Works matching IS 07410395 AND DT 2011 AND VI 35

Results: 104

Detecting multiple causal rare variants in exome sequence data.

Published in:

Genetic Epidemiology, 2011, v. 35, p. S18, doi. 10.1002/gepi.20644

By:

Ye, Kenny Q.;
Engelman, Corinne D.

Publication type:

Article

Brief review of regression-based and machine learning methods in genetic epidemiology: the Genetic Analysis Workshop 17 experience.

Published in:

Genetic Epidemiology, 2011, v. 35, p. S5, doi. 10.1002/gepi.20642

By:

Dasgupta, Abhijit;
Sun, Yan V.;
König, Inke R.;
Bailey-Wilson, Joan E.;
Malley, James D.

Publication type:

Article

Dealing with high dimensionality for the identification of common and rare variants as main effects and for gene-environment interaction.

Published in:

Genetic Epidemiology, 2011, v. 35, p. S35, doi. 10.1002/gepi.20647

By:

Bickeböller, Heike;
Houwing-Duistermaat, Jeanine J.;
Wang, Xuefeng;
Yan, Xiting

Publication type:

Article

Population-based and family-based designs to analyze rare variants in complex diseases.

Published in:

Genetic Epidemiology, 2011, v. 35, p. S41, doi. 10.1002/gepi.20648

By:

Kazma, Rémi;
Bailey, Julia N.

Publication type:

Article

Regression and data mining methods for analyses of multiple rare variants in the Genetic Analysis Workshop 17 mini-exome data.

Published in:

Genetic Epidemiology, 2011, v. 35, p. S92, doi. 10.1002/gepi.20657

By:

Bailey-Wilson, Joan E.;
Brennan, Jennifer S.;
Bull, Shelley B.;
Culverhouse, Robert;
Kim, Yoonhee;
Jiang, Yuan;
Jung, Jeesun;
Li, Qing;
Lamina, Claudia;
Liu, Ying;
Mägi, Reedik;
Niu, Yue S.;
Simpson, Claire L.;
Wang, Libo;
Yilmaz, Yildiz E.;
Zhang, Heping;
Zhang, Zhaogong

Publication type:

Article

Identification of genetic association of multiple rare variants using collapsing methods.

Published in:

Genetic Epidemiology, 2011, v. 35, p. S101, doi. 10.1002/gepi.20658

By:

Sun, Yan V.;
Sung, Yun Ju;
Tintle, Nathan;
Ziegler, Andreas

Publication type:

Article

Incorporating biological information into association studies of sequencing data.

Published in:

Genetic Epidemiology, 2011, v. 35, p. S29, doi. 10.1002/gepi.20646

By:

Chen, Gary;
Wei, Peng;
DeStefano, Anita L.

Publication type:

Article

Effect of linkage disequilibrium on the identification of functional variants.

Published in:

Genetic Epidemiology, 2011, v. 35, p. S115, doi. 10.1002/gepi.20660

By:

Thomas, Alun;
Abel, Haley J.;
Di, Yanming;
Faye, Laura L.;
Jin, Jing;
Liu, Jin;
Wu, Zheyan;
Paterson, Andrew D.

Publication type:

Article

Quality control issues and the identification of rare functional variants with next-generation sequencing data.

Published in:

Genetic Epidemiology, 2011, v. 35, p. S22, doi. 10.1002/gepi.20645

By:

Hemmelmann, Claudia;
Daw, E. Warwick;
Wilson, Alexander F.

Publication type:

Article

Joint analyses of disease and correlated quantitative phenotypes using next-generation sequencing data.

Published in:

Genetic Epidemiology, 2011, v. 35, p. S67, doi. 10.1002/gepi.20653

By:

Melton, Phillip E.;
Pankratz, Nathan

Publication type:

Article

Multiple testing in high-throughput sequence data: experiences from Group 8 of Genetic Analysis Workshop 17.

Published in:

Genetic Epidemiology, 2011, v. 35, p. S61, doi. 10.1002/gepi.20651

By:

König, Inke R.;
Nsengimana, Jeremie;
Papachristou, Charalampos;
Simonson, Matthew A.;
Wang, Kai;
Weisburd, Jason A.

