A novel CASR variant in a family with familial hypocalciuric hypercalcaemia and primary hyperparathyroidism von Sagi, Satyanarayana V, Joshi, Hareesh, Trotman, Jamie, Elsey, Terence, Swamy, Ashwini, Rajkanna, Jeyanthy, Bhat, Nazir A, Haddadin, Firas J S, Oyibo, Samson O, Park, Soo-Mi

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Predation of native coccinellids by the invasive alien Harmonia axyridis (Coleoptera: Coccinellidae): detection in Britain by PCR-based gut analysis von THOMAS, ALISON P., TROTMAN, JAMIE, WHEATLEY, ANGELA, AEBI, ALEX, ZINDEL, RENATE, BROWN, PETER M. J.

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A cutaneous spindle cell neoplasm characterized by a COL3A1::PDGFRA fusion von Watkins, James, Jackson, Edward, Tarpey, Patrick, Tadross, John A., Trotman, Jamie, O'Dea, Emily

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Challenging our understanding of B‐cell lymphomagenesis and risk: Paediatric high‐grade B‐cell lymphoma, not otherwise specified with a DDX3X::MLLT10 fusion and an IGH deletion... von Hare, Lucy, Trotman, Jamie, Tarpey, Patrick, Hook, Elizabeth, Burke, G. A. Amos

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Introduction and impact of routine whole genome sequencing in the diagnosis and management of sarcoma von Watkins, James A., Trotman, Jamie, Tadross, John A., Harrington, Jennifer, Hatcher, Helen, Horan, Gail, Prewett, Sarah, Wong, Han H., McDonald, Sarah, Tarpey, Patrick, Roberts, Thomas, Su, Jing, Tischkowitz, Marc, Armstrong, Ruth, Amary, Fernanda, Sosinsky, Alona

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A rare case of paediatric astroblastoma with concomitant MN1‐GTSE1 and EWSR1‐PATZ1 gene fusions altering management von Chadda, Karan R., Holland, Katherine, Scoffings, Daniel, Dean, Andrew, Pickles, Jessica C., Behjati, Sam, Jacques, Thomas S., Trotman, Jamie, Tarpey, Patrick, Allinson, Kieren, Murray, Matthew J.

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Wilms Tumor With Raised Serum Alpha-Fetoprotein: Highlighting the Need for Novel Circulating Biomarkers von Green, Rebecca, Ahmed, Adeeb, Fleming, Ben, Long, Anna-May, Behjati, Sam, Trotman, Jamie, Tarpey, Patrick, Nicholson, James C., Coleman, Nicholas, Elizabeth Hook, C., Murray, Matthew J.

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A diagnosis of Noonan syndrome through routine whole genome sequencing in a child with an intracranial nongerminomatous germ cell tumor von Mahmood, Shathar, Leiter, Sarah M., Phyu, Poe, Craven, Claudia, Horan, Gail, Gains, Jennifer, Briggs, Mayen, Blanco, Esther, Behjati, Sam, Watkins, James, Tadross, John A., Roberts, Thomas, Trotman, Jamie, Tarpey, Patrick, Armstrong, Ruth, Murray, Matthew J.

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Recurrent FOSL1 rearrangements in desmoplastic fibroblastoma von De Noon, Solange, Piggott, Robert, Trotman, Jamie, Tadross, John A, Fittall, Matthew, Hughes, Debbie, Ye, Hongtao, Munasinghe, Emani, Murray, Matthew, Tirabosco, Roberto, Amary, Fernanda, Coleman, Nicholas, Watkins, James, Hubank, Michael, Tarpey, Patrick, Behjati, Sam, Flanagan, Adrienne M

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

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The NHS England 100,000 Genomes Project: feasibility and utility of centralised genome sequencing for children with cancer von Trotman, Jamie, Armstrong, Ruth, Firth, Helen, Trayers, Claire, Watkins, James, Allinson, Kieren, Jacques, Thomas S., Nicholson, James C., Burke, G. A. Amos, Behjati, Sam, Murray, Matthew J., Hook, Catherine E., Tarpey, Patrick

