Andrew Read

12.1k citations
124 papers · 6.1k indexed · 3 hit papers · h-index 38

Andrew Read

120 papers receiving 5.9k citations

Hit Papers

SOX10 mutations in patients with Waardenburg-Hirschsprun...6191983202619972011200400600

Peers

Andrew Read
Comparison fields: 5 of 142
  • Sensory Systems 469
  • Developmental Neuroscience 388
  • Cell Biology 1.1k
  • Genetics 1.7k
  • Molecular Biology 3.0k
Replace Eero Lehtonen with:
Eero Lehtonen Finland
Andreas Kispert Germany
William Reardon United Kingdom
Michel Goossens France
Roger A. Williamson United States
Jean‐Louis Guénet France
Dieter Riethmacher Germany
Roger A. Pedersen United States
Manfred Gessler Germany
Miguel Torres Spain
Andrew Read relative to Eero Lehtonen Finland Eero Lehtonen's profile →
Citations per field
00.5×2.9×
Eero Lehtonen · 1×
Citations per year

Countries citing papers authored by Andrew Read

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network

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.

Border = papers with Andrew Read Line = papers co-authored together Andrew Read links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown
#Work
1 20250
2 2005145
3 20051
4 200412
5 20044
6 20038
7 2000110
8 1999166
9 199914
10 199754
11 19971
12 199511
13 1995172
14 199418
15 199417
16 199123
17 19911
18 19881
19 198836
20 198021

About Andrew Read

Andrew Read is a scholar working on Developmental Neuroscience, Genetics and Cell Biology, having authored 124 papers that have together received 6.1k indexed citations. Recurring topics across this work include RNA regulation and disease (12 papers), Prenatal Screening and Diagnostics (12 papers), melanin and skin pigmentation (12 papers), Muscle Physiology and Disorders (9 papers), Folate and B Vitamins Research (8 papers), Genetic Syndromes and Imprinting (7 papers), Cancer-related gene regulation (7 papers) and RNA modifications and cancer (6 papers). The work is most often cited by research in Sensory Systems (469 citations), Developmental Neuroscience (388 citations) and Cell Biology (1.1k 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, Rudi Balling, N. C. Nevin, R. W. Smithells and S Sheppard. Their work appears in journals such as Journal of Medical Genetics, Human Genetics, The Lancet, Nature Genetics and European 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.

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