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For: Pekkinen M, Terhal PA, Botto LD, Henning P, Mäkitie RE, Roschger P, Jain A, Kol M, Kjellberg MA, Paschalis EP, van Gassen K, Murray M, Bayrak-Toydemir P, Magnusson MK, Jans J, Kausar M, Carey JC, Somerharju P, Lerner UH, Olkkonen VM, Klaushofer K, Holthuis JC, Mäkitie O. Osteoporosis and skeletal dysplasia caused by pathogenic variants in SGMS2. JCI Insight 2019;4:126180. [PMID: 30779713 DOI: 10.1172/jci.insight.126180] [Cited by in Crossref: 26] [Cited by in F6Publishing: 22] [Article Influence: 8.7] [Reference Citation Analysis]
Number Citing Articles
1 During A. Osteoporosis: A role for lipids. Biochimie 2020;178:49-55. [PMID: 32818522 DOI: 10.1016/j.biochi.2020.08.004] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
2 Arshad F, Bishop N. Osteogenesis imperfecta in children. Bone 2021;148:115914. [PMID: 33722772 DOI: 10.1016/j.bone.2021.115914] [Reference Citation Analysis]
3 Garg B, Tomar N, Biswas A, Mehta N, Malhotra R. Understanding Musculoskeletal Disorders Through Next-Generation Sequencing. JBJS Rev 2022;10. [PMID: 35383688 DOI: 10.2106/JBJS.RVW.21.00165] [Reference Citation Analysis]
4 Hartmann MA, Blouin S, Misof BM, Fratzl-Zelman N, Roschger P, Berzlanovich A, Gruber GM, Brugger PC, Zwerina J, Fratzl P. Quantitative Backscattered Electron Imaging of Bone Using a Thermionic or a Field Emission Electron Source. Calcif Tissue Int 2021;109:190-202. [PMID: 33837801 DOI: 10.1007/s00223-021-00832-5] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
5 Chen LR, Ko NY, Chen KH. Medical Treatment for Osteoporosis: From Molecular to Clinical Opinions. Int J Mol Sci 2019;20:E2213. [PMID: 31064048 DOI: 10.3390/ijms20092213] [Cited by in Crossref: 29] [Cited by in F6Publishing: 27] [Article Influence: 9.7] [Reference Citation Analysis]
6 Zhou H, Gong Y, Wu Q, Ye X, Yu B, Lu C, Jiang W, Ye J, Fu Z. Rare Diseases Related with Lipoprotein Metabolism. Adv Exp Med Biol 2020;1276:171-88. [PMID: 32705600 DOI: 10.1007/978-981-15-6082-8_11] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
7 Basalom S, Fiscaletti M, Miranda V, Huber C, Couture G, Drouin R, Monceau É, Wavrant S, Dubé J, Mäkitie O, Cormier-Daire V, Campeau PM. Calvarial doughnut lesions with bone fragility in a French-Canadian family; case report and review of the literature. Bone Rep 2021;15:101121. [PMID: 34504906 DOI: 10.1016/j.bonr.2021.101121] [Reference Citation Analysis]
8 Robinson ME, Rauch F. Mendelian bone fragility disorders. Bone 2019;126:11-7. [PMID: 31039433 DOI: 10.1016/j.bone.2019.04.021] [Cited by in Crossref: 13] [Cited by in F6Publishing: 10] [Article Influence: 4.3] [Reference Citation Analysis]
9 Mäkitie RE, Blouin S, Välimäki VV, Pihlström S, Määttä K, Pekkinen M, Fratzl-Zelman N, Mäkitie O, Hartmann MA. Abnormal Bone Tissue Organization and Osteocyte Lacunocanalicular Network in Early-Onset Osteoporosis Due to SGMS2 Mutations. JBMR Plus 2021;5:e10537. [PMID: 34761145 DOI: 10.1002/jbm4.10537] [Reference Citation Analysis]
10 During A, Coutel X, Bertheaume N, Penel G, Olejnik C. Long Term Ovariectomy-Induced Osteoporosis is Associated with High Stearoyl-CoA Desaturase Indexes in Rat Femur. Calcif Tissue Int 2020;106:315-24. [PMID: 31796982 DOI: 10.1007/s00223-019-00637-7] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 Xiao C, Rossignol F, Vaz FM, Ferreira CR. Inherited disorders of complex lipid metabolism: A clinical review. J Inherit Metab Dis 2021;44:809-25. [PMID: 33594685 DOI: 10.1002/jimd.12369] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
12 Wang J, Liu C, Chen J, Bai Y, Wang K, Wang Y, Fang M. Genome-Wide Analysis Reveals Human-Mediated Introgression from Western Pigs to Indigenous Chinese Breeds. Genes (Basel) 2020;11:E275. [PMID: 32143300 DOI: 10.3390/genes11030275] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
