Rezultaty - Jane Chalker
- Rezultaty 1 - 8 Rezultaty od 8
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1
Does the gene matter? Genotype–phenotype and genotype–outcome associations in congenital melanocytic naevi od Satyamaanasa Polubothu, Nancy McGuire, Lara Al-Olabi, William Baird, Neil Bulstrode, Jane Chalker, Dragana Josifova, Debra Lomas, Justine O’Hara, Juling Ong, Dyanne Rampling, Paulina Stadnik, Anna Thomas, E. Wedgeworth, Neil J. Sebire, Veronica A. Kinsler
Wydane 2019Artigo -
2
Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS od Veronica A. Kinsler, Anna Thomas, Miho Ishida, Neil Bulstrode, Sam Loughlin, Sandra Hing, Jane Chalker, Kathryn J. McKenzie, Sayeda Abu‐Amero, Olga Slater, Estelle Chanudet, Rodger Palmer, Deborah Morrogh, Philip Stanier, Eugene Healy, Neil J. Sebire, Gudrun E. Moore
Wydane 2013Artigo -
3
Comprehensive molecular characterisation of epilepsy-associated glioneuronal tumours od T. J. Stone, Angus Keeley, Alex Virasami, William Harkness, Martin Tisdall, Elisa Izquierdo, Alice Gutteridge, Tony Brooks, Mark Kristiansen, Jane Chalker, Lisa Wilkhu, William Mifsud, John Apps, Maria Thom, Michael Hubank, Tim Forshew, J. Helen Cross, Darren Hargrave, Jonathan Ham, Thomas S. Jacques
Wydane 2017Artigo -
4
Pediatric pan-central nervous system tumor analysis of immune-cell infiltration identifies correlates of antitumor immunity od Yura Grabovska, Alan Mackay, Patricia O’Hare, Stephen Crosier, Martina Finetti, Ed C. Schwalbe, Jessica C. Pickles, Amy R. Fairchild, Aimee Avery, Julia Cockle, Rebecca M. Hill, Janet C. Lindsey, Debbie Hicks, Mark Kristiansen, Jane Chalker, John Anderson, Darren Hargrave, Thomas S. Jacques, Karin Straathof, Simon Bailey, Chris Jones, Steven C. Clifford, Daniel Williamson
Wydane 2020Artigo -
5
Down syndrome acute lymphoblastic leukemia, a highly heterogeneous disease in which aberrant expression of CRLF2 is associated with mutated JAK2: a report from the International BF... od Libi Hertzberg, Elena Vendramini, Ithamar Ganmore, Giovanni Cazzaniga, Maike Schmitz, Jane Chalker, Ruth Shiloh, Ilaria Iacobucci, Chen Shochat, Sharon Zeligson, Gunnar Cario, Martin Stanulla, Sabine Strehl, Lisa J. Russell, Christine J. Harrison, Beat Bornhäuser, Akinori Yoda, Gideon Rechavi, Dani Bercovich, Arndt Borkhardt, Helena Kempski, Geertruy te Kronnie, Jean‐Pierre Bourquin, Eytan Domany, Shai Izraeli
Wydane 2009Artigo -
6
Benefits for children with suspected cancer from routine whole-genome sequencing od 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, C Dryden, Sara Ghorashian, Blanche Griffin, Gail Horan, Michael Hubank, Phillippa May, Joanna McDerra, Rajvi Nagrecha, James C. Nicholson, David O’Connor, Vesna Pavasovic, Annelies Quaegebeur, Anupama Rao, Thomas C. 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 Elizabeth Hook, Patrick Tarpey, Aditi Vedi, Jack Bartram, Sam Behjati
Wydane 2024Artigo -
7
DNA methylation-based profiling for paediatric CNS tumour diagnosis and treatment: a population-based study od Jessica C. Pickles, Amy R. Fairchild, T. J. Stone, Lorelle Brownlee, Ashirwad Merve, Shireena A. Yasin, Aimee Avery, Saira Waqar Ahmed, Olumide Ogunbiyi, Jamie Gonzalez Zapata, Abigail F Peary, Marie Edwards, Lisa Wilkhu, Carryl Dryden, Dariusz Ładoń, Mark Kristiansen, Catherine Rowe, Kathreena M. Kurian, James A. R. Nicoll, Clare Mitchell, Tabitha Bloom, David A. Hilton, Safa Al‐Sarraj, Lawrence J. Doey, Paul Johns, Leslie Bridges, Aruna Chakrabarty, Azzam Ismail, Nitika Rathi, Khaja Syed, G. Alistair Lammie, Clara Limbӓck-Stanic, Colin Smith, Antonia Torgersen, Frances Rae, Rebecca M. Hill, Steven C. Clifford, Yura Grabovska, Daniel Williamson, Matthew Clarke, Chris Jones, David Capper, Martin Sill, Andreas von Deimling, Stefan M. Pfister, David Jones, Darren Hargrave, Jane Chalker, Thomas S. Jacques
Wydane 2019Artigo -
8
Infant High-Grade Gliomas Comprise Multiple Subgroups Characterized by Novel Targetable Gene Fusions and Favorable Outcomes od Matthew Clarke, Alan Mackay, Britta Ismer, Jessica C. Pickles, Ruth Tatevossian, Scott Newman, Tejus Bale, Iris Stoler, Elisa Izquierdo, Sara Temelso, Diana Carvalho, Valeria Molinari, Anna Burford, Louise Howell, Alex Virasami, Amy R. Fairchild, Aimee Avery, Jane Chalker, Mark Kristiansen, Kelly Haupfear, James 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 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 Proszek, Tobey J. MacDonald, Matthias Preusser, Christine Haberler, Irene Slavc, Roger J. Packer, Ho‐Keung Ng, Shani Caspi, Mara Popović, Barbara Faganel Kotnik, Matthew D. Wood, Lissa Baird, Monika A. Davare, David A. Solomon, Thale Kristin Olsen, Petter Brandal, Michael Farrell, Jane 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, Tim Hassall, Stephen P. Lowis, Maria Tsoli, Mark J. Cowley, David S. Ziegler, Matthias A. Karajannis, Kristian Aquilina, Darren Hargrave, Fernando Carceller, Lynley V. Marshall
Wydane 2020Artigo
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