Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate von Beaty, Terri H., Ruczinski, Ingo, Murray, Jeffrey C., Marazita, Mary L., Munger, Ronald G., Hetmanski, Jacqueline B., Murray, Tanda, Redett, Richard J., Fallin, M. Daniele, Liang, Kung Yee, Wu, Tao, Patel, Poorav J., Jin, Sheng-Chih, Zhang, Tian Xiao, Schwender, Holger, Wu-Chou, Yah Huei, Chen, Philip K., Chong, Samuel S., Cheah, Felicia, Yeow, Vincent, Ye, Xiaoqian, Wang, Hong, Huang, Shangzhi, Jabs, Ethylin W., Shi, Bing, Wilcox, Allen J., Lie, Rolv T., Jee, Sun Ha, Christensen, Kaare, Doheny, Kimberley F., Pugh, Elizabeth W., Ling, Hua, Scott, Alan F.

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Between-Hospital Variation in Treatment and Outcomes in Extremely Preterm Infants von Rysavy, Matthew A, Li, Lei, Bell, Edward F, Das, Abhik, Hintz, Susan R, Stoll, Barbara J, Vohr, Betty R, Carlo, Waldemar A, Shankaran, Seetha, Walsh, Michele C, Tyson, Jon E, Cotten, C. Michael, Smith, P. Brian, Murray, Jeffrey C, Colaizy, Tarah T, Brumbaugh, Jane E, Higgins, Rosemary D

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Genetics of Nonsyndromic Orofacial Clefts von Rahimov, Fedik, Jugessur, Astanand, Murray, Jeffrey C.

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Dominant Mutations in GRHL3 Cause Van der Woude Syndrome and Disrupt Oral Periderm Development von Peyrard-Janvid, Myriam, Leslie, Elizabeth J., Kousa, Youssef A., Smith, Tiffany L., Dunnwald, Martine, Magnusson, Måns, Lentz, Brian A., Unneberg, Per, Fransson, Ingegerd, Koillinen, Hannele K., Rautio, Jorma, Pegelow, Marie, Karsten, Agneta, Basel-Vanagaite, Lina, Gordon, William, Andersen, Bogi, Svensson, Thomas, Murray, Jeffrey C., Cornell, Robert A., Kere, Juha, Schutte, Brian C.

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Late-Onset Sepsis in Very Low Birth Weight Infants from Singleton and Multiple-Gestation Births von Boghossian, Nansi S., PhD, MPH, Page, Grier P., PhD, Bell, Edward F., MD, Stoll, Barbara J., MD, Murray, Jeffrey C., MD, Cotten, C. Michael, MD, MHS, Shankaran, Seetha, MD, Walsh, Michele C., MD, MS, Laptook, Abbot R., MD, Newman, Nancy S., RN, Hale, Ellen C., RN, BS, CCRC, McDonald, Scott A., BS, Das, Abhik, PhD, Higgins, Rosemary D., MD

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

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Dissecting maternal and fetal genetic effects underlying the associations between maternal phenotypes, birth outcomes, and adult phenotypes: A mendelian-randomization and haplotype... von Chen, Jing, Bacelis, Jonas, Sole-Navais, Pol, Srivastava, Amit, Juodakis, Julius, Rouse, Amy, Hallman, Mikko, Teramo, Kari, Melbye, Mads, Feenstra, Bjarke, Freathy, Rachel M, Smith, George Davey, Lawlor, Deborah A, Murray, Jeffrey C, Williams, Scott M, Jacobsson, Bo, Muglia, Louis J, Zhang, Ge

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Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology von Shaffer, John R, Orlova, Ekaterina, Lee, Myoung Keun, Leslie, Elizabeth J, Raffensperger, Zachary D, Heike, Carrie L, Cunningham, Michael L, Hecht, Jacqueline T, Kau, Chung How, Nidey, Nichole L, Moreno, Lina M, Wehby, George L, Murray, Jeffrey C, Laurie, Cecelia A, Laurie, Cathy C, Cole, Joanne, Ferrara, Tracey, Santorico, Stephanie, Klein, Ophir, Mio, Washington, Feingold, Eleanor, Hallgrimsson, Benedikt, Spritz, Richard A, Marazita, Mary L, Weinberg, Seth M

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Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios von Bishop, Madison R., Diaz Perez, Kimberly K., Sun, Miranda, Ho, Samantha, Chopra, Pankaj, Mukhopadhyay, Nandita, Hetmanski, Jacqueline B., Taub, Margaret A., Moreno-Uribe, Lina M., Valencia-Ramirez, Luz Consuelo, Restrepo Muñeton, Claudia P., Wehby, George, Hecht, Jacqueline T., Deleyiannis, Frederic, Weinberg, Seth M., Wu-Chou, Yah Huei, Chen, Philip K., Brand, Harrison, Epstein, Michael P., Ruczinski, Ingo, Murray, Jeffrey C., Beaty, Terri H., Feingold, Eleanor, Lipinski, Robert J., Cutler, David J., Marazita, Mary L., Leslie, Elizabeth J.

