Dynamic pathway analysis of genes associated with blood pressure using whole genome sequence data

by Hu, Pingzhao, Paterson, Andrew D
Published 2014

Evaluating outlier loci and their effect on the identification of pedigree errors

by Wang, Ke-Sheng, Liu, Michelle, Paterson, Andrew D
Published 2005

Genetic analysis of common factors underlying cardiovascular disease-related traits

by Liu, Xiao-Qing, Hanley, Anthony JG, Paterson, Andrew D
Published 2003

Transmission ratio distortion in families from the Framingham Heart Study

by Paterson, Andrew D, Sun, Lei, Liu, Xiao-Qing
Published 2003

Factors associated with heterogeneity in microarray gene expression in peripheral blood mononuclear cells from large pedigrees

by Gallaugher, Michael, Canty, Angelo J., Paterson, Andrew D.
Published 2016

Identity-by-descent mapping for diastolic blood pressure in unrelated Mexican Americans

by Liu, Xiao-Qing, Fazio, Jillian, Hu, Pingzhao, Paterson, Andrew D.
Published 2016

Assessment and Selection of Competing Models for Zero-Inflated Microbiome Data

by Xu, Lizhen, Paterson, Andrew D., Turpin, Williams, Xu, Wei
Published 2015

Genetic Analysis Workshop 18 single-nucleotide variant prioritization based on protein impact, sequence conservation, and gene annotation

by Nalpathamkalam, Thomas, Derkach, Andriy, Paterson, Andrew D, Merico, Daniele
Published 2014

ANKH variants associated with ankylosing spondylitis: gender differences

by Tsui, Hing Wo, Inman, Robert D, Paterson, Andrew D, Reveille, John D, Tsui, Florence WL
Published 2005

A genome scan for parent-of-origin linkage effects in alcoholism

by Liu, Xiao-Qing, Greenwood, Celia MT, Wang, Ke-Sheng, Paterson, Andrew D
Published 2005

Pathway-based joint effects analysis of rare genetic variants using Genetic Analysis Workshop 17 exon sequence data

by Hu, Pingzhao, Xu, Wei, Cheng, Lu, Xing, Xiang, Paterson, Andrew D
Published 2011

BR-squared: a practical solution to the winner’s curse in genome-wide scans

by Sun, Lei, Dimitromanolakis, Apostolos, Faye, Laura L., Paterson, Andrew D., Waggott, Daryl, Bull, Shelley B.
Published 2011

GRIN1 polymorphisms do not affect susceptibility or phenotype in NMDA receptor encephalitis

by Day, Gregory S., Prüss, Harald, Benseler, Susanne M., Paton, Tara A., Paterson, Andrew D., Andrade, Danielle M.
Published 2015

Resampling to Address the Winner's Curse in Genetic Association Analysis of Time to Event

by Poirier, Julia G., Faye, Laura L., Dimitromanolakis, Apostolos, Paterson, Andrew D., Sun, Lei, Bull, Shelley B.
Published 2015

Assessing models for genetic prediction of complex traits: a comparison of visualization and quantitative methods

by Gagliano, Sarah A., Paterson, Andrew D., Weale, Michael E., Knight, Jo
Published 2015

Using a Bayesian latent variable approach to detect pleiotropy in the Genetic Analysis Workshop 18 data

by Xu, Lizhen, Craiu, Radu V, Derkach, Andriy, Paterson, Andrew D, Sun, Lei
Published 2014

Evaluation of gene-based association tests for analyzing rare variants using Genetic Analysis Workshop 18 data

by Derkach, Andriy, Lawless , Jerry F, Merico, Daniele, Paterson, Andrew D, Sun, Lei
Published 2014

An analysis of identical single-nucleotide polymorphisms genotyped by two different platforms

by Suarez, Brian K, Taylor, Chelsea, Bertelsen, Sarah, Bierut, Laura J, Dunn, Gerald, Jin, Carol H, Kauwe, John SK, Paterson, Andrew D, Hinrichs, Anthony L
Published 2005

Cortactin is necessary for E-cadherin–mediated contact formation and actin reorganization

by Helwani, Falak M., Kovacs, Eva M., Paterson, Andrew D., Verma, Suzie, Ali, Radiya G., Fanning, Alan S., Weed, Scott A., Yap, Alpha S.
Published 2004

Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism

by Vieland, Veronica J., Hallmayer, Joachim, Huang, Yungui, Pagnamenta, Alistair T., Pinto, Dalila, Khan, Hameed, Monaco, Anthony P., Paterson, Andrew D., Scherer, Stephen W., Sutcliffe, James S., Szatmari, Peter
Published 2011