Andrew Read
Impact in
- Developmental Neuroscience top 0.5%
- Williams Syndrome Research
- Sensory Systems top 0.5%
- Hearing, Cochlea, Tinnitus, Genetics
Papers in
- Genetics 33
- Genetic Associations and Epidemiology 7
- Genomics and Rare Diseases 6
- Genetic and rare skin diseases. 6
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- Hearing, Cochlea, Tinnitus, Genetics 9
- Co-authors
- Valerie Newton (13 shared papers)R Harris (42 shared papers)Mayada Tassabehji (8 shared papers)Tom Strachan (19 shared papers)Dian Donnai (32 shared papers)RICHARD W. SMITHELLS (12 shared papers)S Sheppard (11 shared papers)Norman C. Nevin (11 shared papers)
- Journals
- Journal of Medical Genetics (37 papers)The Lancet (15 papers)Human Molecular Genetics (14 papers)Nature Genetics (10 papers)Human Genetics (10 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Andrew Read
177 papers receiving 10.4k citations
Andrew Read's Hit Papers
Peers
Comparison fields: 5 of 114
- Developmental Neuroscience 432
- Sensory Systems 525
- Nephrology 877
- Cell Biology 696
- Genetics 1.4k
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 190 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic rickets Hit paper breakdown → | 1995 | 944 |
| 2 | SOX10 mutations in patients with Waardenburg-Hirschsprung disease Hit paper breakdown → | 1998 | 691 |
| 3 | Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene Hit paper breakdown → | 1992 | 579 |
| 4 | 1994 | 549 | |
| 5 | Analysis of Human Genetic Linkage Hit paper breakdown → | 1992 | 544 |
| 6 | POSSIBLE PREVENTION OF NEURAL-TUBE DEFECTS BY PERICONCEPTIONAL VITAMIN SUPPLEMENTATION Hit paper breakdown → | 1980 | 503 |
| 7 | 1983 | 408 | |
| 8 | 1999 | 405 | |
| 9 | 1997 | 391 | |
| 10 | 1981 | 311 | |
| 11 | 1994 | 239 | |
| 12 | 1999 | 193 | |
| 13 | 1995 | 184 | |
| 14 | 1993 | 179 | |
| 15 | 1994 | 178 | |
| 16 | 2005 | 158 | |
| 17 | 2005 | 149 | |
| 18 | 1994 | 144 | |
| 19 | 1995 | 134 | |
| 20 | 2000 | 133 |
About Andrew Read
Andrew Read is a scholar working on Genetics, Sensory Systems, Developmental Neuroscience, Pediatrics, Perinatology and Child Health and Nephrology, having authored 190 papers that have together received 11.3k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (10 papers), Parathyroid Disorders and Treatments (9 papers), Hearing, Cochlea, Tinnitus, Genetics (9 papers), Muscle Physiology and Disorders (8 papers), Genetic Associations and Epidemiology (7 papers), Williams Syndrome Research (7 papers), Genomics and Rare Diseases (6 papers) and Genetic and rare skin diseases. (6 papers). The work is most often cited by research in Developmental Neuroscience (432 citations), Sensory Systems (525 citations), Nephrology (877 citations), Cell Biology (696 citations) and Genetics (1.4k citations). Andrew Read has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Valerie Newton, R Harris, Mayada Tassabehji, Tom Strachan, Dian Donnai, RICHARD W. SMITHELLS, S Sheppard, Norman C. Nevin, D W Fielding and Mary J. Seller. Their work appears in journals such as Journal of Medical Genetics, The Lancet, Human Molecular Genetics, Nature Genetics and 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.