| 35595835 | Automated next-generation profiling of genomic alterations in human cancers. | Nat Commun | 2022 |
| 32866655 | Inherited Rare, Deleterious Variants in ATM Increase Lung Adenocarcinoma Risk. | J Thorac Oncol | 2020 |
| 31655296 | Randomized Phase II Study of Paclitaxel plus Alisertib versus Paclitaxel plus Placebo as Second-Line Therapy for SCLC: Primary and Correlative Biomarker Analyses. | J Thorac Oncol | 2020 |
| 31506389 | Noninvasive Detection of Microsatellite Instability and High Tumor Mutation Burden in Cancer Patients Treated with PD-1 Blockade. | Clin Cancer Res | 2019 |
| 30185652 | A machine learning approach for somatic mutation discovery. | Sci Transl Med | 2018 |
| 30027257 | Regarding the Congruence Between 2 Circulating Tumor DNA Sequencing Assays. | JAMA Oncol | 2018 |
| 27340278 | Whole-Exome Sequencing of Salivary Gland Mucoepidermoid Carcinoma. | Clin Cancer Res | 2017 |
| 28814544 | Direct detection of early-stage cancers using circulating tumor DNA. | Sci Transl Med | 2017 |
| 28489996 | Cancer-Associated Mutations in Endometriosis without Cancer. | N Engl J Med | 2017 |
| 29062530 | : Developing individuals with lived-experience of health and social care as facilitators to deliver a course to enhance public involvement in research - a Welsh perspective. | Research Involvement and Engagement | 2017 |
| 29061967 | High grade serous ovarian carcinomas originate in the fallopian tube. | Nat Commun | 2017 |
| 27650546 | CoGAPS matrix factorization algorithm identifies transcriptional changes in AP-2alpha target genes in feedback from therapeutic inhibition of the EGFR network. | Oncotarget | 2016 |
| 27196778 | Genomic and Immunological Tumor Profiling Identifies Targetable Pathways and Extensive CD8+/PDL1+ Immune Infiltration in Inflammatory Breast Cancer Tumors. | Mol Cancer Ther | 2016 |
| 25240578 | Familial and sporadic pancreatic cancer share the same molecular pathogenesis. | Fam Cancer | 2015 |
| 25877891 | Personalized genomic analyses for cancer mutation discovery and interpretation. | Sci Transl Med | 2015 |
| 25406187 | Notch1 mutations are drivers of oral tumorigenesis. | Cancer Prev Res (Phila) | 2015 |
| 25428220 | Activating STAT6 mutations in follicular lymphoma. | Blood | 2015 |
| 26506520 | Prevalence of deleterious ATM germline mutations in gastric cancer patients. | Oncotarget | 2015 |
| 26416732 | The genomic landscape of response to EGFR blockade in colorectal cancer. | Nature | 2015 |
| 26154128 | Clinical implications of genomic alterations in the tumour and circulation of pancreatic cancer patients. | Nat Commun | 2015 |
| 26374070 | Targeted sequencing reveals clonal genetic changes in the progression of early lung neoplasms and paired circulating DNA. | Nat Commun | 2015 |
| 24880341 | Exome sequencing identifies somatic gain-of-function PPM1D mutations in brainstem gliomas. | Nature Genetics | 2014 |
| 25305755 | Somatic mutations of SUZ12 in malignant peripheral nerve sheath tumors. | Nat Genet | 2014 |
| 24435047 | Mutations in linker histone genes HIST1H1 B, C, D, and E; OCT2 (POU2F2); IRF8; and ARID1A underlying the pathogenesis of follicular lymphoma. | Blood | 2014 |
| 24140581 | The genetic landscape of anaplastic astrocytoma. | Oncotarget | 2014 |
| 25233892 | Genomic analyses of gynaecologic carcinosarcomas reveal frequent mutations in chromatin remodelling genes. | Nat Commun | 2014 |
| 24634382 | Integrated next-generation sequencing and avatar mouse models for personalized cancer treatment. | Clin Cancer Res | 2014 |
| 23202128 | Integrated genomic analyses identify ARID1A and ARID1B alterations in the childhood cancer neuroblastoma. | Nat Genet | 2013 |
| 23729402 | Therapeutic potential of the poly(ADP-ribose) polymerase inhibitor rucaparib for the treatment of sporadic human ovarian cancer. | Mol Cancer Ther | 2013 |
| 22102435 | Low-grade serous carcinomas of the ovary contain very few point mutations. | Journal of Pathology | 2012 |
| 22302350 | Somatic mutations in the Notch, NF-KB, PIK3CA, and Hedgehog pathways in human breast cancers. | Genes Chromosomes Cancer | 2012 |
| 22991414 | Clinical significance of the genetic landscape of pancreatic cancer and implications for identification of potential long-term survivors. | Clinical Cancer Research | 2012 |
| 22009941 | Somatic mutations in the chromatin remodeling gene ARID1A occur in several tumor types. | Hum Mutat | 2012 |
| 21278246 | Expression of p16 and retinoblastoma determines response to CDK4/6 inhibition in ovarian cancer. | Clin Cancer Res | 2011 |
| 21435433 | Somatic mutations of PPP2R1A in ovarian and uterine carcinomas. | American Journal of Pathology | 2011 |
| 21163964 | The genetic landscape of the childhood cancer medulloblastoma. | Science | 2011 |
| 21135251 | Personalizing cancer treatment in the age of global genomic analyses: PALB2 gene mutations and the response to DNA damaging agents in pancreatic cancer. | Mol Cancer Ther | 2011 |
| 20826764 | Frequent mutations of chromatin remodeling gene ARID1A in ovarian clear cell carcinoma. | Science | 2010 |
| 20981102 | Distant metastasis occurs late during the genetic evolution of pancreatic cancer. | Nature | 2010 |
| 19701947 | The APC Variant p.Glu1317Gln predisposes to colorectal adenomas by a novel mechanism of relaxing the target for tumorigenic somatic APC mutations. | Human Mutation | 2009 |
| 19264984 | Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene. | Science | 2009 |
| 19584151 | SMAD4 gene mutations are associated with poor prognosis in pancreatic cancer. | Clin Cancer Res | 2009 |
| 19351817 | Genetic mutations associated with cigarette smoking in pancreatic cancer. | Cancer Res | 2009 |
| 19349352 | Frequent activating mutations of PIK3CA in ovarian clear cell carcinoma. | Am J Pathol | 2009 |
| 19228619 | IDH1 and IDH2 mutations in gliomas. | N Engl J Med | 2009 |
| 18852474 | Integrated analysis of homozygous deletions, focal amplifications, and sequence alterations in breast and colorectal cancers. | Proc Natl Acad Sci U S A | 2008 |
| 18515411 | Inherited predisposition to colorectal adenomas caused by multiple rare alleles of MUTYH but not OGG1, NUDT1, NTH1 or NEIL 1, 2 or 3. | Gut | 2008 |
| 18337506 | Comparative lesion sequencing provides insights into tumor evolution. | Proc Natl Acad Sci U S A | 2008 |
| 18380902 | Genome-wide linkage scan for colorectal cancer susceptibility genes supports linkage to chromosome 3q. | BMC Cancer | 2008 |
| 18772397 | Core signaling pathways in human pancreatic cancers revealed by global genomic analyses. | Science | 2008 |