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Items: 1 to 20 of 132

1.

Fine mapping of a region of chromosome 11q23.3 reveals independent locus associated with risk of glioma.

Chen H, Sun B, Zhao Y, Song X, Fan W, Zhou K, Zhou L, Mao Y, Lu D.

PLoS One. 2012;7(12):e52864. doi: 10.1371/journal.pone.0052864. Epub 2012 Dec 31.

2.

Functional analysis of the 11q23.3 glioma susceptibility locus implicates PHLDB1 and DDX6 in glioma susceptibility.

Baskin R, Woods NT, Mendoza-Fandiño G, Forsyth P, Egan KM, Monteiro AN.

Sci Rep. 2015 Nov 27;5:17367. doi: 10.1038/srep17367.

3.

Association of sequence variants on chromosomes 20, 11, and 5 (20q13.33, 11q23.3, and 5p15.33) with glioma susceptibility in a Chinese population.

Chen H, Chen Y, Zhao Y, Fan W, Zhou K, Liu Y, Zhou L, Mao Y, Wei Q, Xu J, Lu D.

Am J Epidemiol. 2011 Apr 15;173(8):915-22. doi: 10.1093/aje/kwq457. Epub 2011 Feb 24.

PMID:
21350045
4.

Fine mapping analysis of a region of 20q13.33 identified five independent susceptibility loci for glioma in a Chinese Han population.

Song X, Zhou K, Zhao Y, Huai C, Zhao Y, Yu H, Chen Y, Chen G, Chen H, Fan W, Mao Y, Lu D.

Carcinogenesis. 2012 May;33(5):1065-71. doi: 10.1093/carcin/bgs117. Epub 2012 Mar 2.

PMID:
22387365
5.

Fine-mapping of a region of chromosome 5p15.33 (TERT-CLPTM1L) suggests a novel locus in TERT and a CLPTM1L haplotype are associated with glioma susceptibility in a Chinese population.

Zhao Y, Chen G, Zhao Y, Song X, Chen H, Mao Y, Lu D.

Int J Cancer. 2012 Oct 1;131(7):1569-76. doi: 10.1002/ijc.27417. Epub 2012 Mar 2.

6.

Three SNPs in chromosome 11q23.3 are independently associated with systemic lupus erythematosus in Asians.

Zhang J, Zhang Y, Yang J, Zhang L, Sun L, Pan HF, Hirankarn N, Ying D, Zeng S, Lee TL, Lau CS, Chan TM, Leung AM, Mok CC, Wong SN, Lee KW, Ho MH, Lee PP, Chung BH, Chong CY, Wong RW, Mok MY, Wong WH, Tong KL, Tse NK, Li XP, Avihingsanon Y, Rianthavorn P, Deekajorndej T, Suphapeetiporn K, Shotelersuk V, Ying SK, Fung SK, Lai WM, Garcia-Barceló MM, Cherny SS, Tam PK, Cui Y, Sham PC, Yang S, Ye DQ, Zhang XJ, Lau YL, Yang W.

Hum Mol Genet. 2014 Jan 15;23(2):524-33. doi: 10.1093/hmg/ddt424. Epub 2013 Sep 2.

PMID:
24001599
7.

RTEL1 tagging SNPs and haplotypes were associated with glioma development.

Li G, Jin T, Liang H, Zhang Z, He S, Tu Y, Yang H, Geng T, Cui G, Chen C, Gao G.

Diagn Pathol. 2013 May 17;8:83. doi: 10.1186/1746-1596-8-83.

8.

PXK locus in systemic lupus erythematosus: fine mapping and functional analysis reveals novel susceptibility gene ABHD6.

Oparina NY, Delgado-Vega AM, Martinez-Bueno M, Magro-Checa C, Fernández C, Castro RO, Pons-Estel BA, D'Alfonso S, Sebastiani GD, Witte T, Lauwerys BR, Endreffy E, Kovács L, Escudero A, López-Pedrera C, Vasconcelos C, da Silva BM, Frostegård J, Truedsson L, Martin J, Raya E, Ortego-Centeno N, de Los Angeles Aguirre M, de Ramón Garrido E, Palma MJ, Alarcon-Riquelme ME, Kozyrev SV.

Ann Rheum Dis. 2015 Mar;74(3):e14. doi: 10.1136/annrheumdis-2013-204909. Epub 2014 Feb 17.

PMID:
24534757
9.

The PHLDB1 rs498872 (11q23.3) polymorphism and glioma risk: A meta-analysis.

Gao X, Mi Y, Yan A, Sha B, Guo N, Hu Z, Zhang N, Jiang F, Gou X.

Asia Pac J Clin Oncol. 2015 Dec;11(4):e13-21. doi: 10.1111/ajco.12211. Epub 2014 Jun 17. Review.

