Search Results - Auer, Paul L.

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  1. 1
    Rare variant association studies: considerations, challenges and opportunities

    Rare variant association studies: considerations, challenges and opportunities by Auer, Paul L, Lettre, Guillaume

    Published 2015
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  2. 2
    Statistical Design and Analysis of RNA Sequencing Data

    Statistical Design and Analysis of RNA Sequencing Data by Auer, Paul L., Doerge, R. W.

    Published 2010
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  3. 3
    From exomes to genomes: challenges and solutions in population-based genetic association studies

    From exomes to genomes: challenges and solutions in population-based genetic association studies by Auer, Paul L, Leal, Suzanne M

    Published 2017
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  4. 4
    Genetic association studies in cardiovascular diseases: do we have enough power?

    Genetic association studies in cardiovascular diseases: do we have enough power? by Auer, Paul L., Stitziel, Nathan O.

    Published 2017
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  5. 5
    Functional Annotation of Putative Regulatory Elements at Cancer Susceptibility Loci

    Functional Annotation of Putative Regulatory Elements at Cancer Susceptibility Loci by Rosse, Stephanie A, Auer, Paul L, Carlson, Christopher S

    Published 2014
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  6. 6
    Testing for Rare Variant Associations in the Presence of Missing Data

    Testing for Rare Variant Associations in the Presence of Missing Data by Auer, Paul L., Wang, Gao, Leal, Suzanne M.

    Published 2013
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  7. 7
    The effect of phenotypic outliers and non-normality on rare-variant association testing

    The effect of phenotypic outliers and non-normality on rare-variant association testing by Auer, Paul L, Reiner, Alex P, Leal, Suzanne M

    Published 2016
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  8. 8
    Exploring drivers of gene expression in the Cancer Genome Atlas

    Exploring drivers of gene expression in the Cancer Genome Atlas by Rau, Andrea, Flister, Michael, Rui, Hallgeir, Auer, Paul L

    Published 2019
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  9. 9
    Capturing microRNA targets using an RNA-induced silencing complex (RISC)-trap approach

    Capturing microRNA targets using an RNA-induced silencing complex (RISC)-trap approach by Cambronne, Xiaolu A., Shen, Rongkun, Auer, Paul L., Goodman, Richard H.

    Published 2012
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  10. 10
    Integrative analysis of sequencing and array genotype data for discovering disease associations with rare mutations

    Integrative analysis of sequencing and array genotype data for discovering disease associations with rare mutations by Hu, Yi-Juan, Li, Yun, Auer, Paul L., Lin, Dan-Yu

    Published 2015
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  11. 11
    Regeneration Rosetta: An Interactive Web Application To Explore Regeneration-Associated Gene Expression and Chromatin Accessibility

    Regeneration Rosetta: An Interactive Web Application To Explore Regeneration-Associated Gene Expression and Chromatin Accessibility by Rau, Andrea, Dhara, Sumona P., Udvadia, Ava J., Auer, Paul L.

    Published 2019
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  12. 12
    Individualized multi-omic pathway deviation scores using multiple factor analysis

    Individualized multi-omic pathway deviation scores using multiple factor analysis by Rau, Andrea, Manansala, Regina, Flister, Michael J, Rui, Hallgeir, Jaffrézic, Florence, Laloë, Denis, Auer, Paul L

    Published 2020
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  13. 13
    Genome-wide Association and Population Genetic Analysis of C-Reactive Protein in African American and Hispanic American Women

    Genome-wide Association and Population Genetic Analysis of C-Reactive Protein in African American and Hispanic American Women by Reiner, Alex P., Beleza, Sandra, Franceschini, Nora, Auer, Paul L., Robinson, Jennifer G., Kooperberg, Charles, Peters, Ulrike, Tang, Hua

    Published 2012
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  14. 14
    Cellular reprogramming for successful CNS axon regeneration is driven by a temporally changing cast of transcription factors

    Cellular reprogramming for successful CNS axon regeneration is driven by a temporally changing cast of transcription factors by Dhara, Sumona P., Rau, Andrea, Flister, Michael J., Recka, Nicole M., Laiosa, Michael D., Auer, Paul L., Udvadia, Ava J.

    Published 2019
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  15. 15
    Effect of Sickle Cell Trait and APOL1 Genotype on the Association of Soluble uPAR with Kidney Function Measures in Black Americans

    Effect of Sickle Cell Trait and APOL1 Genotype on the Association of Soluble uPAR with Kidney Function Measures in Black Americans by Reiner, Alexander P., Raffield, Laura M., Franceschini, Nora, Auer, Paul L., Lange, Ethan M., Nickerson, Deborah A., Zakai, Neil A., Correa, Adolfo, Olson, Nels

    Published 2021
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  16. 16
    Guidelines for Large-Scale Sequence-Based Complex Trait Association Studies: Lessons Learned from the NHLBI Exome Sequencing Project

    Guidelines for Large-Scale Sequence-Based Complex Trait Association Studies: Lessons Learned from the NHLBI Exome Sequencing Project by Auer, Paul L., Reiner, Alex P., Wang, Gao, Kang, Hyun Min, Abecasis, Goncalo R., Altshuler, David, Bamshad, Michael J., Nickerson, Deborah A., Tracy, Russell P., Rich, Stephen S., Leal, Suzanne M.

    Published 2016
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  17. 17
    From GWAS variant to function: A study of ∼148,000 variants for blood cell traits

    From GWAS variant to function: A study of ∼148,000 variants for blood cell traits by Sun, Quan, Crowley, Cheynna A., Huang, Le, Wen, Jia, Chen, Jiawen, Bao, Erik L., Auer, Paul L., Lettre, Guillaume, Reiner, Alexander P., Sankaran, Vijay G., Raffield, Laura M., Li, Yun

    Published 2021
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  18. 18
    Pathogenic Variants for Mendelian and Complex Traits in Exomes of 6,517 European and African Americans: Implications for the Return of Incidental Results

    Pathogenic Variants for Mendelian and Complex Traits in Exomes of 6,517 European and African Americans: Implications for the Return of Incidental Results by Tabor, Holly K., Auer, Paul L., Jamal, Seema M., Chong, Jessica X., Yu, Joon-Ho, Gordon, Adam S., Graubert, Timothy A., O’Donnell, Christopher J., Rich, Stephen S., Nickerson, Deborah A., Bamshad, Michael J.

    Published 2014
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  19. 19
    Rare coding variants pinpoint genes that control human hematological traits

    Rare coding variants pinpoint genes that control human hematological traits by Mousas, Abdou, Ntritsos, Georgios, Chen, Ming-Huei, Song, Ci, Huffman, Jennifer E., Tzoulaki, Ioanna, Elliott, Paul, Psaty, Bruce M., Auer, Paul L., Johnson, Andrew D., Evangelou, Evangelos, Lettre, Guillaume, Reiner, Alexander P.

    Published 2017
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  20. 20
    A common TCN1 loss-of-function variant is associated with lower vitamin B(12) concentration in African Americans

    A common TCN1 loss-of-function variant is associated with lower vitamin B(12) concentration in African Americans by Hu, Yao, Raffield, Laura M., Polfus, Linda M., Moscati, Arden, Nadkarni, Girish, Preuss, Michael H., Zhong, Xue, Wei, Qiang, Rich, Stephen S., Li, Yun, Wilson, James G., Correa, Adolfo, Loos, Ruth J. F., Li, Bingshan, Auer, Paul L., Reiner, Alex P.

    Published 2018
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