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1 Camp, Nicola J.Genome-wide linkage analysis for aggressive prostate cancer in Utah high risk pedigreesResearch has consistently shown that genetics plays a critical role in prostate cancer (CaP) development, but the identification of CaP genes has proven to be very difficult. Hereditary prostate cancer is a complex disease involving numerous genes and variable phenotypic expression. This heterogene...Linkage analysis; Aggressive prostate cancer; CaP genes; ICPCG; Utah; Trapeze Interactive Poster2009
2 Camp, Nicola J.Genetic susceptibility of prostate cancer: genome-wide screen of "non-aggressive" diseaseResearch has consistently shown that genetics plays a critical role in prostate cancer (CaP) development, but the identification of CaP genes has proven to be very difficult. Hereditary prostate cancer is a complex disease believed to involve numerous genes and variable penetrance. It has been propo...CaP genes; Prostate cancer; Non-aggressive; Utah Population Database; Trapeze Interactive Poster2009
3 Camp, Nicola J.Survey of excess familiality in prostate cancerProstate cancer (PCa) is the most commonly diagnosed cancer among men, and has long been recognized to occur in familial clusters. However, identification of genes predisposing individuals to prostate cancer has been difficult. Putative PCa predisposition loci identified by genetic linkage have been...Prostate cancer; Utah Population Database; Linkage analysis; Familial compotent; Excess familiality; Trapeze Interactive Poster2009
4 Mitchell, Joyce A.Effect of physician reminders on preventive care: meta-analysis of randomized clinical trialsThe objective of this study was to assess the clinical value of the physician reminder, an information intervention, in increasing compliance for selected preventive health care measures. Meta-analysis was used to combine the quantitative evidence from randomized controlled clinical trials meeting t...1994-01-01
5 Warner, Homer R.Subtotal Hysterectomy in Modern Gynecology: A Decision AnalysisBiomedical Informatics1997
6 Camp, Nicola J.SumLINK statistic for linkage analysis: application to the ICPCG pooled linkage resourceWe propose a novel, genome-wide, linkagebased statistic, "sumLINK," for identification of disease susceptibility loci. Our approach focuses primarily on "linked" pedigrees (those with pedigree-specific LOD ? 0.588; equivalent to unadjusted p ? 0.05) to identify regions of extreme consistency across ...SumLINK; Linkage analysis; ICPCG; Disease susceptibility loci; Trapeze Interactive Poster2009
7 Mitchell, Joyce A.International efforts in nanoinformatics research applied to nanomedicineBackground: Nanomedicine and nanoinformatics are novel disciplines facing substantial challenges. Since nanomedicine involves complex and massive data analysis and management, a new discipline named nanoinformatics is now emerging to provide the vision and the informatics methods and tools needed fo...2011-01-01
8 Mitchell, Joyce A.Bioinformatics linkage of heterogeneous clinical and genomic information in support of personalized medicineObjectives: Biomedical Informatics as a whole faces a difficult epistemological task, since there is no foundation to explain the complexities of modeling clinical medicine and the many relationships between genotype, phenotype, and environment. This paper discusses current efforts to investigate su...2007-01-01
9 DuVall, Scott L.Understanding the profile of errors that cause duplicate entries in a patient registryDuplicate records are detrimental to the cost-effective and efficient delivery of health care. Manually identifying and resolving duplicates can cost $60 per case. Patterns have been found in the types of errors that occur in patient registries, suggesting that undetected duplicate records may be ...Duplicate records; Duplicate patient records; Profile of errors; Enterprise Data Warehouse; EDW; Utah Population Database; UPDB; Trapeze Interactive Poster2009
10 Mitchell, Joyce A.Nanoinformatics: a new area of research in nanomedicineAbstract: Over a decade ago, nanotechnologists began research on applications of nanomaterials for medicine. This research has revealed a wide range of different challenges, as well as many opportunities. Some of these challenges are strongly related to informatics issues, dealing, for instance, wit...2012-01-01
