G Rumsby

914 total citations
27 papers, 652 citations indexed

About

G Rumsby is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Clinical Biochemistry. According to data from OpenAlex, G Rumsby has authored 27 papers receiving a total of 652 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 9 papers in Pulmonary and Respiratory Medicine and 7 papers in Clinical Biochemistry. Recurrent topics in G Rumsby's work include Sexual Differentiation and Disorders (11 papers), Porphyrin Metabolism and Disorders (9 papers) and Kidney Stones and Urolithiasis Treatments (7 papers). G Rumsby is often cited by papers focused on Sexual Differentiation and Disorders (11 papers), Porphyrin Metabolism and Disorders (9 papers) and Kidney Stones and Urolithiasis Treatments (7 papers). G Rumsby collaborates with scholars based in United Kingdom, United States and Austria. G Rumsby's co-authors include B.A. Gusterson, Anna Casteràs, Gerard S. Conway, John W. Honour, J. W. T. Seakins, C G D Brook, Peter C. Hindmarsh, Uma Ramaswami, Christopher J. Danpure and Tiffany L. Weir and has published in prestigious journals such as Annals of the New York Academy of Sciences, British Journal of Cancer and The Journal of Pediatrics.

In The Last Decade

G Rumsby

27 papers receiving 631 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
G Rumsby United Kingdom 15 465 200 160 142 137 27 652
Vernier Rl United States 12 217 0.5× 24 0.1× 77 0.5× 19 0.1× 126 0.9× 19 570
I Caorsi Chile 14 152 0.3× 98 0.5× 30 0.2× 21 0.1× 80 0.6× 25 648
Patricia R. Wahl Switzerland 12 285 0.6× 29 0.1× 356 2.2× 56 0.4× 40 0.3× 16 628
Høyer United States 9 194 0.4× 15 0.1× 56 0.3× 16 0.1× 108 0.8× 12 486
Jocelyn S. Kasper United States 10 615 1.3× 174 0.9× 95 0.6× 6 0.0× 188 1.4× 12 843
Susana Belli Argentina 11 150 0.3× 164 0.8× 73 0.5× 15 0.1× 7 0.1× 28 515
Cristina Clissa Italy 15 341 0.7× 57 0.3× 54 0.3× 75 0.5× 41 0.3× 31 723
Vera Ray United States 13 304 0.7× 104 0.5× 64 0.4× 3 0.0× 119 0.9× 21 615
Harlan R. Giles United States 13 186 0.4× 24 0.1× 124 0.8× 23 0.2× 60 0.4× 22 534
Audrey Casemayou France 13 215 0.5× 25 0.1× 94 0.6× 12 0.1× 72 0.5× 24 596

