Greg Elgar - School of Biological Sciences, Queen Mary, University of London

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个人简介

Application of genomics technologies to clinical healthcare; in particular diagnosis, prognosis and disease monitoring. Whole genome sequencing using short and long read approaches, transcriptomics and proteomics

研究兴趣

论文共 169 篇作者统计合作学者相似作者

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Clinical Utility of 'shaken' Biopsies for Whole-Genome Sequencing

Rachel Nelan,Martina Mijuskovic, Martina Hughes,Jennifer Becq,Zoya Kingsbury, Eleni Tsogka, Miao He, Dunja Vucenovic,Clare Craig,Greg Elgar, Pauline Levey,Tamara Suaris, Emma Walsh,Mark Ross,J Louise Jones

Journal of clinical pathology (2025)

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SAVANA: Reliable Analysis of Somatic Structural Variants and Copy Number Aberrations in Clinical Samples Using Long-Read Sequencing

Hillary Elrick,Carolin M Sauer,Jose Espejo Valle-Inclan, Katherine Trevers,Melanie Tanguy, Sonia Zumalave,Solange De Noon,Francesc Muyas,Rita Cascão,Angela Afonso, Alistair G Rust,Fernanda Amary,Roberto Tirabosco,Adam Giess, Timothy Freeman,Alona Sosinsky,Katherine Piculell,David T Miller,Claudia C Faria,Greg Elgar,Adrienne M Flanagan,Isidro Cortes-Ciriano

Nature methods (2025)

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Ongoing Chromothripsis Underpins Osteosarcoma Genome Complexity and Clonal Evolution

Jose Espejo Valle-Inclan,Solange De Noon, Katherine Trevers, Hillary Elrick, Ianthe A.E.M. van Belzen, Sonia Zumalave,Carolin M. Sauer,Mélanie Tanguy, Thomas Butters,Francesc Muyas,Alistair G. Rust,Fernanda Amary,Roberto Tirabosco,Adam Giess,Alona Sosinsky,Greg Elgar,Adrienne M. Flanagan,Isidro Cortés-Ciriano

Cell（2025）

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Analysis of RNAseq from 4400 Individuals in the 100,000 Genomes Project Identifies New Potential Diagnoses

Jenny Lord,Carolina Jaramillo Oquendo, Niall McGinness, Alexander Ho,Terena James,Mark Ross, Lily Hoa,Greg Elgar,Diana Baralle

EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 3-4

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A Comparison of Structural Variant Calling from Short-Read and Nanopore-Based Whole-Genome Sequencing Using Optical Genome Mapping As a Benchmark

Yang Pei,Melanie Tanguy,Adam Giess,Abhijit Dixit,Louise C. Wilson,Richard J. Gibbons,Stephen R. F. Twigg,Greg Elgar,Andrew O. M. Wilkie

Genesno. 7 (2024): 925-925

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Large-scale Analysis of Whole Genome Sequencing Data from Formalin-Fixed Paraffin-Embedded Cancer Specimens Demonstrates Preservation of Clinical Utility

Shadi Basyuni, Laura Heskin,Andrea Degasperi,Daniella Black, Gene C. C. Koh, Lucia Chmelova, Giuseppe Rinaldi,Steven Bell,Louise Grybowicz,Greg Elgar,Yasin Memari,Pauline Robbe,Zoya Kingsbury,Carlos Caldas,Jean Abraham,Anna Schuh,Louise Jones,Marc Tischkowitz,Matthew A. Brown,Helen R. Davies,Serena Nik-Zainal

NATURE COMMUNICATIONSno. 1 (2024)

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Characterising Clinically Relevant Complex Structural Variants in Craniosynostosis Using Long-Range Technologies

Yang Pei,Eduardo Calpena, Dagmara Korona,Louise Wilson,Wendy Jones,Tazeen Ashraf,Francesca Forzano,Deborah Shears,David Johnson,Gregory Thomas,Jill Clayton-Smith,Ajoy Sarkar, Urvi Savania,Melanie Tanguy,Adam Giess,Greg Elgar,Richard Gibbons,Stephen Twigg,Andrew Wilkie

EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 37-37

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Long read sequencing characterises a novel structural variant opaque to short reads, with likely functional impact in a case of unexplained severe fatigue

Jamie Oakley,Martin Hill,Adam Giess,M. Tanguy,Greg Elgar

Research Square (Research Square) (2023)

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Long Read Sequencing Characterises a Novel Structural Variant, Revealing Underactive AKR1C1 with Overactive AKR1C2 As a Possible Cause of Severe Chronic Fatigue

Julia Oakley,Martin Hill,Adam Giess,Mélanie Tanguy,Greg Elgar

JOURNAL OF TRANSLATIONAL MEDICINE（2023）

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Long Read Sequencing Characterises a Novel Structural Variant Opaque to Short Reads, with Likely Functional Impact in a Case of Unexplained Severe Fatigue

Julia Oakley,Martin Hill,Adam Giess,Mélanie Tanguy,Greg Elgar

crossref（2023）

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