So Many Correlated Tests, So Little Time! Rapid Adjustment of P Values for Multiple Correlated Tests

Por Conneely, Karen N. , Boehnke, Michael 
Publicado em 2007

META-ANALYSIS OF GENETIC ASSOCIATION STUDIES AND ADJUSTMENT FOR MULTIPLE TESTING OF CORRELATED SNPS AND TRAITS

Por Conneely, Karen N., Boehnke, Michael
Publicado em 2010

A Bayesian hierarchical model to detect differentially methylated loci from single nucleotide resolution sequencing data

Por Feng, Hao, Conneely, Karen N., Wu, Hao
Publicado em 2014

Flexible and Robust Methods for Rare-Variant Testing of Quantitative Traits in Trios and Nuclear Families

Por Jiang, Yunxuan, Conneely, Karen N., Epstein, Michael P.
Publicado em 2014

Assessing the Impact of Population Stratification on Association Studies of Rare Variation

Por Jiang, Yunxuan, Epstein, Michael P., Conneely, Karen N.
Publicado no Hum Hered (2013)

DNA Methylation: An Epigenetic Risk Factor in Preterm Birth

Por Menon, Ramkumar, Conneely, Karen N., Smith, Alicia K.
Publicado no Reprod Sci (2012)

CpGassoc: an R function for analysis of DNA methylation microarray data

Por Barfield, Richard T., Kilaru, Varun, Smith, Alicia K., Conneely, Karen N.
Publicado em 2012

Tandem Repeats and G-Rich Sequences Are Enriched at Human CNV Breakpoints

Por Bose, Promita, Hermetz, Karen E., Conneely, Karen N., Rudd, M. Katharine
Publicado em 2014

MethLAB: A graphical user interface package for the analysis of array-based DNA methylation data

Por Kilaru, Varun, Barfield, Richard T, Schroeder, James W, Smith, Alicia K, Conneely, Karen N
Publicado em 2012

Genome-wide analysis validates aberrant methylation in fragile X syndrome is specific to the FMR1 locus

Por Alisch, Reid S, Wang, Tao, Chopra, Pankaj, Visootsak, Jeannie, Conneely, Karen N, Warren, Stephen T
Publicado em 2013

DNA methylation provides insight into intergenerational risk for preterm birth in African Americans

Por Parets, Sasha E, Conneely, Karen N, Kilaru, Varun, Menon, Ramkumar, Smith, Alicia K
Publicado no Epigenetics (2015)

Powerful and Robust Cross-Phenotype Association Test for Case-Parent Trios

Por Fischer, S. Taylor, Jiang, Yunxuan, Broadaway, K. Alaine, Conneely, Karen N., Epstein, Michael P.
Publicado no Genet Epidemiol (2018)

A Permutation Procedure to Correct for Confounders in Case-Control Studies, Including Tests of Rare Variation

Por Epstein, Michael P., Duncan, Richard, Jiang, Yunxuan, Conneely, Karen N., Allen, Andrew S., Satten, Glen A.
Publicado em 2012

Intergenerational effects of endocrine-disrupting compounds: a review of the Michigan polybrominated biphenyl registry

Por Curtis, Sarah W, Conneely, Karen N, Marder, Mary E, Terrell, Metrecia L, Marcus, Michele, Smith, Alicia K
Publicado no Epigenomics (2018)

The Galanin Receptor 1 Gene Associates with Tobacco Craving in Smokers Seeking Cessation Treatment

Por Lori, Adriana, Tang, Yilang, O'Malley, Stephanie, Picciotto, Marina R, Wu, Ran, Conneely, Karen N, Cubells, Joseph F
Publicado em 2011

Age-associated DNA methylation in pediatric populations

Por Alisch, Reid S., Barwick, Benjamin G., Chopra, Pankaj, Myrick, Leila K., Satten, Glen A., Conneely, Karen N., Warren, Stephen T.
Publicado em 2012

ADCYAP1R1 Genotype Associates With Post-Traumatic Stress Symptoms in Highly Traumatized African-American Females

Por Almli, Lynn M., Mercer, Kristina B., Kerley, Kimberly, Feng, Hao, Bradley, Bekh, Conneely, Karen N., Ressler, Kerry J.
Publicado em 2013

Powerful Genetic Association Analysis for Common or Rare Variants with High-Dimensional Structured Traits

Por Zhan, Xiang, Zhao, Ni, Plantinga, Anna, Thornton, Timothy A., Conneely, Karen N., Epstein, Michael P., Wu, Michael C.
Publicado no Genetics (2017)

Kernel Approach for Modeling Interaction Effects in Genetic Association Studies of Complex Quantitative Traits

Por Broadaway, K. Alaine, Duncan, Richard, Conneely, Karen N., Almli, Lynn M., Bradley, Bekh, Ressler, Kerry J., Epstein, Michael P.
Publicado no Genet Epidemiol (2015)

Detection of differentially methylated regions from whole-genome bisulfite sequencing data without replicates

Por Wu, Hao, Xu, Tianlei, Feng, Hao, Chen, Li, Li, Ben, Yao, Bing, Qin, Zhaohui, Jin, Peng, Conneely, Karen N.
Publicado no Nucleic Acids Res (2015)