Countries citing papers authored by G Rumsby

Since Specialization
Citations

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

Fields of papers citing papers by G Rumsby

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G Rumsby

This figure shows the co-authorship network connecting the top 25 collaborators of G Rumsby. A scholar is included among the top collaborators of G Rumsby 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 G Rumsby. G Rumsby 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.
Croxson, Michael, et al.. (2012). Delayed puberty from partial 17-alpha hydroxylase enzyme deficiency.. PubMed. 125(1355). 71–4. 2 indexed citations
2.
Casteràs, Anna, et al.. (2009). Reassessing fecundity in women with classical congenital adrenal hyperplasia (CAH): normal pregnancy rate but reduced fertility rate. Clinical Endocrinology. 70(6). 833–837. 116 indexed citations
3.
Rumsby, G, et al.. (2004). Two Brothers with Non-Classical 21-Hydroxylase Deficiency: To Treat or Not to Treat?. Hormone Research in Paediatrics. 62(5). 241–244. 1 indexed citations
4.
Coulter-Mackie, Marion B., et al.. (2001). Three Novel Deletions in the Alanine:Glyoxylate Aminotransferase Gene of Three Patients with Type 1 Hyperoxaluria. Molecular Genetics and Metabolism. 74(3). 314–321. 19 indexed citations
5.
Masturzo, Bianca, et al.. (2001). Increased nuchal translucency as a prenatal manifestation of congenital adrenal hyperplasia. Prenatal Diagnosis. 21(4). 314–316. 11 indexed citations
6.
Ramaswami, Uma, G Rumsby, Helen Spoudeas, Peter C. Hindmarsh, & C G D Brook. (1999). Treatment of Achondroplasia with Growth Hormone: Six Years of Experience. Pediatric Research. 46(4). 435–435. 24 indexed citations
7.
Ramaswami, Uma, G Rumsby, Peter C. Hindmarsh, & C G D Brook. (1998). Genotype and phenotype in hypochondroplasia. The Journal of Pediatrics. 133(1). 99–102. 37 indexed citations
8.
OSTLERE, L.S., G Rumsby, Peter Holownia, et al.. (1998). Carrier status for steroid 21‐hydroxylase deficiency is only one factor in the variable phenotype of acne. Clinical Endocrinology. 48(2). 209–215. 48 indexed citations
9.
Schnakenburg, Christian von, et al.. (1997). Linkage of microsatellites to the AGXT gene on chromosome 2q37.3 and their role in prenatal diagnosis of primary hyperoxaluria type 1. Annals of Human Genetics. 61(4). 365–368. 5 indexed citations
10.
Danpure, Christopher J. & G Rumsby. (1996). STRATEGIES FOR THE PRENATAL DIAGNOSIS OF PRIMARY HYPEROXALURIA TYPE 1. Prenatal Diagnosis. 16(7). 587–598. 16 indexed citations
11.
Lhotta, Karl, G Rumsby, W Vogel, et al.. (1996). Primary hyperoxaluria type 1 caused by peroxisome-to-mitochondrion mistargeting of alanine : glyoxylate aminotransferase. Nephrology Dialysis Transplantation. 11(11). 2296–2298. 2 indexed citations
12.
Rumsby, G, et al.. (1996). Non-expression of a common mutation in the 21-hydroxylase gene: implications for prenatal diagnosis and carrier testing.. Journal of Medical Genetics. 33(9). 798–799. 7 indexed citations
13.
Rumsby, G, et al.. (1995). Polymorphisms in the alanine:glyoxylate aminotransferase gene and their application to the prenatal diagnosis of primary hyperoxaluria type 1. Nephrology Dialysis Transplantation. 10(supp8). 30–32. 13 indexed citations
14.
Danpure, Christopher J., Graeme M. Birdsey, G Rumsby, et al.. (1994). Molecular characterization and clinical use of a polymorphic tandem repeat in an intron of the human alanine: Glyoxylate aminotransferase gene. Human Genetics. 94(1). 55–64. 27 indexed citations
15.
Spoudeas, Helen, Jeremy D. Slater, G Rumsby, John W. Honour, & C G D Brook. (1993). Deoxycorticosterone, 11 β‐hydroxylase and the adrenal cortex. Clinical Endocrinology. 39(2). 245–251. 5 indexed citations
16.
Rumsby, G, John W. Honour, & C. H. Rodeck. (1993). Prenatal diagnosis of congenital adrenal hyperplasia by direct detection of mutations in the steroid 21‐hydroxylase gene. Clinical Endocrinology. 38(4). 421–425. 18 indexed citations
17.
Rumsby, G, C. J. Skinner, & John W. Honour. (1992). Genetic analysis of the steroid 21-hydroxylase gene following in vitro amplification of genomic DNA. The Journal of Steroid Biochemistry and Molecular Biology. 41(3-8). 827–829. 3 indexed citations
18.
Rumsby, G, et al.. (1990). Low incidence of ras oncogene activation in human squamous cell carcinomas. British Journal of Cancer. 61(3). 365–368. 87 indexed citations
19.
Seakins, J. W. T. & G Rumsby. (1988). The use of phenylpropionic acid as a loading test for medium‐chain acyl‐CoA dehydrogenase deficiency. Journal of Inherited Metabolic Disease. 11(S2). 221–224. 26 indexed citations
20.
Rumsby, G, A.H.L. Fielder, William M. Hague, & John W. Honour. (1988). Heterogeneity in the gene locus for steroid 21-hydroxylase deficiency.. Journal of Medical Genetics. 25(9). 596–599. 10 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Vernier Rl Breakdown of academic impact, for papers by I Caorsi Breakdown of academic impact, for papers by Patricia R. Wahl Breakdown of academic impact, for papers by Høyer Breakdown of academic impact, for papers by Jocelyn S. Kasper Breakdown of academic impact, for papers by Susana Belli Breakdown of academic impact, for papers by Cristina Clissa Breakdown of academic impact, for papers by Vera Ray Breakdown of academic impact, for papers by Harlan R. Giles Breakdown of academic impact, for papers by Audrey Casemayou
Rankless by CCL
2026