Arabella Smith
Impact in
- Genetics top 2%
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 89
- Genomic variations and chromosomal abnormalities 49
- Genetic Syndromes and Imprinting 48
- Genetics and Neurodevelopmental Disorders 10
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- Prenatal Screening and Diagnostics 45
- Co-authors
- Lisa G. Robson (25 shared papers)Ronald J. Trent (16 shared papers)Stewart Einfeld (6 shared papers)Bruce John Tonge (4 shared papers)Ian Stewart Fraser (3 shared papers)Trevor Woodage (7 shared papers)Peter J. C. Russell (3 shared papers)Joanne W. Dixon (3 shared papers)
- Journals
- The Medical Journal of Australia (17 papers)Human Genetics (10 papers)Journal of Medical Genetics (10 papers)Clinical Genetics (8 papers)Journal of Intellectual Disability Research (7 papers)
- Partner nations
- AustraliaUnited StatesGermany
In The Last Decade
Arabella Smith
135 papers receiving 2.1k citations
Peers
Comparison fields: 5 of 98
- Genetics 1.4k
- Pediatrics, Perinatology and Child Health 615
- Transplantation 49
- Hematology 161
- Clinical Biochemistry 69
Countries citing papers authored by Arabella Smith
This map shows the geographic impact of Arabella Smith'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 Arabella Smith with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Arabella Smith more than expected).
Fields of papers citing papers by Arabella Smith
This network shows the impact of papers produced by Arabella Smith. 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 Arabella Smith. The network helps show where Arabella Smith may publish in the future.
Co-authors
The 25 scholars most cited alongside Arabella Smith, 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 138 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 127 | |
| 2 | 2006 | 120 | |
| 3 | 2003 | 101 | |
| 4 | 1996 | 99 | |
| 5 | 2006 | 97 | |
| 6 | 1999 | 88 | |
| 7 | 1988 | 65 | |
| 8 | 1988 | 65 | |
| 9 | 1994 | 59 | |
| 10 | Bloom syndrome and maternal uniparental disomy for chromosome 15. | 1994 | 54 |
| 11 | 1997 | 53 | |
| 12 | 1980 | 47 | |
| 13 | 1999 | 44 | |
| 14 | 1980 | 40 | |
| 15 | 1994 | 39 | |
| 16 | 1999 | 38 | |
| 17 | 1995 | 36 | |
| 18 | 2006 | 35 | |
| 19 | 2003 | 34 | |
| 20 | 1997 | 34 |
About Arabella Smith
Arabella Smith is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Hematology, Molecular Biology and Developmental Biology, having authored 138 papers that have together received 2.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (49 papers), Genetic Syndromes and Imprinting (48 papers), Prenatal Screening and Diagnostics (45 papers), Epigenetics and DNA Methylation (15 papers), Chromosomal and Genetic Variations (15 papers), Acute Myeloid Leukemia Research (12 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Congenital Anomalies and Fetal Surgery (9 papers). The work is most often cited by research in Genetics (1.4k citations), Pediatrics, Perinatology and Child Health (615 citations), Transplantation (49 citations), Hematology (161 citations) and Clinical Biochemistry (69 citations). Arabella Smith has collaborated with scholars based in Australia, United States and Germany. Frequent co-authors include Lisa G. Robson, Ronald J. Trent, Stewart Einfeld, Bruce John Tonge, Ian Stewart Fraser, Trevor Woodage, Peter J. C. Russell, Joanne W. Dixon, Rodney P. Shearman and Zemin Deng. Their work appears in journals such as The Medical Journal of Australia, Human Genetics, Journal of Medical Genetics, Clinical Genetics and Journal of Intellectual Disability Research.
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.