K. B. Pallister, S. Mason, T. K. Nygaard, B. Liu, S. Griffith, J. Jones, S. Linderman, M. Hughes, D. Erickson, J. M. Voyich, M. F. Davis, E. Wilson. “Bovine CCL28 Mediates Chemotaxis via CCR10 and Demonstrates Direct Antimicrobial Activity against Mastitis Causing Bacteria.” PLoS One. Sep. 2015.
M. F. Davis, J. L. Haines. “The intelligent use and clinical benefits of electronic medical records in multiple sclerosis.” Expert Rev Clin Immunol. Feb. 2015.
M. F. Davis, S. Sriram, W. S. Bush, J. C. Denny, and J. L. Haines. “Automated extraction of clinical traits of multiple sclerosis in electronic medical records.” JAMIA. Dec. 2013.
M. F. Davis, A. C. Cummings, L. N. D'Aoust, L. Jiang, D. R. Velez Edwards, R. Laux, L. Reinhart-Mercer, D. Fuzzell, W. K. Scott, M. A. Pericak-Vance, S. L. Lee, and J. L. Haines, "Parkinson disease loci in the mid-western Amish," Hum. Genet. Nov.2013.
A. H. Beecham, N. A. Patsopoulos, D. K. Xifara, M. F. Davis, A. Kemppinen, C. Cotsapas, T. S. Shah, C. Spencer, D. Booth, A. Goris, A. Oturai, J. Saarela, B. Fontaine, B. Hemmer, C. Martin, F. Zipp, S. D'Alfonso, F. Martinelli-Boneschi, B. Taylor, H. F. Harbo, I. Kockum, J. Hillert, T. Olsson, M. Ban, J. R. Oksenberg, R. Hintzen, L. F. Barcellos, C. Agliardi, L. Alfredsson, M. Alizadeh, C. Anderson, R. Andrews, H. B. Sondergaard, A. Baker, G. Band, S. E. Baranzini, N. Barizzone, J. Barrett, C. Bellenguez, L. Bergamaschi, L. Bernardinelli, A. Berthele, V. Biberacher, T. M. Binder, H. Blackburn, I. L. Bomfim, P. Brambilla, S. Broadley, B. Brochet, L. Brundin, D. Buck, H. Butzkueven, S. J. Caillier, W. Camu, W. Carpentier, P. Cavalla, E. G. Celius, I. Coman, G. Comi, L. Corrado, L. Cosemans, I. Cournu-Rebeix, B. A. Cree, D. Cusi, V. Damotte, G. Defer, S. R. Delgado, P. Deloukas, S. A. di, A. T. Dilthey, P. Donnelly, B. Dubois, M. Duddy, S. Edkins, I. Elovaara, F. Esposito, N. Evangelou, B. Fiddes, J. Field, A. Franke, C. Freeman, I. Y. Frohlich, D. Galimberti, C. Gieger, P. A. Gourraud, C. Graetz, A. Graham, V. Grummel, C. Guaschino, A. Hadjixenofontos, H. Hakonarson, C. Halfpenny, G. Hall, P. Hall, A. Hamsten, J. Harley, T. Harrower, C. Hawkins, G. Hellenthal, C. Hillier, J. Hobart, M. Hoshi, S. E. Hunt, M. Jagodic, I. Jelcic, A. Jochim, B. Kendall, A. Kermode, T. Kilpatrick, K. Koivisto, I. Konidari, T. Korn, H. Kronsbein, C. Langford, M. Larsson, M. Lathrop, C. Lebrun-Frenay, J. Lechner-Scott, M. H. Lee, M. A. Leone, V. Leppa, G. Liberatore, B. A. Lie, C. M. Lill, M. Linden, J. Link, F. Luessi, J. Lycke, F. Macciardi, S. Mannisto, C. P. Manrique, R. Martin, V. Martinelli, D. Mason, G. Mazibrada, C. McCabe, I. L. Mero, J. Mescheriakova, L. Moutsianas, K. M. Myhr, G. Nagels, R. Nicholas, P. Nilsson, F. Piehl, M. Pirinen, S. E. Price, H. Quach, M. Reunanen, W. Robberecht, N. P. Robertson, M. Rodegher, D. Rog, M. Salvetti, N. C. Schnetz-Boutaud, F. Sellebjerg, R. C. Selter, C. Schaefer, S. Shaunak, L. Shen, S. Shields, V. Siffrin, M. Slee, P. S. Sorensen, M. Sorosina, M. Sospedra, A. Spurkland, A. Strange, E. Sundqvist, V. Thijs, J. Thorpe, A. Ticca, P. Tienari, D. C. van, E. M. Visser, S. Vucic, H. Westerlind, J. S. Wiley, A. Wilkins, J. F. Wilson, J. Winkelmann, J. Zajicek, E. Zindler, J. L. Haines, M. A. Pericak-Vance, A. J. Ivinson, G. Stewart, D. Hafler, S. L. Hauser, A. Compston, G. McVean, J. P. De, S. J. Sawcer, and J. L. McCauley, "Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis,"Nat. Genet., Nov. 2013.
