Informatics methods for laboratory evaluation of HPV ordering patterns with an example from a nationwide sample in the United States, 2003-2009

por Shirts, Brian H., Jackson, Brian R.
Publicado 2010

Utilization and utility of clinical laboratory reports with graphical elements

por Shirts, Brian H., Larsen, Nichole, Jackson, Brian R.
Publicado 2012

Using Patients Like My Patient for Clinical Decision Support: Institution-Specific Probability of Celiac Disease Diagnosis Using Simplified Near-Neighbor Classification

por Shirts, Brian H., Bennett, Sterling T., Jackson, Brian R.
Publicado 2013

Family-Specific Variants and the Limits of Human Genetics

por Shirts, Brian H., Pritchard, Colin C., Walsh, Tom
Publicado en Trends Mol Med (2016)

Seropositivity Rates for Measles, Mumps, and Rubella IgG and Costs Associated with Testing and Revaccination

por Shirts, Brian H., Welch, Ryan J., Couturier, Marc Roger
Publicado 2013

A bayesian approach to laboratory utilization management

por Hauser, Ronald G., Jackson, Brian R., Shirts, Brian H.
Publicado en J Pathol Inform (2015)

Pragmatic and Ethical Challenges of Incorporating the Genome into the Electronic Medical Record

por Nishimura, Adam A., Tarczy-Hornoch, Peter, Shirts, Brian H.
Publicado en Curr Genet Med Rep (2014)

Modeling the costs of clinical decision support for genomic precision medicine

por Mathias, Patrick C., Tarczy-Hornoch, Peter, Shirts, Brian H.
Publicado en AMIA Jt Summits Transl Sci Proc (2016)

Power of Pedigree Likelihood Analysis in Extended Pedigrees to Classify Rare Variants of Uncertain Significance in Cancer Risk Genes

por Rosenthal, Elisabeth A., Ranola, John Michael O., Shirts, Brian H.
Publicado en Fam Cancer (2017)

Exploring the effect of ascertainment bias on genetic studies that use clinical pedigrees

por Ranola, John Michael O., Tsai, Ginger J., Shirts, Brian H.
Publicado en Eur J Hum Genet (2019)

Laboratory informatics based evaluation of methylene tetrahydrofolate reductase C677T genetic test overutilization

por Cohen, David A., Shirts, Brian H., Jackson, Brian R., Parker, Lisa S.
Publicado 2013

Large numbers of individuals required to classify and define risk for rare variants in known cancer risk genes

por Shirts, Brian H., Jacobson, Angela, Jarvik, Gail P., Browning, Brian L.
Publicado 2013

Modified Capture-Recapture Estimates of the Number of Families with Lynch Syndrome in Central Ohio

por Ranola, John Michael O., Pearlman, Rachel, Hampel, Heather, Shirts, Brian H.
Publicado en Fam Cancer (2019)

Evaluation of the gene-age interactions in HDL cholesterol, LDL cholesterol, and triglyceride levels: The impact of the SORT1 polymorphism on LDL cholesterol levels is age dependen...

por Shirts, Brian H., Hasstedt, Sandra J., Hopkins, Paul N., Hunt, Steven C.
Publicado 2011

A Comparison of Cosegregation Analysis Methods for the Clinical Setting: Cosegregation Analysis Comparison

por Rañola, John Michael O., Liu, Quanhui, Rosenthal, Elisabeth A., Shirts, Brian H.
Publicado en Fam Cancer (2018)

Experiences of patients seeking to participate in variant of uncertain significance reclassification research

por Makhnoon, Sukh, Garrett, Lauren Thomas, Burke, Wylie, Bowen, Deborah J., Shirts, Brian H.
Publicado en J Community Genet (2018)

Exploring relatives’ perceptions of participation, ethics, and communication in a patient-driven study for hereditary cancer variant reclassification

por Tsai, Ginger J., Chen, Annie T., Garrett, Lauren T., Burke, Wylie, Bowen, Deborah J., Shirts, Brian H.
Publicado en J Genet Couns (2020)

Physician Perspectives of CYP2C19 and Clopidogrel Drug-Gene Interaction Active Clinical Decision Support Alerts

por Nishimura, Adam A., Shirts, Brian H., Salama, Joseph, Smith, Joe W., Devine, Beth, Tarczy-Hornoch, Peter
Publicado en Int J Med Inform (2015)

Simultaneous Genotyping of rs12979860 and rs8099917 Variants Near the IL28B Locus Associated with HCV Clearance and Treatment Response

por Melis, Roberta, Fauron, Christiane, McMillin, Gwendolyn, Lyon, Elaine, Shirts, Brian, Hubley, Lindsey M., Slev, Patricia R.
Publicado 2011

Efficient Detection of Copy Number Mutations in PMS2 Exons with a Close Homolog

por Herman, Daniel S., Smith, Christina, Liu, Chang, Vaughn, Cecily P., Palaniappan, Selvi, Pritchard, Colin C., Shirts, Brian H.
Publicado en J Mol Diagn (2018)