Ruth Krone

616 total citations
23 papers, 176 citations indexed

About

Ruth Krone is a scholar working on Endocrinology, Diabetes and Metabolism, Molecular Biology and Surgery. According to data from OpenAlex, Ruth Krone has authored 23 papers receiving a total of 176 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Endocrinology, Diabetes and Metabolism, 9 papers in Molecular Biology and 5 papers in Surgery. Recurrent topics in Ruth Krone's work include Sexual Differentiation and Disorders (7 papers), Metabolism and Genetic Disorders (5 papers) and Diabetes Management and Research (4 papers). Ruth Krone is often cited by papers focused on Sexual Differentiation and Disorders (7 papers), Metabolism and Genetic Disorders (5 papers) and Diabetes Management and Research (4 papers). Ruth Krone collaborates with scholars based in United Kingdom, United States and Australia. Ruth Krone's co-authors include Timothy Barrett, Suma Uday, Luanne M. Metz, Renuka Dias, Melanie Kershaw, Jeremy Kirk, Nils Krone, John Pemberton, Jan Idkowiak and Maurice P. Zeegers and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and Archives of Disease in Childhood.

In The Last Decade

Ruth Krone

22 papers receiving 168 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ruth Krone United Kingdom 9 82 53 34 29 29 23 176
Melinda Pierce United States 7 59 0.7× 51 1.0× 56 1.6× 60 2.1× 23 0.8× 9 225
Álvaro Martín‐Rivada Spain 9 44 0.5× 71 1.3× 43 1.3× 44 1.5× 12 0.4× 28 212
Franziska Phan-Hug Switzerland 8 82 1.0× 59 1.1× 53 1.6× 25 0.9× 26 0.9× 19 180
Vafa Tabatabaie United States 8 94 1.1× 22 0.4× 23 0.7× 21 0.7× 52 1.8× 15 192
P Mah United Kingdom 5 173 2.1× 39 0.7× 28 0.8× 13 0.4× 27 0.9× 6 244
Akemi Inagaki Japan 8 56 0.7× 53 1.0× 38 1.1× 13 0.4× 36 1.2× 13 149
Sureka Bollepalli United States 8 79 1.0× 40 0.8× 52 1.5× 24 0.8× 16 0.6× 9 198
Anat Tsur Israel 9 197 2.4× 62 1.2× 40 1.2× 13 0.4× 104 3.6× 25 381
Kei Matsushita Japan 10 54 0.7× 60 1.1× 35 1.0× 11 0.4× 43 1.5× 22 313
Maxime M. Bos Netherlands 11 53 0.6× 35 0.7× 51 1.5× 10 0.3× 33 1.1× 19 247

Countries citing papers authored by Ruth Krone

Since Specialization
Citations

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

Fields of papers citing papers by Ruth Krone

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ruth Krone

This figure shows the co-authorship network connecting the top 25 collaborators of Ruth Krone. A scholar is included among the top collaborators of Ruth Krone 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 Ruth Krone. Ruth Krone 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.
Pemberton, John, Louise Collins, Renuka Dias, et al.. (2024). Enhancing equity in access to automated insulin delivery systems in an ethnically and socioeconomically diverse group of children with type 1 diabetes. BMJ Open Diabetes Research & Care. 12(3). e004045–e004045. 4 indexed citations
2.
Shaikh, M Guftar, Timothy Barrett, Nicola Bridges, et al.. (2024). Prader–Willi syndrome: guidance for children and transition into adulthood. Endocrine Connections. 13(8). 3 indexed citations
3.
Lawrence, Neil, Jeremy Dawson, Timothy Cheetham, et al.. (2023). Quality of Life in Children and Young People With Congenital Adrenal Hyperplasia—UK Nationwide Multicenter Assessment. The Journal of Clinical Endocrinology & Metabolism. 109(1). e336–e346. 5 indexed citations
4.
Elhassan, Yasir, et al.. (2023). Management aspects of congenital adrenal hyperplasia during adolescence and transition to adult care. Clinical Endocrinology. 101(4). 332–345. 3 indexed citations
5.
Idkowiak, Jan, Suma Uday, Timothy Barrett, et al.. (2023). Diabetes control is worse in children and young people with type 1 diabetes requiring interpreter support. SHILAP Revista de lepidopterología. 4. 1228820–1228820. 3 indexed citations
6.
Lawrence, Neil, et al.. (2023). Blood Pressure in Children with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency. Hormone Research in Paediatrics. 97(4). 315–325. 1 indexed citations
7.
8.
Maharaj, Avinaash, Jack Williams, Chris Smith, et al.. (2022). A retrospective analysis of endocrine disease in sphingosine-1-phosphate lyase insufficiency: case series and literature review. Endocrine Connections. 11(8). 7 indexed citations
9.
Lawrence, Neil, Tim Cheetham, Elizabeth Crowne, et al.. (2021). Quality of Life in Children and Young People With Congenital Adrenal Hyperplasia in the United Kingdom - Nationwide Multicentre Assessment. Journal of the Endocrine Society. 5(Supplement_1). A720–A720. 1 indexed citations
10.
11.
Adaway, Jo, James Hawley, Ruth Krone, et al.. (2019). Measurement of Salivary Adrenal-Specific Androgens as Biomarkers of Therapy Control in 21-Hydroxylase Deficiency. The Journal of Clinical Endocrinology & Metabolism. 104(12). 6417–6429. 30 indexed citations
12.
Idkowiak, Jan, Vrinda Saraff, Renuka Dias, et al.. (2018). Diabetes control is worse in children and young people with type 1 diabetes requiring interpreter support. Endocrine Abstracts. 1 indexed citations
13.
Idkowiak, Jan, Yasir Elhassan, Karen Smith, et al.. (2018). Causes, patterns and severity of androgen excess in 487 consecutively recruited pre- and post-pubertal children. European Journal of Endocrinology. 180(3). 213–221. 19 indexed citations
14.
Uday, Suma, Nick Shaw, Ruth Krone, & Jeremy Kirk. (2016). Hypopituitarism in children with cerebral palsy. Archives of Disease in Childhood. 102(6). 559–561. 10 indexed citations
15.
Prasad, Rathi, Avinaash Maharaj, Eirini Meimaridou, et al.. (2016). Mutations in SGPL1, encoding sphingosine-1-phosphate lyase, cause a novel form of primary adrenal insufficiency with steroid resistant nephrotic syndrome. Endocrine Abstracts. 1 indexed citations
16.
Nan, Cassandra, et al.. (2013). Trajectories and predictors of developmental skills in healthy twins up to 24 months of age. Infant Behavior and Development. 36(4). 670–678. 18 indexed citations
17.
18.
Krone, Ruth, Andrew K Ewer, Timothy Barrett, et al.. (2006). The Birmingham Registry for Twin and Heritability Studies (BiRTHS). Twin Research and Human Genetics. 9(6). 907–912. 2 indexed citations
19.
Krone, Ruth, et al.. (1990). An investigation into the effects of oral iron supplementation on in vivo Hemoccult stool testing.. PubMed. 85(5). 558–61. 6 indexed citations
20.
Krone, Ruth, et al.. (1957). Pipradrol: combined therapy for geriatric and agitated patients.. PubMed. 170(1). 33–6. 2 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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