Åke Borg
Researcher Next ID · RN-026682
Researcher · Biochemistry, Genetics and Molecular Biology
Lund, Sweden
- Works count
- 640
- Citation count
- 58,685
- H-index
- 108
- i10-index
- 301
Research interests
Publications
Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants.
Kölner Universitäts PublikationsServer (Universität zu Köln) · 2021 · https://doi.org/10.17863/cam.78454
Spatial deconvolution of HER2-positive breast cancer delineates tumor-associated cell type interactions
Nature Communications · 2021 · 10.1038/s41467-021-26271-2
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
Nature Genetics · 2020 · 10.1038/s41588-020-0609-2
Ovarian and Breast Cancer Risks Associated With Pathogenic Variants in RAD51C and RAD51D
JNCI Journal of the National Cancer Institute · 2020 · https://doi.org/10.1093/jnci/djaa030
Integrating spatial gene expression and breast tumour morphology via deep learning
Nature Biomedical Engineering · 2020 · 10.1038/s41551-020-0578-x
High-definition spatial transcriptomics for in situ tissue profiling
Nature Methods · 2019 · https://doi.org/10.1038/s41592-019-0548-y
Cancer Risks Associated With GermlinePALB2Pathogenic Variants: An International Study of 524 Families
Journal of Clinical Oncology · 2019 · https://doi.org/10.1200/jco.19.01907
Somatic mutations reveal asymmetric cellular dynamics in the early human embryo
Nature · 2017 · https://doi.org/10.1038/nature21703
HRDetect is a predictor of BRCA1 and BRCA2 deficiency based on mutational signatures
Nature Medicine · 2017 · https://doi.org/10.1038/nm.4292
Visualization and analysis of gene expression in tissue sections by spatial transcriptomics
Science · 2016 · https://doi.org/10.1126/science.aaf2403
The topography of mutational processes in breast cancer genomes
Nature Communications · 2016 · https://doi.org/10.1038/ncomms11383
Landscape of somatic mutations in 560 breast cancer whole-genome sequences
Nature · 2016 · https://doi.org/10.1038/nature17676
Serial monitoring of circulating tumor DNA in patients with primary breast cancer for detection of occult metastatic disease
EMBO Molecular Medicine · 2015 · 10.15252/emmm.201404913
Signatures of mutational processes in human cancer
Nature · 2013 · 10.1038/nature12477
The Life History of 21 Breast Cancers
Cell · 2012 · https://doi.org/10.1016/j.cell.2012.04.023
Mutational Processes Molding the Genomes of 21 Breast Cancers
Cell · 2012 · https://doi.org/10.1016/j.cell.2012.04.024
GOBO: Gene Expression-Based Outcome for Breast Cancer Online
PLoS ONE · 2011 · 10.1371/journal.pone.0017911
The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions
British Journal of Cancer · 2008 · 10.1038/sj.bjc.6604305
The CD44+/CD24-phenotype is enriched in basal-like breast tumors
Breast Cancer Research · 2008 · https://doi.org/10.1186/bcr2108
Recurrent gross mutations of the PTEN tumor suppressor gene in breast cancers with deficient DSB repair
Nature Genetics · 2007 · 10.1038/ng.2007.39
Poor prognosis in carcinoma is associated with a gene expression signature of aberrant PTEN tumor suppressor pathway activity
Proceedings of the National Academy of Sciences · 2007 · 10.1073/pnas.0702507104
Recruitment of HIF-1α and HIF-2α to common target genes is differentially regulated in neuroblastoma: HIF-2α promotes an aggressive phenotype
Cancer Cell · 2006 · https://doi.org/10.1016/j.ccr.2006.08.026
PIK3CA Mutations Correlate with Hormone Receptors, Node Metastasis, and ERBB2, and Are Mutually Exclusive with PTEN Loss in Human Breast Carcinoma
Cancer Research · 2005 · https://doi.org/10.1158/0008-5472-can-04-3913
Average Risks of Breast and Ovarian Cancer Associated with BRCA1 or BRCA2 Mutations Detected in Case Series Unselected for Family History: A Combined Analysis of 22 Studies
The American Journal of Human Genetics · 2003 · 10.1086/375033
BioArray Software Environment (BASE): a platform for comprehensive management and analysis of microarray data
Genome biology · 2002 · 10.1186/gb-2002-3-8-software0003
Estrogen receptor status in breast cancer is associated with remarkably distinct gene expression patterns.
PubMed · 2001
Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus
Proceedings of the National Academy of Sciences · 2000 · https://doi.org/10.1073/pnas.97.17.9603
Amplification and Deletion of Topoisomerase IIα Associate with ErbB-2 Amplification and Affect Sensitivity to Topoisomerase II Inhibitor Doxorubicin in Breast Cancer
American Journal Of Pathology · 2000 · 10.1016/s0002-9440(10)64952-8
Genetic Heterogeneity and Penetrance Analysis of the BRCA1 and BRCA2 Genes in Breast Cancer Families
The American Journal of Human Genetics · 1998 · https://doi.org/10.1086/301749
High prevalence of the 999del5 mutation in icelandic breast and ovarian cancer patients.
PubMed · 1996
HER-2/neu amplification predicts poor survival in node-positive breast cancer.
PubMed · 1990
Current projects
No projects listed.