Caroline E. Browne
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 16
- Genomic variations and chromosomal abnormalities 12
- 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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- Prenatal Screening and Diagnostics 6
- Co-authors
- P. A. Jacobs (2 shared papers)Nicholas Simon Thomas (7 shared papers)N. Gregson (1 shared paper)Caroline Martha Joyce (1 shared paper)Helen White (1 shared paper)Nichola R. Dennis (2 shared papers)P.A. Jacobs (1 shared paper)Peter Strike (1 shared paper)
- Journals
- Human Genetics (6 papers)Journal of Medical Genetics (2 papers)Cytogenetic and Genome Research (2 papers)The American Journal of Human Genetics (1 paper)Psychiatric Genetics (1 paper)
- Partner nations
- United KingdomAustraliaFrance
In The Last Decade
Caroline E. Browne
18 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 62
- Genetics 1.0k
- Pediatrics, Perinatology and Child Health 352
- Cognitive Neuroscience 266
- Molecular Biology 435
- Developmental Biology 12
Countries citing papers authored by Caroline E. Browne
This map shows the geographic impact of Caroline 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 Caroline 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 Caroline E. Browne more than expected).
Fields of papers citing papers by Caroline E. Browne
This network shows the impact of papers produced by Caroline 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 Caroline E. Browne. The network helps show where Caroline E. Browne may publish in the future.
Co-authors
The 25 scholars most cited alongside Caroline 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 | 299 | |
| 2 | 2001 | 192 | |
| 3 | 2007 | 180 | |
| 4 | 1997 | 171 | |
| 5 | 1999 | 145 | |
| 6 | 2001 | 114 | |
| 7 | 2002 | 101 | |
| 8 | 2004 | 57 | |
| 9 | 1998 | 30 | |
| 10 | 1994 | 25 | |
| 11 | 1999 | 20 | |
| 12 | 1999 | 10 | |
| 13 | 2003 | 9 | |
| 14 | 2009 | 8 | |
| 15 | 2002 | 7 | |
| 16 | 1999 | 6 | |
| 17 | 2009 | 3 | |
| 18 | 2000 | 2 |
About Caroline E. Browne
Caroline E. Browne is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Plant Science, Molecular Biology and Developmental Biology, having authored 18 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 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), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Congenital heart defects research (2 papers) and Chromatin Remodeling and Cancer (2 papers). The work is most often cited by research in Genetics (1.0k citations), Pediatrics, Perinatology and Child Health (352 citations), Cognitive Neuroscience (266 citations), Molecular Biology (435 citations) and Developmental Biology (12 citations). Caroline E. Browne has collaborated with scholars based in United Kingdom, Australia and France. Frequent co-authors include P. A. Jacobs, Nicholas Simon Thomas, N. Gregson, Caroline Martha Joyce, Helen White, Nichola R. Dennis, P.A. Jacobs, Peter Strike, Nicholas Robert Dennis and John C.K. Barber. Their work appears in journals such as Human Genetics, Journal of Medical Genetics, Cytogenetic and Genome Research, The American Journal of Human 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.