Publication type:

Article

Introduction to genetic analysis workshop 17 summaries.

Published in:

Genetic Epidemiology, 2011, v. 35, p. S1, doi. 10.1002/gepi.20641

By:

Ziegler, Andreas;
Ghosh, Saurabh;
Dyer, Thomas D.;
Blangero, John;
MacCluer, Jean;
Almasy, Laura

Publication type:

Article

Detecting rare variant associations: methods for testing haplotypes and multiallelic genotypes.

Published in:

Genetic Epidemiology, 2011, v. 35, p. S85, doi. 10.1002/gepi.20656

By:

Cantor, Rita M.;
Wilcox, Marsha

Publication type:

Article

Analysis of exome sequences with and without incorporating prior biological knowledge.

Published in:

Genetic Epidemiology, 2011, v. 35, p. S48, doi. 10.1002/gepi.20649

By:

Namkung, Junghyun;
Raska, Paola;
Kang, Jia;
Liu, Yunlong;
Lu, Qing;
Zhu, Xiaofeng

Publication type:

Article

Rare variants, common markers: synthetic association and beyond.

Published in:

Genetic Epidemiology, 2011, v. 35, p. S80, doi. 10.1002/gepi.20655

By:

Kent, Jack W.

Publication type:

Article

Multilocus association testing with penalized regression.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 8, p. 755, doi. 10.1002/gepi.20625

By:

Basu, Saonli;
Pan, Wei;
Shen, Xiaotong;
Oetting, William S.

Publication type:

Article

Lessons learned from Genetic Analysis Workshop 17: transitioning from genome-wide association studies to whole-genome statistical genetic analysis.

Published in:

Genetic Epidemiology, 2011, v. 35, p. S107, doi. 10.1002/gepi.20659

By:

Wilson, Alexander F.;
Ziegler, Andreas

Publication type:

Article

Statistical analysis of rare sequence variants: an overview of collapsing methods.

Published in:

Genetic Epidemiology, 2011, v. 35, p. S12, doi. 10.1002/gepi.20643

By:

Dering, Carmen;
Hemmelmann, Claudia;
Pugh, Elizabeth;
Ziegler, Andreas

Publication type:

Article

Incorporating linkage information into a common disease/rare variant framework.

Published in:

Genetic Epidemiology, 2011, v. 35, p. S74, doi. 10.1002/gepi.20654

By:

Hinrichs, Anthony L.;
Suarez, Brian K.

Publication type:

Article

Evaluation of an approximation method for assessment of overall significance of multiple-dependent tests in a genomewide association study.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 8, p. 861, doi. 10.1002/gepi.20636

By:

Moskvina, Valentina;
O'Dushlaine, Colm;
Purcell, Shaun;
Craddock, Nick;
Holmans, Peter;
O'Donovan, Michael C.

Publication type:

Article

Rapid testing of gene-gene interactions in genome-wide association studies of binary and quantitative phenotypes.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 8, p. 800, doi. 10.1002/gepi.20629

By:

Bhattacharya, Kanishka;
McCarthy, Mark I.;
Morris, Andrew P.

Publication type:

Article

Inflated type I error rates when using aggregation methods to analyze rare variants in the 1000 Genomes Project exon sequencing data in unrelated individuals: summary results from Group 7 at Genetic Analysis Workshop 17.

Published in:

Genetic Epidemiology, 2011, v. 35, p. S56, doi. 10.1002/gepi.20650

By:

Tintle, Nathan;
Aschard, Hugues;
Hu, Inchi;
Nock, Nora;
Wang, Haitian;
Pugh, Elizabeth

Publication type:

Article

Improving power and robustness for detecting genetic association with extreme-value sampling design.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 8, p. 823, doi. 10.1002/gepi.20631

By:

Chen, Hua Yun;
Li, Mingyao

Publication type:

Article

Stability selection for genome-wide association.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 7, p. 722, doi. 10.1002/gepi.20623

By:

Alexander, David H.;
Lange, Kenneth

Publication type:

Article

Bayesian semiparametric meta-analysis for genetic association studies.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 5, p. 333, doi. 10.1002/gepi.20581

By:

De Iorio, Maria;
Newcombe, Paul J.;
Tachmazidou, Ioanna;
Verzilli, Claudio J.;
Whittaker, John C.

