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The Development of an Infrastructure to Facilitate the Use of Whole Genome Sequencing for Population Health.
Walton NA, Hafen B, Graceffo S, Sutherland N, Emmerson M, Palmquist R, Formea CM, Purcell M, Heale B, Brown MA, Danford CJ, Rachamadugu SI, Person TN, Shortt KA, Christensen GB, Evans JM, Raghunath S, Johnson CP, Knight S, Le VT, Anderson JL, Van Meter M, Reading T, Haslem DS, Hansen IC, Batcher B, Barker T, Sheffield TJ, Yandava B, Taylor DP, Ranade-Kharkar P, Giauque CC, Eyring KR, Breinholt JW, Miller MR, Carter PR, Gillman JL, Gunn AW, Knowlton KU, Bonkowsky JL, Stefansson K, Nadauld LD, McLeod HL. Walton NA, et al. Among authors: christensen gb. J Pers Med. 2022 Nov 8;12(11):1867. doi: 10.3390/jpm12111867. J Pers Med. 2022. PMID: 36579594 Free PMC article.
HerediGene Population Study IT infrastructure: A model to support genomic research recruitment and precision public health.
Taylor DP, Heale BSE, Chisum B, Christensen GB, Wilcox DF, Banks KM, Tripp JS, Liu T, Ruesch JB, Sheffield TJ, Breinholt JW, Harward JC, Hakoda EC, May T, Bonkowsky JL, Walton NA, McLeod HL, Nadauld LD, Ranade-Kharkar P. Taylor DP, et al. Among authors: christensen gb. AMIA Annu Symp Proc. 2024 Jan 11;2023:689-698. eCollection 2023. AMIA Annu Symp Proc. 2024. PMID: 38222332 Free PMC article.
Ingenol Disoxate: A Novel 4-Isoxazolecarboxylate Ester of Ingenol with Improved Properties for Treatment of Actinic Keratosis and Other Non-Melanoma Skin Cancers.
Bertelsen M, Stahlhut M, Grue-Sørensen G, Liang X, Christensen GB, Skak K, Engell KM, Högberg T. Bertelsen M, et al. Among authors: christensen gb. Dermatol Ther (Heidelb). 2016 Dec;6(4):599-626. doi: 10.1007/s13555-016-0137-2. Epub 2016 Aug 8. Dermatol Ther (Heidelb). 2016. PMID: 27503482 Free PMC article.
Concepts and relevance of genome-wide association studies.
Scherer A, Christensen GB. Scherer A, et al. Among authors: christensen gb. Sci Prog. 2016;99(Pt 1):59-67. doi: 10.3184/003685016X14558068452913. Sci Prog. 2016. PMID: 27120814 Free PMC article. Review.
Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population.
Matsunami N, Hensel CH, Baird L, Stevens J, Otterud B, Leppert T, Varvil T, Hadley D, Glessner JT, Pellegrino R, Kim C, Thomas K, Wang F, Otieno FG, Ho K, Christensen GB, Li D, Prekeris R, Lambert CG, Hakonarson H, Leppert MF. Matsunami N, et al. Among authors: christensen gb. Mol Autism. 2014 Jan 27;5(1):5. doi: 10.1186/2040-2392-5-5. Mol Autism. 2014. PMID: 24467814 Free PMC article.
Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population.
Matsunami N, Hadley D, Hensel CH, Christensen GB, Kim C, Frackelton E, Thomas K, da Silva RP, Stevens J, Baird L, Otterud B, Ho K, Varvil T, Leppert T, Lambert CG, Leppert M, Hakonarson H. Matsunami N, et al. Among authors: christensen gb. PLoS One. 2013;8(1):e52239. doi: 10.1371/journal.pone.0052239. Epub 2013 Jan 14. PLoS One. 2013. PMID: 23341896 Free PMC article.
26 results