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A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females.
Sharma S, Londono D, Eckalbar WL, Gao X, Zhang D, Mauldin K, Kou I, Takahashi A, Matsumoto M, Kamiya N, Murphy KK, Cornelia R; TSRHC Scoliosis Clinical Group; Japan Scoliosis Clinical Research Group; Herring JA, Burns D, Ahituv N, Ikegawa S, Gordon D, Wise CA. Sharma S, et al. Among authors: zhang d. Nat Commun. 2015 Mar 18;6:6452. doi: 10.1038/ncomms7452. Nat Commun. 2015. PMID: 25784220 Free PMC article.
Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes.
Sharma S, Gao X, Londono D, Devroy SE, Mauldin KN, Frankel JT, Brandon JM, Zhang D, Li QZ, Dobbs MB, Gurnett CA, Grant SF, Hakonarson H, Dormans JP, Herring JA, Gordon D, Wise CA. Sharma S, et al. Among authors: zhang d. Hum Mol Genet. 2011 Apr 1;20(7):1456-66. doi: 10.1093/hmg/ddq571. Epub 2011 Jan 7. Hum Mol Genet. 2011. PMID: 21216876 Free PMC article.
CHD7 gene polymorphisms are associated with susceptibility to idiopathic scoliosis.
Gao X, Gordon D, Zhang D, Browne R, Helms C, Gillum J, Weber S, Devroy S, Swaney S, Dobbs M, Morcuende J, Sheffield V, Lovett M, Bowcock A, Herring J, Wise C. Gao X, et al. Among authors: zhang d. Am J Hum Genet. 2007 May;80(5):957-65. doi: 10.1086/513571. Epub 2007 Mar 12. Am J Hum Genet. 2007. PMID: 17436250 Free PMC article.
Mutations responsible for Larsen syndrome cluster in the FLNB protein.
Zhang D, Herring JA, Swaney SS, McClendon TB, Gao X, Browne RH, Rathjen KE, Johnston CE, Harris S, Cain NM, Wise CA. Zhang D, et al. J Med Genet. 2006 May;43(5):e24. doi: 10.1136/jmg.2005.038695. J Med Genet. 2006. PMID: 16648377 Free PMC article.
Clinical, Molecular, and Genetic Characteristics of PAPA Syndrome: A Review.
Smith EJ, Allantaz F, Bennett L, Zhang D, Gao X, Wood G, Kastner DL, Punaro M, Aksentijevich I, Pascual V, Wise CA. Smith EJ, et al. Among authors: zhang d. Curr Genomics. 2010 Nov;11(7):519-27. doi: 10.2174/138920210793175921. Curr Genomics. 2010. PMID: 21532836 Free PMC article.
Mutations Preventing Regulated Exon Skipping in MET Cause Osteofibrous Dysplasia.
Gray MJ, Kannu P, Sharma S, Neyt C, Zhang D, Paria N, Daniel PB, Whetstone H, Sprenger HG, Hammerschmidt P, Weng A, Dupuis L, Jobling R, Mendoza-Londono R, Dray M, Su P, Wilson MJ, Kapur RP, McCarthy EF, Alman BA, Howard A, Somers GR, Marshall CR, Manners S, Flanagan AM, Rathjen KE, Karol LA, Crawford H, Markie DM, Rios JJ, Wise CA, Robertson SP. Gray MJ, et al. Among authors: zhang d. Am J Hum Genet. 2015 Dec 3;97(6):837-47. doi: 10.1016/j.ajhg.2015.11.001. Am J Hum Genet. 2015. PMID: 26637977 Free PMC article.
The susceptibility loci juvenile idiopathic arthritis shares with other autoimmune diseases extend to PTPN2, COG6, and ANGPT1.
Thompson SD, Sudman M, Ramos PS, Marion MC, Ryan M, Tsoras M, Weiler T, Wagner M, Keddache M, Haas JP, Mueller C, Prahalad S, Bohnsack J, Wise CA, Punaro M, Zhang D, Rosé CD, Comeau ME, Divers J, Glass DN, Langefeld CD. Thompson SD, et al. Among authors: zhang d. Arthritis Rheum. 2010 Nov;62(11):3265-76. doi: 10.1002/art.27688. Arthritis Rheum. 2010. PMID: 20722033 Free PMC article.
Flexible progestin-primed ovarian stimulation versus a GnRH antagonist protocol in predicted suboptimal responders undergoing freeze-all cycles: a randomized non-inferiority trial.
Cai H, Shi Z, Liu D, Bai H, Zhou H, Xue X, Li W, Li M, Zhao X, Ma C, Wang H, Wang T, Li N, Wen W, Wang M, Zhang D, Mol BW, Shi J, Tian L. Cai H, et al. Among authors: zhang d. Hum Reprod. 2024 Dec 27:deae286. doi: 10.1093/humrep/deae286. Online ahead of print. Hum Reprod. 2024. PMID: 39729571
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