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Elevated tolerance to aneuploidy in cancer cells: estimating the fitness effects of chromosome number alterations by in silico modelling of somatic genome evolutionThe fetal thymus has a unique genomic copy number profile resulting from physiological T cell receptor gene rearrangementWhole chromosome gain does not in itself confer cancer-like chromosomal instabilityActivation of human telomerase reverse transcriptase through gene fusion in clear cell sarcoma of the kidney.Aberrant epigenetic regulation in clear cell sarcoma of the kidney featuring distinct DNA hypermethylation and EZH2 overexpression.Intratumoral genome diversity parallels progression and predicts outcome in pediatric cancer.Reply to Heng: Inborn aneuploidy and chromosomal instability.Reply to Duesberg: Stability of peritriploid and triploid states in neoplastic and nonneoplastic cellsConfined trisomy 8 mosaicism of meiotic origin: a rare cause of aneuploidy in childhood cancer.Neuroblastoma with flat genomic profile: a question of representativity?Four evolutionary trajectories underlie genetic intratumoral variation in childhood cancerBCOR internal tandem duplication and YWHAE-NUTM2B/E fusion are mutually exclusive events in clear cell sarcoma of the kidneyConvergent evolution of 11p allelic loss in multifocal Wilms tumors arising in WT1 mutation carriersExtensive Clonal Branching Shapes the Evolutionary History of High-Risk Pediatric Cancers
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P50
description
researcher ORCID ID = 0000-0002-1654-6978
@en
wetenschapper
@nl
name
Anders Valind
@ast
Anders Valind
@en
Anders Valind
@es
Anders Valind
@nl
type
label
Anders Valind
@ast
Anders Valind
@en
Anders Valind
@es
Anders Valind
@nl
prefLabel
Anders Valind
@ast
Anders Valind
@en
Anders Valind
@es
Anders Valind
@nl
P106
P108
P1153
55804752000
P31
P496
0000-0002-1654-6978