I. Karen Temple

19.6k total citations
185 papers, 8.2k citations indexed

About

I. Karen Temple is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, I. Karen Temple has authored 185 papers receiving a total of 8.2k indexed citations (citations by other indexed papers that have themselves been cited), including 135 papers in Genetics, 94 papers in Molecular Biology and 47 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in I. Karen Temple's work include Genetic Syndromes and Imprinting (77 papers), Epigenetics and DNA Methylation (52 papers) and Prenatal Screening and Diagnostics (42 papers). I. Karen Temple is often cited by papers focused on Genetic Syndromes and Imprinting (77 papers), Epigenetics and DNA Methylation (52 papers) and Prenatal Screening and Diagnostics (42 papers). I. Karen Temple collaborates with scholars based in United Kingdom, United States and Germany. I. Karen Temple's co-authors include Deborah Mackay, David Robinson, Sian Ellard, Andrew T. Hattersley, Eamonn R. Maher, Julian Hamilton‐Shield, M Baraitser, Sarah E. Flanagan, John Barber and R. J. Bayly and has published in prestigious journals such as Cell, The Lancet and Nature Genetics.

In The Last Decade

I. Karen Temple

181 papers receiving 7.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
I. Karen Temple United Kingdom 49 5.6k 4.6k 2.3k 2.0k 1.2k 185 8.2k
Valérie Cormier‐Daire France 62 7.2k 1.3× 8.4k 1.8× 1.0k 0.4× 1.3k 0.7× 463 0.4× 393 14.3k
Helen V. Firth United Kingdom 38 4.5k 0.8× 3.1k 0.7× 1.1k 0.5× 683 0.3× 242 0.2× 102 6.7k
Michel Vekemans France 44 3.3k 0.6× 4.1k 0.9× 1.7k 0.7× 1.2k 0.6× 216 0.2× 248 8.7k
William Reardon United Kingdom 53 5.2k 0.9× 6.5k 1.4× 938 0.4× 1.2k 0.6× 368 0.3× 195 11.9k
Tania Attié‐Bitach France 42 2.4k 0.4× 3.6k 0.8× 888 0.4× 1.6k 0.8× 217 0.2× 156 6.7k
Martine Le Merrer France 46 4.0k 0.7× 4.6k 1.0× 642 0.3× 809 0.4× 256 0.2× 130 7.9k
Gen Nishimura Japan 41 3.7k 0.7× 3.6k 0.8× 541 0.2× 781 0.4× 328 0.3× 344 7.1k
Dian Donnai United Kingdom 48 3.0k 0.5× 3.1k 0.7× 1.2k 0.5× 1.1k 0.6× 112 0.1× 177 7.8k
Martijn H. Breuning Netherlands 50 5.9k 1.1× 6.2k 1.4× 858 0.4× 735 0.4× 221 0.2× 160 11.0k
Patricia A. Labosky United States 41 2.4k 0.4× 6.7k 1.5× 321 0.1× 2.4k 1.2× 1.1k 0.9× 69 10.0k

Countries citing papers authored by I. Karen Temple

Since Specialization
Citations

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

Fields of papers citing papers by I. Karen Temple

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by I. Karen Temple. 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 I. Karen Temple. The network helps show where I. Karen Temple may publish in the future.

