Identifying genes and genetic variation underlying human diseases and complex phenotypes via recombination mapping

由 Broeckel, Ulrich, Schork, Nicholas J
出版 2004

Personal DNA Testing Increases Pharmacy Students’ Confidence and Competence in Pharmacogenomics

由 Assem, Mahfoud, Broeckel, Ulrich, MacKinnon, George E.
發表在 Am J Pharm Educ (2021)

Variants on Chromosome 6p22.3 Associated with Blood Pressure in the HyperGEN Study: Follow-up of FBPP Quantitative Trait Loci

由 Simino, Jeannette, Shi, Gang, Arnett, Donna, Broeckel, Ulrich, Hunt, Steven C., Rao, Dabeeru
出版 2011

Development of reusable logic for determination of statin exposure-time from electronic health records

由 Miller, Aaron W., McCarty, Catherine A., Broeckel, Ulrich, Hytopoulos, Vangelis, Cross, Deanna S.
發表在 J Biomed Inform (2014)

Comprehensive evaluation of AmpliSeq transcriptome, a novel targeted whole transcriptome RNA sequencing methodology for global gene expression analysis

由 Li, Wenli, Turner, Amy, Aggarwal, Praful, Matter, Andrea, Storvick, Erin, Arnett, Donna K., Broeckel, Ulrich
發表在 BMC Genomics (2015)

Genotype Imputation for African Americans using data from HapMap Phase II versus 1000 Genomes Projects

由 Sung, Yun Ju, Gu, C Charles, Tiwari, Hemant K, Arnett, Donna K, Broeckel, Ulrich, Rao, DC
出版 2012

An Autoinflammatory Disease Due to Homozygous Deletion of the IL1RN Locus

由 Reddy, Sreelatha, Jia, Shuang, Geoffrey, Rhonda, Lorier, Rachel, Suchi, Mariko, Broeckel, Ulrich, Hessner, Martin J., Verbsky, James
出版 2009

Adducin 1 (alpha) Gly460Trp variant is associated with left ventricular geometry in Caucasians and African Americans: The HyperGEN Study

由 Chauhan, Krati, Devereux, Richard B, Rao, DC, Broeckel, Ulrich, Gu, Charles C, Hopkins, Paul, Arnett, Donna K
出版 2010

The introduction of RNA-DNA differences underlies interindividual variation in the human IL12RB1 mRNA repertoire

由 Turner, Amy J., Aggarwal, Praful, Miller, Halli E., Waukau, Jill, Routes, John M., Broeckel, Ulrich, Robinson, Richard T.
發表在 Proc Natl Acad Sci U S A (2015)

Human IL12RB1 expression is allele-biased and produces a novel IL12 response regulator

由 Reeme, Allison E., Claeys, Tiffany A., Aggarwal, Praful, Turner, Amy J., Routes, John M., Broeckel, Ulrich, Robinson, Richard T.
發表在 Genes Immun (2018)

Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: The HyperGEN Study

由 Arnett, Donna K, Li, Na, Tang, Weihong, Rao, Dabeeru C, Devereux, Richard B, Claas, Steven A, Kraemer, Rachel, Broeckel, Ulrich
出版 2009

RNA Expression Profiling of Human iPSC-Derived Cardiomyocytes in a Cardiac Hypertrophy Model

由 Aggarwal, Praful, Turner, Amy, Matter, Andrea, Kattman, Steven J., Stoddard, Alexander, Lorier, Rachel, Swanson, Bradley J., Arnett, Donna K., Broeckel, Ulrich
出版 2014

Identification of CYP2D6 Haplotypes that Interfere with Commonly Used Assays for Copy Number Variation Characterization

由 Turner, Amy J., Aggarwal, Praful, Boone, Erin C., Haidar, Cyrine-Eliana, Relling, Mary V., Derezinski, Ashley D., Broeckel, Ulrich, Gaedigk, Andrea
發表在 J Mol Diagn (2021)

NOVEL GENETIC VARIANTS CONTRIBUTING TO LEFT VENTRICULAR HYPERTROPHY: THE HYPERGEN STUDY: Genetic variants for LV hypertrophy

由 Arnett, Donna K., Devereux, Richard B., Rao, DC, Li, Na, Tang, Weihong, Kraemer, Rachel, Claas, Steven A., Leon, Joanlise M., Broeckel, Ulrich
出版 2009

Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study

由 Wineinger, Nathan E, Patki, Amit, Meyers, Kristin J, Broeckel, Ulrich, Gu, Charles C, Rao, DC, Devereux, Richard B, Arnett, Donna K, Tiwari, Hemant K
出版 2011

Potential Novel Mechanism for Axenfeld-Rieger Syndrome: Deletion of a Distant Region Containing Regulatory Elements of PITX2

由 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.
出版 2011

Donor-specific phenotypic variation in hiPSC cardiomyocyte-derived exosomes impacts endothelial cell function

由 Turner, Amy, Aggarwal, Praful, Matter, Andrea, Olson, Benjamin, Gu, C. Charles, Hunt, Steven C., Lewis, Cora E., Arnett, Donna K., Lorier, Rachel, Broeckel, Ulrich
發表在 Am J Physiol Heart Circ Physiol (2021)

Localization of a Small Genomic Region Associated with Elevated ACE

由 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.
出版 2000

Whole-genome copy number variation analysis in anophthalmia and microphthalmia

由 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.
出版 2013

Copy number variations associated with obesity related traits in African Americans: a joint analysis between GENOA and HyperGEN

由 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.
出版 2012