C.E. Browne
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 14
- Genomic variations and chromosomal abnormalities 10
- Genetic Syndromes and Imprinting 5
- Genetics and Neurodevelopmental Disorders 3
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
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- Genomics and Chromatin Dynamics 2
- Chromatin Remodeling and Cancer 2
- Co-authors
- P. A. Jacobs (2 shared papers)N. Simon Thomas (6 shared papers)Caroline Joyce (1 shared paper)Helen White (1 shared paper)N. Gregson (1 shared paper)N R Dennis (2 shared papers)Peter Strike (1 shared paper)P.A. Jacobs (1 shared paper)
- Journals
- Human Genetics (6 papers)Cytogenetic and Genome Research (2 papers)Psychiatric Genetics (1 paper)The American Journal of Human Genetics (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- United KingdomAustraliaSouth Sudan
In The Last Decade
C.E. Browne
15 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 60
- Genetics 943
- Pediatrics, Perinatology and Child Health 330
- Cognitive Neuroscience 255
- Molecular Biology 388
- Plant Science 174
Countries citing papers authored by C.E. Browne
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
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.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 1992 | 285 | |
| 2 | 2001 | 181 | |
| 3 | 2007 | 171 | |
| 4 | 1997 | 149 | |
| 5 | 1999 | 133 | |
| 6 | 2001 | 109 | |
| 7 | 2002 | 90 | |
| 8 | 2004 | 53 | |
| 9 | 1998 | 28 | |
| 10 | 1994 | 23 | |
| 11 | 1999 | 19 | |
| 12 | 2009 | 8 | |
| 13 | 1999 | 8 | |
| 14 | 1999 | 6 | |
| 15 | 2009 | 3 |
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 1.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (6 papers), Genetic Syndromes and Imprinting (5 papers), Chromosomal and Genetic Variations (5 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genomics and Chromatin Dynamics (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers) and Chromatin Remodeling and Cancer (2 papers). The work is most often cited by research in Genetics (943 citations), Pediatrics, Perinatology and Child Health (330 citations), Cognitive Neuroscience (255 citations), Molecular Biology (388 citations) and Plant Science (174 citations). C.E. Browne has collaborated with scholars based in United Kingdom, Australia and South Sudan. Frequent co-authors include P. A. Jacobs, N. Simon Thomas, Caroline Joyce, Helen White, N. Gregson, N R Dennis, Peter Strike, P.A. Jacobs, Nicholas R. Dennis and Marijcke W. M. Veltman. Their work appears in journals such as Human Genetics, Cytogenetic and Genome Research, Psychiatric Genetics, The American Journal of Human Genetics and Journal of Medical 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.