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Recurrent posterior fossa group A (PFA) ependymoma in a young child with constitutional mismatch repair deficiency (CMMRD) von Briggs, Mayen, Das, Anirban, Firth, Helen, Levine, Adrian, Sánchez‐Ramírez, Santiago, Negm, Logine, Ercan, Ayse B., Chung, Jill, Bianchi, Vanessa, Jalloh, Ibrahim, Phyu, Poe, Thorp, Nicky, Grundy, Richard G., Hawkins, Cynthia, Trotman, Jamie, Tarpey, Patrick, Tabori, Uri, Allinson, Kieren, Murray, Matthew J.

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Identification of an Activating PDGFRA Deletion in a Novel Sinonasal Soft Tissue Neoplasm von Watkins, James A., Hatcher, Helen, Malhotra, Shalini, Amen, Furrat, Bruty, Jonathan, Trotman, Jamie, Tarpey, Patrick, Tadross, John A.

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Malignant Peripheral Nerve Sheath Tumor in Cowden Syndrome: A First Report von Taylor, Amy, Delon, Isabelle, Allinson, Kieren, Trotman, Jamie, Liu, Hongxiang, Abbs, Stephen, Tischkowitz, Marc

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Malignant Peripheral Nerve Sheath Tumor in Cowden Syndrome von Taylor, Amy, Delon, Isabelle, Allinson, Kieren, Trotman, Jamie, Liu, Hongxiang, Abbs, Stephen, Tischkowitz, Marc

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Embryonal tumor with multilayered rosettes: Overview of diagnosis and therapy von Chadda, Karan R, Solano-Páez, Palma, Khan, Sara, Llempén-López, Mercedes, Phyu, Poe, Horan, Gail, Trotman, Jamie, Tarpey, Patrick, Erker, Craig, Lindsay, Holly, Addy, Dilys, Jacques, Thomas S, Allinson, Kieren, Pizer, Barry, Huang, Annie, Murray, Matthew J

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Identification of novel pathogenic variants and features in patients with pseudohypoparathyroidism and acrodysostosis, subtypes of the newly classified inactivating PTH/PTHrP signa... von Truelove, Adam, Mulay, Akhilesh, Prapa, Matina, Casey, Ruth T., Adler, Amanda I., Offiah, Amaka C., Poole, Kenneth E. S., Trotman, Jamie, Al Hasso, Namir, Park, Soo‐Mi

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A diagnosis of Noonan syndrome through routine whole genome sequencing in a child with an intracranial nongerminomatous germ cell tumor von Mahmood, Shathar, Leiter, Sarah M, Phyu, Poe, Craven, Claudia, Horan, Gail, Gains, Jennifer, Briggs, Mayen, Blanco, Esther, Behjati, Sam, Watkins, James, Tadross, John A, Roberts, Thomas, Trotman, Jamie, Tarpey, Patrick, Armstrong, Ruth, Murray, Matthew J

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Wilms Tumor With Raised Serum Alpha-Fetoprotein: Highlighting the Need for Novel Circulating Biomarkers von Green, Rebecca, Ahmed, Adeeb, Fleming, Ben, Long, Anna-May, Behjati, Sam, Trotman, Jamie, Tarpey, Patrick, Nicholson, James C, Coleman, Nicholas, Elizabeth Hook, C, Murray, Matthew J

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Introduction and impact of routine whole genome sequencing in the diagnosis and management of sarcoma von Watkins, James A, Trotman, Jamie, Tadross, John A, Harrington, Jennifer, Hatcher, Helen, Horan, Gail, Prewett, Sarah, Wong, Han H, McDonald, Sarah, Tarpey, Patrick, Roberts, Thomas, Su, Jing, Tischkowitz, Marc, Armstrong, Ruth, Amary, Fernanda, Sosinsky, Alona

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