检索结果 - Eric Boerwinkle

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  1. 1
    A three codon insertion/deletion polymorphism in the signal peptide region of the human apolipoprotein B (APOB) gene directly typed by the polymerase chain reaction

    A three codon insertion/deletion polymorphism in the signal peptide region of the human apolipoprotein B (APOB) gene directly typed by the polymerase chain reaction 由 Eric Boerwinkle, Lawrence Chan

    出版 1989
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  2. 2
    Neighboring-Nucleotide Effects on Single Nucleotide Polymorphisms: A Study of 2.6 Million Polymorphisms Across the Human Genome

    Neighboring-Nucleotide Effects on Single Nucleotide Polymorphisms: A Study of 2.6 Million Polymorphisms Across the Human Genome 由 Zhongming Zhao, Eric Boerwinkle

    出版 2002
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  3. 3
    The use of measured genotype information in the analysis of quantitative phenotypes in man.

    The use of measured genotype information in the analysis of quantitative phenotypes in man. 由 Eric Boerwinkle, Charles F. Sing

    出版 1987
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  4. 4
    In silico tools for splicing defect prediction: a survey from the viewpoint of end users

    In silico tools for splicing defect prediction: a survey from the viewpoint of end users 由 Xueqiu Jian, Eric Boerwinkle, Xiaoming Liu

    出版 2013
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  5. 5
    Generalized T2 Test for Genome Association Studies

    Generalized T2 Test for Genome Association Studies 由 Momiao Xiong, Jinying Zhao, Eric Boerwinkle

    出版 2002
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  6. 6
    dbNSFP v2.0: A Database of Human Non-synonymous SNVs and Their Functional Predictions and Annotations

    dbNSFP v2.0: A Database of Human Non-synonymous SNVs and Their Functional Predictions and Annotations 由 Xiaoming Liu, Xueqiu Jian, Eric Boerwinkle

    出版 2013
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  7. 7
    dbNSFP: A lightweight database of human nonsynonymous SNPs and their functional predictions

    dbNSFP: A lightweight database of human nonsynonymous SNPs and their functional predictions 由 Xiaoming Liu, Xueqiu Jian, Eric Boerwinkle

    出版 2011
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  8. 8
    In silico prediction of splice-altering single nucleotide variants in the human genome

    In silico prediction of splice-altering single nucleotide variants in the human genome 由 Xueqiu Jian, Eric Boerwinkle, Xiaoming Liu

    出版 2014
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  9. 9
    Association studies for next-generation sequencing

    Association studies for next-generation sequencing 由 Li Luo, Eric Boerwinkle, Momiao Xiong

    出版 2011
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  10. 10
    The use of measured genotype information in the analysis of quantitative phenotypes in man

    The use of measured genotype information in the analysis of quantitative phenotypes in man 由 Eric Boerwinkle, Ranajit Chakraborty, Charles F. Sing

    出版 1986
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  11. 11
    High-throughput multiplex SNP genotyping with MALDI-TOF mass spectrometry: Practice, problems and promise

    High-throughput multiplex SNP genotyping with MALDI-TOF mass spectrometry: Practice, problems and promise 由 Molly S. Bray, Eric Boerwinkle, Peter A. Doris

    出版 2001
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  12. 12
    Personalized Medicine for High Blood Pressure

    Personalized Medicine for High Blood Pressure 由 Stephen T. Turner, Gary L. Schwartz, Eric Boerwinkle

    出版 2007
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  13. 13
    Lack of Association of 3 Functional Gene Variants With Hypertension in African Americans

    Lack of Association of 3 Functional Gene Variants With Hypertension in African Americans 由 Nicole Larson, Richard G. Hutchinson, Eric Boerwinkle

    出版 2000
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  14. 14
    A Cladistic Analysis of Phenotypic Associations With Haplotypes Inferred From Restriction Endonuclease Mapping. I. Basic Theory and an Analysis of Alcohol Dehydrogenase Activity in Drosophila

    A Cladistic Analysis of Phenotypic Associations With Haplotypes Inferred From Restriction Endonuclease Mapping. I. Basic Theory and an Analysis of Alcohol Dehydrogenase Activity in... 由 Alan R. Templeton, Eric Boerwinkle, Charles F. Sing

    出版 1987
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  15. 15
    dbNSFP v3.0: A One-Stop Database of Functional Predictions and Annotations for Human Nonsynonymous and Splice-Site SNVs

    dbNSFP v3.0: A One-Stop Database of Functional Predictions and Annotations for Human Nonsynonymous and Splice-Site SNVs 由 Xiaoming Liu, Chunlei Wu, Chang Li, Eric Boerwinkle

    出版 2015
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  16. 16
    Generating a robust statistical causal structure over 13 cardiovascular disease risk factors using genomics data

    Generating a robust statistical causal structure over 13 cardiovascular disease risk factors using genomics data 由 Azam Yazdani, Akram Yazdani, Ahmad Samiei, Eric Boerwinkle

    出版 2016
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  17. 17
    VNTR allele frequency distributions under the stepwise mutation model: a computer simulation approach.

    VNTR allele frequency distributions under the stepwise mutation model: a computer simulation approach. 由 Mark D. Shriver, Jin Li, Ranajit Chakraborty, Eric Boerwinkle

    出版 1993
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  18. 18
    Rapid typing of tandemly repeated hypervariable loci by the polymerase chain reaction: application to the apolipoprotein B 3' hypervariable region.

    Rapid typing of tandemly repeated hypervariable loci by the polymerase chain reaction: application to the apolipoprotein B 3' hypervariable region. 由 Eric Boerwinkle, WanLong Xiong, Eric Fourest, Lawrence Chan

    出版 1989
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  19. 19
    Variation at the M235T locus of the angiotensinogen gene and essential hypertension: a population-based case-control study from Rochester, Minnesota

    Variation at the M235T locus of the angiotensinogen gene and essential hypertension: a population-based case-control study from Rochester, Minnesota 由 Myriam Fornage, StephenT. Turner, Charles F. Sing, Eric Boerwinkle

    出版 1995
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  20. 20
    Direct Estimates of the Genomic Contributions to Blood Pressure Heritability within a Population-Based Cohort (ARIC)

    Direct Estimates of the Genomic Contributions to Blood Pressure Heritability within a Population-Based Cohort (ARIC) 由 Elias Salfati, Alanna C. Morrison, Eric Boerwinkle, Aravinda Chakravarti

    出版 2015
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