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Items: 1 to 20 of 44

1.

Brace wear control of curve progression in adolescent idiopathic scoliosis.

Katz DE, Herring JA, Browne RH, Kelly DM, Birch JG.

J Bone Joint Surg Am. 2010 Jun;92(6):1343-52. doi: 10.2106/JBJS.I.01142.

PMID:
20516309
2.

Drosophila neurexin IV interacts with Roundabout and is required for repulsive midline axon guidance.

Banerjee S, Blauth K, Peters K, Rogers SL, Fanning AS, Bhat MA.

J Neurosci. 2010 Apr 21;30(16):5653-67. doi: 10.1523/JNEUROSCI.6187-09.2010.

3.

Transmission disequilibrium test power and sample size in the presence of locus heterogeneity.

Chen C, Yang G, Buyske S, Matise T, Finch SJ, Gordon D.

Stat Appl Genet Mol Biol. 2009;8:Article 44. doi: 10.2202/1544-6115.1501. Epub 2009 Oct 8.

PMID:
19883370
4.

Understanding genetic factors in idiopathic scoliosis, a complex disease of childhood.

Wise CA, Gao X, Shoemaker S, Gordon D, Herring JA.

Curr Genomics. 2008 Mar;9(1):51-9. doi: 10.2174/138920208783884874.

5.

Common genetic variation and human traits.

Goldstein DB.

N Engl J Med. 2009 Apr 23;360(17):1696-8. doi: 10.1056/NEJMp0806284. Epub 2009 Apr 15. No abstract available.

PMID:
19369660
6.

DSCAM functions as a netrin receptor in commissural axon pathfinding.

Liu G, Li W, Wang L, Kar A, Guan KL, Rao Y, Wu JY.

Proc Natl Acad Sci U S A. 2009 Feb 24;106(8):2951-6. doi: 10.1073/pnas.0811083106. Epub 2009 Feb 5.

7.

Transcription. Gene expression--where to start?

Buratowski S.

Science. 2008 Dec 19;322(5909):1804-5. doi: 10.1126/science.1168805. No abstract available.

8.

Dscam guides embryonic axons by Netrin-dependent and -independent functions.

Andrews GL, Tanglao S, Farmer WT, Morin S, Brotman S, Berberoglu MA, Price H, Fernandez GC, Mastick GS, Charron F, Kidd T.

Development. 2008 Dec;135(23):3839-48. doi: 10.1242/dev.023739. Epub 2008 Oct 23.

9.

L1 and NCAM adhesion molecules as signaling coreceptors in neuronal migration and process outgrowth.

Schmid RS, Maness PF.

Curr Opin Neurobiol. 2008 Jun;18(3):245-50. doi: 10.1016/j.conb.2008.07.015. Review.

10.

Disruption of chromodomain helicase DNA binding protein 2 (CHD2) causes scoliosis.

Kulkarni S, Nagarajan P, Wall J, Donovan DJ, Donell RL, Ligon AH, Venkatachalam S, Quade BJ.

Am J Med Genet A. 2008 May 1;146A(9):1117-27. doi: 10.1002/ajmg.a.32178.

11.

Catmap: case-control and TDT meta-analysis package.

Nicodemus KK.

BMC Bioinformatics. 2008 Feb 28;9:130. doi: 10.1186/1471-2105-9-130.

12.

WGAViewer: software for genomic annotation of whole genome association studies.

Ge D, Zhang K, Need AC, Martin O, Fellay J, Urban TJ, Telenti A, Goldstein DB.

Genome Res. 2008 Apr;18(4):640-3. doi: 10.1101/gr.071571.107. Epub 2008 Feb 6.

13.

Application of ancestry informative markers to association studies in European Americans.

Seldin MF, Price AL.

PLoS Genet. 2008 Jan;4(1):e5. doi: 10.1371/journal.pgen.0040005. No abstract available.

14.

Zebrafish mutations affecting cilia motility share similar cystic phenotypes and suggest a mechanism of cyst formation that differs from pkd2 morphants.

Sullivan-Brown J, Schottenfeld J, Okabe N, Hostetter CL, Serluca FC, Thiberge SY, Burdine RD.

Dev Biol. 2008 Feb 15;314(2):261-75. doi: 10.1016/j.ydbio.2007.11.025. Epub 2007 Dec 3.

15.

Screening for idiopathic scoliosis in adolescents. An information statement.

Richards BS, Vitale MG.

J Bone Joint Surg Am. 2008 Jan;90(1):195-8. doi: 10.2106/JBJS.G.01276. Review. No abstract available.

PMID:
18171974
16.

Close homolog of L1 and neuropilin 1 mediate guidance of thalamocortical axons at the ventral telencephalon.

