Kết quả tìm kiếm - Zoya Kingsbury
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1
Spinal muscular atrophy diagnosis and carrier screening from genome sequencing data Bằng Xiao Chen, Alba Sanchis‐Juan, Courtney E. French, Andrew J. Connell, Isabelle Delon, Zoya Kingsbury, Aditi Chawla, Aaron L. Halpern, Ryan J. Taft, David Bentley, Matthew E.R. Butchbach, F. Lucy Raymond, Michael A. Eberle
Được phát hành 2020Artigo -
2
Microbial Metabolism Shifts Towards an Adverse Profile with Supplementary Iron in the TIM-2 In vitro Model of the Human Colon Bằng Guus A. M. Kortman, Bas E. Dutilh, Annet Maathuis, Udo F. H. Engelke, Jos Boekhorst, Kevin Keegan, Fiona Nielsen, Jason Betley, Jacqueline C. Weir, Zoya Kingsbury, Leo A. J. Kluijtmans, Dorine W. Swinkels, Koen Venema, Harold Tjalsma
Được phát hành 2016Artigo -
3
Monitoring chronic lymphocytic leukemia progression by whole genome sequencing reveals heterogeneous clonal evolution patterns Bằng Anna Schuh, Jennifer Becq, Sean Humphray, Adrian Alexa, Adam Burns, Ruth Clifford, Stephan M. Feller, Russell Grocock, Shirley Henderson, Irina Khrebtukova, Zoya Kingsbury, Shujun Luo, David J. McBride, Lisa Murray, Toshi Menju, Adele Timbs, Mark T. Ross, Jenny C. Taylor, David Bentley
Được phát hành 2012Artigo -
4
Whole genome sequencing provides comprehensive genetic testing in childhood B-cell acute lymphoblastic leukaemia Bằng Sarra L. Ryan, John F. Peden, Zoya Kingsbury, Claire Schwab, Terena James, Petri Pölönen, Martina Mijušković, Jenn Becq, Richard Yim, Ruth E. Cranston, Dale J. Hedges, Kathryn G. Roberts, Charles G. Mullighan, Ajay Vora, Lisa J. Russell, Robert Bain, Anthony V. Moorman, David Bentley, Christine J. Harrison, Mark T. Ross
Được phát hành 2023Artigo -
5
Detection of ctDNA in plasma of patients with clinically localised prostate cancer is associated with rapid disease progression Bằng Edmund Lau, Patrick J. McCoy, Fairleigh Reeves, Ken Chow, Michael J. Clarkson, Edmond M. Kwan, Kate Packwood, Helen Northen, Miao He, Zoya Kingsbury, Stefano Mangiola, Michael Kerger, Marc A. Furrer, Helen Crowe, Anthony J. Costello, David J. McBride, Mark T. Ross, Bernard J. Pope, Christopher M. Hovens, Niall M. Corcoran
Được phát hành 2020Artigo -
6
Integrative genomic analysis of childhood acute lymphoblastic leukaemia lacking a genetic biomarker in the UKALL2003 clinical trial Bằng Claire Schwab, Ruth E. Cranston, Sarra L. Ryan, Ellie Butler, Emily Winterman, Zoe Hawking, Matthew Bashton, Amir Enshaei, Lisa J. Russell, Zoya Kingsbury, John F. Peden, Emilio Barretta, J. C. Murray, Jude Gibson, Andrew C. Hinchliffe, Robert Bain, Ajay Vora, David Bentley, Mark T. Ross, Anthony V. Moorman, Christine J. Harrison
Được phát hành 2022Artigo -
7
Multifocal clonal evolution characterized using circulating tumour DNA in a case of metastatic breast cancer Bằng Muhammed Murtaza, Sarah‐Jane Dawson, Katherine Pogrebniak, Oscar M. Rueda, Elena Provenzano, John W. Grant, Suet‐Feung Chin, Dana W.Y. Tsui, Francesco Marass, Davina Gale, H. Raza Ali, Pankti Shah, Tania Contente‐Cuomo, Hossein Farahani, Karey Shumansky, Zoya Kingsbury, Sean Humphray, David Bentley, Sohrab P. Shah, Matthew Wallis, Nitzan Rosenfeld, Carlos Caldas
