2023 - Research.com Medicine in Finland Leader Award
2023 - Research.com Genetics in Finland Leader Award
2022 - Research.com Genetics and Molecular Biology in Finland Leader Award
Member of the European Molecular Biology Organization (EMBO)
Leena Peltonen mostly deals with Genetics, Genome-wide association study, Internal medicine, Single-nucleotide polymorphism and Genetic association. Her study in Locus, Allele, Linkage disequilibrium, Haplotype and Gene falls under the purview of Genetics. The concepts of her Genome-wide association study study are interwoven with issues in Odds ratio, Bipolar disorder, Coronary artery disease and Quantitative trait locus.
Her studies in Internal medicine integrate themes in fields like Immunology, Endocrinology and Oncology. Her Single-nucleotide polymorphism research is multidisciplinary, relying on both Lung cancer, Autism, Copy-number variation and Genetic architecture. Her Genetic association research integrates issues from Penetrance, Psychosis and Genetic linkage.
Leena Peltonen mainly investigates Genetics, Gene, Locus, Internal medicine and Genome-wide association study. Her study in Allele, Haplotype, Genetic linkage, Single-nucleotide polymorphism and Linkage disequilibrium are all subfields of Genetics. Her study looks at the intersection of Gene and topics like Molecular biology with Mutation.
Her Locus research is multidisciplinary, incorporating elements of Genetic marker and Gene mapping. Her Internal medicine research incorporates themes from Endocrinology and Cardiology. Her work carried out in the field of Genome-wide association study brings together such families of science as Bipolar disorder and Genetic association.
The scientist’s investigation covers issues in Genetics, Genome-wide association study, Dissolution, Nanotechnology and Internal medicine. As a part of the same scientific study, Leena Peltonen usually deals with the Genetics, concentrating on Bipolar disorder and frequently concerns with Psychosis. Her study in Genome-wide association study is interdisciplinary in nature, drawing from both Quantitative trait locus, Schizophrenia and Genetic association.
Leena Peltonen interconnects Case-control study and Genetic architecture in the investigation of issues within Genetic association. Her research integrates issues of Amorphous solid, Nanocrystal, Particle size, Dissolution testing and Solubility in her study of Dissolution. Her Internal medicine study combines topics from a wide range of disciplines, such as Endocrinology and Cardiology.
The scientist’s investigation covers issues in Genetics, Genome-wide association study, Internal medicine, Nanotechnology and Single-nucleotide polymorphism. Her study in Autism extends to Genetics with its themes. Leena Peltonen has included themes like Genetic association, Locus, DiGeorge syndrome, Genetic variation and Type 2 diabetes in her Genome-wide association study study.
Leena Peltonen has researched Genetic association in several fields, including Genomics, Genetic variability, Computational biology and 1000 Genomes Project. Leena Peltonen combines subjects such as Endocrinology and Cardiology with her study of Internal medicine. The various areas that she examines in her Single-nucleotide polymorphism study include Case-control study, Allele and Genetic architecture.
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.
A global reference for human genetic variation.
Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin.
(2015)
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)
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)
Positionally Cloned Gene for a Novel Glomerular Protein—Nephrin—Is Mutated in Congenital Nephrotic Syndrome
Marjo Kestilä;Ulla Lenkkeri;Minna Männikkö;Jane Lamerdin.
Molecular Cell (1998)
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (vol 42, pg 105, 2010)
J Dupuis;C Langenberg;I Prokopenko;R Saxena.
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.
Nature (2011)
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)
Common genetic determinants of vitamin D insufficiency: a genome-wide association study
Thomas J. Wang;Feng Zhang;J. Brent Richards;Bryan Kestenbaum.
The Lancet (2010)
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)
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
Sekar Kathiresan;Benjamin F Voight;Shaun Purcell;Kiran Musunuru.
Nature Genetics (2009)
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