Candidate Pathway Based Analysis for Cleft Lip with or without Cleft Palate

le Zhang, Tian-Xiao, Beaty, Terri H., Ruczinski, Ingo
Foilsithe 2012

Genetic factors influencing risk to orofacial clefts: today’s challenges and tomorrow’s opportunities

le Beaty, Terri H., Marazita, Mary L., Leslie, Elizabeth J.
Foilsithe in F1000Res (2016)

The Evolving Field of Genetic Epidemiology: From Familial Aggregation to Genomic Sequencing

le Duggal, Priya, Ladd-Acosta, Christine, Ray, Debashree, Beaty, Terri H
Foilsithe in Am J Epidemiol (2019)

Multipoint Linkage-Disequilibrium–Mapping Approach Based on the Case-Parent Trio Design

le Liang, Kung-Yee, Hsu, Fang-Chi, Beaty, Terri H., Barnes, Kathleen C.
Foilsithe 2001

Cleft lip and palate: synthesizing genetic and environmental influences

le Dixon, Michael J., Marazita, Mary L., Beaty, Terri H., Murray, Jeffrey C.
Foilsithe 2011

Rapid Testing of SNPs and Gene–Environment Interactions in Case–Parent Trio Data Based on Exact Analytic Parameter Estimation

le Schwender, Holger, Taub, Margaret A., Beaty, Terri H., Marazita, Mary L., Ruczinski, Ingo
Foilsithe 2011

Incorporating Genotype Uncertainties Into the Genotypic TDT for Main Effects and Gene-Environment Interactions

le Taub, Margaret A., Schwender, Holger, Beaty, Terri H., Louis, Thomas A., Ruczinski, Ingo
Foilsithe 2012

Differential Parental Transmission of Markers in BCL3 among Korean Cleft Case-parent Trios

le Park, Beyoung Yun, Sull, Jae Woong, Park, Jung Yong, Jee, Sun Ha, Beaty, Terri H
Foilsithe 2009

Analytic power and sample size calculation for the genotypic transmission/disequilibrium test in case-parent trio studies

le Neumann, Christoph, Taub, Margaret A., Younkin, Samuel G., Beaty, Terri H., Ruczinski, Ingo, Schwender, Holger
Foilsithe 2014

Fast detection of de novo copy number variants from SNP arrays for case-parent trios

le Scharpf, Robert B, Beaty, Terri H, Schwender, Holger, Younkin, Samuel G, Scott, Alan F, Ruczinski, Ingo
Foilsithe 2012

Mixed-model admixture mapping identifies smoking-dependent loci of lung function in African Americans

le Ziyatdinov, Andrey, Parker, Margaret M., Vaysse, Amaury, Beaty, Terri H., Kraft, Peter, Cho, Michael H., Aschard, Hugues
Foilsithe in Eur J Hum Genet (2019)

A colorectal cancer prediction model using traditional and genetic risk scores in Koreans

le Jung, Keum Ji, Won, Daeyoun, Jeon, Christina, Kim, Soriul, Kim, Tae Il, Jee, Sun Ha, Beaty, Terri H
Foilsithe in BMC Genet (2015)

Childhood asthma is associated with COPD and known asthma variants in COPDGene: a genome-wide association study

le Hayden, Lystra P., Cho, Michael H., Raby, Benjamin A., Beaty, Terri H., Silverman, Edwin K., Hersh, Craig P.
Foilsithe in Respir Res (2018)

Genotype Imputation Performance of Three Reference Panels Using African Ancestry Individuals

le Vergara, Candelaria, Parker, Margaret M., Franco, Liliana, Cho, Michael H., Valencia-Duarte, Ana V., Beaty, Terri H., Duggal, Priya
Foilsithe in Hum Genet (2018)

Identification of common non-coding variants at 1p22 that are functional for non-syndromic orofacial clefting

le Liu, Huan, Leslie, Elizabeth J., Carlson, Jenna C., Beaty, Terri H., Marazita, Mary L., Lidral, Andrew C., Cornell, Robert A.
Foilsithe in Nat Commun (2017)

Identifying genetic sources of phenotypic heterogeneity in orofacial clefts by targeted sequencing

le Carlson, Jenna C., Taub, Margaret A., Feingold, Eleanor, Beaty, Terri H., Murray, Jeffrey C., Marazita, Mary L., Leslie, Elizabeth J.
Foilsithe in Birth Defects Res (2017)

A genome-wide study of de novo deletions identifies a candidate locus for non-syndromic isolated cleft lip/palate risk

le Younkin, Samuel G, Scharpf, Robert B, Schwender, Holger, Parker, Margaret M, Scott, Alan F, Marazita, Mary L, Beaty, Terri H, Ruczinski, Ingo
Foilsithe 2014

Dectecting disease variants in case-parent trio studies using the Bioconductor software package trio

le Schwender, Holger, Li, Qing, Neumann, Christoph, Taub, Margaret A., Younkin, Samuel G., Berger, Philipp, Scharpf, Robert B., Beaty, Terri H., Ruczinski, Ingo
Foilsithe 2014

A genome-wide study of inherited deletions identified two regions associated with non-syndromic isolated oral clefts

le Younkin, Samuel G, Scharpf, Robert B, Schwender, Holger, Parker, Margaret M, Scott, Alan F, Marazita, Mary L, Beaty, Terri H, Ruczinski, Ingo
Foilsithe in Birth Defects Res A Clin Mol Teratol (2015)

DSP variants may be associated with longitudinal change in quantitative emphysema

le Kim, Woori, Cho, Michael H., Sakornsakolpat, Phuwanat, Lynch, David A., Coxson, Harvey O., Tal-Singer, Ruth, Silverman, Edwin K., Beaty, Terri H.
Foilsithe in Respir Res (2019)