Search Results - "Willer, J."

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    METAL: fast and efficient meta-analysis of genomewide association scans by Willer, Cristen J., Li, Yun, Abecasis, Gonçalo R.

    Published in Bioinformatics (01-09-2010)
    “…METAL provides a computationally efficient tool for meta-analysis of genome-wide association scans, which is a commonly used approach for improving power…”
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    Journal Article
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    Polygenic Risk Scores for Cardiovascular Disease: A Scientific Statement From the American Heart Association by O’Sullivan, Jack W., Raghavan, Sridharan, Marquez-Luna, Carla, Luzum, Jasmine A., Damrauer, Scott M., Ashley, Euan A., O’Donnell, Christopher J., Willer, Cristen J., Natarajan, Pradeep

    Published in Circulation (New York, N.Y.) (23-08-2022)
    “…Cardiovascular disease is the leading contributor to years lost due to disability or premature death among adults. Current efforts focus on risk prediction and…”
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    Genetic variation across the human olfactory receptor repertoire alters odor perception by Trimmer, C., Keller, A., Murphy, N. R., Snyder, L. L., Willer, J. R., Nagai, M. H., Katsanis, N., Vosshall, L. B., Matsunami, H., Mainland, J. D.

    “…Humans use a family of more than 400 olfactory receptors (ORs) to detect odors, but there is currently no model that can predict olfactory perception from…”
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    MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes by Li, Yun, Willer, Cristen J., Ding, Jun, Scheet, Paul, Abecasis, Gonçalo R.

    Published in Genetic epidemiology (01-12-2010)
    “…Genome‐wide association studies (GWAS) can identify common alleles that contribute to complex disease susceptibility. Despite the large number of SNPs assessed…”
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    Unravelling the genetic architecture of human complex traits through whole genome sequencing by Bocher, Ozvan, Willer, Cristen J., Zeggini, Eleftheria

    Published in Nature communications (14-06-2023)
    “…Whole genome sequencing has enabled new insights into the genetic architecture of complex traits, especially through access to low-frequency and rare…”
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    Exploring and visualizing large-scale genetic associations by using PheWeb by Gagliano Taliun, Sarah A., VandeHaar, Peter, Boughton, Andrew P., Welch, Ryan P., Taliun, Daniel, Schmidt, Ellen M., Zhou, Wei, Nielsen, Jonas B., Willer, Cristen J., Lee, Seunggeun, Fritsche, Lars G., Boehnke, Michael, Abecasis, Gonçalo R.

    Published in Nature genetics (01-06-2020)
    “…The ability of investigators to explore their own data by alternating between these two view types, is an increasingly common feature of large-scale…”
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    LocusZoom: regional visualization of genome-wide association scan results by Pruim, Randall J., Welch, Ryan P., Sanna, Serena, Teslovich, Tanya M., Chines, Peter S., Gliedt, Terry P., Boehnke, Michael, Abecasis, Gonçalo R., Willer, Cristen J.

    Published in Bioinformatics (15-09-2010)
    “…Genome-wide association studies (GWAS) have revealed hundreds of loci associated with common human genetic diseases and traits. We have developed a web-based…”
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    GREGOR: evaluating global enrichment of trait-associated variants in epigenomic features using a systematic, data-driven approach by Schmidt, Ellen M, Zhang, Ji, Zhou, Wei, Chen, Jin, Mohlke, Karen L, Chen, Y Eugene, Willer, Cristen J

    Published in Bioinformatics (15-08-2015)
    “…The majority of variation identified by genome wide association studies falls in non-coding genomic regions and is hypothesized to impact regulatory elements…”
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    Genome-scale CRISPR screening for modifiers of cellular LDL uptake by Emmer, Brian T, Sherman, Emily J, Lascuna, Paul J, Graham, Sarah E, Willer, Cristen J, Ginsburg, David

    Published in PLoS genetics (29-01-2021)
    “…Hypercholesterolemia is a causal and modifiable risk factor for atherosclerotic cardiovascular disease. A critical pathway regulating cholesterol homeostasis…”
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    Timing of birth and risk of multiple sclerosis: population based study by Willer, Cristen J, Dyment, David A, Sadovnick, A Dessa, Rothwell, Peter M, Murray, T Jock, Ebers, George C

    Published in BMJ (15-01-2005)
    “…Abstract Objectives To determine if risk of multiple sclerosis (MS) is associated with month of birth in countries in the northern hemisphere and if factors…”
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    Perhexiline activates KLF14 and reduces atherosclerosis by modulating ApoA-I production by Guo, Yanhong, Fan, Yanbo, Zhang, Jifeng, Lomberk, Gwen A, Zhou, Zhou, Sun, Lijie, Mathison, Angela J, Garcia-Barrio, Minerva T, Zhang, Ji, Zeng, Lixia, Li, Lei, Pennathur, Subramaniam, Willer, Cristen J, Rader, Daniel J, Urrutia, Raul, Chen, Y Eugene

    Published in The Journal of clinical investigation (01-10-2015)
    “…Recent genome-wide association studies have revealed that variations near the gene locus encoding the transcription factor Krüppel-like factor 14 (KLF14) are…”
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    The Power of Meta-Analysis in Genome-Wide Association Studies by Panagiotou, Orestis A, Willer, Cristen J, Hirschhorn, Joel N, Ioannidis, John P.A

    “…Meta-analysis of multiple genome-wide association (GWA) studies has become common practice over the past few years. The main advantage of this technique is the…”
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