Journal articles:

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:

M. Montierth*, J.C. Denny, M. F. Davis. “Effect of Genetic Variants Associated with Uric Acid on Multiple Sclerosis: A Mendelian Randomization Study.”

The Intermountain, Rio Grande, and Rocky Mountain ASM TriBranch Meeting. Durango, CO. April 2018


A. Gosch*, J.C. Denny, M. F. Davis. “Relationship between Essential Tremor and Parkinson’s Disease.” Annual Meeting of the American Society of Human Genetics. Orlando, FL. October 2017.

 M. C. Gardner*, J.C. Denny, M. F. Davis. “Depression and Mental Illness Affect Pre and Post Multiple Sclerosis Diagnosis.” Annual Meeting of the American Society of Human Genetics. Orlando, FL. October 2017.

M. Montierth*, J.C. Denny, M. F. Davis. “Effect of Genetic Variants Associated with Uric Acid on Multiple Sclerosis: A Mendelian Randomization Study.” Annual Meeting of the American Society of Human Genetics. Orlando, FL. October 2017.

J. Adams*, M. F. Davis, R. D. Cordner. “Evaluating the Gap between Training Programs and Hospitals in Medical Laboratory Science Chemistry Testing.” Annual Meeting of the American Society of Clinical Laboratory Science. San Diego, CA. July 2017.

H. Jensen*, J. C. Denny, M. F. Davis. “The Relationship between the Presence of Oligoclonal Bands and the Multiple Sclerosis Severity Score.” Annual Meeting of the American Society of Clinical Laboratory Science. San Diego, CA. July 2017.

R. D. Cordner, C. Dunn, M. F. Davis. “The Education Gap in Clinical Microbiology.” Annual Meeting of the American Society of Clinical Laboratory Science. San Diego, CA. July 2017.

A. Gosch *, J. C. Denny, M. F. Davis. “Uric Acid Levels in Relation to Progression of Multiple Sclerosis.” Biotechnology and Bioinformatics Symposium. Provo, UT. December 2016.

H. Jensen*, J. C. Denny, M. F. Davis. “Effects of HLA Types on Multiple Sclerosis Risk and Age of Onset.” Biotechnology and Bioinformatics Symposium. Provo, UT. December 2016.

M. C. Gardner*, J. C. Denny, M. F. Davis. “Depression and Mental Illness Affect Pre and Post Multiple Sclerosis Diagnosis.” Biotechnology and Bioinformatics Symposium. Provo, UT. December 2016.

S. Frodsham*, J. C. Denny, M. F. Davis. “Characterizing Multiple Sclerosis Subtypes Using the Comprehensive Metabolic Panel-Albumin.” Biotechnology and Bioinformatics Symposium. Provo, UT. December 2016.

D. Rowe*, S. Sutton^, S. Draper*, J. L. Haines, J. C. Denny, M. F. Davis. “Algorithmic Extractions of a Database for Multiple Sclerosis Medication History.” Biotechnology and Bioinformatics Symposium. Provo, UT. December 2016.

M. F. Davis, S. Sutton, L. Bastarache, R. Carroll, J. C. Denny. “EHR data extraction shows utility for microphenotypes in genetic studies.” American Society for Human Genetics Annual Meeting, Vancouver, Canada. October 2016.

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.