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Citing this Article

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Published on 23.02.17 in Vol 6, No 2 (2017): February

This paper is in the following e-collection/theme issue:

Works citing "Rationale and Design of a Genetic Study on Cardiometabolic Risk Factors: Protocol for the Tehran Cardiometabolic Genetic Study (TCGS)"

According to Crossref, the following articles are citing this article (DOI 10.2196/resprot.6050):

(note that this is only a small subset of citations)

  1. Javanrouh N, Khalaj A, Guity K, Sedaghati-khayat B, Valizadeh M, Barzin M, Daneshpour MS. Presence of CC Genotype for rs17773430 Could Affect the Percentage of Excess Weight Loss 1 Year After Bariatric Surgery: Tehran Obesity Treatment Study (TOTS). Obesity Surgery 2019;
    CrossRef
  2. Akbarzadeh M, Moghimbeigi A, Morris N, Daneshpour MS, Mahjub H, Soltanian AR. A Bayesian structural equation model in general pedigree data analysis. Statistical Analysis and Data Mining: The ASA Data Science Journal 2019;12(5):404
    CrossRef
  3. Piri Z, Barzin M, Mahdavi M, Guity K, Azizi F, Hosseinpanah F, Valizadeh M. The role of childhood BMI in predicting early adulthood dysglycemia: Tehran lipid and glucose study. Nutrition, Metabolism and Cardiovascular Diseases 2019;
    CrossRef
  4. Koochakpour G, Esfandiar Z, Hosseini-Esfahani F, Mirmiran P, Daneshpour M, Sedaghati-Khayat B, Azizi F. Evaluating the interaction of common FTO genetic variants, added sugar, and trans-fatty acid intakes in altering obesity phenotypes. Nutrition, Metabolism and Cardiovascular Diseases 2019;29(5):474
    CrossRef
  5. Ramezankhani A, Guity K, Azizi F, Hadaegh F. Sex differences in the association between spousal metabolic risk factors with incidence of type 2 diabetes: a longitudinal study of the Iranian population. Biology of Sex Differences 2019;10(1)
    CrossRef
  6. Javanrouh N, Soltanian AR, Tapak L, Azizi F, Ott J, Daneshpour MS. A novel association of rs13334070 in the RPGRIP1L gene with adiposity factors discovered by joint linkage and linkage disequilibrium analysis in Iranian pedigrees: Tehran Cardiometabolic Genetic Study (TCGS). Genetic Epidemiology 2019;43(3):342
    CrossRef
  7. Hosseini-Esfahani F, Koochakpoor G, Mirmiran P, Daneshpour MS, Azizi F. Dietary patterns modify the association between fat mass and obesity-associated genetic variants and changes in obesity phenotypes. British Journal of Nutrition 2019;121(11):1247
    CrossRef
  8. Hosseinzadeh N, Mehrabi Y, Daneshpour MS, Zayeri F, Guity K, Azizi F. Identifying new associated pleiotropic SNPs with lipids by simultaneous test of multiple longitudinal traits: An Iranian family-based study. Gene 2019;692:156
    CrossRef
  9. Azizi F. Tehran Lipid and Glucose Study: A National Legacy. International Journal of Endocrinology and Metabolism 2018;In Press(In Press)
    CrossRef
  10. Daneshpour MS, Hedayati M, Sedaghati-Khayat B, Guity K, Zarkesh M, Akbarzadeh M, Javanrooh N, Zadeh-Vakili A, Azizi F. Cardio-Metabolic Disease Genetic Risk Factors in Iran: Twenty Years of Tehran Lipid and Glucose Study. International Journal of Endocrinology and Metabolism 2018;In Press(In Press)
    CrossRef
  11. Sedaghati-khayat B, Barzin M, Akbarzadeh M, Guity K, Fallah M, Pourhassan H, Azizi F, Daneshpour MS. Lack of association between FTO gene variations and metabolic healthy obese (MHO) phenotype: Tehran Cardio-metabolic Genetic Study (TCGS). Eating and Weight Disorders - Studies on Anorexia, Bulimia and Obesity 2018;
    CrossRef
  12. Khalili D, Azizi F, Asgari S, Zadeh-Vakili A, Momenan AA, Ghanbarian A, Eskandari F, Sheikholeslami F, Hadaegh F. Outcomes in the Tehran Lipid and Glucose Study (TLGS) as a Longitudinal Population-Based Cohort Study and a Pragmatic Community Trial. International Journal of Endocrinology and Metabolism 2018;In Press(In Press)
    CrossRef
  13. Ramezankhani A, Harati H, Bozorgmanesh M, Tohidi M, Khalili D, Azizi F, Hadaegh F. Diabetes Mellitus: Findings from 20 Years of the Tehran Lipid and Glucose Study. International Journal of Endocrinology and Metabolism 2018;16(Suppl Issue)
    CrossRef
  14. Styrkarsdottir U, Helgason H, Sigurdsson A, Norddahl GL, Agustsdottir AB, Reynard LN, Villalvilla A, Halldorsson GH, Jonasdottir A, Magnusdottir A, Oddson A, Sulem G, Zink F, Sveinbjornsson G, Helgason A, Johannsdottir HS, Helgadottir A, Stefansson H, Gretarsdottir S, Rafnar T, Almdahl IS, Brækhus A, Fladby T, Selbæk G, Hosseinpanah F, Azizi F, Koh JM, Tang NLS, Daneshpour MS, Mayordomo JI, Welt C, Braund PS, Samani NJ, Kiemeney LA, Lohmander LS, Christiansen C, Andreassen OA, Magnusson O, Masson G, Kong A, Jonsdottir I, Gudbjartsson D, Sulem P, Jonsson H, Loughlin J, Ingvarsson T, Thorsteinsdottir U, Stefansson K. Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis. Nature Genetics 2017;49(5):801
    CrossRef