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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. Azizi F. Tehran Lipid and Glucose Study: A National Legacy. International Journal of Endocrinology and Metabolism 2018;In Press(In Press)
    CrossRef
  2. 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
  3. 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
  4. 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
  5. 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
  6. 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