Jong-Young Lee mainly investigates Genome-wide association study, Genetics, Genetic association, Single-nucleotide polymorphism and Polymorphism. His Genome-wide association study research is multidisciplinary, incorporating perspectives in Internal medicine, Blood pressure, Kidney disease, Renal function and Quantitative trait locus. His Genetics study frequently draws connections between adjacent fields such as Glucose homeostasis.
His research investigates the connection between Genetic association and topics such as Genetic architecture that intersect with problems in Imputation and Medical genetics. His Single-nucleotide polymorphism research is multidisciplinary, relying on both Lipid metabolism, Allele, Bioinformatics and Candidate gene. His Polymorphism research includes elements of CDKAL1, Obesity and Case-control study.
His primary scientific interests are in Internal medicine, Genetics, Genome-wide association study, Single-nucleotide polymorphism and Cardiology. His studies in Internal medicine integrate themes in fields like Endocrinology and Radiology. His Genetics study frequently links to other fields, such as Type 2 diabetes.
Jong-Young Lee works mostly in the field of Genome-wide association study, limiting it down to topics relating to Genetic predisposition and, in certain cases, Breast cancer and Oncology, as a part of the same area of interest. His Single-nucleotide polymorphism research focuses on Allele and how it relates to Genotyping. His Coronary artery disease, Percutaneous coronary intervention, Artery and Intravascular ultrasound study in the realm of Cardiology connects with subjects such as In patient.
His primary areas of study are Internal medicine, Genome-wide association study, Genetics, Single-nucleotide polymorphism and Cardiology. His biological study deals with issues like Endocrinology, which deal with fields such as Intracellular and Mitochondrion. His Genome-wide association study study incorporates themes from Bioinformatics, Allele frequency, Genetic association, Glucose homeostasis and Kidney.
His study in Genetic architecture, Genotype, Exome sequencing, Imputation and Polymorphism are all subfields of Genetics. The concepts of his Single-nucleotide polymorphism study are interwoven with issues in Bone density, Osteoporosis, Allele and Candidate gene. He has researched Cardiology in several fields, including Stent and Surgery.
His scientific interests lie mostly in Genome-wide association study, Genetics, Genetic association, Single-nucleotide polymorphism and Allele. His Genome-wide association study research incorporates elements of Genetic architecture, Locus, Glucose homeostasis, Imputation and Candidate gene. His Genetic architecture study which covers Medical genetics that intersects with Blood pressure, Bioinformatics and Framingham Risk Score.
Kidney is the focus of his Genetics research. His Genetic association research is multidisciplinary, relying on both Body mass index, Genome, Obesity and Polymorphism. His Bone remodeling research extends to the thematically linked field of Single-nucleotide polymorphism.
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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.
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.
Large-scale association analysis identifies new risk loci for coronary artery disease
Panos Deloukas;Stavroula Kanoni;Christina Willenborg;Martin Farrall.
Nature Genetics (2013)
The genetic architecture of type 2 diabetes
Christian Fuchsberger;Christian Fuchsberger;Jason A. Flannick;Jason A. Flannick;Tanya M. Teslovich;Anubha Mahajan.
A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits.
Yoon Shin Cho;Min Jin Go;Young Jin Kim;Jee Yeon Heo.
Nature Genetics (2009)
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.
Anubha Mahajan;Min Jin Go;Weihua Zhang;Jennifer E. Below.
Nature Genetics (2014)
Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians
Yoon Shin Cho;Chien Hsiun Chen;Chien Hsiun Chen;Cheng Hu;Jirong Long.
Nature Genetics (2012)
Mapping human genetic diversity in Asia
Mahmood Ameen Abdulla;Ikhlak Ahmed;Anunchai Assawamakin;Anunchai Assawamakin;Jong Bhak.
Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians
Norihiro Kato;Fumihiko Takeuchi;Yasuharu Tabara;Tanika N. Kelly.
Nature Genetics (2011)
Loss-of-function mutations in SLC30A8 protect against type 2 diabetes
Jason Flannick;Jason Flannick;Gudmar Thorleifsson;Nicola L. Beer;Nicola L. Beer;Suzanne B R Jacobs.
Nature Genetics (2014)
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