Olli-Pekka Kallioniemi
Molecular Biology · 2001–2014
A researcher in the Science corpus: 8 papers; trusts 1 researcher and is trusted by 1 researcher here, as inferred from the citation graph.
Subfields
- Molecular Biology — 50 citations into it; #16,817 of 17,773 by trust here, #3,494 by citations
Whom Olli-Pekka Kallioniemi trusts
Their strongest outbound trust, strongest first, inferred from their citations.
- W. James Kent (in Molecular Biology)
Who trusts Olli-Pekka Kallioniemi
- Daniel C. Koboldt (in Cancer Research)
Papers from Olli-Pekka Kallioniemi's perspective
Ordered by how strongly the researchers Olli-Pekka Kallioniemi trusts endorse each paper. Same corpus, a different order for every researcher.
- BLAT--the BLAST-like alignment tool. (Genome Research)
- Fast gapped-read alignment with Bowtie 2
- Distinct and predictive chromatin signatures of transcriptional promoters and enhancers in the human genome (Nature Genetics)
- Ultrafast and memory-efficient alignment of short DNA sequences to the human genome (Genome Biology)
- Model-based Analysis of ChIP-Seq (MACS)
- deFuse: An Algorithm for Gene Fusion Discovery in Tumor RNA-Seq Data (PLoS Comput. Biol.)
- Molecular determinants of resistance to antiandrogen therapy (Nature Medicine)
- Formation of the androgen receptor transcription complex. (Molecules and Cells)
- Opening of compacted chromatin by early developmental transcription factors HNF3 (FoxA) and GATA-4. (Molecules and Cells)
- Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukemia. (New England Journal of Medicine)
Their papers
- High frequency of BRAF mutations in nevi (2003) — 1,713 citations
- International network of cancer genome projects (2010) — 2,229 citations
- Dual role of FoxA1 in androgen receptor binding to chromatin, androgen signalling and prostate cancer (2011) — 400 citations
- Tissue microarrays for rapid linking of molecular changes to clinical endpoints. (2001) — 617 citations
- FusionCatcher – a tool for finding somatic fusion genes in paired-end RNA-sequencing data (2014) — 405 citations
- Somatic STAT3 Mutations in Large Granular Lymphocytic Leukemia (2012) — 856 citations
- 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. (2003) — 3,796 citations
- Gene-expression profiles in hereditary breast cancer. (2001) — 969 citations