| 37260508 | RFcaller: a machine learning approach combined with read-level features to detect somatic mutations. | NAR Genom Bioinform | 2023 |
| 37803049 | MALAT1 expression is associated with aggressive behavior in indolent B-cell neoplasms. | Sci Rep | 2023 |
| 35288589 | PanCancer analysis of somatic mutations in repetitive regions reveals recurrent mutations in snRNA U2. | NPJ Genom Med | 2022 |
| 35672297 | ATM germline variants in a young adult with chronic lymphocytic leukemia: 8â¿¿years of genomic evolution. | Blood Cancer J | 2022 |
| 36470887 | Correction: ATM germline variants in a young adult with chronic lymphocytic leukemia: 8 years of genomic evolution. | Blood Cancer J | 2022 |
| 35962045 | Author Correction: Comparative and demographic analysis of orang-utan genomes. | Nature | 2022 |
| 35927489 | Molecular map of chronic lymphocytic leukemia and its impact on outcome. | Nat Genet | 2022 |
| 35953718 | Detection of early seeding of Richter transformation in chronic lymphocytic leukemia. | Nat Med | 2022 |
| 33211804 | IGLV3-21R110 identifies an aggressive biological subtype of chronic lymphocytic leukemia with intermediate epigenetics. | Blood | 2021 |
| 33782531 | mmsig: a fitting approach to accurately identify somatic mutational signatures in hematological malignancies. | Commun Biol | 2021 |
| 31616059 | Specific NOTCH1 antibody targets DLL4-induced proliferation, migration, and angiogenesis in NOTCH1-mutated CLL cells. | Oncogene | 2020 |
| 34079956 | The proliferative history shapes the DNA methylome of B-cell tumors and predicts clinical outcome. | Nat Cancer | 2020 |
| 31753927 | Cryptic insertions of the immunoglobulin light chain enhancer region near <i>CCND1</i> in t(11;14)-negative mantle cell lymphoma. | Haematologica | 2020 |
| 32020046 | Minimal spatial heterogeneity in chronic lymphocytic leukemia at diagnosis. | Leukemia | 2020 |
| 31977296 | Genomic and Epigenomic Alterations in Chronic Lymphocytic Leukemia. | Annu Rev Pathol | 2020 |
| 32636395 | IgCaller for reconstructing immunoglobulin gene rearrangements and oncogenic translocations from whole-genome sequencing in lymphoid neoplasms. | Nat Commun | 2020 |
| 32584970 | Genomic and epigenomic insights into the origin, pathogenesis, and clinical behavior of mantle cell lymphoma subtypes. | Blood | 2020 |
| 30808002 | Withdrawal: Human autophagins, a family of cysteine proteinases potentially implicated in cell degradation by autophagy. | J Biol Chem | 2019 |
| 31213465 | Chromosome 12p Amplification in Triple-Negative/<i>BRCA1-</i>Mutated Breast Cancer Associates with Emergence of Docetaxel Resistance and Carboplatin Sensitivity. | Cancer Res | 2019 |
| 31346173 | Author Correction: A practical guide for mutational signature analysis in hematological malignancies. | Nat Commun | 2019 |
| 31399598 | Insight into genetic predisposition to chronic lymphocytic leukemia from integrative epigenomics. | Nat Commun | 2019 |
| 31597163 | The U1 spliceosomal RNA is recurrently mutated in multiple cancers. | Nature | 2019 |
| 31278357 | A practical guide for mutational signature analysis in hematological malignancies. | Nat Commun | 2019 |
| 28924241 | Clinical impact of the subclonal architecture and mutational complexity in chronic lymphocytic leukemia. | Leukemia | 2018 |
| 29900613 | Germline variation in the oxidative DNA repair genes NUDT1 and OGG1 is not associated with hereditary colorectal cancer or polyposis. | Hum Mutat | 2018 |
