Wise C - Search Results

1

A missense variant in SLC39A8 is associated with severe idiopathic scoliosis.

Haller G, McCall K, Jenkitkasemwong S, Sadler B, Antunes L, Nikolov M, Whittle J, Upshaw Z, Shin J, Baschal E, Cruchaga C, Harms M, Raggio C, Morcuende JA, Giampietro P, Miller NH, Wise C, Gray RS, Solnica-Krezel L, Knutson M, Dobbs MB, Gurnett CA. Haller G, et al. Among authors: wise c. Nat Commun. 2018 Oct 9;9(1):4171. doi: 10.1038/s41467-018-06705-0. Nat Commun. 2018. PMID: 30301978 Free PMC article.

2

Localization of susceptibility to familial idiopathic scoliosis.

Wise CA, Barnes R, Gillum J, Herring JA, Bowcock AM, Lovett M. Wise CA, et al. Spine (Phila Pa 1976). 2000 Sep 15;25(18):2372-80. doi: 10.1097/00007632-200009150-00017. Spine (Phila Pa 1976). 2000. PMID: 10984791

3

SNTG1, the gene encoding gamma1-syntrophin: a candidate gene for idiopathic scoliosis.

Bashiardes S, Veile R, Allen M, Wise CA, Dobbs M, Morcuende JA, Szappanos L, Herring JA, Bowcock AM, Lovett M. Bashiardes S, et al. Hum Genet. 2004 Jun;115(1):81-9. doi: 10.1007/s00439-004-1121-y. Epub 2004 Apr 16. Hum Genet. 2004. PMID: 15088139

4

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: wise c. 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.

5

Asymmetric lower-limb malformations in individuals with homeobox PITX1 gene mutation.

Gurnett CA, Alaee F, Kruse LM, Desruisseau DM, Hecht JT, Wise CA, Bowcock AM, Dobbs MB. Gurnett CA, et al. Am J Hum Genet. 2008 Nov;83(5):616-22. doi: 10.1016/j.ajhg.2008.10.004. Epub 2008 Oct 23. Am J Hum Genet. 2008. PMID: 18950742 Free PMC article.

6

Altered transmission of HOX and apoptotic SNPs identify a potential common pathway for clubfoot.

Ester AR, Weymouth KS, Burt A, Wise CA, Scott A, Gurnett CA, Dobbs MB, Blanton SH, Hecht JT. Ester AR, et al. Am J Med Genet A. 2009 Dec;149A(12):2745-52. doi: 10.1002/ajmg.a.33130. Am J Med Genet A. 2009. PMID: 19938081 Free PMC article.

7

Evaluation of GPR50, hMel-1B, and ROR-alpha melatonin-related receptors and the etiology of adolescent idiopathic scoliosis.

Shyy W, Wang K, Gurnett CA, Dobbs MB, Miller NH, Wise C, Sheffield VC, Morcuende JA. Shyy W, et al. Among authors: wise c. J Pediatr Orthop. 2010 Sep;30(6):539-43. doi: 10.1097/BPO.0b013e3181e7902c. J Pediatr Orthop. 2010. PMID: 20733416 Free PMC article.

8

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. 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.

9

Common polymorphisms in human lysyl oxidase genes are not associated with the adolescent idiopathic scoliosis phenotype.

McGregor TL, Gurnett CA, Dobbs MB, Wise CA, Morcuende JA, Morgan TM, Menon R, Muglia LJ. McGregor TL, et al. BMC Med Genet. 2011 Jul 8;12:92. doi: 10.1186/1471-2350-12-92. BMC Med Genet. 2011. PMID: 21740577 Free PMC article.

10

Genetic variants in GPR126 are associated with adolescent idiopathic scoliosis.

Kou I, Takahashi Y, Johnson TA, Takahashi A, Guo L, Dai J, Qiu X, Sharma S, Takimoto A, Ogura Y, Jiang H, Yan H, Kono K, Kawakami N, Uno K, Ito M, Minami S, Yanagida H, Taneichi H, Hosono N, Tsuji T, Suzuki T, Sudo H, Kotani T, Yonezawa I, Londono D, Gordon D, Herring JA, Watanabe K, Chiba K, Kamatani N, Jiang Q, Hiraki Y, Kubo M, Toyama Y, Tsunoda T, Wise CA, Qiu Y, Shukunami C, Matsumoto M, Ikegawa S. Kou I, et al. Among authors: wise ca. Nat Genet. 2013 Jun;45(6):676-9. doi: 10.1038/ng.2639. Epub 2013 May 12. Nat Genet. 2013. PMID: 23666238

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