2022 - Research.com Best Female Scientist Award
2022 - Research.com Best Scientist Award
2022 - Research.com Medicine in Iceland Leader Award
2022 - Research.com Genetics and Molecular Biology in Iceland Leader Award
Unnur Thorsteinsdottir focuses on Genetics, Genome-wide association study, Single-nucleotide polymorphism, Allele and Genetic association. Her research integrates issues of Body mass index and Glucose homeostasis in her study of Genetics. The concepts of her Genome-wide association study study are interwoven with issues in Endocrinology, Internal medicine, Locus, Type 2 diabetes and Genetic architecture.
Unnur Thorsteinsdottir has researched Single-nucleotide polymorphism in several fields, including Human genome, Copy-number variation, Case-control study, Autism and Cholesterol. Her Allele research is multidisciplinary, incorporating elements of Disease and Immunology. Her Genetic association study also includes fields such as
Unnur Thorsteinsdottir mostly deals with Genetics, Genome-wide association study, Internal medicine, Genetic association and Single-nucleotide polymorphism. Her Genetics study focuses on Allele, Gene, Locus, Genotype and Linkage disequilibrium in particular. Her research combines Genetic variation and Allele.
Her research on Genome-wide association study also deals with topics like
Her primary areas of study are Genome-wide association study, Genetics, Internal medicine, Genetic association and Bioinformatics. Her studies deal with areas such as Missense mutation, Heart failure, Coronary artery disease, Disease and Atrial fibrillation as well as Genome-wide association study. Her research related to Allele, Gene, Locus, Genetic architecture and Genotype might be considered part of Genetics.
Unnur Thorsteinsdottir interconnects Bioelectrical impedance analysis, Lean body mass and Single-nucleotide polymorphism in the investigation of issues within Locus. The study incorporates disciplines such as Endocrinology, Oncology and Cardiology in addition to Internal medicine. Her work deals with themes such as Quantitative trait locus, Type 2 diabetes and Homeostasis, which intersect with Genetic association.
Unnur Thorsteinsdottir mainly investigates Genetics, Genome-wide association study, Allele, Internal medicine and Phenotype. Her study in Genetics is interdisciplinary in nature, drawing from both PCSK9 and Genetic diversity. Her Genome-wide association study research integrates issues from Immunology, Pathogenesis, Bioinformatics, Case-control study and Atrial fibrillation.
Her Bioinformatics research focuses on Mendelian Randomization Analysis and how it connects with Heart failure and Genetic association. Her research in Allele intersects with topics in Bioelectrical impedance analysis, Lean body mass, Single-nucleotide polymorphism and Locus. In her study, which falls under the umbrella issue of Internal medicine, Odds ratio is strongly linked to Endocrinology.
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.
Nature (2010)
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)
Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes.
Struan F. A. Grant;Gudmar Thorleifsson;Inga Reynisdottir;Rafil Benediktsson.
Nature Genetics (2006)
Erratum: Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer (Nature Genetics (2009) 41 (991-995))
Xifeng Wu;Yuanqing Ye;Lambertus A. Kiemeney;Patrick Sulem.
Nature Genetics (2009)
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
E Zeggini;L J Scott;R Saxena;B F Voight.
Nature Genetics (2008)
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.
Nature (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)
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)
Large recurrent microdeletions associated with schizophrenia
Hreinn Stefansson;Dan Rujescu;Sven Cichon;Olli P. H. Pietilainen.
Nature (2008)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
deCODE Genetics (Iceland)
deCODE Genetics (Iceland)
deCODE Genetics (Iceland)
deCODE Genetics (Iceland)
University of Oxford
Erasmus University Rotterdam
Finnish Institute for Health and Welfare
University of Oxford
King's College London
Harvard University
Virginia Tech
Salesforce (United States)
University at Buffalo, State University of New York
Government College University, Lahore
Karolinska Institute
Michigan State University
University of Otago
Yale University
Ottawa Hospital
University of Bristol
University of Queensland
National Institute of Geophysics and Volcanology
Stanford University
National Institutes of Health
University of Freiburg
Leiden University