Gill Rumsby

4.6k total citations · 1 hit paper
84 papers, 3.1k citations indexed

About

Gill Rumsby is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Pathology and Forensic Medicine. According to data from OpenAlex, Gill Rumsby has authored 84 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 65 papers in Molecular Biology, 52 papers in Pulmonary and Respiratory Medicine and 31 papers in Pathology and Forensic Medicine. Recurrent topics in Gill Rumsby's work include Kidney Stones and Urolithiasis Treatments (52 papers), Porphyrin Metabolism and Disorders (43 papers) and Biomedical Research and Pathophysiology (31 papers). Gill Rumsby is often cited by papers focused on Kidney Stones and Urolithiasis Treatments (52 papers), Porphyrin Metabolism and Disorders (43 papers) and Biomedical Research and Pathophysiology (31 papers). Gill Rumsby collaborates with scholars based in United Kingdom, United States and Netherlands. Gill Rumsby's co-authors include Pierre Cochat, Emma L. Williams, Christopher J. Danpure, Gerard S. Conway, Sonia Fargue, Marion B. Coulter-Mackie, John W. Honour, Christian von Schnakenburg, Sally A. Hulton and Sally‐Anne Hulton and has published in prestigious journals such as New England Journal of Medicine, Journal of Biological Chemistry and Journal of Molecular Biology.

In The Last Decade

Gill Rumsby

81 papers receiving 3.1k citations

Hit Papers

align trajectories

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Gill Rumsby United Kingdom	34	2.1k	2.0k	954	682	462	84	3.1k
Mabel L. Purkerson United States	28	488 0.2×	526 0.3×	79 0.1×	373 0.5×	207 0.4×	49	2.2k
Tarek M. El‐Achkar United States	27	641 0.3×	596 0.3×	150 0.2×	303 0.4×	102 0.2×	84	2.4k
Michel Tsimaratos France	22	550 0.3×	302 0.2×	148 0.2×	349 0.5×	104 0.2×	67	1.7k
Gopala K. Rangan Australia	22	751 0.4×	211 0.1×	359 0.4×	143 0.2×	117 0.3×	85	2.2k
Tracy E. Hunley United States	23	455 0.2×	254 0.1×	127 0.1×	325 0.5×	328 0.7×	45	1.7k
Michal Herman‐Edelstein Israel	19	1.1k 0.5×	228 0.1×	156 0.2×	201 0.3×	570 1.2×	33	2.9k
Ayhan Özcan Türkiye	23	545 0.3×	454 0.2×	248 0.3×	69 0.1×	199 0.4×	84	1.8k
B. D. Myers United States	13	486 0.2×	261 0.1×	140 0.1×	184 0.3×	212 0.5×	16	2.0k
María C. Izquierdo Spain	17	643 0.3×	161 0.1×	147 0.2×	140 0.2×	88 0.2×	26	1.8k
Lijun Sun China	15	556 0.3×	140 0.1×	136 0.1×	84 0.1×	193 0.4×	24	1.7k

Countries citing papers authored by Gill Rumsby

Since Specialization

Citations

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

Fields of papers citing papers by Gill Rumsby

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gill Rumsby

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

All Works

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20 of 20 papers shown

1.

Mandrile, Giorgia, Bodo B. Beck, Cécile Acquaviva, et al.. (2022). Genetic assessment in primary hyperoxaluria: why it matters. Pediatric Nephrology. 38(3). 625–634. 34 indexed citations

2.

Acquaviva, Cécile, et al.. (2020). Plasma oxalate: comparison of methodologies. Urolithiasis. 48(6). 473–480. 14 indexed citations

3.

Rumsby, Gill, et al.. (2017). Glycolate oxidase deficiency in a patient with congenital hyperinsulinism and unexplained hyperoxaluria. Pediatric Nephrology. 32(11). 2159–2163. 11 indexed citations

4.

Fargue, Sonia, John Knight, Ross P. Holmes, Gill Rumsby, & Christopher J. Danpure. (2016). Effects of alanine:glyoxylate aminotransferase variants and pyridoxine sensitivity on oxalate metabolism in a cell-based cytotoxicity assay. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1862(6). 1055–1062. 20 indexed citations

5.

