C.E. Browne

1.8k citations
15 papers · 1.1k · h-index 11

Impact in

  • Genetics top 2%
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Genetic Syndromes and Imprinting
    • Genomics and Rare Diseases
    • Prenatal Screening and Diagnostics

Papers in

    • Genomic variations and chromosomal abnormalities 11
    • Genetic Syndromes and Imprinting 5
    • Genetics and Neurodevelopmental Disorders 4
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
    • Genomics and Chromatin Dynamics 2
    • Chromatin Remodeling and Cancer 2

C.E. Browne

15 papers receiving 1.0k citations

Peers

C.E. Browne
Comparison fields: 5 of 58
  • Genetics 938
  • Pediatrics, Perinatology and Child Health 324
  • Cognitive Neuroscience 273
  • Molecular Biology 415
  • Plant Science 186
Replace Nicholas R. Dennis with:
Nicholas R. Dennis United Kingdom
David Francis Australia
S. L. Sherman United States
Trent Burgess Australia
Ilia V. Soloviev Russia
Art Daniel Australia
Dorothy Pettay United States
A Kleczkowska Belgium
M. Lance Cooper United States
Sheila Youings United Kingdom
C.E. Browne relative to Nicholas R. Dennis United Kingdom Nicholas R. Dennis's profile →
Citations per field
00.5×2.6×
Nicholas R. Dennis · 1×
Citations per year

Countries citing papers authored by C.E. Browne

Since Specialization
Citations

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

Fields of papers citing papers by C.E. Browne

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by C.E. Browne. 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 C.E. Browne. The network helps show where C.E. Browne may publish in the future.

Co-authors

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

All Works

15 of 15 papers shown
#Work
1 1992246
2 2001155
3 2007144
4 1997143
5 1999126
6 200190
7 200271
8 200450
9 199825
10 199423
11 199918
12 20098
13 19998
14 19995
15 20093

About C.E. Browne

C.E. Browne is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Neurology, having authored 15 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (6 papers), Chromosomal and Genetic Variations (5 papers), Genetic Syndromes and Imprinting (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Chromatin Dynamics (2 papers), Chromatin Remodeling and Cancer (2 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). The work is most often cited by research in Genetics (938 citations), Pediatrics, Perinatology and Child Health (324 citations), Cognitive Neuroscience (273 citations), Molecular Biology (415 citations) and Plant Science (186 citations). C.E. Browne has collaborated with scholars based in United Kingdom, Australia and France. Frequent co-authors include P. A. Jacobs, N. Simon Thomas, N. Gregson, Helen White, Caroline Joyce, N R Dennis, P.A. Jacobs, Peter Strike, Nicholas R. Dennis and John Barber. Their work appears in journals such as Human Genetics, Cytogenetic and Genome Research, The American Journal of Human Genetics, Journal of Medical Genetics and Psychiatric Genetics.

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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