John Barber
Impact in
- Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic Syndromes and Imprinting
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 51
- Genomic variations and chromosomal abnormalities 45
- Congenital Ear and Nasal Anomalies 11
- Genetics and Neurodevelopmental Disorders 7
- Genomics and Rare Diseases 6
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- Congenital heart defects research 12
- Genomics and Chromatin Dynamics 8
- Co-authors
- Edward J. Hollox (4 shared papers)John A.L. Armour (3 shared papers)I. Karen Temple (8 shared papers)N R Dennis (5 shared papers)Ronald D. Miller (1 shared paper)Viv Maloney (11 shared papers)David Robinson (2 shared papers)R J Gardner (2 shared papers)
- Journals
- Journal of Medical Genetics (11 papers)European Journal of Human Genetics (9 papers)Human Genetics (5 papers)Cytogenetic and Genome Research (5 papers)The American Journal of Human Genetics (5 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
John Barber
102 papers receiving 3.0k citations
Peers
Comparison fields: 5 of 126
- Genetics 1.9k
- Pediatrics, Perinatology and Child Health 457
- Microbiology 157
- Ophthalmology 183
- Molecular Biology 1.1k
Countries citing papers authored by John Barber
This map shows the geographic impact of John Barber'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 John Barber with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites John Barber more than expected).
Fields of papers citing papers by John Barber
This network shows the impact of papers produced by John Barber. 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 John Barber. The network helps show where John Barber may publish in the future.
Co-authors
The 25 scholars most cited alongside John Barber, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 107 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2003 | 288 | |
| 2 | 2000 | 199 | |
| 3 | 2005 | 190 | |
| 4 | 2002 | 187 | |
| 5 | Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene. | 1996 | 158 |
| 6 | 2005 | 153 | |
| 7 | 1997 | 149 | |
| 8 | 1989 | 127 | |
| 9 | 2008 | 95 | |
| 10 | 1996 | 84 | |
| 11 | 2007 | 84 | |
| 12 | 1994 | 82 | |
| 13 | 1981 | 82 | |
| 14 | 1998 | 73 | |
| 15 | 2009 | 73 | |
| 16 | Corneal ulceration and the serum antiproteases. I. Alpha 1-antitrypsin. | 1973 | 63 |
| 17 | 2005 | 62 | |
| 18 | 1988 | 61 | |
| 19 | 2008 | 61 | |
| 20 | 2003 | 60 |
About John Barber
John Barber is a scholar working on Genetics, Molecular Biology, Plant Science, Genetics and Pediatrics, Perinatology and Child Health, having authored 107 papers that have together received 3.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (45 papers), Chromosomal and Genetic Variations (17 papers), Congenital heart defects research (12 papers), Congenital Ear and Nasal Anomalies (11 papers), Prenatal Screening and Diagnostics (11 papers), Genomics and Chromatin Dynamics (8 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genomics and Rare Diseases (6 papers). The work is most often cited by research in Genetics (1.9k citations), Pediatrics, Perinatology and Child Health (457 citations), Microbiology (157 citations), Ophthalmology (183 citations) and Molecular Biology (1.1k citations). John Barber has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Edward J. Hollox, John A.L. Armour, I. Karen Temple, N R Dennis, Ronald D. Miller, Viv Maloney, David Robinson, R J Gardner, James C. Nicholson and Deborah Mackay. Their work appears in journals such as Journal of Medical Genetics, European Journal of Human Genetics, Human Genetics, Cytogenetic and Genome Research and The American Journal of Human 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.