Brian Coppin
Impact in
- Genetics top 5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Cognitive Neuroscience top 10%
- Autism Spectrum Disorder Research
Papers in
- Genetics 7
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Genetics and Neurodevelopmental Disorders 2
- Genetic Syndromes and Imprinting 2
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- Sexual Differentiation and Disorders 2
- Ubiquitin and proteasome pathways 1
- Co-authors
- P. A. Jacobs (6 shared papers)R S James (4 shared papers)Pamela Dalton (3 shared papers)David Skuse (1 shared paper)Dorothy Bishop (2 shared papers)Cathy Creswell (2 shared papers)Rhona McGurk (2 shared papers)I. Karen Temple (1 shared paper)
- Journals
- Journal of Medical Genetics (3 papers)Human Genetics (1 paper)Annals of Human Genetics (1 paper)Clinical Genetics (1 paper)Nature (1 paper)
- Partner nations
- United KingdomGreece
In The Last Decade
Brian Coppin
8 papers receiving 687 citations
Brian Coppin's Hit Papers
Peers
Comparison fields: 5 of 77
- Genetics 530
- Cognitive Neuroscience 158
- Gender Studies 52
- Pediatrics, Perinatology and Child Health 89
- Molecular Biology 335
Countries citing papers authored by Brian Coppin
This map shows the geographic impact of Brian Coppin'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 Brian Coppin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Brian Coppin more than expected).
Fields of papers citing papers by Brian Coppin
This network shows the impact of papers produced by Brian Coppin. 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 Brian Coppin. The network helps show where Brian Coppin may publish in the future.
Co-authors
The 19 scholars most cited alongside Brian Coppin, 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 | Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function Hit paper breakdown → | 1997 | 587 |
| 2 | 1997 | 70 | |
| 3 | 1998 | 55 | |
| 4 | 1997 | 21 | |
| 5 | 1997 | 20 | |
| 6 | 2000 | 19 | |
| 7 | 1998 | 11 | |
| 8 | 2002 | 7 |
About Brian Coppin
Brian Coppin is a scholar working on Genetics, Molecular Biology, Plant Science, Surgery and Cognitive Neuroscience, having authored 8 papers that have together received 790 indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (2 papers), Sexual Differentiation and Disorders (2 papers), Genetic Syndromes and Imprinting (2 papers), Chromosomal and Genetic Variations (2 papers), Ubiquitin and proteasome pathways (1 paper), Autism Spectrum Disorder Research (1 paper) and Galectins and Cancer Biology (1 paper). The work is most often cited by research in Genetics (530 citations), Cognitive Neuroscience (158 citations), Gender Studies (52 citations), Pediatrics, Perinatology and Child Health (89 citations) and Molecular Biology (335 citations). Brian Coppin has collaborated with scholars based in United Kingdom and Greece. Frequent co-authors include P. A. Jacobs, R S James, Pamela Dalton, David Skuse, Dorothy Bishop, Cathy Creswell, Rhona McGurk, I. Karen Temple, Andrew J. Sharp and Isabella Moore. Their work appears in journals such as Journal of Medical Genetics, Human Genetics, Annals of Human Genetics, Clinical Genetics and Nature.
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.