G.R. Sutherland
Impact in
- Genetics top 0.1%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Molecular Biology top 1%
- DNA Repair Mechanisms
- Ubiquitin and proteasome pathways
- RNA modifications and cancer
Papers in
- Genetics 78
- Genetics and Neurodevelopmental Disorders 49
- Genomic variations and chromosomal abnormalities 39
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- Genomics and Chromatin Dynamics 11
- DNA Repair Mechanisms 9
- Co-authors
- Robert I. Richards (30 shared papers)Elizabeth Baker (33 shared papers)K. Holman (11 shared papers)John C. Mulley (24 shared papers)David F. Callen (36 shared papers)Eric J. Kremer (7 shared papers)Melanie Pritchard (5 shared papers)Michael Lynch (5 shared papers)
- Journals
- Human Genetics (16 papers)Genomics (11 papers)Heart (11 papers)Journal of Medical Genetics (8 papers)European Heart Journal - Cardiovascular Imaging (8 papers)
- Partner nations
- AustraliaUnited KingdomUnited States
In The Last Decade
G.R. Sutherland
212 papers receiving 8.3k citations
G.R. Sutherland's Hit Papers
Peers
Comparison fields: 5 of 148
- Genetics 4.2k
- Molecular Biology 4.1k
- Cellular and Molecular Neuroscience 1.0k
- Cognitive Neuroscience 951
- Physiology 195
Countries citing papers authored by G.R. Sutherland
This map shows the geographic impact of G.R. Sutherland'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 G.R. Sutherland with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites G.R. Sutherland more than expected).
Fields of papers citing papers by G.R. Sutherland
This network shows the impact of papers produced by G.R. Sutherland. 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 G.R. Sutherland. The network helps show where G.R. Sutherland may publish in the future.
Co-authors
The 25 scholars most cited alongside G.R. Sutherland, 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 225 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Mapping of DNA Instability at the Fragile X to a Trinucleotide Repeat Sequence P(CCG) n Hit paper breakdown → | 1991 | 738 |
| 2 | Fragile X Genotype Characterized by an Unstable Region of DNA Hit paper breakdown → | 1991 | 641 |
| 3 | Incidence and origin of "null" alleles in the (AC)n microsatellite markers. Hit paper breakdown → | 1993 | 558 |
| 4 | Heritable fragile sites on human chromosomes I. Factors affecting expression in lymphocyte culture. Hit paper breakdown → | 1979 | 424 |
| 5 | 2001 | 273 | |
| 6 | 1995 | 266 | |
| 7 | Two novel mucin genes down-regulated in colorectal cancer identified by differential display. | 1999 | 263 |
| 8 | Molecular characterization of murine and human OX40/OX40 ligand systems: identification of a human OX40 ligand as the HTLV‐1‐regulated protein gp34. Hit paper breakdown → | 1994 | 252 |
| 9 | 1994 | 213 | |
| 10 | 1992 | 166 | |
| 11 | 1996 | 159 | |
| 12 | 1992 | 152 | |
| 13 | Heritable fragile sites on human chromosomes II. Distribution, phenotypic effects, and cytogenetics. | 1979 | 146 |
| 14 | 1991 | 120 | |
| 15 | 2002 | 120 | |
| 16 | 1994 | 118 | |
| 17 | 1994 | 112 | |
| 18 | 1993 | 104 | |
| 19 | 2000 | 95 | |
| 20 | Heritable fragile sites on human chromosomes. VIII. Preliminary population cytogenetic data on the folic-acid-sensitive fragile sites. | 1982 | 93 |
About G.R. Sutherland
G.R. Sutherland is a scholar working on Genetics, Molecular Biology, Radiology, Nuclear Medicine and Imaging, Cardiology and Cardiovascular Medicine and Epidemiology, having authored 225 papers that have together received 8.7k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (49 papers), Genomic variations and chromosomal abnormalities (39 papers), Cardiac Imaging and Diagnostics (14 papers), Congenital Heart Disease Studies (12 papers), Cardiac Valve Diseases and Treatments (12 papers), Cardiovascular Function and Risk Factors (11 papers), Genomics and Chromatin Dynamics (11 papers) and DNA Repair Mechanisms (9 papers). The work is most often cited by research in Genetics (4.2k citations), Molecular Biology (4.1k citations), Cellular and Molecular Neuroscience (1.0k citations), Cognitive Neuroscience (951 citations) and Physiology (195 citations). G.R. Sutherland has collaborated with scholars based in Australia, United Kingdom and United States. Frequent co-authors include Robert I. Richards, Elizabeth Baker, K. Holman, John C. Mulley, David F. Callen, Eric J. Kremer, Melanie Pritchard, Michael Lynch, Shuancang Yu and David Schlessinger. Their work appears in journals such as Human Genetics, Genomics, Heart, Journal of Medical Genetics and European Heart Journal - Cardiovascular Imaging.
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.