Ruth Armstrong - East Anglian Medical Genetics Service, Addenbrooke’s Hospital

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论文共 44 篇作者统计合作学者相似作者

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Abstract A011 Molecular Analysis Improves the Diagnosis of Young People with Renal Tumors

Cancer Researchno. 17_Supplement (2024)

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Benefits for Children with Suspected Cancer from Routine Whole-Genome Sequencing

Angus Hodder,Sarah M. Leiter, Jonathan Kennedy,Dilys Addy,Munaza Ahmed,Thankamma Ajithkumar,Kieren Allinson,Phil Ancliff,Shivani Bailey, Gemma Barnard,G. A. Amos Burke, Charlotte Burns,Julian Cano-Flanagan,Jane Chalker,Nicholas Coleman,Danny Cheng, Yasmin Clinch, Caryl Dryden,Sara Ghorashian,Blanche Griffin,Gail Horan,Michael Hubank, Phillippa May, Joanna McDerra, Rajvi Nagrecha,James Nicholson,David O'Connor,Vesna Pavasovic,Annelies Quaegebeur,Anupama Rao,Thomas Roberts,Sujith Samarasinghe, Iryna Stasevich,John A. Tadross,Claire Trayers,Jamie Trotman,Ajay Vora,James Watkins,Lyn S. Chitty,Sarah Bowdin,Ruth Armstrong,Matthew J. Murray,Catherine E. Hook,Patrick Tarpey,Aditi Vedi,Jack Bartram,Sam Behjati

NATURE MEDICINE（2024）

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Developing a Paired Whole Genome Sequencing Service for Children with Cancer

Lyndall Sarkies, Philippa Thomas, Ebehireme Ann Edeko,Sarah Leiter,Jamie Trotman,Ruth Armstrong,Aditi Vedi

Clinical Oncology (2024)

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Introduction and Impact of Routine Whole Genome Sequencing in the Diagnosis and Management of Sarcoma

James A. Watkins,Jamie Trotman,John A. Tadross, Jennifer Harrington,Helen Hatcher,Gail Horan,Sarah Prewett, Han H. Wong,Sarah McDonald,Patrick Tarpey,Thomas Roberts, Jing Su,Marc Tischkowitz,Ruth Armstrong,Fernanda Amary,Alona Sosinsky

British journal of cancerno. 5 (2024): 860-869

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A Diagnosis of Noonan Syndrome Through Routine Whole Genome Sequencing in a Child with an Intracranial Nongerminomatous Germ Cell Tumor

Shathar Mahmood,Sarah M Leiter,Poe Phyu, Claudia Craven,Gail Horan,Jennifer Gains,Mayen Briggs, Esther Blanco,Sam Behjati,James Watkins,John A Tadross,Thomas Roberts,Jamie Trotman,Patrick Tarpey,Ruth Armstrong,Matthew J Murray

Pediatric blood & cancerno. 12 (2024): e31368-e31368

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Avoiding Premature Diagnostic Closure: Lessons from Two Children with Neurotransmitter Disorders Associated with Dual Pathology

Ainara Salazar-Villacorta,Robert Spaull,Samyami Chowdhury, Bina Mukhtyar,Manali Chitre,Ruth Armstrong,Mario Sa, Saleel Chandratre,Usha Kini, Ravi Chinthapalli,Kshitij Mankad,Sniya Sudhakar, Simon Pope,Simon Heales,Manju A. Kurian

Movement Disorders Clinical Practice (2024)

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Identifying Barriers and Opportunities to Facilitate the Uptake of Whole Genome Sequencing in Paediatric Haematology and Oncology Practice

Michelle Bishop,Aditi Vedi,Sarah Bowdin,Ruth Armstrong,Jack Bartram,David Bentley,Mark Ross,C. Elizabeth Hook, Brian Hon Yin Chung, Parker Moss,David H. Rowitch,Patrick Tarpey,Sam Behjati,Matthew J. Murray

BMC MEDICAL EDUCATIONno. 1 (2024)

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Abstract B030: Whole Genome Sequencing Provides Practice-Changing Benefits when Performed on Consecutive, Unselected Children with Suspected Cancer

CANCER RESEARCHno. 17 (2024)

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Approach to the Paediatric Patient with Suspected Pheochromocytoma or Paraganglioma Versus Neuroblastoma

A. Emile J. Hendriks, Charlotte Burns,Ben Fleming,Ines Harper,Elizabeth Hook,Ruth Armstrong,Christina Pamporaki,Graeme Eisenhofer,Matthew J. Murray,Ruth T. Casey

The Journal of Clinical Endocrinology & Metabolism (2024)

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Molecular Analysis Improves the Diagnosis of Young People with Renal Tumors

Sarah M. Leiter, Aisosa Guobadia,Ben Fleming,Thankamma Ajithkumar, James Armitage,Ruth Armstrong,G. A. Amos Burke, Charlotte Burns,Tanzina Chowdhury,Nicholas Coleman,Helen Hatcher,Gail Horan,Lisa Howell,Anna-May Long,Sarah McDonald,Thomas J. Mitchell,James C. Nicholson,Thomas Roberts,Grant D. Stewart,John A. Tadross,Patrick Tarpey,Claire Trayers,Jamie Trotman,James Watkins,Anne Y. Warren, Godran Vujanic,C. Elizabeth Hook,Sam Behjati,Matthew J. Murray

CANCER RESEARCHno. 17 (2024)

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