Lucas D. Ward
Molecular Biology · 2011–2017
A researcher in the Science corpus: 7 papers; trusts 9 researchers and is trusted by 2 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 215 citations into it; #8,072 of 17,773 by trust here, #2,001 by citations
- Genetics — 101 citations into it; #2,812 of 6,854 by trust here, #2,063 by citations
Whom Lucas D. Ward trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Gerd Kempermann
- Pouya Kheradpour
- ENCODEConsortium
- Manolis Kellis
- Zongli Xu
- J. Harrow
- Donna Karolchik
- Stephen B. Montgomery
- Martin Renqiang Min
- Jack A. Taylor
Who trusts Lucas D. Ward overall
Papers from Lucas D. Ward's perspective
Ordered by how strongly the researchers Lucas D. Ward trusts endorse each paper. Same corpus, a different order for every researcher.
- 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)
- Distinct and predictive chromatin signatures of transcriptional promoters and enhancers in the human genome (Nature Genetics)
- Mapping and quantifying mammalian transcriptomes by RNA-Seq (Nature Methods)
- Transcriptional regulatory elements in the human genome. (Annual review of genomics and human genetics (Print))
- FAIRE (Formaldehyde-Assisted Isolation of Regulatory Elements) isolates active regulatory elements from human chromatin. (Genome Research)
- Genome-scale DNA methylation maps of pluripotent and differentiated cells (Nature)
- Measuring reproducibility of high-throughput experiments
- Distribution and intensity of constraint in mammalian genomic sequence. (Genome Research)
- Finding the missing heritability of complex diseases (Nature)
- Ensembl’s 10th year (Nucleic Acids Res.)
Their papers
- Integrative analysis of 111 reference human epigenomes (2015) — 6,046 citations
- Defining functional DNA elements in the human genome (2014) — 696 citations
- HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants (2011) — 2,261 citations
- A User's Guide to the Encyclopedia of DNA Elements (ENCODE) (2011) — 1,042 citations
- Parental influence on human germline de novo mutations in 1,548 trios from Iceland (2017) — 505 citations
- Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers (2015) — 661 citations
- HaploReg v4: systematic mining of putative causal variants, cell types, regulators and target genes for human complex traits and disease (2015) — 882 citations