Publication type:

Article

Identity-by-descent-based phasing and imputation in founder populations using graphical models.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 8, p. 853, doi. 10.1002/gepi.20635

By:

Palin, Kimmo;
Campbell, Harry;
Wright, Alan F.;
Wilson, James F.;
Durbin, Richard

Publication type:

Article

Transethnic meta-analysis of genomewide association studies.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 8, p. 809, doi. 10.1002/gepi.20630

By:

Morris, Andrew P.

Publication type:

Article

Sifting the wheat from the chaff: prioritizing GWAS results by identifying consistency across analytical methods.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 8, p. 745, doi. 10.1002/gepi.20622

By:

Oldmeadow, Christopher;
Riveros, Carlos;
Holliday, Elizabeth G.;
Scott, Rodney;
Moscato, Pablo;
Wang, Jie Jin;
Mitchell, Paul;
Buitendijk, Gabrielle H.S.;
Vingerling, Johannes R.;
Klaver, Caroline C.W.;
Klein, Ronald;
Attia, John

Publication type:

Article

Approximate and exact tests of Hardy-Weinberg equilibrium using uncertain genotypes.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 7, p. 632, doi. 10.1002/gepi.20612

By:

Shriner, Daniel

Publication type:

Article

Using extreme phenotype sampling to identify the rare causal variants of quantitative traits in association studies.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 8, p. 790, doi. 10.1002/gepi.20628

By:

Li, Dalin;
Lewinger, Juan Pablo;
Gauderman, William J.;
Murcray, Cassandra Elizabeth;
Conti, David

Publication type:

Article

Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 8, p. 887, doi. 10.1002/gepi.20639

By:

Zuvich, Rebecca L.;
Armstrong, Loren L.;
Bielinski, Suzette J.;
Bradford, Yuki;
Carlson, Christopher S.;
Crawford, Dana C.;
Crenshaw, Andrew T.;
de Andrade, Mariza;
Doheny, Kimberly F.;
Haines, Jonathan L.;
Hayes, M. Geoffrey;
Jarvik, Gail P.;
Jiang, Lan;
Kullo, Iftikhar J.;
Li, Rongling;
Ling, Hua;
Manolio, Teri A.;
Matsumoto, Martha E.;
McCarty, Catherine A.;
McDavid, Andrew N.

Publication type:

Article

Genetic epidemiology with a Capital E, ten years after.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 8, p. 845, doi. 10.1002/gepi.20634

By:

Khoury, Muin J.;
Gwinn, Marta;
Clyne, Mindy;
Yu, Wei

Publication type:

Article

On the analysis of sequence data: testing for disease susceptibility loci using patterns of linkage disequilibrium.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 8, p. 880, doi. 10.1002/gepi.20638

By:

Lipman, Peter J.;
Yip, Wai-Ki;
AlChawa, Taofik;
Ludwig, Kerstin U.;
Mangold, Elisabeth;
Lange, Christoph

Publication type:

Article

Defining the power limits of genome-wide association scan meta-analyses.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 8, p. 781, doi. 10.1002/gepi.20627

By:

Chapman, Kay;
Ferreira, Teresa;
Morris, Andrew;
Asimit, Jennifer;
Zeggini, Eleftheria

Publication type:

Article

PlatinumCNV: A Bayesian Gaussian mixture model for genotyping copy number polymorphisms using SNP array signal intensity data.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 8, p. 831, doi. 10.1002/gepi.20633

By:

Kumasaka, Natsuhiko;
Fujisawa, Hironori;
Hosono, Naoya;
Okada, Yukinori;
Takahashi, Atsushi;
Nakamura, Yusuke;
Kubo, Michiaki;
Kamatani, Naoyuki

Publication type:

Article

Haplotype variation and genotype imputation in African populations.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 8, p. 766, doi. 10.1002/gepi.20626

By:

Huang, Lucy;
Jakobsson, Mattias;
Pemberton, Trevor J.;
Ibrahim, Muntaser;
Nyambo, Thomas;
Omar, Sabah;
Pritchard, Jonathan K.;
Tishkoff, Sarah A.;
Rosenberg, Noah A.