Được phát hành 2015Artigo -
8
Rapid Whole-Genome Sequencing for Genetic Disease Diagnosis in Neonatal Intensive Care Units Bằng Carol Saunders, Neil Miller, Sarah Soden, Darrell L. Dinwiddie, Aaron Noll, Noor Abu Alnadi, Nevene Andraws, Melanie Patterson, Lisa Ann Krivohlavek, Joel Fellis, Sean Humphray, Peter Saffrey, Zoya Kingsbury, Jacqueline C. Weir, Jason Betley, Russell Grocock, Elliott H. Margulies, Emily Farrow, Michael Artman, Nicole P. Safina, Joshua E. Petrikin, Kevin P. Hall, Stephen F. Kingsmore
Được phát hành 2012Artigo -
9
Glioblastoma adaptation traced through decline of an IDH1 clonal driver and macro-evolution of a double-minute chromosome Bằng Francesco Favero, Nicholas McGranahan, Maximilian P Salm, Nicolai J. Birkbak, Zack Sanborn, Stephen C. Benz, Jennifer Becq, John F. Peden, Zoya Kingsbury, R.J. Grocok, Sean Humphray, D. R. Bentley, Bradley Spencer‐Dene, Alice Gutteridge, M. Brada, Sébastien Roger, Pierre‐Yves Dietrich, Tim Forshew, Marco Gerlinger, Andrew Rowan, Gordon Stamp, Aron C. Eklund, Zoltán Szállási, Charles Swanton
Được phát hành 2015Artigo -
10
X-linked hypomyelination with spondylometaphyseal dysplasia (H-SMD) associated with mutations in AIFM1 Bằng Noriko Miyake, Nicole I. Wolf, Ferdy Kurniawan Cayami, Joanna Crawford, Annette Bley, Dorothy Bulas, Alex Conant, Stephen J. Bent, Karen W. Gripp, Andreas Hahn, Sean Humphray, Shihoko Kimura‐Ohba, Zoya Kingsbury, Bryan R. Lajoie, Dennis Lal, Dimitra Micha, Amy Pizzino, Richard J. Sinke, Deborah A. Sival, Irene Stolte‐Dijkstra, Andrea Superti‐Furga, Nicole Ulrick, Ryan J. Taft, Tsutomu Ogata, Keiichi Ozono, Naomichi Matsumoto, Bernd A. Neubauer, Cas Simons, Adeline Vanderver
Được phát hành 2017Artigo -
11
Clinical whole-genome sequencing from routine formalin-fixed, paraffin-embedded specimens: pilot study for the 100,000 Genomes Project Bằng Pauline Robbe, Niko Popitsch, Samantha J.L. Knight, Pavlos Antoniou, Jennifer Becq, Miao He, Alexander Kanapin, Anastasia Samsonova, Dimitrios V. Vavoulis, Mark T. Ross, Zoya Kingsbury, Maité Cabes, Sara D.C. Ramos, Suzanne Page, Hélène Dreau, Kate Ridout, J. Louise Jones, Alice Tuff-Lacey, Shirley Henderson, Joanne Mason, Francesca M. Buffa, Clare Verrill, David Maldonado‐Pérez, Ioannis Roxanis, Elena Collantes, Lisa Browning, Sunanda Dhar, Stephen Damato, S. J. Davies, Mark J. Caulfield, David Bentley, Jenny C. Taylor, Clare Turnbull, Anna Schuh
Được phát hành 2018Artigo -
12
The genomic landscape of acute lymphoblastic leukemia with intrachromosomal amplification of chromosome 21 Bằng Qingsong Gao, Sarra L. Ryan, Ilaria Iacobucci, Pankaj S. Ghate, Ruth E. Cranston, Claire Schwab, Abdelrahman H. Elsayed, Lei Shi, Stanley Pounds, Shaohua Lei, Pradyuamna Baviskar, Deqing Pei, Cheng Cheng, Matthew Bashton, Paul Sinclair, David Bentley, Mark T. Ross, Zoya Kingsbury, Terena James, Kathryn G. Roberts, Meenakshi Devidas, Yiping Fan, Wenan Chen, Ti‐Cheng Chang, Gang Wu, Andrew J. Carroll, Nyla A. Heerema, Virginia Valentine, Marcus Valentine, Wenjian Yang, Jun J. Yang, Anthony V. Moorman, Christine J. Harrison, Charles G. Mullighan
