about
Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinomaMutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardationMutational processes molding the genomes of 21 breast cancersMutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardationMutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephalyMutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a Marfanoid habitusSomatic SF3B1 mutation in myelodysplasia with ring sideroblastsGenomic Classification and Prognosis in Acute Myeloid Leukemia.Intratumor Heterogeneity and Branched Evolution Revealed by Multiregion SequencingMutations 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 tremorSignatures of mutational processes in human cancerPatterns of somatic mutation in human cancer genomesThe landscape of cancer genes and mutational processes in breast cancerThe life history of 21 breast cancersWhole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemiaSingle-cell paired-end genome sequencing reveals structural variation per cell cycle.Genome sequencing and analysis of the Tasmanian devil and its transmissible cancer.Landscape of somatic mutations in 560 breast cancer whole-genome sequences.DNA deaminases induce break-associated mutation showers with implication of APOBEC3B and 3A in breast cancer kataegisC. elegans whole-genome sequencing reveals mutational signatures related to carcinogens and DNA repair deficiencyLung cancer: intragenic ERBB2 kinase mutations in tumours.Aging as accelerated accumulation of somatic variants: whole-genome sequencing of centenarian and middle-aged monozygotic twin pairs.Polygenic in vivo validation of cancer mutations using transposons.Sequence analysis of the protein kinase gene family in human testicular germ-cell tumors of adolescents and adults.Mobile DNA in cancer. Extensive transduction of nonrepetitive DNA mediated by L1 retrotransposition in cancer genomes.Analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue.Subclonal diversification of primary breast cancer revealed by multiregion sequencing.Tandem duplication of chromosomal segments is common in ovarian and breast cancer genomesFrequent mutation of the major cartilage collagen gene COL2A1 in chondrosarcoma.Direct Transcriptional Consequences of Somatic Mutation in Breast CancerMutation analysis of 24 known cancer genes in the NCI-60 cell line set.Clinical and biological implications of driver mutations in myelodysplastic syndromes.The genetic heterogeneity and mutational burden of engineered melanomas in zebrafish models.Processed pseudogenes acquired somatically during cancer development.Whole exome sequencing of adenoid cystic carcinoma.RAG-mediated recombination is the predominant driver of oncogenic rearrangement in ETV6-RUNX1 acute lymphoblastic leukemia.Genomic Evolution of Breast Cancer Metastasis and Relapse.A somatic-mutational process recurrently duplicates germline susceptibility loci and tissue-specific super-enhancers in breast cancers.Somatic mutations of the protein kinase gene family in human lung cancer.HRDetect is a predictor of BRCA1 and BRCA2 deficiency based on mutational signatures.
P50
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P50
description
onderzoeker
@nl
name
Keiran Raine
@ast
Keiran Raine
@en
Keiran Raine
@es
Keiran Raine
@nl
Keiran Raine
@sl
type
label
Keiran Raine
@ast
Keiran Raine
@en
Keiran Raine
@es
Keiran Raine
@nl
Keiran Raine
@sl
prefLabel
Keiran Raine
@ast
Keiran Raine
@en
Keiran Raine
@es
Keiran Raine
@nl
Keiran Raine
@sl