R. Bjornson
Nature · 2009–2017
A researcher in the Science corpus: 6 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Whom R. Bjornson trusts
Their strongest outbound trust, strongest first, inferred from their citations.
- John D. Storey (in Statistics and Probability)
Papers from R. Bjornson's perspective
Ordered by how strongly the researchers R. Bjornson trusts endorse each paper. Same corpus, a different order for every researcher.
- Mapping and quantifying mammalian transcriptomes by RNA-Seq (Nature Methods)
- Genome-wide profiles of STAT1 DNA association using chromatin immunoprecipitation and massively parallel sequencing (Nature Methods)
- Genome-Wide Mapping of in Vivo Protein-DNA Interactions (Science)
- Ultrafast and memory-efficient alignment of short DNA sequences to the human genome (Genome Biology)
- Variation in Transcription Factor Binding Among Humans (Science)
- PeakSeq: Systematic Scoring of ChIP-Seq Experiments Relative to Controls (Nature Biotechnology)
- GENCODE: producing a reference annotation for ENCODE (Genome Biology)
- Networks Network Motifs : Simple Building Blocks of Complex
- Transcriptome genetics using second generation sequencing in a Caucasian population (Nature)
- Understanding mechanisms underlying human gene expression variation with RNA sequencing (Nature)
Their papers
- PeakSeq: Systematic Scoring of ChIP-Seq Experiments Relative to Controls (2009) — 589 citations
- AlleleSeq: analysis of allele-specific expression and binding in a network framework (2011) — 352 citations
- De novo mutations in histone modifying genes in congenital heart disease (2013) — 900 citations
- Mutations in Kelch-like 3 and Cullin 3 cause hypertension and electrolyte abnormalities (2012) — 605 citations
- Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands (2017) — 773 citations
- De novo mutations revealed by whole-exome sequencing are strongly associated with autism (2012) — 2,079 citations