Comparison of significance level at the true location using two linkage approaches: LODPAL and GENEFINDER

by Hsu, Fang-Chi, Hetmanski, Jacqueline B, Li, Lan, Markakis, Diane, Jacobs, Kevin, Shugart, Yin Yao
Published 2003

Genome-wide site-specific differential methylation in the blood of individuals with Klinefelter Syndrome

by Wan, Emily S., Qiu, Weiliang, Morrow, Jarrett, Beaty, Terri H., Hetmanski, Jacqueline, Make, Barry J., Lomas, David A., Silverman, Edwin K., DeMeo, Dawn L.
Published in Mol Reprod Dev (2015)

Evidence for SNP-SNP interaction identified through targeted sequencing of cleft case-parent trios

by Xiao, Yanzi, Taub, Margaret A., Ruczinski, Ingo, Begum, Ferdouse, Hetmanski, Jacqueline B., Schwender, Holger, Leslie, Elizabeth J., Koboldt, Daniel C., Murray, Jeffrey C., Marazita, Mary L., Beaty, Terri H.
Published in Genet Epidemiol (2016)

Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios

by Ray, Debashree, Venkataraghavan, Sowmya, Zhang, Wanying, Leslie, Elizabeth J., Hetmanski, Jacqueline B., Weinberg, Seth M., Murray, Jeffrey C., Marazita, Mary L., Ruczinski, Ingo, Taub, Margaret A., Beaty, Terri H.
Published in PLoS Genet (2021)

Hemizygous Deletion on Chromosome 3p26.1 Is Associated with Heavy Smoking among African American Subjects in the COPDGene Study

by Begum, Ferdouse, Ruczinski, Ingo, Hokanson, John E., Lutz, Sharon M., Parker, Margaret M., Cho, Michael H., Hetmanski, Jacqueline B., Scharpf, Robert B., Crapo, James D., Silverman, Edwin K., Beaty, Terri H.
Published in PLoS One (2016)

Detecting Gene-Environment Interaction for Maternal Exposures Using Case-Parent Trios Ascertained Through a Case With Non-Syndromic Orofacial Cleft

by Zhang, Wanying, Venkataraghavan, Sowmya, Hetmanski, Jacqueline B., Leslie, Elizabeth J., Marazita, Mary L., Feingold, Eleanor, Weinberg, Seth M., Ruczinski, Ingo, Taub, Margaret A., Scott, Alan F., Ray, Debashree, Beaty, Terri H.
Published in Front Cell Dev Biol (2021)

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

by Bureau, Alexandre, Begum, Ferdouse, Taub, Margaret A., Hetmanski, Jacqueline, Parker, Margaret M., Albacha-Hejazi, Hasan, Scott, Alan F., Murray, Jeffrey C., Marazita, Mary L., Bailey-Wilson, Joan E., Beaty, Terri H., Ruczinski, Ingo
Published in Genet Epidemiol (2018)

Novel evidence of association with NSCL/P was shown for SNPs in FOXF2 gene in an Asian population

by Bu, Lingxue, Chen, Qianqian, Wang, Hong, Zhang, Tianxiao, Hetmanski, Jacqueline B., Schwender, Holger, Parker, Margaret, Chou, Yah-Huei Wu, Yeow, Vincent, Chong, Samuel S., Zhang, Bo, Jabs, Ethylin Wang, Scott, Alan F., Beaty, Terri H.
Published in Birth Defects Res A Clin Mol Teratol (2015)

Joint Testing of Genotypic and Gene-Environment Interaction Identified Novel Association for BMP4 with Non-Syndromic CL/P in an Asian Population Using Data from an International Cl...

by Chen, Qianqian, Wang, Hong, Schwender, Holger, Zhang, Tianxiao, Hetmanski, Jacqueline B., Chou, Yah-Huei Wu, Ye, Xiaoqian, Yeow, Vincent, Chong, Samuel S., Zhang, Bo, Jabs, Ethylin Wang, Parker, Margaret M., Scott, Alan F., Beaty, Terri H.
Published 2014

Identifying a deletion affecting total lung capacity among subjects in the COPDGene study cohort

by Begum, Ferdouse, Ruczinski, Ingo, Li, Shengchao, Silverman, Edwin K., Cho, Michael H., Lynch, David A., Curran-Everett, Douglas, Crapo, James, Scharpf, Robert B., Parker, Margaret M., Hetmanski, Jacqueline B., Beatyon behalf of the COPDGene investigators, Terri H.
Published in Genet Epidemiol (2015)

Whole Exome Association of Rare Deletions in Multiplex Oral Cleft Families

by Fu, Jack, Beaty, Terri H., Scott, Alan F., Hetmanski, Jacqueline, Parker, Margaret M., Wilson, Joan E. Bailey, Marazita, Mary L., Mangold, Elisabeth, Albacha-Hejazi, Hasan, Murray, Jeffrey C., Bureau, Alexandre, Carey, Jacob, Cristiano, Stephen, Ruczinski, Ingo, Scharpf, Robert B.
Published in Genet Epidemiol (2016)