Wright AG, Demyanenko GP, Powell A, Schachner M, Enriquez-Barreto L, Tran TS, Polleux F, Maness PF.

J Neurosci. 2007 Dec 12;27(50):13667-79.

17.

A second generation human haplotype map of over 3.1 million SNPs.

International HapMap Consortium, Frazer KA, Ballinger DG, Cox DR, Hinds DA, Stuve LL, Gibbs RA, Belmont JW, Boudreau A, Hardenbol P, Leal SM, Pasternak S, Wheeler DA, Willis TD, Yu F, Yang H, Zeng C, Gao Y, Hu H, Hu W, Li C, Lin W, Liu S, Pan H, Tang X, Wang J, Wang W, Yu J, Zhang B, Zhang Q, Zhao H, Zhao H, Zhou J, Gabriel SB, Barry R, Blumenstiel B, Camargo A, Defelice M, Faggart M, Goyette M, Gupta S, Moore J, Nguyen H, Onofrio RC, Parkin M, Roy J, Stahl E, Winchester E, Ziaugra L, Altshuler D, Shen Y, Yao Z, Huang W, Chu X, He Y, Jin L, Liu Y, Shen Y, Sun W, Wang H, Wang Y, Wang Y, Xiong X, Xu L, Waye MM, Tsui SK, Xue H, Wong JT, Galver LM, Fan JB, Gunderson K, Murray SS, Oliphant AR, Chee MS, Montpetit A, Chagnon F, Ferretti V, Leboeuf M, Olivier JF, Phillips MS, Roumy S, Sallée C, Verner A, Hudson TJ, Kwok PY, Cai D, Koboldt DC, Miller RD, Pawlikowska L, Taillon-Miller P, Xiao M, Tsui LC, Mak W, Song YQ, Tam PK, Nakamura Y, Kawaguchi T, Kitamoto T, Morizono T, Nagashima A, Ohnishi Y, Sekine A, Tanaka T, Tsunoda T, Deloukas P, Bird CP, Delgado M, Dermitzakis ET, Gwilliam R, Hunt S, Morrison J, Powell D, Stranger BE, Whittaker P, Bentley DR, Daly MJ, de Bakker PI, Barrett J, Chretien YR, Maller J, McCarroll S, Patterson N, Pe'er I, Price A, Purcell S, Richter DJ, Sabeti P, Saxena R, Schaffner SF, Sham PC, Varilly P, Altshuler D, Stein LD, Krishnan L, Smith AV, Tello-Ruiz MK, Thorisson GA, Chakravarti A, Chen PE, Cutler DJ, Kashuk CS, Lin S, Abecasis GR, Guan W, Li Y, Munro HM, Qin ZS, Thomas DJ, McVean G, Auton A, Bottolo L, Cardin N, Eyheramendy S, Freeman C, Marchini J, Myers S, Spencer C, Stephens M, Donnelly P, Cardon LR, Clarke G, Evans DM, Morris AP, Weir BS, Tsunoda T, Mullikin JC, Sherry ST, Feolo M, Skol A, Zhang H, Zeng C, Zhao H, Matsuda I, Fukushima Y, Macer DR, Suda E, Rotimi CN, Adebamowo CA, Ajayi I, Aniagwu T, Marshall PA, Nkwodimmah C, Royal CD, Leppert MF, Dixon M, Peiffer A, Qiu R, Kent A, Kato K, Niikawa N, Adewole IF, Knoppers BM, Foster MW, Clayton EW, Watkin J, Gibbs RA, Belmont JW, Muzny D, Nazareth L, Sodergren E, Weinstock GM, Wheeler DA, Yakub I, Gabriel SB, Onofrio RC, Richter DJ, Ziaugra L, Birren BW, Daly MJ, Altshuler D, Wilson RK, Fulton LL, Rogers J, Burton J, Carter NP, Clee CM, Griffiths M, Jones MC, McLay K, Plumb RW, Ross MT, Sims SK, Willey DL, Chen Z, Han H, Kang L, Godbout M, Wallenburg JC, L'Archevêque P, Bellemare G, Saeki K, Wang H, An D, Fu H, Li Q, Wang Z, Wang R, Holden AL, Brooks LD, McEwen JE, Guyer MS, Wang VO, Peterson JL, Shi M, Spiegel J, Sung LM, Zacharia LF, Collins FS, Kennedy K, Jamieson R, Stewart J.

Nature. 2007 Oct 18;449(7164):851-61.

18.

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
19.

PLINK: a tool set for whole-genome association and population-based linkage analyses.

Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, Maller J, Sklar P, de Bakker PI, Daly MJ, Sham PC.

Am J Hum Genet. 2007 Sep;81(3):559-75. Epub 2007 Jul 25.

20.

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.

Am J Hum Genet. 2007 May;80(5):957-65. Epub 2007 Mar 12.

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