Được phát hành 2023Artigo -
13
APOBEC3B Upregulation and Genomic Mutation Patterns in Serous Ovarian Carcinoma Bằng Brandon Leonard, Steven N. Hart, Michael B. Burns, Michael A. Carpenter, Nuri A. Temiz, Anurag S. Rathore, Rachel I. Vogel, Jason B. Nikas, Emily K. Law, William L. Brown, Ying Li, Yuji Zhang, Matthew J. Maurer, Ann L. Oberg, Julie M. Cunningham, Viji Shridhar, Debra A. Bell, Craig April, David Bentley, Marina Bibikova, R. Keira Cheetham, Jian‐Bing Fan, Russell Grocock, Sean Humphray, Zoya Kingsbury, John F. Peden, Jeremy Chien, Elizabeth M. Swisher, Lynn C. Hartmann, Kimberly R. Kalli, Ellen L. Goode, Hugues Sicotte, Scott H. Kaufmann, Reuben S. Harris
Được phát hành 2013Artigo -
14
A comprehensive catalogue of somatic mutations from a human cancer genome Bằng Erin Pleasance, R. Keira Cheetham, Philip J. Stephens, David J. McBride, Sean Humphray, Chris Greenman, Ignacio Varela, Meng‐Lay Lin, Gonzalo R. Ordóñez, Graham R. Bignell, Kai Ye, Julie A. Alipaz, Markus Bauer, David Beare, Adam P. Butler, Richard J. Carter, Lina Chen, Anthony J. Cox, Sarah Edkins, Paula I. Kokko-Gonzales, Niall Gormley, Russell Grocock, Christian Haudenschild, Matthew M. Hims, Terena James, Mingming Jia, Zoya Kingsbury, Catherine Leroy, John Marshall, Andrew Menzies, Laura Mudie, Zemin Ning, Tom Royce, Ole Schulz-Trieglaff, Anastassia Spiridou, Lucy Stebbings, Lukasz Szajkowski, Jon W. Teague, David Williamson, Lynda Chin, Mark T. Ross, Peter J. Campbell, David Bentley, P. Andrew Futreal, Michael R. Stratton
Được phát hành 2009Artigo -
15
Detection of long repeat expansions from PCR-free whole-genome sequence data Bằng Egor Dolzhenko, Joke J.F.A. van Vugt, Richard J. Shaw, Mitchell A. Bekritsky, Marka van Blitterswijk, Giuseppe Narzisi, Subramanian S. Ajay, Vani Rajan, Bryan R. Lajoie, Nathan Johnson, Zoya Kingsbury, Sean Humphray, Raymond D. Schellevis, William J. Brands, Matt Baker, Rosa Rademakers, Maarten Kooyman, Gijs H.P. Tazelaar, Michael A. van Es, Russell L. McLaughlin, William Sproviero, Aleksey Shatunov, Ashley Jones, Ahmad Al Khleifat, Alan Pittman, Sarah Morgan, Orla Hardiman, Ammar Al‐Chalabi, Christopher E. Shaw, Bradley Smith, Edmund Jin Rui Neo, Karen Morrison, Pamela J. Shaw, Catherine Reeves, Lara Winterkorn, Nancy S. Wexler, David E. Housman, Christopher Ng, Alina L. Li, Ryan J. Taft, Leonard H. van den Berg, David Bentley, Jan H. Veldink, Michael A. Eberle
Được phát hành 2017Artigo -
16
