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Items: 1 to 20 of 344

1.

Imputation of missing genotypes within LD-blocks relying on the basic coalescent and beyond: consideration of population growth and structure.

Kabisch M, Hamann U, Lorenzo Bermejo J.

BMC Genomics. 2017 Oct 17;18(1):798. doi: 10.1186/s12864-017-4208-2.

2.

SOCS1 and pattern recognition receptors: TLR9 and RIG-I; novel haplotype associations in Egyptian fibrotic/cirrhotic patients with HCV genotype 4.

Youssef SS, Hamdy NM.

Arch Virol. 2017 Nov;162(11):3347-3354. doi: 10.1007/s00705-017-3498-7. Epub 2017 Jul 31.

PMID:
28762092
3.

Non-additive and epistatic effects of HLA polymorphisms contributing to risk of adult glioma.

Zhang C, de Smith AJ, Smirnov IV, Wiencke JK, Wiemels JL, Witte JS, Walsh KM.

J Neurooncol. 2017 Nov;135(2):237-244. doi: 10.1007/s11060-017-2569-7. Epub 2017 Jul 18.

PMID:
28721485
4.

LMWH in IVF - Biomarkers and benefits.

Fishel S, Baker DJ, Greer IA.

Thromb Res. 2017 Mar;151 Suppl 1:S65-S69. doi: 10.1016/S0049-3848(17)30071-3. Review.

PMID:
28262239
5.

DQB1*060101 may contribute to susceptibility to immunoglobulin A nephropathy in southern Han Chinese.

Wang W, Li M, Wang L, Yu X.

Front Med. 2016 Dec;10(4):507-516. doi: 10.1007/s11684-016-0475-6. Epub 2016 Dec 23.

PMID:
27896619
6.

Associations of DNMT3B -149C>T and -2437T>A polymorphisms and lung cancer risk in Chinese population.

Gao M, He D, Meng F, Li J, Shen Y.

World J Surg Oncol. 2016 Nov 22;14(1):293.

7.

Relationships between Common and Novel Interleukin-6 Gene Polymorphisms and Risk of Cervical Cancer: a Case-Control Study.

Zidi S, Stayoussef M, Alsaleh BL, Gazouani E, Mezlini A, Ebrahim BH, Yacoubi-Loueslati B, Almawi WY.

Pathol Oncol Res. 2017 Apr;23(2):385-392. doi: 10.1007/s12253-016-0127-9. Epub 2016 Oct 8.

PMID:
27722983
8.

Are Interactions between cis-Regulatory Variants Evidence for Biological Epistasis or Statistical Artifacts?

Fish AE, Capra JA, Bush WS.

Am J Hum Genet. 2016 Oct 6;99(4):817-830. doi: 10.1016/j.ajhg.2016.07.022. Epub 2016 Sep 15.

9.

Association between genetic polymorphisms of MMP8 and the risk of steroid-induced osteonecrosis of the femoral head in the population of northern China.

Du J, Jin T, Cao Y, Chen J, Guo Y, Sun M, Li J, Zhang X, Wang G, Wang J.

Medicine (Baltimore). 2016 Sep;95(37):e4794. doi: 10.1097/MD.0000000000004794.

10.

Association study of two functional single nucleotide polymorphisms of neuropeptide y gene with multiple sclerosis.

Mohammadi SM, Shirvani Farsani Z, Dosti R, Sahraian MA, Behmanesh M.

Neuropeptides. 2016 Dec;60:45-50. doi: 10.1016/j.npep.2016.08.004. Epub 2016 Aug 8.

PMID:
27559040
11.

Meta-Analysis of Mitochondrial DNA Variation in the Iberian Peninsula.

Barral-Arca R, Pischedda S, Gómez-Carballa A, Pastoriza A, Mosquera-Miguel A, López-Soto M, Martinón-Torres F, Álvarez-Iglesias V, Salas A.

PLoS One. 2016 Jul 21;11(7):e0159735. doi: 10.1371/journal.pone.0159735. eCollection 2016.

12.

Associations between ERAP1 polymorphisms and susceptibility to ankylosing spondylitis: a meta-analysis.

Lee YH, Song GG.