| 29448935 | Germline mutations in the spindle assembly checkpoint genes BUB1 and BUB3 are infrequent in familial colorectal cancer and polyposis. | Mol Cancer | 2018 |
| 29666142 | Tumor xenograft modeling identifies an association between TCF4 loss and breast cancer chemoresistance. | Dis Model Mech | 2018 |
| 29666114 | Chronic lymphocytic leukemia and mantle cell lymphoma: crossroads of genetic and microenvironment interactions. | Blood | 2018 |
| 29511213 | Decapping protein EDC4 regulates DNA repair and phenocopies BRCA1. | Nat Commun | 2018 |
| 29785028 | The reference epigenome and regulatory chromatin landscape of chronic lymphocytic leukemia. | Nat Med | 2018 |
| 29318538 | Dissecting Degradomes: Analysis of Protease-Coding Genes. | Methods Mol Biol | 2018 |
| 29115891 | The mutational landscape of small lymphocytic lymphoma compared to non-early stage chronic lymphocytic leukemia. | Leuk Lymphoma | 2018 |
| 28912018 | Association Between Germline Mutations in BRF1, a Subunit of the RNA Polymerase III Transcription Complex, and Hereditary Colorectal Cancer. | Gastroenterology | 2018 |
| 26991857 | Impact of the functional CD5 polymorphism A471V on the response of chronic lymphocytic leukaemia to conventional chemotherapy regimens. | Br J Haematol | 2017 |
| 28935846 | A t(1;9) translocation involving <i>CSF3R</i> as a novel mechanism in unclassifiable chronic myeloproliferative neoplasm. | Haematologica | 2017 |
| 28797648 | Overview of transcriptomic analysis of all human proteases, non-proteolytic homologs and inhibitors: Organ, tissue and ovarian cancer cell line expression profiling of the human protease degradome by the CLIP-CHIPâ¿¢ DNA microarray. | Biochim Biophys Acta Mol Cell Res | 2017 |
| 27991928 | Stem cell-like transcriptional reprogramming mediates metastatic resistance to mTOR inhibition. | Oncogene | 2017 |
| 26133394 | POLE and POLD1 mutations in 529 kindred with familial colorectal cancer and/or polyposis: review of reported cases and recommendations for genetic testing and surveillance. | Genet Med | 2016 |
| 26611460 | Chronic lymphocytic leukemia: looking into the dark side of the genome. | Cell Death Differ | 2016 |
| 27601210 | Congenital dilated cardiomyopathy caused by biallelic mutations in Filamin C. | Eur J Hum Genet | 2016 |
| 27524613 | Genetic Predisposition to Chronic Lymphocytic Leukemia Is Mediated by a BMF Super-Enhancer Polymorphism. | Cell Rep | 2016 |
| 27512155 | Transplacental transfer of essential thrombocythemia in monozygotic twins. | Blood | 2016 |
| 27096942 | Erratum: Scarce evidence of the causal role of germline mutations in UNC5C in hereditary colorectal cancer and polyposis. | Sci Rep | 2016 |
| 26852919 | Scarce evidence of the causal role of germline mutations in UNC5C in hereditary colorectal cancer and polyposis. | Sci Rep | 2016 |
| 26837699 | Clinical impact of clonal and subclonal TP53, SF3B1, BIRC3, NOTCH1, and ATM mutations in chronic lymphocytic leukemia. | Blood | 2016 |
| 24691292 | Exome sequencing identifies MUTYH mutations in a family with colorectal cancer and an atypical phenotype. | Gut | 2015 |
| 26647970 | A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing. | Nat Commun | 2015 |
| 26052075 | Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA Repair. | Gastroenterology | 2015 |
| 26200345 | Non-coding recurrent mutations in chronic lymphocytic leukaemia. | Nature | 2015 |
| 25903372 | Common and rare variants of microRNA genes in autism spectrum disorders. | World J Biol Psychiatry | 2015 |