Scott Newman
TitleCited byYear
Spatial and temporal heterogeneity in high-grade serous ovarian cancer: a phylogenetic analysis
RF Schwarz, CKY Ng, SL Cooke, S Newman, J Temple, AM Piskorz, ...
PLoS medicine 12 (2), e1001789, 2015
1902015
Aberrant chromosome morphology in human cells defective for Holliday junction resolution
T Wechsler, S Newman, SC West
Nature 471 (7340), 642, 2011
1762011
Amplification of the driving oncogene, KRAS or BRAF, underpins acquired resistance to MEK1/2 inhibitors in colorectal cancer cells.
AS Little, K Balmanno, MJ Sale, S Newman, JR Dry, M Hampson, ...
Science signaling 4 (166), ra17, 2011
1742011
Independence of Repressive Histone Marks and Chromatin Compaction during Senescent Heterochromatic Layer Formation
T Chandra, K Kirschner, JY Thuret, BD Pope, T Ryba, S Newman, ...
Molecular Cell, 2012
1732012
Estimation of rearrangement phylogeny for cancer genomes
CD Greenman, ED Pleasance, S Newman, F Yang, B Fu, S Nik-Zainal, ...
Genome research, 2011
1052011
Deregulation of DUX4 and ERG in acute lymphoblastic leukemia
J Zhang, K McCastlain, H Yoshihara, B Xu, Y Chang, ML Churchman, ...
Nature genetics 48 (12), 1481, 2016
812016
Next-generation sequencing of duplication CNVs reveals that most are tandem and some create fusion genes at breakpoints
S Newman, KE Hermetz, B Weckselblatt, MK Rudd
The American Journal of Human Genetics 96 (2), 208-220, 2015
782015
The NRG1 gene is frequently silenced by methylation in breast cancers and is a strong candidate for the 8p tumour suppressor gene
YL Chua, Y Ito, JCM Pole, S Newman, SF Chin, RC Stein, IO Ellis, ...
Oncogene 28 (46), 4041, 2009
712009
The role of tandem duplicator phenotype in tumour evolution in high‐grade serous ovarian cancer
CKY Ng, SL Cooke, K Howe, S Newman, J Xian, J Temple, EM Batty, ...
The Journal of Pathology, 2011
562011
Large duplications at reciprocal translocation breakpoints that might be the counterpart of large deletions and could arise from stalled replication bubbles
KD Howarth, JCM Pole, JC Beavis, EM Batty, S Newman, GR Bignell, ...
Genome research 21 (4), 525-534, 2011
432011
Large inverted duplications in the human genome form via a fold-back mechanism
KE Hermetz, S Newman, KN Conneely, CL Martin, BC Ballif, LG Shaffer, ...
PLoS genetics 10 (1), e1004139, 2014
352014
Clinical validation and implementation of a targeted next-generation sequencing assay to detect somatic variants in non-small cell lung, melanoma, and gastrointestinal malignancies
KE Fisher, L Zhang, J Wang, GH Smith, S Newman, TM Schneider, ...
The Journal of Molecular Diagnostics 18 (2), 299-315, 2016
302016
Heregulin and HER3 are prognostic biomarkers in oropharyngeal squamous cell carcinoma
G Qian, N Jiang, D Wang, S Newman, S Kim, Z Chen, G Garcia, ...
Cancer 121 (20), 3600-3611, 2015
272015
The genetic basis and cell of origin of mixed phenotype acute leukaemia
TB Alexander, Z Gu, I Iacobucci, K Dickerson, JK Choi, B Xu, ...
Nature 562 (7727), 373, 2018
212018
Farewell to GBM-O: genomic and transcriptomic profiling of glioblastoma with oligodendroglioma component reveals distinct molecular subgroups
BH Hinrichs, S Newman, CL Appin, W Dunn, L Cooper, R Pauly, ...
Acta neuropathologica communications 4 (1), 4, 2016
202016
The relative timing of mutations in a breast cancer genome
S Newman, KD Howarth, CD Greenman, GR Bignell, S Tavaré, ...
PloS one 8 (6), e64991, 2013
192013
PAX5-driven subtypes of B-progenitor acute lymphoblastic leukemia
Z Gu, ML Churchman, KG Roberts, I Moore, X Zhou, J Nakitandwe, ...
Nature genetics 51 (2), 296, 2019
142019
St. Jude Children’s Research Hospital–Washington University Pediatric Cancer Genome Project. Deregulation of DUX4 and ERG in acute lymphoblastic leukemia
J Zhang, K McCastlain, H Yoshihara, B Xu, Y Chang, ML Churchman, ...
Nat Genet 48 (12), 1481-1489, 2016
142016
Mutation and transcriptional profiling of formalin-fixed paraffin embedded specimens as companion methods to immunohistochemistry for determining therapeutic targets in …
NF Saba, M Wilson, G Doho, J DaSilva, RB Isett, S Newman, ZG Chen, ...
Head and neck pathology 9 (2), 223-235, 2015
122015
Integrated analysis of whole-genome paired-end and mate-pair sequencing data for identifying genomic structural variations in multiple myeloma
R Yang, L Chen, S Newman, K Gandhi, G Doho, CS Moreno, PM Vertino, ...
Cancer informatics 13, CIN. S13783, 2014
112014
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Articles 1–20