Clin Rheumatol. 2016 Aug;35(8):2009-2015. doi: 10.1007/s10067-016-3287-9. Epub 2016 Apr 25. Review.

PMID:
27108589
13.

Genetic Investigation of Complement Pathway Genes in Type 2 Diabetic Retinopathy: An Inflammatory Perspective.

Yang MM, Wang J, Ren H, Sun YD, Fan JJ, Teng Y, Li YB.

Mediators Inflamm. 2016;2016:1313027. doi: 10.1155/2016/1313027. Epub 2016 Feb 16.

14.

Rapid Detection of the Three Celiac Disease Risk Genotypes HLA-DQ2.2, HLA-DQ2.5, and HLA-DQ8 by Multiplex Ligation-Dependent Probe Amplification.

Vijzelaar R, van der Zwan E, van Gammeren A, Yilmaz R, Verheul A, van Hoogstraten I, de Baar E, Schrauwen L, Kortlandt W.

Genet Test Mol Biomarkers. 2016 Mar;20(3):158-61. doi: 10.1089/gtmb.2015.0233. Epub 2016 Jan 22.

PMID:
26798991
15.

Association of Apolipoprotein A5 Gene Polymorphisms with Metabolic Syndrome in the Korean Population.

Kim YR, Hong SH.

Genet Test Mol Biomarkers. 2016 Mar;20(3):130-6. doi: 10.1089/gtmb.2015.0250. Epub 2016 Jan 13.

PMID:
26760709
16.

Female genetic distribution bias in mitochondrial genome observed in Parkinson's Disease patients in northern China.

Chu Q, Luo X, Zhan X, Ren Y, Pang H.

Sci Rep. 2015 Nov 25;5:17170. doi: 10.1038/srep17170.

17.

Polymorphisms and minihaplotypes in the VvNAC26 gene associate with berry size variation in grapevine.

Tello J, Torres-Pérez R, Grimplet J, Carbonell-Bejerano P, Martínez-Zapater JM, Ibáñez J.

BMC Plant Biol. 2015 Oct 23;15:253. doi: 10.1186/s12870-015-0622-2.

18.

Association of haplotypes of the TLR8 locus with susceptibility to Crohn's and Behçet's diseases.

Ortiz-Fernández L, García-Lozano JR, Montes-Cano MA, Conde-Jaldón M, Leo E, Ortego-Centeno N, Gómez-García M, García-Hernández FJ, Márquez JL, Espinosa G, Graña-Gil G, Sánchez-Bursón J, Juliá MR, Blanco R, Barnosi-Marín AC, Solans R, Fanlo P, Rodríguez-Carballeira M, Camps T, Castañeda S, Martín J, González-Escribano MF.

Clin Exp Rheumatol. 2015 Nov-Dec;33(6 Suppl 94):S117-22. Epub 2015 Oct 19.

PMID:
26486764
19.

Association between susceptibility to rheumatoid arthritis and PADI4 polymorphisms: a meta-analysis.

Lee YH, Bae SC.

Clin Rheumatol. 2016 Apr;35(4):961-71. doi: 10.1007/s10067-015-3098-4. Epub 2015 Oct 16.

PMID:
26474773
20.

MAPT H1 Haplotype is Associated with Late-Onset Alzheimer's Disease Risk in APOEɛ4 Noncarriers: Results from the Dementia Genetics Spanish Consortium.

Pastor P, Moreno F, Clarimón J, Ruiz A, Combarros O, Calero M, López de Munain A, Bullido MJ, de Pancorbo MM, Carro E, Antonell A, Coto E, Ortega-Cubero S, Hernandez I, Tárraga L, Boada M, Lleó A, Dols-Icardo O, Kulisevsky J, Vázquez-Higuera JL, Infante J, Rábano A, Fernández-Blázquez MÁ, Valentí M, Indakoetxea B, Barandiarán M, Gorostidi A, Frank-García A, Sastre I, Lorenzo E, Pastor MA, Elcoroaristizabal X, Lennarz M, Maier W, Rámirez A, Serrano-Ríos M, Lee SE, Sánchez-Juan P; Dementia Genetic Spanish Consortium (DEGESCO).

J Alzheimers Dis. 2016;49(2):343-52. doi: 10.3233/JAD-150555.

PMID:
26444794

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