|
| 36481818 | Author Correction: Genomic footprints of activated telomere maintenance mechanisms in cancer. | Nat Commun | 2022 |
| 35418684 | Somatic mutation rates scale with lifespan across mammals. | Nature | 2022 |
| 34264955 | Brigatinib causes tumor shrinkage in both NF2-deficient meningioma and schwannoma through inhibition of multiple tyrosine kinases but not ALK. | PLoS One | 2021 |
| 33911282 | Somatic mutation landscapes at single-molecule resolution. | Nature | 2021 |
| 34663923 | Mutational signatures in esophageal squamous cell carcinoma from eight countries with varying incidence. | Nat Genet | 2021 |
| 30849372 | Characterizing Mutational Signatures in Human Cancer Cell Lines Reveals Episodic APOBEC Mutagenesis. | Cell | 2019 |
| 29662167 | Sequencing of prostate cancers identifies new cancer genes, routes of progression and drug targets. | Nat Genet | 2018 |
| 29988082 | Prediction of acute myeloid leukaemia risk in healthy individuals. | Nature | 2018 |
| 28369776 | Clonal haematopoiesis is not prevalent in survivors of childhood cancer. | Br J Haematol | 2018 |
| 28810143 | Genomic Evolution of Breast Cancer Metastasis and Relapse. | Cancer Cell | 2017 |
| 28945760 | Appraising the relevance of DNA copy number loss and gain in prostate cancer using whole genome DNA sequence data. | PLoS Genet | 2017 |
| 27276561 | Genomic Classification and Prognosis in Acute Myeloid Leukemia. | N Engl J Med | 2016 |
| 27615322 | Mutational signatures of ionizing radiation in second malignancies. | Nat Commun | 2016 |
| 27588520 | A DNA target-enrichment approach to detect mutations, copy number changes and immunoglobulin translocations in multiple myeloma. | Blood Cancer J | 2016 |
| 27930809 | ascatNgs: Identifying Somatically Acquired Copy-Number Alterations from Whole-Genome Sequencing Data. | Curr Protoc Bioinformatics | 2016 |
| 27930805 | cgpCaVEManWrapper: Simple Execution of CaVEMan in Order to Detect Somatic Single Nucleotide Variants in NGS Data. | Curr Protoc Bioinformatics | 2016 |
| 27498871 | Direct Transcriptional Consequences of Somatic Mutation in Breast Cancer. | Cell Rep | 2016 |
| 27135926 | Landscape of somatic mutations in 560 breast cancer whole-genome sequences. | Nature | 2016 |
| 25730763 | Analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue. | Nat Genet | 2015 |
| 26647970 | A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing. | Nat Commun | 2015 |
| 26099045 | Subclonal diversification of primary breast cancer revealed by multiregion sequencing. | Nat Med | 2015 |
| 26018901 | Corrigendum: analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue. | Nat Genet | 2015 |
| 24413735 | RAG-mediated recombination is the predominant driver of oncogenic rearrangement in ETV6-RUNX1 acute lymphoblastic leukemia. | Nat Genet | 2014 |
| 25260652 | Polygenic in vivo validation of cancer mutations using transposons. | Genome Biol | 2014 |
| 25301630 | Spatial and temporal diversity in genomic instability processes defines lung cancer evolution. | Science | 2014 |
| 23770606 | Frequent mutation of the major cartilage collagen gene COL2A1 in chondrosarcoma. | Nat Genet | 2013 |
| 24325359 | Somatic CALR mutations in myeloproliferative neoplasms with nonmutated JAK2. | N Engl J Med | 2013 |
| 24182360 | Aging as accelerated accumulation of somatic variants: whole-genome sequencing of centenarian and middle-aged monozygotic twin pairs. | Twin Res Hum Genet | 2013 |
| 24148783 | The genetic heterogeneity and mutational burden of engineered melanomas in zebrafish models. | Genome Biol | 2013 |
| 23778141 | Whole exome sequencing of adenoid cystic carcinoma. | J Clin Invest | 2013 |
| 21994251 | Estimation of rearrangement phylogeny for cancer genomes. | Genome Res | 2012 |
| 22722201 | The landscape of cancer genes and mutational processes in breast cancer. | Nature | 2012 |
| 22608084 | Mutational processes molding the genomes of 21 breast cancers. | Cell | 2012 |
| 22608083 | The life history of 21 breast cancers. | Cell | 2012 |
| 22397650 | Intratumor heterogeneity and branched evolution revealed by multiregion sequencing. | N Engl J Med | 2012 |
| 21248752 | Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma. | Nature | 2011 |
| 21995386 | Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts. | N Engl J Med | 2011 |
| 20016488 | A small-cell lung cancer genome with complex signatures of tobacco exposure. | Nature | 2010 |
| 20054297 | Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genes. | Nature | 2010 |
| 19377476 | A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation. | Nat Genet | 2009 |
| 19330029 | Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer. | Nat Genet | 2009 |
| 18469813 | X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment. | Nat Genet | 2008 |
| 17236139 | Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremor. | Am J Hum Genet | 2007 |
| 17704778 | Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation. | Nat Genet | 2007 |
| 17668385 | Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephaly. | Am J Hum Genet | 2007 |
| 17344846 | Patterns of somatic mutation in human cancer genomes. | Nature | 2007 |
| 17436253 | Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a Marfanoid habitus. | Am J Hum Genet | 2007 |
| 16175573 | Sequence analysis of the protein kinase gene family in human testicular germ-cell tumors of adolescents and adults. | Genes Chromosomes Cancer | 2006 |
| 17088437 | Mutation analysis of 24 known cancer genes in the NCI-60 cell line set. | Mol Cancer Ther | 2006 |
| 17186471 | Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardation. | Am J Hum Genet | 2006 |