Evidence of gene–environment interaction for the IRF6 gene and maternal multivitamin supplementation in controlling the risk of cleft lip with/without cleft palate

by Wu, Tao, Liang, Kung Yee, Hetmanski, Jacqueline B., Ruczinski, Ingo, Fallin, Margaret Daniele, Ingersoll, Roxann G., Wang, Hong, Huang, Shangzhi, Ye, Xiaoqian, Wu-Chou, Yah-Huei, Chen, Philip K., Jabs, Ethylin W., Shi, Bing, Redett, Richard, Scott, Alan F., Beaty, Terri H.
Published 2010

ROR2 gene is associated with risk of non-syndromic cleft palate in an Asian population

by WANG, Hong, Hetmanski, Jacqueline B., Ruczinski, Ingo, Liang, Kung Yee, Fallin, M. Daniele, Redett, Richard J., Raymond, Gerald V., Wu Chou, Yah-Huei, Chen, Philip Kuo-Ting, Yeow, Vincent, Chong, Samuel S., Cheah, Felicia SH, Jabs, Ethylin Wang, Scott, Alan F., Beaty, Terri H.
Published 2012

Association between IRF6 and nonsyndromic cleft lip with or without cleft palate in four populations

by Park, Ji Wan, McIntosh, Iain, Hetmanski, Jacqueline B., Jabs, Ethylin Wang, Vander Kolk, Craig A., Wu-Chou, Yah-Huei, Chen, Philip K., Chong, Samuel S., Yeow, Vincent, Jee, Sun Ha, Park, Beyoung Yun, Fallin, M. Daniele, Ingersoll, Roxann, Scott, Alan F., Beaty, Terri H.
Published 2007

Maternal transmission effects of the PAX genes among cleft case–parent trios from four populations

by Sull, Jae Woong, Liang, Kung-Yee, Hetmanski, Jacqueline B, Fallin, Margaret Daniele, Ingersoll, Roxanne G, Park, Jiwan, Wu-Chou, Yah-Huei, Chen, Philip K, Chong, Samuel S, Cheah, Felicia, Yeow, Vincent, Park, Beyoung Yun, Jee, Sun Ha, Jabs, Ethylin W, Redett, Richard, Scott, Alan F, Beaty, Terri H
Published 2009

Excess Maternal Transmission of Markers in TCOF1 Among Cleft Palate Case-Parent Trios From Three Populations

by Sull, Jae Woong, Liang, Kung-Yee, Hetmanski, Jacqueline B., Fallin, M. Daniele, Ingersoll, Roxanne G., Park, Ji Wan, Wu-Chou, Yah-Huei, Chen, Philip K., Chong, Samuel S., Cheah, Felicia, Yeow, Vincent, Park, Beyoung Yun, Jee, Sun Ha, Jabs, Ethylin W., Redett, Richard, Scott, Alan F., Beaty, Terri H.
Published 2008

BMP4 Was Associated with NSCL/P in an Asian Population

by Chen, Qianqian, Wang, Hong, Hetmanski, Jacqueline B., Zhang, Tianxiao, Ruczinski, Ingo, Schwender, Holger, Liang, Kung Yee, Fallin, M. Daniele, Redett, Richard J., Raymond, Gerald V., Wu Chou, Yah-Huei, Chen, Philip Kuo-Ting, Yeow, Vincent, Chong, Samuel S., Cheah, Felicia S. H., Jabs, Ethylin Wang, Scott, Alan F., Beaty, Terri H.
Published 2012

Analysis of sequence data to identify potential risk variants for oral clefts in multiplex families

by Holzinger, Emily R., Li, Qing, Parker, Margaret M., Hetmanski, Jacqueline B., Marazita, Mary L., Mangold, Elisabeth, Ludwig, Kerstin U., Taub, Margaret A., Begum, Ferdouse, Murray, Jeffrey C., Albacha‐Hejazi, Hasan, Alqosayer, Khalid, Al‐Souki, Giath, Albasha Hejazi, Abdullatiff, Scott, Alan F., Beaty, Terri H., Bailey‐Wilson, Joan E.
Published in Mol Genet Genomic Med (2017)

Whole genome sequencing of orofacial cleft trios from the Gabriella Miller Kids First Pediatric Research Consortium identifies a new locus on chromosome 21

by Mukhopadhyay, Nandita, Bishop, Madison, Mortillo, Michael, Chopra, Pankaj, Hetmanski, Jacqueline B., Taub, Margaret A., Moreno, Lina M., Valencia-Ramirez, Luz Consuelo, Restrepo, Claudia, Wehby, George L., Hecht, Jacqueline T., Deleyiannis, Frederic, Butali, Azeez, Weinberg, Seth M., Beaty, Terri H., Murray, Jeffrey C., Leslie, Elizabeth J., Feingold, Eleanor, Marazita, Mary L.
Published in Hum Genet (2019)

Differential Parental Transmission of Markers in RUNX2 Among Cleft Case-Parent Trios From Four Populations

by Sull, Jae Woong, Liang, Kung-Yee, Hetmanski, Jacqueline B., Fallin, Margaret Daniele, Ingersoll, Roxann G., Park, Jiwan, Wu-Chou, Yah-Huei, Chen, Philip K., Chong, Samuel S., Cheah, Felicia, Yeow, Vincent, Park, Beyoung Yun, Jee, Sun Ha, Jabs, Ethylin Wang, Redett, Richard, Jung, Euiju, Ruczinski, Ingo, Scott, Alan F., Beaty, Terri H.
Published 2008