2022 - Research.com Best Scientist Award
2022 - Research.com Medicine in Netherlands Leader Award
2022 - Research.com Genetics and Molecular Biology in Netherlands Leader Award
His scientific interests lie mostly in Genome-wide association study, Genetics, Internal medicine, Single-nucleotide polymorphism and Genetic association. His research integrates issues of SNP, Bioinformatics, Case-control study and Quantitative trait locus, Genetic architecture in his study of Genome-wide association study. As a member of one scientific family, André G. Uitterlinden mostly works in the field of Genetics, focusing on Body mass index and, on occasion, Obesity and FTO gene.
His studies examine the connections between Internal medicine and genetics, as well as such issues in Endocrinology, with regards to Polymorphism and Haplotype. His study in Single-nucleotide polymorphism is interdisciplinary in nature, drawing from both Framingham Risk Score and Genetic variation. His Genetic association research includes elements of Imputation, Computational biology, Osteoporosis and Atrial fibrillation.
André G. Uitterlinden mostly deals with Genome-wide association study, Genetics, Internal medicine, Single-nucleotide polymorphism and Genetic association. The Genome-wide association study study combines topics in areas such as Bioinformatics, Case-control study, Meta-analysis, Quantitative trait locus and Minor allele frequency. His study in Genetics concentrates on Gene, Locus, Allele, Candidate gene and Genetic variation.
His Internal medicine research incorporates themes from Endocrinology and Oncology. His Endocrinology study integrates concerns from other disciplines, such as Genotype and Haplotype. His Genetic association study combines topics from a wide range of disciplines, such as Disease and Genetic architecture.
His main research concerns Genome-wide association study, Genetics, Internal medicine, Genetic association and Single-nucleotide polymorphism. His work carried out in the field of Genome-wide association study brings together such families of science as Candidate gene, Medical genetics, Meta-analysis and Quantitative trait locus, Genetic architecture. His Internal medicine research includes themes of Endocrinology and Oncology.
His Genetic association research is multidisciplinary, incorporating perspectives in DNA methylation, Bioinformatics, Disease, Minor allele frequency and Computational biology. André G. Uitterlinden is involved in the study of Single-nucleotide polymorphism that focuses on SNP in particular. André G. Uitterlinden works mostly in the field of Rotterdam Study, limiting it down to topics relating to Bone mineral and, in certain cases, Bone density.
The scientist’s investigation covers issues in Genome-wide association study, Genetics, Genetic association, Medical genetics and Internal medicine. His Genome-wide association study study is related to the wider topic of Single-nucleotide polymorphism. His Single-nucleotide polymorphism study deals with QRS complex intersecting with Cardiac conduction.
The various areas that André G. Uitterlinden examines in his Genetic association study include Genetic correlation, Coronary artery disease, Case-control study, Disease and Minor allele frequency. André G. Uitterlinden has included themes like Pulse pressure, Blood pressure and Mendelian randomization in his Medical genetics study. His Internal medicine course of study focuses on DNA methylation and Body mass index.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Biological, clinical and population relevance of 95 loci for blood lipids
Tanya M. Teslovich;Kiran Musunuru;Albert V. Smith;Andrew C. Edmondson.
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)
Genome-wide association study identifies novel breast cancer susceptibility loci
Douglas F. Easton;Karen A. Pooley;Alison M. Dunning;Paul D. P. Pharoah.
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)
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.
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation
Cristen J. Willer;Elizabeth K. Speliotes;Elizabeth K. Speliotes;Ruth J. F. Loos;Shengxu Li.
Nature Genetics (2009)
Discovery and refinement of loci associated with lipid levels
Cristen J. Willer;Ellen M. Schmidt;Sebanti Sengupta;Gina M. Peloso;Gina M. Peloso;Gina M. Peloso.
Nature Genetics (2013)
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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