The scientist’s investigation covers issues in Genome-wide association study, Genetics, Internal medicine, Single-nucleotide polymorphism and Genetic association. His Genome-wide association study research is multidisciplinary, incorporating perspectives in Gout, Bioinformatics, SLC22A12, Locus and Genetic variation. The Genetics study combines topics in areas such as Hyperuricemia and Cohort.
His work carried out in the field of Internal medicine brings together such families of science as Endocrinology and SLC2A9. The concepts of his Endocrinology study are interwoven with issues in Framingham Heart Study, Biochemistry and Allele. His Single-nucleotide polymorphism research is multidisciplinary, relying on both Statistical hypothesis testing, Univariate and Disease.
His primary areas of study are Genome-wide association study, Internal medicine, Genetics, Framingham Heart Study and Genetic association. To a larger extent, Qiong Yang studies Single-nucleotide polymorphism with the aim of understanding Genome-wide association study. His Internal medicine research is multidisciplinary, incorporating elements of Endocrinology and Oncology.
His biological study spans a wide range of topics, including Body mass index, Odds ratio, Cohort study, Prospective cohort study and Cohort. Qiong Yang combines subjects such as Apolipoprotein E and 1000 Genomes Project with his study of Genetic association. He interconnects Creatinine and Kidney in the investigation of issues within Renal function.
His scientific interests lie mostly in Genome-wide association study, Internal medicine, Disease, Genetic association and Genetics. His studies deal with areas such as Cerebral cortex, Parietal lobe, Neuroscience and Pathology as well as Genome-wide association study. His Internal medicine research is multidisciplinary, incorporating perspectives in Gastroenterology, Single-nucleotide polymorphism and Cardiology.
His research in Disease intersects with topics in Evolutionary biology, Heritability, Biobank, Bioinformatics and Genetic heterogeneity. The study incorporates disciplines such as Apolipoprotein E, Allele and Medical genetics in addition to Genetic association. His work on Renal function expands to the thematically related Genetics.
Qiong Yang mainly investigates Genetics, Genome-wide association study, Bioinformatics, Gene and Genetic association. As part of his studies on Genetics, Qiong Yang frequently links adjacent subjects like Renal function. He has researched Genome-wide association study in several fields, including Kidney metabolism, Genetic marker, HNF1A, Neuroscience and Genetic architecture.
The concepts of his Bioinformatics study are interwoven with issues in Gene prioritization, Dementia and Amyloid. When carried out as part of a general Gene research project, his work on Genetic etiology, Pleiotropy and Gene expression is frequently linked to work in Temporal lobe, therefore connecting diverse disciplines of study. His Genetic association study incorporates themes from Diabetes mellitus genetics, Gene knockdown, Medical genetics, Albuminuria and Regulation of gene expression.
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.
Common variants at 30 loci contribute to polygenic dyslipidemia.
Sekar Kathiresan;Sekar Kathiresan;Sekar Kathiresan;Cristen J. Willer;Gina M. Peloso;Serkalem Demissie.
Nature Genetics (2009)
The Third Generation Cohort of the National Heart, Lung, and Blood Institute's Framingham Heart Study: Design, Recruitment, and Initial Examination
Greta Lee Splansky;Diane Corey;Qiong Yang;Larry D. Atwood.
American Journal of Epidemiology (2007)
New loci associated with kidney function and chronic kidney disease
Anna Köttgen;Anna Köttgen;Cristian Pattaro;Carsten A. Böger;Christian Fuchsberger.
Nature Genetics (2010)
Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study
Abbas Dehghan;Anna Köttgen;Qiong Yang;Shih Jen Hwang.
The Lancet (2008)
Multiple loci associated with indices of renal function and chronic kidney disease
Anna Köttgen;Nicole L. Glazer;Abbas Dehghan;Shih Jen Hwang.
Nature Genetics (2009)
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)
Novel Associations of Multiple Genetic Loci With Plasma Levels of Factor VII, Factor VIII, and von Willebrand Factor The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium
Nicholas L. Smith;Ming Huei Chen;Abbas Dehghan;David P. Strachan.
Circulation (2010)
Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
Santhi K. Ganesh;Santhi K. Ganesh;Neil A. Zakai;Frank J A Van Rooij;Nicole Soranzo;Nicole Soranzo.
Nature Genetics (2009)
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
Rebecca Sims;Sven J. Van Der Lee;Adam C. Naj;Céline Bellenguez;Céline Bellenguez.
Nature Genetics (2017)
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