Åke Borg

发表

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.

Carsten Peterson, Carl Troein, Johan Vallon-Christersson, 2011 .

Frequent Amplification of Chromosomal Region 20 q 12-q 13 in Ovarian Cancer 1

Åke Borg, P. Meltzer, Å. Borg, 2000 .

Multiregion Whole-Exome Sequencing Uncovers the Genetic Evolution and Mutational Heterogeneity of Early-Stage Metastatic Melanoma.

Frida Rosengren, Helena Cirenajwis, Martin Lauss, 2016, Cancer research.

High-definition spatial transcriptomics for in situ tissue profiling

Richard Bonneau, Aviv Regev, Ludvig Bergenstråhle, 2019, Nature Methods.

Molecular subtypes of breast cancer are associated with characteristic DNA methylation patterns

Johan Staaf, Markus Ringnér, Johan Vallon-Christersson, 2010, Breast Cancer Research.

Genome-wide DNA Methylation Analysis of Lung Carcinoma Reveals One Neuroendocrine and Four Adenocarcinoma Epitypes Associated with Patient Outcome

Johan Staaf, Hans Brunnström, Mats Jönsson, 2014, Clinical Cancer Research.

Screening for copy‐number alterations and loss of heterozygosity in chronic lymphocytic leukemia—A comparative study of four differently designed, high resolution microarray platforms

Hanna Göransson, Anders Isaksson, Johan Staaf, 2008, Genes, chromosomes & cancer.

Microarray analysis of gliomas reveals chromosomal position-associated gene expression patterns and identifies potential immunotherapy targets

Elisabet Englund, Oscar Persson, Morten Krogh, 2007, Journal of Neuro-Oncology.

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.

Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer

Wei Lu, Wei Zheng, Mads Thomassen, 2013, Nature Genetics.

The Life History of 21 Breast Cancers

Kenric Leung, Andrew Menzies, Adam P. Butler, 2015, Cell.

Detection of submicroscopic constitutional chromosome aberrations in clinical diagnostics: a validation of the practical performance of different array platforms

Johan Staaf, Åke Borg, Sok Kean Khoo, 2008, European Journal of Human Genetics.

Expression profiling to predict outcome in breast cancer: the influence of sample selection

Carsten Peterson, Patrik Edén, Mårten Fernö, 2002, Breast Cancer Research.

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.

Corrigendum: Frequent somatic transfer of mitochondrial DNA into the nuclear genome of human cancer cells.

Carlos Caldas, Fengtang Yang, Rosalind Eeles, 2016, Genome research.

Molecular stratification of metastatic melanoma using gene expression profiling : Prediction of survival outcome and benefit from molecular targeted therapy

Johan Staaf, Frida Rosengren, Markus Ringnér, 2015, Oncotarget.

Metachronous and Synchronous Occurrence of 5 Primary Malignancies in a Female Patient between 1997 and 2013: A Case Report with Germline and Somatic Genetic Analysis

Fredrik Persson, Åke Borg, Per Karlsson, 2017, Case Reports in Oncology.

Erratum: The Life History of 21 Breast Cancers (Cell 149 (994-1007))

Kenric Leung, Jon W. Teague, Peter J. Campbell, 2015 .

Multidimensional transcriptomics provides detailed information about immune cell distribution and identity in HER2+ breast tumors

Joakim Lundeberg, Jari Häkkinen, Johan Vallon-Christersson, 2018, bioRxiv.

Characterization of topoisomerase IIα gene amplification and deletion in breast cancer

Jorma Isola, Åke Borg, Å. Borg, 1999 .

Association Between BRCA1 and BRCA2 Mutations and Survival in Women With Invasive Epithelial Ovarian Cancer

Gord Glendon, Lesley McGuffog, Daniel Barrowdale, 2012 .

Clinical Value of RNA Sequencing–Based Classifiers for Prediction of the Five Conventional Breast Cancer Biomarkers: A Report From the Population-Based Multicenter Sweden Cancerome Analysis Network—Breast Initiative

Christian Brueffer, Martin Malmberg, Jari Häkkinen, 2018, JCO precision oncology.

Frequent somatic transfer of mitochondrial DNA into the nuclear genome of human cancer cells

Carlos Caldas, Fengtang Yang, Rosalind Eeles, 2015, Genome research.

Correction to: Landscape of somatic mutations in 560 breast cancer whole-genome sequences (Nature, (2016), 534, 7605, (47-54), 10.1038/nature17676)

Ville Mustonen, Sung-Min Ahn, Stefania Tommasi, 2019 .

Frequent miRNA-convergent fusion gene events in breast cancer

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

Integrating spatial gene expression and breast tumour morphology via deep learning

Ludvig Bergenstråhle, Joakim Lundeberg, Abubakar Abid, 2020, Nature Biomedical Engineering.

Serial monitoring of circulating tumor DNA in patients with primary breast cancer for detection of occult metastatic disease

Mårten Fernö, Helena Jernström, Christian Ingvar, 2015, EMBO molecular medicine.

GOBO: Gene Expression-Based Outcome for Breast Cancer Online

Johan Staaf, Markus Ringnér, Jari Häkkinen, 2011, PloS one.

Predicting the future of breast cancer

Carsten Peterson, Mårten Fernö, Åke Borg, 2003, Nature Medicine.

The non-coding RNA of the multidrug resistance-linked vault particle encodes multiple regulatory small RNAs

Johan Vallon-Christersson, Carlos Rovira, Åke Borg, 2009, Nature Cell Biology.

The Sweden Cancerome Analysis Network - Breast (SCAN-B) Initiative: a large-scale multicenter infrastructure towards implementation of breast cancer genomic analyses in the clinical routine

Christian Brueffer, Martin Malmberg, Jari Häkkinen, 2015, Genome Medicine.

Landscape of somatic allelic imbalances and copy number alterations in HER2-amplified breast cancer

Johan Staaf, Markus Ringnér, Åke Borg, 2011, Breast Cancer Research.