Found: 33
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The importance of escalating molecular diagnostics in patients with low-grade pediatric brain cancer.
- Published in:
- Cold Spring Harbor Molecular Case Studies, 2023, v. 9, n. 4, p. 1, doi. 10.1101/mcs.a006275
- By:
- Publication type:
- Article
Association of BRAF V600E mutations with vasoactive intestinal peptide syndrome in MYCN-amplified neuroblastoma.
- Published in:
- 2021
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- Publication type:
- journal article
Isabl Platform, a digital biobank for processing multimodal patient data.
- Published in:
- BMC Bioinformatics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12859-020-03879-7
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- Publication type:
- Article
Baseline VDJ clonotype detection using a targeted sequencing NGS assay: allowing for subsequent MRD assessment.
- Published in:
- 2020
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- Publication type:
- Letter
Timing the initiation of multiple myeloma.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-15740-9
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- Publication type:
- Article
Correction: Comprehensive detection of recurring genomic abnormalities: a targeted sequencing approach for multiple myeloma.
- Published in:
- 2020
- By:
- Publication type:
- Correction Notice
Epigenetic therapy of myelodysplastic syndromes connects to cellular differentiation independently of endogenous retroelement derepression.
- Published in:
- Genome Medicine, 2019, v. 11, n. 1, p. 1, doi. 10.1186/s13073-019-0707-x
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- Publication type:
- Article
Comprehensive detection of recurring genomic abnormalities: a targeted sequencing approach for multiple myeloma.
- Published in:
- Blood Cancer Journal, 2019, v. 9, n. 12, p. 1, doi. 10.1038/s41408-019-0264-y
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- Publication type:
- Article
Timing the initiation of multiple myeloma.
- Published in:
- Clinical Lymphoma, Myeloma & Leukemia, 2019, v. 19, p. e6, doi. 10.1016/j.clml.2019.09.008
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- Publication type:
- Article
Baseline identification of clonal V(D)J sequences for DNA-based minimal residual disease detection in multiple myeloma.
- Published in:
- PLoS ONE, 2019, v. 14, n. 3, p. 1, doi. 10.1371/journal.pone.0211600
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- Publication type:
- Article
Characterisation of the genomic landscape of CRLF2-rearranged acute lymphoblastic leukemia.
- Published in:
- Genes, Chromosomes & Cancer, 2017, v. 56, n. 5, p. 363, doi. 10.1002/gcc.22439
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- Publication type:
- Article
Impact of socioeconomic status on disease phenotype, genomic landscape and outcomes in myelodysplastic syndromes.
- Published in:
- British Journal of Haematology, 2016, v. 174, n. 2, p. 227, doi. 10.1111/bjh.14042
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- Publication type:
- Article
Aberrant splicing of genes involved in haemoglobin synthesis and impaired terminal erythroid maturation in SF3B1 mutated refractory anaemia with ring sideroblasts.
- Published in:
- British Journal of Haematology, 2015, v. 171, n. 4, p. 478, doi. 10.1111/bjh.13610
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- Publication type:
- Article
Mechanisms of clonal evolution in childhood acute lymphoblastic leukemia.
- Published in:
- Nature Immunology, 2015, v. 16, n. 7, p. 766, doi. 10.1038/ni.3160
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- Publication type:
- Article
The evolutionary history of lethal metastatic prostate cancer.
- Published in:
- Nature, 2015, v. 520, n. 7547, p. 353, doi. 10.1038/nature14347
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- Publication type:
- Article
Combining gene mutation with gene expression data improves outcome prediction in myelodysplastic syndromes.
- Published in:
- Nature Communications, 2015, v. 6, n. 1, p. 5901, doi. 10.1038/ncomms6901
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- Publication type:
- Article
Subclonal variant calling with multiple samples and prior knowledge.
- Published in:
- Bioinformatics, 2014, v. 30, n. 9, p. 1198, doi. 10.1093/bioinformatics/btt750
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- Publication type:
- Article
Association of a germline copy number polymorphism of APOBEC3A and APOBEC3B with burden of putative APOBEC-dependent mutations in breast cancer.
- Published in:
- Nature Genetics, 2014, v. 46, n. 5, p. 487, doi. 10.1038/ng.2955
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- Publication type:
- Article
Constitutional and somatic rearrangement of chromosome 21 in acute lymphoblastic leukaemia.
- Published in:
- Nature, 2014, v. 508, n. 7494, p. 98, doi. 10.1038/nature13115
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- Publication type:
- Article
Processed pseudogenes acquired somatically during cancer development.
- Published in:
- Nature Communications, 2014, v. 5, n. 4, p. 3644, doi. 10.1038/ncomms4644
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- Publication type:
- Article
Recurrent PTPRB and PLCG1 mutations in angiosarcoma.
- Published in:
- Nature Genetics, 2014, v. 46, n. 4, p. 376, doi. 10.1038/ng.2921
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- Publication type:
- Article
RAG-mediated recombination is the predominant driver of oncogenic rearrangement in ETV6-RUNX1 acute lymphoblastic leukemia.
- Published in:
- Nature Genetics, 2014, v. 46, n. 2, p. 116, doi. 10.1038/ng.2874
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- Publication type:
- Article
Inactivating CUX1 mutations promote tumorigenesis.
- Published in:
- Nature Genetics, 2014, v. 46, n. 1, p. 33, doi. 10.1038/ng.2846
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- Publication type:
- Article
Whole exome sequencing of adenoid cystic carcinoma.
- Published in:
- 2013
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- Publication type:
- journal article
Whole exome sequencing of adenoid cystic carcinoma.
- Published in:
- Journal of Clinical Investigation, 2013, v. 123, n. 7, p. 2965, doi. 10.1172/JCI67201
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- Publication type:
- Article
Recurrent SETBP1 mutations in atypical chronic myeloid leukemia.
- Published in:
- Nature Genetics, 2013, v. 45, n. 1, p. 18, doi. 10.1038/ng.2495
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- Publication type:
- Article
The landscape of cancer genes and mutational processes in breast cancer.
- Published in:
- Nature, 2012, v. 486, n. 7403, p. 400, doi. 10.1038/nature11017
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- Publication type:
- Article
Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk.
- Published in:
- Nature Genetics, 2010, v. 42, n. 6, p. 492, doi. 10.1038/ng.585
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- Publication type:
- Article
Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia.
- Published in:
- Nature Genetics, 2009, v. 41, n. 9, p. 1006, doi. 10.1038/ng.430
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- Publication type:
- Article
Analysis of a large multi-generational family provides insight into the genetics of chronic lymphocytic leukemia.
- Published in:
- British Journal of Haematology, 2008, v. 142, n. 2, p. 238, doi. 10.1111/j.1365-2141.2008.07188.x
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- Publication type:
- Article
A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk.
- Published in:
- Nature Genetics, 2007, v. 39, n. 11, p. 1315, doi. 10.1038/ng.2007.18
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- Publication type:
- Article
Evidence for a colorectal cancer susceptibility locus on chromosome 3q21–q24 from a high-density SNP genome-wide linkage scan.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 24, p. 3592, doi. 10.1093/hmg/ddl435
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- Publication type:
- Article
Evidence for a colorectal cancer susceptibility locus on chromosome 3q21–q24 from a high-density SNP genome-wide linkage scan.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 19, p. 2903, doi. 10.1093/hmg/ddl231
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- Publication type:
- Article