Catherine Owen

2.3k total citations · 1 hit paper
22 papers, 1.5k citations indexed

About

Catherine Owen is a scholar working on Genetics, Endocrinology, Diabetes and Metabolism and Immunology. According to data from OpenAlex, Catherine Owen has authored 22 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 8 papers in Endocrinology, Diabetes and Metabolism and 8 papers in Immunology. Recurrent topics in Catherine Owen's work include Diabetes and associated disorders (8 papers), Adrenal Hormones and Disorders (5 papers) and T-cell and B-cell Immunology (4 papers). Catherine Owen is often cited by papers focused on Diabetes and associated disorders (8 papers), Adrenal Hormones and Disorders (5 papers) and T-cell and B-cell Immunology (4 papers). Catherine Owen collaborates with scholars based in United Kingdom, United States and Australia. Catherine Owen's co-authors include Simon H. S. Pearce, Claire Jennings, Valerie Wilson, Petros Perros, Peter T. Donaldson, Robert A. James, Richard Quinton, Tim Cheetham, Steve Ball and Sharlene D. Herington and has published in prestigious journals such as Nature Genetics, The Journal of Clinical Endocrinology & Metabolism and Nature Reviews Disease Primers.

In The Last Decade

Catherine Owen

21 papers receiving 1.5k citations

Hit Papers

1 papers align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Large-vessel vasculitis

2022 127 citations Dan Pugh, Neil Basu et al. Nature Reviews Disease Primers profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Catherine Owen United Kingdom	15	782	571	521	339	220	22	1.5k
Andrew Demaine United Kingdom	25	426 0.5×	459 0.8×	453 0.9×	226 0.7×	112 0.5×	47	1.6k
Tauro Maria Neri Italy	21	332 0.4×	496 0.9×	591 1.1×	222 0.7×	338 1.5×	51	2.2k
Meiko Takahashi Japan	22	223 0.3×	141 0.2×	699 1.3×	290 0.9×	149 0.7×	46	1.7k
Kathy L. Sivils United States	21	325 0.4×	532 0.9×	336 0.6×	130 0.4×	552 2.5×	49	1.8k
François Cornélis France	29	311 0.4×	685 1.2×	422 0.8×	85 0.3×	877 4.0×	62	1.8k
Christopher J. Lessard United States	19	240 0.3×	552 1.0×	245 0.5×	74 0.2×	476 2.2×	35	1.3k
P. Martin van Hagen Netherlands	21	165 0.2×	457 0.8×	210 0.4×	70 0.2×	267 1.2×	62	1.2k
P. A. Dyer United Kingdom	18	174 0.2×	442 0.8×	215 0.4×	86 0.3×	248 1.1×	50	1.1k
Jena D. French United States	16	175 0.2×	650 1.1×	294 0.6×	762 2.2×	40 0.2×	27	1.7k
Gwenny M. Verstappen Netherlands	19	198 0.3×	456 0.8×	198 0.4×	82 0.2×	288 1.3×	67	1.4k

Countries citing papers authored by Catherine Owen

Since Specialization

Citations

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

Fields of papers citing papers by Catherine Owen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Catherine Owen

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Hummel, Sandra, Peter Achenbach, Reinhard Berner, et al.. (2025). Anti-viral action against type 1 diabetes autoimmunity: The GPPAD-AVAnT1A study protocol. Contemporary Clinical Trials Communications. 44. 101434–101434.

Pugh, Dan, Neil Basu, María C. Cid, et al.. (2022). Large-vessel vasculitis. Nature Reviews Disease Primers. 7(1). 93–93. 127 indexed citations breakdown →

Coles, Jennifer, et al.. (2020). Hyperphosphatemic familial tumoral calcinosis complicated by pica. Archives of Disease in Childhood. 106(8). 790–790. 1 indexed citations

Smith, Kath, Martin Christian, Talat Mushtaq, et al.. (2019). Phenotypic diversity and correlation with the genotypes of pseudohypoaldosteronism type 1. Journal of Pediatric Endocrinology and Metabolism. 32(9). 959–967. 17 indexed citations

Pham, Trang Thanh, Catherine Owen, Val Gebski, et al.. (2016). Left‐sided breast cancer loco‐regional radiotherapy with deep inspiration breath‐hold: Does volumetric‐modulated arc radiotherapy reduce heart dose further compared with tangential intensity‐modulated radiotherapy?. Journal of Medical Imaging and Radiation Oncology. 60(4). 545–553. 42 indexed citations

