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Items: 1 to 20 of 88


A forest-based feature screening approach for large-scale genome data with complex structures.

Wang G, Fu G, Corcoran C.

BMC Genet. 2015 Dec 23;16:148. doi: 10.1186/s12863-015-0294-9.


A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females.

Sharma S, Londono D, Eckalbar WL, Gao X, Zhang D, Mauldin K, Kou I, Takahashi A, Matsumoto M, Kamiya N, Murphy KK, Cornelia R; TSRHC Scoliosis Clinical Group; Japan Scoliosis Clinical Research Group, Herring JA, Burns D, Ahituv N, Ikegawa S, Gordon D, Wise CA.

Nat Commun. 2015 Mar 18;6:6452. doi: 10.1038/ncomms7452.


Analysis of baseline, average, and longitudinally measured blood pressure data using linear mixed models.

Hossain A, Beyene J.

BMC Proc. 2014 Jun 17;8(Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S80. doi: 10.1186/1753-6561-8-S1-S80. eCollection 2014.


A set-based association test identifies sex-specific gene sets associated with type 2 diabetes.

He T, Zhong PS, Cui Y.

Front Genet. 2014 Nov 12;5:395. doi: 10.3389/fgene.2014.00395. eCollection 2014.


The polymorphism in the promoter of HSP70 gene is associated with heat tolerance of two congener endemic bay scallops (Argopecten irradians irradians and A. i. concentricus).

Yang C, Wang L, Wang J, Jiang Q, Qiu L, Zhang H, Song L.

PLoS One. 2014 Jul 16;9(7):e102332. doi: 10.1371/journal.pone.0102332. eCollection 2014.


Antioxidant defense enzyme genes and asthma susceptibility: gender-specific effects and heterogeneity in gene-gene interactions between pathogenetic variants of the disease.

Polonikov AV, Ivanov VP, Bogomazov AD, Freidin MB, Illig T, Solodilova MA.

Biomed Res Int. 2014;2014:708903. doi: 10.1155/2014/708903. Epub 2014 May 5.


An omnibus permutation test on ensembles of two-locus analyses can detect pure epistasis and genetic heterogeneity in genome-wide association studies.

Setsirichok D, Tienboon P, Jaroonruang N, Kittichaijaroen S, Wongseree W, Piroonratana T, Usavanarong T, Limwongse C, Aporntewan C, Phadoongsidhi M, Chaiyaratana N.

Springerplus. 2013 May 19;2:230. doi: 10.1186/2193-1801-2-230. eCollection 2013.


A Simple Scalable Association Hypothesis Test Combining Gene-wide Evidence From Multiple Polymorphisms.

Vaidya D, Yanek LR, Mathias RA, Moy TF, Becker DM, Becker LC.

Br J Med Med Res. 2014 Mar;4(6):1413-1422.


Supervised categorical principal component analysis for genome-wide association analyses.

Lu M, Lee HS, Hadley D, Huang JZ, Qian X.

BMC Genomics. 2014;15 Suppl 1:S10. doi: 10.1186/1471-2164-15-S1-S10. Epub 2014 Jan 24.


An approach to predict the risk of glaucoma development by integrating different attribute data.

Tokuda Y, Yagi T, Yoshii K, Ikeda Y, Fuwa M, Ueno M, Nakano M, Omi N, Tanaka M, Mori K, Kageyama M, Nagasaki I, Yagi K, Kinoshita S, Tashiro K.

Springerplus. 2012 Oct 24;1:41. doi: 10.1186/2193-1801-1-41. eCollection 2012.


Genetics of the connectome.

Thompson PM, Ge T, Glahn DC, Jahanshad N, Nichols TE.

Neuroimage. 2013 Oct 15;80:475-88. doi: 10.1016/j.neuroimage.2013.05.013. Epub 2013 May 21. Review.


Single-variant and multi-variant trend tests for genetic association with next-generation sequencing that are robust to sequencing error.

Kim W, Londono D, Zhou L, Xing J, Nato AQ, Musolf A, Matise TC, Finch SJ, Gordon D.

Hum Hered. 2012;74(3-4):172-83. doi: 10.1159/000346824. Epub 2013 Apr 11.


Systems genetics of alcoholism.

Sloan CD, Sayarath V, Moore JH.

Alcohol Res Health. 2008;31(1):14-25. Review.


Genotype patterns at PICALM, CR1, BIN1, CLU, and APOE genes are associated with episodic memory.

Barral S, Bird T, Goate A, Farlow MR, Diaz-Arrastia R, Bennett DA, Graff-Radford N, Boeve BF, Sweet RA, Stern Y, Wilson RS, Foroud T, Ott J, Mayeux R; National Institute on Aging Late-Onset Alzheimer's Disease Genetics Study.

Neurology. 2012 May 8;78(19):1464-71. doi: 10.1212/WNL.0b013e3182553c48. Epub 2012 Apr 25.


Gene-based Higher Criticism methods for large-scale exonic single-nucleotide polymorphism data.

He S, Wu Z.

BMC Proc. 2011 Nov 29;5 Suppl 9:S65. doi: 10.1186/1753-6561-5-S9-S65.


Reconsidering association testing methods using single-variant test statistics as alternatives to pooling tests for sequence data with rare variants.

Kinnamon DD, Hershberger RE, Martin ER.

PLoS One. 2012;7(2):e30238. doi: 10.1371/journal.pone.0030238. Epub 2012 Feb 17.


Multifactor dimensionality reduction as a filter-based approach for genome wide association studies.

Oki NO, Motsinger-Reif AA.

Front Genet. 2011 Nov 21;2:80. doi: 10.3389/fgene.2011.00080. eCollection 2011.


Multilocus genetic analysis of brain images.

Hibar DP, Kohannim O, Stein JL, Chiang MC, Thompson PM.

Front Genet. 2011 Oct 21;2:73. doi: 10.3389/fgene.2011.00073. eCollection 2011.


Schizophrenia risk gene ZNF804A does not influence macroscopic brain structure: an MRI study in 892 volunteers.

Cousijn H, Rijpkema M, Harteveld A, Harrison PJ, Fernández G, Franke B, Arias-Vásquez A.

Mol Psychiatry. 2012 Dec;17(12):1155-7. doi: 10.1038/mp.2011.181. Epub 2012 Jan 24. No abstract available.


TDT-HET: a new transmission disequilibrium test that incorporates locus heterogeneity into the analysis of family-based association data.

Londono D, Buyske S, Finch SJ, Sharma S, Wise CA, Gordon D.

BMC Bioinformatics. 2012 Jan 20;13:13. doi: 10.1186/1471-2105-13-13.

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