2022 - Research.com Genetics and Molecular Biology in Finland Leader Award
Samuli Ripatti spends much of his time researching Genome-wide association study, Genetics, Single-nucleotide polymorphism, Genetic association and Internal medicine. His study on Genome-wide association study is covered under Gene. In Genetics, Samuli Ripatti works on issues like Type 2 diabetes, which are connected to Insulin resistance.
His Single-nucleotide polymorphism research includes themes of Odds ratio, Case-control study, Polymorphism and Genetic variation. His Genetic association study which covers Heritability that intersects with Bipolar disorder, Clinical psychology, Major depressive disorder and Genetic heterogeneity. He interconnects Immunology, Endocrinology and Oncology in the investigation of issues within Internal medicine.
Samuli Ripatti mainly investigates Genome-wide association study, Genetics, Internal medicine, Single-nucleotide polymorphism and Genetic association. His Genome-wide association study study also includes fields such as
His Internal medicine research incorporates elements of Endocrinology, Type 2 diabetes, Oncology and Cardiology. The various areas that Samuli Ripatti examines in his Single-nucleotide polymorphism study include Odds ratio and Allele frequency. In his research, Biobank is intimately related to Disease, which falls under the overarching field of Genetic association.
Samuli Ripatti mostly deals with Internal medicine, Genetics, Genome-wide association study, Disease and Genetic architecture. His Internal medicine study integrates concerns from other disciplines, such as Cardiology, Type 2 diabetes and Hyperlipidemia. His Locus, Single-nucleotide polymorphism, Allele, Exome sequencing and Phenotype investigations are all subjects of Genetics research.
Samuli Ripatti has researched Single-nucleotide polymorphism in several fields, including Bioelectrical impedance analysis and Lean body mass. The concepts of his Genome-wide association study study are interwoven with issues in Mendelian randomization, Multivariate statistics, Genetic association, Imputation and Computational biology. His Genetic architecture research incorporates elements of Pleiotropy and Cytokine.
His primary areas of study are Genome-wide association study, Genetics, Internal medicine, Genetic association and Disease. Samuli Ripatti performs integrative Genome-wide association study and CYP2A6 research in his work. His study involves Genetic architecture, Allele, Medical genetics, Locus and Single-nucleotide polymorphism, a branch of Genetics.
His Medical genetics research focuses on subjects like Adiponectin, which are linked to Gene. He focuses mostly in the field of Genetic association, narrowing it down to topics relating to Imputation and, in certain cases, Minor allele frequency, 1000 Genomes Project and Colorectal cancer. His research in Disease focuses on subjects like Biobank, which are connected to Biomarker, Mendelian randomization and Genetic variants.
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)
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.
Plasma HDL cholesterol and risk of myocardial infarction: A mendelian randomisation study
Benjamin F. Voight;Benjamin F. Voight;Benjamin F. Voight;Gina M. Peloso;Gina M. Peloso;Marju Orho-Melander;Ruth Frikke-Schmidt.
web science (2012)
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)
A genome-wide association search for type 2 diabetes genes in African Americans.
N D Palmer;C W McDonough;P J Hicks;B H Roh.
PLOS ONE (2012)
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)
Systematic identification of trans eQTLs as putative drivers of known disease associations
Harm-Jan Westra;Marjolein J Peters;Tõnu Esko;Hanieh Yaghootkar.
Nature Genetics (2013)
Prostate cancer and supplementation with alpha-tocopherol and beta-carotene: incidence and mortality in a controlled trial
Heinonen Op;Albanes D;Virtamo J;Taylor Pr.
Journal of the National Cancer Institute (1998)
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