Lucas D. Ward
Affiliations: | 2000-2004 | University of Virginia, Charlottesville, VA | |
| 2004-2010 | Columbia University, New York, NY | ||
| 2010-2014 | Massachusetts Institute of Technology, Cambridge, MA, United States | ||
| 2015-2019 | Amgen Inc., Thousand Oaks, CA, United States | ||
| 2016-2016 | deCode Genetics Inc | ||
| 2019- | Alnylam Pharmaceuticals |
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"Lucas D. Ward"Parents
Sign in to add mentor| Joel G. Belasco | research assistant | 2003 | (Microtree) |
| Anne Beyer | research assistant | 2002-2003 | UVA (Neurotree) |
| Virginia W. Cornish | research assistant | 2004 | (Chemistry Tree) |
| Iva Susan Greenwald | research assistant | 2005 | (GenetiTree) |
| Harmen J. Bussemaker | grad student | 2010 | Columbia (Physics Tree) |
| Manolis Kellis | post-doc | 2010-2014 | MIT |
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Publications
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| Hoffing RA, Deaton AM, Holleman AM, et al. (2024) Transcript-aware analysis of rare predicted loss-of-function variants in the UK Biobank elucidate new isoform-trait associations. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 29: 247-260 |
| Sun BB, Chiou J, Traylor M, et al. (2023) Plasma proteomic associations with genetics and health in the UK Biobank. Nature. 622: 329-338 |
| Carss KJ, Deaton AM, Del Rio-Espinola A, et al. (2022) Using human genetics to improve safety assessment of therapeutics. Nature Reviews. Drug Discovery |
| Nguyen PA, Born DA, Deaton AM, et al. (2019) Phenotypes associated with genes encoding drug targets are predictive of clinical trial side effects. Nature Communications. 10: 1579 |
| Fielden MR, Ward LD, Minocherhomji S, et al. (2017) Modernizing Human Cancer Risk Assessment of Therapeutics. Trends in Pharmacological Sciences |
| Jónsson H, Sulem P, Kehr B, et al. (2017) Parental influence on human germline de novo mutations in 1,548 trios from Iceland. Nature. 549: 519-522 |
| Jónsson H, Sulem P, Kehr B, et al. (2017) Whole genome characterization of sequence diversity of 15,220 Icelanders. Scientific Data. 4: 170115 |
| Benonisdottir S, Oddsson A, Helgason A, et al. (2016) Epigenetic and genetic components of height regulation. Nature Communications. 7: 13490 |
| Ward LD, Kellis M. (2016) HaploReg v4: systematic mining of putative causal variants, cell types, regulators and target genes for human complex traits and disease. Nucleic Acids Research. 44: D877-81 |
| Onengut-Gumuscu S, Chen WM, Burren O, et al. (2015) Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers. Nature Genetics. 47: 381-6 |