Christopher M. Watson - Univ Leeds, St Jamess Univ Hosp

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论文共 63 篇作者统计合作学者相似作者

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Inherited CD19 Deficiency Does Not Impair Plasma Cell Formation or Response to CXCL12

Kieran Walker,Anoop Mistry,Christopher M. Watson,Fatima Nadat, Eleanor O’Callaghan,Matthew Care,Laura A. Crinnion,Gururaj Arumugakani,David T. Bonthron,Clive Carter,Gina M. Doody,Sinisa Savic

Journal of Clinical Immunologyno. 1 (2025): 1-2

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AgileMultiIdeogram: Rapid Identification and Visualization of Autozygous Regions Using Illumina Short-Read Sequencing Data

Christopher M. Watson,Carolina Lascelles, Morag Raynor, Marilena Elpidorou, Ummey Hany, Laura Crinnion,Colin A. Johnson,Eamonn Sheridan,Alexander F. Markham,James A. Poulter,David T. Bonthron,Ian M. Carr

Biologyno. 6 (2025): 666

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Heterozygous COL17A1 Variants Are a Frequent Cause of Amelogenesis Imperfecta

Ummey Hany,Christopher M. Watson, Lu Liu,Claire E. L. Smith, Asmaa Harfoush,James A. Poulter,Georgios Nikolopoulos,Richard Balmer,Catriona J. Brown,Anesha Patel, Jenny Simmonds,Ruth Charlton,Maria Gabriela Acosta de Camargo,Helen D. Rodd,Hussain Jafri,Agne Antanaviciute, Michelle Moffat,Maisoon Al-Jawad,Chris F. Inglehearn,Alan J. Mighell

JOURNAL OF MEDICAL GENETICSno. 4 (2024): 347-355

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Biallelic Variants in Plexin B2 (PLXNB2) Cause Amelogenesis Imperfecta, Hearing Loss and Intellectual Disability

Claire E. L. Smith,Virginie Laugel-Haushalter, Ummey Hany,Sunayna Best,Rachel L. Taylor,James A. Poulter,Saskia B. Wortmann,Rene G. Feichtinger,Johannes A. Mayr,Suhaila Al Bahlani,Georgios Nikolopoulos, Alice Rigby,Graeme C. Black,Christopher M. Watson,Sahar Mansour,Chris F. Inglehearn,Alan J. Mighell,Agnes Bloch-Zupan

Journal of Medical Geneticsno. 7 (2024): 689-698

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Characterization of Genetic Landscape and Novel Inflammatory Biomarkers in Patients with Adult-Onset Still's Disease

Joanne Topping,Leon Chang,Fatima Nadat,James A. Poulter, Alice Ibbotson,Samuel Lara-Reyna,Christopher M. Watson,Clive Carter, Linda P. Pournara,Jan Zernicke,Rebecca L. Ross,Catherine Cargo,Paul A. Lyons,Kenneth G. C. Smith,Francesco Del Galdo,Juergen Rech,Bruno Fautrel,Eugen Feist,Michael F. Mcdermott,Sinisa Savic, ImmunAID Consortium

ARTHRITIS & RHEUMATOLOGY (2024)

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Using Long-Read Nanopore Sequencing to Study the Genetic Basis of Fuchs Endothelial Corneal Dystrophy

Bushra Alayed,Christopher M. Watson,Seema Anand,Salina Siddiqui,Chris F. Inglehearn,Manir Ali

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCEno. 7 (2024)

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Effective Smmips-Based Sequencing of Maculopathy-Associated Genes in Stargardt Disease Cases and Allied Maculopathies from the UK

Benjamin Mc Clinton,Zelia Corradi,Martin McKibbin,Daan M. Panneman,Susanne Roosing,Erica G. M. Boonen,Manir Ali,Christopher M. Watson,David H. Steel,Frans P. M. Cremers,Chris F. Inglehearn,Rebekkah J. Hitti-Malin,Carmel Toomes

Genes（2023）

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Targeted Nanopore Sequencing Enables Complete Characterisation of Structural Deletions Initially Identified Using Exon-Based Short-Read Sequencing Strategies

Benjamin McClinton,Laura A. Crinnion,Martin McKibbin,Rajarshi Mukherjee,James A. Poulter,Claire E. L. Smith,Manir Ali,Christopher M. Watson,Chris F. Inglehearn,Carmel Toomes

Molecular Genetics & Genomic Medicine（2023）

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Long-Read Nanopore Sequencing of RPGR ORF15 is Enhanced Following DNase I Treatment of MinION Flow Cells

Samar Yahya,Christopher M. Watson,Ian Carr,Martin McKibbin,Laura A. Crinnion,Morag Taylor, Hope Bonin,Tracy Fletcher,Mohammed E. El-Asrag,Manir Ali,Carmel Toomes,Chris F. Inglehearn

Molecular Diagnosis & Therapyno. 4 (2023): 525-535

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Haplotyping Using Long-Range PCR and Nanopore Sequencing to Phase Variants: Lessons Learned from the ABCA4 Locus

Benjamin McClinton,Christopher M. Watson,Laura A. Crinnion,Martin McKibbin,Manir Ali,Chris F. Inglehearn,Carmel Toomes

LABORATORY INVESTIGATIONno. 8 (2023)

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