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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Cleft lip and palate: understanding genetic and environmental influences von Murray, Jeffrey C, Dixon, Michael J, Marazita, Mary L, 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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Genetics of Nonsyndromic Orofacial Clefts von Rahimov, Fedik, Jugessur, Astanand, Murray, Jeffrey C.

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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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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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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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Academic performance in adolescence after inguinal hernia repair in infancy: a nationwide cohort study von Hansen, Tom G, Pedersen, Jacob K, Henneberg, Steen W, Pedersen, Dorthe A, Murray, Jeffrey C, Morton, Neil S, Christensen, Kaare

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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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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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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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Ibalizumab in Multidrug-Resistant HIV — Accepting Uncertainty von Sheikh, Virginia, Murray, Jeffrey S, Sherwat, Adam

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Hyperglycemia as a risk factor for the development of retinopathy of prematurity von Mohamed, Shakir, Murray, Jeffrey C, Dagle, John M, Colaizy, Tarah

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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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Challenges to the study of gender dysphoria von Stevenson, David K., Murray, Jeffrey C., Muglia, Louis J., Wong, Ronald J., Katz, Michael

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Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysis von Haataja, Ritva, Karjalainen, Minna K, Luukkonen, Aino, Teramo, Kari, Puttonen, Hilkka, Ojaniemi, Marja, Varilo, Teppo, Chaudhari, Bimal P, Plunkett, Jevon, Murray, Jeffrey C, McCarroll, Steven A, Peltonen, Leena, Muglia, Louis J, Palotie, Aarno, Hallman, Mikko

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Polymorphisms of CYP51A1 from cholesterol synthesis: associations with birth weight and maternal lipid levels and impact on CYP51 protein structure von Lewińska, Monika, Zelenko, Urska, Merzel, Franci, Golic Grdadolnik, Simona, Murray, Jeffrey C, Rozman, Damjana

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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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