Jane Fleming

619 citations
31 papers · 377 · h-index 9

Impact in

Papers in

    • Neurofibromatosis and Schwannoma Cases 9
    • BRCA gene mutations in cancer 5
    • Genomics and Rare Diseases 3
    • Genetics and Neurodevelopmental Disorders 2

Jane Fleming

28 papers receiving 364 citations

Peers

Jane Fleming
Comparison fields: 5 of 72
  • Sensory Systems 19
  • Genetics 108
  • Cellular and Molecular Neuroscience 59
  • Molecular Biology 183
  • Neurology 36
Replace Julie L. Lauzon with:
Julie L. Lauzon Canada
Nicolas Chatron France
Heraldo Mendes Garmes Brazil
Kate Sinclair Australia
Esther A. R. Nibbeling Netherlands
Igor Medica Slovenia
Maria Tereza Matias Baptista Brazil
May Sanyoura United States
Rita Igorevna Khusainova Russia
Hervé Testard France
Jane Fleming relative to Julie L. Lauzon Canada Julie L. Lauzon's profile →
Citations per field
00.5×1.5×2×2.5×
Julie L. Lauzon · 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 31 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1993110
2 200155
3 200532
4 200331
5 202325
6 199920
7 202015
8 20239
9 20229
10 20209
11 20218
12 19867
13 20236
14 20206
15 20214
16 20244
17 20204
18 19613
19 20163
20 20203

About Jane Fleming

Jane Fleming is a scholar working on Neurology, Genetics, Pathology and Forensic Medicine, Pediatrics, Perinatology and Child Health and Rheumatology, having authored 31 papers that have together received 377 indexed citations. Recurring topics across this work include Neurofibromatosis and Schwannoma Cases (9 papers), BRCA gene mutations in cancer (5 papers), Prenatal Screening and Diagnostics (3 papers), Soft tissue tumor case studies (3 papers), Genomics and Rare Diseases (3 papers), Ethics in Clinical Research (2 papers), Genetic factors in colorectal cancer (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). The work is most often cited by research in Sensory Systems (19 citations), Genetics (108 citations), Cellular and Molecular Neuroscience (59 citations), Molecular Biology (183 citations) and Neurology (36 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, Joseph H. Nadeau, Peter B. Rowe, Martyn Goulding, Rudi Balling, Sylvia Sterrer, Karen P. Steel, Karen J. Moore and S.D.M. Brown. Their work appears in journals such as Human Gene Therapy, Familial Cancer, Journal of Investigative Dermatology, Genomics and American Journal of Veterinary Research.

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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