Wood, Claire, C. Marini Bettolo, Kate Bushby, et al.. (2016). Bisphosphonate use in Duchenne Muscular Dystrophy – why, when to start and when to stop?. Expert Opinion on Orphan Drugs. 4(4). 407–416. 5 indexed citations

Cheetham, Tim, Michela Guglieri, Kate Bushby, et al.. (2015). Testosterone Treatment of Pubertal Delay in Duchenne Muscular Dystrophy. Neuropediatrics. 46(6). 371–376. 24 indexed citations

Sárközy, Anna, Ramesh Srinivasan, David J. Rawlings, et al.. (2014). G.P.97. Neuromuscular Disorders. 24(9-10). 824–824. 3 indexed citations

Gomes, Lavier, et al.. (2014). Clinical equipoise: Protons and the child with craniopharyngioma. Journal of Medical Imaging and Radiation Oncology. 59(3). 379–385. 12 indexed citations

10.

Owen, Catherine & Tim Cheetham. (2009). Diagnosis and Management of Polyendocrinopathy Syndromes. Endocrinology and Metabolism Clinics of North America. 38(2). 419–436. 18 indexed citations

11.

Owen, Catherine, Simon H. S. Pearce, Michael Wright, et al.. (2009). Discordance for X-Linked Hypophosphataemic Rickets in Identical Twin Girls. Hormone Research in Paediatrics. 71(4). 237–244. 10 indexed citations

12.

Owen, Catherine, et al.. (2007). Analysis of the Fc Receptor-Like-3 (FCRL3) Locus in Caucasians with Autoimmune Disorders Suggests a Complex Pattern of Disease Association. The Journal of Clinical Endocrinology & Metabolism. 92(3). 1106–1111. 77 indexed citations

13.

Fanciulli, Manuela, Penny J. Norsworthy, Enrico Petretto, et al.. (2007). FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity. Nature Genetics. 39(6). 721–723. 352 indexed citations

14.

Owen, Catherine, et al.. (2006). Genetic association studies of the FOXP3 gene in Graves’ disease and autoimmune Addison’s disease in the United Kingdom population. Journal of Molecular Endocrinology. 37(1). 97–104. 64 indexed citations

15.

Lin, Lin, Wen-Xia Gu, Gökhan Özışık, et al.. (2006). Analysis of DAX1 (NR0B1) and Steroidogenic Factor-1 (NR5A1) in Children and Adults with Primary Adrenal Failure: Ten Years’ Experience. The Journal of Clinical Endocrinology & Metabolism. 91(8). 3048–3054. 138 indexed citations

16.

Jennings, Claire, Catherine Owen, Valerie Wilson, & Simon H. S. Pearce. (2005). A haplotype of the CYP27B1 promoter is associated with autoimmune Addison’s disease but not with Graves’ disease in a UK population. Journal of Molecular Endocrinology. 34(3). 859–863. 31 indexed citations

17.

Jennings, Claire, Catherine Owen, Valerie Wilson, & Simon H. S. Pearce. (2005). No association of the codon 55 methionine to valine polymorphism in the SUMO4 gene with Graves’ disease. Clinical Endocrinology. 62(3). 362–365. 13 indexed citations

18.

Wilson, Valerie, Claire Jennings, Catherine Owen, et al.. (2004). The Codon 620 Tryptophan Allele of the Lymphoid Tyrosine Phosphatase (LYP) Gene Is a Major Determinant of Graves’ Disease. The Journal of Clinical Endocrinology & Metabolism. 89(11). 5862–5865. 357 indexed citations

19.

Wilson, Valerie, Claire Jennings, Catherine Owen, et al.. (2004). Role of the CD40 Locus in Graves' Disease. Thyroid. 14(7). 506–509. 46 indexed citations

20.

Owen, Catherine, Claire Jennings, Helen Imrie, et al.. (2003). Mutational Analysis of the FOXP3 Gene and Evidence for Genetic Heterogeneity in the Immunodysregulation, Polyendocrinopathy, Enteropathy Syndrome. The Journal of Clinical Endocrinology & Metabolism. 88(12). 6034–6039. 85 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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