Epigenetic regulator genes direct lineage switching in <i>MLL/AF4</i> leukemia Bằng Ricky Tirtakusuma, Katarzyna Szołtysek, Paul Milne, Vasily V. Grinev, Anetta Ptasinska, Paulynn Suyin Chin, Claus Meyer, Sirintra Nakjang, Jayne Y. Hehir‐Kwa, Daniel Williamson, Pierre Cauchy, Peter Keane, Salam A. Assi, Minoo Ashtiani, Sophie G. Kellaway, Maria Rosaria Imperato, Fotini Vogiatzi, Elizabeth K. Schweighart, Shan Lin, Mark Wunderlich, Janine Stutterheim, Alexander Komkov, Elena Zerkalenkova, Paul Evans, Hesta McNeill, Alex Elder, Natalia Martinez-Soria, Sarah Fordham, Yuzhe Shi, Lisa J. Russell, Deepali Pal, Alexandra Smith, Zoya Kingsbury, Jennifer Becq, Cornelia Eckert, Oskar A. Haas, Peter Carey, Simon Bailey, Roderick Skinner, Natalia Miakova, Matthew Collin, Venetia Bigley, Muzlifah Haniffa, Rolf Marschalek, Christine J. Harrison, Catherine Cargo, Denis M. Schewe, Yulia Olshanskaya, Michael J. Thirman, Peter N. Cockerill, James C. Mulloy, Helen J. Blair, Josef Vormoor, James M. Allan, Constanze Bonifer, Olaf Heidenreich, Simon Bomken
Được phát hành 2022Artigo -
17
Whole-genome sequencing of bladder cancers reveals somatic CDKN1A mutations and clinicopathological associations with mutation burden Bằng Jean‐Baptiste Cazier, Srinivasa R. Rao, Chelsea McLean, Alexandra K. Walker, Ben Wright, E Jaeger, Christiana Kartsonaki, Luke Marsden, Christopher Yau, Carme Camps, Pamela J. Kaisaki, Christopher Allan, Moustafa Attar, John Bell, David L. Bentley, John Broxholme, David Buck, Jean‐Baptiste Cazier, Richard R. Copley, Richard J. Cornall, Peter Donnelly, Simon Fiddy, Angie Green, Lorna Gregory, Russell Grocock, Edouard Hatton, Chris Holmes, Linda Hughes, Peter Humburg, Sean Humphray, Alexander Kanapin, Zoya Kingsbury, Julian C. Knight, Sarah Lamble, Stefano Lise, Lorne Lonie, Gerton Lunter, Hilary C. Martin, Lisa Murray, Davis J. McCarthy, Gil McVean, Alistair T. Pagnamenta, Paolo Piazza, Guadelupe Polanco, Peter J. Ratcliffe, Andy Rimmer, Natasha Sahgal, Jenny C. Taylor, Ian Tomlinson, Amy Trebes, Andrew O.M. Wilkie, Ben Wright, Christopher Yau, Jenny C. Taylor, James W.F. Catto, Ian Tomlinson, Anne E. Kiltie, Freddie C. Hamdy
Được phát hành 2014Artigo -
18
Genome Sequencing and Analysis of the Tasmanian Devil and Its Transmissible Cancer Bằng Elizabeth P. Murchison, Ole Schulz-Trieglaff, Zemin Ning, Ludmil B. Alexandrov, Markus Bauer, Beiyuan Fu, Matthew M. Hims, Zhihao Ding, Sergii Ivakhno, Caitlin M. Stewart, Bee Ling Ng, Wendy S.W. Wong, Bronwen Aken, Simon White, Amber E. Alsop, Jennifer Becq, Graham R. Bignell, R. Keira Cheetham, William Cheng, Thomas R. Connor, Anthony J. Cox, Zhiping Feng, Yong Gu, Russell Grocock, Simon R. Harris, Irina Khrebtukova, Zoya Kingsbury, Mark Kowarsky, Alexandre Kreiss, Shujun Luo, John Marshall, David J. McBride, Lisa Murray, Anne‐Maree Pearse, Keiran Raine, Isabelle Rasolonjatovo, Richard J. Shaw, Philip Tedder, Carolyn Tregidgo, Albert J. Vilella, David C. Wedge, GM Woods, Niall Gormley, Sean Humphray, Gary P. Schroth, Geoffrey Smith, Kevin P. Hall, Stephen M. J. Searle, Nigel P. Carter, Anthony T. Papenfuss, P. Andrew Futreal, Peter J. Campbell, Fengtang Yang, David Bentley, Dirk J. Evers, Michael R. Stratton
Được phát hành 2012Artigo -
19
