Jane Fleming

594 citations
30 papers · 348 · h-index 9

Impact in

Papers in

    • BRCA gene mutations in cancer 5
    • Genomics and Rare Diseases 3
    • Virus-based gene therapy research 2
    • Neurofibromatosis and Schwannoma Cases 8

Jane Fleming

29 papers receiving 339 citations

Peers

Jane Fleming
Comparison fields: 5 of 82
  • Genetics 111
  • Sensory Systems 17
  • Cellular and Molecular Neuroscience 57
  • Molecular Biology 184
  • Neurology 28
Replace Kate Sinclair with:
Kate Sinclair Australia
Selwa A.F. Al-Hazzaa Saudi Arabia
Andrew T. Timberlake United States
Julie Sarfati France
Ji Yoon Han South Korea
Igor Medica Slovenia
Sandra P. Toelle Switzerland
Alice S. Brooks Netherlands
Piotr Gasperowicz Poland
Fabien Guimiot France
Jane Fleming relative to Kate Sinclair Australia Kate Sinclair's profile →
Citations per field
00.5×3.4×
Kate Sinclair · 1×
Citations per year

Countries citing papers authored by Jane Fleming

Since Specialization
Citations

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

Fields of papers citing papers by Jane Fleming

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Jane Fleming, 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 Jane Fleming Line = papers co-authored together Jane Fleming links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 30 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1993105
2 200152
3 200331
4 200527
5 199920
6 202319
7 202013
8 20218
9 20228
10 20208
11 19757
12 20236
13 19865
14 20235
15 20204
16 20204
17 20193
18 19613
19 20213
20 20163

About Jane Fleming

Jane Fleming is a scholar working on Genetics, Neurology, Pediatrics, Perinatology and Child Health, Pathology and Forensic Medicine and Epidemiology, having authored 30 papers that have together received 348 indexed citations. Recurring topics across this work include Neurofibromatosis and Schwannoma Cases (8 papers), BRCA gene mutations in cancer (5 papers), Prenatal Screening and Diagnostics (5 papers), Soft tissue tumor case studies (4 papers), Genomics and Rare Diseases (3 papers), Genetic factors in colorectal cancer (2 papers), Virus-based gene therapy research (2 papers) and Ethics in Clinical Research (2 papers). The work is most often cited by research in Genetics (111 citations), Sensory Systems (17 citations), Cellular and Molecular Neuroscience (57 citations), Molecular Biology (184 citations) and Neurology (28 citations). Jane Fleming has collaborated with scholars based in Australia, United Kingdom and United States. Frequent co-authors include Samantha L. Ginn, Ian E. Alexander, Karen J. Moore, S. Sterrer, Karen P. Steel, Rudi Balling, S.D.M. Brown, Martyn Goulding, Joseph H. Nadeau and Peter B. Rowe. Their work appears in journals such as Human Gene Therapy, Familial Cancer, European Journal of Human Genetics, Clinical and Experimental Dermatology and Journal of Investigative Dermatology.

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