Fargue, Sonia, Gill Rumsby, & Christopher J. Danpure. (2013). Multiple mechanisms of action of pyridoxine in primary hyperoxaluria type 1. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1832(10). 1776–1783. 85 indexed citations

6.

Fargue, Sonia, Jackie Lewin, Gill Rumsby, & Christopher J. Danpure. (2012). Four of the Most Common Mutations in Primary Hyperoxaluria Type 1 Unmask the Cryptic Mitochondrial Targeting Sequence of Alanine:glyoxylate Aminotransferase Encoded by the Polymorphic Minor Allele. Journal of Biological Chemistry. 288(4). 2475–2484. 76 indexed citations

7.

Berra, Marta, Emma L. Williams, Sarah Creighton, et al.. (2011). Recognition of 5α-reductase-2 deficiency in an adult female 46XY DSD clinic. European Journal of Endocrinology. 164(6). 1019–1025. 33 indexed citations

8.

Pietrancosta, Nicolas, et al.. (2007). Purification and characterization of recombinant human liver glycolate oxidase. Archives of Biochemistry and Biophysics. 465(2). 410–416. 25 indexed citations

9.

Brooke, Antonia, Norman Taylor, J. H. Shepherd, et al.. (2006). A Novel Point Mutation in P450c17 (CYP17) Causing Combined 17α-Hydroxylase/17,20-Lyase Deficiency. The Journal of Clinical Endocrinology & Metabolism. 91(6). 2428–2431. 34 indexed citations

10.

Conners, Rebecca, et al.. (2006). Structural Basis of Substrate Specificity in Human Glyoxylate Reductase/Hydroxypyruvate Reductase. Journal of Molecular Biology. 360(1). 178–189. 51 indexed citations

11.

Brady, R.L., et al.. (2005). A preliminary account of the properties of recombinant human Glyoxylate reductase (GRHPR), LDHA and LDHB with glyoxylate, and their potential roles in its metabolism. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1753(2). 209–216. 53 indexed citations

12.

Rumsby, Gill. (2005). An overview of the role of genotyping in the diagnosis of the primary hyperoxalurias. Urological Research. 33(5). 318–320. 11 indexed citations

13.

Frishberg, Yaacov, Choni Rinat, Adel Shalata, et al.. (2005). Intra-Familial Clinical Heterogeneity: Absence of Genotype-Phenotype Correlation in Primary Hyperoxaluria Type 1 in Israel. American Journal of Nephrology. 25(3). 269–275. 33 indexed citations

14.

Rumsby, Gill, Emma L. Williams, & Marion B. Coulter-Mackie. (2004). Evaluation of mutation screening as a first line test for the diagnosis of the primary hyperoxalurias. Kidney International. 66(3). 959–963. 85 indexed citations

15.

Rumsby, Gill, et al.. (2001). Primary hyperoxaluria type 2 without l‐glycericaciduria: is the disease under‐diagnosed?. Nephrology Dialysis Transplantation. 16(8). 1697–1699. 25 indexed citations

16.

Yousaf, Nasim, et al.. (1998). Characterization of polymorphisms at the 11β‐hydroxylase (CYP11B1) locus. Annals of Human Genetics. 62(2). 181–183. 4 indexed citations

17.

Schnakenburg, Christian von, Todd H. Weir, & Gill Rumsby. (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. 9 indexed citations

18.

Höppe, Bernd, Christopher J. Danpure, Gill Rumsby, et al.. (1997). A vertical (pseudodominant) pattern of inheritance in the autosomal recessive disease primary hyperoxaluria type 1: Lack of relationship between genotype, enzymic phenotype, and disease severity. American Journal of Kidney Diseases. 29(1). 36–44. 53 indexed citations

19.

Rumsby, Gill, et al.. (1994). Steroid 11β-hydroxylase deficiency caused by a five base pair duplication in the CYP11B1 gene. Human Molecular Genetics. 3(2). 377–378. 23 indexed citations

20.

Honour, John W. & Gill Rumsby. (1993). Problems in diagnosis and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. The Journal of Steroid Biochemistry and Molecular Biology. 45(1-3). 69–74. 23 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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