David R. FitzPatrick

According to our database, David R. FitzPatrick authored at least 3 papers between 2014 and 2022.

Collaborative distances:

• Dijkstra number of four.
• Erdős number of three.

2022

Creation and evaluation of full-text literature-derived, feature-weighted disease models of genetically determined developmental disorders.

Thabo M. Yates, A. Laine, Jennifer Campbell, David R. FitzPatrick, T. Ian Simpson

Database J. Biol. Databases Curation, 2022

2014

The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data.

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

Nucleic Acids Res., 2014

Variant detection sensitivity and biases in whole genome and exome sequencing.

Alison M. Meynert, Morad Ansari, David R. FitzPatrick, Martin S. Taylor

BMC Bioinform., 2014