Amanda Stride

1.6k total citations
14 papers, 1.1k citations indexed

About

Amanda Stride is a scholar working on Surgery, Genetics and Molecular Biology. According to data from OpenAlex, Amanda Stride has authored 14 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Surgery, 10 papers in Genetics and 7 papers in Molecular Biology. Recurrent topics in Amanda Stride's work include Pancreatic function and diabetes (12 papers), Diabetes and associated disorders (7 papers) and Metabolism, Diabetes, and Cancer (5 papers). Amanda Stride is often cited by papers focused on Pancreatic function and diabetes (12 papers), Diabetes and associated disorders (7 papers) and Metabolism, Diabetes, and Cancer (5 papers). Amanda Stride collaborates with scholars based in United Kingdom, Denmark and Finland. Amanda Stride's co-authors include Andrew T. Hattersley, Sian Ellard, Maggie Shepherd, Katharine R. Owen, Lorna W. Harries, Ali Chakera, Noel G. Morgan, Kevin Colclough, Beverley M. Shields and Oluf Pedersen and has published in prestigious journals such as Diabetes Care, Kidney International and Human Molecular Genetics.

In The Last Decade

Amanda Stride

14 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Amanda Stride United Kingdom 13 889 744 475 452 89 14 1.1k
Lisa I.S. Allen United Kingdom 12 993 1.1× 829 1.1× 375 0.8× 725 1.6× 167 1.9× 12 1.3k
Anne Lienhardt France 12 161 0.2× 177 0.2× 175 0.4× 173 0.4× 85 1.0× 26 636
Sara Ernst United States 7 320 0.4× 123 0.2× 103 0.2× 96 0.2× 81 0.9× 9 481
Fredrik Lindgren Sweden 16 497 0.6× 608 0.8× 506 1.1× 71 0.2× 31 0.3× 22 817
Doris Taha United States 13 331 0.4× 378 0.5× 266 0.6× 238 0.5× 51 0.6× 27 655
Erling Tjora Norway 14 542 0.6× 220 0.3× 119 0.3× 208 0.5× 14 0.2× 47 675
Travis Monchamp United States 6 752 0.8× 420 0.6× 418 0.9× 201 0.4× 50 0.6× 8 915
Dalong Zhu China 12 393 0.4× 332 0.4× 378 0.8× 138 0.3× 11 0.1× 19 649
Christine H Albini United States 10 242 0.3× 252 0.3× 334 0.7× 58 0.1× 72 0.8× 21 528
Marion Shattock United Kingdom 11 1.2k 1.3× 1.4k 1.9× 1.2k 2.5× 100 0.2× 21 0.2× 13 1.5k

Countries citing papers authored by Amanda Stride

Since Specialization
Citations

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

Fields of papers citing papers by Amanda Stride

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amanda Stride

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

All Works

14 of 14 papers shown
1.
Stride, Amanda, Beverley M. Shields, Ali Chakera, et al.. (2013). Cross-sectional and longitudinal studies suggest pharmacological treatment used in patients with glucokinase mutations does not alter glycaemia. Diabetologia. 57(1). 54–56. 139 indexed citations
2.
Cuesta‐Muñoz, Antonio L., Nadia Cobo‐Vuilleumier, Hanna Koskela, et al.. (2009). Clinical Heterogeneity in Monogenic Diabetes Caused by Mutations in the Glucokinase Gene (GCK-MODY). Diabetes Care. 33(2). 290–292. 35 indexed citations
3.
Ellard, Sian, Emma L. Edghill, Martina Owens, et al.. (2007). Partial and whole gene deletion mutations of the GCK and HNF1A genes in maturity-onset diabetes of the young. Diabetologia. 50(11). 2313–2317. 56 indexed citations
4.
Harries, Lorna W., Sian Ellard, Amanda Stride, Noel G. Morgan, & Andrew T. Hattersley. (2006). Isomers of the TCF1 gene encoding hepatocyte nuclear factor-1 alpha show differential expression in the pancreas and define the relationship between mutation position and clinical phenotype in monogenic diabetes. Human Molecular Genetics. 15(14). 2216–2224. 99 indexed citations
5.
Stride, Amanda, et al.. (2005). β-Cell Dysfunction, Insulin Sensitivity, and Glycosuria Precede Diabetes in Hepatocyte Nuclear Factor-1α Mutation Carriers. Diabetes Care. 28(7). 1751–1756. 95 indexed citations
6.
Dobson, Lee, et al.. (2004). Microalbuminuria as a screening tool in cystic fibrosis-related diabetes. Pediatric Pulmonology. 39(2). 103–107. 19 indexed citations
7.
Stride, Amanda, et al.. (2004). Serum amino acids in patients with mutations in the hepatocyte nuclear factor‐1 alpha gene. Diabetic Medicine. 21(8). 928–930. 5 indexed citations
8.
Bingham, Coralie, Sian Ellard, William G. van’t Hoff, et al.. (2003). Atypical familial juvenile hyperuricemic nephropathy associated with a hepatocyte nuclear factor-1β gene mutation. Kidney International. 63(5). 1645–1651. 110 indexed citations
9.
Owen, Katharine R., Amanda Stride, Sian Ellard, & Andrew T. Hattersley. (2003). Etiological Investigation of Diabetes in Young Adults Presenting With Apparent Type 2 Diabetes. Diabetes Care. 26(7). 2088–2093. 44 indexed citations
10.
Stride, Amanda, Martine Vaxillaire, Fabrizio Barbetti, et al.. (2002). The genetic abnormality in the beta cell determines the response to an oral glucose load. Diabetologia. 45(3). 427–435. 197 indexed citations
11.
Owen, Katharine R., Maggie Shepherd, Amanda Stride, Sian Ellard, & Andrew T. Hattersley. (2002). Heterogeneity in young adult onset diabetes: aetiology alters clinical characteristics. Diabetic Medicine. 19(9). 758–761. 42 indexed citations
12.
Stride, Amanda & Andrew T. Hattersley. (2002). Different genes, different diabetes: lessons from maturity-onset diabetes of the young. Annals of Medicine. 34(3). 207–216. 137 indexed citations
13.
Stride, Amanda, et al.. (2002). Intrauterine Hyperglycemia Is Associated With an Earlier Diagnosis of Diabetes in HNF-1α Gene Mutation Carriers. Diabetes Care. 25(12). 2287–2291. 82 indexed citations
14.
Stride, Amanda & Andrew T. Hattersley. (2002). Different genes, different diabetes: lessons from maturity-onset diabetes of the young. Annals of Medicine. 34(3). 207–216. 31 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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