2022 - Research.com Best Female Scientist Award
2022 - Research.com Best Scientist Award
2022 - Research.com Genetics and Molecular Biology in United Kingdom Leader Award
Cornelia M. van Duijn focuses on Genetics, Genome-wide association study, Single-nucleotide polymorphism, Internal medicine and Genetic association. Genetics is closely attributed to Body mass index in her study. The concepts of her Genome-wide association study study are interwoven with issues in Bioinformatics, Linkage disequilibrium, Quantitative trait locus, Genetic architecture and Disease.
Cornelia M. van Duijn has researched Single-nucleotide polymorphism in several fields, including Meta-analysis and Coronary artery disease. Her work carried out in the field of Internal medicine brings together such families of science as Endocrinology, Type 2 diabetes and Cardiology. Her Genetic association research is multidisciplinary, incorporating perspectives in Genome and Candidate gene.
The scientist’s investigation covers issues in Genetics, Genome-wide association study, Internal medicine, Single-nucleotide polymorphism and Genetic association. Her research links Disease with Genetics. Disease is represented through her Dementia and Apolipoprotein E research.
Her Genome-wide association study research includes elements of SNP, Polymorphism, Bioinformatics, Quantitative trait locus and Meta-analysis. Her Internal medicine research incorporates themes from Endocrinology, Oncology and Genotype. Her research related to Diabetes mellitus, Type 2 diabetes and Body mass index might be considered part of Endocrinology.
Her main research concerns Genome-wide association study, Genetics, Internal medicine, Disease and Genetic association. In her work, Obesity and Computational biology is strongly intertwined with Mendelian randomization, which is a subfield of Genome-wide association study. Her work in Genetics tackles topics such as Inbreeding which are related to areas like Genetic model.
Her Internal medicine research integrates issues from Diabetes mellitus, Endocrinology and Oncology. Her Disease research is multidisciplinary, incorporating elements of Pathogenesis and Genomics. Her Odds ratio research includes themes of Alzheimer's disease and PRNP.
Her primary areas of investigation include Genome-wide association study, Genetics, Internal medicine, Mendelian randomization and Disease. Her Genome-wide association study study deals with the bigger picture of Gene. Her research in Linkage disequilibrium, Haplotype, HNF1A, Locus and Epigenetics are components of Genetics.
Her work deals with themes such as Endocrinology, Neuroimaging and Open angle glaucoma, which intersect with Internal medicine. Her research integrates issues of Pharmaceutical sciences, Clinical trial and Clinical psychology in her study of Mendelian randomization. Her Disease study combines topics from a wide range of disciplines, such as Telomere, Thyroid cancer, Metabolomics and Medical genetics.
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.
Effects of Age, Sex, and Ethnicity on the Association Between Apolipoprotein E Genotype and Alzheimer Disease: A Meta-analysis
Lindsay A. Farrer;L. Adrienne Cupples;Jonathan L. Haines;Bradley T Hyman.
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)
Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism
Vincenzo Bonifati;Patrizia Rizzu;Marijke J. van Baren;Onno Schaap.
Genetic studies of body mass index yield new insights for obesity biology
Adam E. Locke;Bratati Kahali;Sonja I. Berndt;Anne E. Justice.
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)
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.
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