Sandy Raeburn
Impact in
- Neurology top 10%
- Neurological diseases and metabolism
-
- Hereditary Neurological Disorders
Papers in
- Genetics 10
- Genomics and Rare Diseases 5
- BRCA gene mutations in cancer 5
-
- Neurological diseases and metabolism 2
- Co-authors
- Katherine DickAndrew H. CrosbyMartin BobrowPeter FarndonChristos ProukakisNaomi SibtainSégolène AyméCoro Paisán‐Ruíz
- Journals
- European Journal of Human Genetics (2 papers)Journal of Medical Ethics (2 papers)Public Health Genomics (2 papers)Family Practice (1 paper)Neurology (1 paper)
- Partner nations
- United KingdomOmanUnited States
In The Last Decade
Sandy Raeburn
21 papers receiving 510 citations
Peers
Comparison fields: 5 of 78
- Neurology 114
- Cellular and Molecular Neuroscience 107
- Clinical Biochemistry 35
- Pathology and Forensic Medicine 84
- Genetics 128
Countries citing papers authored by Sandy Raeburn
This map shows the geographic impact of Sandy Raeburn'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 Sandy Raeburn with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sandy Raeburn more than expected).
Fields of papers citing papers by Sandy Raeburn
This network shows the impact of papers produced by Sandy Raeburn. 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 Sandy Raeburn. The network helps show where Sandy Raeburn may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Sandy Raeburn, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 147 | |
| 2 | Clinically-Defined Maturity Onset Diabetes of the Young in Omanis: Absence of the common Caucasian gene mutations. | 2010 | 8 |
| 3 | 2010 | 4 | |
| 4 | 2009 | 2 | |
| 5 | Molecular analysis of CYP1B1 in Omani patients with primary congenital glaucoma: a pilot study. | 2009 | 19 |
| 6 | 2008 | 28 | |
| 7 | 2008 | 66 | |
| 8 | 2008 | 2 | |
| 9 | 2006 | 22 | |
| 10 | 2005 | 1 | |
| 11 | 2005 | 62 | |
| 12 | 2005 | 13 | |
| 13 | 2003 | 62 | |
| 14 | 2002 | 3 | |
| 15 | 2000 | 19 | |
| 16 | Population genetic screening programmes. Proposed recommendations of the European Society of Human Genetics (vol 8, pg 998, 2000) | 2000 | 1 |
| 17 | 1998 | 1 | |
| 18 | Genetic services in the United Kingdom. | 1997 | 4 |
| 19 | 1994 | 17 | |
| 20 | 1991 | 0 |
About Sandy Raeburn
Sandy Raeburn is a scholar working on Genetics, Neurology, Reproductive Medicine, Cellular and Molecular Neuroscience and Genetics, having authored 22 papers that have together received 526 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (5 papers), BRCA gene mutations in cancer (5 papers), Genetic factors in colorectal cancer (3 papers), Biomedical Ethics and Regulation (2 papers), Neurological diseases and metabolism (2 papers), Reproductive Health and Technologies (2 papers), Colorectal Cancer Screening and Detection (2 papers) and Hereditary Neurological Disorders (2 papers). The work is most often cited by research in Neurology (114 citations), Cellular and Molecular Neuroscience (107 citations), Clinical Biochemistry (35 citations), Pathology and Forensic Medicine (84 citations) and Genetics (128 citations). Sandy Raeburn has collaborated with scholars based in United Kingdom, Oman and United States. Frequent co-authors include Katherine Dick, Andrew H. Crosby, Martin Bobrow, Peter Farndon, Christos Proukakis, Naomi Sibtain, Ségolène Aymé, Coro Paisán‐Ruíz, Reza Seyed Sharifi and Béatrice Godard. Their work appears in journals such as European Journal of Human Genetics, Journal of Medical Ethics, Public Health Genomics, Family Practice and Neurology.
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.