Joan E Bailey-Wilson

发表

Inferring Disease Risk Genes from Sequencing Data in Multiplex Pedigrees Through Sharing of Rare Variants

Ingo Ruczinski, Alexandre Bureau, Ferdouse Begum, 2018, bioRxiv.

Comparison of results from tests of association in unrelated individuals with uncollapsed and collapsed sequence variants using tiled regression

Qing Li, Heejong Sung, Yoonhee Kim, 2011, BMC proceedings.

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

Abhijit Dasgupta, Joan E Bailey-Wilson, James D Malley, 2011, Genetic epidemiology.

A comparison study of multivariate fixed models and Gene Association with Multiple Traits (GAMuT) for next‐generation sequencing

Momiao Xiong, Joan E Bailey-Wilson, Ruzong Fan, 2017, Genetic epidemiology.

Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error.

Christian Gieger, Thomas Meitinger, Paul Mitchell, 2013, Human molecular genetics.

Normalization of microarray expression data using within-pedigree pool and its effect on linkage analysis

Joan E Bailey-Wilson, Betty Q Doan, J. Bailey-Wilson, 2007, BMC proceedings.

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

Heping Zhang, Ying Liu, Joan E Bailey-Wilson, 2011, Genetic epidemiology.

Evaluation of random forests performance for genome-wide association studies in the presence of interaction effects

Li Wang, Heejong Sung, Joan E Bailey-Wilson, 2009, BMC proceedings.

Genome-wide scan for myopia in the Old Order Amish.

Joan E Bailey-Wilson, Dwight Stambolian, J. Bailey-Wilson, 2005, American journal of ophthalmology.

Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error.

Thomas Meitinger, Toomas Haller, Andres Metspalu, 2013, American journal of human genetics.

Genetic Analysis Workshop 13: Analysis of Longitudinal Family Data for Complex Diseases and Related Risk Factors

Joan E Bailey-Wilson, Christopher I Amos, Rita M Cantor, 2003, BMC Genetics.

Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy

Nathan J Morris, Xuejun Qin, Joan E Bailey-Wilson, 2017, Nature Communications.

Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association

Joan E Bailey-Wilson, Cheryl D Cropp, Alexander F Wilson, 2012, Proceedings of the National Academy of Sciences.

Inferring relationships between pairs of individuals from locus heterozygosities

Joan E Bailey-Wilson, Francesco De Stefano, Silvano Presciuttini, 2002, BMC Genetics.

Haplotypic structure of the X chromosome in the COGA population sample and the quality of its reconstruction by extant software packages

Joan E Bailey-Wilson, Silvano Presciuttini, Chiara Toni, 2005, BMC Genetics.

REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants.

Trevor Hastie, Predrag Radivojac, Saurabh Baheti, 2016, American journal of human genetics.

DNA Identifications After the 9/11 World Trade Center Attack

Bruce Budowle, Joan E Bailey-Wilson, Leslie G Biesecker, 2005, Science.

Genome-wide association study of familial lung cancer

Paul Brennan, Mariza de Andrade, Maria Teresa Landi, 2018, Carcinogenesis.

ARLTS1 germline variants and the risk for breast, prostate, and colorectal cancer

Joan E Bailey-Wilson, Heli Nevanlinna, Rainer Fagerholm, 2008, European Journal of Human Genetics.

Pleiotropy Analysis of Quantitative Traits at Gene Level by Multivariate Functional Linear Models

Momiao Xiong, Joan E Bailey-Wilson, Ruzong Fan, 2015, Genetic epidemiology.

Establishing an adjusted p-value threshold to control the family-wide type 1 error in genome wide association studies

Joan E Bailey-Wilson, Elizabeth M Gillanders, E. Gillanders, 2008, BMC Genomics.