A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis by Justice, CM, Cuellar, A, Bala, K, Sabourin, JA, Cunningham, ML, Crawford, K, Phipps, JM, Zhou, Y, Cilliers, D, Byren, JC, Johnson, D, Wall, SA, Morton, JEV, Noons, P, Sweeney, E, Weber, A, Rees, KEM, Wilson, LC, Simeonov, E, Kaneva, R, Yaneva, N, Georgiev, K, Bussarsky, A, Senders, C, Zwienenberg, M, Boggan, J, Roscioli, T, Tamburrini, G, Barba, M, Conway, K, Sheffield, VC, Brody, L, Mills, JL, Kay, D, Sicko, RJ, Langlois, PH, Tittle, RK, Botto, LD, Jenkins, MM, LaSalle, JM, Lattanzi, W, Wilkie, AOM, Wilson, AF, Romitti, PA, Boyadjiev, SA, National Birth Defects Prevention Study

Regulatory elements in SEM1–DLX5–DLX6 (7q21.3) locus contribute to genetic control of coronal nonsyndromic craniosynostosis and bone density-related traits by Nicoletti, P, Zafer, S, Matok, L, Irron, I, Patrick, M, Haklai, R, Evangelista, JE, Marino, GB, Ma'ayan, A, Sewda, A, Holmes, G, Britton, SR, Lee, WJ, Wu, M, Ru, Y, Arnaud, E, Botto, L, Brody, LC, Byren, JC, Caggana, M, Carmichael, S, Cilliers, D, Conway, K, Crawford, K, Cuellar, A, Di Rocco, F, Engel, M, Fearon, J, Feldkamp, ML, Finnell, R, Fisher, S, Freudlsperger, C, Garcia-Fructuoso, G, Hagge, R, Heuzé, Y, Harshbarger, RJ, Hobbs, C, Howley, M, Jenkins, MM, Johnson, D, Justice, CM, Kane, A, Kay, D, Gosain, AK, Langlois, P, Legal-Mallet, L, Lin, AE, Mills, JL, Morton, JEV, Noons, P, Phipps, J, Wilkie, AOM