Co-authorship network of co-authors of I. Karen Temple

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

All Works

20 of 20 papers shown
1.
Iotova, Violeta, et al.. (2023). A Long-term Follow-up of a Late Diagnosed Patient with Temple Syndrome – a Case Report. Journal of Clinical Research in Pediatric Endocrinology. 16(4). 475–480.
2.
Lim, Derek, Shane McKee, Meriel McEntagart, et al.. (2021). Whole-genome analysis as a diagnostic tool for patients referred for diagnosis of Silver-Russell syndrome: a real-world study. Journal of Medical Genetics. 59(6). 613–622. 13 indexed citations
3.
Mackay, Deborah, Jet Bliek, Maria Lombardi, et al.. (2019). Discrepant molecular and clinical diagnoses in Beckwith-Wiedemann and Silver-Russell syndromes. Genetics Research. 101. e3–e3. 16 indexed citations
4.
Fenwick, Angela, et al.. (2016). Falling short? The psychosocial impact of living with Russell-Silver syndrome. Journal of Aesthetic Nursing. 5(7). 340–342. 2 indexed citations
5.
Eggermann, Thomas, Guiomar Pérez de Nanclares, Eamonn R. Maher, et al.. (2015). Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci. Clinical Epigenetics. 7(1). 123–123. 130 indexed citations
6.
Rezwan, Faisal I., Louise E Docherty, Rebecca Poole, et al.. (2015). A statistical method for single sample analysis of HumanMethylation450 array data: genome-wide methylation analysis of patients with imprinting disorders. Clinical Epigenetics. 7(1). 48–48. 13 indexed citations
7.
Gregory, Louise, Rachel Besser, I. Karen Temple, Justin E. Davies, & Mehul Dattani. (2015). Mutations inBRAFare associated with septo-optic dysplasia and cardiofaciocutaneous syndrome. Endocrine Abstracts.
8.
Tapper, William, Nicola Foulds, Nicholas C.P. Cross, et al.. (2014). Megalencephaly Syndromes: Exome Pipeline Strategies for Detecting Low-Level Mosaic Mutations. PLoS ONE. 9(1). e86940–e86940. 16 indexed citations
9.
Naik, Swati, N. Simon Thomas, Justin H. Davies, et al.. (2011). Novel Tandem Duplication in Exon 1 of the SNURF/SNRPN Gene in a Child with Transient Excessive Eating Behaviour and Weight Gain. Molecular Syndromology. 2(2). 76–80. 4 indexed citations
10.
Maas, Saskia M., Maria Lombardi, A. J. van Essen, et al.. (2009). Phenotype and genotype in 17 patients with Goltz–Gorlin syndrome. Journal of Medical Genetics. 46(10). 716–720. 53 indexed citations
11.
Temple, I. Karen & Greta Westwood. (2006). Do Once and Share: clinical genetics. ePrints Soton (University of Southampton). 6(6). 523–535. 2 indexed citations
12.
Tatton‐Brown, Katrina, Jenny Douglas, Kim Coleman, et al.. (2005). Genotype-Phenotype Associations in Sotos Syndrome: An Analysis of 266 Individuals with NSD1 Aberrations. The American Journal of Human Genetics. 77(2). 193–204. 221 indexed citations
13.
Cox, Helen, H. Bullman, & I. Karen Temple. (2003). Maternal UPD(14) in the patient with a normal karyotype: Clinical report and a systematic search for cases in samples sent for testing for Prader–Willi syndrome. American Journal of Medical Genetics Part A. 127A(1). 21–25. 24 indexed citations
14.
Дедов, И. И., et al.. (2002). ? Tranzitornyy? neonatal'nyy diabet vsledstvie duplikatsii v 6-y khromosome [dup(6)(q24.2q24.2) de novo]. Diabetes Mellitus. 5(2). 18–23.
15.
Elanko, Navaratnam, et al.. (2001). A survey of TWIST for mutations in craniosynostosis reveals a variable length polyglycine tract in asymptomatic individuals.. The American Journal of Human Genetics. 69. 653–653. 2 indexed citations
16.
Fisher, Andrew, Simon Thomas, Caroline Joyce, Peter Strike, & I. Karen Temple. (2001). A patient with growth retardation and a duplication of the Beckwith Wiedemann critical region of maternal origin. ePrints Soton (University of Southampton). 2 indexed citations
17.
Gloyn, Anna L., Sian Ellard, Julian Hamilton‐Shield, et al.. (2001). Complete glucokinase deficiency is not a common cause of permanent neonatal diabetes in European cases of neonatal diabetes. ePrints Soton (University of Southampton). 1 indexed citations
18.
Hatchwell, Eli, et al.. (1998). Molecular confirmation of germ line mosaicism for a submicroscopic deletion of chromosome 22q11. American Journal of Medical Genetics. 78(2). 103–106. 23 indexed citations
19.
Coppin, Brian & I. Karen Temple. (1997). Multiple lentigines syndrome (LEOPARD syndrome or progressive cardiomyopathic lentiginosis).. Journal of Medical Genetics. 34(7). 582–586. 60 indexed citations
20.
Temple, I. Karen, et al.. (1991). Pitfalls in counselling: the craniosynostoses.. Journal of Medical Genetics. 28(2). 117–121. 8 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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