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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. Among authors: wise ca. J Med Genet. 2006 May;43(5):e24. doi: 10.1136/jmg.2005.038695. J Med Genet. 2006. PMID: 16648377 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. 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.
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: wise ca. 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.
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: wise ca. Curr Genomics. 2010 Nov;11(7):519-27. doi: 10.2174/138920210793175921. Curr Genomics. 2010. PMID: 21532836 Free PMC article.
Whole-exome sequencing: discovering genetic causes of orthopaedic disorders.
Paria N, Copley LA, Herring JA, Kim HK, Richards BS, Sucato DJ, Wise CA, Rios JJ. Paria N, et al. Among authors: wise ca. J Bone Joint Surg Am. 2013 Dec 4;95(23):e1851-8. doi: 10.2106/JBJS.L.01620. J Bone Joint Surg Am. 2013. PMID: 24306708 Review. No abstract available.
125 results