T. Daniel Andrews

Molecular Biology · 2004–2020

A researcher in the Science corpus: 8 papers; trusts 1 researcher and is trusted by 1 researcher here, as inferred from the citation graph.

Subfields

• Molecular Biology — 94 citations into it; #16,252 of 17,773 by trust here, #5,041 by citations

Whom T. Daniel Andrews trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

1. W. James Kent

Who trusts T. Daniel Andrews overall

1. Ryan E. Mills
2. James R. Brown
3. Kai Wang

Papers from T. Daniel Andrews's perspective

Ordered by how strongly the researchers T. Daniel Andrews trusts endorse each paper. Same corpus, a different order for every researcher.

1. Basic local alignment search tool.
2. EnsMart: a generic system for fast and flexible access to biological data. (Genome Research)
3. BLAT--the BLAST-like alignment tool. (Genome Research)
4. Detection of large-scale variation in the human genome (Nature Genetics)
5. Improved prediction of signal peptides: SignalP 3.0. (Journal of Molecular Biology)
6. GeneWise and Genomewise. (Genome Research)
7. Regulation of lifespan in Drosophila by modulation of genes in the TOR signaling pathway. (Current Biology)
8. Discovery of functional elements in 12 Drosophila genomes using evolutionary signatures (Nature)
9. Integrated detection and population-genetic analysis of SNPs and copy number variation (Nature Genetics)
10. Longer lifespan, altered metabolism, and stress resistance in Drosophila from ablation of cells making insulin-like ligands. (Proceedings of the National Academy of Sciences of the United States of America)

Their papers

• The Ensembl automatic gene annotation system. (2004) — 428 citations
• A high-resolution survey of deletion polymorphism in the human genome (2006) — 717 citations
• The DNA sequence of the human X chromosome (2005) — 1,099 citations
• NINJ1 mediates plasma membrane rupture during lytic cell death (2020) — 675 citations
• Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls (2010) — 710 citations
• Molecular Evolution and Functional Characterization of Drosophila Insulin-Like Peptides (2010) — 620 citations
• Origins and functional impact of copy number variation in the human genome (2009) — 1,997 citations
• Global variation in copy number in the human genome (2006) — 4,423 citations