G.R. Sutherland
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Immunology and Allergy top 10%
- Cell Adhesion Molecules Research
Papers in
-
- Genomics and Chromatin Dynamics 2
- RNA regulation and disease 2
- Genetics 13
- Genetics and Neurodevelopmental Disorders 9
- Genomic variations and chromosomal abnormalities 6
- Co-authors
- David F. Callen (9 shared papers)John C. Mulley (5 shared papers)V.J. Hyland (4 shared papers)Danuta Z. Loesch (2 shared papers)Ági K. Gedeon (2 shared papers)Robert I. Richards (7 shared papers)John Shine (2 shared papers)Elizabeth Baker (3 shared papers)
- Journals
- Genomics (6 papers)Cytogenetic and Genome Research (2 papers)Journal of Medical Genetics (1 paper)Genes Brain & Behavior (1 paper)Current Opinion in Genetics & Development (1 paper)
- Partner nations
- AustraliaFranceUnited Kingdom
In The Last Decade
G.R. Sutherland
22 papers receiving 679 citations
Peers
Comparison fields: 5 of 70
- Genetics 355
- Immunology and Allergy 46
- Molecular Biology 396
- Cognitive Neuroscience 110
- Cellular and Molecular Neuroscience 78
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 22 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2003 | 73 | |
| 2 | Genotype-phenotype relationships in fragile X syndrome: a family study. | 1993 | 68 |
| 3 | Chromosomal localization of the human alpha-L-iduronidase gene (IDUA) to 4p16.3. | 1990 | 59 |
| 4 | 1989 | 54 | |
| 5 | 1996 | 49 | |
| 6 | The gene for human leukemia inhibitory factor (LIF) maps to 22q12. | 1989 | 47 |
| 7 | 2007 | 44 | |
| 8 | 1992 | 40 | |
| 9 | Fragile X syndrome: diagnosis using highly polymorphic microsatellite markers. | 1991 | 38 |
| 10 | 1991 | 35 | |
| 11 | 1991 | 33 | |
| 12 | 1994 | 28 | |
| 13 | 1994 | 28 | |
| 14 | 1991 | 23 | |
| 15 | Organization and chromosomal localization of the human interleukin 5 receptor alpha-chain gene. | 1993 | 23 |
| 16 | 1999 | 20 | |
| 17 | 2004 | 13 | |
| 18 | 1991 | 13 | |
| 19 | 1992 | 7 | |
| 20 | 1993 | 4 |
About G.R. Sutherland
G.R. Sutherland is a scholar working on Molecular Biology, Genetics, Oncology, Cellular and Molecular Neuroscience and Cognitive Neuroscience, having authored 22 papers that have together received 703 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (9 papers), Genomic variations and chromosomal abnormalities (6 papers), Cell Adhesion Molecules Research (3 papers), Autism Spectrum Disorder Research (3 papers), Cytokine Signaling Pathways and Interactions (2 papers), Genomics and Chromatin Dynamics (2 papers), RNA regulation and disease (2 papers) and Genetic Neurodegenerative Diseases (2 papers). The work is most often cited by research in Genetics (355 citations), Immunology and Allergy (46 citations), Molecular Biology (396 citations), Cognitive Neuroscience (110 citations) and Cellular and Molecular Neuroscience (78 citations). G.R. Sutherland has collaborated with scholars based in Australia, France and United Kingdom. Frequent co-authors include David F. Callen, John C. Mulley, V.J. Hyland, Danuta Z. Loesch, Ági K. Gedeon, Robert I. Richards, John Shine, Elizabeth Baker, H.M. Kozman and Richard Huggins. Their work appears in journals such as Genomics, Cytogenetic and Genome Research, Journal of Medical Genetics, Genes Brain & Behavior and Current Opinion in Genetics & Development.
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.