13 Wen C, Zhou Y, Xu Y, Tan H, Pang C, Liu H, Liu K, Wei L, Luo H, Qin T, He C, Liu C, Zhou C. The Regulatory Role of GBF1 on Osteoclast Activation Through EIF2a Mediated ER Stress and Novel Marker FAM129A Induction. Front Cell Dev Biol 2021;9:706768. [PMID: 34513838 DOI: 10.3389/fcell.2021.706768] [Reference Citation Analysis]
14 Costantini A, Muurinen MH, Mäkitie O. New gene discoveries in skeletal diseases with short stature. Endocr Connect 2021;10:R160-74. [PMID: 33830070 DOI: 10.1530/EC-21-0083] [Reference Citation Analysis]
15 Elsebaie H, Mansour MA, Elsayed SM, Mahmoud S, El-Sobky TA. Multicentric Osteolysis, Nodulosis, and Arthropathy in two unrelated children with matrix metalloproteinase 2 variants: Genetic-skeletal correlations. Bone Rep 2021;15:101106. [PMID: 34307793 DOI: 10.1016/j.bonr.2021.101106] [Reference Citation Analysis]
16 Qi T, Li L, Weidong T. The Role of Sphingolipid Metabolism in Bone Remodeling. Front Cell Dev Biol 2021;9:752540. [PMID: 34912800 DOI: 10.3389/fcell.2021.752540] [Reference Citation Analysis]
17 Yoshioka H, Okita S, Nakano M, Minamizaki T, Nubukiyo A, Sotomaru Y, Bonnelye E, Kozai K, Tanimoto K, Aubin JE, Yoshiko Y. Single-Cell RNA-Sequencing Reveals the Breadth of Osteoblast Heterogeneity. JBMR Plus 2021;5:e10496. [PMID: 34189385 DOI: 10.1002/jbm4.10496] [Reference Citation Analysis]
18 Robinson ME, Bardai G, Veilleux LN, Glorieux FH, Rauch F. Musculoskeletal phenotype in two unrelated individuals with a recurrent nonsense variant in SGMS2. Bone 2020;134:115261. [PMID: 32028018 DOI: 10.1016/j.bone.2020.115261] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 4.0] [Reference Citation Analysis]
19 Sandal S, Arora V, Verma IC. ANO5-associated Gnathodiaphyseal dysplasia with calvarial doughnut lesions: First report in an Asian Indian with an expanded phenotype. Congenit Anom (Kyoto) 2021;61:25-6. [PMID: 32902009 DOI: 10.1111/cga.12391] [Reference Citation Analysis]
20 Bäck M, Michel JB. From organic and inorganic phosphates to valvular and vascular calcifications. Cardiovasc Res 2021;117:2016-29. [PMID: 33576771 DOI: 10.1093/cvr/cvab038] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
21 Taniguchi M, Okazaki T. Ceramide/Sphingomyelin Rheostat Regulated by Sphingomyelin Synthases and Chronic Diseases in Murine Models. J Lipid Atheroscler 2020;9:380-405. [PMID: 33024732 DOI: 10.12997/jla.2020.9.3.380] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
22 Chetty M, Roomaney IA, Beighton P. The evolution of the nosology of osteogenesis imperfecta. Clin Genet 2021;99:42-52. [PMID: 32901963 DOI: 10.1111/cge.13846] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 2.5] [Reference Citation Analysis]
23 Costantini A, Alm JJ, Tonelli F, Valta H, Huber C, Tran AN, Daponte V, Kirova N, Kwon YU, Bae JY, Chung WY, Tan S, Sznajer Y, Nishimura G, Näreoja T, Warren AJ, Cormier-Daire V, Kim OH, Forlino A, Cho TJ, Mäkitie O. Novel RPL13 Variants and Variable Clinical Expressivity in a Human Ribosomopathy With Spondyloepimetaphyseal Dysplasia. J Bone Miner Res 2021;36:283-97. [PMID: 32916022 DOI: 10.1002/jbmr.4177] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
24 Hannan FM, Newey PJ, Whyte MP, Thakker RV. Genetics of Skeletal Disorders. Handb Exp Pharmacol 2020;262:325-51. [PMID: 32166388 DOI: 10.1007/164_2020_350] [Reference Citation Analysis]
25 Indellicato R, Trinchera M. The Link between Gaucher Disease and Parkinson's Disease Sheds Light on Old and Novel Disorders of Sphingolipid Metabolism. Int J Mol Sci 2019;20:E3304. [PMID: 31284408 DOI: 10.3390/ijms20133304] [Cited by in Crossref: 16] [Cited by in F6Publishing: 14] [Article Influence: 5.3] [Reference Citation Analysis]