PMID:
24935770
10.

Evaluation of 6 candidate genes on chromosome 11q23 for coeliac disease susceptibility: a case control study.

Brophy K, Ryan AW, Turner G, Trimble V, Patel KD, O'Morain C, Kennedy NP, Egan B, Close E, Lawlor G, MacMathuna P, Stevens FM, Abuzakouk M, Feighery C, Kelleher D, McManus R.

BMC Med Genet. 2010 May 17;11:76. doi: 10.1186/1471-2350-11-76.

11.
12.

Association of genetic variants in the retinoblastoma binding protein 6 gene with the risk of glioma: a case-control study in a Chinese Han population.

Hu D, Zhang S, Zhao Y, Wang S, Wang Q, Song X, Lu D, Mao Y, Chen H.

J Neurosurg. 2014 Nov;121(5):1209-18. doi: 10.3171/2014.6.JNS132240. Epub 2014 Aug 15.

PMID:
25127414
13.

Genetic polymorphisms of the HCR gene and a genomic segment in close proximity to HLA-C are associated with patients with psoriasis in Taiwan.

Chang YT, Shiao YM, Chin PJ, Liu YL, Chou FC, Wu S, Lin YF, Li LH, Lin MW, Liu HN, Tsai SF.

Br J Dermatol. 2004 Jun;150(6):1104-11.

PMID:
15214895
14.

Genetic variants of 6q25 and breast cancer susceptibility: a two-stage fine mapping study in a Chinese population.

Han J, Jiang T, Bai H, Gu H, Dong J, Ma H, Hu Z, Shen H.

Breast Cancer Res Treat. 2011 Oct;129(3):901-7. doi: 10.1007/s10549-011-1527-x. Epub 2011 Apr 28.

PMID:
21528353
15.

Investigation of established genetic risk variants for glioma in prediagnostic samples from a population-based nested case-control study.

Wibom C, Späth F, Dahlin AM, Langseth H, Hovig E, Rajaraman P, Johannesen TB, Andersson U, Melin B.

Cancer Epidemiol Biomarkers Prev. 2015 May;24(5):810-6. doi: 10.1158/1055-9965.EPI-14-1106. Epub 2015 Feb 20.

16.

Inherited variant on chromosome 11q23 increases susceptibility to IDH-mutated but not IDH-normal gliomas regardless of grade or histology.

Rice T, Zheng S, Decker PA, Walsh KM, Bracci P, Xiao Y, McCoy LS, Smirnov I, Patoka JS, Hansen HM, Hsuang G, Wiemels JL, Tihan T, Pico AR, Prados MD, Chang SM, Berger MS, Caron A, Fink S, Kollmeyer T, Rynearson A, Voss J, Kosel ML, Fridley BL, Lachance DH, Eckel-Passow JE, Sicotte H, O'Neill BP, Giannini C, Wiencke JK, Jenkins RB, Wrensch MR.

Neuro Oncol. 2013 May;15(5):535-41. doi: 10.1093/neuonc/nos324. Epub 2013 Jan 29.

17.

A novel low-penetrance locus for familial glioma at 15q23-q26.3.

Paunu N, Lahermo P, Onkamo P, Ollikainen V, Rantala I, Helén P, Simola KO, Kere J, Haapasalo H.

Cancer Res. 2002 Jul 1;62(13):3798-802.

18.

Confirmation of the genetic association between the U2AF homology motif (UHM) kinase 1 (UHMK1) gene and schizophrenia on chromosome 1q23.3.

Puri V, McQuillin A, Datta S, Choudhury K, Pimm J, Thirumalai S, Krasucki R, Lawrence J, Quested D, Bass N, Crombie C, Fraser G, Walker N, Moorey H, Ray MK, Sule A, Curtis D, St Clair D, Gurling H.

Eur J Hum Genet. 2008 Oct;16(10):1275-82. doi: 10.1038/ejhg.2008.76. Epub 2008 Apr 16.

19.

Possible association between genetic variants in the H2AFX promoter region and risk of adult glioma in a Chinese Han population.

Fan W, Zhou K, Zhao Y, Wu W, Chen H, Jin L, Chen G, Shi J, Wei Q, Zhang T, Du G, Mao Y, Lu D, Zhou L.

J Neurooncol. 2011 Nov;105(2):211-8. doi: 10.1007/s11060-011-0586-5. Epub 2011 Apr 22.

PMID:
21512825
20.

Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia.

Cope N, Harold D, Hill G, Moskvina V, Stevenson J, Holmans P, Owen MJ, O'Donovan MC, Williams J.

Am J Hum Genet. 2005 Apr;76(4):581-91. Epub 2005 Feb 16. Erratum in: Am J Hum Genet. 2005 Nov;77(5):898.

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