Andrew Read
Impact in
- Nephrology top 0.5%
- Parathyroid Disorders and Treatments
- Developmental Neuroscience top 1%
- Williams Syndrome Research
Papers in
- Genetics 42
- Genetic Syndromes and Imprinting 9
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- RNA regulation and disease 12
- Muscle Physiology and Disorders 10
- RNA modifications and cancer 6
- Co-authors
- Mayada Tassabehji (10 shared papers)Rodney E. Harris (33 shared papers)Tom Strachan (15 shared papers)Valerie Newton (11 shared papers)Dian Donnai (26 shared papers)RICHARD W. SMITHELLS (11 shared papers)Simon G. Sheppard (11 shared papers)Norman C. Nevin (11 shared papers)
- Journals
- Journal of Medical Genetics (19 papers)The Lancet (12 papers)Human Molecular Genetics (11 papers)Nature Genetics (10 papers)Human Genetics (9 papers)
- Partner nations
- United KingdomUnited StatesSouth Africa
In The Last Decade
Andrew Read
143 papers receiving 9.0k citations
Andrew Read's Hit Papers
Peers
Comparison fields: 5 of 152
- Nephrology 911
- Developmental Neuroscience 509
- Sensory Systems 496
- Genetics 2.5k
- Rheumatology 1.2k
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 153 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 | 952 |
| 2 | SOX10 mutations in patients with Waardenburg-Hirschsprung disease Hit paper breakdown → | 1998 | 690 |
| 3 | 1992 | 585 | |
| 4 | 1994 | 554 | |
| 5 | 1980 | 505 | |
| 6 | FURTHER EXPERIENCE OF VITAMIN SUPPLEMENTATION FOR PREVENTION OF NEURAL TUBE DEFECT RECURRENCES Hit paper breakdown → | 1983 | 410 |
| 7 | 1999 | 406 | |
| 8 | 1981 | 315 | |
| 9 | 1994 | 238 | |
| 10 | 1999 | 195 | |
| 11 | 1995 | 187 | |
| 12 | 1993 | 180 | |
| 13 | 1994 | 179 | |
| 14 | 2013 | 175 | |
| 15 | 2005 | 157 | |
| 16 | 2005 | 149 | |
| 17 | 1994 | 145 | |
| 18 | 2012 | 143 | |
| 19 | 1995 | 135 | |
| 20 | 2000 | 132 |
About Andrew Read
Andrew Read is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Cell Biology and Developmental Neuroscience, having authored 153 papers that have together received 9.7k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (15 papers), melanin and skin pigmentation (12 papers), RNA regulation and disease (12 papers), Muscle Physiology and Disorders (10 papers), Genetic Syndromes and Imprinting (9 papers), Folate and B Vitamins Research (8 papers), Assisted Reproductive Technology and Twin Pregnancy (7 papers) and RNA modifications and cancer (6 papers). The work is most often cited by research in Nephrology (911 citations), Developmental Neuroscience (509 citations), Sensory Systems (496 citations), Genetics (2.5k citations) and Rheumatology (1.2k citations). Andrew Read has collaborated with scholars based in United Kingdom, United States and South Africa. Frequent co-authors include Mayada Tassabehji, Rodney E. Harris, Tom Strachan, Valerie Newton, Dian Donnai, RICHARD W. SMITHELLS, Simon G. Sheppard, Norman C. Nevin, D W Fielding and Christopher J. Schorah. 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.