Osteoprotegerin gene polymorphisms and otosclerosis: an additional genetic association study, multilocus interaction and meta-analysis-Reference-Cited by-同舟云学术

Osteoprotegerin gene polymorphisms and otosclerosis: an additional genetic association study, multilocus interaction and meta-analysis

Published:2020-06-03 Issue:1 Volume:21 Page:
ISSN:1471-2350
Container-title:BMC Medical Genetics
language:en
Short-container-title:BMC Med Genet

Author:

Bouzid Amal^ORCID,Tekari Adel,Jbeli Fida,Chakroun Amine,Hansdah Kirtal,Souissi Amal,Singh Neha,Mosrati Mohamed Ali,Achour Imen,Ghorbel Abdelmonem,Charfeddine Ilhem,Ramchander Puppala Venkat,Masmoudi Saber

Funder

Grant under the Tunisia/India agreement on science and technology cooperation

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1186/s12881-020-01036-8.pdf

Reference49 articles.

1. Ealy M, Smith RJH. The genetics of otosclerosis. Hear Res. 2010;266:70–4.

2. Harada S, Rodan GA. Control of osteoblast function and regulation of bone mass. Nature. 2003;423:349–55.

3. Teitelbaum SL, Ross FP. Genetic regulation of osteoclast development and function. Nat Rev Genet. 2003;4:638–49.

4. Rodan GA. Introduction to bone biology. Bone. 1992;13(Suppl 1):S3–6.

5. Feng X, McDonald JM. Disorders of bone remodeling. Annu Rev Pathol. 2011;6:121–45.

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Brazilian Society of Otology task force – Otosclerosis: evaluation and treatment;Brazilian Journal of Otorhinolaryngology;2023-09

2. SMARCA4mutation causes human otosclerosis and a similar phenotype in mice;Journal of Medical Genetics;2023-06-30

3. Genetic variants and altered expression of SERPINF1 confer disease susceptibility in patients with otosclerosis;Journal of Human Genetics;2023-05-18

4. The risks of RELN polymorphisms and its expression in the development of otosclerosis;PLOS ONE;2022-06-03

5. Genetic Association of rs1021188 and DNA Methylation Signatures of TNFSF11 in the Risk of Conductive Hearing Loss;Frontiers in Medicine;2022-04-18