Luke Ward
Luke Ward
Alnylam Pharmaceuticals
Verified email at alnylam.com - Homepage
Title
Cited by
Cited by
Year
An integrated encyclopedia of DNA elements in the human genome
ENCODE Project Consortium
Nature, 2012
10526*2012
Integrative analysis of 111 reference human epigenomes
A Kundaje, W Meuleman, J Ernst, M Bilenky, A Yen, A Heravi-Moussavi, ...
Nature 518 (7539), 317-330, 2015
32812015
Mapping and analysis of chromatin state dynamics in nine human cell types
J Ernst, P Kheradpour, TS Mikkelsen, N Shoresh, LD Ward, CB Epstein, ...
Nature 473 (7345), 43-49, 2011
25242011
The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans
KG Ardlie, DS Deluca, AV Segrè, TJ Sullivan, TR Young, ET Gelfand, ...
Science 348 (6235), 648-660, 2015
25122015
HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants
LD Ward, M Kellis
Nucleic Acids Research, 2011
16992011
A user's guide to the encyclopedia of DNA elements (ENCODE)
EP Consortium
PLoS Biology 9 (4), e1001046, 2011
11612011
A high-resolution map of human evolutionary constraint using 29 mammals
K Lindblad-Toh, M Garber, O Zuk, MF Lin, BJ Parker, S Washietl, ...
Nature 478 (7370), 476-482, 2011
9372011
Systematic Protein Location Mapping Reveals Five Principal Chromatin Types in Drosophila Cells
GJ Filion, JG van Bemmel, U Braunschweig, W Talhout, J Kind, LD Ward, ...
Cell 145 (1), 160-160, 2011
9152011
Defining functional DNA elements in the human genome
M Kellis, B Wold, MP Snyder, BE Bernstein, A Kundaje, GK Marinov, ...
Proceedings of the National Academy of Sciences 111 (17), 6131-6138, 2014
6032014
HaploReg v4: systematic mining of putative causal variants, cell types, regulators and target genes for human complex traits and disease
LD Ward, M Kellis
Nucleic acids research 44 (D1), D877-D881, 2016
4162016
Interpreting noncoding genetic variation in complex traits and human disease
LD Ward, M Kellis
Nature biotechnology 30 (11), 1095-1106, 2012
4162012
Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers
S Onengut-Gumuscu, WM Chen, O Burren, NJ Cooper, AR Quinlan, ...
Nature genetics 47 (4), 381-386, 2015
3512015
Common genetic variants modulate pathogen-sensing responses in human dendritic cells
MN Lee, C Ye, AC Villani, T Raj, W Li, TM Eisenhaure, SH Imboywa, ...
Science 343 (6175), 2014
3212014
Hotspots of transcription factor colocalization in the genome of Drosophila melanogaster
C Moorman, LV Sun, J Wang, E de Wit, W Talhout, LD Ward, F Greil, ...
Proceedings of the National Academy of Sciences 103 (32), 12027-12032, 2006
2032006
Evidence of abundant purifying selection in humans for recently acquired regulatory functions
LD Ward, M Kellis
Science, 2012
2022012
Parental influence on human germline de novo mutations in 1,548 trios from Iceland
H Jónsson, P Sulem, B Kehr, S Kristmundsdottir, F Zink, E Hjartarson, ...
Nature 549 (7673), 519-522, 2017
1822017
Effect of predicted protein-truncating genetic variants on the human transcriptome
MA Rivas, M Pirinen, DF Conrad, M Lek, EK Tsang, KJ Karczewski, ...
Science 348 (6235), 666-669, 2015
1802015
Predictive modeling of genome-wide mRNA expression: from modules to molecules
HJ Bussemaker, BC Foat, LD Ward
Annual review of biophysics and biomolecular structure 36, 2007
992007
Predicting functional transcription factor binding through alignment-free and affinity-based analysis of orthologous promoter sequences
LD Ward, HJ Bussemaker
Bioinformatics 24 (13), i165-i171, 2008
632008
Broad Institute Sequencing Platform and Whole Genome Assembly Team; Baylor College of Medicine Human Genome Sequencing Center Sequencing Team; Genome Institute at Washington …
K Lindblad-Toh, M Garber, O Zuk, MF Lin, BJ Parker, S Washietl, ...
Nature 478 (7370), 476-482, 0
61
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