His main research concerns Genetics, Quantitative trait locus, Genetic linkage, Internal medicine and Locus. His is doing research in Genome-wide association study, Gene, Genetic association, Genetic determinism and Single-nucleotide polymorphism, both of which are found in Genetics. His research integrates issues of Pedigree chart, Bivariate analysis, Statistics, Heritability and Linkage in his study of Quantitative trait locus.
His work in Genetic linkage addresses issues such as Genotype, which are connected to fields such as Genetic analysis. His Internal medicine study integrates concerns from other disciplines, such as Endocrinology and Allele. His Locus research includes themes of Diabetes mellitus genetics, Meta-analysis, FTO gene, Gene mapping and Alzheimer's disease.
His scientific interests lie mostly in Genetics, Quantitative trait locus, Internal medicine, Genetic linkage and Endocrinology. His Genetics research focuses on Gene, Locus, Genome-wide association study, Single-nucleotide polymorphism and Genotype. His Single-nucleotide polymorphism research incorporates themes from Genetic variation and Allele.
John Blangero works mostly in the field of Quantitative trait locus, limiting it down to topics relating to Heritability and, in certain cases, Genetic correlation, as a part of the same area of interest. His studies in Internal medicine integrate themes in fields like Diabetes mellitus and Type 2 diabetes. The Genetic linkage study combines topics in areas such as Genetic marker, Chromosome and Microsatellite.
John Blangero spends much of his time researching Genetics, Genome-wide association study, Computational biology, Internal medicine and Heritability. Minor allele frequency, Single-nucleotide polymorphism, Genetic variation, Genetic association and Gene are the subjects of his Genetics studies. His study in Genome-wide association study is interdisciplinary in nature, drawing from both Quantitative trait locus and Bioinformatics.
His Computational biology research is multidisciplinary, incorporating elements of Genome, Whole genome sequencing, Inference, Pedigree chart and Mixed model. His Internal medicine research integrates issues from Endocrinology, Mexican americans and Oncology. His research investigates the connection between Heritability and topics such as Genetic linkage that intersect with issues in Genotype.
His primary areas of study are Genetics, Genome-wide association study, Genetic variation, Locus and Single-nucleotide polymorphism. As a part of the same scientific study, John Blangero usually deals with the Genetics, concentrating on Body mass index and frequently concerns with Carotenoid. His biological study spans a wide range of topics, including Evolutionary biology, Medical genetics, Quantitative trait locus, Genetic association and Imputation.
His Locus research is multidisciplinary, incorporating perspectives in Endocrinology, Germline, Meta-analysis, Internal medicine and Genotype. His Endocrinology course of study focuses on Genome wide linkage and Genetic linkage. His Single-nucleotide polymorphism research incorporates themes from Exome and DISC1.
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Multipoint Quantitative-Trait Linkage Analysis in General Pedigrees
Laura Almasy;John Blangero.
American Journal of Human Genetics (1998)
Defining the role of common variation in the genomic and biological architecture of adult human height
Andrew R. Wood;Tonu Esko;Jian Yang;Sailaja Vedantam.
Nature Genetics (2014)
Genetic studies of body mass index yield new insights for obesity biology
Adam E. Locke;Bratati Kahali;Sonja I. Berndt;Anne E. Justice.
Faculty of Health; Institute of Health and Biomedical Innovation (2015)
Cortical Thickness or Grey Matter Volume? The Importance of Selecting the Phenotype for Imaging Genetics Studies
Anderson M. Winkler;Peter V. Kochunov;John Blangero;Laura Almasy.
Quantitative trait loci on chromosomes 3 and 17 influence phenotypes of the metabolic syndrome
Ahmed H. Kissebah;Gabriele E. Sonnenberg;Joel Myklebust;Michael Goldstein.
Proceedings of the National Academy of Sciences of the United States of America (2000)
The genetic architecture of type 2 diabetes
Christian Fuchsberger;Christian Fuchsberger;Jason A. Flannick;Jason A. Flannick;Tanya M. Teslovich;Anubha Mahajan.
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.
Alisa K. Manning;Alisa K. Manning;Alisa K. Manning;Robert A. Scott;Jonna L. Grimsby.
Nature Genetics (2012)
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants
Lars G. Fritsche;Wilmar Igl;Jessica N.Cooke Bailey;Felix Grassmann.
Nature Genetics (2016)
Discovery of expression QTLs using large-scale transcriptional profiling in human lymphocytes.
Harald H H Göring;Joanne E Curran;Matthew P Johnson;Thomas D Dyer.
Nature Genetics (2007)
Identification of common variants associated with human hippocampal and intracranial volumes
Jason L Stein;Sarah E Medland;Sarah E Medland;Alejandro Arias Vasquez;Alejandro Arias Vasquez;Derrek P Hibar.
Nature Genetics (2012)
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