Helen Storey

1.3k total citations
14 papers, 690 citations indexed

About

Helen Storey is a scholar working on Immunology and Allergy, Hematology and Molecular Biology. According to data from OpenAlex, Helen Storey has authored 14 papers receiving a total of 690 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Immunology and Allergy, 8 papers in Hematology and 7 papers in Molecular Biology. Recurrent topics in Helen Storey's work include Cell Adhesion Molecules Research (12 papers), Platelet Disorders and Treatments (8 papers) and Renal and related cancers (5 papers). Helen Storey is often cited by papers focused on Cell Adhesion Molecules Research (12 papers), Platelet Disorders and Treatments (8 papers) and Renal and related cancers (5 papers). Helen Storey collaborates with scholars based in United Kingdom, Australia and Spain. Helen Storey's co-authors include Frances Flinter, Judy Savige, Stephen Abbs, Mads Thomassen, Jens Michael Hertz, Daniel P. Gale, Anton V. Persikov, Francesca Mari, Valerio Izzi and Roser Torrá and has published in prestigious journals such as PLoS ONE, Biochemical Journal and Journal of the American Society of Nephrology.

In The Last Decade

Helen Storey

14 papers receiving 675 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Helen Storey United Kingdom	12	469	358	238	200	178	14	690
C E Kashtan United States	12	430 0.9×	234 0.7×	178 0.7×	183 0.9×	162 0.9×	13	636
Marie Christine Verpont France	5	118 0.3×	126 0.4×	84 0.4×	36 0.2×	79 0.4×	6	325
Kamila Bledzka United States	14	440 0.9×	315 0.9×	10 0.0×	200 1.0×	52 0.3×	19	783
Aruna M. Somasiri Canada	8	96 0.2×	438 1.2×	30 0.1×	29 0.1×	51 0.3×	11	681
Roland Bosse Germany	7	322 0.7×	260 0.7×	7 0.0×	74 0.4×	21 0.1×	8	593
Nancy E. Kirschbaum United States	9	160 0.3×	310 0.9×	5 0.0×	249 1.2×	43 0.2×	13	635
Maya Damianovich Israel	8	52 0.1×	81 0.2×	36 0.2×	71 0.4×	15 0.1×	11	341
Ismo Virtanen Finland	11	214 0.5×	161 0.4×	11 0.0×	32 0.2×	23 0.1×	11	470
Rongfeng Fu China	13	31 0.1×	149 0.4×	18 0.1×	258 1.3×	26 0.1×	71	468
J H Spragg United Kingdom	8	205 0.4×	142 0.4×	9 0.0×	89 0.4×	20 0.1×	12	397

Countries citing papers authored by Helen Storey

Since Specialization

Citations

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

Fields of papers citing papers by Helen Storey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Helen Storey

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

All Works

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14 of 14 papers shown

Gibson, Joel T., Melanie Chan, Omid Sadeghi‐Alavijeh, et al.. (2021). Prevalence Estimates of Predicted Pathogenic COL4A3–COL4A5 Variants in a Population Sequencing Database and Their Implications for Alport Syndrome. Journal of the American Society of Nephrology. 32(9). 2273–2290. 98 indexed citations

Savige, Judy, Francesca Ariani, Francesca Mari, et al.. (2018). Expert consensus guidelines for the genetic diagnosis of Alport syndrome. Pediatric Nephrology. 34(7). 1175–1189. 85 indexed citations

Savige, Judy, Helen Storey, Hae Il Cheong, et al.. (2016). X-Linked and Autosomal Recessive Alport Syndrome: Pathogenic Variant Features and Further Genotype-Phenotype Correlations. PLoS ONE. 11(9). e0161802–e0161802. 63 indexed citations

Mencarelli, Maria Antonietta, Laurence Heidet, Helen Storey, et al.. (2015). Evidence of digenic inheritance in Alport syndrome. Journal of Medical Genetics. 52(3). 163–174. 107 indexed citations

Lennon, Rachel, Helen M. Stuart, Agnieszka Bierżyńska, et al.. (2015). Coinheritance of COL4A5 and MYO1E mutations accentuate the severity of kidney disease. Pediatric Nephrology. 30(9). 1459–1465. 33 indexed citations

Hertz, Jens Michael, Mads Thomassen, Helen Storey, & Frances Flinter. (2014). Clinical utility gene card for: Alport syndrome – update 2014. European Journal of Human Genetics. 23(9). 1269–1269. 36 indexed citations

Savige, Judy, Elisabet Ars, Richard G.H. Cotton, et al.. (2013). DNA variant databases improve test accuracy and phenotype prediction in Alport syndrome. Pediatric Nephrology. 29(6). 971–977. 16 indexed citations

Storey, Helen, et al.. (2013). COL4A3/COL4A4 Mutations and Features in Individuals with Autosomal Recessive Alport Syndrome. Journal of the American Society of Nephrology. 24(12). 1945–1954. 106 indexed citations

Wang, Yanyan, Deb Colville, Helen Storey, et al.. (2013). Clinical and genetic features in autosomal recessive and X-linked Alport syndrome. Pediatric Nephrology. 29(3). 391–396. 28 indexed citations

10.

Nanra, R. S., Deb Colville, Paul Trevillian, et al.. (2013). A female with X-linked Alport syndrome and compound heterozygous COL4A5 mutations. Pediatric Nephrology. 29(3). 481–485. 11 indexed citations

11.

Hertz, Jens Michael, Mads Thomassen, Helen Storey, & Frances Flinter. (2011). Clinical utility gene card for: Alport syndrome. European Journal of Human Genetics. 20(6). 713–713. 35 indexed citations

12.

Hanson, Helen, et al.. (2010). The Value of Clinical Criteria in Identifying Patients with X-Linked Alport Syndrome. Clinical Journal of the American Society of Nephrology. 6(1). 198–203. 31 indexed citations

13.

Rajakulendran, Sanjeev, Thierry Küntzer, Shu C. Yau, et al.. (2010). Marked Hemiatrophy in Carriers of Duchenne Muscular Dystrophy. Archives of Neurology. 67(4). 497–500. 9 indexed citations

14.

Storey, Helen, Abigail Stewart, Peter Vandenabeele, & J. Paul Luzio. (2002). The p55 tumour necrosis factor receptor TNFR1 contains a trans-Golgi network localization signal in the C-terminal region of its cytoplasmic tail. Biochemical Journal. 366(1). 15–22. 32 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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