Publication type:

Article

To stratify or not to stratify: power considerations for population-based genome-wide association studies of quantitative traits.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 8, p. 867, doi. 10.1002/gepi.20637

By:

Behrens, Gundula;
Winkler, Thomas W.;
Gorski, Mathias;
Leitzmann, Michael F.;
Heid, Iris M.

Publication type:

Article

A comparison of strategies for analyzing dichotomous outcomes in genome-wide association studies with general pedigrees.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 7, p. 650, doi. 10.1002/gepi.20614

By:

Chen, Ming-Huei;
Liu, Xuan;
Wei, Fengrong;
Larson, Martin G.;
Fox, Caroline S.;
Vasan, Ramachandran S.;
Yang, Qiong

Publication type:

Article

Robust Mantel-Haenszel test under genetic model uncertainty allowing for covariates in case-control association studies.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 7, p. 695, doi. 10.1002/gepi.20620

By:

Zang, Yong;
Fung, Wing Kam

Publication type:

Article

Incorporating model uncertainty in detecting rare variants: the Bayesian risk index.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 7, p. 638, doi. 10.1002/gepi.20613

By:

Quintana, Melanie A.;
Berstein, Jonine L.;
Thomas, Duncan C.;
Conti, David V.

Publication type:

Article

A fast algorithm to optimize SNP prioritization for gene-gene and gene-environment interactions.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 7, p. 729, doi. 10.1002/gepi.20624

By:

Q. Deng, Wei;
Paré, Guillaume

Publication type:

Article

A test of Hardy-Weinberg equilibrium in structured populations.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 7, p. 671, doi. 10.1002/gepi.20617

By:

Sha, Qiuying;
Zhang, Shuanglin

Publication type:

Article

A data-driven method for identifying rare variants with heterogeneous trait effects.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 7, p. 679, doi. 10.1002/gepi.20618

By:

Zhang, Qunyuan;
Irvin, Marguerite R.;
Arnett, Donna K.;
Province, Michael A.;
Borecki, Ingrid

Publication type:

Article

Detecting genetic interactions for quantitative traits with U-statistics.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 6, p. 457, doi. 10.1002/gepi.20594

By:

Li, Ming;
Ye, Chengyin;
Fu, Wenjiang;
Elston, Robert C.;
Lu, Qing

Publication type:

Article

X chromosome association testing in genome wide association studies.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 7, p. 664, doi. 10.1002/gepi.20616

By:

Hickey, Peter F.;
Bahlo, Melanie

Publication type:

Article

Comparison of statistical tests for disease association with rare variants.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 7, p. 606, doi. 10.1002/gepi.20609

By:

Basu, Saonli;
Pan, Wei

Publication type:

Article

Power and type I error results for a bias-correction approach recently shown to provide accurate odds ratios of genetic variants for the secondary phenotypes associated with primary diseases.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 7, p. 739, doi. 10.1002/gepi.20611

By:

Wang, Jian;
Shete, Sanjay

Publication type:

Article

Identification of association between disease and multiple markers via sparse partial least-squares regression.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 6, p. 479, doi. 10.1002/gepi.20596

By:

Chun, Hyonho;
Ballard, David H.;
Cho, Judy;
Zhao, Hongyu

Publication type:

Article

A new association test based on Chi-square partition for case-control GWA studies.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 7, p. 658, doi. 10.1002/gepi.20615

By:

Chen, Zhongxue

Publication type:

Article

The use of imputed values in the meta-analysis of genome-wide association studies.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 7, p. 597, doi. 10.1002/gepi.20608

By:

Jiao, Shuo;
Hsu, Li;
Hutter, Carolyn M.;
Peters, Ulrike

Publication type:

Article