PubMed

Evidence of a linkage between matrilin-1 gene (MATN1) and idiopathic scoliosis.

Montanaro L, Parisini P, Greggi T, Di Silvestre M, Campoccia D, Rizzi S, Arciola CR.

Scoliosis. 2006 Dec 18;1:21.PMID: 17176459 [PubMed]Related articlesFree article

Promoter polymorphism of matrilin-1 gene predisposes to adolescent idiopathic scoliosis in a Chinese population.

Chen Z, Tang NL, Cao X, Qiao D, Yi L, Cheng JC, Qiu Y.

Eur J Hum Genet. 2009 Apr;17(4):525-32. Epub 2008 Nov 5.PMID: 18985072 [PubMed - indexed for MEDLINE]Related articles

[Association between polymorphism of Matrilin-1 gene (MATN1) with susceptibility to adolescent idiopathic scoliosis]

Chen ZJ, Qiu Y, Yu Y, Wang B, Zhu ZZ.

Zhonghua Wai Ke Za Zhi. 2009 Sep 1;47(17):1332-5. Chinese. PMID: 20092731 [PubMed - in process]Related articles

Congenital and idiopathic scoliosis: clinical and genetic aspects.

Giampietro PF, Blank RD, Raggio CL, Merchant S, Jacobsen FS, Faciszewski T, Shukla SK, Greenlee AR, Reynolds C, Schowalter DB.

Clin Med Res. 2003 Apr;1(2):125-36. Review.PMID: 15931299 [PubMed - indexed for MEDLINE]Related articlesFree article

Family-based association study of Tim-1 and Tim-3 gene polymorphisms with childhood asthma in Chinese trios.

Wu QW, Cai PC, Wang L, Li YR, Kong LL, Hu LH.

Int Arch Allergy Immunol. 2009;150(3):252-60. Epub 2009 Jun 4.PMID: 19494522 [PubMed - indexed for MEDLINE]Related articles

Melatonin receptor 1B (MTNR1B) gene polymorphism is associated with the occurrence of adolescent idiopathic scoliosis.

Qiu XS, Tang NL, Yeung HY, Lee KM, Hung VW, Ng BK, Ma SL, Kwok RH, Qin L, Qiu Y, Cheng JC.

Spine (Phila Pa 1976). 2007 Jul 15;32(16):1748-53.PMID: 17632395 [PubMed - indexed for MEDLINE]Related articles

Synteny-defined candidate genes for congenital and idiopathic scoliosis.

Giampietro PF, Raggio CL, Blank RD.

Am J Med Genet. 1999 Mar 19;83(3):164-77.PMID: 10096591 [PubMed - indexed for MEDLINE]Related articles

[Association analysis of neuregulin 1 gene polymorphism with schizophrenia in Chinese Han population]

Zhang HX, Li WQ, Zhang Y, Zhao JP, Lv LX, Yang G.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Feb;26(1):16-20. Chinese. PMID: 19199244 [PubMed - indexed for MEDLINE]Related articles

Family-based association study of 5-HTTLPR and the 5-HT2A receptor gene polymorphisms with autism spectrum disorder in Korean trios.

Cho IH, Yoo HJ, Park M, Lee YS, Kim SA.

Brain Res. 2007 Mar 30;1139:34-41. Epub 2007 Jan 8.PMID: 17280648 [PubMed - indexed for MEDLINE]Related articles

[Transmission disequilibrium test for congenital dislocation of the hip and HOXB9 gene or COL1AI gene]

Jiang J, Ma HW, Lu Y, Wang YP, Wang Y, Li QW, Ji SJ.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Jun;20(3):193-5. Chinese. PMID: 12778441 [PubMed - indexed for MEDLINE]Related articles

Exclusion of positional candidate gene coding region mutations in the common posterior polymorphous corneal dystrophy 1 candidate gene interval.

