Genetics, Genome-wide association study, Single-nucleotide polymorphism, Polymorphism and Allele are his primary areas of study. His Genetics study combines topics in areas such as Internal medicine and Case-control study. As a part of the same scientific study, Gudmar Thorleifsson usually deals with the Internal medicine, concentrating on Endocrinology and frequently concerns with SLC30A8, CDKAL1 and TCF7L2.
Gudmar Thorleifsson has included themes like Bioinformatics, Disease, Genetic association, Locus and Genetic architecture in his Genome-wide association study study. Gudmar Thorleifsson interconnects Eye pigmentation, Genetics of obesity and Eye color in the investigation of issues within Single-nucleotide polymorphism. The various areas that Gudmar Thorleifsson examines in his Polymorphism study include SNP, OCA2, Heart disease and Genomic imprinting.
The scientist’s investigation covers issues in Genome-wide association study, Genetics, Internal medicine, Genetic association and Single-nucleotide polymorphism. His Genome-wide association study research is multidisciplinary, relying on both Odds ratio, Bioinformatics, Case-control study, Meta-analysis and Quantitative trait locus. His Genetics study frequently links to other fields, such as Type 2 diabetes.
The concepts of his Internal medicine study are interwoven with issues in Endocrinology, Oncology and Cardiology. The study of Single-nucleotide polymorphism is intertwined with the study of Bone density in a number of ways. His Allele study combines topics from a wide range of disciplines, such as Genetic variation and Genetic predisposition.
His primary areas of investigation include Genome-wide association study, Genetics, Internal medicine, Genetic association and Endocrinology. His study in Genome-wide association study is interdisciplinary in nature, drawing from both Cancer, Minor allele frequency, Allele frequency and Case-control study. His studies link Multiple myeloma with Genetics.
His Internal medicine research includes themes of Missense mutation, Oncology and Cardiology. Single-nucleotide polymorphism covers Gudmar Thorleifsson research in Genetic association. In the field of Endocrinology, his study on Cholesterol and Diabetes mellitus overlaps with subjects such as Non hdl cholesterol and Absorption.
His primary areas of study are Genome-wide association study, Genetics, Internal medicine, Genetic association and Missense mutation. His study with Genome-wide association study involves better knowledge in Genotype. His Genetics research includes elements of Stroke and Renal function.
Internal medicine is closely attributed to Allele in his study. His biological study spans a wide range of topics, including Leiomyoma and Breast cancer. His Case-control study research incorporates elements of Odds ratio, Cancer, Uterine leiomyoma and Bioinformatics.
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Biological, clinical and population relevance of 95 loci for blood lipids
Tanya M. Teslovich;Kiran Musunuru;Albert V. Smith;Andrew C. Edmondson.
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)
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)
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)
Hundreds of variants clustered in genomic loci and biological pathways affect human height
Hana Lango Allen;Karol Estrada;Guillaume Lettre;Sonja I. Berndt.
Rate of de novo mutations and the importance of father’s age to disease risk
Augustine Kong;Michael L. Frigge;Gisli Masson;Soren Besenbacher;Soren Besenbacher.
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)
Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity
Gudmar Thorleifsson;G Bragi Walters;Daniel F Gudbjartsson;Valgerdur Steinthorsdottir.
Nature Genetics (2009)
Genetics of gene expression and its effect on disease
Valur Emilsson;Gudmar Thorleifsson;Bin Zhang;Amy S. Leonardson.
A variant in CDKAL1 influences insulin response and risk of type 2 diabetes.
Valgerdur Steinthorsdottir;Gudmar Thorleifsson;Inga Reynisdottir;Rafn Benediktsson.
Nature Genetics (2007)
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