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

Por Zhang, Tian-Xiao, Beaty, Terri H., Ruczinski, Ingo
Publicado em 2012

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

Por Beaty, Terri H., Marazita, Mary L., Leslie, Elizabeth J.
Publicado no F1000Res (2016)

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

Por Duggal, Priya, Ladd-Acosta, Christine, Ray, Debashree, Beaty, Terri H
Publicado no Am J Epidemiol (2019)

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

Por Liang, Kung-Yee, Hsu, Fang-Chi, Beaty, Terri H., Barnes, Kathleen C.
Publicado em 2001

Cleft lip and palate: synthesizing genetic and environmental influences

Por Dixon, Michael J., Marazita, Mary L., Beaty, Terri H., Murray, Jeffrey C.
Publicado em 2011

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

Por Schwender, Holger, Taub, Margaret A., Beaty, Terri H., Marazita, Mary L., Ruczinski, Ingo
Publicado em 2011

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

Por Taub, Margaret A., Schwender, Holger, Beaty, Terri H., Louis, Thomas A., Ruczinski, Ingo
Publicado em 2012

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

Por Park, Beyoung Yun, Sull, Jae Woong, Park, Jung Yong, Jee, Sun Ha, Beaty, Terri H
Publicado em 2009

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

Por Neumann, Christoph, Taub, Margaret A., Younkin, Samuel G., Beaty, Terri H., Ruczinski, Ingo, Schwender, Holger
Publicado em 2014

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

Por Scharpf, Robert B, Beaty, Terri H, Schwender, Holger, Younkin, Samuel G, Scott, Alan F, Ruczinski, Ingo
Publicado em 2012

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

Por Ziyatdinov, Andrey, Parker, Margaret M., Vaysse, Amaury, Beaty, Terri H., Kraft, Peter, Cho, Michael H., Aschard, Hugues
Publicado no Eur J Hum Genet (2019)

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

Por Jung, Keum Ji, Won, Daeyoun, Jeon, Christina, Kim, Soriul, Kim, Tae Il, Jee, Sun Ha, Beaty, Terri H
Publicado no BMC Genet (2015)

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

Por Hayden, Lystra P., Cho, Michael H., Raby, Benjamin A., Beaty, Terri H., Silverman, Edwin K., Hersh, Craig P.
Publicado no Respir Res (2018)

Genotype Imputation Performance of Three Reference Panels Using African Ancestry Individuals

Por Vergara, Candelaria, Parker, Margaret M., Franco, Liliana, Cho, Michael H., Valencia-Duarte, Ana V., Beaty, Terri H., Duggal, Priya
Publicado no Hum Genet (2018)

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

Por Liu, Huan, Leslie, Elizabeth J., Carlson, Jenna C., Beaty, Terri H., Marazita, Mary L., Lidral, Andrew C., Cornell, Robert A.
Publicado no Nat Commun (2017)

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

Por Carlson, Jenna C., Taub, Margaret A., Feingold, Eleanor, Beaty, Terri H., Murray, Jeffrey C., Marazita, Mary L., Leslie, Elizabeth J.
Publicado no Birth Defects Res (2017)

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

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

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

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

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

Por Younkin, Samuel G, Scharpf, Robert B, Schwender, Holger, Parker, Margaret M, Scott, Alan F, Marazita, Mary L, Beaty, Terri H, Ruczinski, Ingo
Publicado no Birth Defects Res A Clin Mol Teratol (2015)

DSP variants may be associated with longitudinal change in quantitative emphysema

Por Kim, Woori, Cho, Michael H., Sakornsakolpat, Phuwanat, Lynch, David A., Coxson, Harvey O., Tal-Singer, Ruth, Silverman, Edwin K., Beaty, Terri H.
Publicado no Respir Res (2019)