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Items: 1 to 20 of 160

1.

Genetic linkage localizes an adolescent idiopathic scoliosis and pectus excavatum gene to chromosome 18 q.

Gurnett CA, Alaee F, Bowcock A, Kruse L, Lenke LG, Bridwell KH, Kuklo T, Luhmann SJ, Dobbs MB.

Spine (Phila Pa 1976). 2009 Jan 15;34(2):E94-100. doi: 10.1097/BRS.0b013e31818b88a5.

2.

A novel locus for adolescent idiopathic scoliosis on chromosome 12p.

Raggio CL, Giampietro PF, Dobrin S, Zhao C, Dorshorst D, Ghebranious N, Weber JL, Blank RD.

J Orthop Res. 2009 Oct;27(10):1366-72. doi: 10.1002/jor.20885.

3.

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
4.

Correlations of adolescent idiopathic scoliosis and pectus excavatum.

Hong JY, Suh SW, Park HJ, Kim YH, Park JH, Park SY.

J Pediatr Orthop. 2011 Dec;31(8):870-4. doi: 10.1097/BPO.0b013e31822da7d5.

PMID:
22101666
5.

Idiopathic scoliosis: identification of candidate regions on chromosome 19p13.

Alden KJ, Marosy B, Nzegwu N, Justice CM, Wilson AF, Miller NH.

Spine (Phila Pa 1976). 2006 Jul 15;31(16):1815-9.

PMID:
16845357
6.

Gpr126/Adgrg6 deletion in cartilage models idiopathic scoliosis and pectus excavatum in mice.

Karner CM, Long F, Solnica-Krezel L, Monk KR, Gray RS.

Hum Mol Genet. 2015 Aug 1;24(15):4365-73. doi: 10.1093/hmg/ddv170. Epub 2015 May 7.

7.

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
8.

A genetic locus for adolescent idiopathic scoliosis linked to chromosome 19p13.3.

Chan V, Fong GC, Luk KD, Yip B, Lee MK, Wong MS, Lu DD, Chan TK.

Am J Hum Genet. 2002 Aug;71(2):401-6. Epub 2002 Jun 28.

9.

Are copy number variants associated with adolescent idiopathic scoliosis?

Buchan JG, Alvarado DM, Haller G, Aferol H, Miller NH, Dobbs MB, Gurnett CA.

Clin Orthop Relat Res. 2014 Oct;472(10):3216-25. doi: 10.1007/s11999-014-3766-8. Epub 2014 Jul 9.

10.

Allelic variants of human melatonin 1A receptor in patients with familial adolescent idiopathic scoliosis.

Morcuende JA, Minhas R, Dolan L, Stevens J, Beck J, Wang K, Weinstein SL, Sheffield V.

Spine (Phila Pa 1976). 2003 Sep 1;28(17):2025-8; discussion 2029.

PMID:
12973153
11.

Model-based linkage analyses confirm chromosome 19q13.3 as a susceptibility locus for intracranial aneurysm.

Mineharu Y, Inoue K, Inoue S, Yamada S, Nozaki K, Hashimoto N, Koizumi A.

Stroke. 2007 Apr;38(4):1174-8. Epub 2007 Feb 22.

12.

Genome-wide linkage scan of a large family with IgA nephropathy localizes a novel susceptibility locus to chromosome 2q36.

Paterson AD, Liu XQ, Wang K, Magistroni R, Song X, Kappel J, Klassen J, Cattran D, St George-Hyslop P, Pei Y.

J Am Soc Nephrol. 2007 Aug;18(8):2408-15. Epub 2007 Jul 18.

13.

Autosomal dominant partial epilepsy with auditory features: a new locus on chromosome 19q13.11-q13.31.

Bisulli F, Naldi I, Baldassari S, Magini P, Licchetta L, Castegnaro G, Fabbri M, Stipa C, Ferrari S, Seri M, Gonçalves Silva GE, Tinuper P, Pippucci T.

Epilepsia. 2014 Jun;55(6):841-8. doi: 10.1111/epi.12560. Epub 2014 Mar 1.

14.

Autosomal dominant progressive sensorineural hearing loss due to a novel mutation in the KCNQ4 gene.

Arnett J, Emery SB, Kim TB, Boerst AK, Lee K, Leal SM, Lesperance MM.

Arch Otolaryngol Head Neck Surg. 2011 Jan;137(1):54-9. doi: 10.1001/archoto.2010.234. Erratum in: Arch Otolaryngol Head Neck Surg. 2011 Jul;137(7):711.

15.

Localization of susceptibility to familial idiopathic scoliosis.

Wise CA, Barnes R, Gillum J, Herring JA, Bowcock AM, Lovett M.

Spine (Phila Pa 1976). 2000 Sep 15;25(18):2372-80.

PMID:
10984791
16.

Identification of 2 Loci at chromosomes 9 and 14 in a multiplex family with frontotemporal lobar degeneration and amyotrophic lateral sclerosis.

Gijselinck I, Engelborghs S, Maes G, Cuijt I, Peeters K, Mattheijssens M, Joris G, Cras P, Martin JJ, De Deyn PP, Kumar-Singh S, Van Broeckhoven C, Cruts M.

Arch Neurol. 2010 May;67(5):606-16. doi: 10.1001/archneurol.2010.82.

PMID:
20457961
17.

Males with familial idiopathic scoliosis: a distinct phenotypic subgroup.

Clough M, Justice CM, Marosy B, Miller NH.

Spine (Phila Pa 1976). 2010 Jan 15;35(2):162-8. doi: 10.1097/BRS.0b013e3181b7f1a7.

18.

Identification of susceptibility loci for scoliosis in FIS families with triple curves.

Marosy B, Justice CM, Vu C, Zorn A, Nzegwu N, Wilson AF, Miller NH.

Am J Med Genet A. 2010 Apr;152A(4):846-55. doi: 10.1002/ajmg.a.33222.

19.

Linkage analysis of genetic loci for kyphoscoliosis on chromosomes 5p13, 13q13.3, and 13q32.

Miller NH, Marosy B, Justice CM, Novak SM, Tang EY, Boyce P, Pettengil J, Doheny KF, Pugh EW, Wilson AF.

Am J Med Genet A. 2006 May 15;140(10):1059-68.

PMID:
16596674
20.

Identification of a susceptibility locus for severe adolescent idiopathic scoliosis on chromosome 17q24.3.

Miyake A, Kou I, Takahashi Y, Johnson TA, Ogura Y, Dai J, Qiu X, Takahashi A, 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, Kubo M, Tsunoda T, Watanabe K, Chiba K, Toyama Y, Qiu Y, Matsumoto M, Ikegawa S.

PLoS One. 2013 Sep 4;8(9):e72802. doi: 10.1371/journal.pone.0072802. eCollection 2013.

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