Erythrocytosis associated with a novel missense mutation in the BPGM gene Bằng Nayia Petousi, Richard R. Copley, Terence R.J. Lappin, S.E. Haggan, Celeste Bento, Holger Cario, Melanie J. Percy, Peter J. Ratcliffe, Peter A. Robbins, M. F. McMullin, Peter Donnelly, John I. Bell, D. R. Bentley, Gil McVean, Peter J. Ratcliffe, Jenny C. Taylor, Andrew O.M. Wilkie, P. Donelly, John Broxholme, David Buck, Jean‐Baptiste Cazier, Richard J. Cornall, Lynn Gregory, Julian C. Knight, Gerton Lunter, Gil McVean, Ian Tomlinson, Andrew O.M. Wilkie, David Buck, Christopher Allan, Moustafa Attar, Andrew Green, Lynn Gregory, Sean Humphray, Zoya Kingsbury, Sarah Lamble, Lorne Lonie, Alistair T. Pagnamenta, Paolo Piazza, Guadelupe Polanco, Amy Trebes, Gil McVean, Peter Donnelly, Jean‐Baptiste Cazier, John Broxholme, Richard R. Copley, Simon Fiddy, Russell Grocock, Edouard Hatton, Chris Holmes, L. Hughes, Peter Humburg, Alexander Kanapin, Stefano Lise, Gerton Lunter, Hilary C. Martin, Lisa Murray, Davis J. McCarthy, Andy Rimmer, Natasha Sahgal, Bruce Wright, Christopher Yau
Được phát hành 2014Carta -
20
Whole-genome sequencing provides new insights into the clonal architecture of Barrett's esophagus and esophageal adenocarcinoma Bằng Caryn S. Ross-Innes, Jennifer Becq, Andrew Warren, R. Keira Cheetham, Helen Northen, Maria O’Donovan, Shalini Malhotra, Massimiliano di Pietro, Sergii Ivakhno, Miao He, Jamie Weaver, Andy G. Lynch, Zoya Kingsbury, Mark T. Ross, Sean Humphray, David Bentley, Rebecca C. Fitzgerald, Stephen J. Hayes, Yeng Ang, Ian Welch, Shaun R. Preston, Sarah Oakes, Vicki Save, Richard J. E. Skipworth, Olga Tucker, Jim Davies, Charles Crichton, Christian Schusterreiter, Tim Underwood, Fergus Noble, Bernard Stacey, Jamie Kelly, James D. Byrne, Annette Haydon, Donna Sharland, Jack Owsley, Hugh Barr, Jesper Lagergren, James Gossage, Andrew Davies, Robert C. Mason, Fuju Chang, Janine Zylstra, Grant Sanders, Tim Wheatley, Richard Berrisford, Tim Bracey, Catherine Harden, David Bunting, Tom Roques, Jenny Nobes, Suat Loo, Mike Lewis, Ed Cheong, Oliver Priest, Simon L. Parsons, Irshad Soomro, Philip Kaye, J. Saunders, Junxiong Pang, Neil T. Welch, James Catton, John P. Duffy, Krish Ragunath, Laurence Lovat, Rehan Haidry, Haroon Miah, Sarah Kerr, Victor Eneh, Rommel Butawan, Tom Roques, Michael Lewis, Edward Cheong, Bhaskar Kumar, Laszlo Igali, Sharon Walton, Adela Dann, Peter Safranek, Andrew Hindmarsh, Vijayendran Sudjendran, Michael Scott, Alison D. Cluroe, Ahmad Miremadi, Betania Mahler‐Araujo, Barbara Nutzinger, Christopher J. Peters, Zarah Abdullahi, Jason Crawte, Shona MacRae, Ayesha Noorani, Rachael Fels Elliott, Lawrence Bower, Paul A. Edwards, Simon Tavaré, Matthew Eldridge, Jan Bornschein, Maria Secrier, Yeng Ang, J. Robert O’Neill, Kasia Adamczuk
Được phát hành 2015Artigo
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Các môn học liên quan
Biology
Genetics
Gene
Genome
Medicine
Cancer
Mutation
Computational biology
Internal medicine
Cancer research
DNA sequencing
Disease
Whole genome sequencing
Bioinformatics
Genotype
Oncology
Pathology
Single-nucleotide polymorphism
1000 Genomes Project
Computer science
DNA
Evolutionary biology
Exome sequencing
Human genome
Indel
Phenotype
Somatic cell
Somatic evolution in cancer
Allele
Biochemistry