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John Blangero

Researcher Next ID · RN-025773

Researcher · Biochemistry, Genetics and Molecular Biology

The University of Texas at San Antonio Health Science Center

San Antonio, Taiwan

Not currently recruitingFunding unknown
Works count
1,163
Citation count
74,909
H-index
119
i10-index
654

Research interests

Biochemistry, Genetics and Molecular Biology
Neuroscience
Medicine
Genetic Associations and Epidemiology
Genetic Mapping and Diversity in Plants and Animals
Genetic and phenotypic traits in livestock
Functional Brain Connectivity Studies
Advanced Neuroimaging Techniques and Applications

Publications

  • Clonal haematopoiesis and risk of chronic liver disease

    Nature · 2023 · https://doi.org/10.1038/s41586-023-05857-4

  • Genetic diversity fuels gene discovery for tobacco and alcohol use

    Nature · 2022 · 10.1038/s41586-022-05477-4

  • Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention

    Nature Genetics · 2022 · https://doi.org/10.1038/s41588-022-01165-1

  • Brain charts for the human lifespan

    Nature · 2022 · https://doi.org/10.1038/s41586-022-04554-y

  • Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

    Nature · 2021 · https://doi.org/10.1038/s41586-021-03205-y

  • A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

    Nature Genetics · 2021 · https://doi.org/10.1038/s41588-021-00935-7

  • Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale

    Nature Genetics · 2020 · https://doi.org/10.1038/s41588-020-0676-4

  • Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale

    Nature Genetics · 2020 · https://doi.org/10.1038/s41588-020-0676-4

  • Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls

    Nature · 2019 · 10.1038/s41586-019-1231-2

  • Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

    PLoS Genetics · 2019 · https://doi.org/10.1371/journal.pgen.1008500

  • Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits

    Nature Communications · 2017 · https://doi.org/10.1038/ncomms14977

  • Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults

    PLoS Genetics · 2017 · 10.1371/journal.pgen.1006528

  • Long-term neural and physiological phenotyping of a single human

    Nature Communications · 2015 · 10.1038/ncomms9885

  • Loss-of-function mutations in SLC30A8 protect against type 2 diabetes

    Nature Genetics · 2014 · https://doi.org/10.1038/ng.2915

  • The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

    Brain Imaging and Behavior · 2014 · https://doi.org/10.1007/s11682-013-9269-5

  • Plasma lipid profiling in a large population-based cohort

    Journal of Lipid Research · 2013 · 10.1194/jlr.p035808

  • Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: A pilot project of the ENIGMA–DTI working group

    NeuroImage · 2013 · 10.1016/j.neuroimage.2013.04.061

  • A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

    Nature Genetics · 2012 · https://doi.org/10.1038/ng.2274

  • Fractional anisotropy of water diffusion in cerebral white matter across the lifespan

    Neurobiology of Aging · 2010 · 10.1016/j.neurobiolaging.2010.01.014

  • Genetic control over the resting brain

    Proceedings of the National Academy of Sciences · 2010 · 10.1073/pnas.0909969107

  • Cortical thickness or grey matter volume? The importance of selecting the phenotype for imaging genetics studies

    NeuroImage · 2009 · 10.1016/j.neuroimage.2009.12.028

  • Discovery of expression QTLs using large-scale transcriptional profiling in human lymphocytes

    Nature Genetics · 2007 · 10.1038/ng2119

  • Genetic variation in selenoprotein S influences inflammatory response

    Nature Genetics · 2005 · 10.1038/ng1655

  • Linkage of Plasma Aβ42 to a Quantitative Locus on Chromosome 10 in Late-Onset Alzheimer's Disease Pedigrees

    Science · 2000 · 10.1126/science.290.5500.2303

  • Quantitative trait loci on chromosomes 3 and 17 influence phenotypes of the metabolic syndrome

    Proceedings of the National Academy of Sciences · 2000 · 10.1073/pnas.97.26.14478

  • Linkage of Type 2 Diabetes Mellitus and of Age at Onset to a Genetic Location on Chromosome 10q in Mexican Americans

    The American Journal of Human Genetics · 1999 · 10.1086/302316

  • An Autosomal Genomic Scan for Loci Linked to Type II Diabetes Mellitus and Body-Mass Index in Pima Indians

    The American Journal of Human Genetics · 1998 · 10.1086/302061

  • Multipoint Quantitative-Trait Linkage Analysis in General Pedigrees

    The American Journal of Human Genetics · 1998 · 10.1086/301844

  • Bivariate quantitative trait linkage analysis: Pleiotropy versus co-incident linkages

    Genetic Epidemiology · 1997 · 10.1002/(sici)1098-2272(1997)14:6<953::aid-gepi65>3.0.co;2-k

  • A major quantitative trait locus determining serum leptin levels and fat mass is located on human chromosome 2

    Nature Genetics · 1997 · 10.1038/ng0397-273

  • Genetic and Environmental Contributions to Cardiovascular Risk Factors in Mexican Americans

    Circulation · 1996 · 10.1161/01.cir.94.9.2159

Current projects

    No projects listed.