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Tiling resolution array CGH and high density expression profiling of urothelial carcinomas delineate genomic amplicons and candidate target genes specific for advanced tumorsDistinct evolutionary mechanisms for genomic imbalances in high-risk and low-risk neuroblastomasCharacterization of the CHOP breakpoints and fusion transcripts in myxoid liposarcomas with the 12;16 translocationFusion of the EWS and CHOP genes in myxoid liposarcomaExpression patterns of the human sarcoma-associated genes FUS and EWS and the genomic structure of FUSMiRNA expression in urothelial carcinomas: important roles of miR-10a, miR-222, miR-125b, miR-7 and miR-452 for tumor stage and metastasis, and frequent homozygous losses of miR-31Approximate geodesic distances reveal biologically relevant structures in microarray data.Dissecting karyotypic patterns in renal cell carcinoma: an analysis of the accumulated cytogenetic data.The isolation of evolutionarily conserved Eag I end-clones from mouse chromosome 17 using cloned DNA.Independent component analysis reveals new and biologically significant structures in micro array data.Analysis of promoter regions of co-expressed genes identified by microarray analysis.High-resolution genomic profiles of breast cancer cell lines assessed by tiling BAC array comparative genomic hybridization.Recurrent and multiple bladder tumors show conserved expression profilesNormalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios.Non-negative matrix factorization for the analysis of complex gene expression data: identification of clinically relevant tumor subtypesAssociation between polymorphisms in RMI1, TOP3A, and BLM and risk of cancer, a case-control study.Genome-wide transcription factor binding site/promoter databases for the analysis of gene sets and co-occurrence of transcription factor binding motifsMolecular classification of urothelial carcinoma: global mRNA classification versus tumour-cell phenotype classification.Prediction of stage, grade, and survival in bladder cancer using genome-wide expression data: a validation study.Robust assignment of cancer subtypes from expression data using a uni-variate gene expression average as classifier.A systematic study of gene mutations in urothelial carcinoma; inactivating mutations in TSC2 and PIK3R1.The breakpoint region of the most common isochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeatsStructural and numerical chromosome changes in colon cancer develop through telomere-mediated anaphase bridges, not through mitotic multipolarity.Telomere dysfunction triggers extensive DNA fragmentation and evolution of complex chromosome abnormalities in human malignant tumors.Molecular signatures in childhood acute leukemia and their correlations to expression patterns in normal hematopoietic subpopulations.Integrated genomic and gene expression profiling identifies two major genomic circuits in urothelial carcinoma.Deletions of CDKN1B and ETV6 in acute myeloid leukemia and myelodysplastic syndromes without cytogenetic evidence of 12p abnormalities.Genetic variant of the human homologous recombination-associated gene RMI1 (S455N) impacts the risk of AML/MDS and malignant melanoma.Coping with complexity. multivariate analysis of tumor karyotypes.Acute myeloid leukemia with inv(16)(p13q22): involvement of cervical lymph nodes and tonsils is common and may be a negative prognostic sign.Clustering of deletions on chromosome 13 in benign and low-malignant lipomatous tumors.Molecular subtypes of urothelial carcinoma are defined by specific gene regulatory systemsAbnormal nuclear shape in solid tumors reflects mitotic instability.Hibernomas are characterized by homozygous deletions in the multiple endocrine neoplasia type I region. Metaphase fluorescence in situ hybridization reveals complex rearrangements not detected by conventional cytogeneticsStatistical behavior of complex cancer karyotypes.Cytogenetic and molecular genetic demonstration of polyclonality in an acinic cell carcinoma.DNA methylation analyses of urothelial carcinoma reveal distinct epigenetic subtypes and an association between gene copy number and methylation statusCytogenetic and FISH analyses of pancreatic carcinoma reveal breaks in 18q11 with consistent loss of 18q12-qter and frequent gain of 18p.Molecular profiling reveals low- and high-grade forms of primary melanoma.New probabilistic network models and algorithms for oncogenesis.
P50
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description
Professor vid BioCARE
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Zweeds onderzoeker
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hulumtues
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researcher
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taighdeoir
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հետազոտող
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name
Mattias Höglund
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Mattias Höglund
@en
Mattias Höglund
@es
Mattias Höglund
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Mattias Höglund
@nl
Mattias Höglund
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Mattias Höglund
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Mattias Höglund
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type
label
Mattias Höglund
@ast
Mattias Höglund
@en
Mattias Höglund
@es
Mattias Höglund
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Mattias Höglund
@nl
Mattias Höglund
@sl
Mattias Höglund
@sq
Mattias Höglund
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prefLabel
Mattias Höglund
@ast
Mattias Höglund
@en
Mattias Höglund
@es
Mattias Höglund
@ga
Mattias Höglund
@nl
Mattias Höglund
@sl
Mattias Höglund
@sq
Mattias Höglund
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P106
P21
P27
P31
P496
0000-0001-9283-4421