2022 - Research.com Best Female Scientist Award
Her primary areas of study are Genetics, Genome-wide association study, Single-nucleotide polymorphism, Genetic association and Internal medicine. Her Genome-wide association study research integrates issues from Polymorphism, DNA methylation, Bioinformatics, Medical genetics and Epigenetics. The various areas that Myriam Fornage examines in her Single-nucleotide polymorphism study include Hyperintensity, Immunology and Allelic heterogeneity.
The Genetic association study combines topics in areas such as Blood pressure, Genotyping, Glucose homeostasis, Human genetics and Genetic architecture. Her study looks at the relationship between Internal medicine and topics such as Endocrinology, which overlap with Case-control study and Mendelian Randomization Analysis. Her Stroke research is multidisciplinary, relying on both Cohort and MEDLINE.
Genetics, Genome-wide association study, Internal medicine, Genetic association and Single-nucleotide polymorphism are her primary areas of study. Her Genetics study frequently draws connections to other fields, such as Blood pressure. Her study looks at the relationship between Genome-wide association study and fields such as Bioinformatics, as well as how they intersect with chemical problems.
Particularly relevant to Stroke is her body of work in Internal medicine. Her Stroke course of study focuses on Epidemiology and Dementia. Her Genetic association research is multidisciplinary, incorporating perspectives in Apolipoprotein E, Disease and Genetic architecture.
Her primary scientific interests are in Genetics, Genome-wide association study, Internal medicine, Genetic association and Gene. The study of Genetics is intertwined with the study of Blood pressure in a number of ways. Her Genome-wide association study study improves the overall literature in Single-nucleotide polymorphism.
Her Internal medicine study combines topics in areas such as Endocrinology, Oncology and Cardiology. Her Genetic association study combines topics from a wide range of disciplines, such as Cognition, Genomics, Imputation, Apolipoprotein E and Epigenome. Her research in Disease focuses on subjects like Bioinformatics, which are connected to Mendelian randomization.
Her scientific interests lie mostly in Genome-wide association study, Genetics, Genetic variation, Genetic architecture and Genetic association. Her Genome-wide association study research is included under the broader classification of Single-nucleotide polymorphism. In her study, which falls under the umbrella issue of Genetic variation, Feces, Host and Genotype is strongly linked to Microbiome.
Her research investigates the connection with Genetic architecture and areas like Genome which intersect with concerns in Epigenetics, Ageing, dNaM and Parental longevity. Myriam Fornage has included themes like Apolipoprotein E, Case-control study, Oncology and Age of onset in her Genetic association study. Her research on Mendelian randomization also deals with topics like
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.
Heart Disease and Stroke Statistics-2018 Update: A Report From the American Heart Association.
Emelia J. Benjamin;Salim S. Virani;Clifton W. Callaway;Alanna M. Chamberlain.
Heart Disease and Stroke Statistics—2019 Update: A Report From the American Heart Association
Emelia J. Benjamin;Paul Muntner;Alvaro Alonso;Marcio S. Bittencourt.
Heart Disease and Stroke Statistics—2017 Update: A Report From the American Heart Association
Emelia J. Benjamin;Michael J. Blaha;Stephanie E. Chiuve;Mary Cushman.
Heart Disease and Stroke Statistics—2020 Update: A Report From the American Heart Association
Salim S. Virani;Alvaro Alonso;Emelia J. Benjamin;Marcio S. Bittencourt.
Association between alcohol and cardiovascular disease:Mendelian randomisation analysis based on individual participant data
Michael V Holmes;Michael V Holmes;Caroline E Dale;Luisa Zuccolo;Richard J Silverwood.
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations
Anna Köttgen;Anna Köttgen;Eva Albrecht;Alexander Teumer;Veronique Vitart.
Nature Genetics (2013)
Genomewide Association Studies of Stroke
M. Arfan Ikram;Sudha Seshadri;Joshua C. Bis;Myriam Fornage.
The New England Journal of Medicine (2009)
HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials.
Daniel I Swerdlow;David Preiss;Karoline B Kuchenbaecker;Michael Holmes.
The Lancet (2015)
DNA methylation-based measures of biological age: meta-analysis predicting time to death
Brian H. Chen;Riccardo E. Marioni;Riccardo E. Marioni;Elena Colicino;Marjolein J. Peters.
Aging (Albany NY) , 8 (9) pp. 1844-1865. (2016) (2016)
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies.
Matthew Traylor;Martin Farrall;Elizabeth G Holliday;Cathie Sudlow.
Lancet Neurology (2012)
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