Resultados de procura - Fuchsberger, Christian

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

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

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

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

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

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

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

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

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

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

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

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

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

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Sequencing and imputation in GWAS: Cost‐effective strategies to increase power and genomic coverage across diverse populations por 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

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

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

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

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Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort por 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

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Reference-based phasing using the Haplotype Reference Consortium panel por 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

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

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