Søgeresultater - Fuchsberger, Christian

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  1. 1
    Improving power for rare variant tests by integrating external controls

    Improving power for rare variant tests by integrating external controls af Lee, Seunggeun, Kim, Sehee, Fuchsberger, Christian

    Udgivet 2017
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  2. 2
    Combining sequence data from multiple studies: impact of analysis strategies on rare variant calling and association results

    Combining sequence data from multiple studies: impact of analysis strategies on rare variant calling and association results af Chen, Zhongsheng, Boehnke, Michael, Fuchsberger, Christian

    Udgivet 2019
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  3. 3
    minimac2: faster genotype imputation

    minimac2: faster genotype imputation af Fuchsberger, Christian, Abecasis, Gonçalo R., Hinds, David A.

    Udgivet 2015
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  4. 4
    Fast and accurate genotype imputation in genome-wide association studies through pre-phasing

    Fast and accurate genotype imputation in genome-wide association studies through pre-phasing af Howie, Bryan, Fuchsberger, Christian, Stephens, Matthew, Marchini, Jonathan, Abecasis, Gonçalo R.

    Udgivet 2012
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  5. 5
    emeraLD: rapid linkage disequilibrium estimation with massive datasets

    emeraLD: rapid linkage disequilibrium estimation with massive datasets af Quick, Corbin, Fuchsberger, Christian, Taliun, Daniel, Abecasis, Gonçalo, Boehnke, Michael, Kang, Hyun Min

    Udgivet 2019
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  6. 6
    OR05-1 Genetic Discovery and Translational Decision Support from Exome Sequencing of 45,231 Type 2 Diabetes Cases and Controls from Five Ancestries

    OR05-1 Genetic Discovery and Translational Decision Support from Exome Sequencing of 45,231 Type 2 Diabetes Cases and Controls from Five Ancestries af Udler, Miriam, Flannick, Jason, Mercader, Josep, Fuchsberger, Christian, Mahajan, Anubha, Consortium, for the AMP-T2D

    Udgivet 2019
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  7. 7
    Drawing the history of the Hutterite population on a genetic landscape: inference from Y-chromosome and mtDNA genotypes

    Drawing the history of the Hutterite population on a genetic landscape: inference from Y-chromosome and mtDNA genotypes af Pichler, Irene, Fuchsberger, Christian, Platzer, Christa, Çalişkan, Minal, Marroni, Fabio, Pramstaller, Peter P, Ober, Carole

    Udgivet 2010
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  8. 8
    Drawing the history of the Hutterite population on a genetic landscape: inference from Y-chromosome and mtDNA genotypes

    Drawing the history of the Hutterite population on a genetic landscape: inference from Y-chromosome and mtDNA genotypes af Pichler, Irene, Fuchsberger, Christian, Platzer, Christa, Çalişkan, Minal, Marroni, Fabio, Pramstaller, Peter P, Ober, Carole

    Udgivet 2010
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  9. 9
    Genetic association studies for gene expressions: permutation-based mutual information in a comparison with standard ANOVA and as a novel approach for feature selection

    Genetic association studies for gene expressions: permutation-based mutual information in a comparison with standard ANOVA and as a novel approach for feature selection af Szymczak, Silke, Nuzzo, Angelo, Fuchsberger, Christian, Schwarz, Daniel F, Ziegler, Andreas, Bellazzi, Riccardo, Igl, Bernd-Wolfgang

    Udgivet 2007
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  10. 10
    mtDNA-Server: next-generation sequencing data analysis of human mitochondrial DNA in the cloud

    mtDNA-Server: next-generation sequencing data analysis of human mitochondrial DNA in the cloud af Weissensteiner, Hansi, Forer, Lukas, Fuchsberger, Christian, Schöpf, Bernd, Kloss-Brandstätter, Anita, Specht, Günther, Kronenberg, Florian, Schönherr, Sebastian

    Udgivet 2016
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  11. 11
    Evaluation of the role of STAP1 in Familial Hypercholesterolemia

    Evaluation of the role of STAP1 in Familial Hypercholesterolemia af Danyel, Magdalena, Ott, Claus-Eric, Grenkowitz, Thomas, Salewsky, Bastian, Hicks, Andrew A., Fuchsberger, Christian, Steinhagen-Thiessen, Elisabeth, Bobbert, Thomas, Kassner, Ursula, Demuth, Ilja

    Udgivet 2019
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  12. 12
    Meta-imputation: An efficient method to combine genotype data after imputation with multiple reference panels

    Meta-imputation: An efficient method to combine genotype data after imputation with multiple reference panels af Yu, Ketian, Das, Sayantan, LeFaive, Jonathon, Kwong, Alan, Pleiness, Jacob, Forer, Lukas, Schönherr, Sebastian, Fuchsberger, Christian, Smith, Albert Vernon, Abecasis, Gonçalo Rocha

    Udgivet 2022
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  13. 13
    A Common Functional Regulatory Variant at a Type 2 Diabetes Locus Upregulates ARAP1 Expression in the Pancreatic Beta Cell

    A Common Functional Regulatory Variant at a Type 2 Diabetes Locus Upregulates ARAP1 Expression in the Pancreatic Beta Cell af Kulzer, Jennifer R., Stitzel, Michael L., Morken, Mario A., Huyghe, Jeroen R., Fuchsberger, Christian, Kuusisto, Johanna, Laakso, Markku, Boehnke, Michael, Collins, Francis S., Mohlke, Karen L.

