Assistant Professor at University of Washington
Pathology
Dr. Brian H. Shirts, MD
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Doctor Brian H. Shirts, MD works in the field of Pathology. He attended University of Pittsburgh School of Medicine. Brian Shirts is also published. He has 41 publications published. The lastest publication: "Improving performance of multigene panels for genomic analysis of cancer predisposition.'
Publications
- Physician perspectives of CYP2C19 and clopidogrel drug-gene interaction active clinical decision support alerts.
- Improving performance of multigene panels for genomic analysis of cancer predisposition.
- CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record.
- Actionable exomic incidental findings in 6503 participants: challenges of variant classification.
- Development of clinical decision support alerts for pharmacogenomic incidental findings from exome sequencing.
- Do We Now Know What Inappropriate Laboratory Utilization Is? An Expanded Systematic Review of Laboratory Clinical Audits.
- Deep sequencing with intronic capture enables identification of an APC exon 10 inversion in a patient with polyposis.
- Large numbers of individuals are required to classify and define risk for rare variants in known cancer risk genes.
- Actionable, Pathogenic Incidental Findings in 1,000 Participants' Exomes.
- Using Patients Like My Patient for Clinical Decision Support: Institution-Specific Probability of Celiac Disease Diagnosis Using Simplified Near-Neighbor Classification.
- Seropositivity Rates for Measles, Mumps, and Rubella IgG and Associated Cost with Testing and Revaccination.
- Prothrombin time, activated partial thromboplastin time and dilute Russell's Viper Venom times are not shorter in patients with the prothrombin G20210A mutation, and d...
- Vitamin D dependent effects of APOA5 polymorphisms on HDL cholesterol.
- Cervical Ribs are More Prevalent in Stillborn Fetuses than in Liveborn Infants and are Strongly Associated with Fetal Aneuploidy.
- 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...
- Partitioning reference intervals by use of genetic information.
- A population-based description of familial clustering of pancreatic cancer.
- Informatics methods for laboratory evaluation of HPV ordering patterns with an example from a nationwide sample in the United States, 2003-2009.
- Pilot study of linking Web-based supplemental interpretive information to laboratory test reports.
- Provider management of and satisfaction with laboratory testing in the nursing home setting: results of a national internet-based survey.
- Changing interpretations, stable genes: responsibilities of patients, professionals, and policy makers in the clinical interpretation of complex genetic information.
- Frequency of laboratory monitoring of chronic medications administered to nursing facility residents: results of a national Internet-based study.
- Comprehensive evaluation of positional candidates in the IL-18 pathway reveals suggestive associations with schizophrenia and herpes virus seropositivity.
- The genes for schizophrenia: finally a breakthrough?
- Clinical laboratory analytics: Challenges and promise for an emerging discipline.
- A bayesian approach to laboratory utilization management.
- The 2013 symposium on pathology data integration and clinical decision support and the current state of field.
- Laboratory informatics based evaluation of methylene tetrahydrofolate reductase C677T genetic test overutilization.
- Brain morphological changes associated with exposure to HSV1 in first-episode schizophrenia.
- Cell culture analysis of the regulatory frameshift event required for the expression of mammalian antizymes.
- Sequence specificity of aminoglycoside-induced stop condon readthrough: potential implications for treatment of Duchenne muscular dystrophy.
- Antibodies to cytomegalovirus and Herpes Simplex Virus 1 associated with cognitive function in schizophrenia.
- A network of dopaminergic gene variations implicated as risk factors for schizophrenia.
- Polymorphisms in MICB are associated with human herpes virus seropositivity and schizophrenia risk.
- Are exposure to cytomegalovirus and genetic variation on chromosome 6p joint risk factors for schizophrenia?
- Association study of IL10, IL1beta, and IL1RN and schizophrenia using tag SNPs from a comprehensive database: suggestive association with rs16944 at IL1beta.
- A comprehensive genetic association and functional study of TNF in schizophrenia risk.
- Simultaneous genotyping of rs12979860 and rs8099917 variants near the IL28B locus associated with HCV clearance and treatment response.
- Grey matter changes associated with host genetic variation and exposure to Herpes Simplex Virus 1 (HSV1) in first episode schizophrenia.
- Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathy.
Schools
University of Pittsburgh Main Campus
Doctors Specialties
- Molecular Genetic Pathology
- Pathology
Accepted Insurances
- Blue Card PPO
- Coop Core
- Choice Plus POS
- Navigate HMO
- Navigate POS
- Options PPO
Education
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University of Utah -
University of Pittsburgh School of Medicine
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