Integrating common and rare genetic variation in diverse human populations. by Altshuler, D, Gibbs, R, Peltonen, L, Altshuler, D, Gibbs, R, Peltonen, L, Dermitzakis, E, Schaffner, S, Yu, F, Peltonen, L, Dermitzakis, E, Bonnen, P, Altshuler, D, Gibbs, R, de Bakker, P, Deloukas, P, Gabriel, S, Gwilliam, R, Hunt, S, Inouye, M, Jia, X, Palotie, A, Parkin, M, Whittaker, P, Yu, F, Chang, K, Hawes, A, Lewis, L, Ren, Y, Wheeler, D, Gibbs, R, Muzny, D, Barnes, C, Darvishi, K, Hurles, M, Korn, J, Kristiansson, K, Lee, C, McCarrol, SA, Nemesh, J, Dermitzakis, E, Keinan, A, Montgomery, S, Pollack, S, Price, A, Soranzo, N, Bonnen, P, Gibbs, R, Gonzaga-Jauregui, C, Keinan, A, Price, A, Yu, F, Anttila, V, Brodeur, W, Daly, M, Leslie, S, McVean, G, Moutsianas, L, Nguyen, H, Schaffner, S, Zhang, Q, Ghori, M, McGinnis, R, McLaren, W, Pollack, S, Price, A, Schaffner, S, Takeuchi, F, Grossman, SR, Shlyakhter, I, Hostetter, E, Sabeti, P, Adebamowo, C, Foster, M, Gordon, DR, Licinio, J, Manca, M, Marshall, P, Matsuda, I, Ngare, D, Wang, V, Reddy, D, Rotimi, C, Royal, C, Sharp, R, Zeng, C, Brooks, L, McEwen, J

TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities by Wiszniewski, W, Hunter, J, Hanchard, N, Willer, JR, Shaw, C, Tian, Q, Illner, A, Wang, X, Cheung, S, Patel, A, Campbell, I, Gelowani, V, Hixson, P, Ester, A, Azamian, MS, Potocki, L, Zapata, G, Hernandez, P, Ramocki, M, Santos-Cortez, R, Wang, G, York, M, Justice, M, Chu, Z, Bader, P, Omo-Griffith, L, Madduri, N, Scharer, G, Crawford, H, Yanatatsaneejit, P, Eifert, A, Kerr, J, Bacino, C, Franklin, A, Goin-Kochel, R, Simpson, G, Immken, L, Haque, M, Stosic, M, Williams, MD, Morgan, T, Pruthi, S, Omary, R, Boyadjiev, SA, Win, K, Thida, A, Hurles, M, Hibberd, M, Khor, C, Van Vinh Chau, N, Gallagher, T, Mutirangura, A, Stankiewicz, P, Beaudet, A, Maletic-Savatic, M, Rosenfeld, J, Shaffer, L, Davis, E, Belmont, J, Dunstan, S, Simmons, C, Bonnen, P, Leal, S, Katsanis, N, Lupski, JR, Lalani, SR

TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities. by Wiszniewski, W, Hunter, J, Hanchard, N, Willer, JR, Shaw, C, Tian, Q, Illner, A, Wang, X, Cheung, S, Patel, A, Campbell, I, Gelowani, V, Hixson, P, Ester, A, Azamian, MS, Potocki, L, Zapata, G, Hernandez, P, Ramocki, M, Santos-Cortez, R, Wang, G, York, M, Justice, M, Chu, Z, Bader, P, Omo-Griffith, L, Madduri, N, Scharer, G, Crawford, H, Yanatatsaneejit, P, Eifert, A, Kerr, J, Bacino, C, Franklin, A, Goin-Kochel, R, Simpson, G, Immken, L, Haque, M, Stosic, M, Williams, MD, Morgan, T, Pruthi, S, Omary, R, Boyadjiev, SA, Win, K, Thida, A, Hurles, M, Hibberd, M, Khor, C, Van Vinh Chau, N, Gallagher, T, Mutirangura, A, Stankiewicz, P, Beaudet, A, Maletic-Savatic, M, Rosenfeld, J, Shaffer, L, Davis, E, Belmont, J, Dunstan, S, Simmons, C, Bonnen, P, Leal, S, Katsanis, N, Lupski, JR, Lalani, SR

TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities by Wiszniewski, W, Hunter, J, Hanchard, N, Willer, J, Shaw, C, Tian, Q, Illner, A, Wang, X, Cheung, S, Patel, A, Campbell, I, Gelowani, V, Hixson, P, Ester, A, Azamian, M, Potocki, L, Zapata, G, Hernandez, P, Ramocki, M, Santos-Cortez, R, Wang, G, York, M, Justice, M, Chu, Z, Bader, P, Omo-Griffith, L, Madduri, N, Scharer, G, Crawford, H, Yanatatsaneejit, P, Eifert, A, Kerr, J, Bacino, C, Franklin, A, Goin-Kochel, R, Simpson, G, Immken, L, Haque, M, Stosic, M, Williams, M, Morgan, T, Pruthi, S, Omary, R, Boyadjiev, S, Win, K, Thida, A, Hurles, M, Hibberd, M, Khor, C, Van Vinh Chau, N, Gallagher, T, Mutirangura, A, Stankiewicz, P, Beaudet, A, Maletic-Savatic, M, Rosenfeld, J, Shaffer, L, Davis, E, Belmont, J, Dunstan, S, Simmons, C, Bonnen, P, Leal, S, Katsanis, N, Lupski, J, Lalani, S