Alexander E. Urban
Science · 2004–2019
A researcher in the Science corpus: 7 papers; trusts 2 researchers and is trusted by 1 researcher here, as inferred from the citation graph.
Whom Alexander E. Urban trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Alexander E. Urban overall
Papers from Alexander E. Urban's perspective
Ordered by how strongly the researchers Alexander E. Urban trusts endorse each paper. Same corpus, a different order for every researcher.
- Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry (Nature)
- Transcriptional regulatory elements in the human genome. (Annual review of genomics and human genetics (Print))
- Ultrafast and memory-efficient alignment of short DNA sequences to the human genome (Genome Biology)
- Mean Shift: A Robust Approach Toward Feature Space Analysis
- FAIRE (Formaldehyde-Assisted Isolation of Regulatory Elements) isolates active regulatory elements from human chromatin. (Genome Research)
- Antisense Transcription in the Mammalian Transcriptome (Science)
- Control of developmental regulators by Polycomb in human embryonic stem cells. (Cell)
- Genome sequence of the Brown Norway rat yields insights into mammalian evolution (Nature)
- The RNA polymerase II core promoter. (Annual Review of Biochemistry)
- Transcriptional Maps of 10 Human Chromosomes at 5-Nucleotide Resolution (Science)
Their papers
- Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project (2007) — 5,374 citations
- Global Identification of Human Transcribed Sequences with Genome Tiling Arrays (2004) — 1,120 citations
- Variation in Transcription Factor Binding Among Humans (2010) — 617 citations
- The ENCODE (ENCyclopedia Of DNA Elements) Project (2004) — 2,411 citations
- The NASA Twins Study: A multidimensional analysis of a year-long human spaceflight (2019) — 943 citations
- Mapping copy number variation by population scale genome sequencing (2011) — 1,130 citations
- CNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing. (2011) — 1,610 citations