    Udgivet 2014
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  14. 14
    Sequencing and imputation in GWAS: Cost‐effective strategies to increase power and genomic coverage across diverse populations

    Sequencing and imputation in GWAS: Cost‐effective strategies to increase power and genomic coverage across diverse populations af Quick, Corbin, Anugu, Pramod, Musani, Solomon, Weiss, Scott T., Burchard, Esteban G., White, Marquitta J., Keys, Kevin L., Cucca, Francesco, Sidore, Carlo, Boehnke, Michael, Fuchsberger, Christian

    Udgivet 2020
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  15. 15
    miR-22 and miR-29a Are Members of the Androgen Receptor Cistrome Modulating LAMC1 and Mcl-1 in Prostate Cancer

    miR-22 and miR-29a Are Members of the Androgen Receptor Cistrome Modulating LAMC1 and Mcl-1 in Prostate Cancer af Pasqualini, Lorenza, Bu, Huajie, Puhr, Martin, Narisu, Narisu, Rainer, Johannes, Schlick, Bettina, Schäfer, Georg, Angelova, Mihaela, Trajanoski, Zlatko, Börno, Stefan T., Schweiger, Michal R., Fuchsberger, Christian, Klocker, Helmut

    Udgivet 2015
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  16. 16
    The Power of Gene-Based Rare Variant Methods to Detect Disease-Associated Variation and Test Hypotheses About Complex Disease

    The Power of Gene-Based Rare Variant Methods to Detect Disease-Associated Variation and Test Hypotheses About Complex Disease af Moutsianas, Loukas, Agarwala, Vineeta, Fuchsberger, Christian, Flannick, Jason, Rivas, Manuel A., Gaulton, Kyle J., Albers, Patrick K., McVean, Gil, Boehnke, Michael, Altshuler, David, McCarthy, Mark I.

    Udgivet 2015
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  17. 17
    Frequency of Heterozygous Parkin (PRKN) Variants and Penetrance of Parkinson's Disease Risk Markers in the Population-Based CHRIS Cohort

    Frequency of Heterozygous Parkin (PRKN) Variants and Penetrance of Parkinson's Disease Risk Markers in the Population-Based CHRIS Cohort af Castelo Rueda, Maria Paulina, Raftopoulou, Athina, Gögele, Martin, Borsche, Max, Emmert, David, Fuchsberger, Christian, Hantikainen, Essi M., Vukovic, Vladimir, Klein, Christine, Pramstaller, Peter P., Pichler, Irene, Hicks, Andrew A.

    Udgivet 2021
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  18. 18
    Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort

    Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort af König, Eva, Rainer, Johannes, Hernandes, Vinicius Verri, Paglia, Giuseppe, Del Greco M., Fabiola, Bottigliengo, Daniele, Yin, Xianyong, Chan, Lap Sum, Teumer, Alexander, Pramstaller, Peter P., Locke, Adam E., Fuchsberger, Christian

    Udgivet 2022
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  19. 19
    Reference-based phasing using the Haplotype Reference Consortium panel

    Reference-based phasing using the Haplotype Reference Consortium panel af Loh, Po-Ru, Danecek, Petr, Palamara, Pier Francesco, Fuchsberger, Christian, Reshef, Yakir A, Finucane, Hilary K, Schoenherr, Sebastian, Forer, Lukas, McCarthy, Shane, Abecasis, Goncalo R, Durbin, Richard, Price, Alkes L

    Udgivet 2016
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  20. 20
    Imputation-Aware Tag SNP Selection To Improve Power for Large-Scale, Multi-ethnic Association Studies

    Imputation-Aware Tag SNP Selection To Improve Power for Large-Scale, Multi-ethnic Association Studies af Wojcik, Genevieve L., Fuchsberger, Christian, Taliun, Daniel, Welch, Ryan, Martin, Alicia R, Shringarpure, Suyash, Carlson, Christopher S., Abecasis, Goncalo, Kang, Hyun Min, Boehnke, Michael, Bustamante, Carlos D., Gignoux, Christopher R., Kenny, Eimear E.

    Udgivet 2018
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