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Cited In for PubMed (Select 19474294)


Implications of pleiotropy: challenges and opportunities for mining Big Data in biomedicine.

Yang C, Li C, Wang Q, Chung D, Zhao H.

Front Genet. 2015 Jun 30;6:229. doi: 10.3389/fgene.2015.00229. eCollection 2015. Review.


Mutations Causing Complex Disease May under Certain Circumstances Be Protective in an Epidemiological Sense.

Siegert S, Wolf A, Cooper DN, Krawczak M, Nothnagel M.

PLoS One. 2015 Jul 10;10(7):e0132150. doi: 10.1371/journal.pone.0132150. eCollection 2015.


The Use of Non-Variant Sites to Improve the Clinical Assessment of Whole-Genome Sequence Data.

Ferrarini A, Xumerle L, Griggio F, Garonzi M, Cantaloni C, Centomo C, Vargas SM, Descombes P, Marquis J, Collino S, Franceschi C, Garagnani P, Salisbury BA, Harvey JM, Delledonne M.

PLoS One. 2015 Jul 6;10(7):e0132180. doi: 10.1371/journal.pone.0132180. eCollection 2015.


Phenome-Wide Association Studies: Leveraging Comprehensive Phenotypic and Genotypic Data for Discovery.

Pendergrass SA, Ritchie MD.

Curr Genet Med Rep. 2015 Jun 1;3(2):92-100.


Genomic Scans of Zygotic Disequilibrium and Epistatic SNPs in HapMap Phase III Populations.

Hu XS, Hu Y.

PLoS One. 2015 Jun 30;10(6):e0131039. doi: 10.1371/journal.pone.0131039. eCollection 2015.


dbEMT: an epithelial-mesenchymal transition associated gene resource.

Zhao M, Kong L, Liu Y, Qu H.

Sci Rep. 2015 Jun 23;5:11459. doi: 10.1038/srep11459.


Genome-Wide Association Identifies SLC2A9 and NLN Gene Regions as Associated with Entropion in Domestic Sheep.

Mousel MR, Reynolds JO, White SN.

PLoS One. 2015 Jun 22;10(6):e0128909. doi: 10.1371/journal.pone.0128909. eCollection 2015.


Deciphering Signaling Pathway Networks to Understand the Molecular Mechanisms of Metformin Action.

Sun J, Zhao M, Jia P, Wang L, Wu Y, Iverson C, Zhou Y, Bowton E, Roden DM, Denny JC, Aldrich MC, Xu H, Zhao Z.

PLoS Comput Biol. 2015 Jun 17;11(6):e1004202. doi: 10.1371/journal.pcbi.1004202. eCollection 2015 Jun.


The Associations between RNA Splicing Complex Gene SF3A1 Polymorphisms and Colorectal Cancer Risk in a Chinese Population.

Chen X, Du H, Liu B, Zou L, Chen W, Yang Y, Zhu Y, Gong Y, Tian J, Li F, Zhong S.

PLoS One. 2015 Jun 16;10(6):e0130377. doi: 10.1371/journal.pone.0130377. eCollection 2015.


Common variants of NFE2L2 gene predisposes to acute respiratory distress syndrome in patients with severe sepsis.

Acosta-Herrera M, Pino-Yanes M, Blanco J, Ballesteros JC, Ambrós A, Corrales A, Gandía F, Subirá C, Domínguez D, Baluja A, Añón JM, Adalia R, Pérez-Méndez L, Flores C, Villar J; GRECIA and GEN-SEP networks.

Crit Care. 2015 Jun 16;19:256. doi: 10.1186/s13054-015-0981-y.


Pedican: an online gene resource for pediatric cancers with literature evidence.

Zhao M, Ma L, Liu Y, Qu H.

Sci Rep. 2015 Jun 15;5:11435. doi: 10.1038/srep11435.


The genetic architecture of NAFLD among inbred strains of mice.

Hui ST, Parks BW, Org E, Norheim F, Che N, Pan C, Castellani LW, Charugundla S, Dirks DL, Psychogios N, Neuhaus I, Gerszten RE, Kirchgessner T, Gargalovic PS, Lusis AJ.

Elife. 2015 Jun 12;4. doi: 10.7554/eLife.05607.


Powerful Tukey's One Degree-of-Freedom Test for Detecting Gene-Gene and Gene-Environment Interactions.

Wang Y, Li D, Wei P.

Cancer Inform. 2015 Jun 4;14(Suppl 2):209-18. doi: 10.4137/CIN.S17305. eCollection 2015.


Pharmacogenomic and clinical data link non-pharmacokinetic metabolic dysregulation to drug side effect pathogenesis.

Zielinski DC, Filipp FV, Bordbar A, Jensen K, Smith JW, Herrgard MJ, Mo ML, Palsson BO.

Nat Commun. 2015 Jun 9;6:7101. doi: 10.1038/ncomms8101.


Detection and analysis of disease-associated single nucleotide polymorphism influencing post-translational modification.

Kim Y, Kang C, Min B, Yi GS.

BMC Med Genomics. 2015;8 Suppl 2:S7. doi: 10.1186/1755-8794-8-S2-S7. Epub 2015 May 29.


Human fertility, molecular genetics, and natural selection in modern societies.

Tropf FC, Stulp G, Barban N, Visscher PM, Yang J, Snieder H, Mills MC.

PLoS One. 2015 Jun 3;10(6):e0126821. doi: 10.1371/journal.pone.0126821. eCollection 2015.


Genetic basis of autoimmunity.

Marson A, Housley WJ, Hafler DA.

J Clin Invest. 2015 Jun 1;125(6):2234-41. doi: 10.1172/JCI78086. Epub 2015 Jun 1.


Improved Ancestry Estimation for both Genotyping and Sequencing Data using Projection Procrustes Analysis and Genotype Imputation.

Wang C, Zhan X, Liang L, Abecasis GR, Lin X.

Am J Hum Genet. 2015 Jun 4;96(6):926-37. doi: 10.1016/j.ajhg.2015.04.018. Epub 2015 May 28.


A statistical framework to predict functional non-coding regions in the human genome through integrated analysis of annotation data.

Lu Q, Hu Y, Sun J, Cheng Y, Cheung KH, Zhao H.

Sci Rep. 2015 May 27;5:10576. doi: 10.1038/srep10576.

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