Albert V. Smith mainly focuses on Genome-wide association study, Genetics, Genetic association, Internal medicine and Single-nucleotide polymorphism. The various areas that Albert V. Smith examines in his Genome-wide association study study include Odds ratio, Allele, Polymorphism, Disease and Genetic architecture. His research links Body mass index with Genetics.
Albert V. Smith has researched Genetic association in several fields, including Cohort, Case-control study, Meta-analysis, Atrial fibrillation and Femoral neck. His Internal medicine research includes themes of Endocrinology and Cardiology. The study incorporates disciplines such as Lipid metabolism, Genetic variation and Haplotype in addition to Single-nucleotide polymorphism.
His primary areas of study are Genome-wide association study, Genetics, Genetic association, Internal medicine and Single-nucleotide polymorphism. His Genome-wide association study study combines topics from a wide range of disciplines, such as Bioinformatics, Meta-analysis, Quantitative trait locus, Allele and Locus. Gene, Candidate gene, Genetic variation, Genetic architecture and SNP are among the areas of Genetics where the researcher is concentrating his efforts.
His Genetic association study combines topics in areas such as Linkage disequilibrium, Blood pressure, Medical genetics, 1000 Genomes Project and Heritability. His Internal medicine research integrates issues from Diabetes mellitus, Endocrinology, Oncology and Cardiology. His studies in Single-nucleotide polymorphism integrate themes in fields like Body mass index and Polymorphism.
Albert V. Smith focuses on Genome-wide association study, Genetics, Internal medicine, Disease and Genetic architecture. He interconnects Bioinformatics, PR interval, Medical genetics, Blood lipids and Genetic association in the investigation of issues within Genome-wide association study. His Blood pressure research extends to the thematically linked field of Genetics.
The study incorporates disciplines such as Diabetes mellitus, Endocrinology, Single-nucleotide polymorphism and Oncology in addition to Internal medicine. His study in Single-nucleotide polymorphism is interdisciplinary in nature, drawing from both Odds ratio and Allele. His research investigates the link between Disease and topics such as Epidemiology that cross with problems in Cohort and Coronary artery disease.
His main research concerns Genome-wide association study, Genetics, Genetic architecture, Internal medicine and Locus. His Genome-wide association study study integrates concerns from other disciplines, such as Genetic association and Medical genetics. His research in Genetics intersects with topics in Blood lipids, Cholesterol and Lipid metabolism.
His Genetic architecture research includes themes of Caudate nucleus, Neuroscience and Putamen. His Internal medicine study combines topics in areas such as Diabetes mellitus, Oncology and Linoleic acid. His Locus research focuses on Somatic cell and how it relates to Genetic variation, Stem cell, Hematopoietic stem cell and Haematopoiesis.
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Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33)
R C Turner;R R Holman;C A Cull;I M Stratton.
The Lancet (1998)
A haplotype map of the human genome
John W. Belmont;Andrew Boudreau;Suzanne M. Leal;Paul Hardenbol.
Nature (2003)
A second generation human haplotype map of over 3.1 million SNPs
Kelly A. Frazer;Dennis G. Ballinger;David R. Cox;David A. Hinds.
Nature (2007)
Biological, clinical and population relevance of 95 loci for blood lipids
Tanya M. Teslovich;Kiran Musunuru;Albert V. Smith;Andrew C. Edmondson.
Nature (2010)
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
Elizabeth K. Speliotes;Elizabeth K. Speliotes;Cristen J. Willer;Sonja I. Berndt;Keri L. Monda.
Nature Genetics (2010)
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
Jean-Charles Lambert;Jean-Charles Lambert;Jean-Charles Lambert;Carla A Ibrahim-Verbaas;Denise Harold;Adam C Naj.
Nature Genetics (2013)
Genome-wide detection and characterization of positive selection in human populations
Pardis C. Sabeti;Pardis C. Sabeti;Patrick Varilly;Patrick Varilly;Ben Fry;Jason Lohmueller.
(2007)
Hundreds of variants clustered in genomic loci and biological pathways affect human height
Hana Lango Allen;Karol Estrada;Guillaume Lettre;Sonja I. Berndt.
Nature (2010)
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Georg B. Ehret;Georg B. Ehret;Georg B. Ehret;Patricia B. Munroe;Kenneth M. Rice;Murielle Bochud.
Nature (2011)
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Heribert Schunkert;Inke R. König;Sekar Kathiresan;Muredach P. Reilly.
Nature Genetics (2011)
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