Search Results - "Plenge, Robert M."

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    Disciplined approach to drug discovery and early development by Plenge, Robert M

    Published in Science translational medicine (27-07-2016)
    “…Our modern health care system demands therapeutic interventions that improve the lives of patients. Unfortunately, decreased productivity in therapeutics…”
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    Validating therapeutic targets through human genetics by Plenge, Robert M., Scolnick, Edward M., Altshuler, David

    Published in Nature reviews. Drug discovery (01-08-2013)
    “…Key Points Existing preclinical models have a limited ability to test 'therapeutic hypotheses'; that is, whether perturbing a target in a given manner would…”
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    Principal components analysis corrects for stratification in genome-wide association studies by Price, Alkes L, Patterson, Nick J, Plenge, Robert M, Weinblatt, Michael E, Shadick, Nancy A, Reich, David

    Published in Nature genetics (01-08-2006)
    “…Population stratification--allele frequency differences between cases and controls due to systematic ancestry differences-can cause spurious associations in…”
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    Defining the role of the MHC in autoimmunity: a review and pooled analysis by Fernando, Michelle M A, Stevens, Christine R, Walsh, Emily C, De Jager, Philip L, Goyette, Philippe, Plenge, Robert M, Vyse, Timothy J, Rioux, John D

    Published in PLoS genetics (01-04-2008)
    “…The major histocompatibility complex (MHC) is one of the most extensively studied regions in the human genome because of the association of variants at this…”
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    Recent progress in rheumatoid arthritis genetics: one step towards improved patient care by Plenge, Robert M

    Published in Current opinion in rheumatology (01-05-2009)
    “…PURPOSE OF REVIEWRecent human genetic discoveries have increased our understanding of rheumatoid arthritis (RA) susceptibility. These discoveries are reviewed…”
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    The Rheumatoid Arthritis Risk Variant CCR6DNP Regulates CCR6 via PARP-1 by Li, Gang, Cunin, Pierre, Wu, Di, Diogo, Dorothée, Yang, Yu, Okada, Yukinori, Plenge, Robert M, Nigrovic, Peter A

    Published in PLoS genetics (14-09-2016)
    “…Understanding the implications of genome-wide association studies (GWAS) for disease biology requires both identification of causal variants and definition of…”
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    X Chromosome–Inactivation Patterns of 1,005 Phenotypically Unaffected Females by Amos-Landgraf, James M., Cottle, Amy, Plenge, Robert M., Friez, Mike, Schwartz, Charles E., Longshore, John, Willard, Huntington F.

    Published in American journal of human genetics (01-09-2006)
    “…X-chromosome inactivation is widely believed to be random in early female development and to result in a mosaic distribution of cells, approximately half with…”
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    Automatic prediction of rheumatoid arthritis disease activity from the electronic medical records by Lin, Chen, Karlson, Elizabeth W, Canhao, Helena, Miller, Timothy A, Dligach, Dmitriy, Chen, Pei Jun, Perez, Raul Natanael Guzman, Shen, Yuanyan, Weinblatt, Michael E, Shadick, Nancy A, Plenge, Robert M, Savova, Guergana K

    Published in PloS one (16-08-2013)
    “…We aimed to mine the data in the Electronic Medical Record to automatically discover patients' Rheumatoid Arthritis disease activity at discrete rheumatology…”
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    Quantifying missing heritability at known GWAS loci by Gusev, Alexander, Bhatia, Gaurav, Zaitlen, Noah, Vilhjalmsson, Bjarni J, Diogo, Dorothée, Stahl, Eli A, Gregersen, Peter K, Worthington, Jane, Klareskog, Lars, Raychaudhuri, Soumya, Plenge, Robert M, Pasaniuc, Bogdan, Price, Alkes L

    Published in PLoS genetics (01-12-2013)
    “…Recent work has shown that much of the missing heritability of complex traits can be resolved by estimates of heritability explained by all genotyped SNPs…”
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    Analysis and application of European genetic substructure using 300 K SNP information by Tian, Chao, Plenge, Robert M, Ransom, Michael, Lee, Annette, Villoslada, Pablo, Selmi, Carlo, Klareskog, Lars, Pulver, Ann E, Qi, Lihong, Gregersen, Peter K, Seldin, Michael F

    Published in PLoS genetics (2008)
    “…European population genetic substructure was examined in a diverse set of >1,000 individuals of European descent, each genotyped with >300 K SNPs. Both…”
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    Priority index for human genetics and drug discovery by Plenge, Robert M.

    Published in Nature genetics (01-07-2019)
    “…Although human genetics can help identify new drug targets, the best way to prioritize genes as therapeutic targets is uncertain. A new study describes a…”
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