Steven Hardy

1.8k total citations
28 papers, 777 citations indexed

About

Steven Hardy is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Steven Hardy has authored 28 papers receiving a total of 777 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 9 papers in Clinical Biochemistry and 5 papers in Genetics. Recurrent topics in Steven Hardy's work include Mitochondrial Function and Pathology (14 papers), Metabolism and Genetic Disorders (9 papers) and RNA modifications and cancer (8 papers). Steven Hardy is often cited by papers focused on Mitochondrial Function and Pathology (14 papers), Metabolism and Genetic Disorders (9 papers) and RNA modifications and cancer (8 papers). Steven Hardy collaborates with scholars based in United Kingdom, United States and Germany. Steven Hardy's co-authors include Daniel J. Maltman, Stefan Przyborski, Chun-Ya Han, Bruce K. Lin, Henry J. Lin, Robert W. Taylor, Stefan Przyborski, Yi Shiau Ng, Robert McFarland and Douglass M. Turnbull and has published in prestigious journals such as SHILAP Revista de lepidopterología, Cancer Research and Scientific Reports.

In The Last Decade

Steven Hardy

27 papers receiving 763 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Steven Hardy United Kingdom 13 498 219 142 94 82 28 777
Daniella Magen Israel 16 518 1.0× 53 0.2× 32 0.2× 55 0.6× 45 0.5× 46 941
Belén Bornstein Spain 19 1.2k 2.5× 297 1.4× 66 0.5× 53 0.6× 29 0.4× 49 1.6k
Rosa Aledo Spain 20 507 1.0× 79 0.4× 67 0.5× 17 0.2× 166 2.0× 36 882
Haiyan Fan China 17 449 0.9× 34 0.2× 31 0.2× 32 0.3× 142 1.7× 36 822
Mohga El‐Abbadi United States 14 439 0.9× 55 0.3× 77 0.5× 17 0.2× 231 2.8× 15 1.1k
Silvia Di Giandomenico Italy 10 499 1.0× 130 0.6× 30 0.2× 119 1.3× 58 0.7× 11 741
Oleg A. Shchelochkov United States 24 746 1.5× 460 2.1× 52 0.4× 31 0.3× 60 0.7× 47 1.3k
Robert Mott United States 11 519 1.0× 162 0.7× 32 0.2× 35 0.4× 84 1.0× 14 1.0k
HP Hammes Germany 12 299 0.6× 265 1.2× 36 0.3× 29 0.3× 47 0.6× 22 888
Jianning Zhang China 15 470 0.9× 15 0.1× 99 0.7× 43 0.5× 243 3.0× 28 839

Countries citing papers authored by Steven Hardy

Since Specialization
Citations

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

Fields of papers citing papers by Steven Hardy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Steven Hardy

