Elena Prigmore

11.4k total citations
27 papers, 1.4k citations indexed

About

Elena Prigmore is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Elena Prigmore has authored 27 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 12 papers in Molecular Biology and 7 papers in Plant Science. Recurrent topics in Elena Prigmore's work include Genomic variations and chromosomal abnormalities (16 papers), Genomics and Rare Diseases (8 papers) and Chromosomal and Genetic Variations (7 papers). Elena Prigmore is often cited by papers focused on Genomic variations and chromosomal abnormalities (16 papers), Genomics and Rare Diseases (8 papers) and Chromosomal and Genetic Variations (7 papers). Elena Prigmore collaborates with scholars based in United Kingdom, Spain and Brazil. Elena Prigmore's co-authors include Nigel P. Carter, Susan Gribble, Helen V. Firth, Matthew E. Hurles, Tomas Fitzgerald, David Fitzpatrick, Jeremy F. McRae, Louis Lim, Anthony W. Segal and Júlia Baptista and has published in prestigious journals such as Nature, Journal of Biological Chemistry and Nature Medicine.

In The Last Decade

Elena Prigmore

27 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Elena Prigmore United Kingdom	18	758	742	225	164	153	27	1.4k
H F Willard United States	22	804 1.1×	1.2k 1.6×	545 2.4×	124 0.8×	76 0.5×	28	1.8k
Judy Fantes United Kingdom	20	942 1.2×	1.3k 1.8×	281 1.2×	114 0.7×	36 0.2×	26	1.8k
David J. Picketts Canada	28	934 1.2×	2.2k 2.9×	107 0.5×	82 0.5×	241 1.6×	64	2.7k
Hanan E. Shamseldin Saudi Arabia	24	590 0.8×	981 1.3×	33 0.1×	106 0.6×	127 0.8×	55	1.5k
Andreas Massouras Switzerland	8	571 0.8×	746 1.0×	45 0.2×	44 0.3×	102 0.7×	9	1.4k
Kevin Huang United States	17	228 0.3×	1.4k 1.9×	65 0.3×	99 0.6×	113 0.7×	19	1.8k
Melanie M. Mahtani United States	14	705 0.9×	818 1.1×	252 1.1×	56 0.3×	60 0.4×	18	1.4k
Francesca Cole United States	20	636 0.8×	2.2k 3.0×	298 1.3×	73 0.4×	69 0.5×	30	2.5k
Diana Rajan United Kingdom	7	1.4k 1.8×	955 1.3×	199 0.9×	205 1.3×	61 0.4×	10	1.8k
Evica Rajcan‐Separovic Canada	24	770 1.0×	775 1.0×	178 0.8×	386 2.4×	166 1.1×	58	1.6k

Countries citing papers authored by Elena Prigmore

Since Specialization

Citations

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

Fields of papers citing papers by Elena Prigmore

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elena Prigmore

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

All Works

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20 of 20 papers shown

Rodríguez‐Ubreva, Javier, Josep Calafell-Segura, Baerbel Keller, et al.. (2024). COVID-19 progression and convalescence in common variable immunodeficiency patients show dysregulated adaptive immune responses and persistent type I interferon and inflammasome activation. Nature Communications. 15(1). 10344–10344. 1 indexed citations

Lawrence, John E., Kenny Roberts, Elizabeth Tuck, et al.. (2024). HOX gene expression in the developing human spine. Nature Communications. 15(1). 10023–10023. 5 indexed citations

Elmentaite, Rasa, Stijn van Dongen, Christine Thevanesan, et al.. (2024). Transcriptional signals of transformation in human cancer. Genome Medicine. 16(1). 8–8. 3 indexed citations

Thevanesan, Christine, Alice Piapi, Kirsty Ambridge, et al.. (2022). Precise identification of cancer cells from allelic imbalances in single cell transcriptomes. Communications Biology. 5(1). 884–884. 3 indexed citations

Khabirova, Eleonora, Laura Jardine, Tim Coorens, et al.. (2022). Single-cell transcriptomics reveals a distinct developmental state of KMT2A-rearranged infant B-cell acute lymphoblastic leukemia. Nature Medicine. 28(4). 743–751. 39 indexed citations