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Identification of Functional Variants for Cleft Lip with or without Cleft Palate in or near PAX7, FGFR2, and NOG by Targeted Sequencing of GWAS Loci von Leslie, Elizabeth J., Taub, Margaret A., Liu, Huan, Steinberg, Karyn Meltz, Koboldt, Daniel C., Zhang, Qunyuan, Carlson, Jenna C., Hetmanski, Jacqueline B., Wang, Hang, Larson, David E., Fulton, Robert S., Kousa, Youssef A., Fakhouri, Walid D., Naji, Ali, Ruczinski, Ingo, Begum, Ferdouse, Parker, Margaret M., Busch, Tamara, Standley, Jennifer, Rigdon, Jennifer, Hecht, Jacqueline T., Scott, Alan F., Wehby, George L., Christensen, Kaare, Czeizel, Andrew E., Deleyiannis, Frederic W.-B., Schutte, Brian C., Wilson, Richard K., Cornell, Robert A., Lidral, Andrew C., Weinstock, George M., Beaty, Terri H., Marazita, Mary L., Murray, Jeffrey C.

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Transcriptome landscape of the human placenta von Kim, Jinsil, Zhao, Keyan, Jiang, Peng, Lu, Zhi-xiang, Wang, Jinkai, Murray, Jeffrey C, Xing, Yi

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Psychiatric Diagnoses in Individuals with Non-Syndromic Oral Clefts: A Danish Population-Based Cohort Study von Pedersen, Dorthe Almind, Wehby, George L, Murray, Jeffrey C, Christensen, Kaare

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Integrated Genomic Analyses in Bronchopulmonary Dysplasia von Ambalavanan, Namasivayam, MD, Cotten, C. Michael, MD, Page, Grier P., PhD, Carlo, Waldemar A., MD, Murray, Jeffrey C., MD, Bhattacharya, Soumyaroop, MS, MEd, Mariani, Thomas J., PhD, Cuna, Alain C., MD, Faye-Petersen, Ona M., MD, Kelly, David, MD, Higgins, Rosemary D., MD

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Disruption of an AP-2α binding site in an IRF6 enhancer is associated with cleft lip von Rahimov, Fedik, Marazita, Mary L, Visel, Axel, Cooper, Margaret E, Hitchler, Michael J, Rubini, Michele, Domann, Frederick E, Govil, Manika, Christensen, Kaare, Bille, Camille, Melbye, Mads, Jugessur, Astanand, Lie, Rolv T, Wilcox, Allen J, Fitzpatrick, David R, Green, Eric D, Mossey, Peter A, Little, Julian, Steegers-Theunissen, Regine P, Pennacchio, Len A, Schutte, Brian C, Murray, Jeffrey C

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Using an aquatic model, Xenopus laevis, to uncover the role of chromodomain 1 in craniofacial disorders von Wyatt, Brent H., Raymond, Thomas O., Lansdon, Lisa A., Darbro, Benjamin W., Murray, Jeffrey C., Manak, John Robert, Dickinson, Amanda J. G.

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The 3D Facial Norms Database: Part 1. A Web-Based Craniofacial Anthropometric and Image Repository for the Clinical and Research Community von Weinberg, Seth M., Raffensperger, Zachary D., Kesterke, Matthew J., Heike, Carrie L., Cunningham, Michael L., Hecht, Jacqueline T., Kau, Chung How, Murray, Jeffrey C., Wehby, George L., Moreno, Lina M., Marazita, Mary L.

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Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 ( Irf6 ) von Schutte, Brian C, Ingraham, Christopher R, Kinoshita, Akira, Kondo, Shinji, Yang, Baoli, Sajan, Samin, Trout, Kurt J, Malik, Margaret I, Dunnwald, Martine, Goudy, Stephen L, Lovett, Michael, Murray, Jeffrey C

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Integrative genetic, genomic and transcriptomic analysis of heat shock protein and nuclear hormone receptor gene associations with spontaneous preterm birth von Huusko, Johanna M., Tiensuu, Heli, Haapalainen, Antti M., Pasanen, Anu, Tissarinen, Pinja, Karjalainen, Minna K., Zhang, Ge, Christensen, Kaare, Ryckman, Kelli K., Jacobsson, Bo, Murray, Jeffrey C., Kingsmore, Stephen F., Hallman, Mikko, Muglia, Louis J., Rämet, Mika

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Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome von O'Sullivan, James, Bitu, Carolina C., Daly, Sarah B., Urquhart, Jill E., Barron, Martin J., Bhaskar, Sanjeev S., Martelli-Júnior, Hercilio, dos Santos Neto, Pedro Eleuterio, Mansilla, Maria A., Murray, Jeffrey C., Coletta, Ricardo D., Black, Graeme C.M., Dixon, Michael J.

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Genome-wide association studies in dogs and humans identify ADAMTS20 as a risk variant for cleft lip and palate von Wolf, Zena T, Brand, Harrison A, Shaffer, John R, Leslie, Elizabeth J, Arzi, Boaz, Willet, Cali E, Cox, Timothy C, McHenry, Toby, Narayan, Nicole, Feingold, Eleanor, Wang, Xioajing, Sliskovic, Saundra, Karmi, Nili, Safra, Noa, Sanchez, Carla, Deleyiannis, Frederic W B, Murray, Jeffrey C, Wade, Claire M, Marazita, Mary L, Bannasch, Danika L

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