Resultats de la cerca - David Altshuler

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  1. 1
    Once and Again—Issues Surrounding Replication in Genetic Association Studies

    Once and Again—Issues Surrounding Replication in Genetic Association Studies per Joel N. Hirschhorn, David Altshuler

    Publicat 2002
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  2. 2
    Genetic Polymorphisms and Disease

    Genetic Polymorphisms and Disease per David Altshuler, Leonid Kruglyak, Eric S. Lander

    Publicat 1998
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  3. 3
    Quality and completeness of SNP databases

    Quality and completeness of SNP databases per David Reich, Stacey B. Gabriel, David Altshuler

    Publicat 2003
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  4. 4
    Genetic Mapping in Human Disease

    Genetic Mapping in Human Disease per David Altshuler, Mark J. Daly, Eric S. Lander

    Publicat 2008
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  5. 5
    Evaluating empirical bounds on complex disease genetic architecture

    Evaluating empirical bounds on complex disease genetic architecture per Vineeta Agarwala, Jason Flannick, Shamil Sunyaev, David Altshuler

    Publicat 2013
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  6. 6
    Common Inherited Variation in Mitochondrial Genes Is Not Enriched for Associations with Type 2 Diabetes or Related Glycemic Traits

    Common Inherited Variation in Mitochondrial Genes Is Not Enriched for Associations with Type 2 Diabetes or Related Glycemic Traits per Ayellet V. Segrè, Leif Groop, Vamsi K. Mootha, Mark J. Daly, David Altshuler

    Publicat 2010
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  7. 7
    Calibrating a coalescent simulation of human genome sequence variation

    Calibrating a coalescent simulation of human genome sequence variation per S. F. Schaffner, Catherine K. Foo, Stacey Gabriel, David Reich, Mark J. Daly, David Altshuler

    Publicat 2005
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  8. 8
    Accurately Assessing the Risk of Schizophrenia Conferred by Rare Copy-Number Variation Affecting Genes with Brain Function

    Accurately Assessing the Risk of Schizophrenia Conferred by Rare Copy-Number Variation Affecting Genes with Brain Function per Soumya Raychaudhuri, Joshua M. Korn, Steven A. McCarroll, David Altshuler, Pamela Sklar, Shaun Purcell, Mark J. Daly

    Publicat 2010
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  9. 9
    Challenges and standards in integrating surveys of structural variation

    Challenges and standards in integrating surveys of structural variation per Stephen W. Scherer, Charles Lee, Ewan Birney, David Altshuler, Evan E. Eichler, Nigel P. Carter, Matthew E. Hurles, Lars Feuk

    Publicat 2007
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  10. 10
    Systematic Evaluation of Genetic Variation at the Androgen Receptor Locus and Risk of Prostate Cancer in a Multiethnic Cohort Study

    Systematic Evaluation of Genetic Variation at the Androgen Receptor Locus and Risk of Prostate Cancer in a Multiethnic Cohort Study per Matthew L. Freedman, Celeste Leigh Pearce, Kathryn L. Penney, Joel N. Hirschhorn, Laurence N. Kolonel, Brian E. Henderson, David Altshuler

    Publicat 2004
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  11. 11
    Clinical Risk Factors, DNA Variants, and the Development of Type 2 Diabetes

    Clinical Risk Factors, DNA Variants, and the Development of Type 2 Diabetes per Valeriya Lyssenko, Anna Jonsson, Peter Almgren, Nicolò Pulizzi, Bo Isomaa, Jaakko Tuomilehto, Göran Berglund, David Altshuler, Peter M. Nilsson, Leif Groop

    Publicat 2008
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  12. 12
    Whole population, genome-wide mapping of hidden relatedness

    Whole population, genome-wide mapping of hidden relatedness per Alexander Gusev, Jennifer K. Lowe, Markus Stoffel, Mark J. Daly, David Altshuler, Jan L. Breslow, Jeffrey M. Friedman, Itsik Pe’er