Kaplanis, Joanna, Rashesh Sanghvi, Matthew D. C. Neville, et al.. (2022). Genetic and chemotherapeutic influences on germline hypermutation. Nature. 605(7910). 503–508. 49 indexed citations

Gardner, Eugene J., Alejandro Sifrim, Sarah Lindsay, et al.. (2021). Detecting cryptic clinically relevant structural variation in exome-sequencing data increases diagnostic yield for developmental disorders. The American Journal of Human Genetics. 108(11). 2186–2194. 11 indexed citations

Wright, Caroline F., Elena Prigmore, Jeremy F. McRae, et al.. (2019). Clinically-relevant postzygotic mosaicism in parents and children with developmental disorders in trio exome sequencing data. Nature Communications. 10(1). 2985–2985. 54 indexed citations

Gardner, Eugene J., Elena Prigmore, Giuseppe Gallone, et al.. (2019). Contribution of retrotransposition to developmental disorders. Nature Communications. 10(1). 4630–4630. 39 indexed citations

10.

Wright, Caroline F., Jeremy F. McRae, Stephen Clayton, et al.. (2018). Making new genetic diagnoses with old data: iterative reanalysis and reporting from genome-wide data in 1,133 families with developmental disorders. Genetics in Medicine. 20(10). 1216–1223. 193 indexed citations

11.

Quinlan-Jones, E, Jenny Lord, Denise Williams, et al.. (2018). Molecular autopsy by trio exome sequencing (ES) and postmortem examination in fetuses and neonates with prenatally identified structural anomalies. Genetics in Medicine. 21(5). 1065–1073. 41 indexed citations

12.

Freitas, Érika L., Susan Gribble, Milena Simioni, et al.. (2012). A familial case with interstitial 2q36 deletion: Variable phenotypic expression in full and mosaic state. European Journal of Medical Genetics. 55(11). 660–665. 4 indexed citations

13.

Freitas, Érika L., Susan Gribble, Milena Simioni, et al.. (2011). Maternally inherited partial monosomy 9p (pter → p24.1) and partial trisomy 20p (pter → p12.1) characterized by microarray comparative genomic hybridization. American Journal of Medical Genetics Part A. 155(11). 2754–2761. 8 indexed citations

14.

Gribble, Susan, Bee Ling Ng, Elena Prigmore, Tomas Fitzgerald, & Nigel P. Carter. (2009). Array painting: a protocol for the rapid analysis of aberrant chromosomes using DNA microarrays. Nature Protocols. 4(12). 1722–1736. 21 indexed citations

15.

El-Aziz, Mai M. Abd, Isabel Barragán, Salud Borrego, et al.. (2008). Large‐scale Molecular Analysis of a 34 Mb Interval on Chromosome 6q: Major Refinement of the RP25 Interval. Annals of Human Genetics. 72(4). 463–477. 5 indexed citations

16.

El-Aziz, Mai M. Abd, Isabel Barragán, Leo Goodstadt, et al.. (2008). EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosa. Nature Genetics. 40(11). 1285–1287. 150 indexed citations

17.

Baptista, Júlia, Catherine Mercer, Elena Prigmore, et al.. (2008). Breakpoint Mapping and Array CGH in Translocations: Comparison of a Phenotypically Normal and an Abnormal Cohort. The American Journal of Human Genetics. 82(4). 927–936. 127 indexed citations

18.

Abdulrahman, Mahera, Mark R. Morris, Elena Prigmore, et al.. (2007). Characterization of a 3;6 translocation associated with renal cell carcinoma. Genes Chromosomes and Cancer. 46(4). 311–317. 26 indexed citations

19.

Baptista, Júlia, Elena Prigmore, Susan Gribble, et al.. (2005). Molecular cytogenetic analyses of breakpoints in apparently balanced reciprocal translocations carried by phenotypically normal individuals. European Journal of Human Genetics. 13(11). 1205–1212. 21 indexed citations

20.

Ahmed, Sohail, Elena Prigmore, Sheila Govind, et al.. (1998). Cryptic Rac-binding and p21 -activated Kinase Phosphorylation Sites of NADPH Oxidase Component p67. Journal of Biological Chemistry. 273(25). 15693–15701. 69 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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