A. F. Brady
Impact in
- Genetics top 10%
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
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- Prenatal Screening and Diagnostics
Papers in
-
- RNA modifications and cancer 2
- Genetics 2
- Genetic Syndromes and Imprinting 1
- Neurogenetic and Muscular Disorders Research 1
- Connective tissue disorders research 1
- Co-authors
- K G Burnand (1 shared paper)Peter Mortimer (1 shared paper)M. Sarfarazi (1 shared paper)R. Bryan Bell (1 shared paper)Anne H. Child (1 shared paper)Sahar Mansour (1 shared paper)Steven Jeffery (1 shared paper)J. R. O. Collin (1 shared paper)
- Journals
- Journal of Medical Genetics (3 papers)Human Molecular Genetics (1 paper)Clinical Dysmorphology (1 paper)
- Partner nations
- United KingdomNetherlandsUnited States
In The Last Decade
A. F. Brady
5 papers receiving 466 citations
Peers
Comparison fields: 5 of 48
- Genetics 206
- Pediatrics, Perinatology and Child Health 114
- Internal Medicine 17
- Oncology 121
- Molecular Biology 208
Countries citing papers authored by A. F. Brady
This map shows the geographic impact of A. F. Brady'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 A. F. Brady with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A. F. Brady more than expected).
Fields of papers citing papers by A. F. Brady
This network shows the impact of papers produced by A. F. Brady. 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 A. F. Brady. The network helps show where A. F. Brady may publish in the future.
Co-authors
The 25 scholars most cited alongside A. F. Brady, 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 | 2009 | 218 | |
| 2 | 2002 | 194 | |
| 3 | 1998 | 72 | |
| 4 | 1997 | 14 | |
| 5 | Elucidating the aetiology of Prader-Willi syndrome: deletion of the HBII-85 class of snoRNA is associated with hyperphagia, obesity and hypogonadism | 2009 | 1 |
About A. F. Brady
A. F. Brady is a scholar working on Molecular Biology, Genetics, Infectious Diseases, Surgery and Genetics, having authored 5 papers that have together received 499 indexed citations. Recurring topics across this work include RNA modifications and cancer (2 papers), Congenital Anomalies and Fetal Surgery (1 paper), MicroRNA in disease regulation (1 paper), Genetic Syndromes and Imprinting (1 paper), Prenatal Screening and Diagnostics (1 paper), Neurogenetic and Muscular Disorders Research (1 paper), Parvovirus B19 Infection Studies (1 paper) and Connective tissue disorders research (1 paper). The work is most often cited by research in Genetics (206 citations), Pediatrics, Perinatology and Child Health (114 citations), Internal Medicine (17 citations), Oncology (121 citations) and Molecular Biology (208 citations). A. F. Brady has collaborated with scholars based in United Kingdom, Netherlands and United States. Frequent co-authors include K G Burnand, Peter Mortimer, M. Sarfarazi, R. Bryan Bell, Anne H. Child, Sahar Mansour, Steven Jeffery, J. R. O. Collin, Victoria A. Murday and Glen Brice. Their work appears in journals such as Journal of Medical Genetics, Human Molecular Genetics and Clinical Dysmorphology.
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.