    Publicat 2008
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  13. 13
    Current State and Future Prospects of Immunotherapy for Glioma

    Current State and Future Prospects of Immunotherapy for Glioma per Neha Kamran, Mahmoud S. Alghamri, Felipe J. Núñez, Diana Shah, Antonela S. Asad, Marianela Candolfi, David Altshuler, Pedro R. Löwenstein, María G. Castro

    Publicat 2018
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  14. 14
    High-Throughput Luminescent Reporter of Insulin Secretion for Discovering Regulators of Pancreatic Beta-Cell Function

    High-Throughput Luminescent Reporter of Insulin Secretion for Discovering Regulators of Pancreatic Beta-Cell Function per Sean M. Burns, Amedeo Vetere, Deepika Walpita, Vlado Dančík, Carol Khodier, José R. Perez, Paul A. Clemons, Bridget K. Wagner, David Altshuler

    Publicat 2015
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  15. 15
    The Pro12Ala variant at the peroxisome proliferator-activated receptor γ gene and change in obesity-related traits in the Diabetes Prevention Program

    The Pro12Ala variant at the peroxisome proliferator-activated receptor γ gene and change in obesity-related traits in the Diabetes Prevention Program per Paul W. Franks, K. A. Jablonski, Linda M. Delahanty, Robert L. Hanson, Steven E. Kahn, David Altshuler, William C. Knowler, José C. Florez

    Publicat 2007
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  16. 16
    Testing of diabetes-associated WFS1 polymorphisms in the Diabetes Prevention Program

    Testing of diabetes-associated WFS1 polymorphisms in the Diabetes Prevention Program per José C. Florez, K. A. Jablonski, J. B. McAteer, Manjinder S. Sandhu, Nicholas J. Wareham, Inês Barroso, Paul W. Franks, David Altshuler, William C. Knowler

    Publicat 2007
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  17. 17
    DASH: A Method for Identical-by-Descent Haplotype Mapping Uncovers Association with Recent Variation

    DASH: A Method for Identical-by-Descent Haplotype Mapping Uncovers Association with Recent Variation per Alexander Gusev, Eimear E. Kenny, Jennifer K. Lowe, Jaqueline Salit, Richa Saxena, Sekar Kathiresan, David Altshuler, Jeffrey M. Friedman, Jan L. Breslow, Itsik Pe’er

    Publicat 2011
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  18. 18
    Identifying Relationships among Genomic Disease Regions: Predicting Genes at Pathogenic SNP Associations and Rare Deletions

    Identifying Relationships among Genomic Disease Regions: Predicting Genes at Pathogenic SNP Associations and Rare Deletions per Soumya Raychaudhuri, Robert M. Plenge, Elizabeth J. Rossin, Aylwin Ng, Shaun Purcell, Pamela Sklar, Edward M. Scolnick, Ramnik J. Xavier, David Altshuler, Mark J. Daly

    Publicat 2009
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  19. 19
    Testing for an Unusual Distribution of Rare Variants

    Testing for an Unusual Distribution of Rare Variants per Benjamin M. Neale, Manuel A. Rivas, Benjamin F. Voight, David Altshuler, Bernie Devlin, Marju Orho‐Melander, Sekar Kathiresan, Shaun Purcell, Kathryn Roeder, Mark J. Daly

    Publicat 2011
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  20. 20
    Type 2 Diabetes–Associated Missense Polymorphisms <i>KCNJ11</i> E23K and <i>ABCC8</i> A1369S Influence Progression to Diabetes and Response to Interventions in the Diabetes Prevention Program

    Type 2 Diabetes–Associated Missense Polymorphisms <i>KCNJ11</i> E23K and <i>ABCC8</i> A1369S Influence Progression to Diabetes and Response to Interventions in the Diabetes Prevent... per José C. Florez, Kathleen A. Jablonski, Steven E. Kahn, Paul W. Franks, Dana Dabelea, Richard F. Hamman, William C. Knowler, David M. Nathan, David Altshuler

    Publicat 2007
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