Хайлтын үр дүнгүүд - Broeckel, Ulrich

Identifying genes and genetic variation underlying human diseases and complex phenotypes via recombination mapping -н Broeckel, Ulrich, Schork, Nicholas J

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Personal DNA Testing Increases Pharmacy Students’ Confidence and Competence in Pharmacogenomics -н Assem, Mahfoud, Broeckel, Ulrich, MacKinnon, George E.

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Variants on Chromosome 6p22.3 Associated with Blood Pressure in the HyperGEN Study: Follow-up of FBPP Quantitative Trait Loci -н Simino, Jeannette, Shi, Gang, Arnett, Donna, Broeckel, Ulrich, Hunt, Steven C., Rao, Dabeeru

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Development of reusable logic for determination of statin exposure-time from electronic health records -н Miller, Aaron W., McCarty, Catherine A., Broeckel, Ulrich, Hytopoulos, Vangelis, Cross, Deanna S.

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Genotype Imputation for African Americans using data from HapMap Phase II versus 1000 Genomes Projects -н Sung, Yun Ju, Gu, C Charles, Tiwari, Hemant K, Arnett, Donna K, Broeckel, Ulrich, Rao, DC

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An Autoinflammatory Disease Due to Homozygous Deletion of the IL1RN Locus -н Reddy, Sreelatha, Jia, Shuang, Geoffrey, Rhonda, Lorier, Rachel, Suchi, Mariko, Broeckel, Ulrich, Hessner, Martin J., Verbsky, James

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Adducin 1 (alpha) Gly460Trp variant is associated with left ventricular geometry in Caucasians and African Americans: The HyperGEN Study -н Chauhan, Krati, Devereux, Richard B, Rao, DC, Broeckel, Ulrich, Gu, Charles C, Hopkins, Paul, Arnett, Donna K

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Human IL12RB1 expression is allele-biased and produces a novel IL12 response regulator -н Reeme, Allison E., Claeys, Tiffany A., Aggarwal, Praful, Turner, Amy J., Routes, John M., Broeckel, Ulrich, Robinson, Richard T.

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Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: The HyperGEN Study -н Arnett, Donna K, Li, Na, Tang, Weihong, Rao, Dabeeru C, Devereux, Richard B, Claas, Steven A, Kraemer, Rachel, Broeckel, Ulrich

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RNA Expression Profiling of Human iPSC-Derived Cardiomyocytes in a Cardiac Hypertrophy Model -н Aggarwal, Praful, Turner, Amy, Matter, Andrea, Kattman, Steven J., Stoddard, Alexander, Lorier, Rachel, Swanson, Bradley J., Arnett, Donna K., Broeckel, Ulrich

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Identification of CYP2D6 Haplotypes that Interfere with Commonly Used Assays for Copy Number Variation Characterization -н Turner, Amy J., Aggarwal, Praful, Boone, Erin C., Haidar, Cyrine-Eliana, Relling, Mary V., Derezinski, Ashley D., Broeckel, Ulrich, Gaedigk, Andrea

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NOVEL GENETIC VARIANTS CONTRIBUTING TO LEFT VENTRICULAR HYPERTROPHY: THE HYPERGEN STUDY: Genetic variants for LV hypertrophy -н Arnett, Donna K., Devereux, Richard B., Rao, DC, Li, Na, Tang, Weihong, Kraemer, Rachel, Claas, Steven A., Leon, Joanlise M., Broeckel, Ulrich

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Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study -н Wineinger, Nathan E, Patki, Amit, Meyers, Kristin J, Broeckel, Ulrich, Gu, Charles C, Rao, DC, Devereux, Richard B, Arnett, Donna K, Tiwari, Hemant K

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Potential Novel Mechanism for Axenfeld-Rieger Syndrome: Deletion of a Distant Region Containing Regulatory Elements of PITX2 -н Volkmann, Bethany A., Zinkevich, Natalya S., Mustonen, Aki, Schilter, Kala F., Bosenko, Dmitry V., Reis, Linda M., Broeckel, Ulrich, Link, Brian A., Semina, Elena V.

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Donor-specific phenotypic variation in hiPSC cardiomyocyte-derived exosomes impacts endothelial cell function -н Turner, Amy, Aggarwal, Praful, Matter, Andrea, Olson, Benjamin, Gu, C. Charles, Hunt, Steven C., Lewis, Cora E., Arnett, Donna K., Lorier, Rachel, Broeckel, Ulrich

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Incorporating G6PD genotyping to identify patients with G6PD deficiency -н Morris, Sarah A., Crews, Kristine R., Hayden, Randall T., Takemoto, Clifford M., Yang, Wenjian, Baker, Donald K., Broeckel, Ulrich, Relling, Mary V., Haidar, Cyrine E.

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Localization of a Small Genomic Region Associated with Elevated ACE -н Zhu, Xiaofeng, McKenzie, Colin A., Forrester, Terrence, Nickerson, Deborah A., Broeckel, Ulrich, Schunkert , Heribert, Doering, Angela, Jacob, Howard J., Cooper, Richard S., Rieder, Mark J.

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Whole-genome copy number variation analysis in anophthalmia and microphthalmia -н Schilter, Kala F., Reis, Linda M., Schneider, Adele, Bardakjian, Tanya M., Abdul-Rahman, Omar, Kozel, Beth A., Zimmerman, Holly H., Broeckel, Ulrich, Semina, Elena V.

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Copy number variations associated with obesity related traits in African Americans: a joint analysis between GENOA and HyperGEN -н Zhao, Wei, Wineinger, Nathan E., Tiwari, Hemant K., Mosley, Thomas H., Broeckel, Ulrich, Arnett, Donna K., Kardia, Sharon L. R., Kabagambe, Edmond K., Sun, Yan V.

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Pharmacokinetics and pharmacogenomics of daunorubicin in children: a report from the Children’s Oncology Group -н Thompson, Patrick, Wheeler, Heather E., Delaney, Shannon M., Lorier, Rachel, Broeckel, Ulrich, Devidas, Meenakshi, Reaman, Gregory H., Scorsone, Kathleen, Sung, Lillian, Dolan, M. Eileen, Berg, Stacey L.

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