Steven Hardy

1.8k citations
29 papers · 805 · h-index 14

Impact in

Papers in

    • Mitochondrial Function and Pathology 14
    • RNA modifications and cancer 7
    • Ubiquitin and proteasome pathways 2
    • ATP Synthase and ATPases Research 2
    • Metabolism and Genetic Disorders 7

Steven Hardy

28 papers receiving 791 citations

Peers

Steven Hardy
Comparison fields: 5 of 68
  • Clinical Biochemistry 176
  • Developmental Neuroscience 61
  • Genetics 125
  • Molecular Biology 485
  • Cancer Research 73
Replace Rosa Aledo with:
Rosa Aledo Spain
Qiong Ke China
Steven Messina‐Graham United States
Jianning Zhang China
Mary Blonski United States
Haiyan Fan China
Ali‐Reza Moslemi Sweden
Naser Jaleel United States
Tomoko Asashima Japan
Leonardo Romorini Argentina
Steven Hardy relative to Rosa Aledo Spain Rosa Aledo's profile →
Citations per field
00.5×
Rosa Aledo · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Steven Hardy, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Steven Hardy Line = papers co-authored together Steven Hardy links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 29 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2018199
2 1994137
3 2011113
4 200875
5 201548
6 201430
7 201625
8 201624
9 201521
10 201319
11 202017
12 202314
13 201514
14 201913
15 202311
16 20179
17 20248
18 20176
19 20245
20 20165

About Steven Hardy

Steven Hardy is a scholar working on Molecular Biology, Clinical Biochemistry, Pathology and Forensic Medicine, Cancer Research and Genetics, having authored 29 papers that have together received 805 indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (14 papers), Metabolism and Genetic Disorders (7 papers), RNA modifications and cancer (7 papers), Genetic factors in colorectal cancer (4 papers), Cancer Genomics and Diagnostics (2 papers), Ubiquitin and proteasome pathways (2 papers), Mesenchymal stem cell research (2 papers) and ATP Synthase and ATPases Research (2 papers). The work is most often cited by research in Clinical Biochemistry (176 citations), Developmental Neuroscience (61 citations), Genetics (125 citations), Molecular Biology (485 citations) and Cancer Research (73 citations). Steven Hardy has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Daniel J. Maltman, Stefan Przyborski, Bruce K. Lin, Chun-Ya Han, Henry J. Lin, Robert W. Taylor, Stefan Przyborski, Yi Shiau Ng, Emma L. Blakely and Gráinne S. Gorman. Their work appears in journals such as Neurology Genetics, Neuromuscular Disorders, Frontiers in Genetics, European Journal of Human Genetics and Current Stem Cell Research & Therapy.

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