检索结果 - Paul I.W. de Bakker

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  1. 1
    Interrogating the major histocompatibility complex with high-throughput genomics

    Interrogating the major histocompatibility complex with high-throughput genomics 由 Paul I. W. de Bakker, Soumya Raychaudhuri

    出版 2012
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  2. 2
    Genome‐wide meta‐analysis identifies novel multiple sclerosis susceptibility loci

    Genome‐wide meta‐analysis identifies novel multiple sclerosis susceptibility loci 由 Nikolaos A. Patsopoulos, Paul I.W. de Bakker

    出版 2011
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  3. 3
    Multiethnic Genetic Association Studies Improve Power for Locus Discovery

    Multiethnic Genetic Association Studies Improve Power for Locus Discovery 由 Sara L. Pulit, Benjamin F. Voight, Paul I. W. de Bakker

    出版 2010
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  4. 4
    Resetting the bar: Statistical significance in whole‐genome sequencing‐based association studies of global populations

    Resetting the bar: Statistical significance in whole‐genome sequencing‐based association studies of global populations 由 Sara L. Pulit, Sera A. J. de With, Paul I. W. de Bakker

    出版 2016
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  5. 5
    A general framework for meta-analyzing dependent studies with overlapping subjects in association mapping

    A general framework for meta-analyzing dependent studies with overlapping subjects in association mapping 由 Buhm Han, Dat Duong, Jae Hoon Sul, Paul I. W. de Bakker, Eleazar Eskin, Soumya Raychaudhuri

    出版 2016
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  6. 6
    Behçet disease-associated MHC class I residues implicate antigen binding and regulation of cell-mediated cytotoxicity

    Behçet disease-associated MHC class I residues implicate antigen binding and regulation of cell-mediated cytotoxicity 由 Michael J. Ombrello, Yohei Kirino, Paul I.W. de Bakker, Ahmet Gül, Daniel L. Kastner, Elaine F. Remmers

    出版 2014
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  7. 7
    Practical aspects of imputation-driven meta-analysis of genome-wide association studies

    Practical aspects of imputation-driven meta-analysis of genome-wide association studies 由 Paul I. W. de Bakker, Manuel A. R. Ferreira, Xiaoming Jia, Benjamin M. Neale, Soumya Raychaudhuri, Benjamin F. Voight

    出版 2008
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  8. 8
    Pooled Association Tests for Rare Variants in Exon-Resequencing Studies

    Pooled Association Tests for Rare Variants in Exon-Resequencing Studies 由 Alkes L. Price, Gregory V. Kryukov, Paul I.W. de Bakker, Shaun Purcell, Jeff Staples, L. J. Wei, Shamil Sunyaev

    出版 2010
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  9. 9
    Imputing Amino Acid Polymorphisms in Human Leukocyte Antigens

    Imputing Amino Acid Polymorphisms in Human Leukocyte Antigens 由 Xiaoming Jia, Buhm Han, Suna Önengüt-Gümüşcü, Wei‐Min Chen, Patrick Concannon, Stephen S. Rich, Soumya Raychaudhuri, Paul I. W. de Bakker

    出版 2013
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  10. 10
    SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap

    SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap 由 Andrew D. Johnson, Robert E. Handsaker, Sara L. Pulit, Marcia M. Nizzari, Christopher J. O’Donnell, Paul I. W. de Bakker

    出版 2008
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  11. 11
    Impact of carotid atherosclerosis loci on cardiovascular events

    Impact of carotid atherosclerosis loci on cardiovascular events 由 Daiane Hemerich, Sander W. van der Laan, Vinicius Tragante, Hester M. den Ruijter, Gert J. de Borst, Gerard Pasterkamp, Paul I. W. de Bakker, Folkert W. Asselbergs

    出版 2015
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  12. 12
    <i>TCF7L2</i>Polymorphisms and Progression to Diabetes in the Diabetes Prevention Program

    <i>TCF7L2</i>Polymorphisms and Progression to Diabetes in the Diabetes Prevention Program 由 José C. Florez, Kathleen A. Jablonski, Nick Bayley, Toni I. Pollin, Paul I. W. de Bakker, Alan R. Shuldiner, William C. Knowler, David M. Nathan, David Altshuler

