Tara C. Matise American geneticist
Matise, Tara
VIAF ID: 28970739 (Personal)
Permalink: http://viaf.org/viaf/28970739
Preferred Forms
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Matise, Tara
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Tara C. Matise
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American geneticist
4xx's: Alternate Name Forms (2)
Works
| Title | Sources |
|---|---|
| Association of functional polymorphism rs2231142 (Q141K) in the ABCG2 gene with serum uric acid and gout in 4 US populations: the PAGE Study |
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| Cognitive traits link to human chromosomal regions |
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| Construction of a 5000(rad) whole-genome radiation hybrid panel in the horse and generation of a comprehensive and comparative map for ECA11. |
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| Contrasting methods of quantifying fine structure of human recombination. |
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| Defining the role of common variation in the genomic and biological architecture of adult human height |
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| Enabling Data and Compute Intensive Workflows in Bioinformatics |
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| Enhanced genetic maps from family-based disease studies: population-specific comparisons |
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| Evaluation of the metabochip genotyping array in African Americans and implications for fine mapping of GWAS-identified loci: the PAGE study |
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| Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects |
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| The Future of Genomic Studies Must Be Globally Representative: Perspectives from PAGE |
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| Generalization and dilution of association results from European GWAS in populations of non-European ancestry: the PAGE study |
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| Genetic analyses of diverse populations improves discovery for complex traits |
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| Genetic determinants of age-related macular degeneration in diverse populations from the PAGE study |
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| Genetic Diversity Turns a New PAGE in Our Understanding of Complex Traits |
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| Genetic studies of body mass index yield new insights for obesity biology |
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| Genetics of Chronic Kidney Disease Stages Across Ancestries: The PAGE Study |
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| Genome scan of European-American schizophrenia pedigrees: Results of the NIMH genetics initiative and millennium consortium |
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| Genotype imputation of Metabochip SNPs using a study-specific reference panel of ~4,000 haplotypes in African Americans from the Women's Health Initiative |
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| Imputation of coding variants in African Americans: better performance using data from the exome sequencing project |
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| The influence of obesity-related single nucleotide polymorphisms on BMI across the life course: the PAGE study |
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| Insights into genetics, human biology and disease gleaned from family based genomic studies |
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| Lack of associations of ten candidate coronary heart disease risk genetic variants and subclinical atherosclerosis in four US populations: the Population Architecture using Genomics and Epidemiology |
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| Linkage disequilibrium and inference of ancestral recombination in 538 single-nucleotide polymorphism clusters across the human genome |
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| The map problem: a comparison of genetic and sequence-based physical maps |
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| Mapping and characterization of structural variation in 17,795 human genomes |
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| Mapping genes with longitudinal phenotypes via Bayesian posterior probabilities |
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| Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study |
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| New genetic loci link adipose and insulin biology to body fat distribution |
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| A novel method for analyzing genetic association with longitudinal phenotypes |
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| Nucleotide sequence database policies |
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| The orphan GPCR, Gpr161, regulates the retinoic acid and canonical Wnt pathways during neurulation |
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| Phenome-wide association study |
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| Pleiotropy of cancer susceptibility variants on the risk of non-Hodgkin lymphoma: the PAGE consortium |
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| A second-generation combined linkage physical map of the human genome |
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| Single-variant and multi-variant trend tests for genetic association with next-generation sequencing that are robust to sequencing error. |
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| Strategies for Enriching Variant Coverage in Candidate Disease Loci on a Multiethnic Genotyping Array |
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| Systematic evaluation of map quality: human chromosome 22. |
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| Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained |
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| Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium |
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| When a case is not a case: effects of phenotype misclassification on power and sample size requirements for the transmission disequilibrium test with affected child trios |
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| Widespread RNA editing of embedded alu elements in the human transcriptome |
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