Associated Papers
Gestational Weight Gain: Is the Role of Genetic Variants a Determinant? A Review.
Sámano R et al.
International Journal of Molecular Sciences, 2024
Frequency of PPAR-γ, FTO and ABCC8 genetic variation in Pakistani cardiovascular smokers.
Rehman K et al.
Environmental Science and Pollution Research International, 2020
Single-nucleotide polymorphisms in inflammatory bowel disease.
Neuman MG et al.
Translational Research : the Journal of Laboratory and Clinical Medicine, 2012
Pharmacogenomic analysis of ATP-sensitive potassium channels coexpressing the common type 2 diabetes risk variants E23K and S1369A.
Lang VY et al.
Pharmacogenetics and Genomics, 2012
Genetic variations in the pancreatic ATP-sensitive potassium channel, beta-cell dysfunction, and susceptibility to type 2 diabetes.
Chistiakov DA et al.
Acta Diabetologica, 2009
Genetic variants associated with insulin resistance and metabolic syndrome in young Asian Indians with myocardial infarction.
Ranjith N et al.
Metabolic Syndrome and Related Disorders, 2008
Association of TCF7L2 polymorphism with diabetes mellitus, metabolic syndrome, and markers of beta cell function and insulin resistance in a population-based sample of Emirati subjects.
Saadi H et al.
Diabetes Research and Clinical Practice, 2008
Association between KCNJ11 E23K genotype and cardiovascular and glucose metabolism phenotypes in older men and women.
Yi Y et al.
Experimental Physiology, 2008
Challenges in studies of the genetic basis of Type 2 diabetes.
Laakso M
Expert Review of Endocrinology & Metabolism, 2007
KCNJ11 E23K polymorphism and diabetes mellitus with adult onset in Czech patients.
Cejková P et al.
Folia Biologica, 2007
Common variants in the ATP-sensitive K+ channel genes KCNJ11 (Kir6.2) and ABCC8 (SUR1) in relation to glucose intolerance: population-based studies and meta-analyses.
van Dam RM et al.
Diabetic Medicine : a Journal of the British Diabetic Association, 2005
Is glutamate decarboxylase 2 (GAD2) a genetic link between low birth weight and subsequent development of obesity in children?
Meyre D et al.
The Journal of Clinical Endocrinology and Metabolism, 2005
Association of an insulin gene promoter insertion polymorphism with type 2 diabetes and diabetic nephropathy in African Americans.
Karim MA et al.
Molecular Genetics and Metabolism, 2004
Phenotypic consequences of the peroxisome proliferator-activated receptor-gamma Pro12Ala polymorphism: the weight of the evidence in genetic association studies.
Florez JC
The Journal of Clinical Endocrinology and Metabolism, 2004
Meta-analysis and a large association study confirm a role for calpain-10 variation in type 2 diabetes susceptibility.
Weedon MN et al.
American Journal of Human Genetics, 2003
E23K single nucleotide polymorphism in the islet ATP-sensitive potassium channel gene (Kir6.2) contributes as much to the risk of Type II diabetes in Caucasians as the PPARgamma Pro12Ala variant.
Love-Gregory L et al.
Diabetologia, 2003