Miranda Splitt

508 total citations
5 papers, 63 citations indexed

About

Miranda Splitt is a scholar working on Surgery, Molecular Biology and Genetics. According to data from OpenAlex, Miranda Splitt has authored 5 papers receiving a total of 63 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Surgery, 2 papers in Molecular Biology and 2 papers in Genetics. Recurrent topics in Miranda Splitt's work include Epigenetics and DNA Methylation (1 paper), Genetic Syndromes and Imprinting (1 paper) and Vascular Malformations and Hemangiomas (1 paper). Miranda Splitt is often cited by papers focused on Epigenetics and DNA Methylation (1 paper), Genetic Syndromes and Imprinting (1 paper) and Vascular Malformations and Hemangiomas (1 paper). Miranda Splitt collaborates with scholars based in United Kingdom and Australia. Miranda Splitt's co-authors include Christine Gicquel, Rebecca Poole, I. Karen Temple, Deborah Mackay, Alan Fenton, Aileen Taylor, Neil Rajan, S. Leech, D. J. Maxwell and S. C. Whitaker and has published in prestigious journals such as European Journal of Human Genetics, Clinical and Experimental Dermatology and BMJ Case Reports.

In The Last Decade

Miranda Splitt

5 papers receiving 63 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Miranda Splitt United Kingdom	4	52	41	29	6	6	5	63
Rosa Baldinger Switzerland	5	41 0.8×	54 1.3×	36 1.2×	7 1.2×	3 0.5×	5	90
Debra Rita United States	4	32 0.6×	50 1.2×	32 1.1×	6 1.0×	6 1.0×	5	78
Melissa A Dempsey United States	5	63 1.2×	47 1.1×	11 0.4×	5 0.8×	2 0.3×	8	86
Florence Démurger France	5	40 0.8×	50 1.2×	33 1.1×	5 0.8×	2 0.3×	7	78
Dagmar Huhle Germany	4	22 0.4×	22 0.5×	26 0.9×	3 0.5×	3 0.5×	5	48
Elyse Mitchell United States	4	20 0.4×	45 1.1×	17 0.6×	10 1.7×	4 0.7×	5	65
Valerie Banks United States	3	56 1.1×	56 1.4×	10 0.3×	4 0.7×	9 1.5×	3	77
Andrea Seeley United States	5	17 0.3×	31 0.8×	13 0.4×	5 0.8×	7 1.2×	8	57
Anna Wilsdon United Kingdom	3	42 0.8×	40 1.0×	10 0.3×	3 0.5×	4 0.7×	6	76
Mary‐Louise Freckmann Australia	6	145 2.8×	52 1.3×	13 0.4×	5 0.8×	2 0.3×	8	164

Countries citing papers authored by Miranda Splitt

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Miranda Splitt

This figure shows the co-authorship network connecting the top 25 collaborators of Miranda Splitt. A scholar is included among the top collaborators of Miranda Splitt based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Miranda Splitt. Miranda Splitt is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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5 of 5 papers shown

1.

Fenton, Alan, et al.. (2015). Cornelia de Lange syndrome due to mosaic NIPBL mutation: antenatal presentation with sacrococcygeal teratoma. BMJ Case Reports. 2015. bcr2015211006–bcr2015211006. 5 indexed citations

2.

Whitaker, S. C., S. Leech, Aileen Taylor, et al.. (2015). Multifocal capillary malformations in an older, asymptomatic child with a novel RASA 1 mutation. Clinical and Experimental Dermatology. 41(2). 156–158. 3 indexed citations

3.

Poole, Rebecca, et al.. (2011). Beckwith–Wiedemann syndrome caused by maternally inherited mutation of an OCT-binding motif in the IGF2/H19-imprinting control region, ICR1. European Journal of Human Genetics. 20(2). 240–243. 48 indexed citations

4.

Beysen, Diane, Jean‐Pierre Fryns, Miranda Splitt, et al.. (2004). Genomic deletions account for more than 10% of the FOXL2 mutations in BPES families and can be revealed by MLPA analysis. European Journal of Human Genetics. 12. 248–248. 2 indexed citations

5.

Splitt, Miranda, et al.. (2003). Class II neocentromeres: a putative common neocentromere site in band 4q21.2. European Journal of Human Genetics. 11(10). 749–753. 5 indexed citations

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.

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