His main research concerns Genetics, Internal medicine, Endocrinology, Genome-wide association study and Longevity. His Genetics study deals with Population genetics intersecting with Gene flow. As a part of the same scientific family, Gil Atzmon mostly works in the field of Endocrinology, focusing on Ashkenazi jews and, on occasion, National Health and Nutrition Examination Survey and Thyroid-stimulating hormone.
His biological study spans a wide range of topics, including Exome sequencing, Allele, Haplotype, Genetic association and Genetic architecture. His Longevity research integrates issues from Offspring, Body mass index and Cohort. His research investigates the connection with Imputation and areas like Common disease-common variant which intersect with concerns in Exome.
Gil Atzmon focuses on Genetics, Longevity, Internal medicine, Genome-wide association study and Endocrinology. His study in Single-nucleotide polymorphism, Gene, Genotype, Exome sequencing and Allele is carried out as part of his studies in Genetics. His research in Single-nucleotide polymorphism intersects with topics in Locus and Haplotype.
Gil Atzmon combines subjects such as Offspring, Ashkenazi jews and Cohort with his study of Longevity. His Internal medicine research incorporates themes from Pregnancy, Type 2 diabetes and Oncology. His studies in Genome-wide association study integrate themes in fields like SNP, Allele frequency, Genetic association, Genetic variation and Genetic architecture.
His scientific interests lie mostly in Genetics, Longevity, Genome-wide association study, Gene and Founder effect. Genetics is closely attributed to Type 2 diabetes in his work. His study in Longevity is interdisciplinary in nature, drawing from both Telomere, Odds, Evolutionary biology and Genomics.
His Odds study integrates concerns from other disciplines, such as Allele and Genetic association. His Genome-wide association study study incorporates themes from Child and adolescent psychiatry, Allele frequency, Meta-analysis, Drug discovery and Genetic architecture. His research integrates issues of Ashkenazi jews, Cohort and Mutation in his study of Offspring.
His primary areas of investigation include Longevity, Odds, Genetics, Allele and Genetic association. The study of Longevity is intertwined with the study of Offspring in a number of ways. His Genetics study is mostly concerned with Genetic architecture, Genome-wide association study, Telomere, Biomarker and Methylation.
His work carried out in the field of Genetic architecture brings together such families of science as Genetic correlation, Percentile, Meta-analysis, Tourette's syndrome and Tourette syndrome. His Genome-wide association study study combines topics from a wide range of disciplines, such as Child and adolescent psychiatry and Copy-number variation. His Allele research includes themes of Odds ratio, Apolipoprotein E and Genetic genealogy.
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Age-Related Clonal Hematopoiesis Associated with Adverse Outcomes
Siddhartha Jaiswal;Pierre Fontanillas;Jason Flannick;Jason Flannick;Alisa Manning.
The New England Journal of Medicine (2014)
The genetic architecture of type 2 diabetes
Christian Fuchsberger;Christian Fuchsberger;Jason A. Flannick;Jason A. Flannick;Tanya M. Teslovich;Anubha Mahajan.
Functionally significant insulin-like growth factor I receptor mutations in centenarians
Yousin Suh;Gil Atzmon;Mi Ook Cho;David Hwang.
Proceedings of the National Academy of Sciences of the United States of America (2008)
Unique Lipoprotein Phenotype and Genotype Associated With Exceptional Longevity
Nir Barzilai;Gil Atzmon;Clyde Schechter;Ernst J. Schaefer.
Removal of visceral fat prevents insulin resistance and glucose intolerance of aging: An adipokine-mediated process?
Ilan Gabriely;Xiao Hui Ma;Xiao Man Yang;Gil Atzmon.
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)
Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico
A. L. Williams Amy;A. L. Williams Amy;S. B R Jacobs Suzanne;Hortensia Moreno-Macías;Alicia Huerta-Chagoya.
Association of common genetic variation in the insulin/IGF1 signaling pathway with human longevity.
Ludmila Pawlikowska;Donglei Hu;Scott Huntsman;Andrew Sung.
Aging Cell (2009)
Association Between a Functional Variant of the KLOTHO Gene and High-Density Lipoprotein Cholesterol, Blood Pressure, Stroke, and Longevity
Dan E. Arking;Gil Atzmon;Albert Arking;Nir Barzilai.
Circulation Research (2005)
Genetic variation in human telomerase is associated with telomere length in Ashkenazi centenarians
Gil Atzmon;Miook Cho;Richard M. Cawthon;Temuri Budagov.
Proceedings of the National Academy of Sciences of the United States of America (2010)
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