Miranda Splitt
Impact in
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- Prenatal Screening and Diagnostics
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- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
Papers in
- Surgery 2
- Vascular Malformations and Hemangiomas 1
- Teratomas and Epidermoid Cysts 1
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- Epigenetics and DNA Methylation 1
- Genomics and Chromatin Dynamics 1
- Co-authors
- I. Karen Temple (1 shared paper)Christine Gicquel (1 shared paper)Rebecca Poole (1 shared paper)Deborah Mackay (1 shared paper)Alan Fenton (1 shared paper)Neil Rajan (1 shared paper)D. J. Maxwell (1 shared paper)S. C. Whitaker (1 shared paper)
- Journals
- European Journal of Human Genetics (3 papers)Clinical and Experimental Dermatology (1 paper)BMJ Case Reports (1 paper)
- Partner nations
- United KingdomAustralia
In The Last Decade
Miranda Splitt
5 papers receiving 63 citations
Peers
Comparison fields: 5 of 21
- Pediatrics, Perinatology and Child Health 29
- Genetics 41
- Molecular Biology 52
- Cancer Research 6
- Neurology 3
Countries citing papers authored by Miranda Splitt
This map shows the geographic impact of Miranda Splitt'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 Miranda Splitt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Miranda Splitt more than expected).
Fields of papers citing papers by Miranda Splitt
This network shows the impact of papers produced by Miranda Splitt. 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 Miranda Splitt. The network helps show where Miranda Splitt may publish in the future.
Co-authors
The 22 scholars most cited alongside Miranda Splitt, 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 | 2011 | 48 | |
| 2 | 2015 | 5 | |
| 3 | 2003 | 5 | |
| 4 | 2015 | 3 | |
| 5 | Genomic deletions account for more than 10% of the FOXL2 mutations in BPES families and can be revealed by MLPA analysis | 2004 | 2 |
About Miranda Splitt
Miranda Splitt is a scholar working on Surgery, Molecular Biology, Genetics, Pathology and Forensic Medicine and Neurology, having authored 5 papers that have together received 63 indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (1 paper), Genomics and Chromatin Dynamics (1 paper), Vascular Malformations and Hemangiomas (1 paper), Teratomas and Epidermoid Cysts (1 paper), Vascular Malformations Diagnosis and Treatment (1 paper), Retinal and Macular Surgery (1 paper), Chromosomal and Genetic Variations (1 paper) and Tumors and Oncological Cases (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (29 citations), Genetics (41 citations), Molecular Biology (52 citations), Cancer Research (6 citations) and Neurology (3 citations). Miranda Splitt has collaborated with scholars based in United Kingdom and Australia. Frequent co-authors include I. Karen Temple, Christine Gicquel, Rebecca Poole, Deborah Mackay, Alan Fenton, Neil Rajan, D. J. Maxwell, S. C. Whitaker, S. Leech and S. Natarajan. Their work appears in journals such as European Journal of Human Genetics, Clinical and Experimental Dermatology and BMJ Case Reports.
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.