Resultados de búsqueda - Qiao, Dandi
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On Association Analysis of Rare Variants Under Population Substructure: An Approach for the Detection of Subjects That Can Cause Bias in the Analysis—T(opt): An Outlier Detection M... por Qiao, Dandi, Mattheisen, Manuel, Lange, Christoph
Publicado 2013Texto -
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metaFARVAT: An Efficient Tool for Meta-Analysis of Family-Based, Case-Control, and Population-Based Rare Variant Association Studies por Wang, Longfei, Lee, Sungyoung, Qiao, Dandi, Cho, Michael H., Silverman, Edwin K., Lange, Christoph, Won, Sungho
Publicado 2019Texto -
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Family-based Rare Variant Association Analysis: a Fast and Efficient Method of Multivariate Phenotype Association Analysis por Wang, Longfei, Lee, Sungyoung, Gim, Jungsoo, Qiao, Dandi, Cho, Michael, Elston, Robert C, Silverman, Edwin K, Won, Sungho
Publicado 2016Texto -
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Heterozygosity of the Alpha 1‐Antitrypsin Pi*Z Allele and Risk of Liver Disease por Hakim, Aaron, Moll, Matthew, Qiao, Dandi, Liu, Jiangyuan, Lasky‐Su, Jessica A., Silverman, Edwin K., Vilarinho, Silvia, Jiang, Z. Gordon, Hobbs, Brian D., Cho, Michael H.
Publicado 2021Texto -
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Genome-wide assessment of gene-by-smoking interactions in COPD por Park, Boram, Koo, So-My, An, Jaehoon, Lee, MoonGyu, Kang, Hae Yeon, Qiao, Dandi, Cho, Michael H., Sung, Joohon, Silverman, Edwin K., Yang, Hyeon-Jong, Won, Sungho
Publicado 2018Texto -
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Identification of Functional Variants in the FAM13A Chronic Obstructive Pulmonary Disease Genome-Wide Association Study Locus by Massively Parallel Reporter Assays por Castaldi, Peter J., Guo, Feng, Qiao, Dandi, Du, Fei, Naing, Zun Zar Chi, Li, Yan, Pham, Betty, Mikkelsen, Tarjei S., Cho, Michael H., Silverman, Edwin K., Zhou, Xiaobo
Publicado 2019Texto -
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Gene-based Segregation Method for Identifying Rare Variants in Family-based Sequencing Studies por Qiao, Dandi, Lange, Christoph, Laird, Nan M., Won, Sungho, Hersh, Craig P., Morrow, Jarrett, Hobbs, Brian D., Lutz, Sharon M., Ruczinski, Ingo, Beaty, Terri H., Silverman, Edwin K., Cho, Michael H.
Publicado 2017Texto -
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The rare TREM2 R47H variant exerts only a modest effect on Alzheimer disease risk por Hooli, Basavaraj V., Parrado, Antonio R., Mullin, Kristina, Yip, Wai-Ki, Liu, Tian, Roehr, Johannes T., Qiao, Dandi, Jessen, Frank, Peters, Oliver, Becker, Tim, Ramirez, Alfredo, Lange, Christoph, Bertram, Lars, Tanzi, Rudolph E.
Publicado 2014Texto