Showing 391 - 405 of 611 results
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Shukla SK, Pantrangi M, Stahl B, Briska AM, Stemper ME, Wagner TK,...Dykes CW. (2012 November). Comparative whole genome mapping to determine staphylococcus aureus genome size, virulence motifs and clonality. JOURNAL OF CLINICAL MICROBIOLOGY. 50(11):3526-33.
PubMed ID: 22915603
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Duellman T, Warren CL, Peissig PL, Wynn M, Yang J. (2012 October). Matrix metalloproteinase-9 genotype as a potential genetic marker for abdominal aortic aneurysm. Circ Cardiovasc Genet.. 5(5):529-37.
PubMed ID: 22942228
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Browne ML, Carter TC, Kay DM, Kuehn D, Brody LC, Romitti PA,...Mills JL. (2012 October). Evaluation of genes involved in limb development, angiogenesis, and coagulation as risk factors for congenital limb deficiencies. Am J Med Genet A. 158A(10):2463-72.
PubMed ID: 22965740
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Ji Y, Nordgren KK, Chai Y, Hebbring SJ, Jenkins GD, Abo RP,...Weinshilboum RM. (2012 October). Human liver methionine cycle: MAT1A and GNMT gene resequencing, functional genomics, and hepatic genotype-phenotype correlation. Drug Metab. Dispos.. 40(10):1984-92.
PubMed ID: 22807109
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Rose WE, Schulz LT, Andes D, Striker R, Berti AD, Hutson PR, Shukla SK. (2012 October). Addition of ceftaroline to daptomycin after emergence of daptomycin-nonsusceptible Staphylococcus aureus during therapy improves antibacterial activity. Antimicrob Agents Chemother. 56(10):5296-302.
PubMed ID: 22869564
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Burmeister B, Zaleski C, Cold C, McPherson E. (2012 October). Wisconsin Stillbirth Service Program: analysis of large for gestational age cases. Am J Med Genet A. 158A(10):2493-8.
PubMed ID: 22965821
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Foth WS, Waudby CJ, Brilliant MH. (2012 August). Certificates of Confidentiality and the Marshfield Clinic’s Personalized Medicine Research Project Virtual Mentor. 14(8):653-656.
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Cross DS, Foth WS, Neumann A, McCarty CA, Ritter M. (2012 August). PS1-18: Development and Characterization of a Cohort for Determining Long Term Secondary Side Effects Due to Radiation Treatment for Prostate Cancer Using an Electronic Health Record. Clinical Medicine & Research. 10(3):149.
PubMed ID: 22904396
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Anderson ER, Burmester JK, Caldwell MD. (2012 August). Evaluation of a Mitochondrial DNA Mutation in Maternally Inherited and Sporadic Cases of Dupuytren’s Disease. Clinical Medicine & Research. 10(3):122-6.
PubMed ID: 22634541
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Carter TC, Kay DM, Browne ML, Liu A, Romitti PA, Kuehn D,...Mills JL. (2012 August). Hirschsprung's disease and variants in genes that regulate enteric neural crest cell proliferation, migration and differentiation. J. Hum. Genet.. 57(8):485-93.
PubMed ID: 22648184
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Rosenfeld J, Traylor R, Schaefer G, McPherson EW, Ballif B, Klopocki E,...1q21.1 Study Group. (2012 July). Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes. EUROPEAN JOURNAL OF HUMAN GENETICS. 20(7):754-61.
PubMed ID: 22317977
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Rasmussen LV, Peissig PL, McCarty CA, Starren JB. (2012 June). Development of an optical character recognition pipeline for handwritten form fields from an electronic health record. J Am Med Inform Assoc. 19(e1):e90-e95.
PubMed ID: 21890871
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Bailey-Wilson J, Childs E, Cropp C, Schaid DJ, Xu J, Camp N,...International Consortium for Prostate Cancer Genetics [including Hebbring S.] (2012 June). Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPCG) families. BMC Medical Genetics. 13(46)
PubMed ID: 22712434
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Peissig PL, Rasmussen LV, Berg RL, Linneman JG, McCarty CA, Waudby CJ,...Starren JB [including Chen L.] (2012 March). Importance of multi-modal approaches to effectively identify cataract cases from electronic health records. JOURNAL OF THE AMERICAN MEDICAL INFORMATICS ASSOCIATION. 19(2):225-34.
PubMed ID: 22319176
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Kho A, Hayes M, Rasmussen-Torvik L, Pacheco J, Thompson WK, Armstrong L,...Lowe W [including Peissig PL, Miller AW.] (2012 March). Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study. JOURNAL OF THE AMERICAN MEDICAL INFORMATICS ASSOCIATION. 19(2):212-8.
PubMed ID: 22101970