    出版 2006
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  13. 13
    Fine mapping in the MHC region accounts for 18% additional genetic risk for celiac disease

    Fine mapping in the MHC region accounts for 18% additional genetic risk for celiac disease 由 Javier Gutierrez‐Achury, Alexandra Zhernakova, Sara L. Pulit, Gosia Trynka, Karen A. Hunt, Jihane Romanos, Soumya Raychaudhuri, David A. van Heel, Cisca Wijmenga, Paul I. W. de Bakker

    出版 2015
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  14. 14
    Effective Detection of Human Leukocyte Antigen Risk Alleles in Celiac Disease Using Tag Single Nucleotide Polymorphisms

    Effective Detection of Human Leukocyte Antigen Risk Alleles in Celiac Disease Using Tag Single Nucleotide Polymorphisms 由 Alienke J. Monsuur, Paul I. W. de Bakker, Alexandra Zhernakova, Dalila Pinto, Willem Verduijn, Jihane Romanos, Renata Auricchio, Ana López, David A. van Heel, J. Bart A. Crusius, Cisca Wijmenga

    出版 2008
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  15. 15
    Comprehensive Association Testing of Common Mitochondrial DNA Variation in Metabolic Disease

    Comprehensive Association Testing of Common Mitochondrial DNA Variation in Metabolic Disease 由 Richa Saxena, Paul I.W. de Bakker, Karyn Singer, Vamsi K. Mootha, Noël P. Burtt, Joel N. Hirschhorn, Daniel Gaudet, Bo Isomaa, Mark J. Daly, Leif Groop, Kristin Ardlie, David Altshuler

    出版 2006
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  16. 16
    Association Testing of Variants in the Hepatocyte Nuclear Factor 4α Gene With Risk of Type 2 Diabetes in 7,883 People

    Association Testing of Variants in the Hepatocyte Nuclear Factor 4α Gene With Risk of Type 2 Diabetes in 7,883 People 由 Wendy Winckler, Robert Graham, Paul I.W. de Bakker, Maria Sun, Peter Almgren, Jaakko Tuomilehto, Daniel Gaudet, Thomas J. Hudson, Kristin Ardlie, Mark J. Daly, Joel N. Hirschhorn, Leif Groop, David Altshuler

    出版 2005
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  17. 17
    Leveraging Distant Relatedness to Quantify Human Mutation and Gene-Conversion Rates

    Leveraging Distant Relatedness to Quantify Human Mutation and Gene-Conversion Rates 由 Pier Francesco Palamara, Laurent C. Francioli, Peter Wilton, Giulio Genovese, Alexander Gusev, Hilary K. Finucane, Sriram Sankararaman, Shamil Sunyaev, Paul I. W. de Bakker, John Wakeley, Itsik Pe’er, Alkes L. Price

    出版 2015
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  18. 18
    Additive and interaction effects at three amino acid positions in HLA-DQ and HLA-DR molecules drive type 1 diabetes risk

    Additive and interaction effects at three amino acid positions in HLA-DQ and HLA-DR molecules drive type 1 diabetes risk 由 Xinli Hu, Aaron J. Deutsch, Tobias L. Lenz, Suna Önengüt-Gümüşcü, Buhm Han, Wei‐Min Chen, Joanna M. M. Howson, John A. Todd, Paul I. W. de Bakker, Stephen S. Rich, Soumya Raychaudhuri

    出版 2015
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  19. 19
    PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses

    PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses 由 Shaun Purcell, Benjamin M. Neale, Katherine EO Todd-Brown, L. Odong Thomas, Manuel A. R. Ferreira, D.B. Bender, Julian Maller, Pamela Sklar, Paul I. W. de Bakker, Mark J. Daly, Pak C. Sham

    出版 2007
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  20. 20
    Population-specific genotype imputations using minimac or IMPUTE2

    Population-specific genotype imputations using minimac or IMPUTE2 由 Jin‐Moo Lee, Alexandros Kanterakis, Patrick Deelen, Mathijs Kattenberg, P. Eline Slagboom, Paul I. W. de Bakker, Cisca Wijmenga, Morris A. Swertz, Dorret I. Boomsma, Cornelia M. van Duijn, Lennart C. Karssen, Jouke‐Jan Hottenga

    出版 2015
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