Miranda Splitt
Impact in
- Developmental Neuroscience top 5%
- Williams Syndrome Research
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 15
- Genetics and Neurodevelopmental Disorders 7
- Genomic variations and chromosomal abnormalities 7
- Genomics and Rare Diseases 6
- Craniofacial Disorders and Treatments 2
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- Congenital heart defects research 4
- RNA modifications and cancer 4
- Ubiquitin and proteasome pathways 2
- Hedgehog Signaling Pathway Studies 2
- Co-authors
- John Burn (5 shared papers)Harinder Gill (2 shared papers)Judith Goodship (2 shared papers)Gurleen Sharland (2 shared papers)John Simpson (1 shared paper)Susan Lindsay (2 shared papers)Bruno Marino (1 shared paper)Richard N. Bamford (1 shared paper)
- Journals
- The American Journal of Human Genetics (4 papers)European Journal of Human Genetics (2 papers)Journal of Medical Genetics (2 papers)European Journal of Medical Genetics (1 paper)Neuromuscular Disorders (1 paper)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Miranda Splitt
29 papers receiving 1.0k citations
Peers
Comparison fields: 5 of 78
- Developmental Neuroscience 142
- Genetics 406
- Molecular Biology 566
- Epidemiology 172
- Cognitive Neuroscience 101
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 25 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
Showing the 20 most-cited of 29 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2000 | 251 | |
| 2 | 1999 | 167 | |
| 3 | 2003 | 121 | |
| 4 | 2002 | 102 | |
| 5 | 2000 | 76 | |
| 6 | 1996 | 55 | |
| 7 | PPM-X: a new X-linked mental retardation syndrome with psychosis, pyramidal signs, and macroorchidism maps to Xq28. | 1996 | 33 |
| 8 | 2008 | 31 | |
| 9 | 2018 | 29 | |
| 10 | 2016 | 29 | |
| 11 | 2009 | 21 | |
| 12 | 2017 | 21 | |
| 13 | 2016 | 19 | |
| 14 | 1997 | 19 | |
| 15 | 2018 | 18 | |
| 16 | 2006 | 14 | |
| 17 | 2017 | 12 | |
| 18 | 2007 | 11 | |
| 19 | 1994 | 11 | |
| 20 | 2018 | 6 |
About Miranda Splitt
Miranda Splitt is a scholar working on Genetics, Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health and Epidemiology, having authored 29 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (7 papers), Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (6 papers), Congenital heart defects research (4 papers), RNA modifications and cancer (4 papers), Ubiquitin and proteasome pathways (2 papers), Hedgehog Signaling Pathway Studies (2 papers) and Craniofacial Disorders and Treatments (2 papers). The work is most often cited by research in Developmental Neuroscience (142 citations), Genetics (406 citations), Molecular Biology (566 citations), Epidemiology (172 citations) and Cognitive Neuroscience (101 citations). Miranda Splitt has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include John Burn, Harinder Gill, Judith Goodship, Gurleen Sharland, John Simpson, Susan Lindsay, Bruno Marino, Richard N. Bamford, Brett Casey and Michael M. Shen. Their work appears in journals such as The American Journal of Human Genetics, European Journal of Human Genetics, Journal of Medical Genetics, European Journal of Medical Genetics and Neuromuscular Disorders.
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.