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Ralston, S.H., Uitterlinden, A.G., Brandi, M.L., Balcells, S., Langdahl, B.L., Lips, P., Lorenc, R., Obermayer-Pietsch, B., Scollen, S., Bustamante, M., Husted, L.B., Carey, A.H., Diez-Perez, A., Dunning, A.M., Falchetti, A., Karczmarewicz, E., Kruk, M., van Leeuwen, J.P., van Meurs, J.B., Mangion, J., McGuigan, F.E., Mellibovsky, L., del Monte, F., Pols, H.A., Reeve, J., Reid, D.M., Renner, W., Rivadeneira, F., van Schoor, N.M., Sherlock, R.E. and Ioannidis, J.P. (2006) Large-Scale Evidence for the Effect of the COLIA1 Sp1 Polymorphism on Osteoporosis Outcomes: The GENOMOS Study. PLOS Medicine, 3, e90.
https://doi.org/10.1371/journal.pmed.0030090

has been cited by the following article:

• TITLE: Association of COL1A1 rs180012 SNP and Fibromyalgia Suggests the Implication of Collagen Structure in Musculoskeletal Pain

  AUTHORS: Isabel Navarro-Vera, José Antonio Casajús, Manuel J. López-Pérez, Carmen Díez-Sánchez

  KEYWORDS: Fibromyalgia, Genotype, Collagen, Bone Mineral Density, SP1

  JOURNAL NAME: Advances in Bioscience and Biotechnology, Vol.9 No.2, February 23, 2018

  ABSTRACT: Fibromyalgia (FM) is a complex, chronic condition, which causes widespread musculoskeletal pain, fatigue and a variety of other symptoms. Many polymorphisms related to neuroendocrine system function as the ApoE isoforms, Val158Met polymorphism in COMT, as well as a 44 bp deletion located in 5-HTTLPR, have been studied. Other polymorphisms have been related to inflammatory response such as the 70 bp VNTR in IL-4 or to citokine levels. Furthermore, some studies focused on finding out new FM related SNPs, have been performed by genome wide association scan (GWAS). The target of this work was to study a possible linkage of a collagen type I polymorphism (COL1A1 rs180012 SNP) affecting bone mineralization, with fibromyalgia. Results obtained show a clear association of ss homozygous genotype with FM patients no dependent on bone mineralization.