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] Evaluation of the association between the PPARGC1A genetic polymorphisms and type 2 diabetes in Han Chinese population
[PMID 16642433] Polymorphism in maternal LRP8 gene is associated with fetal growth.
[PMID 17187763] Analysis of PGC-1alpha variants Gly482Ser and Thr612Met concerning their PPARgamma2-coactivation function.
[PMID 18162502] PPARGC1A variation associated with DNA damage, diabetes, and cardiovascular diseases: the Boston Puerto Rican Health Study.
[PMID 18588668] Association between PPARGC1A polymorphisms and the occurrence of nonalcoholic fatty liver disease (NAFLD).
[PMID 18599530] Ser1369Ala variant in sulfonylurea receptor gene ABCC8 is associated with antidiabetic efficacy of gliclazide in Chinese type 2 diabetic patients.
[PMID 19133136] The gene coding for PGC-1alpha modifies age at onset in Huntington's Disease.
[PMID 20426853] Association and interaction of PPAR-complex gene variants with latent traits of left ventricular diastolic function.
[PMID 23741228] Lack of Genetic Associations of PPAR-γ and PGC-1α with Alzheimer's Disease and Parkinson's Disease with Dementia
[PMID 24383721] A single nucleotide polymorphism in the coding region of PGC-1alpha is a male-specific modifier of Huntington disease age-at-onset in a large European cohort