexed citations
16.
Ferrante, Maria Immacolata, Sally Feather, Alessandro Bulfone, et al.. (2001). Identification of the Gene for Oral-Facial-Digital Type I Syndrome. The American Journal of Human Genetics. 68(3). 569–576. 239 indexed citations
17.
Andreu, Núria, M. Escarceller, Sally Feather, et al.. (2001). PALML, a novel paralemmin-related gene mapping on human chromosome 1p21. Gene. 278(1-2). 33–40. 10 indexed citations
18.
Feather, Sally. (1997). The oral-facial-digital syndrome type 1 (OFD1), a cause of polycystic kidney disease and associated malformations, maps to Xp22.2-Xp22.3. Human Molecular Genetics. 6(7). 1163–1167. 73 indexed citations
19.
Feather, Sally, Paul J.D. Winyard, Susan Dodd, & Adrian S. Woolf. (1997). Oral-facial-digital syndrome type 1 is another dominant polycystic kidney disease: clinical, radiological and histopathological features of a new kindred. Nephrology Dialysis Transplantation. 12(7). 1354–1361. 57 indexed citations
20.
Winyard, Paul J.D. & Sally Feather. (1996). Genetics of human kidney malformations. Nephrology Dialysis Transplantation. 11(6). 976–978. 1 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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