S. M. Forrest
Impact in
- Genetics top 5%
- Virus-based gene therapy research
- Neurogenetic and Muscular Disorders Research
- Molecular Biology top 5%
- Muscle Physiology and Disorders
- Mitochondrial Function and Pathology
- CRISPR and Genetic Engineering
Papers in
-
- Muscle Physiology and Disorders 11
- Mitochondrial Function and Pathology 8
- DNA Repair Mechanisms 4
- Nuclear Structure and Function 4
- RNA Research and Splicing 3
-
- Genetic Neurodegenerative Diseases 9
- Co-authors
- K. E. Davies (6 shared papers)Andreas Speer (7 shared papers)Gareth Cross (5 shared papers)Donald R. Love (3 shared papers)Kay E. Davies (5 shared papers)Sarah England (3 shared papers)J.B. Harris (1 shared paper)Mark Johnson (1 shared paper)
- Journals
- Journal of Medical Genetics (5 papers)Human Genetics (3 papers)Neurology (2 papers)Nucleic Acids Research (2 papers)Molecular Diagnosis (2 papers)
- Partner nations
- AustraliaUnited KingdomUnited States
In The Last Decade
S. M. Forrest
38 papers receiving 1.6k citations
Peers
Comparison fields: 5 of 88
- Genetics 227
- Molecular Biology 1.3k
- Genetics 474
- Cellular and Molecular Neuroscience 278
- Clinical Biochemistry 95
Countries citing papers authored by S. M. Forrest
This map shows the geographic impact of S. M. Forrest'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 S. M. Forrest with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites S. M. Forrest more than expected).
Fields of papers citing papers by S. M. Forrest
This network shows the impact of papers produced by S. M. Forrest. 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 S. M. Forrest. The network helps show where S. M. Forrest may publish in the future.
Co-authors
The 25 scholars most cited alongside S. M. Forrest, 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 39 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1990 | 485 | |
| 2 | 1987 | 164 | |
| 3 | 1988 | 147 | |
| 4 | 2000 | 62 | |
| 5 | Mutation detection in phenylketonuria by using chemical cleavage of mismatch: importance of using probes from both normal and patient samples. | 1991 | 56 |
| 6 | 1994 | 55 | |
| 7 | 2001 | 53 | |
| 8 | 2008 | 51 | |
| 9 | X-linked recessive panhypopituitarism associated with a regional duplication in Xq25-q26. | 1997 | 45 |
| 10 | 1987 | 41 | |
| 11 | 1987 | 40 | |
| 12 | 1984 | 37 | |
| 13 | 1988 | 36 | |
| 14 | 2009 | 34 | |
| 15 | 1991 | 34 | |
| 16 | 1999 | 34 | |
| 17 | 1999 | 34 | |
| 18 | 1996 | 33 | |
| 19 | 2004 | 33 | |
| 20 | 1998 | 31 |
About S. M. Forrest
S. M. Forrest is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Genetics, Clinical Biochemistry and Cell Biology, having authored 39 papers that have together received 1.7k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (11 papers), Genetic Neurodegenerative Diseases (9 papers), Mitochondrial Function and Pathology (8 papers), Metabolism and Genetic Disorders (7 papers), DNA Repair Mechanisms (4 papers), Nuclear Structure and Function (4 papers), Biotin and Related Studies (3 papers) and RNA Research and Splicing (3 papers). The work is most often cited by research in Genetics (227 citations), Molecular Biology (1.3k citations), Genetics (474 citations), Cellular and Molecular Neuroscience (278 citations) and Clinical Biochemistry (95 citations). S. M. Forrest has collaborated with scholars based in Australia, United Kingdom and United States. Frequent co-authors include K. E. Davies, Andreas Speer, Gareth Cross, Donald R. Love, Kay E. Davies, Sarah England, J.B. Harris, Mark Johnson, Elizabeth E. Zubrzycka‐Gaarn and Dennis E. Bulman. Their work appears in journals such as Journal of Medical Genetics, Human Genetics, Neurology, Nucleic Acids Research and Molecular Diagnosis.
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.