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Showing 1–9 of 9 results
Advanced filters: Author: David O Willenborg Clear advanced filters

  • Timothy Frayling, Joel Hirschhorn, Peter Visscher and colleagues report a meta-analysis of genome-wide association studies for adult height in 253,288 individuals. They identify 697 variants in 423 loci significantly associated with adult height and find that these variants cluster in pathways involved in growth and together explain one-fifth of the heritability for this trait.

    • Andrew R Wood
    • Tonu Esko
    • Timothy M Frayling
    Research
    Nature Genetics
    Volume: 46, P: 1173-1186

  • Panos Deloukas, Nilesh Samani and colleagues report a large-scale association analysis using the Metabochip array in 63,746 coronary artery disease cases and 130,681 controls. They identify 15 susceptibility loci, refine previous associations and use network analysis to highlight biological pathways.

    • Panos Deloukas
    • Stavroula Kanoni
    • Nilesh J Samani
    Research
    Nature Genetics
    Volume: 45, P: 25-33

  • A genome-wide association study and Metabochip meta-analysis of body mass index (BMI) detects 97 BMI-associated loci, of which 56 were novel, and many loci have effects on other metabolic phenotypes; pathway analyses implicate the central nervous system in obesity susceptibility and new pathways such as those related to synaptic function, energy metabolism, lipid biology and adipogenesis.

    • Adam E. Locke
    • Bratati Kahali
    • Elizabeth K. Speliotes
    Research
    Nature
    Volume: 518, P: 197-206

  • Reduced glomerular filtration rate (eGFR) is a hallmark of chronic kidney disease. Here, Pattaro et al. conduct a meta-analysis to discover several new loci associated with variation in eGFR and find that genes associated with eGFR loci often encode proteins potentially related to kidney development.

    • Cristian Pattaro
    • Alexander Teumer
    • Caroline S. Fox
    ResearchOpen Access
    Nature Communications
    Volume: 7, P: 1-19

  • Nicole Soranzo and colleagues report a meta-analysis of genome-wide association datasets identifying 22 associations to 8 clinically relevant hematological traits. They also identify a long-range haplotype at 12q24 that includes variants associated with platelet counts as well as coronary artery disease and shows evidence of a selective sweep in Europeans.

    • Nicole Soranzo
    • Tim D Spector
    • Christian Gieger
    Research
    Nature Genetics
    Volume: 41, P: 1182-1190

  • Hugh Watkins, Sekar Kathiresan, Ruth McPherson, Martin Farrall and colleagues report the results of a large genome-wide association meta-analysis of coronary artery disease based on 1000 Genomes imputation. They identify ten new risk loci and show that susceptibility to this disease is largely determined by common SNPs with small effect sizes.

    • Majid Nikpay
    • Anuj Goel
    • Martin Farrall
    Research
    Nature Genetics
    Volume: 47, P: 1121-1130

  • During cytokinesis, the intercellular bridge connecting the mother and daughter cell is thinned by a process called secondary ingression before it is eventually severed in an ESCRT-III-dependent manner. Prekeris and colleagues report that FIP3-positive endosomes deliver p50RhoGAP and SCAMP2/3 proteins to the intercellular bridge, which promote actin depolymerization to decrease the bridge diameter and allow ESCRT-III binding.

    • John A. Schiel
    • Glenn C. Simon
    • Rytis Prekeris
    Research
    Nature Cell Biology
    Volume: 14, P: 1068-1078