Andrew Green
Impact in
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- Neuroscience and Neuropharmacology Research
- Neuropeptides and Animal Physiology
- Neurotransmitter Receptor Influence on Behavior
- Neurology top 1%
- Amyotrophic Lateral Sclerosis Research
Papers in
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- DNA Repair Mechanisms 11
- Genetics 56
- Genomic variations and chromosomal abnormalities 15
- BRCA gene mutations in cancer 11
- Co-authors
- John R.W. Yates (2 shared papers)Alan Wise (4 shared papers)Fiona H. Marshall (2 shared papers)Neil J. Fraser (1 shared paper)Ashley Barnes (1 shared paper)Piers C. Emson (1 shared paper)G. H. Disney (1 shared paper)Steven M. Foord (1 shared paper)
- Journals
- Journal of Medical Genetics (11 papers)Neuropharmacology (10 papers)Human Mutation (5 papers)The Lancet (5 papers)Environmental Toxicology and Chemistry (4 papers)
- Partner nations
- United KingdomIrelandUnited States
In The Last Decade
Andrew Green
213 papers receiving 8.3k citations
Andrew Green's Hit Papers
Peers
Comparison fields: 5 of 187
- Cellular and Molecular Neuroscience 1.5k
- Neurology 881
- Genetics 1.4k
- Molecular Biology 3.3k
- Genetics 478
Countries citing papers authored by Andrew Green
This map shows the geographic impact of Andrew Green'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 Green with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andrew Green more than expected).
Fields of papers citing papers by Andrew Green
This network shows the impact of papers produced by Andrew Green. 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 Green. The network helps show where Andrew Green may publish in the future.
Co-authors
The 25 scholars most cited alongside Andrew Green, 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 224 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Heterodimerization is required for the formation of a functional GABAB receptor Hit paper breakdown → | 1998 | 973 |
| 2 | ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis Hit paper breakdown → | 2006 | 520 |
| 3 | 2003 | 409 | |
| 4 | 1994 | 284 | |
| 5 | 2013 | 226 | |
| 6 | 2017 | 194 | |
| 7 | 2010 | 175 | |
| 8 | 1997 | 172 | |
| 9 | 2007 | 168 | |
| 10 | 1983 | 144 | |
| 11 | 1994 | 143 | |
| 12 | 2004 | 143 | |
| 13 | 1979 | 129 | |
| 14 | 1996 | 127 | |
| 15 | 1999 | 122 | |
| 16 | 1984 | 110 | |
| 17 | 2001 | 102 | |
| 18 | 1984 | 98 | |
| 19 | 1996 | 95 | |
| 20 | 1992 | 90 |
About Andrew Green
Andrew Green is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Pathology and Forensic Medicine and Physiology, having authored 224 papers that have together received 8.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (15 papers), BRCA gene mutations in cancer (11 papers), DNA Repair Mechanisms (11 papers), Prenatal Screening and Diagnostics (10 papers), Genetic factors in colorectal cancer (10 papers), Urological Disorders and Treatments (9 papers), Pediatric Urology and Nephrology Studies (9 papers) and Tuberous Sclerosis Complex Research (8 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.5k citations), Neurology (881 citations), Genetics (1.4k citations), Molecular Biology (3.3k citations) and Genetics (478 citations). Andrew Green has collaborated with scholars based in United Kingdom, Ireland and United States. Frequent co-authors include John R.W. Yates, Alan Wise, Fiona H. Marshall, Neil J. Fraser, Ashley Barnes, Piers C. Emson, G. H. Disney, Steven M. Foord, Julia H. White and Martin J. Main. Their work appears in journals such as Journal of Medical Genetics, Neuropharmacology, Human Mutation, The Lancet and Environmental Toxicology and Chemistry.
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.