Andrew Read
Impact in
- Developmental Neuroscience top 1%
- Sensory Systems top 0.5%
- Hearing, Cochlea, Tinnitus, Genetics
Papers in
-
- RNA regulation and disease 12
- Muscle Physiology and Disorders 9
- Cancer-related gene regulation 7
- Congenital heart defects research 6
- Genetics 36
- Genetic Syndromes and Imprinting 7
- Co-authors
- Mayada Tassabehji (9 shared papers)Tom Strachan (15 shared papers)R Harris (26 shared papers)Valerie Newton (12 shared papers)Dian Donnai (20 shared papers)Peter Gruß (2 shared papers)R. W. Smithells (8 shared papers)N. C. Nevin (8 shared papers)
- Journals
- Journal of Medical Genetics (18 papers)Human Molecular Genetics (11 papers)Human Genetics (10 papers)The Lancet (6 papers)Nature Genetics (6 papers)
- Partner nations
- United KingdomUnited StatesSouth Africa
In The Last Decade
Andrew Read
126 papers receiving 6.3k citations
Andrew Read's Hit Papers
Peers
Comparison fields: 5 of 142
- Developmental Neuroscience 409
- Sensory Systems 490
- Cell Biology 1.1k
- Genetics 1.8k
- Rheumatology 628
Countries citing papers authored by Andrew Read
This map shows the geographic impact of Andrew Read'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 Andrew Read with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andrew Read more than expected).
Fields of papers citing papers by Andrew Read
This network shows the impact of papers produced by Andrew Read. 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 Andrew Read. The network helps show where Andrew Read may publish in the future.
Co-authors
The 25 scholars most cited alongside Andrew Read, 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 134 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | SOX10 mutations in patients with Waardenburg-Hirschsprung disease Hit paper breakdown → | 1998 | 668 |
| 2 | Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene Hit paper breakdown → | 1992 | 587 |
| 3 | Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene Hit paper breakdown → | 1994 | 540 |
| 4 | FURTHER EXPERIENCE OF VITAMIN SUPPLEMENTATION FOR PREVENTION OF NEURAL TUBE DEFECT RECURRENCES Hit paper breakdown → | 1983 | 392 |
| 5 | 1981 | 290 | |
| 6 | 1994 | 183 | |
| 7 | 1993 | 182 | |
| 8 | 1999 | 180 | |
| 9 | 1995 | 177 | |
| 10 | 2013 | 173 | |
| 11 | 2005 | 149 | |
| 12 | 1994 | 146 | |
| 13 | 2012 | 139 | |
| 14 | 1995 | 129 | |
| 15 | 2000 | 127 | |
| 16 | Assignment of the locus for Waardenburg syndrome type I to human chromosome 2q37 and possible homology to the Splotch mouse. | 1990 | 100 |
| 17 | 1994 | 99 | |
| 18 | 2018 | 99 | |
| 19 | Allelic imbalance on chromosome 3p in oral dysplastic lesions: an early event in oral carcinogenesis. | 1996 | 94 |
| 20 | 2003 | 87 |
About Andrew Read
Andrew Read is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Cell Biology and Surgery, having authored 134 papers that have together received 6.7k indexed citations. Recurring topics across this work include melanin and skin pigmentation (12 papers), RNA regulation and disease (12 papers), Prenatal Screening and Diagnostics (12 papers), Muscle Physiology and Disorders (9 papers), Folate and B Vitamins Research (8 papers), Cancer-related gene regulation (7 papers), Genetic Syndromes and Imprinting (7 papers) and Congenital heart defects research (6 papers). The work is most often cited by research in Developmental Neuroscience (409 citations), Sensory Systems (490 citations), Cell Biology (1.1k citations), Genetics (1.8k citations) and Rheumatology (628 citations). Andrew Read has collaborated with scholars based in United Kingdom, United States and South Africa. Frequent co-authors include Mayada Tassabehji, Tom Strachan, R Harris, Valerie Newton, Dian Donnai, Peter Gruß, R. W. Smithells, N. C. Nevin, S Sheppard and D W Fielding. Their work appears in journals such as Journal of Medical Genetics, Human Molecular Genetics, Human Genetics, The Lancet and Nature 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.