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363 results

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Page 1
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: herring j. 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.
Localization of susceptibility to familial idiopathic scoliosis.
Wise CA, Barnes R, Gillum J, Herring JA, Bowcock AM, Lovett M. Wise CA, et al. Among authors: herring ja. Spine (Phila Pa 1976). 2000 Sep 15;25(18):2372-80. doi: 10.1097/00007632-200009150-00017. Spine (Phila Pa 1976). 2000. PMID: 10984791
A meta-analysis identifies adolescent idiopathic scoliosis association with LBX1 locus in multiple ethnic groups.
Londono D, Kou I, Johnson TA, Sharma S, Ogura Y, Tsunoda T, Takahashi A, Matsumoto M, Herring JA, Lam TP, Wang X, Tam EM, Song YQ, Fan YH, Chan D, Cheah KS, Qiu X, Jiang H, Huang D; Japanese Scoliosis Clinical Research Group; TSRHC IS Clinical Group, International Consortium for Scoliosis Genetics, Su P, Sham P, Cheung KM, Luk KD, Gordon D, Qiu Y, Cheng J, Tang N, Ikegawa S, Wise CA. Londono D, et al. Among authors: herring ja. J Med Genet. 2014 Jun;51(6):401-6. doi: 10.1136/jmedgenet-2013-102067. Epub 2014 Apr 10. J Med Genet. 2014. PMID: 24721834
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. Nat Commun. 2015 Mar 18;6:6452. doi: 10.1038/ncomms7452. Nat Commun. 2015. PMID: 25784220 Free PMC article.
Genome-wide meta-analysis and replication studies in multiple ethnicities identify novel adolescent idiopathic scoliosis susceptibility loci.
Khanshour AM, Kou I, Fan Y, Einarsdottir E, Makki N, Kidane YH, Kere J, Grauers A, Johnson TA, Paria N, Patel C, Singhania R, Kamiya N, Takeda K, Otomo N, Watanabe K, Luk KDK, Cheung KMC, Herring JA, Rios JJ, Ahituv N, Gerdhem P, Gurnett CA, Song YQ, Ikegawa S, Wise CA. Khanshour AM, et al. Among authors: herring ja. Hum Mol Genet. 2018 Nov 15;27(22):3986-3998. doi: 10.1093/hmg/ddy306. Hum Mol Genet. 2018. PMID: 30395268 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. Among authors: herring ja. J Med Genet. 2006 May;43(5):e24. doi: 10.1136/jmg.2005.038695. J Med Genet. 2006. PMID: 16648377 Free PMC article.
363 results