Claire Turner

3.2k total citations
14 papers, 578 citations indexed

About

Claire Turner is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Claire Turner has authored 14 papers receiving a total of 578 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 7 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Claire Turner's work include Genetic Syndromes and Imprinting (5 papers), Prenatal Screening and Diagnostics (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Claire Turner is often cited by papers focused on Genetic Syndromes and Imprinting (5 papers), Prenatal Screening and Diagnostics (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Claire Turner collaborates with scholars based in United Kingdom, United States and New Zealand. Claire Turner's co-authors include I. Karen Temple, Deborah Mackay, Michael N. Weedon, Peter D. Turnpenny, David J. Bunyan, Timothy M. Frayling, Louise E Docherty, Emma Wakeling, Rebecca Poole and Nicola Foulds and has published in prestigious journals such as Diabetes, Scientific Reports and Kidney International.

In The Last Decade

Claire Turner

13 papers receiving 538 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Claire Turner United Kingdom	13	414	304	183	61	48	14	578
Diana Carli Italy	14	272 0.7×	279 0.9×	152 0.8×	124 2.0×	40 0.8×	51	599
Mariana F.A. Funari Brazil	17	400 1.0×	368 1.2×	91 0.5×	44 0.7×	57 1.2×	35	736
Mark E. Nuñes United States	12	211 0.5×	202 0.7×	87 0.5×	89 1.5×	59 1.2×	24	644
J. W. E. Oorthuys Netherlands	12	345 0.8×	211 0.7×	87 0.5×	66 1.1×	41 0.9×	25	558
Shari Fallet United States	12	179 0.4×	389 1.3×	71 0.4×	40 0.7×	58 1.2×	18	739
María Juliana Ballesta‐Martínez Spain	14	274 0.7×	308 1.0×	82 0.4×	29 0.5×	18 0.4×	33	569
Anna Baroncini Italy	13	256 0.6×	149 0.5×	128 0.7×	61 1.0×	14 0.3×	29	458
Mariangela Cisternino Italy	14	228 0.6×	274 0.9×	82 0.4×	71 1.2×	16 0.3×	23	594
Eusebiu Vlad Gorduza Romania	12	149 0.4×	161 0.5×	72 0.4×	65 1.1×	24 0.5×	49	385
Intza Garin Spain	17	506 1.2×	476 1.6×	114 0.6×	91 1.5×	41 0.9×	32	638

Countries citing papers authored by Claire Turner

Since Specialization

Citations

This map shows the geographic impact of Claire Turner'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 Claire Turner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Claire Turner more than expected).

Fields of papers citing papers by Claire Turner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Claire Turner. 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 Claire Turner. The network helps show where Claire Turner may publish in the future.

Co-authorship network of co-authors of Claire Turner

This figure shows the co-authorship network connecting the top 25 collaborators of Claire Turner. A scholar is included among the top collaborators of Claire Turner 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 Claire Turner. Claire Turner is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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14 of 14 papers shown

Dasyam, Nathaniel, Claire Turner, Alfonso Schmidt, et al.. (2025). Jurkat T-cell lines exhibit marked genomic instability affecting karyotype, mutational profile, gene expression, immunophenotype and function. Scientific Reports. 15(1). 22426–22426.

Tuke, Marcus A., Katherine S. Ruth, Andrew R. Wood, et al.. (2018). Mosaic Turner syndrome shows reduced penetrance in an adult population study. Genetics in Medicine. 21(4). 877–886. 86 indexed citations

Barber, John, Jill A. Rosenfeld, John M. Graham, et al.. (2015). Inside the 8p23.1 duplication syndrome; eight microduplications of likely or uncertain clinical significance. American Journal of Medical Genetics Part A. 167(9). 2052–2064. 28 indexed citations

Mulchandani, Surabhi, Elizabeth Bhoj, Minjie Luo, et al.. (2015). Maternal uniparental disomy of chromosome 20: a novel imprinting disorder of growth failure. Genetics in Medicine. 18(4). 309–315. 73 indexed citations

Allen, Hana Lango, Richard Caswell, Weijia Xie, et al.. (2014). Next generation sequencing of chromosomal rearrangements in patients with split-hand/split-foot malformation provides evidence for DYNC1I1 exonic enhancers of DLX5/6 expression in humans. Journal of Medical Genetics. 51(4). 264–267. 47 indexed citations

Poole, Rebecca, Louise E Docherty, Almuth Caliebe, et al.. (2013). Targeted methylation testing of a patient cohort broadens the epigenetic and clinical description of imprinting disorders. American Journal of Medical Genetics Part A. 161(9). 2174–2182. 56 indexed citations

Scurr, Ingrid, Louise C. Wilson, Melissa Lees, et al.. (2011). Cantú syndrome: Report of nine new cases and expansion of the clinical phenotype. American Journal of Medical Genetics Part A. 155(3). 508–518. 54 indexed citations

Turner, Claire, Deborah Mackay, Jonathan L A Callaway, et al.. (2010). Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci. European Journal of Human Genetics. 18(6). 648–655. 73 indexed citations

Turner, Claire, et al.. (2009). Detection of 53 FBN1 mutations (41 novel and 12 recurrent) and genotype–phenotype correlations in 113 unrelated probands referred with Marfan syndrome, or a related fibrillinopathy. American Journal of Medical Genetics Part A. 149A(2). 161–170. 29 indexed citations

10.

Gilbert, Rodney D., Claire Turner, Jane Whitney Gibson, et al.. (2008). Mutations in phospholipase C epsilon 1 are not sufficient to cause diffuse mesangial sclerosis. Kidney International. 75(4). 415–419. 22 indexed citations

11.

Blyth, Moira, Nicola Foulds, Claire Turner, & David J. Bunyan. (2008). Severe Marfan syndrome due to FBN1 exon deletions. American Journal of Medical Genetics Part A. 146A(10). 1320–1324. 19 indexed citations

12.

Turner, Claire, David J. Bunyan, N. Simon Thomas, et al.. (2007). Zellweger syndrome resulting from maternal isodisomy of chromosome 1. American Journal of Medical Genetics Part A. 143A(18). 2172–2177. 18 indexed citations

13.

Turner, Claire, Katherine Lachlan, Nishani Amerasinghe, et al.. (2005). Kabuki syndrome: new ocular findings but no evidence of 8p22-p23.1 duplications in a clinically defined cohort. European Journal of Human Genetics. 13(6). 716–720. 31 indexed citations

14.

Frayling, Timothy M., Mark Walker, Mark I. McCarthy, et al.. (1999). Parent-offspring trios: a resource to facilitate the identification of type 2 diabetes genes.. Diabetes. 48(12). 2475–2479. 42 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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