Adrian R. Krainer
Molecular Biology · 2002–2016
A researcher in the Science corpus: 10 papers; trusts 4 researchers and is trusted by 18 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 115 citations into it; #2,967 of 17,773 by trust here, #2,446 by citations
- Genetics — 35 citations into it; #3,145 of 6,854 by trust here, #2,712 by citations
Whom Adrian R. Krainer trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Adrian R. Krainer overall
Papers from Adrian R. Krainer's perspective
Ordered by how strongly the researchers Adrian R. Krainer trusts endorse each paper. Same corpus, a different order for every researcher.
- Listening to silence and understanding nonsense: exonic mutations that affect splicing (Nature reviews genetics)
- Understanding alternative splicing: towards a cellular code (Nature reviews. Molecular cell biology)
- Drosophila Dscam is an axon guidance receptor exhibiting extraordinary molecular diversity. (Cell)
- dbSNP: the NCBI database of genetic variation
- A genomic view of alternative splicing (Nature Genetics)
- Mechanisms of alternative pre-messenger RNA splicing. (Annual Review of Biochemistry)
- A compendium of RNA-binding motifs for decoding gene regulation (Nature)
- Potential etiologic and functional implications of genome-wide association loci for human diseases and traits (Proceedings of the National Academy of Sciences of the United States of America)
- The Human Gene Mutation Database: 2008 update
- Local dystrophin restoration with antisense oligonucleotide PRO051. (New England Journal of Medicine)
Their papers
- Listening to silence and understanding nonsense: exonic mutations that affect splicing (2002) — 2,297 citations
- The human splicing code reveals new insights into the genetic determinants of disease (2014) — 1,219 citations
- CRISPR Inversion of CTCF Sites Alters Genome Topology and Enhancer/Promoter Function (2015) — 905 citations
- ESEfinder: a web resource to identify exonic splicing enhancers (2003) — 1,656 citations
- Disruption of an SF2/ASF-dependent exonic splicing enhancer in SMN2 causes spinal muscular atrophy in the absence of SMN1 (2002) — 758 citations
- The gene encoding the splicing factor SF2/ASF is a proto-oncogene (2007) — 937 citations
- RNA therapeutics: Beyond RNA interference and antisense oligonucleotides (2012) — 1,108 citations
- Comprehensive splice-site analysis using comparative genomics (2006) — 401 citations
- A Broad Set of Chromatin Factors Influences Splicing (2016) — 43 citations
- Antisense correction of SMN2 splicing in the CNS rescues necrosis in a type III SMA mouse model. (2010) — 643 citations