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Items: 16


Innovative strategies for annotating the "relationSNP" between variants and molecular phenotypes.

Miller JE, Veturi Y, Ritchie MD.

BioData Min. 2019 May 14;12:10. doi: 10.1186/s13040-019-0197-9. eCollection 2019. Review.


Influence of tissue context on gene prioritization for predicted transcriptome-wide association studies.

Li B, Veturi Y, Bradford Y, Verma SS, Verma A, Lucas AM, Haas DW, Ritchie MD.

Pac Symp Biocomput. 2019;24:296-307.


Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43,870 individuals from the eMERGE network.

Zhang X, Veturi Y, Verma S, Bone W, Verma A, Lucas A, Hebbring S, Denny JC, Stanaway IB, Jarvik GP, Crosslin D, Larson EB, Rasmussen-Torvik L, Pendergrass SA, Smoller JW, Hakonarson H, Sleiman P, Weng C, Fasel D, Wei WQ, Kullo I, Schaid D, Chung WK, Ritchie MD.

Pac Symp Biocomput. 2019;24:272-283.


Modeling Heterogeneity in the Genetic Architecture of Ethnically Diverse Groups Using Random Effect Interaction Models.

Veturi Y, de Los Campos G, Yi N, Huang W, Vazquez AI, Kühnel B.

Genetics. 2019 Apr;211(4):1395-1407. doi: 10.1534/genetics.119.301909. Epub 2019 Feb 22.


Using Adipose Measures from Health Care Provider-Based Imaging Data for Discovery.

Cha EDK, Veturi Y, Agarwal C, Patel A, Arbabshirani MR, Pendergrass SA.

J Obes. 2018 Sep 27;2018:3253096. doi: 10.1155/2018/3253096. eCollection 2018.


Author Correction: Rare variants in drug target genes contributing to complex diseases, phenome-wide.

Verma SS, Josyula N, Verma A, Zhang X, Veturi Y, Dewey FE, Hartzel DN, Lavage DR, Leader J, Ritchie MD, Pendergrass SA.

Sci Rep. 2018 Oct 23;8(1):15911. doi: 10.1038/s41598-018-27936-7.


Collective feature selection to identify crucial epistatic variants.

Verma SS, Lucas A, Zhang X, Veturi Y, Dudek S, Li B, Li R, Urbanowicz R, Moore JH, Kim D, Ritchie MD.

BioData Min. 2018 Apr 19;11:5. doi: 10.1186/s13040-018-0168-6. eCollection 2018.


Rare variants in drug target genes contributing to complex diseases, phenome-wide.

Verma SS, Josyula N, Verma A, Zhang X, Veturi Y, Dewey FE, Hartzel DN, Lavage DR, Leader J, Ritchie MD, Pendergrass SA.

Sci Rep. 2018 Mar 15;8(1):4624. doi: 10.1038/s41598-018-22834-4. Erratum in: Sci Rep. 2018 Oct 23;8(1):15911.


Evaluation of PrediXcan for prioritizing GWAS associations and predicting gene expression.

Li B, Verma SS, Veturi YC, Verma A, Bradford Y, Haas DW, Ritchie MD.

Pac Symp Biocomput. 2018;23:448-459.


Increased Proportion of Variance Explained and Prediction Accuracy of Survival of Breast Cancer Patients with Use of Whole-Genome Multiomic Profiles.

Vazquez AI, Veturi Y, Behring M, Shrestha S, Kirst M, Resende MF Jr, de Los Campos G.

Genetics. 2016 Jul;203(3):1425-38. doi: 10.1534/genetics.115.185181. Epub 2016 Apr 29.


Incorporating Genetic Heterogeneity in Whole-Genome Regressions Using Interactions.

de Los Campos G, Veturi Y, Vazquez AI, Lehermeier C, Pérez-Rodríguez P.

J Agric Biol Environ Stat. 2015;20(4):467-490. Epub 2015 Nov 9.


Assessment of whole-genome regression for type II diabetes.

Vazquez AI, Klimentidis YC, Dhurandhar EJ, Veturi YC, Paérez-Rodríguez P.

PLoS One. 2015 Apr 17;10(4):e0123818. doi: 10.1371/journal.pone.0123818. eCollection 2015.


Effectiveness of shrinkage and variable selection methods for the prediction of complex human traits using data from distantly related individuals.

Berger S, Pérez-Rodríguez P, Veturi Y, Simianer H, de los Campos G.

Ann Hum Genet. 2015 Mar;79(2):122-35. doi: 10.1111/ahg.12099. Epub 2015 Jan 20. Erratum in: Ann Hum Genet. 2018 Mar;82(2):127.


Multivariate mixed linear model analysis of longitudinal data: an information-rich statistical technique for analyzing plant disease resistance.

Veturi Y, Kump K, Walsh E, Ott O, Poland J, Kolkman JM, Balint-Kurti PJ, Holland JB, Wisser RJ.

Phytopathology. 2012 Nov;102(11):1016-25. doi: 10.1094/PHYTO-10-11-0268.


A Database Developed with Information Extracted from Chemotherapy Drug Package Inserts to Enhance Future Prescriptions.

D'Souza MJ, Alabed GJ, Wheatley JM, Roberts N, Veturi Y, Bi X, Continisio CH.

Conf Comput Vis Pattern Recognit Workshops. 2011;2011:219-226.

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