11 Warner, Homer R.Some Changes in Medical Informatics (Editorial)Biomedical Informatics1990
12 Frey, Lewis J.ca! - emergency and disaster recovery system extensions to caBIG™During Hurricane Katrina, US Federal and State Agencies had disparate data acquisition systems, separate data networks and unique incompatible applications. •System incompatibilities exist even between various Federal agencies. •Consistent data available to one agency should be available to an...caBIG; Data acquisition systems; Data sharing; Information sharing; Trapeze Interactive Poster2009-09-23
13 Burton, CharlesBiomedical Instrumentation in the Soviet UnionBiomedical Informatics1977
14 Gardner, Reed M.Medical Informatics at the University of Utah: Applying Research to Real-Life IssuesBiomedical Informatics1999
15 Mitchell, Joyce A.Computational Feature of Selection and Classification of RET Phenotypic SeverityAlthough many reported mutations in the RET oncogene have been directly associated with hereditary thyroid carcinoma, other mutations are labelled as uncertain gene variants because they have not been clearly associated with a clinical phenotype. The process of determining the severity of a mutation...2010-01-01
16 Mitchell, Joyce A.Retrieval from full-text medical literature: the dream & the realityWhile the retrieval of the full-text of a document might seem to end all the hassle of using traditional retrieval systems, the results of the MEDLINE/Full-Text Project indicate that retrieval from the current full-text databases of biomedical journal literature does not match the dream. During the ...1991-01-01
17 Mitchell, Joyce A.Predicting phenotypic severity of uncertain gene variants in the RET Proto-OncogeneAlthough reported gene variants in the RET oncogene have been directly associated with multiple endocrine neoplasia type 2 and hereditary medullary thyroid carcinoma, other mutations are classified as variants of uncertain significance (VUS) until the associated clinical phenotype is made clear. Cur...2011-01-01
18 Warner, Homer R.On Confiding in ComputersBiomedical Informatics1975
19 Gardner, Reed M.Prospective Comparison of Arterial Catheter Blood and Catheter-Tip Cultures in Critically Ill PatientsBiomedical Informatics1984
20 Robison, Reid Justin; Farley, Megan A.; Cannon, Dale Sherman; Allen Brady, Kristina Lisa; Matsunami, Norisada; Stevens, Jeffery; Baird, Lisa M.; Varvil, Tena; Leppert, Mark F.; McMahon, William M.; Coon, Hilary H.Copy number variation in a follow-up of adults with ASD: a behavioral phenotype-genotype studyAutistic Spectrum Disorders (ASD) are a set of complex, early-onset neurodevelopmental disorders. Recent studies have revealed a complex genetic landscape for ASD, with many potential genes involved. Little is known about the long-term outcome of individuals with ASD who were diagnosed in childhoo...Autistic spectrum disorders; Copy number variation; Genotyping; Trapeze Interactive Poster2010-03-15
21 Huser, Vojtech; Rocha, Roberto A.RetroGuide: Conducting Time Series Analyses on Large Data Sets: a Case Study With LymphomaWe describe the application of our previously developed analytical infrastructure called RetroGuide to conduct an observational retrospective cohort study using a clinician friendly flowchart approach.Retroguide; Analysis of data; Biomedical informatics; EHR; lymphoma; Case study; Knowledge representation; Cancer; Retrospective study2008-03-28
22 Warner, Homer R.A Mathematical Approach to Medical Diagnosis: Application to Polycythemic States Utilizing Clinical Findings with Values Continuously DistributedBiomedical Informatics1969
23 Mitchell, Joyce A.From phenotype to genotype: issues in navigating the available information resourcesObjectives-As part of an investigation of connecting health professionals and the lay public to both disease and genomic information, we assessed the availability and nature of the data from the Human Genome Project relating to human genetic diseases. Methods-We focused on a set of single gene disea...2003-01-01
24 Warner, Homer R.Automated Transformation of Probabilistic Knowledge for a Medical Diagnostic SystemBiomedical Informatics1994
25 Warner, Homer R.Automated Transformation of Probablistic Knowledge for a Medical Diagnostic SystemBiomedical Informatics1994
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