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Field, Matt A. (2022) Bioinformatic Challenges Detecting Genetic Variation in Precision Medicine Programs. Frontiers in Medicine, 9. 806696.

McConnell, Hannah, Andrews, T. Daniel, and Field, Matt A. (2021) Efficacy of computational predictions of the functional effect of idiosyncratic pharmacogenetic variants. PeerJ, 9. e11774.

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Marthick, James R., Raspin, Kelsie, Foley, Georgea R., Blackburn, Nicholas B., Banks, Annette, Donovan, Shaun, Malley, Roslyn C., Field, Matthew A., Stanford, Janet L., Ostrander, Elaine A., FitzGerald, Liesel M., and Dickinson, Joanne L. (2021) Massively parallel sequencing in hereditary prostate cancer families reveals a rare risk variant in the DNA repair gene, RAD51C. European Journal of Cancer, 159. pp. 52-55.

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Raspin, Kelsie, FitzGerald, Liesel M., Marthick, James R., Field, Matt A., Malley, Roslyn C., Banks, Annette, Donovan, Shaun, Thomson, Russell J., Foley, Georgea R., Stanford, Janet L., and Dickinson, Joanne L. (2021) A rare variant in EZH2 is associated with prostate cancer risk. International Journal of Cancer, 149 (5). pp. 1089-1099.

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Sriwichai, Patchara, Karl, Stephan, Samung, Yudthana, Kiattibuti, Kirakorn, Sirichaisinthop, Jeeraphat, Mueller, Ivo, Cui, Liwang, and Sattabongkot, Jetsumon (2017) Imported Plasmodium falciparum and locally transmitted Plasmodium vivax: cross-border malaria transmission scenario in northwestern Thailand. Malaria Journal, 16. 258.

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Wong, Justin J.-L., Au, Amy Y.M., Gao, Dada, Pinello, Natalia, Kwok, Chau-To, Thoeng, Annora, Lau, Katherine A., Gordon, Jane E.A., Schmitz, Ulf, Feng, Yue, Nguyen, Trung V., Middleton, Robert, Bailey, Charles G., Holst, Jeff, Rasko, John E.J., and Ritchie, William (2016) RBM3 regulates temperature sensitive miR-142-5p and miR-143 (thermomiRs), which target immune genes and control fever. Nucleic Acids Research, 44 (6). pp. 2888-2897.

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Knoll, Susanne, Fürst, Katharina, Kowtharapu, Bhavani, Schmitz, Ulf, Marquardt, Stephan, Wolkenhauer, Olaf, Martin, Hubert, and Pützer, Brigitte (2014) E2F1 induces miR-224/452 expression to drive EMT through TXNIP downregulation. EMBO Reports, 15. pp. 1315-1329.

Book Chapter

Hamzeh, Abdul Rezzak, Andrews, T. Daniel, and Field, Matt A. (2021) Detecting Causal Variants in Mendelian Disorders Using Whole-Genome Sequencing. In: Noam, Shomron, (ed.) Deep Sequencing Data Analysis. Methods in Molecular Biology, 2243 . Humana Press, New York, NY, USA, pp. 1-25.

Book

Schmitz, Ulf, and Wolkenhauer, Olaf (2016) Systems medicine. Methods in Molecular Biology, 1386 . Springer, New York, USA.