This figure shows the co-authorship network connecting the top 25 collaborators of Steven Hardy. A scholar is included among the top collaborators of Steven Hardy 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 Steven Hardy. Steven Hardy 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.
Knott, Craig, Catherine Huntley, Yvonne Walburga Joko-Fru, et al.. (2025). Long-term outcomes of bilateral salpingo-oophorectomy in women with personal history of breast cancer. PubMed. 4(1). e000574–e000574. 1 indexed citations
2.
Ramakrishnan, Rema, Steven Hardy, Jennifer M. Broughan, et al.. (2024). Implementation of a national rapid prenatal exome sequencing service in England: evaluation of service outcomes and factors associated with regional variation. Frontiers in Genetics. 15. 1485306–1485306. 2 indexed citations
3.
Hill, Melissa, et al.. (2024). Implementation of a National Prenatal Exome Sequencing Service in England: Cost‐Effectiveness Analysis. BJOG An International Journal of Obstetrics & Gynaecology. 132(4). 483–491. 2 indexed citations
4.
McRonald, Fiona E., Joanna Pethick, Margreet Lüchtenborg, et al.. (2024). Identification of people with Lynch syndrome from those presenting with colorectal cancer in England: baseline analysis of the diagnostic pathway. European Journal of Human Genetics. 32(5). 529–538. 7 indexed citations
5.
Monahan, Kevin, Adam Shaw, Laura Monje‐Garcia, et al.. (2023). P293 Finding the missing 95%: the English national lynch syndrome transformation project. Poster presentations. A204.2–A204. 3 indexed citations
6.
Monahan, Kevin, Neil Ryan, Laura Monje‐Garcia, et al.. (2023). The English National Lynch Syndrome transformation project: an NHS Genomic Medicine Service Alliance (GMSA) programme. SHILAP Revista de lepidopterología. 2(1). e000124–e000124. 9 indexed citations
7.
8.
Ng, Yi Shiau, Kyle Thompson, Sila Hopton, et al.. (2020). Novel MT-ND Gene Variants Causing Adult-Onset Mitochondrial Disease and Isolated Complex I Deficiency. Frontiers in Genetics. 11. 24–24. 16 indexed citations
9.
Hellebrekers, Debby M.E.I., Emma L. Blakely, Alexandra T.M. Hendrickx, et al.. (2019). A novel mitochondrial m.4414T>C MT-TM gene variant causing progressive external ophthalmoplegia and myopathy. Neuromuscular Disorders. 29(9). 693–697. 2 indexed citations
10.
Perli, Elena, Annalinda Pisano, Steven Hardy, et al.. (2019). Novel compound mutations in the mitochondrial translation elongation factor (TSFM) gene cause severe cardiomyopathy with myocardial fibro-adipose replacement. Scientific Reports. 9(1). 5108–5108. 12 indexed citations
11.
Grady, John P., Sarah J. Pickett, Yi Shiau Ng, et al.. (2018). mt DNA heteroplasmy level and copy number indicate disease burden in m.3243A>G mitochondrial disease. EMBO Molecular Medicine. 10(6). 190 indexed citations
12.
Hardy, Steven, Emma L. Blakely, Sila Hopton, et al.. (2017). Pigmentary retinopathy, rod–cone dysfunction and sensorineural deafness associated with a rare mitochondrial tRNALys(m.8340G>A) gene variant. British Journal of Ophthalmology. 101(9). 1298–1302. 6 indexed citations
13.
Rocha, Mariana C., Steven Hardy, Amy E. Vincent, et al.. (2017). Disclosing the functional changes of two genetic alterations in a patient with Chronic Progressive External Ophthalmoplegia: Report of the novel mtDNA m.7486G>A variant. Neuromuscular Disorders. 28(4). 350–360. 8 indexed citations
14.
Reimann, Jens, Diana Lehmann, Steven Hardy, et al.. (2017). Camptocormia and shuffling gait due to a novel MT-TV mutation: Diagnostic pitfalls. Neurology Genetics. 3(3). e147–e147. 1 indexed citations
15.
Sommerville, Ewen W., Rachel L. Jones, Steven Hardy, et al.. (2017). Opening One's Eyes to Mosaicism in Progressive External Ophthalmoplegia. Neurology Genetics. 3(6). e202–e202. 1 indexed citations
16.
Ng, Yi Shiau, Steven Hardy, Gerardine Quaghebeur, et al.. (2016). Clinical features of the pathogenic m.5540G>A mitochondrial transfer RNA tryptophan gene mutation. Neuromuscular Disorders. 26(10). 702–705. 5 indexed citations
17.
Oláhová, Monika, Kyle Thompson, Steven Hardy, et al.. (2016). Pathogenic variants in HTRA2 cause an early‐onset mitochondrial syndrome associated with 3‐methylglutaconic aciduria. Journal of Inherited Metabolic Disease. 40(1). 121–130. 23 indexed citations
18.
Lehmann, Diana, Pushpa Raj Joshi, Steven Hardy, et al.. (2015). Pathogenic mitochondrial mt-tRNAAla variants are uniquely associated with isolated myopathy. European Journal of Human Genetics. 23(12). 1735–1738. 20 indexed citations
19.
Gilbert, Rodney D., et al.. (2013). Cisplatin-induced haemolytic uraemic syndrome associated with a novel intronic mutation ofCD46treated with eculizumab. Clinical Kidney Journal. 6(4). 421–425. 19 indexed citations
20.
Maltman, Daniel J., Steven Hardy, & Stefan Przyborski. (2011). Role of mesenchymal stem cells in neurogenesis and nervous system repair. Neurochemistry International. 59(3). 347–56. 113 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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