A. C. Cummings, E. Torstenson, M. F. Davis, L. N. D'Aoust, W. K. Scott, M. A. Pericak-Vance, W. S. Bush, and J. L. Haines, "Evaluating power and type 1 error in large pedigree analyses of binary traits," PLoS. One. May 2013.
Oral and Poster presentations:
Genetic Associations to Microphenotypes in Electronic Health Records: Identifying Causes of Multiple Sclerosis Progression. M. F. Davis. University of Utah Department of Biomedical Informatics Invited Seminar. Salt Lake City, UT. March 2, 2016.
Microphenotypes in Electronic Health Records: Mining the Way for Personalized Medicine. M. F. Davis. BYU Department of Plant and Wildlife Science Seminar. Provo, UT. October 22, 2015.
Using iPads to Document Work in a Clinical Microbiology Course. Mary F. Davis. ASMCUE. Austin, TX. May 30, 2015.
Improving Phenotypic Granularity with NLP-PheWAS in Multiple Sclerosis P. Teixeira, M. F. Davis, L. Wiley, L. Bastarache, J. Smith, R. Carroll, D. Fabbri, D. Roden, J. Denny. Joint Summits on Translational Science. San Francisco, CA. March 2015.
Extraction and analysis of clinical traits of multiple sclerosis using electronic medical records. American Society for Human Genetics Annual Meeting. October 23, 2013.
Genetic analysis of MS using EMR and BioVU—A template for clinical research. Vanderbilt Neurology Grand Rounds. October 4, 2013.
M. F. Davis, B. Peaden*, S. Sriram, J. L. Haines, J. C. Denny. “Genetic involvement in progression of MS disease course.” American Society for Human Genetics Annual Meeting. Baltimore, MD. October 2015.
S. Frodsham*, J. C. Denny, M. F. Davis. “Analysis of Comorbidities of Multiple Sclerosis Patients using an Electronic Medical Record-linked DNA Biobank.” American Society for Human Genetics Annual Meeting. Baltimore, MD. October 2015.
M. G. Durrant*, J. C. Denny, M. F. Davis. “Analysis of pathways associated with Body Mass Index in individuals with multiple sclerosis.” American Society for Human Genetics Annual Meeting. Baltimore, MD. October 2015.
T. Gallion*, J. C. Denny, M. F. Davis. “Relapsing-Remitting Multiple Sclerosis Genotypes Correlated with Copaxone-Induced Hepatotoxicity.” American Society of Clinical Laboratory Science Annual Meeting. Atlanta, GA. July 2015.
T. Gallion*, J. C. Denny, M. F. Davis. “RRMS Patient Genotype Correlated with Copaxone-Induced Hepatotoxicity.” Utah Conference for Undergraduate Research. St. George, UT. February 2015.
S. Frodsham*, J. C. Denny, M. F. Davis. “A Genetic Analysis of the Multiple Sclerosis Disease Course as Influenced by Rheumatoid Arthritis.” Utah Conference for Undergraduate Research. St. George, UT. February 2015.
Genetic enrichment of multiple sclerosis risk loci in multiple sclerosis patients with co-morbid diseases. American Society for Human Genetics Annual Meeting. San Diego, CA. October 21, 2014.
Reported values for oligoclonal bands in an electronic medical record system. American Society for Clinical Laboratory Science. Houston, TX. July 31, 2013.
Defining the use of electronic medical records in genetic studies of multiple sclerosis. American Society for Human Genetics Annual Meeting. San Francisco, CA. November 8, 2012.
Genome-wide association study for Parkinson’s disease in the mid-western US Amish. International Congress for Human Genetics Meeting. Montreal, CA. October 12, 2011.
Defining the use of electronic medical records in genetic studies of multiple sclerosis. Genetics, Immunology and Repair in Multiple Sclerosis--Keystone Symposium. Taos, NM. February 16, 2011.