2014 - Fellow of the Royal Society of Canada Academy of Science
Genetics, Genome-wide association study, Gene, Allele and Single-nucleotide polymorphism are his primary areas of study. His research on Genetics often connects related topics like Molecular biology. His Genome-wide association study research incorporates elements of Linkage disequilibrium, Case-control study, Allele frequency, Cohort and SLC30A8.
The Allelic heterogeneity, Variable number tandem repeat, Untranslated region and Imprinting research Constantin Polychronakos does as part of his general Gene study is frequently linked to other disciplines of science, such as Minisatellite, therefore creating a link between diverse domains of science. His Allele research is multidisciplinary, incorporating perspectives in Endocrinology, Insulin, Internal medicine, Genotype and Regulation of gene expression. His work in Single-nucleotide polymorphism addresses issues such as Genotyping, which are connected to fields such as Autoantibody.
Constantin Polychronakos mainly focuses on Genetics, Internal medicine, Endocrinology, Type 1 diabetes and Gene. Allele, Single-nucleotide polymorphism, Locus, Genome-wide association study and Linkage disequilibrium are subfields of Genetics in which his conducts study. Constantin Polychronakos has researched Genome-wide association study in several fields, including Computational biology, Genetic association, Allele frequency and Human genetics.
The Internal medicine study combines topics in areas such as Diabetes mellitus, Cell and Phenotype. His research investigates the connection between Endocrinology and topics such as Receptor that intersect with issues in Cell culture. His research investigates the link between Type 1 diabetes and topics such as Immunology that cross with problems in Disease.
His primary areas of study are Genetics, Internal medicine, Genome-wide association study, Endocrinology and Type 1 diabetes. His Genetics study focuses mostly on Single-nucleotide polymorphism, Allele frequency, Genome, Exome sequencing and Genotype. He focuses mostly in the field of Internal medicine, narrowing it down to matters related to Diabetes mellitus and, in some cases, Epilepsy, Bioinformatics and Mutation.
He has included themes like Case-control study, Rheumatoid arthritis, Allele, Genetic association and Genetic architecture in his Genome-wide association study study. His Endocrinology study combines topics in areas such as Phenotype and Cell biology. His work in Type 1 diabetes covers topics such as Insulin which are related to areas like Autoimmune regulator.
His main research concerns Genetics, Genome-wide association study, Genetic association, Single-nucleotide polymorphism and Disease. Point mutation, Gene, Autoimmunity, Genotyping and Major histocompatibility complex are the subjects of his Genetics studies. The various areas that he examines in his Genome-wide association study study include Inflammatory bowel disease, Autoantibody, Case-control study, Rheumatoid arthritis and Candidate gene.
His study focuses on the intersection of Rheumatoid arthritis and fields such as Coronary artery disease with connections in the field of Endocrinology. His Genetic association research includes themes of Schizophrenia, Linkage disequilibrium, Immune system, Quantitative trait locus and Allele. Constantin Polychronakos combines subjects such as Exome sequencing and Genetic heterogeneity with his study of Disease.
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A genome-wide association study identifies novel risk loci for type 2 diabetes
Robert Sladek;Ghislain Rocheleau;Johan Rung;Christian Dina.
Nature (2007)
Insulin expression in human thymus is modulated by INS VNTR alleles at the IDDM2 locus
Petros Vafiadis;Simon T. Bennett;John A. Todd;Joseph Nadeau.
Nature Genetics (1997)
Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations
David Meyre;Jérôme Delplanque;Jean-Claude Chèvre;Cécile Lecoeur.
Nature Genetics (2009)
A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene
Hakon Hakonarson;Struan F A Grant;Jonathan P. Bradfield;Luc Marchand.
Nature (2007)
Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease
David Neil Cooper;Michael Krawczak;Constantin Polychronakos;Chris Tyler-Smith.
Human Genetics (2013)
Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers.
Suna Onengut-Gumuscu;Wei-Min Chen;Oliver Burren;Nick J Cooper.
Nature Genetics (2015)
Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia.
Johan Rung;Stéphane Cauchi;Anders Albrechtsen;Lishuang Shen;Lishuang Shen.
Nature Genetics (2009)
Parental genomic imprinting of the human IGF2 gene.
Nick Giannoukakis;Cheri Deal;Jean Paquette;Cynthia G. Goodyer.
Nature Genetics (1993)
Guidelines for Growth Hormone and Insulin-Like Growth Factor-I Treatment in Children and Adolescents: Growth Hormone Deficiency, Idiopathic Short Stature, and Primary Insulin-Like Growth Factor-I Deficiency.
Adda Grimberg;Sara A. DiVall;Constantin Polychronakos;David B. Allen.
Hormone Research in Paediatrics (2016)
Divergence between genetic determinants of IGF2 transcription levels in leukocytes and of IDDM2-encoded susceptibility to type 1 diabetes.
Petros Vafiadis;Simon T. Bennett;John A. Todd;Rosemarie Grabs.
The Journal of Clinical Endocrinology and Metabolism (1998)
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