Aldave AJ, Yellore VS, Vo RC, Kamal KM, Rayner SA, Plaisier CL, Chen MC, Damani MR, Pham MN, Gorin MB, Sobel E, Papp J.

Cornea. 2009 Aug;28(7):801-7.PMID: 19574904 [PubMed - indexed for MEDLINE]Related articles

[Transmission disequilibrium test for nonsyndromic cleft lip and palate and segment homeobox gene-1 gene]

Wu PA, Li YL, Wu HJ, Wang K, Fan GZ.

Zhonghua Kou Qiang Yi Xue Za Zhi. 2007 Sep;42(9):561-3. Chinese. PMID: 18070437 [PubMed - in process]Related articles

Linkage and mutational analysis of CLCN2 in childhood absence epilepsy.

Everett K, Chioza B, Aicardi J, Aschauer H, Brouwer O, Callenbach P, Covanis A, Dooley J, Dulac O, Durner M, Eeg-Olofsson O, Feucht M, Friis M, Guerrini R, Heils A, Kjeldsen M, Nabbout R, Sander T, Wirrell E, McKeigue P, Robinson R, Taske N, Gardiner M.

Epilepsy Res. 2007 Jul;75(2-3):145-53. Epub 2007 Jun 18.PMID: 17580110 [PubMed - indexed for MEDLINE]Related articles

Genetic association study of synphilin-1 in idiopathic Parkinson's disease.

Myhre R, Klungland H, Farrer MJ, Aasly JO.

BMC Med Genet. 2008 Mar 21;9:19.PMID: 18366718 [PubMed - indexed for MEDLINE]Related articlesFree article

Association study between adolescent idiopathic scoliosis and the DPP9 gene which is located in the candidate region identified by linkage analysis.

Qiu XS, Tang NL, Yeung HY, Qiu Y, Cheng JC.

Postgrad Med J. 2008 Sep;84(995):498-501.PMID: 18940951 [PubMed - indexed for MEDLINE]Related articles

Genetic association study of growth hormone receptor and idiopathic scoliosis.

Qiu XS, Tang NL, Yeung HY, Qiu Y, Cheng JC.

Clin Orthop Relat Res. 2007 Sep;462:53-8.PMID: 17514010 [PubMed - indexed for MEDLINE]Related articles

Chromosome 7p linkage and GPR154 gene association in Italian families with allergic asthma.

Malerba G, Lindgren CM, Xumerle L, Kiviluoma P, Trabetti E, Laitinen T, Galavotti R, Pescollderungg L, Boner AL, Kere J, Pignatti PF.

Clin Exp Allergy. 2007 Jan;37(1):83-9.PMID: 17210045 [PubMed - indexed for MEDLINE]Related articles

Genes on bovine chromosome 18 associated with bilateral convergent strabismus with exophthalmos in German Brown cattle.

Fink S, Mömke S, Wöhlke A, Distl O.

Mol Vis. 2008 Sep 22;14:1737-51.PMID: 18836565 [PubMed - indexed for MEDLINE]Related articlesFree article

Association of estrogen receptor beta gene polymorphisms with susceptibility to adolescent idiopathic scoliosis.

Zhang HQ, Lu SJ, Tang MX, Chen LQ, Liu SH, Guo CF, Wang XY, Chen J, Xie L.

Spine (Phila Pa 1976). 2009 Apr 15;34(8):760-4.PMID: 19337134 [PubMed - indexed for MEDLINE]Related articles

Assignment of two loci for autosomal dominant adolescent idiopathic scoliosis to chromosomes 9q31.2-q34.2 and 17q25.3-qtel.

Ocaka L, Zhao C, Reed JA, Ebenezer ND, Brice G, Morley T, Mehta M, O'Dowd J, Weber JL, Hardcastle AJ, Child AH.

J Med Genet. 2008 Feb;45(2):87-92. Epub 2007 Oct 11.PMID: 17932119 [PubMed - indexed for MEDLINE]Related articles