G. Asimenos
Molecular Biology · 2004–2019
A researcher in the Science corpus: 5 papers; trusts 2 researchers and is trusted by 9 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 118 citations into it; #5,213 of 17,773 by trust here, #1,044 by citations
Whom G. Asimenos trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts G. Asimenos overall
- Patrick D. Schloss
- Kazutaka Katoh
- Paschalia Kapli
- Bibiana Moncada
- K. Dijkstra
- Daron M. Standley
- Céline Mouginot
Papers from G. Asimenos's perspective
Ordered by how strongly the researchers G. Asimenos trusts endorse each paper. Same corpus, a different order for every researcher.
- Transcriptional regulatory elements in the human genome. (Annual review of genomics and human genetics (Print))
- Distribution and intensity of constraint in mammalian genomic sequence. (Genome Research)
- Scanning Human Gene Deserts for Long-Range Enhancers (Science)
- [Structural variation in the human genome]. (Yi chuan = Hereditas)
- FAIRE (Formaldehyde-Assisted Isolation of Regulatory Elements) isolates active regulatory elements from human chromatin. (Genome Research)
- Control of developmental regulators by Polycomb in human embryonic stem cells. (Cell)
- Transcriptional Maps of 10 Human Chromosomes at 5-Nucleotide Resolution (Science)
- Antisense Transcription in the Mammalian Transcriptome (Science)
- Widespread occurrence of antisense transcription in the human genome (Nature Biotechnology)
- The RNA polymerase II core promoter. (Annual Review of Biochemistry)
Their papers
- Distribution and intensity of constraint in mammalian genomic sequence. (2005) — 1,400 citations
- Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project (2007) — 5,374 citations
- Multiple alignment of DNA sequences with MAFFT. (2009) — 1,420 citations
- The ENCODE (ENCyclopedia Of DNA Elements) Project (2004) — 2,411 citations
- Best Practices for Benchmarking Germline Small Variant Calls in Human Genomes (2019) — 350 citations