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ORCIDAndrew P. Jackson
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- affiliation: University of Edinburgh, MRC Institute of Genetics and Molecular Medicine, UK
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2010 – 2019
- 2015
[j3]Martin A. M. Reijns
, Harriet Kemp, James Ding, Sophie Marion de Procé, Andrew P. Jackson, Martin S. Taylor:
Lagging-strand replication shapes the mutational landscape of the genome. Nat. 518(7540): 502-506 (2015)- 2014
- [j2]Sebastian Köhler, Sandra C. Doelken, Christopher J. Mungall, Sebastian Bauer, Helen V. Firth, Isabelle Bailleul-Forestier, Graeme C. M. Black, Danielle L. Brown, Michael Brudno, Jennifer Campbell, David R. FitzPatrick, Janan T. Eppig, Andrew P. Jackson, Kathleen Freson, Marta Gîrdea, Ingo Helbig, Jane A. Hurst, Johanna Jähn, Laird G. Jackson, Anne M. Kelly, David H. Ledbetter, Sahar Mansour, Christa L. Martin, Celia Moss, Andrew D. Mumford, Willem H. Ouwehand, Soo-Mi Park, Erin Rooney Riggs, Richard H. Scott, Sanjay Sisodiya, Steven Van Vooren, Ronald J. Wapner, Andrew O. M. Wilkie, Caroline F. Wright, Anneke T. Vulto-van Silfhout, Nicole de Leeuw, Bert B. A. de Vries, Nicole L. Washington, Cynthia L. Smith, Monte Westerfield, Paul N. Schofield, Barbara J. Ruef, Georgios V. Gkoutos, Melissa A. Haendel, Damian Smedley, Suzanna E. Lewis, Peter N. Robinson:
The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data. Nucleic Acids Res. 42(Database-Issue): 966-974 (2014) - 2013
- [j1]Alison M. Meynert, Louise S. Bicknell, Matthew E. Hurles, Andrew P. Jackson, Martin S. Taylor:
Quantifying single nucleotide variant detection sensitivity in exome sequencing. BMC Bioinform. 14: 195 (2013)
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