Stephen Kingsmore
Molecular Biology · 2002–2012
A researcher in the Science corpus: 5 papers; trusts 5 researchers and is trusted by 2 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 41 citations into it; #13,139 of 17,773 by trust here, #2,983 by citations
- Genetics — 17 citations into it
Whom Stephen Kingsmore trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Stephen Kingsmore overall
Papers from Stephen Kingsmore's perspective
Ordered by how strongly the researchers Stephen Kingsmore trusts endorse each paper. Same corpus, a different order for every researcher.
- Causal Protein-Signaling Networks Derived from Multiparameter Single-Cell Data
- The Human Gene Mutation Database: 2008 update
- Solution Hybrid Selection with Ultra-long Oligonucleotides for Massively Parallel Targeted Sequencing (Nature Biotechnology)
- A computational algebra approach to the reverse engineering of gene regulatory networks. (Journal of Theoretical Biology)
- Mechanisms of alternative pre-messenger RNA splicing. (Annual Review of Biochemistry)
- Human breast cancer cells generated by oncogenic transformation of primary mammary epithelial cells. (Genes & Development)
- Genome-Wide Survey of Human Alternative Pre-mRNA Splicing with Exon Junction Microarrays (Science)
- Fast and SNP-tolerant detection of complex variants and splicing in short reads (Bioinform.)
- The complete genome of an individual by massively parallel DNA sequencing (Nature)
- Bioinformatics Applications Note Databases and Ontologies Deriving the Consequences of Genomic Variants with the Ensembl Api and Snp Effect Predictor
Their papers
- Alternative Isoform Regulation in Human Tissue Transcriptomes (2008) — 5,160 citations
- Comprehensive human genome amplification using multiple displacement amplification (2002) — 1,491 citations
- Multiplexed protein measurement: technologies and applications of protein and antibody arrays (2006) — 698 citations
- Rapid Whole-Genome Sequencing for Genetic Disease Diagnosis in Neonatal Intensive Care Units (2012) — 637 citations
- Carrier Testing for Severe Childhood Recessive Diseases by Next-Generation Sequencing (2011) — 657 citations