Mattias Höglund

发表

Approximate geodesic distances reveal biologically relevant structures in microarray data

Jens Nilsson, Magnus Fontes, Thoas Fioretos, 2004, Bioinform..

Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios

Johan Staaf, David Lindgren, Mattias Höglund, 2008, BMC Bioinformatics.

Analysis of promoter regions of co-expressed genes identified by microarray analysis

Mattias Höglund, Srinivas Veerla, M. Höglund, 2006, BMC Bioinformatics.

Independent component analysis reveals new and biologically significant structures in micro array data

David Lindgren, Mattias Höglund, Srinivas Veerla, 2006, BMC Bioinformatics.

A Global Structural EM Algorithm for a Model of Cancer Progression

Erik Sjölund, Jens Lagergren, Mattias Höglund, 2011, NIPS.

Monitoring of Technical Variation in Quantitative High-Throughput Datasets

Albert Kriegner, Mattias Höglund, Markus Ringnér, 2013, Cancer informatics.

New Probabilistic Network Models and Algorithms for Oncogenesis

Jens Lagergren, Mattias Höglund, Marcus Hjelm, 2006, J. Comput. Biol..

Power law distribution of chromosome aberrations in cancer.

Mattias Höglund, Attila Frigyesi, David Gisselsson, 2003, Cancer research.

Statistical behavior of complex cancer karyotypes

Mattias Höglund, Attila Frigyesi, David Gisselsson, 2005, Genes, chromosomes & cancer.

Integrated Genomic and Gene Expression Profiling Identifies Two Major Genomic Circuits in Urothelial Carcinoma

Johan Staaf, Mårten Fernö, Mattias Höglund, 2012, PloS one.

Molecular signatures in childhood acute leukemia and their correlations to expression patterns in normal hematopoietic subpopulations.

Patrik Edén, Björn Nilsson, Thoas Fioretos, 2005, Proceedings of the National Academy of Sciences of the United States of America.

Tiling resolution array CGH and high density expression profiling of urothelial carcinomas delineate genomic amplicons and candidate target genes specific for advanced tumors

Mattias Höglund, Srinivas Veerla, Åke Borg, 2008, BMC Medical Genomics.

Frequent amplification of 8q24, 11q, 17q, and 20q‐specific genes in pancreatic cancer

Mattias Höglund, Anne Kallioniemi, M. Höglund, 2002, Genes, chromosomes & cancer.

Dissecting karyotypic patterns in colorectal tumors: two distinct but overlapping pathways in the adenoma-carcinoma transition.

Mattias Höglund, Mef Nilbert, David Gisselsson, 2002, Cancer research.

Non-Negative Matrix Factorization for the Analysis of Complex Gene Expression Data: Identification of Clinically Relevant Tumor Subtypes

Mattias Höglund, Attila Frigyesi, M. Höglund, 2008, Cancer informatics.

High‐resolution genomic profiles of breast cancer cell lines assessed by tiling BAC array comparative genomic hybridization

Johan Staaf, Mattias Höglund, Markus Ringnér, 2007, Genes, chromosomes & cancer.

Association between polymorphisms in RMI1, TOP3A, and BLM and risk of cancer, a case-control study

Jonas Björk, Mattias Höglund, Christian Ingvar, 2009, BMC Cancer.

Identification of cytogenetic subgroups and karyotypic pathways of clonal evolution in follicular lymphomas

Mattias Höglund, Reiner Siebert, Randy D Gascoyne, 2004, Genes, chromosomes & cancer.

Robust assignment of cancer subtypes from expression data using a uni-variate gene expression average as classifier

Mattias Höglund, Martin Lauss, Attila Frigyesi, 2010, BMC Cancer.

Cell-Type-Specific Gene Programs of the Normal Human Nephron Define Kidney Cancer Subtypes.

Pontus Eriksson, Mattias Höglund, Srinivas Veerla, 2017, Cell reports.

Statistical analyses of karyotypic complexity in head and neck squamous cell carcinoma.

Mattias Höglund, David Gisselsson, D. Gisselsson, 2004, Cancer genetics and cytogenetics.

Coping with complexity. multivariate analysis of tumor karyotypes.

Mattias Höglund, David Gisselsson, D. Gisselsson, 2002, Cancer genetics and cytogenetics.

Genome-wide transcription factor binding site/promoter databases for the analysis of gene sets and co-occurrence of transcription factor binding motifs

Mattias Höglund, Markus Ringnér, Srinivas Veerla, 2010, BMC Genomics.

Microarray analyses reveal strong influence of DNA copy number alterations on the transcriptional patterns in pancreatic cancer: implications for the interpretation of genomic amplifications

Mattias Höglund, David Lindgren, J. Veltman, 2005, Oncogene.

Multivariate analysis of chromosomal imbalances in breast cancer delineates cytogenetic pathways and reveals complex relationships among imbalances.

Mattias Höglund, David Gisselsson, D. Gisselsson, 2002, Cancer research.

Frequent miRNA-convergent fusion gene events in breast cancer

Mattias Höglund, Jari Häkkinen, Johan Vallon-Christersson, 2017, Nature Communications.

Dissecting karyotypic patterns in malignant melanomas: Temporal clustering of losses and gains in melanoma karyotypic evolution

Mattias Höglund, David Gisselsson, D. Horsman, 2004, International journal of cancer.

Combined gene expression and genomic profiling define two intrinsic molecular subtypes of urothelial carcinoma and gene signatures for molecular grading and outcome.

Mattias Höglund, Srinivas Veerla, Attila Frigyesi, 2010, Cancer research.

A Molecular Taxonomy for Urothelial Carcinoma

Mårten Fernö, Mattias Höglund, Markus Ringnér, 2012, Clinical Cancer Research.

Promoter analysis of epigenetically controlled genes in bladder cancer

Ioannis Panagopoulos, Mattias Höglund, Srinivas Veerla, 2008, Genes, chromosomes & cancer.

Dissecting karyotypic patterns in renal cell carcinoma: an analysis of the accumulated cytogenetic data.

Mattias Höglund, David Gisselsson, D. Gisselsson, 2004, Cancer genetics and cytogenetics.