Andrew P. Morris spends much of his time researching Genome-wide association study, Genetics, Genetic association, Single-nucleotide polymorphism and Genetic architecture. Andrew P. Morris has researched Genome-wide association study in several fields, including Allele frequency, Medical genetics, Glucose homeostasis, Imputation and Type 2 diabetes. The Type 2 diabetes study combines topics in areas such as CDKAL1, Internal medicine and SLC30A8.
In most of his Genetics studies, his work intersects topics such as Body mass index. His studies in Genetic association integrate themes in fields like Multiple comparisons problem, Bioinformatics, Case-control study, Blood pressure and Disease. His Genetic architecture research integrates issues from Common disease-common variant, Minor allele frequency, Genetic predisposition and Allelic heterogeneity.
His main research concerns Genetics, Genome-wide association study, Genetic association, Single-nucleotide polymorphism and Locus. His study on Genetics is mostly dedicated to connecting different topics, such as Type 2 diabetes. His Type 2 diabetes research is multidisciplinary, incorporating elements of Susceptibility locus and Glucose homeostasis.
His Genome-wide association study study incorporates themes from Bioinformatics, Medical genetics, Quantitative trait locus, Internal medicine and Computational biology. His work deals with themes such as Meta-analysis, Disease, Imputation, Minor allele frequency and Genetic variation, which intersect with Genetic association. His Single-nucleotide polymorphism study combines topics in areas such as Exome and Haplotype.
His primary scientific interests are in Genome-wide association study, Genetic association, Genetics, Internal medicine and Locus. His study in Genome-wide association study is interdisciplinary in nature, drawing from both Mendelian randomization, Bioinformatics, Medical genetics, Disease and Atrial fibrillation. His Genetic association research incorporates themes from DNA methylation, Minor allele frequency, Case-control study and Confounding.
His biological study spans a wide range of topics, including Diabetes mellitus, Endocrinology and Cardiology. His research integrates issues of Single-nucleotide polymorphism and Type 2 diabetes in his study of Locus. His Single-nucleotide polymorphism research is multidisciplinary, incorporating perspectives in Odds ratio and Allele.
Andrew P. Morris mainly investigates Genome-wide association study, Genetics, Genetic association, Bioinformatics and Mendelian randomization. His Genome-wide association study study combines topics from a wide range of disciplines, such as Polymorphism, Mendelian Randomization Analysis, Medical genetics, Meta-analysis and Heritability. His work on Genetics is being expanded to include thematically relevant topics such as Pathogenesis.
His work carried out in the field of Genetic association brings together such families of science as Renal function, Case-control study, Disease, Minor allele frequency and Kidney. Andrew P. Morris combines subjects such as Diabetes mellitus genetics, Gene knockdown, Kidney disease, Quantitative trait locus and Regulation of gene expression with his study of Bioinformatics. In Locus, he works on issues like Allele, which are connected to Bioelectrical impedance analysis, Lean body mass and Single-nucleotide polymorphism.
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Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
Paul R. Burton;David G. Clayton;Lon R. Cardon;Nick Craddock.
The International HapMap Project
John W. Belmont;Paul Hardenbol;Thomas D. Willis;Fuli Yu.
A haplotype map of the human genome
John W. Belmont;Andrew Boudreau;Suzanne M. Leal;Paul Hardenbol.
A second generation human haplotype map of over 3.1 million SNPs
Kelly A. Frazer;Dennis G. Ballinger;David R. Cox;David A. Hinds.
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)
Replication of Genome-Wide Association Signals in UK Samples Reveals Risk Loci for Type 2 Diabetes
Eleftheria Zeggini;Michael N Weedon;Cecilia M Lindgren;Timothy M Frayling.
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
Josée Dupuis;Josée Dupuis;Claudia Langenberg;Inga Prokopenko;Richa Saxena;Richa Saxena.
Nature Genetics (2010)
Hundreds of variants clustered in genomic loci and biological pathways affect human height
Hana Lango Allen;Karol Estrada;Guillaume Lettre;Sonja I. Berndt.
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
Benjamin F. Voight;Benjamin F. Voight;Laura J. Scott;Valgerdur Steinthorsdottir;Andrew P. Morris.
Nature Genetics (2010)
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
Andrew P Morris;Benjamin F Voight;Benjamin F Voight;Tanya M Teslovich;Teresa Ferreira.
Nature Genetics (2012)
Profile was last updated on December 6th, 2021.
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