Jane Chalker - Great Ormond St Hosp Children NHS Fdn Trust, Specialist Integrated Haematol & Malignancy Diagn, London, England

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论文共 58 篇作者统计合作学者相似作者

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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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Decision Making for Health-Related Research Outcomes That Alter Diagnosis: A Model from Paediatric Brain Tumours

Jessica C. Pickles,Kristian Aquilina,Jane Chalker,Christine Dahl,Abel Devadass,Kshitij Mankad,Ashirwad Merve,Munaza Ahmed,James A. R. Nicoll,Tabitha Bloom,David A. Hilton,Neil J. Sebire,Darren Hargrave,Thomas S. Jacques

Neuropathology and Applied Neurobiologyno. 4 (2024)

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Recurrent Adamantinomatous Craniopharyngiomas Show MAPK Pathway Activation, Clonal Evolution and Rare TP53-loss-mediated Malignant Progression

Acta Neuropathologica Communicationsno. 1 (2024)

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MAPK PATHWAY ACTIVATION, CLONAL EVOLUTION, INCLUDING RARE TP53 LOSS, AND THE IMMUNE ENVIRONMENT OF RECURRENT CRANIOPHARYNGIOMA

John R. Apps, Mario Gonzalez-Meljem,Romain Guiho,Jessica C. Pickles,Eric Prince,Edward Schwalbe, Nikhil Joshi,Thomas J. Stone,Olumide Ogunbiyi,Jane Chalker, Akang Bassey,Georg Otto, Rosalind Davies,Debbie Hughes,Enrica Tan,Sebastian Brandner, Victoria Lee,Caroline Hayhurst, Cassie Kline,Sergi Castellano,Todd C. Hankinson,Timo Deutschbein,Thomas S. Jacques, Juan Pedro Martinez-Barbera

NEURO-ONCOLOGY (2024)

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

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

CANCER RESEARCHno. 17 (2024)

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CP-05. MAPK PATHWAY ACTIVATION, CLONAL EVOLUTION, INCLUDING RARE TP53 LOSS, AND THE IMMUNE ENVIRONMENT OF RECURRENT CRANIOPHARYNGIOMA

John Apps, Mario Gonzalez-Meljem,Romain Guiho,Jessica C. Pickles,Eric D. Prince,Ed C. Schwalbe, Nikhil Joshi,T. J. Stone,Olumide Ogunbiyi,Jane Chalker, Akang Leonard Bassey,Georg Otto, Rosalind Davies,Debbie Hughes,Enrica Ee Kar Tan,Sebastian Brandner, Victoria Lee,Caroline Hayhurst, Cassie Kline,Sergi Castellano,Todd C. Hankinson,Timo Deutschbein,Thomas S. Jacques,Juan Pedro Martı́nez-Barberá

Neuro-oncologyno. Supplement_4 (2024): 0-0

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Supplementary Table S2 from Infant High-Grade Gliomas Comprise Multiple Subgroups Characterized by Novel Targetable Gene Fusions and Favorable Outcomes

Matthew Clarke,Alan Mackay,Britta Ismer,Jessica C. Pickles,Ruth G. Tatevossian,Scott Newman,Tejus A. Bale,Iris Stoler,Elisa Izquierdo,Sara Temelso,Diana M. Carvalho,Valeria Molinari,Anna Burford,Louise Howell,Alex Virasami,Amy R. Fairchild,Aimee Avery,Jane Chalker,Mark Kristiansen,Kelly Haupfear,James D. Dalton,Wilda Orisme,Ji Wen,Michael Hubank,Kathreena M. Kurian,Catherine Rowe,Mellissa Maybury,Stephen Crosier,Jeffrey Knipstein,Ulrich Schüller,Uwe Kordes,David E. Kram,Matija Snuderl,Leslie Bridges,Andrew J. Martin,Lawrence J. Doey,Safa Al-Sarraj,Christopher Chandler,Bassel Zebian,Claire Cairns,Rachael Natrajan,Jessica K.R. Boult,Simon P. Robinson,Martin Sill,Ira J. Dunkel,Stephen W. Gilheeney,Marc K. Rosenblum,Debbie Hughes,Paula Z. Proszek,Tobey J. Macdonald,Matthias Preusser,Christine Haberler,Irene Slavc,Roger Packer,Ho-Keung Ng,Shani Caspi,Mara Popović,Barbara Faganel Kotnik,Matthew D. Wood,Lissa Baird,Monika Ashok Davare,David A. Solomon,Thale Kristin Olsen,Petter Brandal,Michael Farrell,Jane B. Cryan,Michael Capra,Michael Karremann,Jens Schittenhelm,Martin U. Schuhmann,Martin Ebinger,Winand N.M. Dinjens,Kornelius Kerl,Simone Hettmer,Torsten Pietsch,Felipe Andreiuolo,Pablo Hernáiz Driever,Andrey Korshunov,Lotte Hiddingh,Barbara C. Worst,Dominik Sturm,Marc Zuckermann, Olaf Witt,Tabitha Bloom,Clare Mitchell,Evelina Miele,Giovanna Stefania Colafati,Francesca Diomedi-Camassei,Simon Bailey,Andrew S. Moore,Timothy E.G. Hassall,Stephen P. Lowis,Maria Tsoli,Mark J. Cowley,David S. Ziegler,Matthias A. Karajannis,Kristian Aquilina,Darren R. Hargrave,Fernando Carceller,Lynley V. Marshall,Andreas von Deimling,Christof M. Kramm,Stefan M. Pfister,Felix Sahm,Suzanne J. Baker,Angela Mastronuzzi,Andrea Carai,Maria Vinci,David Capper,Sergey Popov,David W. Ellison,Thomas S. Jacques,David T.W. Jones,Chris Jones

crossref（2023）

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Routine Whole Genome Sequencing for All Children with Hematological Malignancies Defines a New Standard of Care - Data of the First 152 Cases from the NHS England Genomic Medicine Service

Angus Hodder, Sarah Leiter,Aditi Vedi, Phillipa May,Dilys Addy,Phil Ancliff,Julian Cano-Flanagan,Jane Chalker,Danny Cheng, Yasmin Clinch, Caryl Dryden,Sara Ghorashian,David O'Connor,Vesna Pavasovic,Anupama Rao,Sujith Samarasinghe, Iryna Stasevich,Ajay Vora,Michael Hubank, Dame Lyn Chitty,Sam Behjati,Jack Bartram

BLOOD（2023）

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